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4-chloro-N-(1-(pyridin-2-yl)-1H-pyrazol-5-yl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1620335-76-3

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1620335-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620335-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,3,3 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1620335-76:
(9*1)+(8*6)+(7*2)+(6*0)+(5*3)+(4*3)+(3*5)+(2*7)+(1*6)=133
133 % 10 = 3
So 1620335-76-3 is a valid CAS Registry Number.

1620335-76-3Downstream Products

1620335-76-3Relevant academic research and scientific papers

Investigation of pyrazolo-sulfonamides as putative small molecule oxytocin receptor agonists

Katte, Timothy A.,Reekie, Tristan A.,Werry, Eryn L.,Jorgensen, William T.,Boyd, Rochelle,Wong, Erick C.N.,Gulliver, Damien W.,Connor, Mark,Kassiou, Michael

, p. 330 - 333 (2017/06/09)

The neuropeptide oxytocin has been implicated in multiple central nervous system functions in mammalian species. Increased levels have been reported to improve trust, alleviate symptoms related to autism and social phobias, and reduce social anxiety. Hoffman-La Roche published a patent claiming to have found potent small molecule oxytocin receptor agonists, smaller than the first non-peptide oxytocin agonist reported, WAY 267,464. We selected two of the more potent compounds from the patent and, in addition, created WAY 267,464 hybrid structures and determined their oxytocin and vasopressin receptor activity. Human embryonic kidney and Chinese hamster ovary cells were used for the expression of oxytocin or vasopressin 1a receptors and activity assessed via IP1 accumulation assays and calcium FLIPR assays. The results concluded that the reported compounds in the patent and the hybrid structures have no activity at the oxytocin or vasopressin 1a receptors.

OXYTOCIN RECEPTOR AGONISTS FOR THE TREATMENT OF CNS DISEASES

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Page/Page column 9, (2014/08/06)

The invention relates to the use of a compound of formula I wherein A1 is phenyl or a five or six membered hereroaryl group, containing 1, 2 or 3 heteroatoms, selected from N or S; R1 is hydrogen, lower alkyl, halogen, lower alkyl substituted by halogen or cycloalkyl; A2 is phenyl; R2 is halogen, lower alkyl, lower alkyl substituted by halogen, lower alkoxy substituted by halogen, cyano, S-lower alkyl substituted by halogen, S(O)2-lower alkyl substituted by halogen; n is 1 or 2; or a to pharmaceutically acceptable acid addition salt, to a racemic mixture or to its corresponding enantiomer and/or optical isomers thereof for the treatment of autism, stress, including post traumatic stress disorder, anxiety, including anxiety disorders and depression, schizophrenia, psychiatric disorders and memory loss, alcohol withdrawel, drug addiction and for the treatment of Prader-Willi Syndrom.

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