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Design, synthesis, and bioevaluation of 1 h -pyrrolo[3,2- c ]pyridine derivatives as colchicine-binding site inhibitors with potent anticancer activities

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2302320

2024

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Design, synthesis and biological evaluation of novel podophyllotoxin derivatives as tubulin-targeting anticancer agents

Pharmaceutical biology, 2024-12, Vol.62 (1), p.233-249

2024

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3-aryl-4-(3,4,5-trimethoxyphenyl)pyridines inhibit tubulin polymerisation and act as anticancer agents

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2286939-2286939

2024

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Discovery of novel FGFR4 inhibitors through a build-up fragment strategy

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2343350-2343350

2024

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Development of certain benzylidene coumarin derivatives as anti-prostate cancer agents targeting EGFR and PI3Kβ kinases

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2311157-2311157

2024

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The activity of pyrazolo[4,3- e ][1,2,4]triazine and pyrazolo[4,3- e ]tetrazolo[1,5- b ][1,2,4]triazine sulphonamide derivatives in monolayer and spheroid breast cancer cell cultures

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2343352-2343352

2024

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Design, synthesis, molecular modelling and biological evaluation of novel 6-amino-5-cyano-2-thiopyrimidine derivatives as potent anticancer agents against leukemia and apoptotic inducers

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2304625-2304625

2024

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Design, synthesis, and apoptotic antiproliferative action of new 1,2,3-triazole/1,2,4-oxadiazole hybrids as dual EGFR/VEGFR-2 inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2305856-2305856

2024

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Imparting aromaticity to 2-pyridone derivatives by O -alkylation resulted in new competitive and non-competitive PIM-1 kinase inhibitors with caspase-activated apoptosis

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2304044-2304044

2024

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Multicore iron oxide nanoparticles for magnetic hyperthermia and combination therapy against cancer cells

Journal of colloid and interface science, 2024-09, Vol.670, p.73-85

2024

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A novel acceptor–donor–acceptor structured molecule-based nanosystem for tumor mild photothermal therapy

Journal of colloid and interface science, 2024-09, Vol.670, p.762-773

2024

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J-aggregates of multi-groups cyanine dye for NIR-IIa fluorescence-guided mild photothermal therapy under 1064 nm irradiation

Journal of colloid and interface science, 2024-09, Vol.670, p.751-761

2024

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Glutathione-depleting polyprodrug nanoparticle for enhanced photodynamic therapy and cascaded locoregional chemotherapy

Journal of colloid and interface science, 2024-09, Vol.670, p.279-287

2024

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Polyphosphoester-stabilized cubosomes encapsulating a Ru(II) complex for the photodynamic treatment of lung adenocarcinoma

Journal of colloid and interface science, 2024-09, Vol.670, p.234-245

2024

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Cholesterol sulfate-mediated ion-pairing facilitates the self-nanoassembly of hydrophilic cationic mitoxantrone

Journal of colloid and interface science, 2024-09, Vol.669, p.731-739

2024

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Zinc peroxide-based nanotheranostic platform with endogenous hydrogen peroxide/oxygen generation for enhanced photodynamic-chemo therapy of tumors

Journal of colloid and interface science, 2024-08, Vol.668, p.88-97

2024

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Enhanced catalytic activity of Fe 3 O 4 -carbon dots complex in the Fenton reaction for enhanced immunotherapeutic and oxygenation effects

Journal of colloid and interface science, 2024-08, Vol.668, p.618

2024

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Orchestrating apoptosis and ferroptosis through enhanced sonodynamic therapy using amorphous UIO-66-CoO x

Journal of colloid and interface science, 2024-08, Vol.667, p.91

2024

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Blocking SIG1R Along with Low Cadmium Exposure Display Anti-cancer Qualities in Both MCF7 and MDA-MB-231 Cells

Biological trace element research, 2024-08, Vol.202 (8), p.3588-3600

2024

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Boric Acid Affects Cell Proliferation, Apoptosis, and Oxidative Stress in ALL Cells

Biological trace element research, 2024-08, Vol.202 (8), p.3614-3622

2024

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Empowering hydrophobic anticancer drugs by ultrashort peptides: General Co-assembly strategy for improved solubility, targeted efficacy, and clinical application

