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N,9-dimethyl-3-(phenylsulfonyl)-5,6,7,8-tetrahydropyrazolo-[5,1-b]quinazolin-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173004-23-3

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1173004-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173004-23-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,0,0 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1173004-23:
(9*1)+(8*1)+(7*7)+(6*3)+(5*0)+(4*0)+(3*4)+(2*2)+(1*3)=103
103 % 10 = 3
So 1173004-23-3 is a valid CAS Registry Number.

1173004-23-3Downstream Products

1173004-23-3Relevant academic research and scientific papers

(3-Phenylsulfonylcycloalkano[e and d]pyrazolo[1,5- a]pyrimidin-2-yl)amines: Potent and selective antagonists of the serotonin 5-HT6 receptor

Ivachtchenko, Alexandre V.,Dmitriev, Dmitri E.,Golovina, Elena S.,Kadieva, Madina G.,Koryakova, Angela G.,Kysil, Volodymyr M.,Mitkin, Oleg D.,Okun, Ilya M.,Tkachenko, Sergey E.,Vorobiev, Anton A.

experimental part, p. 5186 - 5196 (2010/09/09)

5-HT6 receptors are exclusively localized in the CNS and have high affinity with many psychotropic agents. Though the role of this receptor in many CNS diseases is widely anticipated, lack of definite progress in the development of 5-HT6 receptor-oriented drugs indicates a need for further discoveries of novel chemotypes with high potency and high selectivity to the receptor. Here we present preparations and biological evaluation of a series of (3-phenylsulfonylcycloalkano[e and d]pyrazolo[1,5-a]pyrimidin-2-yl) amines. Phenylsulfonylcyclopentapyrazolopyrimidine 7 was found to be a highly selective 5-HT6 receptor antagonist with high affinity (low picomolar range) and potency. 7 and a few of its analogues were further tested for biological effect on 5-HT2B receptors and hERG potassium channels, potential liability targets. Such liability appears to be minimal, based on the in vitro data.

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