67463-44-9 Usage
General Description
N-ME-CIS-HYDROXYPROLINE, also known as N-methyl-L-cis-hydroxyproline, is a chemical compound derived from the amino acid proline. It is a natural product found in collagen, and it plays a crucial role in the stability and structure of collagen molecules. N-ME-CIS-HYDROXYPROLINE has been the subject of research for its potential medical applications, particularly in the development of pharmaceuticals for wound healing and tissue repair. Its unique structure and properties make it a valuable component in the study of collagen-related diseases and in the development of new drugs for skin and connective tissue disorders. Additionally, it has been investigated for its potential use in cosmetic formulations and skincare products due to its ability to promote collagen synthesis and improve skin elasticity.
Check Digit Verification of cas no
The CAS Registry Mumber 67463-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,6 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67463-44:
(7*6)+(6*7)+(5*4)+(4*6)+(3*3)+(2*4)+(1*4)=149
149 % 10 = 9
So 67463-44-9 is a valid CAS Registry Number.
67463-44-9Relevant articles and documents
PROLINE DERIVATIVES USED AS PHARMACEUTICAL ACTIVE INGREDIENTS FOR THE TREATMENT OF TUMOURS
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Page/Page column 39-40, (2008/06/13)
The invention relates to proline derivatives and their salts, to pharmaceutical agents containing said derivatives and to the use of said agents for treating tumours. The invention also relates to methods for producing said compounds and pharmaceutical ag
Enantioselective Solvent Extraction of Neutral DL-Amino Acids in Two-Phase Systems Containing N-n-Alkyl-L-proline Derivatives and Copper(II) Ion
Takeuchi, Toshifumi,Horikawa, Rikizo,Tanimura, Takenori
, p. 1152 - 1155 (2007/10/02)
Distribution behavior of neutral amino acid enantiomers was examined in the aqueous and organic solvent of a two-phase system containing cupric ion and N-n-dodecyl-L-proline or N-n-alkyl-L-hydroxyproline.Significant enentioselectivity was observed when n-butyl, n-amyl, or n-octyl alcohol was used as the organic solvent.Equilibrium constants of ligand exchange reaction for several amino acid enantiomers were estimated for the n-butyl alcohol-water system.The enantioselectivity seems to depend primarily on the difference of the stability of mixed ligand complexes in the organic phase.
