CHEBI:85360 - L-dihydroanticapsin

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ChEBI Name L-dihydroanticapsin ChEBI ID CHEBI:85360 ChEBI ASCII Name L-dihydroanticapsin Definition An L-alanine derivative in which one of the methyl hydrogens of L-alanine is replaced by a 5-hydroxy-7-oxabicyclo[4.1.0]heptan-2-yl group. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C9H15NO4 Net Charge 0 Average Mass 201.21970 Monoisotopic Mass 201.10011 InChI InChI=1S/C9H15NO4/c10-5(9(12)13)3-4-1-2-6(11)8-7(4)14-8/h4-8,11H,1-3,10H2,(H,12,13)/t4-,5-,6+,7+,8-/m0/s1 InChIKey YMLXTGCTHGQQKS-TXXZRHAASA-N SMILES N[C@@H](C[C@@H]1CC[C@@H](O)[C@@H]2O[C@H]12)C(O)=O Metabolite of Species Details Bacillus subtilis (NCBI:txid1423) 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): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing L-dihydroanticapsin (CHEBI:85360) has role bacterial metabolite (CHEBI:76969) L-dihydroanticapsin (CHEBI:85360) is a L-alanine derivative (CHEBI:83943) L-dihydroanticapsin (CHEBI:85360) is a epoxide (CHEBI:32955) L-dihydroanticapsin (CHEBI:85360) is a non-proteinogenic L-α-amino acid (CHEBI:83822) L-dihydroanticapsin (CHEBI:85360) is a oxabicycloalkane (CHEBI:46733) L-dihydroanticapsin (CHEBI:85360) is a secondary alcohol (CHEBI:35681) L-dihydroanticapsin (CHEBI:85360) is tautomer of L-dihydroanticapsin zwitterion (CHEBI:84358) Incoming L-dihydroanticapsin zwitterion (CHEBI:84358) is tautomer of L-dihydroanticapsin (CHEBI:85360) IUPAC Name 3-[(1R,2S,5R,6S )-5-hydroxy-7-oxabicyclo[4.1.0]heptan-2-yl]-L-alanine Manual Xref Database CPD-17531 MetaCyc View more database links Registry Number Type Source 27406393 Reaxys Registry Number Reaxys Citation Type Source 23317005 PubMed citation Europe PMC Last Modified 31 March 2015