CARBENICILLIN

Carbenicillin is a penicillin antibiotic effective against gram‑negative bacteria. Side effects include rash, diarrhea, and hypersensitivity.

SKU: f98644411dde Category: Tag:

Product Description


Mechanism of action

Carbenicillin is a broad‑spectrum β‑lactam antibiotic belonging to the carboxypenicillin class. It inhibits bacterial cell‑wall synthesis by binding to penicillin‑binding proteins (PBPs), preventing crosslinking of peptidoglycan layers. It is particularly active against *Pseudomonas* species and gram‑negative rods.

Benefits and advantages

Used in antibacterial‑mechanism research, PBP‑binding assays, β‑lactam resistance studies, gram‑negative metabolism modelling, biofilm‑formation studies and comparative β‑lactam SAR research.

Side effects and risks

Risks include hypersensitivity reactions, bleeding tendencies (platelet dysfunction), electrolyte disturbances due to sodium load, and nephrotoxicity. Handle with antimicrobial compound safety precautions.

Datasheet


Molecular Formula

C17H18N2O6S

Molecular Weight

378.4 g/mol

CAS Number

428863-50-7

Storage Condition

Carbenicillin indanyl sodium tablets should be protected from moisture and stored in tight containers at a temperature not exceeding 30 °C. /Carbenicillin indanyl sodium/

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

carbenicillin; Carboxybenzylpenicillin; 4697-36-3; Carbenicilina; Carbenicilline

IUPAC/Chemical Name

(2S,5R,6R)-6-[(2-carboxy-2-phenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid

InChl Key

FPPNZSSZRUTDAP-UWFZAAFLSA-N

InChl Code

InChI=1S/C17H18N2O6S/c1-17(2)11(16(24)25)19-13(21)10(14(19)26-17)18-12(20)9(15(22)23)8-6-4-3-5-7-8/h3-7,9-11,14H,1-2H3,(H,18,20)(H,22,23)(H,24,25)/t9?,10-,11+,14-/m1/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/20824;

3D Conformer.

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