BRAF-Targeted Anticancer Agents: Synthesis, Molecular Docking, and In Vitro Evaluation of Novel 1,3,4-Thiadiazolyl-Benzamide Derivatives

Indhumathy P., Gandhimathi Rathinasamy

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DOI: 10.2174/0115701638478360261020053650
Published: 2026-10-22
Container: Current Drug Discovery Technologies
Publisher: Bentham Science Publishers Ltd.
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.2174/0115701638478360261020053650,
  title = {BRAF-Targeted Anticancer Agents: Synthesis, Molecular Docking, and In Vitro Evaluation of Novel 1,3,4-Thiadiazolyl-Benzamide Derivatives},
  author = {Indhumathy P. and Gandhimathi Rathinasamy},
  year = {2026},
  journal = {Current Drug Discovery Technologies},
  doi = {10.2174/0115701638478360261020053650},
  url = {https://doi.org/10.2174/0115701638478360261020053650}
}

RIS

TY  - JOUR
TI  - BRAF-Targeted Anticancer Agents: Synthesis, Molecular Docking, and In Vitro Evaluation of Novel 1,3,4-Thiadiazolyl-Benzamide Derivatives
AU  - Indhumathy P.
AU  - Gandhimathi Rathinasamy
PY  - 2026
JO  - Current Drug Discovery Technologies
DO  - 10.2174/0115701638478360261020053650
UR  - https://doi.org/10.2174/0115701638478360261020053650
ER  -

APA

P., I., & Rathinasamy, G. (2026). BRAF-Targeted Anticancer Agents: Synthesis, Molecular Docking, and In Vitro Evaluation of Novel 1,3,4-Thiadiazolyl-Benzamide Derivatives. Current Drug Discovery Technologies. https://doi.org/10.2174/0115701638478360261020053650

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crossref · retrieved 2026-11-04T13:27:41.864Z