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2-Butenoic acid, 4-oxo-4-[[4-[(2E)-1-oxo-3-phenyl-2-propenyl]phenyl]amino]-, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

569646-63-5

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569646-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 569646-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,9,6,4 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 569646-63:
(8*5)+(7*6)+(6*9)+(5*6)+(4*4)+(3*6)+(2*6)+(1*3)=215
215 % 10 = 5
So 569646-63-5 is a valid CAS Registry Number.

569646-63-5Downstream Products

569646-63-5Relevant academic research and scientific papers

Cytostatic activity of novel 4′-aminochalcone-based imides

Jha, Amitabh,Mukherjee, Chandrani,Rolle, Alfred J.,De Clercq, Erik,Balzarini, Jan,Stables, James P.

, p. 4545 - 4550 (2007)

A series of nine 1-(4-((E)-3-arylacryloyl)phenyl)-1H-pyrrole-2,5-diones 3a-i (4′-aminochalcone-based maleimides) was synthesized as candidate cytotoxic agents. The efficacy of these potential cytotoxics were evaluated against three representative cell lin

Cytotoxic 4′-aminochalcones and related compounds

Dimmock,Jha,Zello,Allen,Santos,Balzarini,De Clercq,Manavathu,Stables

, p. 227 - 232 (2007/10/03)

A series of 4′-aminochalcones 1 and related maleamic acids 2 and Schiff bases 3 were designed and synthesized as candidate cytotoxic agents. The atomic charges on different atoms of representative compounds were calculated. Evaluation of the enones 1-3 against human Molt 4/C8 and CEM T-lymphocytes as well as murine P388 and L1210 leukemic cells revealed that approximately 40% of the IC50 values generated were less than 10 μM. In some cases cytotoxicity was correlated with the Hammett σ values of the aryl substituents and less frequently with the aryl Hansch π values. Evidence was obtained that in general these compounds displayed selective toxicity for certain malignant cells and were well tolerated in mice. This study has revealed various directions whereby the project may be amplified in the future with a view to finding compounds with increased cytotoxicity to tumour cells.

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