Synthesis and Anti-Breast Cancer Potency of Mono- and Bis-(pyrazolyl[1,2,4]triazolo[3,4-<i>b</i>][1,3,4]thiadiazine) Derivatives as EGFR/CDK-2 Target Inhibitors-Reference-Cited by-同舟云学术

Synthesis and Anti-Breast Cancer Potency of Mono- and Bis-(pyrazolyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine) Derivatives as EGFR/CDK-2 Target Inhibitors

Published:2023-09-11 Issue:38 Volume:8 Page:35359-35369
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Salem Mostafa E.¹²,Mahrous Esraa M.¹,Ragab Eman A.¹,Nafie Mohamed S.³⁴^ORCID,Dawood Kamal M.¹^ORCID

Affiliation:

1. Department of Chemistry, Faculty of Science, Cairo University, Giza 12613, Egypt

2. Department of Chemistry, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh 11623, Saudi Arabia

3. Chemistry Department, College of Sciences, University of Sharjah, P. O. Box 27272, Sharjah 27272, United Arab Emirates

4. Department of Chemistry (Biochemistry Program), Faculty of Science, Suez Canal University, Ismailia 41522, Egypt

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsomega.3c05309

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4. Synthesis, biological evaluation and molecular docking studies of aminochalcone derivatives as potential anticancer agents by targeting tubulin colchicine binding site

5. Synthesis, biological evaluation, and molecular modelling of new naphthalene-chalcone derivatives as potential anticancer agents on MCF-7 breast cancer cells by targeting tubulin colchicine binding site

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