Selective phosphodiesterase inhibition and alterations of cardiac function by alkylated xanthines

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Determination of amino acid residues that are accessible from the ligand binding crevice in the seventh transmembrane-spanning region of the human A(1) adenosine receptor.

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Serine and alanine mutagenesis of the nine native cysteine residues of the human A(1) adenosine receptor.

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Molecular basis for state-dependent drug block of Kv11.1 (human ether-à-go-go-related gene) potassium channels.

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Piezo1 agonists are potent off-target inhibitors of the Kv1.3 channel via gating modification.

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Diallyl sulfide pretreatment protects against DSS-induced colitis by reshaping the gut microbiota and enhancing microbiota-associated tryptophan metabolism.

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Balancing efficacy and risk: A toxicological review and safety transformation of Berberis plants and their alkaloids.

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Selective phosphodiesterase inhibition and alterations of cardiac function by alkylated xanthines

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Helping patients manage cancer-related fatigue.

Inhibition of human mast cell activation with the novel selective adenosine A(2B) receptor antagonist 3-isobutyl-8-pyrrolidinoxanthine (IPDX)(2).

Psychometric evaluation of Breast Health Behavior Questionnaire: Spanish version.

Assessment of hepatic function in cystic fibrosis by lidocaine metabolism.

Determination of amino acid residues that are accessible from the ligand binding crevice in the seventh transmembrane-spanning region of the human A(1) adenosine receptor.

Serine and alanine mutagenesis of the nine native cysteine residues of the human A(1) adenosine receptor.

Promotion of tumor cell senescence by the antibody-drug conjugate, sacituzumab govitecan.

Molecular basis for state-dependent drug block of Kv11.1 (human ether-à-go-go-related gene) potassium channels.

AKAP6β-a conductor in the orchestra of pathological cardiomyocyte gene transcription.

ZD-4009, a novel B-cell lymphoma 9 inhibitor, is associated with ameliorated pulmonary fibrosis and reduced hypoxia-inducible factor 1α-mediated glycolysis and transforming growth factor-β/SMAD signaling.

Piezo1 agonists are potent off-target inhibitors of the Kv1.3 channel via gating modification.

Panoramic characterization of proposed ligands for GPR3: oleoylethanolamide as a pharmacological chaperone.

Chemical components with antitumour activity from Inula britannica.

Diallyl sulfide pretreatment protects against DSS-induced colitis by reshaping the gut microbiota and enhancing microbiota-associated tryptophan metabolism.

(S)-SA, a bioactive flavonoid from Dalbergiae Odoriferae Lignum, alleviates cerebral ischemia-reperfusion injury via SLC11A2-mediated ferroptosis inhibition.

Balancing efficacy and risk: A toxicological review and safety transformation of Berberis plants and their alkaloids.

Experimental and theoretical approaches on structural, electronic, thermal and conductivity properties of ethynylated versus alkoxylated chalcones and elucidation of their cytotoxicity mechanisms in Acanthamoeba cells.

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Selective phosphodiesterase inhibition and alterations of cardiac function by alkylated xanthines

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