Keywords: انزازول; A; adenine; AcO; acetate; Atox1; antioxidant protein 1; BEOV; bis(ethyl-maltolato)oxovanadium(IV); bipy; bipyridine; bipydmb; 6-(1,1-dimethylbenzyl)-2,20-bipyridine); BMOV; bis(maltolato)oxovanadium(IV); cbdca; 1,1-cyclobutanedicarboxylate; CE; capillary
مقالات ISI انزازول (ترجمه نشده)
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Keywords: انزازول; XIZYTDLDJKWLOW-UHFFFAOYSA-N; Glucagon receptor antagonist; Indazole; Indole; Diabetes; Glucose lowering;
Keywords: انزازول; 2,6-NITpy; 2,6-bis-(3â²-oxide-1â²-oxyl-4â²,4â²,5â²,5â²-tetramethylimidazolin-2â²-yl)pyridine; 2pyNO; tert-butyl 2-pyridyl nitroxide; 3,5-DBSQ; 3,5-di-tert-butyl-o-semiquinone; 3,6-DBSQ; 3,6-di-tert-butyl-o-semiquinone; 6,6â²-NITbpy; 6,6â²-bis-(3â
Keywords: انزازول; Indazole; 1,3,4-Thiadiazoles; Anticonvulsant activity; Neurotoxicity;
Strong emission properties of 7-hydroxyindazolo[2,3-b]isoquinolin-12(7H)-one derivatives in aqueous solution
Keywords: انزازول; Functional dyes; Emission; Water solution; Indazole; Isoquinolinone; (TD)DFT calculation;
Ruthenium anticancer agent KP1019 binds more tightly than NAMI-A to tRNAPhe
Keywords: انزازول; KP1019; IndH[trans-RuCl4(Ind)2]; NAMI-A; ImH[trans-RuCl4(dmso)(Im)]; Ind; Indazole; Im; Imidazole; DMSO; Dimethylsulfoxide; tRNA; Transfer RNA; tRNAPhe; Phenylalanine-specific tRNA; FTIR; Fourier transform infrared; PAGE; Polyacrylamide electrophoresis; N
Designing and fabricating of single and double alkyl-chain indazole derivatives self-assembled monolayer for corrosion inhibition of copper
Keywords: انزازول; Self-assemble monolayer; Indazole; Adsorption; Corrosion inhibition; Molecular modeling;
Ruthenium coordination compounds of biological and biomedical significance. DNA binding agents
Keywords: انزازول; 2,3-dpp; 2,3-bis(2-pyridyl)pyrazine; 2-appt; 2-amino-4-phenylamino-6-(2-pyridyl)-1,3,5-triazine; apip; 2-(2-aminophenyl)imidazo[4,5-f][1,10]phenanthroline; bnbp; 2,6-bis-(6-nitrobenzimidazol-2-yl)pyridine; bpm; 2,2â²-bipyrimidine; bpy; 2,2â²-bipyridine;
A series of novel indazole derivatives of Sirt 1 activator as osteogenic regulators
Keywords: انزازول; Sirt 1; Osteoporosis; Osteogeneration; Indazole; HTS;
Synthesis and SAR studies of 3,6-disubstituted indazole derivatives as potent hepcidin production inhibitors
Keywords: انزازول; Hepcidin; Anemia of chronic disease; Indazole; Phenol; Intraperitoneal administration;
Discovery of indazole aldosterone synthase (CYP11B2) inhibitors as potential treatments for hypertension
Keywords: انزازول; Aldosterone synthase; CYP11B2; Indazole; Hit-to-lead; Hypertension;
Discovery of DS28120313 as a potent orally active hepcidin production inhibitor: Design and optimization of novel 4,6-disubstituted indazole derivatives
Keywords: انزازول; Hepcidin; Anemia of chronic disease; Indazole; Pyrazole; Kinase;
Aqueous behavior and reactivity towards nitric oxide of NAMI-A type complexes bearing bulky N-heterocyclic ligands
Keywords: انزازول; Ruthenium complexes; Indazole; Isoquinoline; Nitric oxide; Aquation;
A family of 2p-4f complexes based on indazole radical: Syntheses, structures and magnetic properties
Keywords: انزازول; Indazole; Nitronyl nitroxide radical; Lanthanide complexes; Magnetic property; Single-molecule magnet;
Discovery of methylsulfonyl indazoles as potent and orally active respiratory syncytial Virus(RSV) fusion inhibitors
Keywords: انزازول; Respiratory syncytial virus (RSV); Antiviral; Fusion inhibitors; Indazole; Heterocycle;
Indazole-based ligands for estrogen-related receptor α as potential anti-diabetic agents
Keywords: انزازول; Estrogen-related receptor α; ERRα; Nuclear receptor; Anti-diabetic; Metabolic syndrome; Indazole; Thiazolidenedione; TZD; Insulin resistance; ERR; estrogen-related receptor; ER; estrogen receptor; ERE; estrogen response element; ERRE; estrogen-related r
