98510-71-5 Usage
Description
P-NITROBENZYL-6,6-DIBROMOPENICILLINATE is a chemical compound that is a derivative of penicillin, featuring a nitrobenzyl group and two bromine atoms attached to the penicillin molecule. This modification enhances its potential applications and effectiveness.
Uses
Used in Pharmaceutical Industry:
P-NITROBENZYL-6,6-DIBROMOPENICILLINATE is used as a potential antibiotic for inhibiting the growth of certain bacteria, showcasing its effectiveness in combating bacterial infections.
Used in Drug Delivery Systems:
P-NITROBENZYL-6,6-DIBROMOPENICILLINATE is utilized in the development of drug delivery systems to improve the administration and efficacy of the antibiotic, ensuring targeted delivery and optimized therapeutic outcomes.
Used in Research:
P-NITROBENZYL-6,6-DIBROMOPENICILLINATE serves as a valuable tool for studying penicillin-binding proteins, contributing to a deeper understanding of the mechanisms of action and resistance associated with penicillin-based antibiotics.
Check Digit Verification of cas no
The CAS Registry Mumber 98510-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,1 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 98510-71:
(7*9)+(6*8)+(5*5)+(4*1)+(3*0)+(2*7)+(1*1)=155
155 % 10 = 5
So 98510-71-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H14Br2N2O5S/c1-14(2)10(18-12(21)15(16,17)13(18)25-14)11(20)24-7-8-3-5-9(6-4-8)19(22)23/h3-6,10,13H,7H2,1-2H3
98510-71-5Relevant articles and documents
Synthesis and biological evaluation of penem inhibitors of bacterial signal peptidase
Harris, David A.,Powers, Michael E.,Romesberg, Floyd E.
scheme or table, p. 3787 - 3790 (2010/03/25)
We report the first synthesis of a 5S penem, known to bind bacterial type I signal peptidase, from the commercially available and inexpensive 6-aminopenicillanic acid. We report the first in vivo activity of the compound and use structure-activity relationship studies to begin to define the determinants of signal peptidase binding and also to begin to optimize the penem as an antibiotic.
Phase-transfer esterification of the alkali metal salts of cephalosporins and penicillins
Ganboa,Palomo
, p. 52 - 54 (2007/10/02)
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