ARTICLE;
CRYSTAL STRUCTURE;
CYCLOADDITION;
DRUG SYNTHESIS;
INFRARED SPECTROSCOPY;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
ROOM TEMPERATURE;
X RAY CRYSTALLOGRAPHY;
CHEMISTRY TECHNIQUES, SYNTHETIC;
DRUG DESIGN;
OXADIAZOLES;
QUINOLINES;
THIAZEPINES;
TRIAZOLES;
Effect of diltiazem and lidocaine on arterial pressure or heart rate and the quality of extubation in patients undergoing uvulopalato- pharyngoplasty
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Synthesis of some new 1,4-benzothiazine and 1,5-benzothiazepine tricyclic derivatives with structural analogy with TIBO and their screening for anti-HIV activity
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Vascular effects of calcium channel antagonists: New evidence
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Efficient syntheses of benzothiazepines as antagonists for the mitochondrial sodium-calcium exchanger: Potential therapeutics for type II diabetes
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Synthesis of novel derivative of 1, 5-benzothiazepines from 1, 3-diketones and their antibacterial activity
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Cardiovascular characterization of pyrrolo[2,1-d][1,5]benzothiazepine derivatives binding selectively to the peripheral-type benzodiazepine receptor (PBR): From dual PBR affinity and calcium antagonist activity to novel and selective calcium entry blockers
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Studies on annulated 1, 4-benzothiazines and l, 5- benzothiazepines. IX. Imidazo[2, 1-d] [1, 5]benzothiazepines: Synthesis and in vitro benzodiazepine receptor affinity
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Synthesis and antiproliferative evaluation of certain indeno[1, 2-c]quinoline derivatives
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Synthesis and evaluation of cryptolepine analogues for their potential as new antimalarial agents
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Discovery and structure-activity relationship of 3-aryl-5-aryl-1,2,4- oxadiazoles as a new series of apoptosis inducers and potential anticancer agents
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Synthesis and anti-HIV activity of new metabolically stable alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors incorporating N-methoxy imidoyl halide and 1,2,4-oxadiazole systems
DOI 10.1021/jm070236e
Sakamoto T, Cullen MD, Hartman TL, Watson KM et al (2007) Synthesis and anti-HIV activity of newmetabolically stable alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors incorporating N-methoxy imidoyl halide and 1, 2, 4-oxadiazole systems. J Med Chem 50:3314-3321. doi:10.1021/jm070236e (Pubitemid 47065980)
Structural optimization of azadipeptide nitriles strongly increases association rates and allows the development of selective cathepsin inhibitors
doi:10.1021/jm101272p
FrizlerM, Lohr F, Furtmann N, Klas J, GutschowM (2011) Structural optimization of azadipeptide nitriles strongly increases association rates and allows the development of selective cathepsin inhibitors. J Med Chem 54:396-400. doi:10.1021/jm101272p
Synthesis and Biological Evaluation of Analogues of 7-Chloro-4,5-dihydro- 4-oxo-8-(1,2,4-triazol-4-yl)-1,2,4-triazolo[1,5-a] quinoxaline-2-carboxylic Acid (TQX-173) as Novel Selective AMPA Receptor Antagonists
DOI 10.1021/jm030906q
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Synthesis and pharmacological activity of triazole derivatives inhibiting eosinophilia
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Benzopyran potassium channel activators related to cromakalim- heterocyclic amide replacements at position 4
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α-cyclisation of tertiary amines: Synthesis of some novel annelated quinolines via a three-component reaction under solvent-free conditions
DOI 10.1055/s-2006-951477
Devi I, Baruah B, Bhuyan PJ (2006) α-cyclisation of tertiary amines: synthesis of some novel annelated quinolines via a three-component reaction under solvent-free conditions. Synlett 16:2593-2596. doi:10.1055/s-2006-951477 (Pubitemid 44580492)
Synthesis and biological evaluation of new clofibrate analogues as potential PPARα agonists
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Synthesis and evaluation of furan, thiophene, and azole bis[(carbamoyloxy)methyl] derivatives as potential antineoplastic agents
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Synthesis and crystal structure of 5-pyrazol-4, 5-dihydropyrazoles derivatives
doi:10.1002/jhet.5570450539
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