Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-04-06 16:22:02 UTC
Update Date2021-09-14 15:40:57 UTC
HMDB IDHMDB0012267
Secondary Accession Numbers
  • HMDB12267
Metabolite Identification
Common NameN-Succinyl-L,L-2,6-diaminopimelate
DescriptionN-Succinyl-L,L-2,6-diaminopimelate belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. N-Succinyl-L,L-2,6-diaminopimelate exists in all living organisms, ranging from bacteria to humans. N-Succinyl-L,L-2,6-diaminopimelate has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make N-succinyl-L,L-2,6-diaminopimelate a potential biomarker for the consumption of these foods. N-Succinyl-L,L-2,6-diaminopimelate is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review very few articles have been published on N-Succinyl-L,L-2,6-diaminopimelate.
Structure
Data?1582753035
Synonyms
ValueSource
N-Succinyl-L,L-2,6-diaminopimelic acidGenerator
L,L-SdapHMDB
N-Succinyl-L-2,6-diaminoheptanedioateHMDB
N-Succinyl-L-2,6-diaminoheptanedioic acidHMDB
N-Succinyl-LL-2,6-diaminoheptanedioateHMDB
N-Succinyl-LL-2,6-diaminoheptanedioic acidHMDB
N-Succinyl-LL-2,6-diaminopimelateHMDB
Chemical FormulaC11H18N2O7
Average Molecular Weight290.2698
Monoisotopic Molecular Weight290.11140094
IUPAC Name(6S)-2-amino-6-(3-carboxypropanamido)heptanedioic acid
Traditional Name(6S)-2-amino-6-(3-carboxypropanamido)heptanedioic acid
CAS Registry Number26605-36-7
SMILES
NC(CCC[C@H](NC(=O)CCC(O)=O)C(O)=O)C(O)=O
InChI Identifier
InChI=1S/C11H18N2O7/c12-6(10(17)18)2-1-3-7(11(19)20)13-8(14)4-5-9(15)16/h6-7H,1-5,12H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20)/t6?,7-/m0/s1
InChI KeyGLXUWZBUPATPBR-MLWJPKLSSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated 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 ParentN-acyl-L-alpha-amino acids
Alternative Parents
Substituents
  • N-acyl-l-alpha-amino acid
  • Alpha-amino acid
  • Tricarboxylic acid or derivatives
  • Amino fatty acid
  • Fatty amide
  • N-acyl-amine
  • Fatty acyl
  • Carboxamide group
  • Secondary carboxylic acid amide
  • Amino acid
  • Carboxylic acid
  • Primary amine
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Primary aliphatic amine
  • Organopnictogen compound
  • Carbonyl group
  • Organic oxygen compound
  • Organic nitrogen compound
  • Amine
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
RoleNot Available
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 Solubility5.8 g/LALOGPS
logP-3.1ALOGPS
logP-3.8ChemAxon
logS-1.7ALOGPS
pKa (Strongest Acidic)1.89ChemAxon
pKa (Strongest Basic)9.53ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area167.02 ŲChemAxon
Rotatable Bond Count10ChemAxon
Refractivity63.98 m³·mol⁻¹ChemAxon
Polarizability27.09 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+167.37231661259
DarkChem[M-H]-164.4131661259
DeepCCS[M+H]+164.40230932474
DeepCCS[M-H]-162.04430932474
DeepCCS[M-2H]-194.9330932474
DeepCCS[M+Na]+170.49530932474
AllCCS[M+H]+163.132859911
AllCCS[M+H-H2O]+160.232859911
AllCCS[M+NH4]+165.832859911
AllCCS[M+Na]+166.632859911
AllCCS[M-H]-164.232859911
AllCCS[M+Na-2H]-164.432859911
AllCCS[M+HCOO]-164.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
N-Succinyl-L,L-2,6-diaminopimelateNC(CCC[C@H](NC(=O)CCC(O)=O)C(O)=O)C(O)=O3738.8Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelateNC(CCC[C@H](NC(=O)CCC(O)=O)C(O)=O)C(O)=O2167.4Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelateNC(CCC[C@H](NC(=O)CCC(O)=O)C(O)=O)C(O)=O2826.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
N-Succinyl-L,L-2,6-diaminopimelate,1TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O)C(=O)O2593.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TMS,isomer #2C[Si](C)(C)OC(=O)[C@H](CCCC(N)C(=O)O)NC(=O)CCC(=O)O2561.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TMS,isomer #3C[Si](C)(C)OC(=O)C(N)CCC[C@H](NC(=O)CCC(=O)O)C(=O)O2577.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TMS,isomer #4C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)C(=O)O2660.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TMS,isomer #5C[Si](C)(C)N(C(=O)CCC(=O)O)[C@@H](CCCC(N)C(=O)O)C(=O)O2581.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O[Si](C)(C)C)C(=O)O2521.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #10C[Si](C)(C)N(C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)C(=O)O)[Si](C)(C)C2807.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #11C[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C)C(=O)O2645.7Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #2C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O)C(=O)O[Si](C)(C)C2519.2Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #3C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C)C(=O)O)C(=O)O2664.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #4C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O)C(=O)O)[Si](C)(C)C2528.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #5C[Si](C)(C)OC(=O)C(N)CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C2521.2Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #6C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C)C(=O)O2644.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #7C[Si](C)(C)OC(=O)[C@H](CCCC(N)C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C2541.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #8C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)C(=O)O[Si](C)(C)C2644.7Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TMS,isomer #9C[Si](C)(C)OC(=O)C(N)CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C2509.7Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2524.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)NC(=O)CCC(=O)O2782.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #11C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C)C(=O)O2604.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #12C[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C2795.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #13C[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C)C(=O)O[Si](C)(C)C2575.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #14C[Si](C)(C)N(C(=O)CCC(=O)O)[C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2731.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #2C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C)C(=O)O)C(=O)O[Si](C)(C)C2610.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #3C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C2507.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #4C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O2615.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #5C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C2529.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #6C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2785.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #7C[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O2585.