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1H-Indole-2,3-dione, 1-(4-hydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

683276-76-8

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683276-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 683276-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,3,2,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 683276-76:
(8*6)+(7*8)+(6*3)+(5*2)+(4*7)+(3*6)+(2*7)+(1*6)=198
198 % 10 = 8
So 683276-76-8 is a valid CAS Registry Number.

683276-76-8Relevant academic research and scientific papers

Hydrophobic substituents on isatin derivatives enhance their inhibition against bacterial peptidoglycan glycosyltransferase activity

Chan, Kin-Fai,Chen, Yu Wai,Cheong, Wing-Lam,Liang, Zhiguang,So, Lok-Yan,So, Pui-Kin,Wang, Yong,Wong, Kwok-Yin,Wong, Wing-Leung

, (2020)

Moenomycin A, the well-known natural product inhibitor of peptidoglycan glycosyltransferase (PGT), is a large amphiphilic molecule of molecular mass of 1583 g/mol and its bioavailablity as a drug is relatively poor. In searching for small-molecule ligands

SSAO INHIBITOR

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Paragraph 0154; 0155; 0158; 0300; 0301; 0303, (2020/04/02)

The present invention provides an SSAO inhibitor and an application thereof in preparing a drug for treating a disease related to SSAO. In particular, the present invention provides a compound shown in formula (IV) and a pharmaceutically acceptable salt thereof.

3-IMINO-2-INDOLONES FOR THE TREATMENT OF DEPRESSION AND/OR ANXIETY

-

, (2008/06/13)

This invention is directed to indolone derivatives which are selective antagonists for the GalR3 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutica

3-Imino-2-indolones for the treatement of depression and/or anxiety

-

, (2010/02/06)

This invention is directed to indolone derivatives which are selective antagonists for the GalR3 receptor. The invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of the invention and a pharmaceutica

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