Iodohydroxybenzylpindolol: preparation, purification, localization of its iodine to the indole ring, and characterization as a partial agonist

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Genetic disruption of G proteins, G(i2)alpha or G(o)alpha, does not abolish inotropic and chronotropic effects of stimulating muscarinic cholinoceptors in atrium.

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Phosphodiesterase-4 blunts inotropism and arrhythmias but not sinoatrial tachycardia of (-)-adrenaline mediated through mouse cardiac beta(1)-adrenoceptors.

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Human heart beta-adrenoceptors: beta1-adrenoceptor diversification through 'affinity states' and polymorphism.

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Structurome-wide analysis reveals intracellular loop 2 folding as an activation-associated feature of class A G protein-coupled receptors.

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Mechanism of activity inversion for GluN2B-selective negative allosteric modulators.

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A conserved conformation-dependent mechanism for the TREK two-pore domain potassium channel inhibitors carvedilol and fluphenazine.

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High potency μ-opioid receptor agonists engage sodium-bound receptor states.

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Regulation of transient receptor potential ankyrin-1 agonist-induced airway epithelial cell injury and repair by protein kinase C and p38 mitogen-activated kinase.

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The molecular geography of cell signaling diseases.

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Halogen-bond/hydrogen-bond donor hybrid catalysts for carbon dioxide fixation.

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Novel Borsche-Drechsel type cyclisation of 3-(2-cyclohexylidenehydrazinyl)quinoxalin-2(1H)-ones to construct tetrahydrobenzo[4,5]imidazo[1,2-a]quinoxalin-6(5H)-ones.

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Robust continuous-flow oxidation of aryl-alkyl sulfides to sulfoxides and sulfones over titanium silicalite-1 using diluted hydrogen peroxide.

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Nickel-Catalyzed Enantioselective Carbo-Carbonylation of Alkenes Using Formic Acid as a CO Surrogate: Access to Oxindoles Bearing Chiral Quaternary Carbon.

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Iron-Catalyzed Electrochemical α-C(sp3) Sulfonylation of Ethers and Pyrrolidine Derivatives with Sulfonyl Chlorides.

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Photoinduced Hydrogen Atom Transfer in 2-Formylbenzamides: Amide-Aldehyde 1,2-Transposition and Antioxidant Activity of Isobenzofuranones.

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Iodohydroxybenzylpindolol: preparation, purification, localization of its iodine to the indole ring, and characterization as a partial agonist

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Paediatric and neonatal sepsis and inflammation.

Excipient exposure in very low birth weight preterm neonates.

Membrane depolarization combined with Gq-activated G-protein-coupled receptors induce transient receptor potential channel 1 (TRPC1)- dependent potentiation of catecholamine release.

Genetic disruption of G proteins, G(i2)alpha or G(o)alpha, does not abolish inotropic and chronotropic effects of stimulating muscarinic cholinoceptors in atrium.

Phosphodiesterase-4 blunts inotropism and arrhythmias but not sinoatrial tachycardia of (-)-adrenaline mediated through mouse cardiac beta(1)-adrenoceptors.

Human heart beta-adrenoceptors: beta1-adrenoceptor diversification through 'affinity states' and polymorphism.

Structurome-wide analysis reveals intracellular loop 2 folding as an activation-associated feature of class A G protein-coupled receptors.

Mechanism of activity inversion for GluN2B-selective negative allosteric modulators.

A conserved conformation-dependent mechanism for the TREK two-pore domain potassium channel inhibitors carvedilol and fluphenazine.

High potency μ-opioid receptor agonists engage sodium-bound receptor states.

Regulation of transient receptor potential ankyrin-1 agonist-induced airway epithelial cell injury and repair by protein kinase C and p38 mitogen-activated kinase.

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Halogen-bond/hydrogen-bond donor hybrid catalysts for carbon dioxide fixation.

Novel Borsche-Drechsel type cyclisation of 3-(2-cyclohexylidenehydrazinyl)quinoxalin-2(1H)-ones to construct tetrahydrobenzo[4,5]imidazo[1,2-a]quinoxalin-6(5H)-ones.

Robust continuous-flow oxidation of aryl-alkyl sulfides to sulfoxides and sulfones over titanium silicalite-1 using diluted hydrogen peroxide.

Nickel-Catalyzed Enantioselective Carbo-Carbonylation of Alkenes Using Formic Acid as a CO Surrogate: Access to Oxindoles Bearing Chiral Quaternary Carbon.

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Iodohydroxybenzylpindolol: preparation, purification, localization of its iodine to the indole ring, and characterization as a partial agonist

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