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N-(4-methoxyphenyl)benzisothiazol-3-one-2-amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1423967-86-5

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1423967-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423967-86-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,9,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1423967-86:
(9*1)+(8*4)+(7*2)+(6*3)+(5*9)+(4*6)+(3*7)+(2*8)+(1*6)=185
185 % 10 = 5
So 1423967-86-5 is a valid CAS Registry Number.

1423967-86-5Downstream Products

1423967-86-5Relevant articles and documents

With Caspase - 3 inhibitory activity of benzisothiazole - 3 - one - 2 - amide compounds

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Paragraph 0107; 0112-0114, (2018/11/04)

The invention relates to a benzisothiazole-3-ketone-2-amide compound with Caspase-3 inhibiting activity. The benzisothiazole-3-ketone-2-amide compound has the Caspase-3 inhibiting activity, can be used for treating diseases mediated by Caspase-3, belongs to the field of pharmaceutical chemistry, and has a structural formula (I) as shown in the specification.

Design, synthesis and evaluation of 1,2-benzisothiazol-3-one derivatives as potent caspase-3 inhibitors

Liu, Dazhi,Tian, Zhen,Yan, Zhihui,Wu, Lixin,Ma, Yan,Wang, Quan,Liu, Wei,Zhou, Honggang,Yang, Cheng

, p. 2960 - 2967 (2013/07/28)

A number of 1,2-benzisothiazol-3-one derivatives were prepared through structural modification of the original compound from high-throughput screening. Some analogues (e.g., 6b, 6r, 6s and 6w) were identified as novel and potent caspase inhibitors with IC50 of nanomolar. Structure-activity relationship (SAR) studies for caspase-3 inhibition were evaluated in vitro. Molecular modeling studies provided further insight into the interaction of this class of compounds with activated caspase-3. The present small molecule caspase-3 inhibitor with novel structures different from structures of known caspase inhibitors revealed a new direction for therapeutic strategies directed against diseases involving abnormally up-regulated apoptosis.

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