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Record Information
Version5.0
StatusDetected and Quantified
Creation Date2005-11-16 15:48:42 UTC
Update Date2021-09-14 15:37:02 UTC
HMDB IDHMDB0000569
Secondary Accession Numbers
  • HMDB00569
Metabolite Identification
Common NameDeoxypyridinoline
DescriptionDeoxypyridinoline (DPD) is a breakdown product of type I fibrillar collagen, it occurs mainly in Type I collagen of bone. DPD shows a high specificity for bone, and the measurement of urinary DPD is not influenced by newly collagens and dietary intake. DPD cross-links of type 1 collagen are excreted in urine either as free or peptide-bound moieties. It is the peptide-bound cross-links that decrease by the greatest amount in response to bisphosphonate therapy. DPD is one of the most extensively characterized biochemical bone markers, but the interpretation of results is hampered by biologic and other preanalytical variability. Biochemical bone markers can provide a valuable tool in the management of metabolic bone diseases. Their most recognized application in clinical practice is for monitoring treatment for osteoporosis as an adjunct to bone mineral density measurements. Other applications that have been investigated include their use as a diagnostic tool for bone diseases other than osteoporosis and as predictive markers for bone loss and the risk of bone fracture. DPD measured in urine follow a circadian or diurnal cycle with a peak in the early morning and nadir in the late afternoon to early evening. The magnitude of the diurnal change, i.e., nadir concentration divided by peak concentration, expressed as a percentage is around 70% (range, 53-75%). (PMID: 11805003 , 17229003 , 16751696 ).
Structure
Data?1582752140
Synonyms
ValueSource
4-(2-Amino-2-carboxyethyl)-1-(5-amino-5-carboxypentyl)-3-(3-amino-3-carboxypropyl)-5-hydroxy-pyridinium inner salt stereoisomerHMDB
DeoxipyridinolineHMDB
Deoxy-pyridinolineHMDB
DeoxypiridinolineHMDB
DeoxypirydynolineHMDB
DeoxypyridinoloneHMDB
DeoxypyridolineHMDB
DesoxypyridinolineHMDB
LysylpyridinolineHMDB
N-(5-Amino-5-carboxypentyl)-3-hydroxy-4-(2-amino-2-carboxyethyl)-5-(3-amino-3-carboxypropyl)pyridineHMDB
Chemical FormulaC18H28N4O7
Average Molecular Weight412.4375
Monoisotopic Molecular Weight412.19579927
IUPAC Name4-[(2S)-2-amino-2-carboxyethyl]-3-[(3S)-3-amino-3-carboxypropyl]-1-[(5S)-5-amino-5-carboxypentyl]-5-hydroxypyridin-1-ium
Traditional Name4-[(2S)-2-amino-2-carboxyethyl]-3-[(3S)-3-amino-3-carboxypropyl]-1-[(5S)-5-amino-5-carboxypentyl]-5-hydroxypyridin-1-ium
CAS Registry Number83462-55-9
SMILES
N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C([O-])=O)=C(C[C@H](N)C(O)=O)C(O)=C1)C(O)=O
InChI Identifier
InChI=1S/C18H28N4O7/c19-12(16(24)25)3-1-2-6-22-8-10(4-5-13(20)17(26)27)11(15(23)9-22)7-14(21)18(28)29/h8-9,12-14H,1-7,19-21H2,(H3-,23,24,25,26,27,28,29)/t12-,13-,14-/m0/s1
InChI KeyZAHDXEIQWWLQQL-IHRRRGAJSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentL-alpha-amino acids
Alternative Parents
Substituents
  • L-alpha-amino acid
  • Tricarboxylic acid or derivatives
  • Pyridinolate
  • Aralkylamine
  • Pyridine
  • Pyridinium
  • Heteroaromatic compound
  • Amino acid
  • Carboxylic acid
  • Organoheterocyclic compound
  • Azacycle
  • Organic zwitterion
  • Organopnictogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Primary aliphatic amine
  • Amine
  • Organic oxide
  • Carbonyl group
  • Hydrocarbon derivative
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.15 g/LALOGPS
logP-4.1ALOGPS
logP-12ChemAxon
logS-3.5ALOGPS
pKa (Strongest Acidic)0.83ChemAxon
pKa (Strongest Basic)9.9ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count10ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area216.9 ŲChemAxon
Rotatable Bond Count13ChemAxon
Refractivity113.48 m³·mol⁻¹ChemAxon
Polarizability42.08 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
AllCCS[M+H]+192.07632859911
AllCCS[M-H]-191.6432859911
DeepCCS[M+H]+191.66730932474
DeepCCS[M-H]-189.27130932474
DeepCCS[M-2H]-222.15430932474
DeepCCS[M+Na]+197.5830932474
AllCCS[M+H]+192.132859911
AllCCS[M+H-H2O]+189.932859911
AllCCS[M+NH4]+194.132859911
AllCCS[M+Na]+194.632859911
AllCCS[M-H]-191.632859911
AllCCS[M+Na-2H]-191.232859911
AllCCS[M+HCOO]-190.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
DeoxypyridinolineN[C@@H](CCCC[N+]1=CC(CC[C@H](N)C([O-])=O)=C(C[C@H](N)C(O)=O)C(O)=C1)C(O)=O5132.4Standard polar33892256
DeoxypyridinolineN[C@@H](CCCC[N+]1=CC(CC[C@H](N)C([O-])=O)=C(C[C@H](N)C(O)=O)C(O)=C1)C(O)=O3495.8Standard non polar33892256
DeoxypyridinolineN[C@@H](CCCC[N+]1=CC(CC[C@H](N)C([O-])=O)=C(C[C@H](N)C(O)=O)C(O)=C1)C(O)=O3901.3Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Deoxypyridinoline,1TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-]3613.5Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #2C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O3673.8Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C13599.2Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #4C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3729.9Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #5C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3734.8Semi standard non polar33892256
Deoxypyridinoline,1TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3724.9Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C3555.1Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3554.9Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #11C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3563.0Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #12C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3553.8Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #13C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3693.5Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3700.4Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #15C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C3829.8Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3697.6Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #17C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C3876.8Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #18C[Si](C)(C)N([C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O)[Si](C)(C)C3831.7Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #2C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13470.7Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3556.1Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #4C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3574.3Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #5C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3565.0Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C13537.1Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #7C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3649.9Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #8C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3651.6Semi standard non polar33892256
Deoxypyridinoline,2TMS,isomer #9C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O3652.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C13473.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3689.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3573.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]3696.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3722.9Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3528.3Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3529.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #16C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3549.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #17C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3662.5Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3656.7Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #19C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O3762.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #2C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3538.7Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3658.9Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #21C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O3799.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #22C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3767.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3571.1Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3560.5Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3693.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3568.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13688.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13712.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3713.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3536.7Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #30C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3788.5Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #31C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3795.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3846.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3790.2Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3844.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3792.3Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #4C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3551.9Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3457.8Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3453.6Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3461.4Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3571.3Semi standard non polar33892256
