2,3-Disubstituted-1,4-naphthoquinones, 12H-benzo[b]phenothiazine-6,11-diones and related compounds: synthesis and biological evaluation as potential antiproliferative and antifungal agents.
Vishnu K Tandon, Hardesh K Maurya, Ashutosh Tripathi, G B ShivaKeshava, Praveen K Shukla, Pallavi Srivastava, Dulal Panda, Vishnu K. Tandon, Hardesh K. Maurya, Ashutosh Tripathi, G.B. ShivaKeshava, Praveen K. Shukla, Pallavi Srivastava, Dulal Panda
文献索引:Eur. J. Med. Chem. 44 , 1086-92, (2009)
全文:HTML全文
摘要
A series of 2-chloro-3-arylsulfanyl-[1,4]naphthoquinones (2), 2,3-bis-arylsulfanyl-[1,4]naphthoquinones (3) and 12H-benzo[b]phenothiazine-6,11-diones and their analogs 6-8 were synthesized and evaluated for their antiproliferative activity against human cervical cancer (HeLa) cells. Compounds 3a and 3b were found to possess most potent antiproliferative and cell killing ability. Compounds 1-8 were also evaluated for antifungal activities. The structure-activity relationship of these compounds was studied and the results show that compound 2a (MIC(50)=1.56 microg/mL) exhibited in vitro potent antifungal activity compared to the clinically useful antifungal drug Fluconazole (MIC(50)=2.0 microg/mL) against Sporothrix. schenckii. Compound 2a (MIC(50)=1.56 microg/mL) also exhibited same antifungal activity compared to clinically useful drug Amphotericin-B (MIC(50)=1.56 microg/mL) against Trichophyton. mentagraphytes.
相关化合物
相关文献:
2008-03-27
[J. Med. Chem. 51 , 1706-18, (2008)]
2007-08-01
[Bioorg. Med. Chem. 15 , 5340-50, (2007)]
1988-08-01
[Bull. Environ. Contam. Toxicol. 41(2) , 164-71, (1988)]
2012-12-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 98 , 378-83, (2012)]
1993-01-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 60(7) , 1641-7, (2004)]