Journal of colloid and interface science, 2024-08, Vol.667, p.119-127

2024

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Four-component of double-layer infinite coordination polymer nanocomposites for large tumor trimodal therapy via multi high-efficiency synergies

Journal of colloid and interface science, 2024-07, Vol.666, p.259-275

2024

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Discovery and preclinical evaluations of TQB3616, a novel CDK4-biased inhibitor

Bioorganic & medicinal chemistry letters, 2024-07, Vol.107, p.129769-129769, Article 129769

2024

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Design, synthesis, and bioevaluation of SOS1 PROTACs derived from pyrido[2,3-d]pyrimidin-7-one-based SOS1 inhibitor

Bioorganic & medicinal chemistry letters, 2024-07, Vol.107, p.129780-129780, Article 129780

2024

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Establishment of patient‐derived organoids for guiding personalized therapies in breast cancer patients

International journal of cancer, 2024-07, Vol.155 (2), p.324-338

2024

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Design, synthesis, and bioevaluation of 1 h -pyrrolo[3,2- c ]pyridine derivatives as colchicine-binding site inhibitors with potent anticancer activities

Design, synthesis and biological evaluation of novel podophyllotoxin derivatives as tubulin-targeting anticancer agents

3-aryl-4-(3,4,5-trimethoxyphenyl)pyridines inhibit tubulin polymerisation and act as anticancer agents

Discovery of novel FGFR4 inhibitors through a build-up fragment strategy

Development of certain benzylidene coumarin derivatives as anti-prostate cancer agents targeting EGFR and PI3Kβ kinases

The activity of pyrazolo[4,3- e ][1,2,4]triazine and pyrazolo[4,3- e ]tetrazolo[1,5- b ][1,2,4]triazine sulphonamide derivatives in monolayer and spheroid breast cancer cell cultures

Design, synthesis, molecular modelling and biological evaluation of novel 6-amino-5-cyano-2-thiopyrimidine derivatives as potent anticancer agents against leukemia and apoptotic inducers

Design, synthesis, and apoptotic antiproliferative action of new 1,2,3-triazole/1,2,4-oxadiazole hybrids as dual EGFR/VEGFR-2 inhibitors

Imparting aromaticity to 2-pyridone derivatives by O -alkylation resulted in new competitive and non-competitive PIM-1 kinase inhibitors with caspase-activated apoptosis

Multicore iron oxide nanoparticles for magnetic hyperthermia and combination therapy against cancer cells

A novel acceptor–donor–acceptor structured molecule-based nanosystem for tumor mild photothermal therapy

J-aggregates of multi-groups cyanine dye for NIR-IIa fluorescence-guided mild photothermal therapy under 1064 nm irradiation

Glutathione-depleting polyprodrug nanoparticle for enhanced photodynamic therapy and cascaded locoregional chemotherapy

Polyphosphoester-stabilized cubosomes encapsulating a Ru(II) complex for the photodynamic treatment of lung adenocarcinoma

Cholesterol sulfate-mediated ion-pairing facilitates the self-nanoassembly of hydrophilic cationic mitoxantrone

Zinc peroxide-based nanotheranostic platform with endogenous hydrogen peroxide/oxygen generation for enhanced photodynamic-chemo therapy of tumors

Enhanced catalytic activity of Fe 3 O 4 -carbon dots complex in the Fenton reaction for enhanced immunotherapeutic and oxygenation effects

Orchestrating apoptosis and ferroptosis through enhanced sonodynamic therapy using amorphous UIO-66-CoO x

Blocking SIG1R Along with Low Cadmium Exposure Display Anti-cancer Qualities in Both MCF7 and MDA-MB-231 Cells

Boric Acid Affects Cell Proliferation, Apoptosis, and Oxidative Stress in ALL Cells

Empowering hydrophobic anticancer drugs by ultrashort peptides: General Co-assembly strategy for improved solubility, targeted efficacy, and clinical application

Four-component of double-layer infinite coordination polymer nanocomposites for large tumor trimodal therapy via multi high-efficiency synergies

Discovery and preclinical evaluations of TQB3616, a novel CDK4-biased inhibitor

Design, synthesis, and bioevaluation of SOS1 PROTACs derived from pyrido[2,3-d]pyrimidin-7-one-based SOS1 inhibitor

Establishment of patient‐derived organoids for guiding personalized therapies in breast cancer patients

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