The in vitro evaluation of thieno[3,2-d]pyrimidines identified halogenated compounds 1 and 2 with antiproliferative activity against three different cancer cell lines. A structure activity relationship study indicated the necessity of the chlorine at the C4-position for biological activity. The two most active compounds 1 and 2 were found to induce apoptosis in the leukemia L1210 cell line. Additionally, the compounds were screened against a variety of other microbial targets and as a result, selective activity against several fungi was also observed. The synthesis and preliminary biological results are reported herein.status: publishe
A series of 78 synthetic 7-chloro-(4-thioalkylquinoline) derivatives were investigated for cytotoxic...
Department of Chemistry. Saurashtra Universitty, Rajlot-360 005 Manuscript received 21 December 199...
Two new series of inhibitors of tubulin polymerization based on the 2-(alkoxycarbonyl)-3-(3',4',5'-t...
The in vitro evaluation of thieno[3,2-d]pyrimidines identified halogenated compounds 1 and 2 with an...
Anticancer screening of several novel thienopyrimidines has been performed. The thienopyrimidine der...
In vitro evaluation of the halogenated pyrrolo[3,2-d]pyrimidines identified antiproliferative activi...
The evolution of medicine from alchemy to rationale-based drug design has been instrumental in allev...
Thieno[3,2-d]pyrimidine as an effective pharmacophore has been extensively studied. However, its 2,6...
3-Methyl-6-phenyl-2-thioxo-2,3-dihydrothieno[3,2-d]pyrimidin- 4(1H)-one (2), on treatment with phosp...
International audienceA series of thieno[2,3-d]- and thieno[3,2-d]pyrimidines have been easily synth...
The anticancer activity of the thieno[2,3-b]pyridines was explored by altering the ring size of the ...
From 2-amino-3-ethoxycarbonyl-4,5-dimethyl-, -polymethylenethiophenes (1-4) were synthesized 2,3-dis...
This work describes the synthesis and anticancer activity against kinase enzymes of newly designed t...
Thiazolo[4,5-d]pyrimidine derivatives are considered potential therapeutic agents, particularly in t...
Two new series of inhibitors of tubulin polymerization based on the 2-(alkoxycarbonyl)-3-(3',4',5'-t...
A series of 78 synthetic 7-chloro-(4-thioalkylquinoline) derivatives were investigated for cytotoxic...
Department of Chemistry. Saurashtra Universitty, Rajlot-360 005 Manuscript received 21 December 199...
Two new series of inhibitors of tubulin polymerization based on the 2-(alkoxycarbonyl)-3-(3',4',5'-t...
The in vitro evaluation of thieno[3,2-d]pyrimidines identified halogenated compounds 1 and 2 with an...
Anticancer screening of several novel thienopyrimidines has been performed. The thienopyrimidine der...
In vitro evaluation of the halogenated pyrrolo[3,2-d]pyrimidines identified antiproliferative activi...
The evolution of medicine from alchemy to rationale-based drug design has been instrumental in allev...
Thieno[3,2-d]pyrimidine as an effective pharmacophore has been extensively studied. However, its 2,6...
3-Methyl-6-phenyl-2-thioxo-2,3-dihydrothieno[3,2-d]pyrimidin- 4(1H)-one (2), on treatment with phosp...
International audienceA series of thieno[2,3-d]- and thieno[3,2-d]pyrimidines have been easily synth...
The anticancer activity of the thieno[2,3-b]pyridines was explored by altering the ring size of the ...
From 2-amino-3-ethoxycarbonyl-4,5-dimethyl-, -polymethylenethiophenes (1-4) were synthesized 2,3-dis...
This work describes the synthesis and anticancer activity against kinase enzymes of newly designed t...
Thiazolo[4,5-d]pyrimidine derivatives are considered potential therapeutic agents, particularly in t...
Two new series of inhibitors of tubulin polymerization based on the 2-(alkoxycarbonyl)-3-(3',4',5'-t...
A series of 78 synthetic 7-chloro-(4-thioalkylquinoline) derivatives were investigated for cytotoxic...
Department of Chemistry. Saurashtra Universitty, Rajlot-360 005 Manuscript received 21 December 199...
Two new series of inhibitors of tubulin polymerization based on the 2-(alkoxycarbonyl)-3-(3',4',5'-t...