Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2007-05-23 01:45:11 UTC
Update Date2022-03-07 02:49:31 UTC
HMDB IDHMDB0006354
Secondary Accession Numbers
  • HMDB06354
Metabolite Identification
Common NameDeoxythymidine diphosphate-L-rhamnose
DescriptionDeoxythymidine diphosphate-L-rhamnose (dTDP-L-rhamnose) is the precursor of L-rhamnose, a saccharide required for the virulence of some pathogenic bacteria. In gram-negative bacteria such as Salmonella enterica, Vibrio cholerae, or Escherichia coli 075:K5, L-rhamnose is an important residue in the O-antigen of lipopolysaccharides, which are essential for resistance to serum killing and colonization. In gram-positive bacteria such as streptococci, the capsule is a recognized virulence factor. For example, L-rhamnose is known to be present in the capsule of Streptococcus suis, a causative agent of meningitis in humans. In Streptococcus mutans, L-rhamnose containing polysaccharides have been implicated in tooth surface colonization and adherence to kidney, muscle, and heart tissues. In mycobacteria, L-rhamnose is fundamental to the structural integrity of the cell wall since it connects the inner peptidoglycan layer to the arabinogalactan polysaccharides. dTDP-L-rhamnose is synthesized from glucose-1-phosphate and deoxythymidine triphosphate (dTTP) via a pathway involving four distinct enzymes. Whereas common sugars such as glucose, fructose, and mannose are all D-configured, bacteria commonly utilize the L-configured carbohydrates in pharmacologically active compounds and their cell-wall structures. The bacterial cell wall is unique to bacteria; neither the cell wall nor the enzymes and chemical intermediates in its formation have analogues in humans. The enzymes involved in dTDP-L-rhamnose synthesis are potential targets for the design of new therapeutic agents (PMID: 10802738 , 12773151 ).
Structure
Data?1586448036
Synonyms
ValueSource
dTDP-6-Deoxy-beta-L-mannoseChEBI
dTDP-6-Deoxy-L-mannoseChEBI
dTDP-L-RhamnoseChEBI
Thymidine 5'-(trihydrogen diphosphate), p'-(6-deoxy-beta-L-mannopyranosyl) esterChEBI
Thymidine diphosphate-L-rhamnoseChEBI
dTDP-beta-L-RhamnoseKegg
dTDP-6-Deoxy-b-L-mannoseGenerator
dTDP-6-Deoxy-β-L-mannoseGenerator
Thymidine 5'-(trihydrogen diphosphate), p'-(6-deoxy-b-L-mannopyranosyl) esterGenerator
Thymidine 5'-(trihydrogen diphosphate), p'-(6-deoxy-β-L-mannopyranosyl) esterGenerator
Thymidine 5'-(trihydrogen diphosphoric acid), p'-(6-deoxy-b-L-mannopyranosyl) esterGenerator
Thymidine 5'-(trihydrogen diphosphoric acid), p'-(6-deoxy-beta-L-mannopyranosyl) esterGenerator
Thymidine 5'-(trihydrogen diphosphoric acid), p'-(6-deoxy-β-L-mannopyranosyl) esterGenerator
Thymidine diphosphoric acid-L-rhamnoseGenerator
dTDP-b-L-RhamnoseGenerator
dTDP-Β-L-rhamnoseGenerator
Deoxythymidine diphosphoric acid-L-rhamnoseGenerator
Thymidine diphosphate rhamnoseHMDB
Deoxythymidine diphosphate rhamnoseHMDB
TDP-L-RhamnoseHMDB
TDP-RhamnoseHMDB
dTDP L-RhamnoseHMDB
Deoxythymidine diphosphate-L-rhamnoseHMDB
Chemical FormulaC16H26N2O15P2
Average Molecular Weight548.3296
Monoisotopic Molecular Weight548.080841196
IUPAC Name{[hydroxy({[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methoxy})phosphoryl]oxy}({[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy})phosphinic acid
Traditional Namedtdp-β-L-rhamnose
CAS Registry Number2147-59-3
SMILES
C[C@@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=C(C)C(=O)NC2=O)[C@H](O)[C@H](O)[C@H]1O
InChI Identifier
InChI=1S/C16H26N2O15P2/c1-6-4-18(16(24)17-14(6)23)10-3-8(19)9(31-10)5-29-34(25,26)33-35(27,28)32-15-13(22)12(21)11(20)7(2)30-15/h4,7-13,15,19-22H,3,5H2,1-2H3,(H,25,26)(H,27,28)(H,17,23,24)/t7-,8-,9+,10+,11-,12+,13+,15+/m0/s1
InChI KeyZOSQFDVXNQFKBY-CGAXJHMRSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as pyrimidine nucleotide sugars. These are pyrimidine nucleotides bound to a saccharide derivative through the terminal phosphate group.
