CHEBI:38655 - (S)-2-methylbutyric acid

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ChEBI Name (S)-2-methylbutyric acid ChEBI ID CHEBI:38655 ChEBI ASCII Name (S)-2-methylbutyric acid Definition The (S)-enantiomer of 2-methylbutanoic acid. 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 C5H10O2 Net Charge 0 Average Mass 102.13170 Monoisotopic Mass 102.06808 InChI InChI=1S/C5H10O2/c1-3-4(2)5(6)7/h4H,3H2,1-2H3,(H,6,7)/t4-/m0/s1 InChIKey WLAMNBDJUVNPJU-BYPYZUCNSA-N SMILES CC[C@H](C)C(O)=O Roles Classification Chemical Role(s): 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. (via 2-methylbutyric acid ) human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). (via 2-methylbutyric acid ) View more via ChEBI Ontology ChEBI Ontology Outgoing (S)-2-methylbutyric acid (CHEBI:38655) is a 2-methylbutyric acid (CHEBI:37070) (S)-2-methylbutyric acid (CHEBI:38655) is conjugate acid of (S)-2-methylbutanoate (CHEBI:145932) (S)-2-methylbutyric acid (CHEBI:38655) is enantiomer of (R)-2-methylbutyric acid (CHEBI:45525) Incoming (S)-2-methylbutanoyl-CoA (CHEBI:90222) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) egonol-2ʼʼʼ-methyl butanoate (CHEBI:69550) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) lovastatin (CHEBI:40303) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) mevinolinic acid (CHEBI:82985) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXI (CHEBI:67851) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXII (CHEBI:67852) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXIII (CHEBI:67853) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXIV (CHEBI:67854) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXIX (CHEBI:67859) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXVII (CHEBI:67857) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXVIII (CHEBI:67858) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pescaprein XXX (CHEBI:67860) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pravastatin (CHEBI:63618) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) pravastatin lactone (CHEBI:145933) has functional parent (S)-2-methylbutyric acid (CHEBI:38655) (S)-2-methylbutanoate (CHEBI:145932) is conjugate base of (S)-2-methylbutyric acid (CHEBI:38655) (R)-2-methylbutyric acid (CHEBI:45525) is enantiomer of (S)-2-methylbutyric acid (CHEBI:38655) IUPAC Name (2S)-2-methylbutanoic acid Synonyms Sources (S)-2-methylbutanoic acid NIST Chemistry WebBook (S)-α-methylbutanoic acid ChEBI Registry Numbers Types Sources 1720485 Beilstein Registry Number Beilstein 1730-91-2 CAS Registry Number ChemIDplus 1730-91-2 CAS Registry Number NIST Chemistry WebBook 3648078 Beilstein Registry Number Beilstein 532948 Gmelin Registry Number Gmelin Citation Type Source 2026560 PubMed citation Europe PMC Last Modified 05 November 2015