Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-01-30 15:54:42 UTC
Update Date2021-09-14 15:44:40 UTC
HMDB IDHMDB0011641
Secondary Accession Numbers
  • HMDB11641
Metabolite Identification
Common NameUridine 2'-phosphate
DescriptionUridine 2'- phosphate is a product of the decylclization reaction carried out by the enzyme 2',3'-cyclic nucleotide-3'-phosphodiesterase (CNPase, EC 3.1.4.37) which hydrolyses Uridine 2',3'-cyclic phosphate to Uridine 2'-phosphate. CNPase is a unique RNase in that it only cleaves nucleoside 2',3'-cyclic phosphates and not the RNA internucleotide linkage, like other RNases such as RNase A and RNase T1.
Structure
Data?1582752932
Synonyms
ValueSource
Uridine 2'-monophosphateChEBI
Uridine 2'-monophosphoric acidGenerator
Uridine 2'-phosphoric acidGenerator
2'-PhosphouridineHMDB
2'-UMPHMDB
2'-UridylateHMDB
2'-Uridylic acidHMDB
Uridine 2'-(dihydrogen phosphate)HMDB
Chemical FormulaC9H13N2O9P
Average Molecular Weight324.1813
Monoisotopic Molecular Weight324.035866536
IUPAC Name{[(2R,3R,4R,5R)-2-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-4-hydroxy-5-(hydroxymethyl)oxolan-3-yl]oxy}phosphonic acid
Traditional Nameuridine 2'-phosphate
CAS Registry Number131-83-9
SMILES
OC[C@H]1O[C@H]([C@H](OP(O)(O)=O)[C@@H]1O)N1C=CC(=O)NC1=O
InChI Identifier
InChI=1S/C9H13N2O9P/c12-3-4-6(14)7(20-21(16,17)18)8(19-4)11-2-1-5(13)10-9(11)15/h1-2,4,6-8,12,14H,3H2,(H,10,13,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChI KeyHQIDPEYTETUCNF-XVFCMESISA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as pentose phosphates. These are carbohydrate derivatives containing a pentose substituted by one or more phosphate groups.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentPentose phosphates
Alternative Parents
Substituents
  • Pentose phosphate
  • Glycosyl compound
  • N-glycosyl compound
  • Hydroxypyrimidine
  • Monoalkyl phosphate
  • Pyrimidone
  • Hydropyrimidine
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Pyrimidine
  • Alkyl phosphate
  • Heteroaromatic compound
  • Tetrahydrofuran
  • Secondary alcohol
  • Oxacycle
  • Azacycle
  • Organoheterocyclic compound
  • Alcohol
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Primary alcohol
  • Organic nitrogen compound
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
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 Solubility12.4 g/LALOGPS
logP-1.7ALOGPS
logP-2.5ChemAxon
logS-1.4ALOGPS
pKa (Strongest Acidic)0.72ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area165.86 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity63.44 m³·mol⁻¹ChemAxon
Polarizability26.45 ųChemAxon
Number of Rings2ChemAxon
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]+170.59231661259
DarkChem[M-H]-163.70131661259
DeepCCS[M+H]+166.27830932474
DeepCCS[M-H]-163.9230932474
DeepCCS[M-2H]-197.81430932474
DeepCCS[M+Na]+172.96430932474
AllCCS[M+H]+169.232859911
AllCCS[M+H-H2O]+166.032859911
AllCCS[M+NH4]+172.132859911
AllCCS[M+Na]+173.032859911
AllCCS[M-H]-162.332859911
AllCCS[M+Na-2H]-162.132859911
AllCCS[M+HCOO]-162.032859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Uridine 2'-phosphateOC[C@H]1O[C@H]([C@H](OP(O)(O)=O)[C@@H]1O)N1C=CC(=O)NC1=O3327.3Standard polar33892256
Uridine 2'-phosphateOC[C@H]1O[C@H]([C@H](OP(O)(O)=O)[C@@H]1O)N1C=CC(=O)NC1=O2259.1Standard non polar33892256
Uridine 2'-phosphateOC[C@H]1O[C@H]([C@H](OP(O)(O)=O)[C@@H]1O)N1C=CC(=O)NC1=O3142.8Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Uridine 2'-phosphate,1TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O)[C@@H]1O2659.0Semi standard non polar33892256
Uridine 2'-phosphate,1TMS,isomer #2C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O)O2673.8Semi standard non polar33892256
Uridine 2'-phosphate,1TMS,isomer #3C[Si](C)(C)OP(=O)(O)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)[NH]C1=O2754.3Semi standard non polar33892256
Uridine 2'-phosphate,1TMS,isomer #4C[Si](C)(C)N1C(=O)C=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OP(=O)(O)O)C1=O2731.7Semi standard non polar33892256
Uridine 2'-phosphate,2TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C2606.1Semi standard non polar33892256
Uridine 2'-phosphate,2TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O2716.2Semi standard non polar33892256
Uridine 2'-phosphate,2TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O2714.0Semi standard non polar33892256
Uridine 2'-phosphate,2TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C2706.8Semi standard non polar33892256
Uridine 2'-phosphate,2TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1OP(=O)(O)O2710.9Semi standard non polar33892256
Uridine 2'-phosphate,2TMS,isomer #6C[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)[NH]C1=O)O[Si](C)(C)C2758.6Semi standard non polar33892256
Uridine 2'-phosphate,2TMS,isomer #7C[Si](C)(C)OP(=O)(O)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O2800.5Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2678.9Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2914.3Standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3598.0Standard polar33892256
