furanomycin (CHEBI:79390)

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ChEBI Name	furanomycin

ChEBI ID	CHEBI:79390

Definition	A non-proteinogenic L-α-amino acid that is L-alanine in which the methyl group is replaced by a (2R,5S)-5-methyl-2,5-dihydrofuran-2-yl moiety.

Stars	This entity has been manually annotated by the ChEBI Team.

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Formula

C7H11NO3

Net Charge

Average Mass

157.16710

Monoisotopic Mass

157.07389

InChI

InChI=1S/C7H11NO3/c1-4-2-3-5(11-4)6(8)7(9)10/h2-6H,8H2,1H3,(H,9,10)/t4-,5+,6-/m0/s1

InChIKey

PNOKUGWGMLEAPE-JKUQZMGJSA-N

SMILES

C[C@@H]1O[C@H](C=C1)[C@H](N)C(O)=O

Metabolite of Species	Details
Pseudomonas fluorescens SBW25 (NCBI:txid216595)	of strain SBW25 See: PubMed
Streptomyces threomyceticus L-803 (NCBI:txidATCC 15795)	of strain L-803 See: PubMed

Roles Classification
Chemical Role(s):	Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid )

Biological Role(s):	antimicrobial agent A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans. bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. antibacterial agent A substance (or active part thereof) that kills or slows the growth of bacteria.

ChEBI Ontology
Outgoing	furanomycin (CHEBI:79390) has role antibacterial agent (CHEBI:33282) furanomycin (CHEBI:79390) has role antimicrobial agent (CHEBI:33281) furanomycin (CHEBI:79390) has role bacterial metabolite (CHEBI:76969) furanomycin (CHEBI:79390) is a dihydrofuran (CHEBI:51659) furanomycin (CHEBI:79390) is a non-proteinogenic L-α-amino acid (CHEBI:83822)

IUPAC Name

(2S)-amino[(2R,5S)-5-methyl-2,5-dihydrofuran-2-yl]acetic acid

Synonyms	Sources
(+)-furanomycin	ChEBI
(2S,2'R,5'S)-2-amino-2-(5'-methyl-2',5'-dihydrofuran-2'-yl)acetic acid	ChEBI
(6S)-2-amino-3,6-anhydro-2,4,5-trideoxy-6-methyl-D-threo-hex-4-enonic acid	IUPAC
L-(+)-furanomycin	ChEBI

Last Modified

26 March 2015