Works in Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, Vol 31, Issue 6
Results: 117
Editorial Board.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. ebi, doi. 10.1080/14756366.2016.1216274
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- Article
New light on bacterial carbonic anhydrases phylogeny based on the analysis of signal peptide sequences.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1254, doi. 10.1080/14756366.2016.1201479
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Anti-tubercular and antioxidant activities of C -glycosyl carbonic anhydrase inhibitors: towards the development of novel chemotherapeutic agents against Mycobacterium tuberculosis.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1726, doi. 10.3109/14756366.2016.1172577
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Synthesis of some novel 2-substituted benzothiazole derivatives containing benzylamine moiety as monoamine oxidase inhibitory agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1654, doi. 10.3109/14756366.2016.1161621
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Simple ITC method for activity and inhibition studies on human salivary α-amylase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1648, doi. 10.3109/14756366.2016.1161619
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Evaluation of the analgesic effect of 4-anilidopiperidine scaffold containing ureas and carbamates.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1638, doi. 10.3109/14756366.2016.1160902
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Yeast as a tool to select inhibitors of the cullin deneddylating enzyme Csn5.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1632, doi. 10.3109/14756366.2016.1160901
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Biological activities of Zn(II)- S -methyl-cysteine complex as antiradical, inhibitor of acid phosphatase enzyme and in vivo antidepressant effects.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1625, doi. 10.3109/14756366.2016.1160900
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Synthesis and bioactivity studies on new 4-(3-(4-Substitutedphenyl)-3a,4-dihydro-3 H -indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1619, doi. 10.3109/14756366.2016.1160077
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Synthesis, molecular modeling and NAD(P)H:quinone oxidoreductase 1 inducer activity of novel 2-phenylquinazolin-4-amine derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1612, doi. 10.3109/14756366.2016.1158714
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Structure-based design, synthesis, molecular docking study and biological evaluation of 1,2,4-triazine derivatives acting as COX/15-LOX inhibitors with anti-oxidant activities.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1602, doi. 10.3109/14756366.2016.1158713
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Antiplatelet pyrazolopyridines derivatives: pharmacological, biochemical and toxicological characterization.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1591, doi. 10.3109/14756366.2016.1158712
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Synthesis of new thieno[2,3- b ]pyridine derivatives as pim-1 inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1718, doi. 10.3109/14756366.2016.1158711
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A review of the effects of some endocrinological factors on respiratory mechanics.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 890, doi. 10.3109/14756366.2016.1158174
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In vivo effects of curcumin on the paraoxonase, carbonic anhydrase, glucose-6-phosphate dehydrogenase and β -glucosidase enzyme activities in dextran sulphate sodium-induced ulcerative colitis mice.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1583, doi. 10.3109/14756366.2016.1158173
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Synthesis and anticonvulsant activities of novel 2-(cyclopentylmethylene)hydrazinyl-1,3-thiazoles in mouse models of seizures.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1576, doi. 10.3109/14756366.2016.1158172
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Design and synthesis of antimicrobial, anticoagulant, and anticholinesterase hybrid molecules from 4-methylumbelliferone.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1566, doi. 10.3109/14756366.2016.1158171
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Purification and characterization of a Cys-Gly hydrolase from the gastropod mollusk, Patella caerulea.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1560, doi. 10.3109/14756366.2016.1158170
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Apparent cooperativity and apparent hyperbolic behavior of enzyme mixtures acting on the same substrate.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1556, doi. 10.3109/14756366.2016.1158169
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Synthesis, cyclooxygenase inhibition and anti-inflammatory evaluation of new 1,3,5-triaryl-4,5-dihydro-1 H -pyrazole derivatives possessing methanesulphonyl pharmacophore.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1545, doi. 10.3109/14756366.2016.1158168
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Discovery of Strecker-type α-aminonitriles as a new class of human carbonic anhydrase inhibitors using differential scanning fluorimetry.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1707, doi. 10.3109/14756366.2016.1156676
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Inhibitory effects of benzimidazole containing new phenolic Mannich bases on human carbonic anhydrase isoforms hCA I and II.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1540, doi. 10.3109/14756366.2016.1156675
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A nonmainstream approach against cancer.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 882, doi. 10.3109/14756366.2016.1156105
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Synthesis of some tetrahydropyrimidine-5-carboxylates, determination of their metal chelating effects and inhibition profiles against acetylcholinesterase, butyrylcholinesterase and carbonic anhydrase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1531, doi. 10.3109/14756366.2016.1156104