Uridine 2'-phosphate,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C2680.7Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C2962.2Standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C3819.4Standard polar33892256
Uridine 2'-phosphate,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O2730.9Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O2955.1Standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O3448.6Standard polar33892256
Uridine 2'-phosphate,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O2768.6Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O2948.6Standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O3650.2Standard polar33892256
Uridine 2'-phosphate,3TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C2726.5Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C2904.4Standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C3391.0Standard polar33892256
Uridine 2'-phosphate,3TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C2764.6Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C2910.9Standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C3591.6Standard polar33892256
Uridine 2'-phosphate,3TMS,isomer #7C[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O)O[Si](C)(C)C2801.0Semi standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #7C[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O)O[Si](C)(C)C2932.1Standard non polar33892256
Uridine 2'-phosphate,3TMS,isomer #7C[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C)C1=O)O[Si](C)(C)C3421.5Standard polar33892256
Uridine 2'-phosphate,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2705.3Semi standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2938.0Standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3247.3Standard polar33892256
Uridine 2'-phosphate,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2759.7Semi standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2934.9Standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3356.1Standard polar33892256
Uridine 2'-phosphate,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O2799.1Semi standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O2966.2Standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O3253.6Standard polar33892256
Uridine 2'-phosphate,4TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C2808.8Semi standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C2934.9Standard non polar33892256
Uridine 2'-phosphate,4TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C3203.5Standard polar33892256
Uridine 2'-phosphate,5TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2815.7Semi standard non polar33892256
Uridine 2'-phosphate,5TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2941.0Standard non polar33892256
Uridine 2'-phosphate,5TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3068.3Standard polar33892256
Uridine 2'-phosphate,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O)[C@@H]1O2912.7Semi standard non polar33892256
Uridine 2'-phosphate,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O)O2923.4Semi standard non polar33892256
Uridine 2'-phosphate,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OP(=O)(O)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)[NH]C1=O2997.0Semi standard non polar33892256
Uridine 2'-phosphate,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)N1C(=O)C=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OP(=O)(O)O)C1=O3002.1Semi standard non polar33892256
Uridine 2'-phosphate,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C(C)(C)C3062.7Semi standard non polar33892256
Uridine 2'-phosphate,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O3165.5Semi standard non polar33892256
Uridine 2'-phosphate,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O3198.4Semi standard non polar33892256
Uridine 2'-phosphate,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C(C)(C)C3160.7Semi standard non polar33892256
Uridine 2'-phosphate,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OP(=O)(O)O3202.3Semi standard non polar33892256
Uridine 2'-phosphate,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)[NH]C1=O)O[Si](C)(C)C(C)(C)C3181.0Semi standard non polar33892256
Uridine 2'-phosphate,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OP(=O)(O)O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O3254.3Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3323.0Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3495.8Standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3793.5Standard polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C(C)(C)C3384.5Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C(C)(C)C3553.0Standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O)[C@@H]1O[Si](C)(C)C(C)(C)C3888.1Standard polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O3350.4Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O3496.8Standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O3700.5Standard polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O3440.6Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O3515.2Standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O3781.6Standard polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3336.9Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3463.7Standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)[NH]C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3646.7Standard polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C(C)(C)C3439.4Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C(C)(C)C3483.7Standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OP(=O)(O)O[Si](C)(C)C(C)(C)C3725.9Standard polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O)O[Si](C)(C)C(C)(C)C3447.1Semi standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O)O[Si](C)(C)C(C)(C)C3476.2Standard non polar33892256
