39860-12-3 Usage
General Description
1,5-dimethylbenzoimidazol-2-amine is a type of chemical compound that is also known as DMBA. It is an azo compound with a molecular formula C10H12N2. DMBA is an aromatic amine and has been used in various chemical and pharmaceutical applications. It is commonly used in the synthesis of dyes and pigments, as well as in the production of pharmaceutical drugs. DMBA is also known to exhibit certain biological activities, including anti-inflammatory and antimicrobial properties, making it a potentially important compound in the field of medicine and drug development. Overall, 1,5-dimethylbenzoimidazol-2-amine is a versatile chemical with various uses and potential biomedical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 39860-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,6 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39860-12:
(7*3)+(6*9)+(5*8)+(4*6)+(3*0)+(2*1)+(1*2)=143
143 % 10 = 3
So 39860-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N3/c1-6-3-4-8-7(5-6)11-9(10)12(8)2/h3-5H,1-2H3,(H2,10,11)
39860-12-3Relevant articles and documents
Discovery of 2-iminobenzimidazoles as potent hepatitis C virus inhibitors with a novel mechanism of action
Windisch, Marc Peter,Jo, Suyeon,Kim, Hee-Young,Kim, Soo-Hyun,Kim, Keumhyun,Kong, Sunju,Jeong, Hyangsuk,Ahn, Sujin,No, Zaesung,Hwang, Jong Yeon
, p. 35 - 42 (2014/04/17)
In this report we describe 2-iminobenzimidazole (IBI) analogs, identified during the course of a phenotypic high-throughput screening campaign, as novel hepatitis C virus (HCV) inhibitors. A series of IBI derivatives was synthesized and evaluated for their inhibitory activity against infectious HCV. Among the IBIs derivatives studied in this work, we identified promising compounds with high antiviral efficacy, high selectivity index and good microsomal stability. Noteworthy, the IBI series exhibited inhibitory activity on early and late steps of the viral cycle, but not in the HCV replicon system demonstrating a mechanism of action distinct from clinical-stage and approved anti-HCV drugs. Overall, our results suggest that IBIs are predestinated for further exploration as lead compounds for novel HCV interventions.