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1000370-80-8

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1000370-80-8 Usage

General Description

The chemical compound (R)-3-(2-Amino-phenylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester is a derivative of pyrrolidine-1-carboxylic acid with an amino group attached to the phenylamine moiety. It is commonly used in pharmaceutical research and drug development as a potential therapeutic agent. The tert-butyl ester group provides stability and increased solubility, making it easier to work with in laboratory settings. (R)-3-(2-AMino-phenylaMino)-pyrrolidine-1-carboxylic acid tert-butyl ester may have potential applications in the treatment of various medical conditions, but further research and testing are necessary to fully understand its pharmacological properties and potential benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 1000370-80-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,3,7 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1000370-80:
(9*1)+(8*0)+(7*0)+(6*0)+(5*3)+(4*7)+(3*0)+(2*8)+(1*0)=68
68 % 10 = 8
So 1000370-80-8 is a valid CAS Registry Number.

1000370-80-8Downstream Products

1000370-80-8Relevant articles and documents

(HETERO) ARYL IMIDAZOLONE COMPOUND

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Paragraph 0087; 0090, (2021/08/13)

PROBLEM TO BE SOLVED: To provide a novel compound that has an inhibitory action on prolyl hydroxylases (PHDs), and is useful as a treatment agent for inflammatory bowel diseases such as ulcerative colitis. SOLUTION: The present disclosure provides a (hetero) aryl imidazolone compound represented by the formula (I) or a pharmacologically acceptable salt thereof (where m, u, p, q and r each denote a specific integer, E, G, Q and T each denote a specific group such as N or CH, W and Z each denote a specific ring, R1 and R3 each denote a specific group such as a halogen atom). SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

New 'chemical probes' to examine the role of the hFPRL1 (or ALXR) receptor in inflammation

Frohn, Mike,Xu, Han,Zou, Xiaoming,Chang, Catherine,McElvaine, Michele,Plant, Matthew H.,Wong, Min,Tagari, Philip,Hungate, Randall,Buerli, Roland W.

, p. 6633 - 6637 (2008/03/18)

We report the development of the novel N-substituted benzimidazole 11 as a potent and selective human formyl peptide receptor-like 1 (hFPRL1) agonist. This compound and its less active enantiomer 12 were identified as useful tools for studying receptor function in vitro.

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