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.
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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 |
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