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15839-70-0 molecular structure
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[({[5-(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy][(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phosphinic acid

ChemBase ID: 133523
Molecular Formular: C16H25N5O15P2
Molecular Mass: 589.341722
Monoisotopic Mass: 589.08223839
SMILES and InChIs

SMILES:
CC1C(C(C(C(O1)OP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n1cnc2c1[nH]c(nc2=O)N)O)O)O)O)O
Canonical SMILES:
OC1C(COP(=O)(OP(=O)(OC2OC(C)C(C(C2O)O)O)O)O)OC(C1O)n1cnc2c1[nH]c(N)nc2=O
InChI:
InChI=1S/C16H25N5O15P2/c1-4-7(22)9(24)11(26)15(33-4)35-38(30,31)36-37(28,29)32-2-5-8(23)10(25)14(34-5)21-3-18-6-12(21)19-16(17)20-13(6)27/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H3,17,19,20,27)
InChIKey:
LQEBEXMHBLQMDB-UHFFFAOYSA-N

Cite this record

CBID:133523 http://www.chembase.cn/molecule-133523.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
[({[5-(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy][(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phosphinic acid
IUPAC Traditional name
{[5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphosphinic acid
Synonyms
6-Deoxy-β-L-galactopyranosylguanosine 5′-diphosphate
GDP-Fuc
GDP-fucose
Guanosine 5′-diphospho-β-L-fucose sodium salt
CAS Number
15839-70-0
MDL Number
MFCD00058553
PubChem SID
24895171
162227800
PubChem CID
451

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID Price
Sigma Aldrich
G4401 external link Add to cart Please log in.
Data Source Data ID
PubChem 451 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 1.7326082  H Acceptors 16 
H Donor LogD (pH = 5.5) -8.1417675 
LogD (pH = 7.4) -8.565294  Log P -3.7230635 
Molar Refractivity 116.5342 cm3 Polarizability 47.121407 Å3
Polar Surface Area 307.2 Å2 Rotatable Bonds
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
-20°C expand Show data source
Purity
≥85% expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - G4401 external link
Substrates
Substrate for fucosyltransferase
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. G4401.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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