Keywords: مهار ثابت; THR; Thrombin; EC; Epicatechin; EGC; Epigallocatechin; ECG; Epicatechin gallate; EGCG; Epigallocatechin gallate; CE; Capillary electrophoresis; EMMA; Electrophoretically mediated microanalysis; IMER; Immobilized enzyme microreaction; pNA; para-nitroanilin
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Keywords: مهار ثابت; Phosphodiesterase-6; Inhibitor; Inhibition constant; Retina; Photoreceptors; Ex vivo electroretinography; A; activation coefficient; cAMP; adenosine 3â²,5â² cyclic monophosphate; cGMP; guanosine 3â²,5â² cyclic monophosphate; CNG channel; cyclic nucleo
Keywords: مهار ثابت; Arsenic; Soil acid phosphatase; Soil property; Inhibition constant; Noncompetitive inhibition;
Keywords: مهار ثابت; AD; Alzheimer's disease; DA; dopamine; DAergic; dopaminergic; hMAO-A; human monoamine oxidase A; hMAO-B; human monoamine oxidase B; HRP; horseradish peroxidase; IC50; the half maximal inhibitory concentration; i.p.; intraperitoneal; Ki; inhibition const
Keywords: مهار ثابت; ADAM; advanced dissolution, absorption, and metabolism; AED; antiepileptic drug; AUC; area-under-the-curve; B/P; blood to plasma ratio; BID; twice daily; BMI; body mass index; CBZ; carbamazepine; CLint; intrinsic clearance; CLR; renal clearance; CL; clear
Keywords: مهار ثابت; Dissociation constant; Inhibition constant; Affinity; Nonspecific binding; Nontarget site binding; Adsorption; Ki; enzyme inhibition constant; AChE; acetylcholinesterase; eeAChE; Electrophorus electricus AChE; ATCh; acetylthiocholine chloride; bis(7)-tacr
Keywords: مهار ثابت; Scorpion; Venom; Neurotoxin; Neuropeptide; Ion channels; AC50; toxin concentration for activation to 50%; Cav; voltage-gated calcium channel; EC50; half maximal effective concentration; ED50; median effective dose; ER; endoplasmic reticulum; IC50; half ma
Keywords: مهار ثابت; physiologically based pharmacokinetic modeling; drug interactions; Monte Carlo; in vitro-in vivo correlations (IVIVC); nonlinear regression; biliary excretion; biliary recycling; hepatic metabolism; hepatic transport; AUC; area under the curve of concen
Cathepsin B inhibitors: Further exploration of the nitroxoline core
Keywords: مهار ثابت; Abz; 2-aminobenzoyl; AMC; 7-amido-4-methylcoumarin; catB; cathepsin B; DIPEA; N,N-diisopropylethylamine; DMSO; dimethyl sulfoxide; ECM; extracellular matrix; EDC; 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide; HATU; 1-[bis(dimethylamino)methylene]-1H-1,2,
Anthranilate phosphoribosyltransferase: Binding determinants for 5â²-phospho-alpha-d-ribosyl-1â²-pyrophosphate (PRPP) and the implications for inhibitor design
Keywords: مهار ثابت; AnPRT; anthranilate phosphoribosyltransferase; IC50; absolute IC50, that is the concentration of inhibitor which decreased enzyme activity by 50%; Km; Michaelis-Menten constant; Ki; inhibition constant; Mtb; Mycobacterium tuberculosis; PPi; pyrophosphate;
Synthesis of novel 4-functionalized 1,5-diaryl-1,2,3-triazoles containing benzenesulfonamide moiety as carbonic anhydrase I, II, IV and IX inhibitors
Keywords: مهار ثابت; Carbonic anhydrase inhibitors; Isoforms I, II, IV, IX; Benzenesulfonamide; 1,2,3-Triazole; CA; Carbonic anhydrase; hCA; human carbonic anhydrase; CAIs; Carbonic anhydrase inhibitors; AAZ; Acetazolamide; Ki; Inhibition constant; nM; nanomolar; μM; micromo
An appraisal on synthetic and pharmaceutical perspectives of pyrazolo[4,3-d]pyrimidine scaffold
Keywords: مهار ثابت; A. flavus; Aspergillus flavus; C. albicans; Candida albicans; cAMP; cyclic adenosine monophosphate; CDK; cyclin-dependent kinase; CNS; central nervous system; COX; cyclooxygenase; CRF; corticotropin-releasing hormone; CRK; cdc2-related kinase; CYC6; cycli
Tricyclic antidepressants inhibit hippocampal α7* and α9α10 nicotinic acetylcholine receptors by different mechanisms
