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Phenol, 2-amino-4-(2-thienyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90923-91-4

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90923-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90923-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,9,2 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90923-91:
(7*9)+(6*0)+(5*9)+(4*2)+(3*3)+(2*9)+(1*1)=144
144 % 10 = 4
So 90923-91-4 is a valid CAS Registry Number.

90923-91-4Downstream Products

90923-91-4Relevant academic research and scientific papers

PHOTOSWITCHABLE HDAC INHIBITORS

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, (2014/10/15)

This invention relates to photoswitchable inhibitors of histone deacetylases and methods of using the same. Provided herein are inhibitors of HDAC having photoswitchable modulators of protein function with short thermal relaxation kinetics. The compounds

Novel aminophenyl benzamide-type histone deacetylase inhibitors with enhanced potency and selectivity

Moradei, Oscar M.,Mallais, Tammy C.,Frechette, Sylvie,Paquin, Isabelle,Tessier, Pierre E.,Leit, Silvana M.,Fournel, Marielle,Bonfils, Claire,Trachy-Bourget, Marie-Claude,Liu, Jianhong,Yan, Theresa P.,Lu, Ai-Hua,Rahil, Jubrail,Wang, James,Lefebvre, Sylvain,Li, Zuomei,Vaisburg, Arkadii F.,Besterman, Jeffrey M.

, p. 5543 - 5546 (2008/03/27)

Significant effort is being made to understand the role of HDAC isotypes in human cancer and to develop antitumor agents with better therapeutic windows. A part of this endeavor was the exploration of the 14 ? internal cavity adjacent to the enzyme catalytic site, which led to the design and synthesis of compound 4 with the unusual bis-(aryl)-type pharmacophore. SAR studies around this lead resulted in optimization to potent, selective, nonhydroxamic acid HDAC inhibitors.

INHIBITORS OF HISTONE DEACETYLASE

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Page/Page column 261-262, (2010/02/11)

The invention relates to the inhibition of histone deacetylase. The invention provides compounds and methods for inhibiting histone deacetylase enzymatic activity. The invention also provides compositions and methods for treating cell proliferative diseases and conditions.

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