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Identification of new anti- Candida compounds by ligand-based pharmacophore virtual screening.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1703, doi. 10.3109/14756366.2016.1156103
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Benzimidazolium-based novel silver N -heterocyclic carbene complexes: synthesis, characterisation and in vitro antimicrobial activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1527, doi. 10.3109/14756366.2016.1156102
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Synthesis and anti-inflammatory activity evaluation of novel triazolyl-isatin hybrids.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1520, doi. 10.3109/14756366.2016.1151015
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3,6-Diazaphenothiazines as potential lead molecules – synthesis, characterization and anticancer activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1512, doi. 10.3109/14756366.2016.1151014
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Xylarinase: a novel clot busting enzyme from an endophytic fungus Xylaria curta.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1502, doi. 10.3109/14756366.2016.1151013
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Establishment of an effective TLC bioautographic method for the detection of Mycobacterium tuberculosis H37Ra phosphoglucose isomerase inhibition by phosphoenolpyruvate.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1712, doi. 10.3109/14756366.2016.1151012
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Inhibitory effects of isatin Mannich bases on carbonic anhydrases, acetylcholinesterase, and butyrylcholinesterase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1498, doi. 10.3109/14756366.2016.1149479
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Inhibitory effects of Aphanizomenon flos-aquae constituents on human UDP-glucose dehydrogenase activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1492, doi. 10.3109/14756366.2016.1149478
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Synthesis and inhibitory properties of some carbamates on carbonic anhydrase and acetylcholine esterase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1484, doi. 10.3109/14756366.2016.1149477
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Advances in plant-based inhibitors of P-glycoprotein.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 867, doi. 10.3109/14756366.2016.1149476
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Synthesis and carbonic anhydrase I, II, IV and XII inhibitory properties of N-protected amino acid – sulfonamide conjugates.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1476, doi. 10.3109/14756366.2016.1147438
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Comparative assay of Vipera ammodytes antivenom potency.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1471, doi. 10.3109/14756366.2016.1144598
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Effects of novel acylhydrazones derived from 4-quinolone on the acetylcholinesterase activity and A β 42 peptide fibrils formation.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1464, doi. 10.3109/14756366.2016.1144597
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Synthesis and biological evaluation of novel hydrogen sulfide releasing glycyrrhetic acid derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1457, doi. 10.3109/14756366.2016.1144596
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Niacin esters of chalcones with tumor-selective properties.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1451, doi. 10.3109/14756366.2016.1144595
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Pred-binding: large-scale protein–ligand binding affinity prediction.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1443, doi. 10.3109/14756366.2016.1144594
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Molecular dynamic simulations and structure-based pharmacophore development for farnesyltransferase inhibitors discovery.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1428, doi. 10.3109/14756366.2016.1144593
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Design and synthesis of pyridazinone-substituted benzenesulphonylurea derivatives as anti-hyperglycaemic agents and inhibitors of aldose reductase – an enzyme embroiled in diabetic complications.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1415, doi. 10.3109/14756366.2016.1142986
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Molecular processes in the streptokinase thrombolytic therapy.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1411, doi. 10.3109/14756366.2016.1142985
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Novel agonists of free fatty acid receptor 1 (GPR40) based on 3-(1,3,4-thiadiazol-2-yl)propanoic acid scaffold.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1404, doi. 10.3109/14756366.2016.1142984
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Ultrasonic synthesis of tyramine derivatives as novel inhibitors of α -glucosidase in vitro.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1392, doi. 10.3109/14756366.2016.1142983
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Some coumarins and benzoxazinones as potent paraoxonase 1 inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1386, doi. 10.3109/14756366.2016.1142982
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Ectopic expression of a tobacco vacuolar invertase inhibitor in guard cells confers drought tolerance in Arabidopsis.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1381, doi. 10.3109/14756366.2016.1142981
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Carbonic anhydrase inhibition and cytotoxicity studies of Mannich base derivatives of thymol.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1375, doi. 10.3109/14756366.2016.1140755
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Targeting methionyl tRNA synthetase: design, synthesis and antibacterial activity against Clostridium difficile of novel 3-biaryl- N -benzylpropan-1-amine derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1694, doi. 10.3109/14756366.2016.1140754
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Tumor metabolism, cancer cell transporters, and microenvironmental resistance.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 859, doi. 10.3109/14756366.2016.1140753
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