Keywords: مهار ثابت; AChR; nicotinic acetylcholine receptor; ACh; acetylcholine; TCAs; tricyclic antidepressants; α-BTx; α-bungarotoxin; MLA; methyllycaconitine; RT; room temperature; IC50; ligand concentration that produces 50% inhibition (of binding or of agonist activati
In silico and in vitro analysis of coumarin derivative induced anticancer effects by undergoing intrinsic pathway mediated apoptosis in human stomach cancer
Keywords: مهار ثابت; SBC; Apoptosis; Docking; ADME; Stomach cancer cell line (AGS); Anti-proliferative; MTT; 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide; ADME; absorption, distribution, metabolism and excretion; FBS; fetal bovine serum; RPMI; rosewell park m
Quantitative and systems pharmacology 2. In silico polypharmacology of G protein-coupled receptor ligands via network-based approaches
Keywords: مهار ثابت; GPCR; G protein-coupled receptor; EP4; prostaglandin E2 receptor EP4 subtype; LPAR; lysophosphatidic acid receptor; DTI; drug-target interaction; ADE; adverse drug event; MoA; mechanism of action; Ki; inhibition constant; Kd; dissociation constant; IC50;
Combining in silico and in vitro approaches to evaluate the acetylcholinesterase inhibitory profile of some commercially available flavonoids in the management of Alzheimer's disease
Keywords: مهار ثابت; Alzheimer's disease; Binding energy; Inhibition constant; Amino acid residues; Molecular interactions;
A Novel Antagonist of the Immune Checkpoint Protein Adenosine A2a Receptor Restores Tumor-Infiltrating Lymphocyte Activity in the Context of the Tumor Microenvironment
Keywords: مهار ثابت; A2aR; adenosine A2a receptor; CAF; cancer-associated fibroblast; CHO; Chinese hamster ovary; IC50; concentration of compound that displaces the binding of radioligand by 50%; Kb; binding constant; Ki; inhibition constant; NECA; 5â³-N-ethylcarboxamidoaden
Prediction of renal transporter-mediated drug-drug interactions for a drug which is an OAT substrate and inhibitor using PBPK modelling
Keywords: مهار ثابت; AUC; area under the curve; DDI; drug-drug interaction; fu; fraction unbound; IC50; inhibition constant; IV; intravenous; IVIVE; in vitro/in vivo extrapolation; Ki; inhibition constant; OAT; organic anion transporter; PBPK; physiologically based pharmacoki
Dual Inhibition of Mnk2 and FLT3 for potential treatment of acute myeloid leukaemia
Keywords: مهار ثابت; Mnk inhibitor; FLT3 inhibitor; Dual inhibitor; AML; Drug discovery; Anti-leukaemic agent; AML; acute myeloid leukaemia; CDK; cyclin-dependent kinase; eIF; eukaryotic initiation factor; Erk; extracellular signal-regulated kinase; FLT3; Fms-like tyrosine ki
In Vitro-In Vivo Extrapolation of Metabolism- and Transporter-Mediated Drug-Drug Interactions-Overview of Basic Prediction Methods
Keywords: مهار ثابت; drug interaction; cytochrome P450s; membrane transport/transporters; regulatory; guidance/guideline; ADME; absorption, distribution, metabolism and excretion; BCRP; breast cancer resistance protein; CYP; cytochrome P-450; d; induction calibration factor;
Competitive protein tyrosine phosphatase 1B (PTP1B) inhibitors, prenylated caged xanthones from Garcinia hanburyi and their inhibitory mechanism
Keywords: مهار ثابت; PTP1B; protein tyrosine phosphatase 1B; IC50; the inhibitor concentration leading 50% activity loss; Ki; inhibition constant; Kiapp; apparent Ki; Vmax; maximum velocity; Km; Michaelis-Menten constant; Kobs; apparent first-order rate constant for the trans
Quantitative Analysis of Complex Drug-Drug Interactions Between Repaglinide and Cyclosporin A/Gemfibrozil Using Physiologically Based Pharmacokinetic Models With In Vitro Transporter/Enzyme Inhibition Data
