Synthesis, in-vitro screening, and docking analysis of novel pyrrolidine and piperidine-substituted ethoxy chalcone as anticancer agents
A series of novel-substituted chalcone analogs were synthesized and evaluated for
antiproliferative activity against estrogen receptor-positive MCF-7 breast cancer cell lines …
antiproliferative activity against estrogen receptor-positive MCF-7 breast cancer cell lines …
[引用][C] Synthesis, in-vitro screening, and docking analysis of novel pyrrolidine and piperidine-substituted ethoxy chalcone as anticancer agents
SN Mokale, PN Dube, SA Bhavale, I Sayed… - Medicinal Chemistry …, 2014 - cir.nii.ac.jp
Synthesis, in-vitro screening, and docking analysis of novel pyrrolidine and piperidine-substituted
ethoxy chalcone as anticancer agents | CiNii Research CiNii 国立情報学研究所 学術情報 …
ethoxy chalcone as anticancer agents | CiNii Research CiNii 国立情報学研究所 学術情報 …
[PDF][PDF] Synthesis, in-vitro screening, and docking analysis of novel pyrrolidine and piperidine-substituted ethoxy chalcone as anticancer agents
SN Mokale, PN Dube, SA Bhavale, I Sayed, A Begum… - academia.edu
A series of novel-substituted chalcone analogs were synthesized and evaluated for
antiproliferative activity against estrogen receptor-positive MCF-7 breast cancer cell lines …
antiproliferative activity against estrogen receptor-positive MCF-7 breast cancer cell lines …
Synthesis, in-vitro screening, and docking analysis of novel pyrrolidine and piperidine-substituted ethoxy chalcone as anticancer agents
SN Mokale, PN Dube, SA Bhavale, I Sayed… - Medicinal Chemistry …, 2015 - infona.pl
A series of novel-substituted chalcone analogs were synthesized and evaluated for
antiproliferative activity against estrogen receptor-positive MCF-7 breast cancer cell lines …
antiproliferative activity against estrogen receptor-positive MCF-7 breast cancer cell lines …