CLAVULANIC ACID

Clavulanic acid is a lactamase inhibitor protecting companion antibiotics from enzymatic degradation. Side effects include GI upset, rash, and rare liver disturbances. Only GMP materials will be supplied, logistics all according to GDP.

SKU: f8358751bee4 Category: Tag:

Product Description


Mechanism of Action

Clavulanic acid is a lactamase inhibitor structurally related to penicillins but possessing minimal intrinsic antibacterial activity. It covalently binds serine lactamases, generating inactive acylenzyme intermediates. It restores activity of lactam antibiotics against resistant organisms producing TEM, SHV and certain ESBL-type enzymes.

Benefits and Advantages

Used in inhibitorresistance research, lactamase structural studies, combinationdrug PK/PD modelling, synergy evaluation and enzymemechanism profiling of serinehydrolase inhibition.

Side Effects and Risks

Risks include GI discomfort, hypersensitivity, hepatic dysfunction and rash. Handle with lactamaseinhibitor precautions.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C8H9NO5

Molecular Weight

199.16 g/mol

CAS Number

58001-44-8

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

3.37e+02 g/L

Purity

Purity information is available upon request (COA).

Synonym

CLAVULANIC ACID; 58001-44-8; Acido clavulanico; Acide clavulanique; Clavulansaeure

IUPAC/Chemical Name

(2R,3Z,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

InChl Key

HZZVJAQRINQKSD-PBFISZAISA-N

InChl Code

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

References

https://pubchem.ncbi.nlm.nih.gov/compound/5280980;

3D Conformer.

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