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Escherichia coli K-12 substr. MG1655 Compound: 7,8-dihydroneopterin

Synonyms: 2-amino-4-hydroxy-6-(D-erythro-1,2,3-trihydroxypropyl)-7,8-dihydropteridine, dihydroneopterin, 2-amino-4-hydroxy-6-(D-erythro)-trihydroxypropyldihydropteridin, dihydro-neo-pterin, DHN, 7,8-dihydro-D-neopterin

Superclasses: an organic heterocyclic compoundan organic heterobicyclic compounda pteridinea pterin
an organic heterocyclic compoundan organonitrogen heterocyclic compounda pteridinea pterin


Chemical Formula: C9H13N5O4

Molecular Weight: 255.23 Daltons

Monoisotopic Molecular Weight: 255.0967539317 Daltons

7,8-dihydroneopterin compound structure

SMILES: C1(NC2(N=C(N)NC(=O)C(N=C1C(O)C(O)CO)=2))

InChI: InChI=1S/C9H13N5O4/c10-9-13-7-5(8(18)14-9)12-3(1-11-7)6(17)4(16)2-15/h4,6,15-17H,1-2H2,(H4,10,11,13,14,18)/t4-,6+/m1/s1

InChIKey: InChIKey=YQIFAMYNGGOTFB-XINAWCOVSA-N

Unification Links: ChEBI:17001, ChemSpider:58584, DrugBank:DB04425, HMDB:HMDB02275, IAF1260:44772, KEGG:C04874, MetaboLights:MTBLC17001, PubChem:65074

Standard Gibbs Free Energy of Formation (ΔfG in kcal/mol): -114.21

Reactions known to consume the compound:

6-hydroxymethyl-dihydropterin diphosphate biosynthesis I :
7,8-dihydroneopterin → glycolaldehyde + 6-hydroxymethyl-7,8-dihydropterin

Reactions known to produce the compound:

6-hydroxymethyl-dihydropterin diphosphate biosynthesis I :
7,8-dihydroneopterin 3'-phosphate + H2O → 7,8-dihydroneopterin + phosphate

Reactions known to both consume and produce the compound:

Not in pathways:
7,8-dihydroneopterin ↔ 7,8-dihydromonapterin


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Please cite the following article in publications resulting from the use of EcoCyc: Nucleic Acids Research 41:D605-12 2013
Page generated by Pathway Tools version 19.5 (software by SRI International) on Sat Feb 13, 2016, biocyc13.