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2-((carboxymethyl)amino)-5-hydroxybenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1223385-84-9

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1223385-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1223385-84-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,3,3,8 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1223385-84:
(9*1)+(8*2)+(7*2)+(6*3)+(5*3)+(4*8)+(3*5)+(2*8)+(1*4)=139
139 % 10 = 9
So 1223385-84-9 is a valid CAS Registry Number.

1223385-84-9Downstream Products

1223385-84-9Relevant academic research and scientific papers

INDIRUBIN-3'-OXIME DERIVATIVES AS POTENT CYCLIN DEPENDENT KINASE INHIBITORS

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, (2012/12/13)

The present invention relates to an indirubin-3′-oxime derivative as potent cyclin dependent kinase inhibitor with anti-cancer activity. More particularly, this invention relates to an indirubin-3′-oxime derivative as potent cyclin dependent kinase inhibitor having excellent anti-cancer activity against human lung cancer cell, human fibro sarcoma cell, human colon cancer cell, human leukemia cell, human stomach cancer cell, human nasopharyngeal cancer cell and/or human breast cancer cell.

INDIRUBIN-3'-OXIME DERIVATIVES AS POTENT CYCLIN DEPENDENT KINASE INHIBITORS

-

, (2011/09/14)

The present invention relates to an indirubin-3'-oxime derivative as potent cyclin dependent kinase inhibitor with anti-cancer activity. More particularly, this invention relates to an indirubin-3'-oxime derivative as potent cyclin dependent kinase inhibitor having excellent anti-cancer activity against human lung cancer cell, human fibro sarcoma cell, human colon cancer cell, human leukemia cell, human stomach cancer cell, human nasopharyngeal cancer cell and/or human breast cancer cell.

5,5′-substituted indirubin-3′-oxime derivatives as potent cyclin-dependent kinase inhibitors with anticancer activity

Choi, Soo-Jeong,Lee, Jung-Eun,Jeong, Soon-Young,Im, Isak,Lee, So-Deok,Lee, Eun-Jin,Lee, Sang Kook,Kwon, Seong-Min,Ahn, Sang-Gun,Yoon, Jung-Hoon,Han, Sun-Young,Kim, Jae-Il,Kim, Yong-Chul

experimental part, p. 3696 - 3706 (2010/08/06)

To enhance the ability of indirubin derivatives to inhibit CDK2/cyclin E, a target of anticancer agents, we designed and synthesized a new series of indirubin-3′-oxime derivatives with combined substitutions at the 5 and 5′ positions. A molecular docking

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