Keywords: مهار ثابت; clinical trial simulations; drug interactions; pharmacokinetics; physiologically based pharmacokinetic modeling; organic anion-transporting polypeptide transporters; CYP enzymes; AUC; area under the blood concentration-time curve; AUCR; area under the b
Selectivity of coronaridine congeners at nicotinic acetylcholine receptors and inhibitory activity on mouse medial habenula
Keywords: مهار ثابت; AChR; nicotinic acetylcholine receptor; ACh; acetylcholine; NCA; noncompetitive antagonist; RT; room temperature; MHb; medial habenula; VI; ventral inferior; Ki; inhibition constant; Kd; dissociation constant; IC50; ligand concentration that produces 50%
Kinetics of soil dehydrogenase in response to exogenous Cd toxicity
Keywords: مهار ثابت; Cadmium; Dehydrogenase; Kinetic; Inhibition constant;
Pretreatment With Rifampicin and Tyrosine Kinase Inhibitor Dasatinib Potentiates the Inhibitory Effects Toward OATP1B1- and OATP1B3-Mediated Transport
Keywords: مهار ثابت; drug transport; drug interactions; organic anion-transporting polypeptide transporters; hepatocytes; hepatic transport; pharmacokinetics; physiologically based pharmacokinetic modeling; AUC; area under the plasma concentration-time curve; CsA; cyclosporin
Quantitative Analyses of the Influence of Parameters Governing Rate-Determining Process of Hepatic Elimination of Drugs on the Magnitudes of Drug-Drug Interactions via Hepatic OATPs and CYP3A Using Physiologically Based Pharmacokinetic Models
Keywords: مهار ثابت; cytochrome P450; drug interaction; hepatic clearance; mathematical model; organic anion-transporting polypeptide transporters; pharmacokinetics; AUC; area under the plasma concentration-time curve; CL; clearance; CLint,all; overall hepatic intrinsic cle
Bupropion and its photoreactive analog (±)-SADU-3-72 interact with luminal and non-luminal sites at human α4β2 nicotinic acetylcholine receptors
Keywords: مهار ثابت; Human α4β2 nicotinic acetylcholine receptor; Bupropion; (±)-SADU-3-72; Molecular docking; Luminal and non-luminal sites; Ca2+ influx; AChR; nicotinic acetylcholine receptor; NCA; noncompetitive antagonist; (±)-BP; (±)-bupropion [(±)-2-(tert-butylami
Positive allosteric modulators of α7 nicotinic acetylcholine receptors affect neither the function of other ligand- and voltage-gated ion channels and acetylcholinesterase, nor β-amyloid content
Keywords: مهار ثابت; 5-HT; 5-hydroxytryptamine (serotonin); m5-HT3AR; murine serotonin type 3A receptor; AChR; nicotinic acetylcholine receptor; ACh; acetylcholine; NMDAR; N-methyl-D-aspartate receptor; AMPAR; α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor; NI
Ethnomedical research and review of Q'eqchi Maya women's reproductive health in the Lake Izabal region of Guatemala: Past, present and future prospects
Keywords: مهار ثابت; COX-2; Cyclooxygenase 2; E2; Estradiol; ERα, ERβ; estrogen receptor alpha and beta; ERE; estrogen responsive element; GC; granulosa cells; 5-HT; Serotonin; 5-HT1-7; Serotonin receptors 1-7; IC50; median inhibitory concentration; Ki; Inhibition constant;
Microwave assisted synthesis of novel acridine-acetazolamide conjugates and investigation of their inhibition effects on human carbonic anhydrase isoforms hCA I, II, IV and VII
Keywords: مهار ثابت; CA; carbonic anhydrase; hCA; human carbonic anhydrase; Quinacrine; (RS)-Nâ²-(6-Chloro-2-methoxy-acridin-9-yl)-N,N-diethylpentane-1,4-diamine; Proflavine; acridine-3,6-di-amine; Amsacrine; N-(4-(acridin-9-ylamino)-3-methoxyphenyl)methanesulfonamide; IR; i
Radiosynthesis and in vitro validation of 3H-NS14492 as a novel high affinity alpha7 nicotinic receptor radioligand
Keywords: مهار ثابت; Bmax; maximum density; 125I-BTX; 125I-α-bungarotoxin; Kd; dissociation constant; Ki; inhibition constant; NSB; non-specific binding; OD; optical density; PAM; positive allosteric modulator; SB; specific binding; TB; total binding; TE; tissue equivalent;
