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((R)-1-Benzyl-2-{(S)-2-[2-(4-cyano-phenyl)-ethylcarbamoyl]-pyrrolidin-1-yl}-2-oxo-ethyl)-carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183595-83-7

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183595-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183595-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,5,9 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 183595-83:
(8*1)+(7*8)+(6*3)+(5*5)+(4*9)+(3*5)+(2*8)+(1*3)=177
177 % 10 = 7
So 183595-83-7 is a valid CAS Registry Number.

183595-83-7Downstream Products

183595-83-7Relevant academic research and scientific papers

Design, synthesis, and evaluation of a novel benzamidine-based inhibitor of VEGF-C binding to Neuropilin-2

Parker, Matthew W.,Said, Ahmed M.,Vander Kooi, Craig W.

, (2020/04/28)

The Neuropilin (Nrp) family of cell surface receptors have key physiological and pathological functions. Nrp2 is of particular interest due to its involvement in tumor metastasis. Currently, peptide and small molecule inhibitors that target Nrp utilize ar

D-Phe-Pro-p-amidinobenzylamine: A potent and highly selective thrombin inhibitor

Wiley, Michael R.,Chirgadze, Nickolay Y.,Clawson, David K.,Craft, Trelia J.,Gifford-Moore, Donetta S.,Jones, Noel D.,Olkowski, Jennifer L.,Weir, Leonard C.,Smith, Gerald F.

, p. 2387 - 2392 (2007/10/03)

The design, synthesis, and enzyme inhibitory profile of D-Phe-Pro-p-Amidinobenzylamine are presented. This compound has inhibitory activity equivalent to D-Phe-Pro-Arg-H, two orders of magnitude more potent than D-Phe-Pro-Agmatine. The results indicate that binding energy provided by the covalent bond of a transition-state analog can be replaced with noncovalent interactions.

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