[HTML][HTML] Anticancer potential of alkaloids: a key emphasis to colchicine, vinblastine, vincristine, vindesine, vinorelbine and vincamine
Cancer, one of the leading illnesses, accounts for about 10 million deaths worldwide. The
treatment of cancer includes surgery, chemotherapy, radiation therapy, and drug therapy …
treatment of cancer includes surgery, chemotherapy, radiation therapy, and drug therapy …
[HTML][HTML] HIV Infection: Shaping the Complex, Dynamic, and Interconnected Network of the Cytoskeleton
R Cabrera-Rodríguez, S Pérez-Yanes… - International journal of …, 2023 - mdpi.com
HIV-1 has evolved a plethora of strategies to overcome the cytoskeletal barrier (ie, actin and
intermediate filaments (AFs and IFs) and microtubules (MTs)) to achieve the viral cycle. HIV …
intermediate filaments (AFs and IFs) and microtubules (MTs)) to achieve the viral cycle. HIV …
Discovery of novel benzimidazole and indazole analogues as tubulin polymerization inhibitors with potent anticancer activities
Y Ren, Y Wang, G Li, Z Zhang, L Ma… - Journal of Medicinal …, 2021 - ACS Publications
Novel indazole and benzimidazole analogues were designed and synthesized as tubulin
inhibitors with potent antiproliferative activities. Among them, compound 12b exhibited the …
inhibitors with potent antiproliferative activities. Among them, compound 12b exhibited the …
Novel indole-pyrazole hybrids as potential tubulin-targeting agents; Synthesis, antiproliferative evaluation, and molecular modeling studies
Abstract Structurally diverse indole-3-pyrazole-5-carboxamide analogues (10-29) were
designed, synthesized, and evaluated for their antiproliferative activity against three cancer …
designed, synthesized, and evaluated for their antiproliferative activity against three cancer …
SB226, an inhibitor of tubulin polymerization, inhibits paclitaxel-resistant melanoma growth and spontaneous metastasis
S Deng, S Banerjee, H Chen, S Pochampally, Y Wang… - Cancer letters, 2023 - Elsevier
Extensive preclinical studies have shown that colchicine-binding site inhibitors (CBSIs) are
promising drug candidates for cancer therapy. Although numerous CBSIs were generated …
promising drug candidates for cancer therapy. Although numerous CBSIs were generated …
Design, synthesis and biological evaluation of novel acridine and quinoline derivatives as tubulin polymerization inhibitors with anticancer activities
Y Ren, Y Ruan, B Cheng, L Li, J Liu, Y Fang… - Bioorganic & Medicinal …, 2021 - Elsevier
A series of acridine and quinoline derivatives were designed and synthesized based on our
previous work as novel tubulin inhibitors targeting the colchicine binding site. Among them …
previous work as novel tubulin inhibitors targeting the colchicine binding site. Among them …
[HTML][HTML] Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents
DS Alshaya, RMO Tawakul, I Zaki, AHA Almaaty… - RSC …, 2023 - pubs.rsc.org
A new series of acrylic acid and acrylate ester derivatives as modified analogs of tubulin
polymerization inhibitors were designed and synthesized. The antiproliferative activity of the …
polymerization inhibitors were designed and synthesized. The antiproliferative activity of the …
Microtubule‐targeting agents for cancer treatment: Seven binding sites and three strategies
X Wang, B Gigant, X Zheng, Q Chen - MedComm–Oncology, 2023 - Wiley Online Library
Microtubules are pivotal in diverse cellular functions encompassing cell signaling,
morphology, intracellular trafficking, and cell mitosis/division. They are validated targets for …
morphology, intracellular trafficking, and cell mitosis/division. They are validated targets for …
Design, synthesis, and biological evaluation of novel diphenylamine derivatives as tubulin polymerization inhibitors targeting the colchicine binding site
XY Yan, JF Leng, TT Chen, YJ Zhao, LY Kong… - European Journal of …, 2022 - Elsevier
A novel series of diphenylamine derivatives were designed and synthesized, and their
biological activities were evaluated. The anti-proliferative activities of the derivatives were …
biological activities were evaluated. The anti-proliferative activities of the derivatives were …
Discovery and biological evaluation of 4, 6-pyrimidine analogues with potential anticancer agents as novel colchicine binding site inhibitors
J Zhang, L Tan, C Wu, Y Li, H Chen, Y Liu… - European Journal of …, 2023 - Elsevier
Abstract Novel 4, 6-pyrimidine analogues were designed and synthesized as colchicine
binding site inhibitors (CBSIs) with potent antiproliferative activities. Among them, compound …
binding site inhibitors (CBSIs) with potent antiproliferative activities. Among them, compound …