Keywords: داروهای ضد سرطان; Tankyrase-2; Inverse Virtual Screening; Biomimetic compounds; Tankyrase-2 inhibitors; Anti-cancer drugs;
مقالات ISI داروهای ضد سرطان (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: داروهای ضد سرطان; ARV-825 PubChem CID 92044400; BETd-246 PubChem CID 131698640; dBET1 PubChem CID 91799313; I-BET151 PubChem CID 52912189; I-BET762 PubChem CID 46943432; JQ1 PubChem CID 46907787; MS417 PubChem CID 59190723; OTX015 PubChem CID 9936746; THZ1 PubChem CID 7360
Keywords: داروهای ضد سرطان; Alcohols; Anti-cancer drugs; Glioblastoma;
Keywords: داروهای ضد سرطان; Cancer; Anti-cancer drugs; Drug-resistance; Extracellular vesicles; Exosomes; Microvesicles; Drug delivery vehicles;
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Antitumor activity; Ethnopharmacology; Ethnoguided studies;
Keywords: داروهای ضد سرطان; Copper complexes; Schiff base compounds; Phenanthroline; Interactions with DNA; Anti-cancer drugs; Mechanism of cytotoxicity of Cu-compounds;
Keywords: داروهای ضد سرطان; 6ACM; 6-acetylmorphine; ADI; acceptable daily intake; ALP; alprazolam; AM; amphetamine; ATC; Anatomical Therapeutic Classification; ATS; amphetamine-type stimulant; BE; benzoylecgonine; BQ; benchmark quotient; BW; body weight; CAF; caffeine; CBD; cannabid
Keywords: داروهای ضد سرطان; Drug delivery; Reduced graphene oxide; Anti-cancer drugs; Breast cancer; Poly-l-lysine; Endocytosis;
Keywords: داروهای ضد سرطان; Mangroves; Lung cancer; Anti-cancer drugs; Phytochemicals; Nicotiana tobacum
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Phytotoxicity; Cytotoxicity; Genotoxicity; Mutagenicity;
Keywords: داروهای ضد سرطان; Ceramide; Glucosylceramide synthase (GCS); P-glycoprotein; Multidrug resistance; Anti-cancer drugs
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Polo-like kinase; Structure-based drug design; Homology modelling; Molecular docking; Molecular dynamics simulation
Keywords: داروهای ضد سرطان; Field-effect transistor; Impedance spectroscopy; Cancer cells; Cell adhesion; Anti-cancer drugs;
MicroRNA-195 desensitizes HCT116 human colon cancer cells to 5-fluorouracil
Keywords: داروهای ضد سرطان; microRNAs; 5-Fluouracil; Resistance; Cell survival; Anti-cancer drugs; Cell cycle;
Synthesis and biological evaluation of 20-epi-amino-20-deoxysalinomycin derivatives
Keywords: داروهای ضد سرطان; Salinomycin; Nature product modification; Staudinger reaction; Anti-cancer drugs; 19F MRI; K-ras pathway;
A simultaneous determination of anti-cancer drugs in hospital effluent by DLLME HPLC-FLD, together with a risk assessment
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Hospital effluent; Microextraction; HPLC-FLD; Ecotoxicological risk;
Machineries regulating the activity of the small GTPase Arf6 in cancer cells are potential targets for developing innovative anti-cancer drugs
Keywords: داروهای ضد سرطان; Arf6; GEF; GAP; Invasion; Metastasis; Tumor angiogenesis; Tumor growth; Anti-cancer drugs;
Molecular dynamics study on DNA nanotubes as drug delivery vehicle for anticancer drugs
Keywords: داروهای ضد سرطان; DNA nanotubes; Anti-cancer drugs; Drug delivery; Computational modeling; Molecular dynamics;
A spectroscopic investigation into the binding of novel platinum(IV) and platium(II) anticancer drugs with DNA
Keywords: داروهای ضد سرطان; Attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR); DNA; Anti-cancer drugs; Platinum (II and IV);
Binding affinity of pro-apoptotic BH3 peptides for the anti-apoptotic Mcl-1 and A1 proteins: Molecular dynamics simulations of Mcl-1 and A1 in complex with six different BH3 peptides
Keywords: داروهای ضد سرطان; BH3-mimetics; Programmed cell death; Apoptosis; Anti-cancer drugs; Protein-Protein interactions; Hydrophobic groove; Polar interactions; Structure-based drug design; Bcl-2 family; Molecular dynamics; Flexible binding pocket;
NF-Y in cancer: Impact on cell transformation of a gene essential for proliferation
