879398-80-8 Usage
Molecular structure
1H-Pyrrolo[2,3-c]pyridine-5-carboxylic acid, 3-[[(2S)-2-(aminocarbonyl)-1-pyrrolidinyl]methyl]-1-[(4-fluorophenyl)methyl]-, methyl ester is a complex organic compound consisting of a pyrrolopyridine ring with various functional groups attached to it.
Pyrrolopyridine ring
The core structure of 1H-Pyrrolo[2,3-c]pyridine-5-carboxylic acid,
3-[[(2S)-2-(aminocarbonyl)-1-pyrrolidinyl]methyl]-1-[(4-fluorophenyl)meth
yl]-, methyl ester is a fusion of a pyrrole and a pyridine ring, which are both nitrogen-containing heterocyclic aromatic rings.
Carboxylic acid group
The compound contains a 5-carboxylic acid group, which is a functional group consisting of a carbonyl group (C=O) and a hydroxyl group (OH) bonded to the same carbon atom.
Methyl ester group
A methyl ester group (-COOCH3) is present in the compound, which is formed by the esterification of the carboxylic acid group with methanol (CH3OH).
Substituted phenyl group
The compound has a substituted phenyl group (4-fluorophenyl) attached to the pyrrolopyridine ring, which is an aromatic ring with a fluorine atom at the 4-position.
Potential applications
Due to its unique structure and functional groups, 1H-Pyrrolo[2,3-c]pyridine-5-carboxylic acid,
3-[[(2S)-2-(aminocarbonyl)-1-pyrrolidinyl]methyl]-1-[(4-fluorophenyl)meth
yl]-, methyl ester may have potential applications in the development of pharmaceuticals or other chemical products. Further research is needed to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 879398-80-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,3,9 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 879398-80:
(8*8)+(7*7)+(6*9)+(5*3)+(4*9)+(3*8)+(2*8)+(1*0)=258
258 % 10 = 8
So 879398-80-8 is a valid CAS Registry Number.
879398-80-8Relevant academic research and scientific papers
Azaindole N-methyl hydroxamic acids as HIV-1 integrase inhibitors-II. the impact of physicochemical properties on ADME and PK
Tanis, Steven P.,Plewe, Michael B.,Johnson, Ted W.,Butler, Scott L.,Dalvie, Deepak,Delisle, Dorothy,Dress, Klaus R.,Hu, Qiyue,Huang, Buwen,Kuehler, Jon E.,Kuki, Atsuo,Liu, Wen,Peng, Qinghai,Smith, Graham L.,Solowiej, Jim,Tran, Khanh T.,Wang, Hai,Yang, Anle,Yin, Chunfeng,Yu, Xiaoming,Zhang, Junhu,Zhu, Huichun
supporting information; experimental part, p. 7429 - 7434 (2011/02/26)
HIV-1 integrase is one of three enzymes encoded by the HIV genome and is essential for viral replication, and HIV-1 IN inhibitors have emerged as a new promising class of therapeutics. Recently, we reported the discovery of azaindole hydroxamic acids that
INHIBITORS OF THE HIV INTEGRASE ENZYME
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Page/Page column 84-85, (2010/10/20)
The present invention relates to compounds of formula (I), or a pharmaceutically acceptable salt or solvate thereof, pharmaceutical compositions comprisingm compounds of formula (I), and their methods of use in treating HIV-infected mammals.
