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2-Propen-1-one, 3-(4-chlorophenyl)-1-(1H-indol-3-yl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38470-73-4

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38470-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38470-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,7 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38470-73:
(7*3)+(6*8)+(5*4)+(4*7)+(3*0)+(2*7)+(1*3)=134
134 % 10 = 4
So 38470-73-4 is a valid CAS Registry Number.

38470-73-4Downstream Products

38470-73-4Relevant academic research and scientific papers

Identification of Indole-Based Chalcones: Discovery of a Potent, Selective, and Reversible Class of MAO-B Inhibitors

Sasidharan, Rani,Manju, Sreedharannair Leelabaiamma,U?ar, Gülberk,Baysal, Ipek,Mathew, Bijo

, p. 627 - 637 (2016)

A series of 11 indole-based chalcones (IC1–11) with various electron donating and withdrawing groups at the para position of the phenyl ring B were synthesized. All the compounds were tested for their human monoamine oxidase (hMAO)-A and hMAO-B inhibitory

Synthesis and biological evaluation of novel indole-pyrazoline hybrid derivatives as potential topoisomerase 1 inhibitors

Shu, Bing,Yu, Qian,Hu, De-xuan,Che, Tong,Zhang, Shang-shi,Li, Ding

supporting information, (2020/01/08)

A series of novel indole-pyrazoline hybrid derivatives were designed, synthesized, and evaluated for topoisomerase 1 (Top1) inhibitory activity. Top1-mediated relaxation assays showed that our synthesized compounds had variable Top1 inhibitory activity. A

Design, docking, and synthesis of some new pyrazoline and pyranopyrazole derivatives as anti-inflammatory agents

Ismail, Magda M. F.,Khalifa, Nagy M.,Fahmy, Hoda H.,Nossier, Eman S.,Abdulla, Mohamed M.

, p. 450 - 458 (2014/04/17)

Design and synthesis of some novel pyrazoline and pyranopyrazole derivatives as potential anti-inflammatory agents are described. Most of the compounds were tested for their anti-inflammatory (in vitro and in vivo) and ulcerogenic activities. In all teste

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