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Molecule
ID:131800
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₄N₃O₇P
Molecular Mass
307.197121
Exact Mass
307.05693643
Charge
0
InChI
InChI=1S/C9H14N3O7P/c10-7-1-2-12(9(14)11-7)8-3-5(6(4-13)18-8)19-20(15,16)17/h1-2,5-6,8,13H,3-4H2,(H2,10,11,14)(H2,15,16,17)
InChIKey
FVSAHFFHPOLBLL-UHFFFAOYSA-N
Canonic Smiles
OCC1OC(CC1OP(=O)(O)O)n1ccc(nc1=O)N
Isomeric Smiles
c1cn(c(=O)nc1N)C1CC(C(O1)CO)OP(=O)(O)O
Calculated Properties
JChem
Acid pKa
1.1573411
H Acceptors
8
H Donor
4
LogD (pH = 5.5)
-4.485237
LogD (pH = 7.4)
-5.6634254
Log P
-2.3395295
Molar Refractivity
63.907
Polarizability
25.347824
Polar Surface Area
154.91
Rotatable Bonds
4
Lipinski's Rule of Five
true
Data Source
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
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IUPAC name
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IUPAC Traditional name
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PubChem CID
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PubChem SID
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From Data Sources
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Data Source
Commercial Catalog
Sigma Aldrich
D2134
Academic Data
PubChem
3274948
Names and Identifiers
IUPAC name
{[5-(4-amino-2-oxo-1,2-dihydropyrimidin-1-yl)-2-(hydroxymethyl)oxolan-3-yl]oxy}phosphonic acid
IUPAC Traditional name
[5-(4-amino-2-oxopyrimidin-1-yl)-2-(hydroxymethyl)oxolan-3-yl]oxyphosphonic acid
Synonyms
2′-Deoxycytidine 3′-monophosphate
Registration numbers
CAS Number
6220-63-9
MDL Number
MFCD00070165
PubChem CID
3274948
PubChem SID
162226077
Properties
Safety Information
German water hazard class
3
Source
Storage Temperature
-20°C
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay