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A review on diverse heterocyclic compounds as the privileged scaffolds in non-steroidal aromatase inhibitors
Breast cancer, emerging malignancy is common among women due to overexpression of
estrogen. Estrogens are biosynthesized from androgens by aromatase, a cytochrome P450 …
estrogen. Estrogens are biosynthesized from androgens by aromatase, a cytochrome P450 …
Recent development in indole derivatives as anticancer agent: A mechanistic approach
N Devi, K Kaur, A Biharee… - Anti-Cancer Agents in …, 2021 - benthamdirect.com
Background: Cancer accounts for several deaths each year. There are multiple FDA
approved drugs for cancer treatments. Due to the severe side effects and multiple drug …
approved drugs for cancer treatments. Due to the severe side effects and multiple drug …
Design, synthesis, molecular modeling, DFT, ADME and biological evaluation studies of some new 1, 3, 4-oxadiazole linked benzimidazoles as anticancer agents and …
Breast cancer is the most frequent female cancer and second cause of cancer-related
deaths among women around the world. Two thirds of breast cancer patients have hormone …
deaths among women around the world. Two thirds of breast cancer patients have hormone …
New thieno [3, 2-d] pyrimidine-based derivatives: Design, synthesis and biological evaluation as antiproliferative agents, EGFR and ARO inhibitors inducing apoptosis …
AM Farghaly, OM AboulWafa, HH Baghdadi… - Bioorganic …, 2021 - Elsevier
An array of newly synthesized thieno [3, 2-d] pyrimidine-based derivatives and
thienotriazolopyrimidines hybridized with some pharmacophoric anticancer fragments were …
thienotriazolopyrimidines hybridized with some pharmacophoric anticancer fragments were …
[HTML][HTML] Synthesis, docking studies and biological activity of new benzimidazole-triazolothiadiazine derivatives as aromatase inhibitor
In the last step of estrogen biosynthesis, aromatase enzyme catalyzes the conversion of
androgens to estrogens. Aromatase inhibition is an important way to control estrogen …
androgens to estrogens. Aromatase inhibition is an important way to control estrogen …
Synthesis and docking study of benzimidazole–triazolothiadiazine hybrids as aromatase inhibitors
Aromatase is involved in the biosynthesis of estrogen and thus is a critical target for breast
cancer. In this study, to identify new aromatase enzyme inhibitors, seven 3‐[4‐(5‐methyl‐1H …
cancer. In this study, to identify new aromatase enzyme inhibitors, seven 3‐[4‐(5‐methyl‐1H …
Benzoxazole derivatives as new generation of anti-breast cancer agents
AMME Omar, OM AboulWafa, MS El-Shoukrofy… - Bioorganic …, 2020 - Elsevier
New 2-substituted benzoxazole derivatives were synthesized and screened for their in vitro
anti-proliferative activities against MCF-7 and MDA-MB-231 cell lines. Compounds 4b, 4d …
anti-proliferative activities against MCF-7 and MDA-MB-231 cell lines. Compounds 4b, 4d …
New imidazole derivatives as aromatase inhibitor: Design, synthesis, biological activity, molecular docking, and computational ADME-Tox studies
In this study, a series of imidazole derivatives was designed, synthesized, and evaluated for
in vitro biological activity on the human breast cancer cell line MCF7 by MTT assay. To …
in vitro biological activity on the human breast cancer cell line MCF7 by MTT assay. To …
Antiproliferative activity, enzymatic inhibition and apoptosis-promoting effects of benzoxazole-based hybrids on human breast cancer cells
AMME Omar, OM AboulWafa, ME Amr… - Bioorganic …, 2021 - Elsevier
Abstract New benzoxazole derivatives containing 1, 3, 4-oxadiazole, 1, 2, 4-triazole or
triazolothiadiazine rings were synthesized and screened for their in vitro antiproliferative …
triazolothiadiazine rings were synthesized and screened for their in vitro antiproliferative …
Enantioselective synthesis of indole derivatives by Rh/Pd relay catalysis and their anti-inflammatory evaluation
S Li, Z Wang, H **ao, Z Bian, JJ Wang - Chemical Communications, 2020 - pubs.rsc.org
An efficient Rh/Pd relay catalyzed intermolecular and cascade intramolecular
hydroamination for the synthesis of exclusive trans 1-indolyl dihydronaphthalenols (up to …
hydroamination for the synthesis of exclusive trans 1-indolyl dihydronaphthalenols (up to …