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3-[(2E)-3-(4-acetoxy-3-methoxyphenyl)prop-2-enoyl]-1,3-bis[2-chloro-4-nitrophenyl]triazene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1600526-99-5

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1600526-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1600526-99-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,0,5,2 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1600526-99:
(9*1)+(8*6)+(7*0)+(6*0)+(5*5)+(4*2)+(3*6)+(2*9)+(1*9)=135
135 % 10 = 5
So 1600526-99-5 is a valid CAS Registry Number.

1600526-99-5Downstream Products

1600526-99-5Relevant academic research and scientific papers

Anti-mycobacterial activity of 1,3-diaryltriazenes

Cappoen, Davie,Vajs, Jure,Uythethofken, Cynthia,Virag, Andrej,Mathys, Vanessa,Ko?evar, Marijan,Verschaeve, Luc,Gazvoda, Martin,Polanc, Slovenko,Huygen, Kris,Ko?mrlj, Janez

, p. 193 - 203 (2014)

The rapid generation and spread of the drug resistant tuberculosis has led to an ongoing demand for novel compounds for therapeutic use. Identification and study of compounds with the ability to inhibit Mycobacterium tuberculosis is of paramount importance. For this reason, a library of substituted 1,3-diaryltriazenes based on the acting component of the anti-trypanosomal drug, diminazene aceturate was created and evaluated for its potential as anti-tubercular agent. Several compounds were identified with sub-micro molar inhibitory concentrations against M. tuberculosis and other clinically relevant mycobacterial species such as Mycobacterium bovis, Mycobacterium avium and Mycobacterium ulcerans. Although the library of the compounds showed a considerable acute cytotoxicity, a genotoxicity could not be observed. Finally, the triazene 14 was selected with the best biological properties (IC 50 = 3.26 μM, NI50 = 24.22 μM, SI = 7.44). The compound 14 showed the ability to inhibit the growth of intracellular replicating and multi-drug resistant M. tuberculosis. The results suggest the molecule to be an interesting scaffold for further study and optimization.

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