81109-85-5 Usage
Uses
Used in Research Applications:
CARBOXYMETHYL-PHE-LEU-OH is used as a molecular tool for studying various biological processes due to its enhanced water solubility and specific functional groups provided by the phenylalanine and leucine residues.
Used in Pharmaceutical Development:
In the pharmaceutical industry, CARBOXYMETHYL-PHE-LEU-OH is used as a building block for creating new drug molecules, leveraging its unique properties to develop innovative therapeutic agents.
Used in Chemistry:
CARBOXYMETHYL-PHE-LEU-OH is utilized in chemical research for its potential to interact with biological targets, contributing to the advancement of chemical sciences and the discovery of novel compounds.
Used in Biology:
CARBOXYMETHYL-PHE-LEU-OH is employed in biological studies to understand its interactions with biological systems, which can lead to insights into new mechanisms of action and potential therapeutic applications.
Used in Medicine:
CARBOXYMETHYL-PHE-LEU-OH has potential applications in medicine, particularly in the development of new drugs and therapies, thanks to its unique properties and ability to engage with biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 81109-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,0 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81109-85:
(7*8)+(6*1)+(5*1)+(4*0)+(3*9)+(2*8)+(1*5)=115
115 % 10 = 5
So 81109-85-5 is a valid CAS Registry Number.
81109-85-5Relevant academic research and scientific papers
New carboxyalkyl inhibitors of brain enkephalinase: Synthesis, biological activity, and analgesic properties
Fournie Zaluski,Chaillet,Soroca Lucas,Fournie-Zaluski,Marcais-Collado,Costentin,Roques
, p. 60 - 65 (2007/10/02)
New carboxylalkyl compounds derived from Phe-Leu and Phe-Ala were synthesized and checked as inhibitors of enkephalinase, a metalloendopeptidase cleaving the Gly3-Phe4 bond of enkephalins from mouse striatal membranes. Differential r
