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1,2,4-Triazolidine-3-thione, 5-methyl-2,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39263-76-8

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39263-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39263-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,6 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39263-76:
(7*3)+(6*9)+(5*2)+(4*6)+(3*3)+(2*7)+(1*6)=138
138 % 10 = 8
So 39263-76-8 is a valid CAS Registry Number.

39263-76-8Relevant academic research and scientific papers

1,2,4-TRIAZOLIDINE-3-THIONE DERIVATIVES AND USES THEREOF

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Page/Page column 34; 49, (2018/03/09)

The present invention relates to 1,2,4-triazolidine-3-thione compounds, compositions, and methods for the treatment or prevention of bacterial infections (for example, bacterial infections due to Acinetobacter).

1,2,4-Triazolidine-3-thiones as narrow spectrum antibiotics against multidrug-resistant acinetobacter baumannii

Huggins, William M.,Minrovic, Bradley M.,Corey, Brendan W.,Jacobs, Anna C.,Melander, Roberta J.,Sommer, Roger D.,Zurawski, Daniel V.,Melander, Christian

supporting information, p. 27 - 31 (2017/12/12)

With only two new classes of antibiotics developed in the last 40 years, novel antibiotics are desperately needed to combat the growing problem of multidrug-resistant and extensively drug resistant bacteria, particularly Gram-negative bacteria. Described in this letter is the synthesis and antibiotic activity of 1,2,4-triazolidine-3-thiones as narrow spectrum antibiotics. Optimization of the 1,2,4-triazolidine-3-thione scaffold identified a small molecule with potent antibiotic activity against multiple strains of multidrug-resistant and extensively drug-resistant Acinetobacter baumannii. This small molecule also shows single dose, in vivo activity in a Galleria mellonella infection model with A. baumannii and represents a promising start in the development of a class of drugs that can target this bacterial pathogen.

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