Works matching DE "ANTINEOPLASTIC agents"
Results: 5000
Revisiting the association between sodium-glucose cotransporter-2 inhibitors and the risk of neoplasm in patients with type 2 diabetes: new insights from an updated systematic review and meta-analysis of randomized controlled trials.
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- Expert Review of Clinical Pharmacology, 2025, v. 18, n. 3, p. 165, doi. 10.1080/17512433.2024.2439970
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Improvement of assessment in surrogate endpoint and safety outcome of single-arm trials for anticancer drugs.
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- Expert Review of Clinical Pharmacology, 2024, v. 17, n. 5/6, p. 477, doi. 10.1080/17512433.2024.2344669
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The application of snake venom in anticancer drug discovery: an overview of the latest developments.
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- Expert Opinion on Drug Discovery, 2025, v. 20, n. 3, p. 317, doi. 10.1080/17460441.2025.2465364
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Omega-3 polyunsaturated fatty acid derived lipid mediators: a comprehensive update on their application in anti-cancer drug discovery.
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- Expert Opinion on Drug Discovery, 2024, v. 19, n. 5, p. 617, doi. 10.1080/17460441.2024.2340493
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Relacorilant in recurrent ovarian cancer: clinical evidence and future perspectives.
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- Expert Review of Anticancer Therapy, 2024, v. 24, n. 8, p. 649, doi. 10.1080/14737140.2024.2362178
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Are statins onco- suppressive agents for every type of tumor? A systematic review of literature.
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- Expert Review of Anticancer Therapy, 2024, v. 24, n. 6, p. 435, doi. 10.1080/14737140.2024.2343338
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Post‐marketing surveillance data for avelumab + axitinib treatment in patients with advanced renal cell carcinoma in Japan: Subgroup analyses by pathological classification.
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- International Journal of Urology, 2025, v. 32, n. 3, p. 293, doi. 10.1111/iju.15646
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Current status of endoscopic ultrasound‐guided antitumor treatment for pancreatic cancer.
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- Digestive Endoscopy, 2025, v. 37, n. 1, p. 18, doi. 10.1111/den.14815
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Construction of oral squamous cell carcinoma organoids in vitro 3D‐culture for drug screening.
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- Oral Diseases, 2025, v. 31, n. 1, p. 99, doi. 10.1111/odi.15044
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Assessment of pain prevalence in cancer patients undergoing anticancer treatments and in cancer survivors after completion of anticancer treatments: A French nationwide cross‐sectional study.
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- International Journal of Cancer, 2025, v. 156, n. 10, p. 1873, doi. 10.1002/ijc.35280
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Anticancer (cytotoxic, anticlonogenic, antimetastatic, immunomodulatory actions) properties of 3,5‐dibromosalicylaldehyde against glioblastoma cells and DFT analyses (FT‐IR, Raman, NMR, UV) as well as a molecular docking study.
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- Biology of the Cell (Wiley-Blackwell), 2025, v. 117, n. 2, p. 1, doi. 10.1111/boc.202400138
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A phase 2 basket study of talabostat, a small‐molecule inhibitor of dipeptidyl peptidases, administered in combination with pembrolizumab in patients with advanced solid cancers.
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- Cancer (0008543X), 2025, v. 131, n. 3, p. 1, doi. 10.1002/cncr.35728
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Impact of Acid‐Reducing Agents on Sotorasib Pharmacokinetics and Potential Mitigation of the Impact by Coadministration With an Acidic Beverage.
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- Clinical Pharmacology in Drug Development, 2025, v. 14, n. 2, p. 167, doi. 10.1002/cpdd.1489
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Impact of oncologic diseases on outcome in patients with severe isolated tricuspid regurgitation.
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- European Journal of Clinical Investigation, 2025, v. 55, n. 3, p. 1, doi. 10.1111/eci.14367
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Antitumor Effect of Apilactobacillus kosoi 10H by Inducing Immunostimulatory Macrophages.
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- Cellular Microbiology, 2025, v. 2025, p. 1, doi. 10.1155/cmi/4115145
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Cutaneous Toxicities of MEK Inhibitor Use in Children: A Comparison of Binimetinib and Selumetinib.
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- Pediatric Dermatology, 2025, v. 42, n. 1, p. 67, doi. 10.1111/pde.15792
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BF‐BOIN‐ET: A Backfill Bayesian Optimal Interval Design Using Efficacy and Toxicity Outcomes for Dose Optimization.