Keywords: داروهای ضد سرطان; NF-Y; CCAAT box; Cell proliferation; p53; Cancer; Anti-cancer drugs;
Recent advances in the development of dual VEGFR and c-Met small molecule inhibitors as anticancer drugs
Keywords: داروهای ضد سرطان; VEGFR; c-Met; Dual inhibitor; Anti-cancer drugs
A Smart pH-responsive Nano-Carrier as a Drug Delivery System: A hybrid system comprised of mesoporous nanosilica MCM-41 (as a nano-container) & a pH-sensitive polymer (as smart reversible gatekeepers): Preparation, characterization and in vitro release st
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Drug delivery systems; MCM-41; pH-sensitive nano-carriers; Sol-gel process;
Drug-eluting biodegradable ureteral stent: New approach for urothelial tumors of upper urinary tract cancer
Keywords: داروهای ضد سرطان; Ureteral stents; Upper tract urothelial carcinoma; Anti-cancer drugs; T24 cell line; Biodegradable polymers; Supercritical fluid technology;
Luteolin inhibits the Nrf2 signaling pathway and tumor growth in vivo
Keywords: داروهای ضد سرطان; Luteolin; Nrf2; Glutathione; Non-small-cell lung cancer; Anti-cancer drugs; Drug resistance;
Histone deacetylase inhibition enhances the lymphomacidal activity of the anti-CD22 monoclonal antibody HB22.7
Keywords: داروهای ضد سرطان; AR42; HB22.7; Lymphoma; Anti-cancer drugs; CD22; NHL
Magnetic core-mesoporous shell nanocarriers with drug anchorages suspended in mesopore interior for cisplatin delivery
Keywords: داروهای ضد سرطان; Mesoporous nanocarriers; Carboxylic groups; Magnetic core-shell structure; Anti-cancer drugs; Cisplatin delivery
Lovastatin inhibits human B lymphoma cell proliferation by reducing intracellular ROS and TRPC6 expression
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Cell cycle; Membrane cholesterol; Oxidative stress; Intracellular calcium; Confocal microscopy;
4,5,6,7-Tetrahydro-isoxazolo-[4,5-c]-pyridines as a new class of cytotoxic Hsp90 inhibitors
Keywords: داروهای ضد سرطان; Heat shock protein 90; Anti-cancer drugs; 4,5,6,7-Tetrahydro-isoxazolo-[4,5-c]-pyridines
2-(4-Chlorobenzyl)-6-arylimidazo[2,1-b][1,3,4]thiadiazoles: Synthesis, cytotoxic activity and mechanism of action
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Cancer therapeutics; Cytotoxicity; Apoptosis; Cell death
Synthesis, spectroscopic and DFT structural characterization of two novel ruthenium(III) oxicam complexes. In vivo evaluation of anti-inflammatory and gastric damaging activities
Keywords: داروهای ضد سرطان; Ruthenium complexes; Anti-inflammatory drugs; Anti-cancer drugs; Density functional; Spectroscopy
Recent syntheses of PI3K/Akt/mTOR signaling pathway inhibitors
Keywords: داروهای ضد سرطان; PI3K/Akt/mTor inhibitor; Protein kinase inhibitor; Anti-cancer drugs;
Lycorine hydrochloride selectively inhibits human ovarian cancer cell proliferation and tumor neovascularization with very low toxicity
Keywords: داروهای ضد سرطان; LH, lycorine hydrochloride; VEGF, vascular endothelial growth factorCell proliferation; Neovascularization; Angiogenesis; Ovarian cancer; Lycorine hydrochloride; Anti-cancer drugs
Liposomal drug delivery systems: From concept to clinical applications
Keywords: داروهای ضد سرطان; Liposome; Lipidic nanoparticle; Polyethylene glycol; Anti-cancer drugs; siRNA; Pharmacokinetics; Biodistribution; Ligand-targeted
Putting together a plasma membrane NADH oxidase: A tale of three laboratories
Keywords: داروهای ضد سرطان; VDAC; voltage dependent anion channel; NOX; NADH oxidase (plasma membrane); CNOX, ENOX1; NADH oxidase of normal cells; tNOX, ENOX 2; NADH oxidase of tumor cells; PDI; protein disulfide isomerase; AFR; ascorbate free radical; Cell growth; ENOX; CNOX; PMOR;
In vitro inhibition of translation initiation by N,Nâ²-diarylureas-potential anti-cancer agents
Keywords: داروهای ضد سرطان; SAR study; N,Nâ²-Diarylureas; Inhibition of translation initiation; Ternary complex; Phosphorylation of eIF2α; Anti-cancer drugs;
