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tert-butyl (6R,7R)-7-(2-((tert-butoxycarbonyl)amino)-2-phenylacetamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo-[4.2.0]oct-2-ene-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34632-03-6

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34632-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34632-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,3 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34632-03:
(7*3)+(6*4)+(5*6)+(4*3)+(3*2)+(2*0)+(1*3)=96
96 % 10 = 6
So 34632-03-6 is a valid CAS Registry Number.

34632-03-6Relevant academic research and scientific papers

A Synthetic Dual Drug Sideromycin Induces Gram-Negative Bacteria to Commit Suicide with a Gram-Positive Antibiotic

Liu, Rui,Miller, Patricia A.,Vakulenko, Sergei B.,Stewart, Nichole K.,Boggess, William C.,Miller, Marvin J.

, p. 3845 - 3854 (2018)

Many antibiotics lack activity against Gram-negative bacteria because they cannot permeate the outer membrane or suffer from efflux and, in the case of β-lactams, are degraded by β-lactamases. Herein, we describe the synthesis and studies of a dual drug conjugate (1) of a siderophore linked to a cephalosporin with an attached oxazolidinone. The cephalosporin component of 1 is rapidly hydrolyzed by purified ADC-1 β-lactamase to release the oxazolidinone. Conjugate 1 is active against clinical isolates of Acinetobacter baumannii as well as strains producing large amounts of ADC-1 β-lactamase. Overall, the results are consistent with siderophore-mediated active uptake, inherent activity of the delivered dual drug, and in the presence of β-lactamases, intracellular release of the oxazolidinone upon cleavage of the cephalosporin to allow the freed oxazolidinone to inactivate its target. The ultimate result demonstrates that Gram-positive oxazolidinone antibiotics can be made to be effective against Gram-negative bacteria by β-lactamase triggered release.

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