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({[({[(2S,3R,4R,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)(sulfanylidene)phosphonous acid
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ChemBase ID:
1634
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Molecular Formular:
C10H16N5O13P3S
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Molecular Mass:
539.246023
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Monoisotopic Mass:
538.96781649
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SMILES and InChIs
SMILES:
Nc1nc2c(ncn2[C@@H]2O[C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OP(=S)(O)O)[C@H](O)[C@H]2O)c(=O)[nH]1
Canonical SMILES:
O[C@H]1[C@H](CO[P@](=O)(O[P@@](=O)(OP(=S)(O)O)O)O)O[C@H]([C@@H]1O)n1cnc2c1nc(N)[nH]c2=O
InChI:
InChI=1S/C10H16N5O13P3S/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(26-9)1-25-29(19,20)27-30(21,22)28-31(23,24)32/h2-3,5-6,9,16-17H,1H2,(H,19,20)(H,21,22)(H2,23,24,32)(H3,11,13,14,18)/t3-,5-,6+,9+/m0/s1
InChIKey:
XOFLBQFBSOEHOG-BZKDHIKHSA-N
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Cite this record
CBID:1634 http://www.chembase.cn/molecule-1634.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
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IUPAC name
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({[({[(2S,3R,4R,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)(sulfanylidene)phosphonous acid
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IUPAC Traditional name
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({[(2S,3R,4R,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy(sulfanylidene)phosphonous acid
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Synonyms
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5'-Guanosine-Diphosphate-Monothiophosphate
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
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Data Source
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Data ID
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Price
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CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
ALOGPS 2.1
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Acid pKa
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0.8959188
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H Acceptors
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13
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H Donor
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8
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LogD (pH = 5.5)
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-9.715189
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LogD (pH = 7.4)
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-11.171269
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Log P
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-2.812619
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Molar Refractivity
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105.2307 cm3
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Polarizability
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41.63349 Å3
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Polar Surface Area
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277.74 Å2
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Rotatable Bonds
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8
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Lipinski's Rule of Five
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false
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Log P
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-0.24
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LOG S
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-1.83
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Solubility (Water)
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7.89e+00 g/l
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PROPERTIES
PROPERTIES
Bioassay(PubChem)
DETAILS
DETAILS
DrugBank
DrugBank -
DB01864
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Information |
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Drug Groups
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experimental |
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Description
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Guanosine 5'-(trihydrogen diphosphate), monoanhydride with phosphorothioic acid. A stable GTP analog which enjoys a variety of physiological actions such as stimulation of guanine nucleotide-binding proteins, phosphoinositide hydrolysis, cyclic AMP accumulation, and activation of specific proto-oncogenes. [PubChem] |
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PATENTS
PATENTS
PubChem Patent
Google Patent