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(Z)-5-((1-(4-methylbenzyl)-1H-indol-3-yl)methylene)imidazolidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1207615-72-2

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1207615-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207615-72-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,6,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1207615-72:
(9*1)+(8*2)+(7*0)+(6*7)+(5*6)+(4*1)+(3*5)+(2*7)+(1*2)=132
132 % 10 = 2
So 1207615-72-2 is a valid CAS Registry Number.

1207615-72-2Downstream Products

1207615-72-2Relevant articles and documents

INDOLE COMPOUNDS AND THEIR USE AS RADIATION SENSITIZING AGENTS AND CHEMOTHERAPEUTIC AGENTS

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Page/Page column 8, (2010/04/25)

Indole derivatives that are useful in the treatment of cancer as a chemotherapeutic agent or radiosensitizing agent.

Aplysinopsin analogs: Synthesis and anti-proliferative activity of substituted (Z)-5-(N-benzylindol-3-ylmethylene)imidazolidine-2,4-diones

Thirupathi Reddy,Narsimha Reddy,Koduru, Srinivas,Damodaran, Chendil,Crooks, Peter A.

experimental part, p. 3570 - 3574 (2010/07/17)

A series of substituted (Z)-5-(N-benzylindol-3-ylmethylene)imidazolidine-2,4-dione (3) analogs structurally related to aplysinopsin, and that incorporate a variety of substituents in both the indole and N-benzyl moieties have been synthesized under microwave irradiation and conventional heating methods These analogs were evaluated for their anti-proliferative activity against MCF-7 and MDA-231 breast cancer cell lines, and A549 and H460 lung cancer cell lines. Two analogs, 3f and 3j had IC50 values of 4.4 and 5.2 μM, respectively, compared to 5-fluorouracil (IC50 = 15.2 μM) against MCF-7 cells.

Novel substituted (Z)-5-((N-benzyl-1H-indol-3-yl)methylene)imidazolidine-2,4-diones and 5-((N-benzyl-1H-indol-3-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-triones as potent radio-sensitizing agents

Reddy, Y. Thirupathi,Sekhar, Konjeti R.,Sasi, Nidhish,Reddy, P. Narsimha,Freeman, Michael L.,Crooks, Peter A.

scheme or table, p. 600 - 602 (2010/04/26)

A series of (Z)-5-((N-benzyl-1H-indol-3-yl)methylene)imidazolidine-2,4-dione (9a-9m) and 5-((N-benzyl-1H-indol-3-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-trione (10a-10i) derivatives that incorporate a variety of aromatic substituents in both the indole and N-benzyl moieties have been synthesized. These analogs were evaluated for their radiosensitization activity against the HT-29 cell line. Three analogs, 10a, 10b, and 10c were identified as the most potent radiosensitizing agents.

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