KingdomOrganic compounds
Super ClassNucleosides, nucleotides, and analogues
ClassPyrimidine nucleotides
Sub ClassPyrimidine nucleotide sugars
Direct ParentPyrimidine nucleotide sugars
Alternative Parents
Substituents
  • Pyrimidine nucleotide sugar
  • Pentose phosphate
  • Monosaccharide phosphate
  • Organic pyrophosphate
  • Pyrimidone
  • Monoalkyl phosphate
  • Hydroxypyrimidine
  • Oxane
  • Monosaccharide
  • Phosphoric acid ester
  • Pyrimidine
  • Alkyl phosphate
  • Organic phosphoric acid derivative
  • Hydropyrimidine
  • Tetrahydrofuran
  • Heteroaromatic compound
  • Secondary alcohol
  • Oxacycle
  • Azacycle
  • Organoheterocyclic compound
  • Polyol
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Alcohol
  • Organic nitrogen compound
  • Organic oxygen compound
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Ontology
Not AvailableNot 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 Solubility11.6 g/LALOGPS
logP-1.1ALOGPS
logP-2.7ChemAxon
logS-1.7ALOGPS
pKa (Strongest Acidic)1.73ChemAxon
pKa (Strongest Basic)-3.2ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count12ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area251.08 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity107.76 m³·mol⁻¹ChemAxon
Polarizability45.89 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+192.46130932474
DeepCCS[M-H]-190.46530932474
DeepCCS[M-2H]-223.70430932474
DeepCCS[M+Na]+198.2130932474
AllCCS[M+H]+213.232859911
AllCCS[M+H-H2O]+211.632859911
AllCCS[M+NH4]+214.632859911
AllCCS[M+Na]+214.932859911
AllCCS[M-H]-207.232859911
AllCCS[M+Na-2H]-208.532859911
AllCCS[M+HCOO]-210.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Deoxythymidine diphosphate-L-rhamnoseC[C@@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=C(C)C(=O)NC2=O)[C@H](O)[C@H](O)[C@H]1O4697.5Standard polar33892256
Deoxythymidine diphosphate-L-rhamnoseC[C@@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=C(C)C(=O)NC2=O)[C@H](O)[C@H](O)[C@H]1O3187.9Standard non polar33892256
Deoxythymidine diphosphate-L-rhamnoseC[C@@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H](C[C@@H]2O)N2C=C(C)C(=O)NC2=O)[C@H](O)[C@H](O)[C@H]1O4582.8Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Deoxythymidine diphosphate-L-rhamnose,1TMS,isomer #1CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O3976.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TMS,isomer #2CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3913.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TMS,isomer #3CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3884.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TMS,isomer #4CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O3928.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TMS,isomer #5CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O4048.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TMS,isomer #6CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4041.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TMS,isomer #7CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O4060.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #1CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O3843.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #10CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3880.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #11CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3914.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #12CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3786.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #13CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3848.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #14CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3855.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #15CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3882.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #16CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O3895.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #17CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3902.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #18CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3931.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #19CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3990.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #2CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3801.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #20CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O4022.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #21CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O4020.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #3CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3825.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #4CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O3928.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #5CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3936.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #6CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3984.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #7CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3799.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #8CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3796.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TMS,isomer #9CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3875.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #1CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3734.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #10CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3803.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #11CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3813.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #12CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3834.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #13CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3895.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #14CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3916.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #15CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3919.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #16CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3745.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #17CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3788.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #18CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3797.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #19CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3806.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #2CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3747.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #20CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3786.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #21CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3797.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #22CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3807.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #23CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3862.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #24CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3864.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #25CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3871.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #26CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3774.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #27CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3786.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #28CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3799.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #29CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3845.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #3CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O3820.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #30CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3847.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #31CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3850.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #32CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3877.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #33CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3888.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #34CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3888.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #35CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3950.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #4CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3831.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #5CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3852.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #6CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3743.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #7CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3788.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #8CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3798.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TMS,isomer #9CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3819.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #1CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3728.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #10CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3856.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #11CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3753.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #12CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3763.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #13CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3802.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #14CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3809.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #15CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3837.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #16CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3840.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #17CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3801.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #18CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3833.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #19CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3836.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #2CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O3751.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #20CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3893.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #21CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3765.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #22CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3776.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #23CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3807.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #24CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3811.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #25CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3836.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #26CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3839.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #27CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3808.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #28CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3832.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #29CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3833.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #3CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3765.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #30CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3870.