Welcome to LookChem.com Sign In|Join Free
  • or
ethyl 1-(3-broMophenyl)-3-Methyl-1H-pyrazole-5-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

209958-55-4

Post Buying Request

209958-55-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

209958-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209958-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,9,5 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 209958-55:
(8*2)+(7*0)+(6*9)+(5*9)+(4*5)+(3*8)+(2*5)+(1*5)=174
174 % 10 = 4
So 209958-55-4 is a valid CAS Registry Number.

209958-55-4Relevant academic research and scientific papers

CALPAIN MODULATORS AND THERAPEUTIC USES THEREOF

-

Paragraph 0705, (2018/04/17)

Disclosed herein are small molecule calpain modulator compositions, pharmaceutical compositions, the use and preparation thereof.

Substituted biaryl pyrazoles as sodium channel blockers

Tyagarajan, Sriram,Chakravarty, Prasun K.,Zhou, Bishan,Taylor, Brett,Fisher, Michael H.,Wyvratt, Mathew J.,Lyons, Kathy,Klatt, Tracy,Li, Xiaohua,Kumar, Sanjeev,Williams, Brande,Felix, John,Priest, Birgit T.,Brochu, Richard M.,Warren, Vivien,Smith, McHardy,Garcia, Maria,Kaczorowski, Gregory J.,Martin, William J.,Abbadie, Catherine,McGowan, Erin,Jochnowitz, Nina,Parsons, William H.

scheme or table, p. 5480 - 5483 (2010/12/24)

Voltage-gated sodium channels have been shown to play a critical role in neuropathic pain. A series of low molecular weight biaryl substituted pyrazole carboxamides were identified with good in-vitro potency and in-vivo efficacy. Compound 26, a Nav1.7 blocker has excellent efficacy in the Chung model of neuropathic pain.

Structure-based design of novel guanidine/benzamidine mimics: Potent and orally bioavailable factor Xa inhibitors as novel anticoagulants

Lam, Patrick Y. S.,Clark, Charles G.,Li, Renhua,Pinto, Donald J. P.,Orwat, Michael J.,Galemmo, Robert A.,Fevig, John M.,Teleha, Christopher A.,Alexander, Richard S.,Smallwood, Angela M.,Rossi, Karen A.,Wright, Matthew R.,Bai, Stephen A.,He, Kan,Luettgen, Joseph M.,Wong, Pancras C.,Knabb, Robert M.,Wexler, Ruth R.

, p. 4405 - 4418 (2007/10/03)

As part of an ongoing effort to prepare orally active factor Xa inhibitors using structure-based drug design techniques and molecular recognition principles, a systematic study has been performed on the pharmacokinetic profile resulting from replacing the

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 209958-55-4