Vitamin E TPGS prodrug micelles for hydrophilic drug delivery with neuroprotective effects
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Biodegradable polymers; Cancer nanotechnology; Drug formulation; Nanomedicine;
Meta analysis of gene expression changes upon treatment of A549 cells with anti-cancer drugs to identify universal responses
Keywords: داروهای ضد سرطان; Meta-analysis; Gene expression; FDXR; CDKN1A; PARVB; MYC; HBP1; LDLR; SIM2; ALX1; GPHN; A549 lung adenocarcinoma cell line; Anti-cancer drugs;
An in vitro comparative assessment with a series of new triphenyltin(IV) 2-/4-[(E)-2-(aryl)-1-diazenyl]benzoates endowed with anticancer activities: Structural modifications, analysis of efficacy and cytotoxicity involving human tumor cell lines
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Triphenyltin(IV) benzoates; Triphenyltin(IV) 2-/4-[(E)-2-(aryl)-1-diazenyl]benzoates; Cell lines; QSAR
Digitoxin and a synthetic monosaccharide analog inhibit cell viability in lung cancer cells
Keywords: داروهای ضد سرطان; Digitoxin; D6-MA analog; Increased potency; Sub-therapeutic concentrations; Anti-cancer drugs
Hybrids of privileged structures benzothiazoles and pyrrolo[2,1-c] [1,4]benzodiazepin-5-one, and diversity-oriented synthesis of benzothiazoles
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Privileged structures; Benzothiazoles; Pyrrolobenzodiazepines; Diversity-oriented synthesis
Liposomal paclitaxel formulations
Keywords: داروهای ضد سرطان; Cr-P; paclitaxel solubilized in Cremophor EL®; DCP; dicetylphosphate; DEPC; dielaidoyl phosphatidyl choline; DLPC; dilauroyl phosphatidyl choline; DLPE; dilauroyl phosphatidyl ethanolamine; DLPG; dilauroyl phosphatidyl glycerol; DLTs; dose-limiting toxic
An ion-current-based, comprehensive and reproducible proteomic strategy for comparative characterization of the cellular responses to novel anti-cancer agents in a prostate cell model
Keywords: داروهای ضد سرطان; Drug mechanism of action; Drug-responsive proteomics signatures; Anti-cancer drugs; False-positive biomarker discovery rate; Peptide ion current areas
Design, synthesis, and in vitro characterization of novel hybrid peptidomimetic inhibitors of STAT3 protein
Keywords: داروهای ضد سرطان; STAT3; Peptidomimetics; SH2 domain; Molecular recognition; Anti-cancer drugs; Protein-protein interactions;
A new series of titanocene dichloride derivatives bearing chiral alkylammonium groups; assessment of their cytotoxic properties
Keywords: داروهای ضد سرطان; Anti-cancer drugs; Titanocene dichloride; Metallocenes
Design and synthesis of chloroquine analogs with anti-breast cancer property
Keywords: داروهای ضد سرطان; Chloroquine analogs; 4-Aminoquinoline; Anti-cancer drugs; Breast cancer; Repositioning approach
Platinum speciation used for elucidating activation or inhibition of Pt-containing anti-cancer drugs
Keywords: داروهای ضد سرطان; Platinum speciation; Anti-cancer drugs; Cisplatin; Carboplatin; Oxaliplatin
Fabrication of gold nanoparticles for targeted therapy in pancreatic cancer
Keywords: داروهای ضد سرطان; Gold nanoparticles; Drug delivery; EGFR; Tyrosine kinase; Anti-cancer drugs; Pancreatic cancer; Colloidal gold nanoparticles; AuNPs; Fabrication; Targeted therapy
Molecular basis of the interaction of novel tributyltin(IV) 2/4-[(E)-2-(aryl)-1-diazenyl]benzoates endowed with an improved cytotoxic profile: Synthesis, structure, biological efficacy and QSAR studies
Keywords: داروهای ضد سرطان; Tributyltin(IV) compounds; Arylazobenzoate; Spectroscopy; X-ray crystallography; Cell lines; Anti-cancer drugs; Hydrophobicity; QSAR; Docking studies
Bioenergetic pathways in tumor mitochondria as targets for cancer therapy and the importance of the ROS-induced apoptotic trigger
Keywords: داروهای ضد سرطان; Mitochondria; Apoptosis; Cancer; Bioenergetic pathways; Reactive oxygen species (ROS); Mitocans; Bioenergetics; Warburg effect; Carcinogenesis; Anti-cancer drugs