Deoxypyridinoline,3TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3556.1Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #1C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3476.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #1C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3516.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #1C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C5406.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3479.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3663.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #10C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C5025.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3487.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3635.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #11C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4877.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]3610.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]3674.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #12C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-]5452.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3482.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3648.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4964.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #14C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13605.2Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #14C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13692.8Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #14C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C15526.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13617.1Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13636.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #15C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C15392.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3617.2Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3731.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4668.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #17C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3685.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #17C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3757.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #17C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C5108.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3693.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3760.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #18C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O5144.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3721.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3732.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C5170.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3478.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3492.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #2C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]5379.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3689.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3754.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]5194.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3735.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3709.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4972.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3694.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3729.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4960.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3563.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3600.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5047.8Standard polar33892256
Deoxypyridinoline,4TMS,isomer #24C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3574.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #24C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3636.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #24C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O5065.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3671.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3650.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C5566.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3582.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3613.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #26C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]5008.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C13693.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C13603.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #27C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C15508.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13672.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13654.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C15507.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3711.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3711.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4740.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3478.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3527.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #3C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C5470.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3802.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3690.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O5138.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3752.7Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3712.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5127.6Standard polar33892256
Deoxypyridinoline,4TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3747.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3738.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O5149.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #33C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3754.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #33C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3743.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #33C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O5148.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O3800.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O3705.0Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #34C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O5210.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3754.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3731.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]5198.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3616.7Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3732.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4651.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #37C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3691.9Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #37C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3763.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #37C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C5102.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #38C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3686.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #38C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3754.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #38C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O5138.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #39C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3725.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #39C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3715.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #39C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C5088.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3560.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3618.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]5118.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #40C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3688.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #40C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]3732.3Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #40C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]5113.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #41C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3721.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #41C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3721.8Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #41C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O5053.4Standard polar33892256
Deoxypyridinoline,4TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3686.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3746.7Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]5040.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #43C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3862.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #43C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3773.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #43C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4801.8Standard polar33892256
Deoxypyridinoline,4TMS,isomer #44C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3796.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #44C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3802.4Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #44C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4796.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #45C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3802.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #45C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3806.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #45C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4797.3Standard polar33892256
Deoxypyridinoline,4TMS,isomer #46C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C3880.5Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #46C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C3860.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #46C[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C5200.7Standard polar33892256
Deoxypyridinoline,4TMS,isomer #47C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C3953.8Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #47C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C3813.9Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #47C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C5186.0Standard polar33892256
Deoxypyridinoline,4TMS,isomer #48C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C3958.4Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #48C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C3827.2Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #48C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C5265.5Standard polar33892256
Deoxypyridinoline,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3575.2Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3634.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O5066.9Standard polar33892256
Deoxypyridinoline,4TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3671.0Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3669.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #6C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C5629.1Standard polar33892256
Deoxypyridinoline,4TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3587.3Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3599.1Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4931.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C3697.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C3604.6Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #8C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C5504.2Standard polar33892256