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #8C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2607.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TMS,isomer #9C[Si](C)(C)OC(=O)C(N)CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C2530.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #1C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2608.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #1C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2604.8Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #1C[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C3119.7Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C2738.7Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C2702.6Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #10C[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C3378.4Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #11C[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2721.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #11C[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2702.4Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #11C[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3379.2Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2502.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2572.6Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #2C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C3733.9Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2751.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2666.4Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #3C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O3351.8Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #4C[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2546.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #4C[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2646.7Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #4C[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3226.9Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #5C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2758.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #5C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2684.9Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #5C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C3313.5Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #6C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O2560.9Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #6C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O2622.3Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #6C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O3277.0Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C2709.2Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C2741.3Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #7C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C3420.3Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #8C[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2755.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #8C[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2646.1Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #8C[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3258.2Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #9C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C)C(=O)O[Si](C)(C)C2580.9Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #9C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C)C(=O)O[Si](C)(C)C2617.4Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TMS,isomer #9C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C)C(=O)O[Si](C)(C)C3181.7Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2721.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2688.2Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2964.1Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #2C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2551.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #2C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2654.8Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #2C[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2880.2Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C2697.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C2729.7Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #3C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C3069.9Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #4C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2703.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #4C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2730.1Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #4C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C3067.5Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #5C[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2730.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #5C[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C2704.5Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TMS,isomer #5C[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C3030.2Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,6TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2733.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,6TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2741.7Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,6TMS,isomer #1C[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C2821.5Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O)C(=O)O2867.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC(N)C(=O)O)NC(=O)CCC(=O)O2827.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC[C@H](NC(=O)CCC(=O)O)C(=O)O2845.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)C(=O)O2915.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)N(C(=O)CCC(=O)O)[C@@H](CCCC(N)C(=O)O)C(=O)O2828.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O3015.0Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)N(C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C3238.2Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)C(=O)O3099.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O)C(=O)O[Si](C)(C)C(C)(C)C3010.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)O3128.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C3020.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C2986.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O3087.2Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC(N)C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C2997.4Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)C(=O)O[Si](C)(C)C(C)(C)C3108.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C2983.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3224.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)NC(=O)CCC(=O)O3403.