122456-37-5 Usage
Chemical class
Quinoline derivatives
Core structure
Pyrroloquinoline
1-position
2-methylphenyl group
4-position
Methylamino group
6-position
Methyl group
Hydrogenation
2,3-dihydropyrrolo
Potential applications
Pharmaceutical research and drug development
Medicinal properties
Unknown, requires further research
Biological activities
Unknown, requires further research
Structural complexity
High, due to multiple substituents and core structure
Current understanding
Limited, further studies and research needed to fully understand properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 122456-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,5 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 122456-37:
(8*1)+(7*2)+(6*2)+(5*4)+(4*5)+(3*6)+(2*3)+(1*7)=105
105 % 10 = 5
So 122456-37-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H21N3/c1-13-7-4-5-10-17(13)23-12-11-16-19(23)15-9-6-8-14(2)18(15)22-20(16)21-3/h4-10H,11-12H2,1-3H3,(H,21,22)
122456-37-5Relevant articles and documents
Reversible Inhibitors of the Gastric (H+/K+)-ATPase. 2. 1-Arylpyrroloquinolines: Effect of the 4-Substituent
Leach, Colin A.,Brown, Thomas H.,Ife, Robert J.,Keeling, David J.,Laing, Shiona M.,et al.
, p. 1845 - 1852 (2007/10/02)
Further work on compounds 1 has identified the 4-position as a site where substantial modifications are tolerated, leading to analogues which are more potent and less toxic than those described previously.The best compound in the series is 13a (SKandF 963
DIHYDROPYRROLO QUINOLINE DERIVATIVES
-
, (2008/06/13)
1,4-Substituted 2,3-dihydropyrrolo[3,2-c]quinolines which are inhibitors of H+ K+ ATPase activity and useful as inhibitors of gastric acid secretion. A compound of the invention is 1-(2-methylphenyl)-4-amino-6-methyl-2,3-dihydropyrrolo[3,2-c]quinoline.