Deoxypyridinoline,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3677.6Semi standard non polar33892256
Deoxypyridinoline,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3637.5Standard non polar33892256
Deoxypyridinoline,4TMS,isomer #9C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C5438.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3519.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3600.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4669.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #10C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3678.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #10C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3724.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #10C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4880.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #11C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3697.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #11C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3727.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #11C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4912.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3726.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3671.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #12C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4754.5Standard polar33892256
Deoxypyridinoline,5TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3683.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3695.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #13C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4744.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3542.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3749.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #14C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4312.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #15C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3639.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #15C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C3754.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #15C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C4858.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #16C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3633.5Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #16C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C3760.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #16C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C4859.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #17C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3652.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #17C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3707.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #17C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4690.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #18C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3632.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #18C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3724.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #18C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4709.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3647.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3720.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #19C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C4772.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3515.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3630.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4800.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3624.8Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3743.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #20C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4793.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3771.5Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3798.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4461.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3729.8Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3821.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4463.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3735.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3818.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #23C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4492.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3842.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3863.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #24C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C4943.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3895.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3837.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #25C[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4992.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3882.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3806.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #26C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C4781.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #27C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3639.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #27C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3720.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #27C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4402.8Standard polar33892256
Deoxypyridinoline,5TMS,isomer #28C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3717.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #28C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3673.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #28C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4863.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3696.4Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]3692.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #29C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4882.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3644.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3625.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #3C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C5258.7Standard polar33892256
Deoxypyridinoline,5TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3678.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3729.7Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4880.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #31C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3689.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #31C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3722.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #31C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4909.5Standard polar33892256
Deoxypyridinoline,5TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3711.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3683.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #32C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4827.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3673.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3710.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #33C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4818.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #34C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3842.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #34C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O3768.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #34C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O)C(O[Si](C)(C)C)=C1)C(=O)O4538.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3780.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3795.0Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #35C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4539.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3787.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3798.2Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #36C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4540.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #37C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O3932.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #37C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O3783.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #37C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@H](N)C(=O)O4944.7Standard polar33892256
Deoxypyridinoline,5TMS,isomer #38C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3867.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #38C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3837.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #38C[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C4960.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #39C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3946.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #39C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C3801.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #39C[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C5008.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3518.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3611.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #4C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4741.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #40C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3773.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #40C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3798.4Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #40C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O4443.3Standard polar33892256
Deoxypyridinoline,5TMS,isomer #41C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3727.9Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #41C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3811.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #41C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4474.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3726.6Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3826.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #42C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4446.1Standard polar33892256
