Glyceraldehyde 3-phosphate

Glyceraldehyde 3-phosphate
Names
	IUPAC name 2-hydroxy-3-oxopropyl dihydrogen phosphate
Identifiers
CAS Number	591-59-3 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	1725008
ChEBI	CHEBI:17138 ;
ChEMBL	ChEMBL1232918;
ChemSpider	709 (Racemic) ; 393755 (L isomer) ; 388314 (D isomer) ;
DrugBank	DB02263;
ECHA InfoCard	100.008.839
EC Number	209-721-7;
KEGG	C00661 ; C00118 ;
MeSH	Glyceraldehyde+3-Phosphate
PubChem CID	729;
UNII	7466PL1110 ;
CompTox Dashboard (EPA)	DTXSID40861814 ;
	InChI InChI=1S/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h1,3,5H,2H2,(H2,6,7,8) Key: LXJXRIRHZLFYRP-UHFFFAOYSA-N ; InChI=1/C3H7O6P/c4-1-3(5)2-9-10(6,7)8/h1,3,5H,2H2,(H2,6,7,8) Key: LXJXRIRHZLFYRP-UHFFFAOYAH;
	SMILES C([C@H](C=O)O)OP(=O)(O)O;
Properties
Chemical formula	C3H7O6P
Molar mass	170.058
Melting point	102–104 °C
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Glyceraldehyde 3-phosphate, also known as triose phosphate or 3-phosphoglyceraldehyde and abbreviated as G3P, GA3P, GADP, GAP, TP, GALP or PGAL, is a metabolite that occurs as an intermediate in several central pathways of all organisms.^[2]^[3] With the chemical formula H(O)CCH(OH)CH₂OPO₃^{^2-}, this anion is a monophosphate ester of glyceraldehyde.

^ "metabocard for Glycerol 3-phosphate".
^ Berg, Jeremy M.; Tymoczko, Stryer (2002). Biochemistry (5th ed.). New York: W.H. Freeman and Company. ISBN 0-7167-3051-0.
^ Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. ISBN 1-57259-153-6.

[hmdb-1] "metabocard for Glycerol 3-phosphate".

[2] Berg, Jeremy M.; Tymoczko, Stryer (2002). Biochemistry (5th ed.). New York: W.H. Freeman and Company. ISBN 0-7167-3051-0.

[3] Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. ISBN 1-57259-153-6.

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