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Ethyl malonate amides: a diketo acid offspring fragment for HIV integrase inhibition.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2011 Aug 15; Vol. 19 (16), pp. 5000-5. Date of Electronic Publication: 2011 Jun 29. - Publication Year :
- 2011
-
Abstract
- While searching for new HIV integrase inhibitors we discovered that some ethyl malonate amides (EMA) are active against this enzyme. Surprisingly, the main function can only very rarely be found among the reported drug candidates. We synthesised a series of compounds in order to establish and analyse the structure-activity relationship. The similarity to the important classes of HIV integrase inhibitors as well as the synthetic availability of the different targets including this pharmacophore makes EMA compounds an interesting object of investigations.<br /> (Copyright © 2011 Elsevier Ltd. All rights reserved.)
- Subjects :
- Amides chemistry
Antiviral Agents chemistry
Antiviral Agents pharmacology
Carboxylic Acids chemical synthesis
Carboxylic Acids chemistry
Carboxylic Acids pharmacology
Data Mining
Drug Design
HIV Integrase analysis
HIV Integrase metabolism
HIV Integrase Inhibitors chemistry
HIV Integrase Inhibitors pharmacology
HIV-1 enzymology
Humans
Keto Acids chemistry
Malonates chemistry
Malonates pharmacology
Models, Molecular
Molecular Structure
Molecular Targeted Therapy
Quinolines chemical synthesis
Quinolines chemistry
Quinolines pharmacology
Structure-Activity Relationship
Amides chemical synthesis
Antiviral Agents chemical synthesis
HIV Integrase drug effects
HIV Integrase Inhibitors chemical synthesis
HIV-1 drug effects
Keto Acids chemical synthesis
Malonates chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3391
- Volume :
- 19
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 21767953
- Full Text :
- https://doi.org/10.1016/j.bmc.2011.06.054