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2-(methylthio)-5-(2-nitrophenyl)-1,3,4-thiadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51146-73-7

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51146-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51146-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,4 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51146-73:
(7*5)+(6*1)+(5*1)+(4*4)+(3*6)+(2*7)+(1*3)=97
97 % 10 = 7
So 51146-73-7 is a valid CAS Registry Number.

51146-73-7Relevant academic research and scientific papers

AMIDE DERIVATIVES AS SIRTUIN MODULATORS

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Page/Page column 92, (2009/06/27)

Provided herein are novel sirtuin-modulating compounds represented by Structural Formula (I) and methods of use thereof. The sirtuin-modulating compounds may be used for increasing the lifespan of a cell, and treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing as well as diseases or disorders that would benfit from increased mitochondrial activity. Also provided are compositions comprising a sirtuin- modulating compound in combination with another therapeutic agent.

Synthesis and antifungal activity of 2-aryl-1,3,4-thiadiazole-5-sulphides, sulphoxides and sulphones

Foroumadi,Daneshtalab,Mahmoudian,Falahati,Nateghian,Shahsavarani,Shafiee

, p. 95 - 98 (2007/10/03)

2-Aryl-1,3,4-thiadiazole-5-sulphides, sulphoxides and sulphones were synthesized and tested against a variety of fungal strains, Miconazole and fluconazole were used as reference drugs. The most active compounds against Candida albicans, Candida spp., Cryptococcus neoformans and Aspergillus niger were 2-(1-methyl-5-nitro-2-imidazolyl)-5-methylsulphonyl-1 ,3,4-thiadiazole (8h) and 2-(5-nitro-2-furyl)-5-methylsulphonyl-1,3,4-thiadiazole (8f). Our results showed that compounds 8h and 8f were several times more active than fluconazole in most fungal strains.

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