Dissecting the functional roles of the conserved NXXE and HXE motifs of the ADP-dependent glucokinase from Thermococcus litoralis
Keywords: مهار ثابت; ADP; adenosine-diphosphate; ATP; adenosine triphosphate; GK; glucokinase; TlGK; glucokinase from Thermococcus litoralis; glucose-6-P; glucose-6-phosphate; KM; Michaelis constant; kcat; turnover rate; Ki; inhibition constant; Ka; activation constant; KD; d
Cloning, characterization and anion inhibition studies of a γ-carbonic anhydrase from the Antarctic cyanobacterium Nostoc commune
Keywords: مهار ثابت; Carbonic anhydrase; Metalloenzymes; Hydratase activity; Antarctic organisms; Cyanobacteria; Anions; Inhibition constant;
Aqueous extracts and suspensions of restructured pork formulated with Undaria pinnatifida, Himanthalia elongata and Porphyra umbilicalis distinctly affect the in vitro α-glucosidase activity and glucose diffusion
Keywords: مهار ثابت; Alpha-glucosidase; Glucose diffusion; Restructured pork; Inhibition mechanism; Hypoglycaemic effects; CVD; cardiovascular disease; CRP; control-RP; GOD; glucose oxidase; Ki; inhibition constant; Km; Michaelis-Menten constant; NRP; restructured pork cont
Comparative inhibitory effect of prenylated coumarins, ferulenol and ferprenin, contained in the 'poisonous chemotype' of Ferula communis on mammal liver microsomal VKORC1 activity
Keywords: مهار ثابت; VKOR; vitamin K epoxide reductase; VKORC1; vitamin K epoxide reductase complex subunit 1; Vitamin KÂ >Â O; vitamin K epoxide; Ferula communis L. (Apiaceae); Ferulenol; Ferprenin; VKORC1; Inhibition constant; Interspecies variability;
Coronaridine congeners inhibit human α3β4 nicotinic acetylcholine receptors by interacting with luminal and non-luminal sites
Keywords: مهار ثابت; AChR; nicotinic acetylcholine receptor; NCA; noncompetitive antagonist; RT; room temperature; Ki; inhibition constant; Kd; dissociation constant; IC50; ligand concentration that produces 50% inhibition of binding (or of agonist activation); nH; Hill coeff
Functional and structural interaction of (â)-lobeline with human α4β2 and α4β4 nicotinic acetylcholine receptor subtypes
Keywords: مهار ثابت; AChR; nicotinic acetylcholine receptor; (â)-lobeline (α-lobeline) (â); -2S, 6R, 8S-lobeline, Ct-AChBP, acetylcholine binding protein from Capitella teleta; Ac-AChBP; acetylcholine binding protein from Aplysia californica; CCh; carbamylcholine; RT; ro
Bowman-Birk proteinase inhibitor from Clitoria fairchildiana seeds: Isolation, biochemical properties and insecticidal potential
Keywords: مهار ثابت; BBI; Bowman-Birk inhibitor; CD; circular dichroism; DTT; dithiothreitol; RP-HPLC; reversed-phase high performance liquid chromatography; Ki; inhibition constant; MALDI-TOF; matrix assisted laser desorption ionisation time of flight mass spectrometry; PI
Enediynyl peptides and iso-coumarinyl methyl sulfones as inhibitors of proprotein convertases PCSK8/SKI-1/S1P and PCSK4/PC4: Design, synthesis and biological evaluations
Keywords: مهار ثابت; aa; amino acid; AMC; 7-amino 4-methyl coumarin; Amu; atomic mass unit; Au; arbitrary unit; Aufs; absorption units full scale; IMS; iso-coumarinyl methyl sulfone; Eda; enediyne amino acid; h; human; IC50; inhibitor concentration required for 50% inhibition
Binding cooperativity between a ligand carbonyl group and a hydrophobic side chain can be enhanced by additional H-bonds in a distance dependent manner: A case study with thrombin inhibitors
Keywords: مهار ثابت; Cooperativity; Protein-ligand binding; Ligand binding affinity; Scoring functions; B-factor; Thrombin; Non-additivity; Me; methyl; Bn; benzyl; Boc; tert-butoxycarbonyl; ÎGË; standard Gibbs free energy; Ki; inhibition constant; EDCI; 1-(3-dimethylaminopr