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)C(=O)O3269.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3445.7Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3275.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)N(C(=O)CCC(=O)O)[C@@H](CCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3390.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)O[Si](C)(C)C(C)(C)C3298.7Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C3211.9Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O3276.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3202.7Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3446.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3299.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3264.9Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C3192.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3457.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3274.2Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)NC(CCC[C@H](NC(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3421.8Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C3575.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C3306.7Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C3558.1Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3602.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3314.3Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3561.4Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3388.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3264.9Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3766.5Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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)O3653.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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)O3331.6Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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)O3527.2Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3462.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3283.1Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3481.8Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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)C3622.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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)C3320.3Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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)C3501.1Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3443.2Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3282.9Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3511.2Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)C3608.9Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)C3331.8Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)C3579.3Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3631.6Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3299.8Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@H](NC(=O)CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3474.8Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3433.5Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3260.0Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3462.0Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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[Si](C)(C)C(C)(C)C3834.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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[Si](C)(C)C(C)(C)C3477.5Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N[C@@H](CCCC(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[Si](C)(C)C(C)(C)C3366.0Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3612.2Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3434.5Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)NC(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3358.5Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)[Si](C)(C)C(C)(C)C3815.8Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)[Si](C)(C)C(C)(C)C3494.8Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)[Si](C)(C)C(C)(C)C3418.2Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)C)[Si](C)(C)C(C)(C)C3788.1Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)C)[Si](C)(C)C(C)(C)C3490.7Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC(=O)CCC(=O)N([C@@H](CCCC(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)C)[Si](C)(C)C(C)(C)C3417.5Standard polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3799.3Semi standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3478.4Standard non polar33892256
N-Succinyl-L,L-2,6-diaminopimelate,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC(=O)C(CCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CCC(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3402.6Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate GC-MS (Non-derivatized) - 70eV, Positivesplash10-0ukd-7980000000-e443695d136f221c8fcf2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate GC-MS (3 TMS) - 70eV, Positivesplash10-006x-9303600000-53e79d2abfa0f9ef52dd2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 10V, Positive-QTOFsplash10-00fs-0290000000-94b59924e5c6f873d3e92015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 20V, Positive-QTOFsplash10-0002-1960000000-f57f28932db38b283c8c2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 40V, Positive-QTOFsplash10-054k-7900000000-66284b4cc1812fbb9f0c2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 10V, Negative-QTOFsplash10-0079-0190000000-fa97ecde1f805141dc722015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 20V, Negative-QTOFsplash10-00g1-1490000000-777a3c340c9bca9df3ae2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 40V, Negative-QTOFsplash10-006y-9800000000-f1025c9e017254c3c3562015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 10V, Positive-QTOFsplash10-006x-0190000000-2b72340d09586ce940a02021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 20V, Positive-QTOFsplash10-0002-1910000000-e4c34aca88cb0711d6e62021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 40V, Positive-QTOFsplash10-0pb9-8900000000-b3cbfc02281c4466f2de2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 10V, Negative-QTOFsplash10-000i-0090000000-39bd027060b8d3f96cff2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 20V, Negative-QTOFsplash10-000b-2970000000-0ae78022739fec47a2222021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - N-Succinyl-L,L-2,6-diaminopimelate 40V, Negative-QTOFsplash10-00dl-9300000000-79f5f223496e3d1a12742021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB028905
KNApSAcK IDNot Available
Chemspider ID35032427
KEGG Compound IDC04421
BioCyc IDN-SUCCINYLLL-2-6-DIAMINOPIMELATE
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound25202447
PDB IDNot Available
ChEBI ID165894
Food Biomarker OntologyNot Available
VMH IDSL26DA
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available