91640-73-2 Usage
Description
Methyl 2-(1,2,3,4-tetrahydro-1-isoquinolinyl)-acetate is a chemical compound that belongs to the class of isoquinoline derivatives. It is an ester, derived from the combination of an isoquinoline ring structure and a methyl acetate group. Methyl 2-(1,2,3,4-tetrahydro-1-isoquinolinyl)-acetate possesses a unique chemical structure that may contribute to its potential biological activities and applications in pharmaceutical research and drug development.
Uses
Used in Pharmaceutical Research:
Methyl 2-(1,2,3,4-tetrahydro-1-isoquinolinyl)-acetate is used as a research compound for exploring its potential pharmacological activities. Its isoquinoline ring structure and ester functional group may contribute to its antitumor, antibacterial, antifungal, and antiviral properties.
Used in Drug Development:
Methyl 2-(1,2,3,4-tetrahydro-1-isoquinolinyl)-acetate is used as a candidate for drug development due to its potential biological activities. Further studies and research are needed to fully understand its potential uses and effects, which may lead to the development of new therapeutic agents for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 91640-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,4 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91640-73:
(7*9)+(6*1)+(5*6)+(4*4)+(3*0)+(2*7)+(1*3)=132
132 % 10 = 2
So 91640-73-2 is a valid CAS Registry Number.
91640-73-2Relevant articles and documents
Substituted Sulfonamide Compounds
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Page/Page column 43, (2009/10/17)
Substituted sulfonamide compounds corresponding to the formula I: processes for the preparation thereof, pharmaceutical composition containing these compounds and the use of substituted sulfonamide compounds for the preparation of pharmaceutical compositions.
Synthesis and structure-activity relationships of novel dipeptides and reduced dipeptides as ligands for melanocortin subtype-4 receptor
Shi, Qing,Ornstein, Paul L.,Briner, Karin,Richardson, Timothy I.,Arnold, Macklin B.,Backer, Ryan T.,Buckmaster, Jennifer L.,Canada, Emily J.,Doecke, Christopher W.,Hertel, Larry W.,Honigschmidt, Nick,Hsiung, Hansen M.,Husain, Saba,Kuklish, Steve L.,Martinelli, Michael J.,Mullaney, Jeffrey T.,O'Brien, Thomas P.,Reinhard, Matt R.,Rothhaar, Roger,Shah, Jikesh,Wu, Zhipei,Xie, Chaoyu,Zgombick, John M.,Fisher, Matthew J.
, p. 2341 - 2346 (2007/10/03)
A series of benzylic piperazines (e.g., 4 and 5) attached to an 'address element', the dipeptide H-d-Tic-d-p-Cl-Phe-OH, 3 has been identified as ligands for the melanocortin subtype-4 receptor (MC4R). We describe herein the structure-activity relationship (SAR) studies on the N-terminal residue of the 'address element'. Several novel dipeptides and reduced dipeptides with high MC4R binding affinities and selectivity emerged from this SAR study.
