19839-52-2 Usage
Description
1H-Pyrido[3,4-b]indol-1-one, 2,9-dihydrois a chemical compound with a molecular formula of C11H9NO. It is a derivative of indole and is a biologically active compound that has been found to possess anticancer and anti-inflammatory properties. It is also known to exhibit potential neuroprotective effects. 1H-Pyrido[3,4-b]indol-1-one, 2,9-dihydrohas been the subject of research for its potential use in pharmaceuticals and medical treatments due to its wide range of biological activities. Its chemical structure and properties make it a valuable compound for further investigation and potential development of therapeutic applications.
Uses
Used in Pharmaceutical Industry:
1H-Pyrido[3,4-b]indol-1-one, 2,9-dihydrois used as a pharmaceutical compound for its anticancer properties. It has been found to possess potential in treating various types of cancer due to its ability to target and inhibit the growth of cancer cells.
Used in Anti-Inflammatory Applications:
1H-Pyrido[3,4-b]indol-1-one, 2,9-dihydrois used as an anti-inflammatory agent for its ability to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Neuroprotective Applications:
1H-Pyrido[3,4-b]indol-1-one, 2,9-dihydrois used as a neuroprotective agent for its potential to protect neurons and prevent neurodegeneration, making it a promising candidate for the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's.
Check Digit Verification of cas no
The CAS Registry Mumber 19839-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,3 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19839-52:
(7*1)+(6*9)+(5*8)+(4*3)+(3*9)+(2*5)+(1*2)=152
152 % 10 = 2
So 19839-52-2 is a valid CAS Registry Number.
19839-52-2Relevant articles and documents
Inhibition of adenosine 3',5'-cyclic monophosphate phosphodiesterase by alkaloids. II
Ohmoto,Nikaido,Koike,Kohda,Sankawa
, p. 4588 - 4592 (1988)
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An expedient stereoselective route to the ACE tricyclic core of manzamine A via a palladium-catalysed arylative allene spirocyclisation cascade
Hawkins, Alison,Jakubec, Pavol,Ironmonger, Alan,Dixon, Darren J.
, p. 365 - 369 (2013)
Application of a novel palladium-catalysed stereoselective arylative allene spirocyclisation cascade as the key step for the construction of the ACE tricyclic core of manzamine A is described.
Direct Tryptophols Synthesis from 2-Vinylanilines and Alkynes via C - C Triple Bond Cleavage and Dioxygen Activation
Shen, Tao,Zhang, Yiqun,Liang, Yu-Feng,Jiao, Ning
, p. 13147 - 13150 (2016/10/24)
An unexpected metal-free C - C triple bond cleavage, dioxygen activation, and reassembly into tryptophol derivatives has been developed. This chemistry provides a novel, simple, and efficient approach to highly valuable tryptophol derivatives from simple substrates under mild conditions. The mechanistic studies may promote the discovery of new methodologies through C-C bond cleavage and dioxygen activation.
Efficient synthesis of eudistomin U and evaluation of its cytotoxicity
Roggero, Chad M.,Giulietti, Jennifer M.,Mulcahy, Seann P.
, p. 3549 - 3551 (2014/07/22)
Eudistomin U is a member of a subclass of naturally occurring indole alkaloids known as β-carbolines. These molecules are reported to have diverse biological activity and high binding affinity to DNA, which make them attractive targets for total synthesis
