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(Z)-N-(2-chlorophenyl)-2-(2-oxoindolin-3-ylidene)hydrazinecarbothioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

380577-78-6

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380577-78-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 380577-78-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,5,7 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 380577-78:
(8*3)+(7*8)+(6*0)+(5*5)+(4*7)+(3*7)+(2*7)+(1*8)=176
176 % 10 = 6
So 380577-78-6 is a valid CAS Registry Number.

380577-78-6Downstream Products

380577-78-6Relevant academic research and scientific papers

THIOSEMICARBAZONES WITH MDR1 - INVERSE ACTIVITY

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Page/Page column 45, (2012/03/27)

Disclosed herein are drug compounds that have MDR-inverse activity and thus are effective against multidrug-resistant cells. Exemplary compounds disclosed herein have the structure;Formula (I). Examples of the disclosed compounds have been found to have,

Isatin-β-thiosemicarbazones as potent herpes simplex virus inhibitors

Kang, Iou-Jiun,Wang, Li-Wen,Hsu, Tsu-An,Yueh, Andrew,Lee, Chung-Chi,Lee, Yen-Chun,Lee, Ching-Yin,Chao, Yu-Sheng,Shih, Shin-Ru,Chern, Jyh-Haur

, p. 1948 - 1952 (2011/05/04)

A series of isatin-β-thiosemicarbazones have been designed and evaluated for antiviral activity against herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) in a plaque reduction assay. Their cytotoxicity was examined using human rhabdomyosarcoma cells (RD cells). Several derivatives of isatin-β-thiosemicarbazone exhibited significant and selective antiviral activity with low cytotoxicity. It was found that the thiourea group at thiosemicarbazone and the NH functionality at isatin were essential for their antiherpetic activity. The synthesis and structure-activity relationship studies are presented.

Synthesis and structure-activity evaluation of isatin-β- thiosemicarbazones with improved selective activity toward multidrug-resistant cells expressing P-glycoprotein

Hall, Matthew D.,Brimacombe, Kyle R.,Varonka, Matthew S.,Pluchino, Kristen M.,Monda, Julie K.,Li, Jiayang,Walsh, Martin J.,Boxer, Matthew B.,Warren, Timothy H.,Fales, Henry M.,Gottesman, Michael M.

experimental part, p. 5878 - 5889 (2011/10/08)

Cancer multidrug resistance (MDR) mediated by ATP-binding cassette (ABC) transporters presents a significant unresolved clinical challenge. One strategy to resolve MDR is to develop compounds that selectively kill cells overexpressing the efflux transport

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