Deoxypyridinoline,5TMS,isomer #43C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3835.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #43C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3861.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #43C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C4937.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #44C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3885.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #44C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3813.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #44C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C4917.8Standard polar33892256
Deoxypyridinoline,5TMS,isomer #45C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13880.0Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #45C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13826.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #45C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C14857.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #46C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3980.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #46C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3879.6Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #46C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O4592.2Standard polar33892256
Deoxypyridinoline,5TMS,isomer #47C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3985.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #47C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3885.5Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #47C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4592.7Standard polar33892256
Deoxypyridinoline,5TMS,isomer #48C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3919.8Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #48C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3910.9Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #48C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4590.4Standard polar33892256
Deoxypyridinoline,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C13641.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C13583.3Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #5C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C15198.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13634.1Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13641.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #6C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C15318.9Standard polar33892256
Deoxypyridinoline,5TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3639.2Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3717.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4413.6Standard polar33892256
Deoxypyridinoline,5TMS,isomer #8C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3719.3Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #8C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3688.8Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #8C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4930.0Standard polar33892256
Deoxypyridinoline,5TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3698.7Semi standard non polar33892256
Deoxypyridinoline,5TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3714.1Standard non polar33892256
Deoxypyridinoline,5TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4951.9Standard polar33892256
Deoxypyridinoline,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3583.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3721.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #1C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4077.4Standard polar33892256
Deoxypyridinoline,6TMS,isomer #10C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3766.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #10C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3794.8Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #10C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4244.1Standard polar33892256
Deoxypyridinoline,6TMS,isomer #11C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3917.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #11C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3792.6Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #11C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4791.9Standard polar33892256
Deoxypyridinoline,6TMS,isomer #12C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3852.3Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #12C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3826.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #12C[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C4757.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3896.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C3773.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #13C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C4616.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3716.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3811.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #14C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4107.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3696.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3827.2Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #15C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4140.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3698.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3834.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #16C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4140.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3815.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C3855.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #17C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C)[Si](C)(C)C4724.8Standard polar33892256
Deoxypyridinoline,6TMS,isomer #18C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3851.1Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #18C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C3801.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #18C[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C4567.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #19C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13851.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #19C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C13821.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #19C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C14645.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3682.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3677.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #2C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4526.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #20C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3943.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #20C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3888.6Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #20C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C4266.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3948.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O3887.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #21C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O4290.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3902.2Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3910.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #22C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4292.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3780.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3773.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #23C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4198.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3756.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]3790.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #24C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O)C(=O)[O-]4229.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #25C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3737.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #25C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3804.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #25C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4209.2Standard polar33892256
Deoxypyridinoline,6TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3907.7Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3774.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #26C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C4730.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3847.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C3826.3Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #27C[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)N([Si](C)(C)C)[Si](C)(C)C4755.1Standard polar33892256
Deoxypyridinoline,6TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13895.2Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C13789.4Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #28C[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C14680.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #29C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3984.5Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #29C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O3854.9Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #29C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O4347.5Standard polar33892256
Deoxypyridinoline,6TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3675.8Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]3693.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #3C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C)C(=O)[O-]4538.7Standard polar33892256
Deoxypyridinoline,6TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3994.1Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3860.0Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #30C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4350.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3930.0Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3886.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #31C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4351.9Standard polar33892256
Deoxypyridinoline,6TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3941.1Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3895.3Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #32C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4248.4Standard polar33892256
