CHEBI:16048 - FMNH2

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ChEBI Name FMNH2
ChEBI ID CHEBI:16048
ChEBI ASCII Name FMNH2
Definition The reduced 1,5-dihydro form of flavin mononucleotide.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:42517, CHEBI:15017, CHEBI:21128, CHEBI:13318, CHEBI:8782
Supplier Information
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Formula C17H23N4O9P
Net Charge 0
Average Mass 458.35984
Monoisotopic Mass 458.120
InChI InChI=1S/C17H23N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,18,22-24H,5-6H2,1-2H3,(H2,27,28,29)(H2,19,20,25,26)/t11-,12+,14-/m0/s1
InChIKey YTNIXZGTHTVJBW-SCRDCRAPSA-N
SMILES Cc1cc2Nc3c([nH]c(=O)[nH]c3=O)N(C[C@H](O)[C@H](O)[C@H](O)COP(O)(O)=O)c2cc1C
Metabolite of Species Details
Escherichia coli (NCBI:562) See: PubMed
Roles Classification
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
cofactor
An organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
(via flavin mononucleotide )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing FMNH2 (CHEBI:16048) has role Escherichia coli metabolite (CHEBI:76971)
FMNH2 (CHEBI:16048) is a flavin mononucleotide (CHEBI:24041)
FMNH2 (CHEBI:16048) is conjugate acid of FMNH2(2−) (CHEBI:57618)
FMNH2 (CHEBI:16048) is conjugate acid of FMNH2(3−) (CHEBI:133886)
Incoming prenyl-FMNH2 (CHEBI:87531) has functional parent FMNH2 (CHEBI:16048)
FMNH2(2−) (CHEBI:57618) is conjugate base of FMNH2 (CHEBI:16048)
FMNH2(3−) (CHEBI:133886) is conjugate base of FMNH2 (CHEBI:16048)
IUPAC Name
1-deoxy-1-(7,8-dimethyl-2,4-dioxo-1,3,4,5-tetrahydrobenzo[g]pteridin-10(2H)-yl)-5-O-phosphono-D-ribitol
Synonyms Sources
1,5-dihydroriboflavin 5'-(dihydrogen phosphate) ChemIDplus
flavin mononucleotide (reduced) ChEBI
FMNH HMDB
FMNH2 KEGG COMPOUND
Reduced FMN KEGG COMPOUND
Database Links Databases
C01847 KEGG COMPOUND
FMNH2 MetaCyc
HMDB0001142 HMDB
MOL000044 COMe
View more database links
Registry Numbers Types Sources
1234695 Beilstein Registry Number Beilstein
1234695 Reaxys Registry Number Reaxys
5666-16-0 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
22770225 PubMed citation Europe PMC
Last Modified
06 March 2017