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4-[(5-Allyl-6-methyl-2-phenyl-4-pyrimidinyl)amino]benzoic acid, also known as AM4503, is a chemical compound with potential pharmaceutical applications. It belongs to the class of benzoic acids and contains a pyrimidine ring. Its structure and properties make it a promising candidate for further drug development and study.
Used in Pharmaceutical Industry:
4-[(5-Allyl-6-methyl-2-phenyl-4-pyrimidinyl)amino]benzoic acid is used as a potent and selective antagonist of the cannabinoid CB2 receptor for its potential therapeutic implications in inflammatory and neurodegenerative conditions.
Used in Drug Development:
4-[(5-Allyl-6-methyl-2-phenyl-4-pyrimidinyl)amino]benzoic acid is used as a candidate for further drug development and study due to its potential in the treatment of various diseases and disorders, particularly those related to the endocannabinoid system.

300837-31-4

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300837-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 300837-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,8,3 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 300837-31:
(8*3)+(7*0)+(6*0)+(5*8)+(4*3)+(3*7)+(2*3)+(1*1)=104
104 % 10 = 4
So 300837-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H19N3O2/c1-3-7-18-14(2)22-19(15-8-5-4-6-9-15)24-20(18)23-17-12-10-16(11-13-17)21(25)26/h3-6,8-13H,1,7H2,2H3,(H,25,26)(H,22,23,24)

300837-31-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(6-methyl-2-phenyl-5-prop-2-enylpyrimidin-4-yl)amino]benzoic acid

1.2 Other means of identification

Product number -
Other names 4-((5-Allyl-6-methyl-2-phenylpyrimidin-4-yl)amino)benzoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:300837-31-4 SDS

300837-31-4Downstream Products

300837-31-4Relevant articles and documents

NURR1:RXR ACTIVATING COMPOUNDS FOR SIMULTANEOUS TREATMENT OF SYMPTOMS AND PATHOLOGY OF PARKINSON'S DISEASE

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Page/Page column 37; 38; 43; 44, (2017/08/01)

The invention provides a series of substituted aryl pyrimidine compounds and the use of these compounds as therapeutics to treat or prevent neurodegenerative disorders, including Parkinson's disease. Compounds of the invention are also able to treat the s

Discovery of selective PDE4B inhibitors

Naganuma, Kenji,Omura, Akifumi,Maekawara, Naomi,Saitoh, Masahiro,Ohkawa, Naoto,Kubota, Takashi,Nagumo, Hiromitsu,Kodama, Toshiyuki,Takemura, Masayoshi,Ohtsuka, Yuji,Nakamura, Junji,Tsujita, Ryuichi,Kawasaki, Koh,Yokoi, Hirotsugu,Kawanishi, Masashi

scheme or table, p. 3174 - 3176 (2010/03/24)

In this study the first PDE4B selective inhibitor is described. Optimization of lead 2-arylpyrimidine derivatives afforded a series of potent PDE4B inhibitors with >100-fold selectivity over the PDE4D isozyme. With a good pharmacokinetic profile, a selected compound exhibited potent anti-inflammatory effects in vivo and showed less emesis compared with Cilomilast.

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