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9-Bromo-7,12-dihydrobenzo[2,3]azepino[4,5-b]indole-6(5H)-thione is a complex organic chemical compound with the molecular formula C14H11BrN2S. It is a derivative of benzoazepinoindole, featuring a 6-membered benzene ring fused to a 7-membered azepine ring, which is further fused to a 5-membered indole ring. The molecule contains a bromine atom at the 9-position, a sulfur atom at the 6-position, and two nitrogen atoms within the azepine and indole rings. 9-bromo-7,12-dihydrobenzo[2,3]azepino[4,5-b]indole-6(5H)-thione is characterized by its unique structure and potential applications in medicinal chemistry, particularly in the development of drugs targeting the central nervous system. Due to its specific chemical properties and structure, it may exhibit various biological activities and serve as a precursor in the synthesis of other related compounds with potential therapeutic uses.

237430-35-2

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237430-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 237430-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,7,4,3 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 237430-35:
(8*2)+(7*3)+(6*7)+(5*4)+(4*3)+(3*0)+(2*3)+(1*5)=122
122 % 10 = 2
So 237430-35-2 is a valid CAS Registry Number.

237430-35-2Upstream product

237430-35-2Downstream Products

237430-35-2Relevant academic research and scientific papers

Tumor-inhibiting anellated azepinone derivatives

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Page/Page column 6-7, (2010/02/15)

This invention relates to anellated azepinone derivatives, a method of their production, metal complexes of the anellated azepinone derivatives as well as their use in the treatment of tumor diseases.

TUMOUR-INHIBITING ANNELLATED AZEPINONE DERIVATIVES

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Page/Page column 19, (2010/02/07)

The invention relates to annellated azepinone derivatives, to a method for the production thereof, to metal complexes of the annellated azepinone derivatives, and to the use of the same for treating tumour diseases.

Fused azepinone cyclin dependent kinase inhibitors

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, (2008/06/13)

A new class of cyclin dependent kinase inhibitors that also have antiproliferative activity in human tumor cell line assays are described. Most of these compounds satisfy the formula wherein A is oxygen or sulfur coupled to the right by a single or double bond; R2 is selected from the group consisting of hydrogen, aryl, lower aliphatic substituents, particularly alkyl and lower alkyl ester; R4-R7 are independently selected from the group consisting of alkoxy, amino, acyl, aliphatic substituents, particularly alkyl, alkenyl and alkinyl substituents, aliphatic alcohols, particularly alkyl alcohols, aliphatic nitriles, particularly alkyl nitriles, cyano, nitro, carboxyl, halogen, hydrogen, hydroxyl, imino, and α, β, unsaturated ketones; R8-R11 are independently selected from the group consisting of aliphatic substituents, particularly alkyl, alkenyl and alkinyl substituents, particularly lower aliphatic substituents, alipahatic alcohols, particularly alkyl alcohols, alkoxy, acyl, cyano, nitro, epoxy, haloalkyl groups, halogen, hydrogen and hydroxyl; R12 is selected from the group consisting of aliphatic groups, particularly lower alkyl groups, aliphatic alcohols, particularly alkyl alcohols, carboxylic acids and hydrogen. Compositions comprising effective amounts of such compounds also are described. These compounds and compositions can be used in a method for inhibiting the proliferation of living cells in a subject comprising administering an effective amount of the compound(s), or composition(s) comprising the compound(s), to a subject to inhibit the proliferation of living cells, such as neoplastic cells.

Paullones, a series of cyclin-dependent kinase inhibitors: Synthesis, evaluation of CDK1/cyclin B inhibition, and in vitro antitumor activity

Schultz, Christiane,Link, Andreas,Leost, Maryse,Zaharevitz, Daniel W.,Gussio, Rick,Sausville, Edward A.,Meijer, Laurent,Kunick, Conrad

, p. 2909 - 2919 (2007/10/03)

The paullones represent a novel class of small molecule cyclin-dependent kinase (CDK) inhibitors. To investigate structure-activity relationships and to develop paullones with antitumor activity, derivatives of the lead structure kenpaullone (9-bromo-7,12

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