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- Pharmaceutical Statistics, 2025, v. 24, n. 2, p. 1, doi. 10.1002/pst.2470
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A Model‐Based Trial Design With a Randomization Scheme Considering Pharmacokinetics Exposure for Dose Optimization in Oncology.
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- Pharmaceutical Statistics, 2025, v. 24, n. 2, p. 1, doi. 10.1002/pst.2454
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Plasma‐Activated Hydrogel Synergies With Paclitaxel to Enhance the Anticancer Efficacy.
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- Plasma Processes & Polymers, 2025, v. 22, n. 2, p. 1, doi. 10.1002/ppap.202400167
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An In Vivo Study of LNS8801, a GPER Agonist, in a Spontaneous Melanoma‐Prone Mouse Model, TGS.
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- Pigment Cell & Melanoma Research, 2025, v. 38, n. 1, p. 1, doi. 10.1111/pcmr.13197
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Unlocking the Chemical Diversity of Plant Catharanthus roseus: Nuclear Magnetic Resonance Spectroscopy Approach.
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- Magnetic Resonance in Chemistry, 2025, v. 63, n. 3, p. 205, doi. 10.1002/mrc.5504
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Structural Elucidation and NMR Spectral Assignments of New Diphenyl Ether Derivatives From Liuweizhiji Gegen‐Sangshen Oral Liquid.
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- Magnetic Resonance in Chemistry, 2025, v. 63, n. 2, p. 151, doi. 10.1002/mrc.5496
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Two New Alkaloids of the Endophytic Fungus Rhizopus oryzae From Atractylodes macrocephala Koidz.
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- Magnetic Resonance in Chemistry, 2025, v. 63, n. 2, p. 122, doi. 10.1002/mrc.5495
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Molecular Docking Studies of Novel Benzimidazole Macromolecules.
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- Macromolecular Symposia, 2025, v. 414, n. 1, p. 1, doi. 10.1002/masy.202400232
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Highly Efficient Ultrasound‐Assisted Synthesis, Characterization, and Antibreast Cancer (Invasive Ductal Carcinoma) of New Chalcone Based Compound and Its Nanohybrid With Silver Nanoparticles.
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- Macromolecular Symposia, 2025, v. 414, n. 1, p. 1, doi. 10.1002/masy.202400235
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Design, Synthesis and Molecular Docking of New Thieno[2,3‑d]Pyrimidin‐4‐One Derivatives as Dual EGFR and FGFR Inhibitors.
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- Drug Development Research, 2025, v. 86, n. 1, p. 1, doi. 10.1002/ddr.70061
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Current Strategies and Future Dimensions in the Development of KRAS Inhibitors for Targeted Anticancer Therapy.
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- Drug Development Research, 2025, v. 86, n. 1, p. 1, doi. 10.1002/ddr.70042
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Design, Synthesis, Docking Studies, and Investigation of Dual EGFR/VEGFR‐2 Inhibitory Potentials of New Pyrazole and Pyrazolopyridine Derivatives.
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- Drug Development Research, 2025, v. 86, n. 1, p. 1, doi. 10.1002/ddr.70056
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Phthalazine Derivatives as VEGFR‐2 Inhibitors: Docking, ADMET, Synthesis, Design, Anticancer Evaluations, and Apoptosis Inducers.
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- Drug Development Research, 2025, v. 86, n. 1, p. 1, doi. 10.1002/ddr.70037
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Design, Synthesis, Biological Evaluation and Molecular Docking Study of New 1,3,4‐Thiadiazole‐Based Compounds as EGFR Inhibitors.
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- Drug Development Research, 2025, v. 86, n. 1, p. 1, doi. 10.1002/ddr.70035
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Anti-cancer activity and brine shrimp lethality assay of the extracts and isolated compounds from Garcinia schomburgkiana Pierre.
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- Journal of Applied Pharmaceutical Science, 2025, v. 15, n. 3, p. 241, doi. 10.7324/JAPS.2025.209800
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Involvement of mitophagy in the anti-cancer activity of melatonin on JURKAT cells.
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- Journal of Applied Pharmaceutical Science, 2025, v. 15, n. 3, p. 218, doi. 10.7324/JAPS.2025.166362
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Rhizospheric actinomycetes from turmeric (Curcuma longa L.): Isolation, detection of the biosynthetic gene clusters, and anticancer activity against T47D cancer cells.
