Tebipenem

Tebipenem Basic information
Product Name:Tebipenem
Synonyms:Tebipenem;(4R,5S,6S)-3-[[1-(4,5-Dihydro-2-thiazolyl)-3-azetidinyl]thio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid;LJC 11036;LJC11036;LJC-11036;Tebipenem Impurity 5;(4R,5S,6S)-3-[1-(4,5-dihydro-1,3-thiazol-2-yl)azetidin-3-yl]sulfanyl-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid;1-Azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid, 3-[[1-(4,5-dihydro-2-thiazolyl)-3-azetidinyl]thio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-, (4R,5S,6S)-
CAS:161715-21-5
MF:C16H21N3O4S2
MW:383.49
EINECS:
Product Categories:API
Mol File:161715-21-5.mol
Tebipenem Structure
Tebipenem Chemical Properties
Boiling point 624.5±65.0 °C(Predicted)
density 1.75
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility insoluble in EtOH; ≥19.15 mg/mL in H2O with gentle warming; ≥24.9 mg/mL in DMSO
form solid
pka4.29±0.60(Predicted)
Safety Information
MSDS Information
Tebipenem Usage And Synthesis
Biological Activitytebipenem is an orally available carbapenem antibiotic. tebipenem is active against a panel of clinical isolates from a variety of bacterial species (mic50s ≤ 0.0039 ~ 8 μg/ml), including methicillin-resistant strains of staphylococcus aureus (s. aureus) and staphylococcus epidermidis (s. epidermidis), as well as penicillin-resistant streptococcus pneumoniae (s. pneumonia). tebipenem also inhibits β-lactamase in a time- and concentration-dependent manner. tebipenem pivoxil, a derivative of tebipenem, has been under development as the first orally available carbapenem antibiotic for the treatment of respiratory and otolaryngological infections caused by drug-resistant s. pneumonia in pediatric patients.1. hazra s, xu h, blanchard js. tebipenem, a new carbapenem antibiotic, is a slow substrate that inhibits the β-lactamase from mycobacterium tuberculosis. biochemistry, 2014, 53(22): 3671-3678.2. fujimoto k, takemoto k, hatano k, et al. novel carbapenem antibiotics for parenteral and oral applications: in vitro and in vivo activities of 2-aryl carbapenems and their pharmacokinetics in laboratory animals. antimicrobial agents and chemotherapy, 2013, 57(2): 697-707.
IBUTILIDE Lambrolizumab RCIMVZWCHLOZJH-RRCSTGOVSA-N 2,2'-[Dithiobis(3,1-azetidinediyl)]bis[4,5-dihydrothiazole] TEBIPENEM PIVOXIL Cefpirome sulfate

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