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #31CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3805.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #32CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3827.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #33CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3832.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #34CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3868.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #35CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3888.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #4CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3797.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #5CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O3757.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #6CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3767.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #7CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O3802.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #8CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O3820.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,4TMS,isomer #9CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O3854.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TBDMS,isomer #1CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4181.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TBDMS,isomer #2CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4123.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TBDMS,isomer #3CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O4101.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TBDMS,isomer #4CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4146.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TBDMS,isomer #5CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4246.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TBDMS,isomer #6CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4241.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,1TBDMS,isomer #7CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4264.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #1CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4254.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #10CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4289.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #11CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4286.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #12CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O4190.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #13CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O4260.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #14CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4277.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #15CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4275.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #16CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4302.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #17CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4312.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #18CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4319.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #19CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4388.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #2CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O4225.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #20CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4386.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #21CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4386.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #3CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4232.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #4CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4333.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #5CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4343.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #6CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4351.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #7CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4206.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #8CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4209.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,2TBDMS,isomer #9CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4276.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #1CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O4366.5Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #10CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4402.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #11CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4414.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #12CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4420.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #13CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4488.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #14CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4495.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #15CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4495.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #16CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4361.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #17CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4385.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #18CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4400.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #19CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4403.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #2CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4376.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #20CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4395.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #21CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4410.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #22CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4408.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #23CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4441.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #24CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4435.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #25CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4444.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #26CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O4375.2Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #27CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4391.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #28CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4393.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #29CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4439.8Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #3CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)[NH]C1=O4425.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #30CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4435.1Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #31CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4446.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #32CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4460.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #33CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4468.3Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #34CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4471.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #35CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4509.9Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #4CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4436.6Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #5CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4456.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #6CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4380.4Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #7CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O4410.0Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #8CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O4421.7Semi standard non polar33892256
Deoxythymidine diphosphate-L-rhamnose,3TBDMS,isomer #9CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@@H](C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O4429.2Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS ("Deoxythymidine diphosphate-L-rhamnose,1TMS,#1" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Deoxythymidine diphosphate-L-rhamnose GC-MS (TMS_2_17) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 10V, Positive-QTOFsplash10-004i-0900000000-43e353abbd92638144fe2017-07-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 20V, Positive-QTOFsplash10-004i-3911000000-cdabd033d59b1aef7f012017-07-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 40V, Positive-QTOFsplash10-004i-3900000000-8f759174f3f6aab6d0e72017-07-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 10V, Negative-QTOFsplash10-0udj-3502490000-5d4d8fa9a27e2cafec772017-07-26Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 20V, Negative-QTOFsplash10-0fb9-3905010000-e8b50977df37869f17012017-07-26Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 40V, Negative-QTOFsplash10-0a6u-4901000000-b718aeb0ca866d681e902017-07-26Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 10V, Positive-QTOFsplash10-0002-0101090000-cd1c8b30ff72e832534a2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 20V, Positive-QTOFsplash10-004i-9743230000-d289a67be04016b750452021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 40V, Positive-QTOFsplash10-002f-9710000000-d43e2745a51f03a29aa32021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 10V, Negative-QTOFsplash10-0002-0000090000-946e334068a1f247b6702021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 20V, Negative-QTOFsplash10-004j-9102210000-d4c75b5cc9c1e379626b2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Deoxythymidine diphosphate-L-rhamnose 40V, Negative-QTOFsplash10-001i-2209000000-9ed146b1b9e4293acc012021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 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, 1000 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, 200 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, 300 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, 400 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, 500 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, 600 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, 700 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, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
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 IDDB03723
Phenol Explorer Compound IDNot Available
FooDB IDFDB030838
KNApSAcK IDC00007662
Chemspider ID108806
KEGG Compound IDC03319
BioCyc IDDTDP-RHAMNOSE
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound121966
PDB IDNot Available
ChEBI ID15774
Food Biomarker OntologyNot Available
VMH IDDTDPRMN
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceShibaev, V. N.; Kusov, Yu. Yu.; Eliseeva, G. I.; Petrenko, V. A. Synthesis of thymidine diphosphate rhamnose analogs. Ref. Dokl. Soobshch. - Mendeleevsk. S'ezd Obshch. Prikl. Khim., 11th (1975), 6 111. CODEN: 37MOAO CAN 88:191313 AN 1978:191313
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Giraud MF, Leonard GA, Field RA, Berlind C, Naismith JH: RmlC, the third enzyme of dTDP-L-rhamnose pathway, is a new class of epimerase. Nat Struct Biol. 2000 May;7(5):398-402. [PubMed:10802738 ]
  2. Dong C, Beis K, Giraud MF, Blankenfeldt W, Allard S, Major LL, Kerr ID, Whitfield C, Naismith JH: A structural perspective on the enzymes that convert dTDP-d-glucose into dTDP-l-rhamnose. Biochem Soc Trans. 2003 Jun;31(Pt 3):532-6. [PubMed:12773151 ]