Uridine 2'-phosphate,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OP(=O)(O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=CC(=O)N([Si](C)(C)C(C)(C)C)C1=O)O[Si](C)(C)C(C)(C)C3627.3Standard polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3500.6Semi standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3608.5Standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)[NH]C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3569.4Standard polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3626.8Semi standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3643.9Standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3592.7Standard polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O3633.5Semi standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O3630.1Standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O3533.2Standard polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3640.0Semi standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3611.5Standard non polar33892256
Uridine 2'-phosphate,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@@H]1OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3484.2Standard polar33892256
Uridine 2'-phosphate,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3792.2Semi standard non polar33892256
Uridine 2'-phosphate,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3707.9Standard non polar33892256
Uridine 2'-phosphate,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](N2C=CC(=O)N([Si](C)(C)C(C)(C)C)C2=O)[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3458.3Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Uridine 2'-phosphate GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-9210000000-6afa45b4a6961e0453e62017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Uridine 2'-phosphate GC-MS (2 TMS) - 70eV, Positivesplash10-00dl-9151200000-e0a01229f4212ff7f3f92017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Uridine 2'-phosphate 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 - Uridine 2'-phosphate 10V, Positive-QTOFsplash10-03di-0910000000-b223591ac37bb4835a0d2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 20V, Positive-QTOFsplash10-03di-6900000000-c0c39b650ce0a7d36d992017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 40V, Positive-QTOFsplash10-03di-2900000000-42691e55ad6cc6b8dbeb2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 10V, Negative-QTOFsplash10-024l-9246000000-91f86f9f2ff06edbdce72017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 20V, Negative-QTOFsplash10-004l-9110000000-85bdfa2e17418427a71d2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 40V, Negative-QTOFsplash10-004i-9000000000-6595c14ab9ca671654472017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 10V, Negative-QTOFsplash10-00di-0009000000-f40929c86dd50c03a6f62021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 20V, Negative-QTOFsplash10-004i-9222000000-33657b40ac572e2680bb2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 40V, Negative-QTOFsplash10-004i-9220000000-622e70c66f0c8ba9cce62021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 10V, Positive-QTOFsplash10-03fr-0917000000-cdfeb50353311b6126082021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 20V, Positive-QTOFsplash10-03di-7902000000-a378bfa03abe7ffe4c782021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Uridine 2'-phosphate 40V, Positive-QTOFsplash10-03dr-9710000000-ca9fbb7e8c8b6d0610332021-09-23Wishart 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 LocationsNot Available
Biospecimen LocationsNot Available
Tissue Locations
  • Placenta
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 IDFDB028338
KNApSAcK IDNot Available
Chemspider ID91808
KEGG Compound IDC03031
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound101609
PDB IDNot Available
ChEBI ID28070
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Elshenawy S, Pinney SE, Stuart T, Doulias PT, Zura G, Parry S, Elovitz MA, Bennett MJ, Bansal A, Strauss JF 3rd, Ischiropoulos H, Simmons RA: The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth. Int J Mol Sci. 2020 Feb 4;21(3). pii: ijms21031043. doi: 10.3390/ijms21031043. [PubMed:32033212 ]

Enzymes

General function:
Involved in 2',3'-cyclic-nucleotide 3'-phosphodiesterase activity
Specific function:
May participate in RNA metabolism in the myelinating cell, CNP is the third most abundant protein in central nervous system myelin (By similarity).
Gene Name:
CNP
Uniprot ID:
P09543
Molecular weight:
47578.22