G6Q

GLUCOSE-6-PHOSPHATE

Created:	2001-09-14
Last modified:	2011-06-04

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22 entries where G6Q is found as a standalone ligand1 entries where G6Q is covalently linked to polymer or other heterogen groups

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Chemical Details
Formal Charge	0
Atom Count	29
Chiral Atom Count	4
Bond Count	28
Aromatic Bond Count	0

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Chemical Component Summary
Name	GLUCOSE-6-PHOSPHATE
Systematic Name (OpenEye OEToolkits)	[(2R,3R,4S,5R)-2,3,4,5-tetrahydroxy-6-oxo-hexyl] dihydrogen phosphate
Formula	C₆ H₁₃ O₉ P
Molecular Weight	260.136
Type	NON-POLYMER

Chemical Descriptors
Type	Program	Version	Descriptor
SMILES	ACDLabs	10.04	O=P(O)(O)OCC(O)C(O)C(O)C(O)C=O
SMILES	CACTVS	3.341	O[CH](CO[P](O)(O)=O)[CH](O)[CH](O)[CH](O)C=O
SMILES	OpenEye OEToolkits	1.5.0	C(C(C(C(C(C=O)O)O)O)O)OP(=O)(O)O
Canonical SMILES	CACTVS	3.341	O[C@H](CO[P](O)(O)=O)[C@@H](O)[C@H](O)[C@@H](O)C=O
Canonical SMILES	OpenEye OEToolkits	1.5.0	C([C@H]([C@H]([C@@H]([C@H](C=O)O)O)O)O)OP(=O)(O)O
InChI	InChI	1.03	InChI=1S/C6H13O9P/c7-1-3(8)5(10)6(11)4(9)2-15-16(12,13)14/h1,3-6,8-11H,2H2,(H2,12,13,14)/t3-,4+,5+,6+/m0/s1
InChIKey	InChI	1.03	VFRROHXSMXFLSN-SLPGGIOYSA-N

Drug Info: DrugBank

DrugBank ID	DB03581
Name	Glucose-6-Phosphate
Groups	experimental
Description	An ester of glucose with phosphoric acid, made in the course of glucose metabolism by mammalian and other cells. It is a normal constituent of resting muscle and probably is in constant equilibrium with fructose-6-phosphate. (Stedman, 26th ed)
Synonyms	Glucose-6-Phosphate
Categories	Carbohydrates Glucosephosphates Hexosephosphates Sugar Phosphates
CAS number	56-73-5

Drug Targets

Name	Target Sequence	Pharmacological Action	Actions
Glutamine--fructose-6-phosphate aminotransferase [isomerizing]	MCGIVGAIAQRDVAEILLEGLRRLEYRGYDSAGLAVVDAEGHMTRLRRLG...	unknown
Glucose-6-phosphate isomerase	MAALTRDPQFQKLQQWYREHRSELNLRRLFDANKDRFNHFSLTLNTNHGH...	unknown
Solute carrier organic anion transporter family member 2A1	MGLLPKLGASQGSDTSTSRAGRCARSVFGNIKVFVLCQGLLQLCQLLYSA...	unknown	inhibitor

Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682