Discovery of potent, reversible MetAP2 inhibitors via fragment based drug discovery and structure based drug design-Part 1
Keywords: انزازول; FBDD; Fragment-based drug discovery; MetAP2; Methionine aminopeptidase 2; Metalloprotease; Indazole;
Synthesis and biological evaluation of substituted indazolyl amide derivatives as S-adenosyl-l-homocysteine hydrolase inhibitors
Keywords: انزازول; S-Adenosylhomocysteine hydrolase; SAHase inhibitors; Amide derivatives; Indazole; Synthesis
Optimization of amide-based EP3 receptor antagonists
Keywords: انزازول; EP3 receptor; PGE2; GPCR; LipE; Metabolites; P-gp; Indazole;
Amine-free melanin-concentrating hormone receptor 1 antagonists: Novel non-basic 1-(2H-indazole-5-yl)pyridin-2(1H)-one derivatives and mitigation of mutagenicity in Ames test
Keywords: انزازول; MCHR1 antagonist; MCH; Antiobesity agent; Indazole; Ames test; Mutagenicity; DNA intercalator;
Antichagasic and trichomonacidal activity of 1-substituted 2-benzyl-5-nitroindazolin-3-ones and 3-alkoxy-2-benzyl-5-nitro-2H-indazoles
Keywords: انزازول; Antiprotozoal drug; Nitroheterocycle; Indazole; Trichomonas vaginalis; Trypanosoma cruzi
Functionalization of indazoles by means of transition metal-catalyzed cross-coupling reactions
Keywords: انزازول; Indazole; Cross-coupling; Sonogashira; Heck; Suzuki-Miyaura; Stille; N-arylation; C-H activation; Direct arylation; Oxidative alkenylation;
Biodistribution of the novel anticancer drug sodium trans-[tetrachloridobis(1H-indazole)ruthenate(III)] KP-1339/IT139 in nude BALB/c mice and implications on its mode of action
Keywords: انزازول; BGE; background electrolyte; CZE; capillary zone electrophoresis; EPR; electron paramagnetic resonance; ESI; electrospray ionization; HSA; human serum albumin; MSA; mouse serum albumin; ICP; inductively coupled plasma; KP1019; indazolium trans-[tetrachlor
Discovery of novel inhibitors of Aurora kinases with indazole scaffold: In silico fragment-based and knowledge-based drug design
Keywords: انزازول; Aurora kinases inhibitor; Indazole; Ligand efficiency; Isoform selectivity; Structure-activity relationship (SAR);
Design, synthesis, and in vivo activity of novel inhibitors of delta-5 desaturase for the treatment of metabolic syndrome
Keywords: انزازول; Delta-5 desaturase; Metabolic syndrome; Indazole; Ring constraint; In vivo efficacy
Synthesis of benzo[6,7][1,4]diazepino[1,2-b]indazol-7(6H)-ones and benzo[f]pyrazolo[1,5-a][1,4]diazepin-4-ones via CuI/l-proline catalyzed intramolecular N2-arylation
Keywords: انزازول; N-arylation; CuI; Indazole; Pyrazole; 1,4-Benzodiazepine;
Discovery and optimization of indazoles as potent and selective interleukin-2 inducible T cell kinase (ITK) inhibitors
Keywords: انزازول; SBDD; ITK; Indazole; X-ray crystallography; Ï-stacking;
A general synthesis of diversely substituted indazoles and hetero-aromatic derivatives from o-halo-(het)arylaldehydes or -phenones
Keywords: انزازول; Heterocycles; Cross-coupling; Palladium; Cyclization; Indazole;
Discovery of 2-(1H-indazol-1-yl)-thiazole derivatives as selective EP1 receptor antagonists for treatment of overactive bladder by core structure replacement
Keywords: انزازول; EP1 antagonist; Indazole; Thiazole; Overactive bladder; Cystometry
Fluorinated analogues of marsanidine, a highly α2-AR/imidazoline I1 binding site-selective hypotensive agent. Synthesis and biological activities
Keywords: انزازول; Marsanidine; Indazole; α2-Adrenoceptor; Selectfluor;
Identification of pyrrolo[2,3-g]indazoles as new Pim kinase inhibitors
Keywords: انزازول; Pyrrolo[2,3-g]indazole; Indazole; Indole; Pim kinase inhibition;
Studies on substituted benzo[h]quinazolines, benzo[g]indazoles, pyrazoles, 2,6-diarylpyridines as anti-tubercular agents