Saccharin: A lead compound for structure-based drug design of carbonic anhydrase IX inhibitors
Keywords: مهار ثابت; CA; carbonic anhydrase; Ki; inhibition constant; ZBG; zinc binding group; Saccharin; Metalloenzyme; Carbonic anhydrase IX; CA IX-mimic; Structure-based drug design;
Novel 4-aryl-pyrido[1,2-c]pyrimidines with dual SSRI and 5-HT1A activity. Part 5
Keywords: مهار ثابت; Pyrido[1,2-c]pyrimidines; Antidepressants; Dual SSRI/5-HT1A activity; Quinoline derivatives; SERT; serotonin transporter; SAR; structure-activity relationship; 5-HT1AR; serotonin 5-HT1A receptors; 8-OH-DPAT; 8-hydroxy-2-(di-n-propylamino)tetralin; Ki; inh
Quantitative determination of active Bowman-Birk isoinhibitors, IBB1 and IBBD2, in commercial soymilks
Keywords: مهار ثابت; BAPNA; N-α-benzoyl-DL-arginine-p-nitroanilide; BBI; Bowman-Birk inhibitors; BBIC; Bowman-Birk inhibitor concentrate; BTEE; N-benzoyl-L-tyrosine ethyl ester; CIA; chymotrypsin inhibitor activity; CIU; chymotrypsin inhibitor units; CRC; colorectal cancer;
Identification of novel drug scaffolds for inhibition of SARS-CoV 3-Chymotrypsin-like protease using virtual and high-throughput screenings
Keywords: مهار ثابت; SARS-CoV; Severe Acute Respiratory Syndrome coronavirus; 3CLpro; 3 Chymotrypsin-like cysteine protease; MD; molecular dynamics; VS; virtual screening; CSM; computational solvent mapping; ROC; receiver operating characteristic; RMSD; root mean square devia
A multivariate approach linking reported side effects of clinical antidepressant and antipsychotic trials to in vitro binding affinities
Keywords: مهار ثابت; 5-HT; 5-hydroxy tryptamine (serotonin); 5-HTT; serotonin transporter; AAP; atypical antipsychotics; ACH; acetylcholine; ADR; adverse drug reaction; AP; antipsychotic; CDSR; cochrane database of systematic reviews; CTZ; chemotrigger zone; DAT; dopamine tra
A hydrophobic residue in position 15 of the rP2X3 receptor slows desensitization and reveals properties beneficial for pharmacological analysis and high-throughput screening
Keywords: مهار ثابت; P2X3 receptor; Desensitization; Mechanism of antagonism; Drug screening; Calcium imaging; αÃ-meATP; αÃ-methylene-ATP; CI; confidence interval; EC50; 50% effective concentration; IC50; 50% inhibitory concentration; Ki; inhibition constant; pA2; negativ
Discovery and SAR studies of methionine-proline anilides as dengue virus NS2B-NS3 protease inhibitors
Keywords: مهار ثابت; HQRJJHXKCFABSI-UONOGXRCSA-N; SAR; structure and activity relationship; NS2B-NS3; nonstructural protein 2B and 3; DENV; dengue virus; Ki; inhibition constant; TFA; trifluoroacetic acid; EtOAc; ethyl acetate; DCM; dichloromethylene; EtOH; ethyl alcohol; DMA
Geranylated flavonoids displaying SARS-CoV papain-like protease inhibition from the fruits of Paulownia tomentosa
Keywords: مهار ثابت; IC50; the inhibitor concentration leading to 50 % activity loss; Ki; inhibition constant; Km; Michaelis-Menten constant; SARS-CoV PLpro; Paulownia tomentosa; Geranylated flavonoids; PLpro inhibitor;
Concentration-dependent inhibitory effects of baicalin on the metabolism of dextromethorphan, a dual probe of CYP2D and CYP3A, in rats
Keywords: مهار ثابت; S. baicalensis; Scutellaria baicalensis; CYP; cytochrome P450; CYP2D; cytochrome P450 2D; CYP3A; cytochrome P450 3A; DXM; dextromethorphan; BG; baicalin; RLMs; rat liver microsomes; Km; substrate concentration at half-maximal product formation rate; Ki; i
Bioinsecticidal activity of a novel Kunitz trypsin inhibitor from Catanduva (Piptadenia moniliformis) seeds
Keywords: مهار ثابت; Bioinsecticidal; Kunitz trypsin inhibitor; Insect pests; Piptadenia moniliformis; ED50; effective dose to inhibit 50% of an enzymatic pool; HPLC; high-performance liquid chromatography; TCA; trichloroacetic acid; Ki; inhibition constant; DTT; dithiothreit