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443661-76-5

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443661-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 443661-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,6,6 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 443661-76:
(8*4)+(7*4)+(6*3)+(5*6)+(4*6)+(3*1)+(2*7)+(1*6)=155
155 % 10 = 5
So 443661-76-5 is a valid CAS Registry Number.

443661-76-5Downstream Products

443661-76-5Relevant academic research and scientific papers

Synthesis, semipreparative HPLC separation, biological evaluation, and 3D-QSAR of hydrazothiazole derivatives as human monoamine oxidase B inhibitors

Chimenti, Franco,Secci, Daniela,Bolasco, Adriana,Chimenti, Paola,Granese, Arianna,Carradori, Simone,MacCioni, Elias,Cardia, M. Cristina,Yanez, Matilde,Orallo, Francisco,Alcaro, Stefano,Ortuso, Francesco,Cirilli, Roberto,Ferretti, Rosella,Distinto, Simona,Kirchmair, Johannes,Langer, Thierry

, p. 5063 - 5070 (2010)

The present study reports on synthesis in high yields (70-99%), HPLC enantioseparation, inhibitory activity against human monoamino oxidases, and molecular modeling including 3D-QSAR studies, of a large series of (4-aryl-thiazol-2-yl)hydrazones (1-45). Most of the synthesized compounds proved to be potent and selective inhibitors of hMAO-B isoform in the micromolar or nanomolar range, thus demonstrating that hydrazothiazole could be considered a good pharmacophore to design new hMAO-B inhibitors. Due to the presence in some derivatives of a chiral center, we also performed a semipreparative chromatographic enantioseparation of these compounds obtained by a stereoconservative pattern. The separated enantiomers were submitted to in vitro biological evaluation to point out the stereorecognition of the active site of the enzyme towards these structures. Finally, a 3D-QSAR study was carried out using Comparative Molecular Field Analysis (CoMFA), aiming to deduce rational guidelines for the further structural modification of these lead compounds.

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