Keywords: انزازول; LFUDVFOVNMIIIB-UHFFFAOYSA-N; CTEHHBOBZOCAIT-UHFFFAOYSA-N; JADFRCNEVYMOAL-UHFFFAOYSA-N; AKKATVMDHBEASX-UHFFFAOYSA-N; AYZGFAJCOVMXLA-UHFFFAOYSA-N; YWQRMQADBLJRKZ-UHFFFAOYSA-N; QLIZWGWIQMJGMB-UHFFFAOYSA-N; DSLIJABHAVBSDV-UHFFFAOYSA-N; HJBWBXRSRQEPRF-UHFFFAOY
Benzofuran-, benzothiophene-, indazole- and benzisoxazole-quinones: Excellent substrates for NAD(P)H:quinone oxidoreductase 1
Keywords: انزازول; Quinone; Benzofuran; Benzothiophene; Indazole; Quinone reductase; NQO1;
Indazoles as potential c-met inhibitors: Design, synthesis and molecular docking studies
Keywords: انزازول; c-Met inhibitor; Indazole; Bioisosterism principles; Molecular docking; Suzuki coupling reaction; IsomerAQKULDWMVLPKPM-RQNOJGIXSA-N; KFHKXMBLOGYCPH-OGESRWMOSA-N; VXDNOGKPNKBTFZ-UHFFFAOYSA-N; KUZAYSZLNQTGIG-UHFFFAOYSA-N; IOEGMAJBPLCGLZ-RQNOJGIXSA-N; LNULRI
2-Arylideneferroceno[e]cyclohexanones and related 3-aryl-3,3a,4,5-tetrahydroferroceno[g]indazoles: Synthesis, NMR-, DFT- and X-ray analysis
Keywords: انزازول; Ferrocene; Indazole; Chalcon; NMR; DFT calculations; X-ray diffractionCRUVJUYXJHHBJM-UHFFFAOYSA-N
Microwave synthesis, characterization and bio-efficacy evaluation of novel chalcone based 6-carbethoxy-2-cyclohexen-1-one and 2H-indazol-3-ol derivatives
Keywords: انزازول; Chalcone; Cyclohexenone; Indazole; Anti-fungal; Anti-bacterial; Anti-oxidant
Phosphorescent cationic iridium(III) complexes with cyclometalating 1H-indazole and 2H-[1,2,3]-triazole ligands
Keywords: انزازول; Iridium; Indazole; [1,2,3]-Triazole; Cyclometalation; Complex; Phosphorescence
New derivatives of indazole as electronically active materials
Keywords: انزازول; Indazole; Diphenylamino; Glass-forming; Thermal stability; Ionization potential; Charge mobility
Flash vacuum pyrolysis of azolylacroleins and azolylbutadienes
Keywords: انزازول; Pyrolysis; Tetrazole; Nitrilimine; Indazole; Nitrogen extrusion;
Study of the different behaviour of thiazolin and thiazin indazole derivatives with palladium(II) acetate
Keywords: انزازول; Palladium(II); Cyclopalladation; Thiazine; Indazole; Thiazoline
Pd- and Cu-catalyzed C-H arylation of indazoles
Keywords: انزازول; Indazole; Catalysis; C-H arylation; Heterobiaryl;
Discovery of indazoles as inhibitors of Tpl2 kinase
Keywords: انزازول; Tpl2 kinase; Indazole; Rheumatoid arthritis
Novel serotonin type 3 receptor partial agonists for the potential treatment of irritable bowel syndrome
Keywords: انزازول; 5-HT3 receptor partial agonist; Irritable bowel syndrome; IBS; Ligand-gated ion channel; Ramosetron; Alosetron; Indole; Indazole;
Discovery and SAR of 2-arylbenzotriazoles and 2-arylindazoles as potential treatments for Duchenne muscular dystrophy
Keywords: انزازول; Duchenne; Muscular; Dystrophy; Benzotriazole; Indazole
Synthesis, characterization and behaviour in solution of organotin complexes based on azole ligands. Single crystal X-ray study of dichlorodimethylbis(1,2,3-benzotriazole)tin(IV)
Keywords: انزازول; Benzotriazole; Indazole; Organotin(IV); Crystal structure; ESI MS
Non-oxime inhibitors of B-RafV600E kinase
Keywords: انزازول; B-Raf; Furopyridine; Indazole
Chemical and biological evaluation of 153Sm and 46/47Sc complexes of indazolebisphosphonates for targeted radiotherapy
Keywords: انزازول; Bisphosphonates; Indazole; 46/47Sc; 153Sm; Hydroxyapatite binding; Radiopharmaceuticals;
Synthesis of 1,6-dihydropyrrolo[2,3-g]indazoles using Larock indole annulation
Keywords: انزازول; Indazole; Larock indole annulation; Pyrroloindazole; Regioselectivity;
Optimization of a pyrazole hit from FBDD into a novel series of indazoles as ketohexokinase inhibitors
Keywords: انزازول; FBDD (fragment based drug discovery); KHK (ketohexokinase); Pyrazole; Indazole
Design, synthesis and SAR of indazole and benzoisoxazole containing 4-azetidinyl-1-aryl-cyclohexanes as CCR2 antagonists
Keywords: انزازول; CCR2; Indazole; Benzoisoxazole