Deoxypyridinoline,6TMS,isomer #33C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3946.2Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #33C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3881.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #33C[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C(=O)O4269.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3894.4Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3910.2Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #34C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4273.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #35C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C4150.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #35C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C3982.4Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #35C[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-])[Si](C)(C)C4400.0Standard polar33892256
Deoxypyridinoline,6TMS,isomer #4C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3676.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #4C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3724.7Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #4C[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4673.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3667.0Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C3731.2Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #5C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O[Si](C)(C)C4676.3Standard polar33892256
Deoxypyridinoline,6TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3684.6Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C3688.8Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #6C[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)C=C1O[Si](C)(C)C)C(=O)O[Si](C)(C)C4592.5Standard polar33892256
Deoxypyridinoline,6TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3667.0Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]3712.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #7C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)[O-]4608.8Standard polar33892256
Deoxypyridinoline,6TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3786.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O3771.5Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #8C[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C)[Si](C)(C)C)=C(C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(=O)O4211.6Standard polar33892256
Deoxypyridinoline,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3743.9Semi standard non polar33892256
Deoxypyridinoline,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]3797.1Standard non polar33892256
Deoxypyridinoline,6TMS,isomer #9C[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)=CC(O[Si](C)(C)C)=C1C[C@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)[O-]4219.5Standard polar33892256
Deoxypyridinoline,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-]3884.3Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O3927.8Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C13869.1Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O3989.1Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4008.1Semi standard non polar33892256
Deoxypyridinoline,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O3995.6Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C4061.2Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4057.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4056.0Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4055.1Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4170.4Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4187.1Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C4262.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4193.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C4309.2Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)N([C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O)[Si](C)(C)C(C)(C)C4275.0Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C13996.5Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4064.7Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4075.9Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4079.3Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C14043.8Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4123.0Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4140.2Semi standard non polar33892256
Deoxypyridinoline,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4132.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C14181.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@H](N)C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4395.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4269.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]4379.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4423.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4223.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4231.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4223.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4343.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4331.5Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@H](N)C(=O)O4438.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4236.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4347.2Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O4489.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(CC[C@H](N)C(=O)[O-])=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4453.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4239.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4246.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@H](N)C(=O)[O-])=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4382.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4251.7Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C14369.4Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C14402.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4394.1Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4244.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4467.4Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4481.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4516.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4473.8Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O4519.5Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4490.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4239.6Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4158.9Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4159.0Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4163.3Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4249.4Semi standard non polar33892256
Deoxypyridinoline,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4255.5Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4339.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4196.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C5357.6Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4334.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4344.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C5029.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4353.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4312.3Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4921.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]4504.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]4328.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-]5348.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4344.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4327.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4989.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C14510.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C14351.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C15406.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C14546.9Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C14287.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C15308.7Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4479.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4394.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4762.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4571.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C4406.6Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O[Si](C)(C)C(C)(C)C5077.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4599.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O4420.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O5099.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4635.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4375.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C5118.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4352.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4177.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]5333.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4614.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4405.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]5131.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4639.5Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4353.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4979.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4588.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4370.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4969.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4421.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4260.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5062.9Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4413.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4290.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O5086.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4566.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4281.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C5464.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4432.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4268.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]5046.1Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C14610.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C14236.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C15424.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C14561.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C14286.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C15427.1Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4580.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4336.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4833.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4340.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C4208.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C5406.6Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4703.