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(R)-3-((1-cyclohexylethyl)amino)benzo[e][1,2,4]triazine-1,4-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1383844-70-9

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1383844-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383844-70-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,8,4 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1383844-70:
(9*1)+(8*3)+(7*8)+(6*3)+(5*8)+(4*4)+(3*4)+(2*7)+(1*0)=189
189 % 10 = 9
So 1383844-70-9 is a valid CAS Registry Number.

1383844-70-9Downstream Products

1383844-70-9Relevant academic research and scientific papers

Benzotriazine Oxides as Drugs Targeting Mycobacterium Tuberculosis

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Paragraph 0080; 0087; 0097, (2013/06/27)

Benzotriazine doxides are disclosed as drugs targeting mycobacterium tuberculosis, including novel compounds of formula I:

Discovery and optimization of benzotriazine Di-N-oxides targeting replicating and nonreplicating mycobacterium tuberculosis

Chopra, Sidharth,Koolpe, Gary A.,Tambo-Ong, Arlyn A.,Matsuyama, Karen N.,Ryan, Kenneth J.,Tran, Tran B.,Doppalapudi, Rupa S.,Riccio, Edward S.,Iyer, Lalitha V.,Green, Carol E.,Wan, Baojie,Franzblau, Scott G.,Madrid, Peter B.

, p. 6047 - 6060 (2012/09/05)

Compounds bactericidal against both replicating and nonreplicating Mtb may shorten the length of TB treatment regimens by eliminating infections more rapidly. Screening of a panel of antimicrobial and anticancer drug classes that are bioreduced into cytotoxic species revealed that 1,2,4-benzotriazine di-N-oxides (BTOs) are potently bactericidal against replicating and nonreplicating Mtb. Medicinal chemistry optimization, guided by semiempirical molecular orbital calculations, identified a new lead compound (20q) from this series with an MIC of 0.31 μg/mL against H37Rv and a cytotoxicity (CC 50) against Vero cells of 25 μg/mL. 20q also had equivalent potency against a panel of single-drug resistant strains of Mtb and remarkably selective activity for Mtb over a panel of other pathogenic bacterial strains. 20q was also negative in a L5178Y MOLY assay, indicating low potential for genetic toxicity. These data along with measurements of the physiochemical properties and pharmacokinetic profile demonstrate that BTOs have the potential to be developed into a new class of antitubercular drugs.

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