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- Journal of Applied Pharmaceutical Science, 2025, v. 15, n. 3, p. 122, doi. 10.7324/JAPS.2025.218990
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Novel Strategies for Synthesis and Assessment of Dextran Conjugated 9Z,11E Linoleic Acid on Cancer Cell Lines Viability via Wnt/Beta‐Catenin Signaling Pathway and Apoptosis.
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- Starch / Staerke, 2025, v. 77, n. 3, p. 1, doi. 10.1002/star.202300281
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Systemic anti‐cancer therapy and anaesthesia: a narrative review.
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- Anaesthesia, 2025, v. 80, n. S2, p. 12, doi. 10.1111/anae.16522
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TAZ‐hTrap: A Rationally Designed, Disulfide‐Stapled Tead Helical Hairpin Trap to Selectively Capture Hippo Signaling Taz With Potent Antigynecological Tumor Activity.
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- Journal of Molecular Recognition, 2025, v. 38, n. 2, p. 1, doi. 10.1002/jmr.3111
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Possible inhibition effects of resveratrol on pancreatic tumorigenesis in the azaserine‐rat model.
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- APMIS, 2025, v. 133, n. 1, p. 1, doi. 10.1111/apm.13498
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Ephedrannin A: A potent dual inhibitor of FAK and Src with anticancer effects.
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- Bulletin of the Korean Chemical Society, 2025, v. 46, n. 3, p. 317, doi. 10.1002/bkcs.70002
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Divergent Total Syntheses of Six Crinipellin‐Type Diterpenoids through Tandem 4π‐Electrocyclization/Dicycloexpansion.
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- Angewandte Chemie, 2025, v. 137, n. 12, p. 1, doi. 10.1002/ange.202501008
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Hypomethylating agents for patients with VEXAS without myelodysplastic syndrome: Clinical outcome and longitudinal follow‐up of vacuolization and UBA1 clonal dynamics.
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- British Journal of Haematology, 2025, v. 206, n. 2, p. 565, doi. 10.1111/bjh.19953
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Preclinical activity of resazurin in acute myeloid leukaemia.
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- British Journal of Haematology, 2025, v. 206, n. 1, p. 109, doi. 10.1111/bjh.19872
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Assessing Etoposide and Cyclophosphamide Contamination and Current Cleaning Practices in Patient Bathrooms.
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- Clinical Journal of Oncology Nursing, 2025, v. 29, n. 2, p. E52, doi. 10.1188/25.CJON.E52-E59
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Optimizing Assessment of and Education About Chemotherapy-Induced Peripheral Neuropathy Among Breast Cancer Survivors.
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- Clinical Journal of Oncology Nursing, 2025, v. 29, n. 2, p. 113, doi. 10.1188/25.CJON.113-118
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Tumor-Infiltrating Lymphocyte Therapy for Melanoma: Nursing Considerations.
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- Clinical Journal of Oncology Nursing, 2025, v. 29, n. 2, p. 125, doi. 10.1188/25.CJON.125-129
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Integrated bulk and single-cell transcriptomic analysis unveiled a novel cuproptosis-related lipid metabolism gene molecular pattern and a risk index for predicting prognosis and antitumor drug sensitivity in breast cancer.
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- Discover Oncology, 2025, v. 16, n. 1, p. 1, doi. 10.1007/s12672-025-02044-x
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Synthesis and reactivity of a Kemp's acid amide as a potential prototype anticancer prodrug.
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- MAI Review, 2009, n. 1, p. 1
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A Metal Chelation Therapy to Effectively Eliminate Breast Cancer and Intratumor Bacteria While Suppressing Tumor Metastasis by Copper Depletion and Zinc Ions Surge.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202417592
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A Mechanical Immune Checkpoint Inhibitor Stiffens Tumor Cells to Potentiate Antitumor Immunity.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202417518
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Targeting Lysosomal Thiols for Immunogenic Cancer Cell Death.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202417509
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Self‐Assembled Peptide‐Derived Proteolysis‐Targeting Chimera (PROTAC) Nanoparticles for Tumor‐Targeted and Durable PD‐L1 Degradation in Cancer Immunotherapy.
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- Angewandte Chemie, 2025, v. 137, n. 5, p. 1, doi. 10.1002/ange.202414146
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