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4304.5Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C(C[C@H](N)C(=O)O)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O5119.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4651.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]4321.5Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O)C(=O)[O-]5109.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4636.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4351.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O5131.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4656.6Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4356.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O5132.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4709.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O4316.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)C(=O)O5173.5Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4676.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4339.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]5164.5Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4464.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4396.2Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #36CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4746.0Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4573.8Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C4412.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #37CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O[Si](C)(C)C(C)(C)C5070.7Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4576.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O4414.5Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #38CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1CC[C@H](N)C(=O)[O-])C(=O)O5090.5Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4620.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C4361.6Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #39CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O[Si](C)(C)C(C)(C)C5055.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4438.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4271.7Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]5118.9Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4589.0Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]4384.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #40CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-]5065.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O4617.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O4370.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #41CC(C)(C)[Si](C)(C)N[C@@H](CC1=C(O)C=[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C=C1CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O5038.8Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4586.1Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4393.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #42CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]5029.6Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4739.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4428.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #43CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(O)=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=C1)C(=O)O4828.7Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4687.9Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4450.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #44CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)[O-]4825.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4706.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4454.6Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #45CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-]4826.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C4776.3Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C4470.1Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #46CC(C)(C)[Si](C)(C)N([C@@H](CCCC[N+]1=CC(O)=C(C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(CC[C@H](N)C(=O)[O-])=C1)C(=O)O)[Si](C)(C)C(C)(C)C5118.9Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C4824.4Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C4425.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #47CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=CC(O)=C1C[C@H](N)C(=O)O)C(=O)[O-])[Si](C)(C)C(C)(C)C5105.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-])[Si](C)(C)C(C)(C)C4842.7Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-])[Si](C)(C)C(C)(C)C4441.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #48CC(C)(C)[Si](C)(C)N([C@@H](CCC1=C[N+](CCCC[C@H](N)C(=O)O)=CC(O)=C1C[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)[O-])[Si](C)(C)C(C)(C)C5162.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4428.3Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O4289.8Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)N[C@@H](CCCC[N+]1=CC(CC[C@H](N)C(=O)[O-])=C(C[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1)C(=O)O5087.4Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4588.3Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4304.0Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C5515.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4451.9Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4254.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)N[C@@H](CCC1=C[N+](CCCC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)O)=CC(O[Si](C)(C)C(C)(C)C)=C1C[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)[O-]4987.2Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C4629.2Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C4237.9Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@@H](C(=O)[O-])N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=[N+](CCCC[C@H](N)C(=O)O)C=C1O[Si](C)(C)C(C)(C)C5421.3Standard polar33892256
Deoxypyridinoline,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4557.5Semi standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4266.4Standard non polar33892256
Deoxypyridinoline,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CC1=C(CC[C@H](N)C(=O)[O-])C=[N+](CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C5373.5Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (Non-derivatized) - 70eV, Positivesplash10-00di-2029000000-bd1b37cf42f6ca53e3fa2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (3 TMS) - 70eV, Positivesplash10-014i-5212591000-a631876ab8a721ce23e22017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxypyridinoline GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-11-05Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 10V, Positive-QTOFsplash10-03di-0001900000-635243e94b1bde7fa2f82016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 20V, Positive-QTOFsplash10-08ir-0009200000-5b2e6b764362837842fc2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 40V, Positive-QTOFsplash10-0uyi-2609000000-85238060df1e37341e992016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 10V, Negative-QTOFsplash10-03di-0000900000-fb17bf7ac61b15c5529b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 20V, Negative-QTOFsplash10-03di-1000900000-953b3f1eb159e9fd568c2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 40V, Negative-QTOFsplash10-00fr-9321000000-2dd743934a01f16230822016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 10V, Positive-QTOFsplash10-03xr-0009400000-306c023ce519cc90c3862021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 20V, Positive-QTOFsplash10-001i-5019000000-a5356bd2aed0616a55532021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 40V, Positive-QTOFsplash10-001i-4091000000-382e57452c8ebe13e2572021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 10V, Negative-QTOFsplash10-03xu-1009400000-ad7e7a69d65e5cce26582021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 20V, Negative-QTOFsplash10-0300-2009100000-132db17dd2c4331eca762021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxypyridinoline 40V, Negative-QTOFsplash10-0596-2192000000-45a922c56b2c7be849c62021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-29Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
Biospecimen Locations
  • Blood
  • Urine
Tissue Locations
  • Kidney
  • Platelet
  • Skeletal Muscle
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.0007 +/- 0.00018 uMAdult (>18 years old)BothNormal details
UrineDetected and Quantified0.005 (0.001 - 0.015) umol/mmol creatinineAdult (>18 years old)Not SpecifiedNormal details
UrineDetected and Quantified0.0086 (0.0004-0.016) umol/mmol creatinineAdult (>18 years old)BothNormal details
UrineDetected and Quantified0.0047 +/- 0.0004 umol/mmol creatinineAdult (>18 years old)BothNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.0006 +/- 0.0001 uMAdult (>18 years old)BothGrowth hormone deficiency details
UrineDetected and Quantified0.015 (0.001 - 0.03) umol/mmol creatinineAdult (>18 years old)Not SpecifiedMultiple myeloma details
UrineDetected and Quantified0.019 +/- 0.0026 umol/mmol creatinineAdult (>18 years old)BothCongestive heart failure details
UrineDetected and Quantified0.0066 +/- 0.0006 umol/mmol creatinineAdult (>18 years old)BothLiver fibrosis details
Associated Disorders and Diseases
Disease References
Growth hormone deficiency
  1. Rodriguez-Arnao J, James I, Jabbar A, Trainer PJ, Perrett D, Besser GM, Ross RJ: Serum collagen crosslinks as markers of bone turn-over during GH replacement therapy in growth hormone deficient adults. Clin Endocrinol (Oxf). 1998 Apr;48(4):455-62. [PubMed:9640412 ]
Multiple myeloma
  1. Dizdar O, Barista I, Kalyoncu U, Karadag O, Hascelik G, Cila A, Pinar A, Celik I, Kars A, Tekuzman G: Biochemical markers of bone turnover in diagnosis of myeloma bone disease. Am J Hematol. 2007 Mar;82(3):185-91. [PubMed:17022050 ]
Congestive heart failure
  1. Shane E, Mancini D, Aaronson K, Silverberg SJ, Seibel MJ, Addesso V, McMahon DJ: Bone mass, vitamin D deficiency, and hyperparathyroidism in congestive heart failure. Am J Med. 1997 Sep;103(3):197-207. [PubMed:9316552 ]
Cirrhosis
  1. Afdhal NH, Keaveny AP, Cohen SB, Nunes DP, Maldonado N, O'Brien M, Stone PJ: Urinary assays for desmosine and hydroxylysylpyridinoline in the detection of cirrhosis. J Hepatol. 1997 Dec;27(6):993-1002. [PubMed:9453424 ]
Associated OMIM IDs
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB013750
KNApSAcK IDNot Available
Chemspider ID9479456
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkDeoxypyridinoline
METLIN ID5552
PubChem Compound11304480
PDB IDNot Available
ChEBI ID89510
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDMDB00000190
Good Scents IDNot Available
References
Synthesis ReferenceHatch, Robert P. Method for the synthesis of deoxypyridinoline. U.S. (1998), 7 pp.
