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Synthesis and biological evaluation of a new class of 4-aminoquinoline- rhodanine hybrid as potent anti-infective agents

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Chauhan, Kuldeep
Sharma, Moni
Saxena, Juhi
Singh, S V
Trivedi, Priyanka
Srivastava, Kumkum
Puri, S K
Saxena, J K
Chaturvedi, Vinita
Chauhan, P M S
 
Date 2013-04-15T08:13:16Z
2013-04-15T08:13:16Z
2013
 
Identifier European Journal of Medicinal Chemistry 2013, 62, 693–704
http://hdl.handle.net/123456789/1047
 
Description Synthesis of novel 4-aminoquinoline-rhodanine hybrid using inexpensive starting materials via easy to operate methodology, and their biological activity is reported. All the compounds were screened for their in vitro antimalarial activity against chloroquine-resistant (K1) and chloroquine-sensitive (3D7) strains of Plasmodium falciparum, and their cytotoxicity towards VERO cell line. Compounds 9, 19, 21 and 23 exhibited excellent antimalarial activity with IC50 value ranging from 13.2-45.5 nM against chloroquine-resistant (K1) strain. Biochemical studies revealed that inhibition of hemozoin formation is the primary mechanism of action of these analogues for their antimalarial activity. Additionally, some derivatives (14, 18 and 26) of this series also exhibited the antimycobacterial activity against H37Rv strain of Mycobacterium tuberculosis with MIC value of 6.25 µM.
 
Format 443783 bytes
application/pdf
 
Language en
 
Relation CDRI Communication No. 8381
 
Subject 4-Aminoquinoline
Rhodanine
Antimalarial
Antitubercular
Cytotoxicity
 
Title Synthesis and biological evaluation of a new class of 4-aminoquinoline- rhodanine hybrid as potent anti-infective agents
 
Type Article