Synthesis and antiproliferative activity of 2-aryl-4-oxo-thiazolidin-3-yl-amides for prostate cancer
We have previously described serine amide phosphates (SAPs) as a novel class of cytotoxic
agents for prostate cancer. Several of them showed potent cytotoxicity against human …
agents for prostate cancer. Several of them showed potent cytotoxicity against human …
Discovery of 2-arylthiazolidine-4-carboxylic acid amides as a new class of cytotoxic agents for prostate cancer
V Gududuru, E Hurh, JT Dalton… - Journal of medicinal …, 2005 - ACS Publications
To improve the selectivity and antiproliferative activity of previously reported serine amide
phosphates (SAPs), we designed a new series of 4-thiazolidinone amides, in which the 4 …
phosphates (SAPs), we designed a new series of 4-thiazolidinone amides, in which the 4 …
Synthesis, in vitro structure–activity relationship, and in vivo studies of 2-arylthiazolidine-4-carboxylic acid amides as anticancer agents
A series of (2RS, 4R)-2-arylthiazolidine-4-carboxylic acid amide (ATCAA) was synthesized.
Antiproliferative activity against melanoma and prostate cancer cells compared with control …
Antiproliferative activity against melanoma and prostate cancer cells compared with control …
Synthesis and antiproliferative activity of thiazolidine analogs for melanoma
We have previously described 2-aryl-thiazolidine-4-carboxylic acid amides as a novel class
of antiproliferative agents for prostate cancer. Screening these compounds with melanoma …
of antiproliferative agents for prostate cancer. Screening these compounds with melanoma …
Design, synthesis and biological evaluation of novel thiosemicarbazone-indole derivatives targeting prostate cancer cells
ZX He, JL Huo, YP Gong, Q An, X Zhang, H Qiao… - European Journal of …, 2021 - Elsevier
To discover novel anticancer agents with potent and low toxicity, we designed and
synthesized a range of new thiosemicarbazone-indole analogues based on lead compound …
synthesized a range of new thiosemicarbazone-indole analogues based on lead compound …
Syntheses and potential anti-prostate cancer activities of ionone-based chalcones
We report the SAR studies of 43 ionone-based chalcones that demonstrate substantial in
vitro anti-proliferative activities in LNCaP, MDA-PCa-2b, 22Rv1, C4-2B and PC-3 prostate …
vitro anti-proliferative activities in LNCaP, MDA-PCa-2b, 22Rv1, C4-2B and PC-3 prostate …
Synthesis and antitumor activities of novel thiourea α-aminophosphonates from dehydroabietic acid
XC Huang, M Wang, YM Pan, GY Yao, HS Wang… - European Journal of …, 2013 - Elsevier
A series of novel thiourea α-aminophosphonate derivatives containing DHA structure was
designed and synthesized as antitumor agents. Their inhibitory activities against the NCI …
designed and synthesized as antitumor agents. Their inhibitory activities against the NCI …
Synthesis and apoptosis inducing ability of new anilino substituted pyrimidine sulfonamides as potential anticancer agents
A series of anilino substituted pyrimidine sulfonamides were prepared and evaluated for
their anticancer activity. These sulfonamides showed promising activity with IC50 values …
their anticancer activity. These sulfonamides showed promising activity with IC50 values …
Synthesis and antitumor activity of α-aminophosphonate derivatives containing thieno [2, 3-d] pyrimidines
YC Guo, J Li, JL Ma, ZR Yu, HW Wang, WJ Zhu… - Chinese Chemical …, 2015 - Elsevier
Abstract Two series of thieno [2, 3-d] pyrimidine derivatives were designed and synthesized,
in which bioactive α-aminophosphonate subunits were introduced at the N3 position through …
in which bioactive α-aminophosphonate subunits were introduced at the N3 position through …
Synthesis and anticancer activity of some novel benzothiazole-thiazolidine derivatives
ABSTRACT Sixteen new 2-(benzothiazol-2-ylthio)-N′-(3-substituted-4-(3, 4-
substitutedphenyl) thiazol-2 (3H)-ylidene) acetohydrazide derivatives (4a-4p) were …
substitutedphenyl) thiazol-2 (3H)-ylidene) acetohydrazide derivatives (4a-4p) were …
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