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Haderslev KV, Tjellesen L, Sorensen HA, Staun M: Alendronate increases lumbar spine bone mineral density in patients with Crohn's disease. Gastroenterology. 2000 Sep;119(3):639-46. [PubMed:10982756 ]
  2. Tanaka K, Inaba M, Goto H, Nagata-Sakurai M, Sakai S, Yamada S, Ueda M, Ishimura E, Nishizawa Y: Paraarticular trabecular bone loss at the ultradistal radius and increased arterial stiffening in postmenopausal patients with rheumatoid arthritis. J Rheumatol. 2006 Apr;33(4):652-8. [PubMed:16583470 ]
  3. Romanello M, Noris Suarez K, Bettica P, Moro L: Detection of pyridinium cross-links in human bile. Calcif Tissue Int. 1995 Dec;57(6):415-8. [PubMed:8581871 ]
  4. Hoff AO, Catala-Lehnen P, Thomas PM, Priemel M, Rueger JM, Nasonkin I, Bradley A, Hughes MR, Ordonez N, Cote GJ, Amling M, Gagel RF: Increased bone mass is an unexpected phenotype associated with deletion of the calcitonin gene. J Clin Invest. 2002 Dec;110(12):1849-57. [PubMed:12488435 ]
  5. Hodsman AB, Fraher LJ, Ostbye T, Adachi JD, Steer BM: An evaluation of several biochemical markers for bone formation and resorption in a protocol utilizing cyclical parathyroid hormone and calcitonin therapy for osteoporosis. J Clin Invest. 1993 Mar;91(3):1138-48. [PubMed:8450043 ]
  6. Kaufmann J, Mueller A, Voigt A, Carl HD, Gursche A, Zacher J, Stein G, Hein G: Hydroxypyridinium collagen crosslinks in serum, urine, synovial fluid and synovial tissue in patients with rheumatoid arthritis compared with osteoarthritis. Rheumatology (Oxford). 2003 Feb;42(2):314-20. [PubMed:12595629 ]
  7. Giangregorio LM, Hicks AL, Webber CE, Phillips SM, Craven BC, Bugaresti JM, McCartney N: Body weight supported treadmill training in acute spinal cord injury: impact on muscle and bone. Spinal Cord. 2005 Nov;43(11):649-57. [PubMed:15968302 ]
  8. Pronchenko IA, Buzulina VP, Tomolina NA, Vedernikova RN, Ermakova IP: [Biochemical markers of bone metabolism and bone tissue losses after allotransplantation of the cadaveric kidney: a cross-sectional]. Klin Lab Diagn. 2005 Nov;(11):3-8. [PubMed:16404967 ]
  9. Yoshihara Y, Tsukazaki T, Osaki M, Nakashima M, Hasui K, Shindo H: Altered expression of inflammatory cytokines in primary osteoarthritis by human T lymphotropic virus type I retrovirus infection: a cross-sectional study. Arthritis Res Ther. 2004;6(4):R347-54. Epub 2004 Jun 7. [PubMed:15225370 ]
  10. Vesper HW, Demers LM, Eastell R, Garnero P, Kleerekoper M, Robins SP, Srivastava AK, Warnick GR, Watts NB, Myers GL: Assessment and recommendations on factors contributing to preanalytical variability of urinary pyridinoline and deoxypyridinoline. Clin Chem. 2002 Feb;48(2):220-35. [PubMed:11805003 ]
  11. Shankar S, Hosking DJ: Biochemical assessment of Paget's disease of bone. J Bone Miner Res. 2006 Dec;21 Suppl 2:P22-7. [PubMed:17229003 ]
  12. Takada J, Imoto K, Iba K, Yamashita T: [Bone and bone related biochemical examinations. Bone and collagen related metabolites. DPD (total, free)]. Clin Calcium. 2006 Jun;16(6):994-1000. [PubMed:16751696 ]