Tebipenem pivoxil hydrochloride

Modify Date: 2024-04-02 19:33:42

Tebipenem pivoxil hydrochloride Structure
Tebipenem pivoxil hydrochloride structure
Common Name Tebipenem pivoxil hydrochloride
CAS Number 211558-19-9 Molecular Weight 534.09
Density N/A Boiling Point N/A
Molecular Formula C22H32ClN3O6S2 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Tebipenem pivoxil hydrochloride


Tebipenem pivoxil (L084) hydrochloride is an orally active antibiotic against a variety of pathogenic bacteria. Tebipenem pivoxil hydrochloride binds penicillin-binding protein (PBP), thereby inhibiting cell wall synthesis[1].

 Names

Name Tebipenem pivoxil hydrochloride

 Tebipenem pivoxil hydrochloride Biological Activity

Description Tebipenem pivoxil (L084) hydrochloride is an orally active antibiotic against a variety of pathogenic bacteria. Tebipenem pivoxil hydrochloride binds penicillin-binding protein (PBP), thereby inhibiting cell wall synthesis[1].
Related Catalog
In Vitro Tebipenem pivoxil hydrochloride (0-128 μg/mL, 18–24 h) displays excellent antibacterial activity against a variety of pathogenic bacteria[1]. Cell Viability Assay[1] Cell Line: Gram-positive and Gram-negative bacteria Concentration: 0-128 μg/mL Incubation Time: 18–24 h Result: Showed inhibition with MIC50s below 64 μg/mL against tested Gram-positive and Gram-negative bacteria.
In Vivo Tebipenem pivoxil (L084) (0-4.00 g/kg; p.o.; once) hydrochloride shows minimal lethal dosage (MLD) of 4.00 g/kg and the maximum tolerance dosage (MTD) of 3.40 g/kg in mice[1]. Tebipenem pivoxil (50 and 100 mg/kg; p.o.; once) hydrochloride significantly protects the sepsis mice challenged with various pathogenic bacteria[1]. Animal Model: KM mice weighing 18–22 g[1] Dosage: 2.89, 3.40 and 4.00 g/kg Administration: Oral administration (tablet), once Result: Within the 14-day observation period, only one mouse was dead in the maximum oral dosage (4.00 g/kg). The minimal lethal dosage (MLD) was 4.00 g/kg and the maximum tolerance dosage (MTD) in the mice was 3.40 g/kg. Showed dose-dependent liver and kidney damage. Animal Model: ICR mice, sepsis mouse models[1] Dosage: 50 and 100 mg/kg Administration: Oral administration (tablet), once Result: Significantly increased the survival number of the sepsis mice within a 168 h observation period.
References

[1]. Yao Q, et al. Antibacterial Properties of Tebipenem Pivoxil Tablet, a New Oral Carbapenem Preparation against a Variety of Pathogenic Bacteria in Vitro and in Vivo. Molecules. 2016 Jan 6;21(1):62.

 Chemical & Physical Properties

Molecular Formula C22H32ClN3O6S2
Molecular Weight 534.09