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N-[(2,4-dimethoxyphenyl)methyl]-2,3,4-trifluoro-N-(pyrimidin-4-yl)benzene-1-sulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1450596-82-3

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1450596-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1450596-82-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,5,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1450596-82:
(9*1)+(8*4)+(7*5)+(6*0)+(5*5)+(4*9)+(3*6)+(2*8)+(1*2)=173
173 % 10 = 3
So 1450596-82-3 is a valid CAS Registry Number.

1450596-82-3Downstream Products

1450596-82-3Relevant academic research and scientific papers

Discovery of DS-1971a, a Potent, Selective NaV1.7 Inhibitor

Shinozuka, Tsuyoshi,Kobayashi, Hiroyuki,Suzuki, Sayaka,Tanaka, Kyosuke,Karanjule, Narayan,Hayashi, Noriyuki,Tsuda, Toshifumi,Tokumaru, Eri,Inoue, Masahiro,Ueda, Kiyono,Kimoto, Hiroko,Domon, Yuki,Takahashi, Sakiko,Kubota, Kazufumi,Yokoyama, Tomihisa,Shimizugawa, Akiko,Koishi, Ryuta,Fujiwara, Chie,Asano, Daigo,Sakakura, Tomoko,Takasuna, Kiyoshi,Abe, Yasuyuki,Watanabe, Toshiyuki,Kitano, Yutaka

, p. 10204 - 10220 (2020/11/02)

A highly potent, selective NaV1.7 inhibitor, DS-1971a, has been discovered. Exploration of the left-hand phenyl ring of sulfonamide derivatives (I and II) led to the discovery of novel series of cycloalkane derivatives with high NaV1.7 inhibitory potency in vitro. As the right-hand heteroaromatic ring affected the mechanism-based inhibition liability of CYP3A4, replacement of this moiety resulted in the generation of 4-pyrimidyl derivatives. Additionally, GSH adducts formation, which can cause idiosyncratic drug toxicity, was successfully avoided by this modification. An additional optimization led to the discovery of DS-1971a. In preclinical studies, DS-1971a demonstrated highly potent selective in vitro profile with robust efficacy in vivo. DS-1971a exhibited a favorable toxicological profile, which enabled multiple-dose studies of up to 600 mg bid or 400 mg tid (1200 mg/day) administered for 14 days to healthy human males. DS-1971a is expected to exert potent efficacy in patients with peripheral neuropathic pain, with a favorable safety profile.

DRUG FOR RESPIRATORY DISEASES

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Paragraph 0520; 0521, (2016/10/08)

It is intended to provide a therapeutic agent and/or a preventive agent for a respiratory disease or a therapeutic agent and/or a preventive agent for a sodium channel associated disease. The present invention provides a pharmaceutical comprising a compound represented by the following formula (I) or a pharmacologically acceptable salt thereof as an active ingredient: Ar 1 and Ar 2 : a heteroaryl group or an aryl group; R 1 , R 2 and R 3 : a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group or a C3-C7 cycloalkyl group or a cyano group; R 4 and R 5 : a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group or a C1-C6 alkoxy group; n: an integer of 1 to 3; and the heteroaryl or aryl group optionally has one or two groups independently selected from a halogen atom, a C1-C6 alkyl group, a halogenated C1-C6 alkyl group, a hydroxyl group, a hydroxy C1-C6 alkyl group, a C1-C6 alkoxy C1-C6 alkyl group, a C3-C7 cycloalkyl group, a carboxyl group, a cyano group, an amino group, a C1-C3 alkylamino group and a di-C1-C3 alkylamino group, and when the heteroaryl or aryl group has two such groups, the two groups are the same as or different from each other.

Cycloalkane Derivatives

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Paragraph 0515; 0634; 0635, (2014/03/21)

Disclosed herein are therapeutic agents and/or preventive agents for pain or therapeutic agents and/or preventive agents for a sodium channel associated disease. The present invention provides compounds represented by the following formula (I) or pharmacologically acceptable salts thereof:

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