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Clavulanic acid

RX-10100
Clavulanic acid
Molecular structure via molpic based on CDK
Rotamer
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Conformer structure via 3Dmol.js
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Physical properties
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199.16 g/mol [1]
Melting point117.5-118 [1]
Solubility3.37e+02 g/L [1]
-1.2 [1]
Structural Identifiers
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C8H9NO5 [1]
(2R,3Z,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid [1]
C1[C@@H]2N(C1=O)[C@H](/C(=C/CO)/O2)C(=O)O [1]
InChI=1S/C8H9NO5/c10-2-1-4-7(8(12)13)9-5(11)3-6(9)14-4/h1,6-7,10H,2-3H2,(H,12,13)/b4-1-/t6-,7-/m1/s1 [1]
InChIKeyHZZVJAQRINQKSD-PBFISZAISA-N [1]
Pharmacokinetics[]
Elimination half-life0.8 – 1.2 hours

(Redirected from Clavulanic acid)

Clavulanic acid (also known as Clavulanic Acid, Acido clavulanico, Acide clavulanique, Antibiotic MM 14151, acidum clavulanicum, Clavulansaeure, MM 14151, BRL-14151, Serdaxin or BRL 14151) is a antibiotic substance of the amine class.

Chemistry

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Clavulanic acid is a absolute mixture.

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  • Australia: Clavulanic acid is a Schedule 4 substance.

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 5280980, Clavulanic acid. Accessed October 16, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/5280980

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Clavulanic acid. UNII: 23521W1S24. Global Substance Registration System. Accessed October 16, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/23521W1S24