(1R,5S,6S)-6-[1(R)-Hydroxyethyl]-1-methyl-2-[1-(2-thiazolin-2-yl)azetidin-3-ylsulfanyl]-1-carba-2-penem-3-carboxylic acid pivaloyloxymethyl ester

99%

Reagent Code: #50670
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CAS Number 161715-24-8

science Other reagents with same CAS 161715-24-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 496.64 g/mol
Formula C₂₃H₃₂N₂O₆S₂
badge Registry Numbers
EC Number 1308068-626-2
MDL Number MFCD17215369
thermostat Physical Properties
Melting Point 140-142℃
Boiling Point 661.9ºC at 760mmHg
inventory_2 Storage & Handling
Density 1.5g/cm3
Storage room temperature

description Product Description

This compound is the pivaloyloxymethyl ester prodrug of a carbapenem antibiotic, primarily utilized in the development of advanced oral antibiotics for treating bacterial infections resistant to conventional treatments. Upon hydrolysis in vivo, the active form effectively inhibits bacterial cell wall synthesis, acting as a potent agent against a wide range of gram-positive and gram-negative bacteria. It is explored in pharmaceutical research to enhance the efficacy and stability of carbapenem antibiotics, with the ester form specifically designed to improve oral bioavailability, making it suitable for oral formulations. Research continues to optimize its pharmacokinetic properties and minimize side effects for more effective, patient-friendly antibacterial therapies, particularly for community-acquired infections.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance white to beige powder
Purity 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿55,990.00
5mg
10-20 days ฿5,410.00
25mg
10-20 days ฿18,990.00
(1R,5S,6S)-6-[1(R)-Hydroxyethyl]-1-methyl-2-[1-(2-thiazolin-2-yl)azetidin-3-ylsulfanyl]-1-carba-2-penem-3-carboxylic acid pivaloyloxymethyl ester
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This compound is the pivaloyloxymethyl ester prodrug of a carbapenem antibiotic, primarily utilized in the development of advanced oral antibiotics for treating bacterial infections resistant to conventional treatments. Upon hydrolysis in vivo, the active form effectively inhibits bacterial cell wall synthesis, acting as a potent agent against a wide range of gram-positive and gram-negative bacteria. It is explored in pharmaceutical research to enhance the efficacy and stability of carbapenem antibiotics

This compound is the pivaloyloxymethyl ester prodrug of a carbapenem antibiotic, primarily utilized in the development of advanced oral antibiotics for treating bacterial infections resistant to conventional treatments. Upon hydrolysis in vivo, the active form effectively inhibits bacterial cell wall synthesis, acting as a potent agent against a wide range of gram-positive and gram-negative bacteria. It is explored in pharmaceutical research to enhance the efficacy and stability of carbapenem antibiotics, with the ester form specifically designed to improve oral bioavailability, making it suitable for oral formulations. Research continues to optimize its pharmacokinetic properties and minimize side effects for more effective, patient-friendly antibacterial therapies, particularly for community-acquired infections.

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