Molecular Pharmacology Q1 Unclaimed

American Society for Pharmacology and Experimental Therapeutics United States
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.


Molecular Pharmacology focuses its scope in these topics and keywords: receptor, human, inhibitor, species, mechanism, inhibitors, regulatory, acetylcholine, characterization, activation, ...

Type: Journal

Type of Copyright: NA

Languages: English

Open Access Policy: NA

Type of publications: NA

Publication frecuency: NA


NA €

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Molecular Pharmacology


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Citable Docs (3 years)


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Aims and Scope

receptor, human, inhibitor, species, mechanism, inhibitors, regulatory, acetylcholine, characterization, activation, drug, basis, cells, oxygen, potent, reactive, acid, pai, t, g, m, carboxylterminal, NA

Best articles

µ Opioid Transactivation and Down-Regulation of the Epidermal Growth Factor Receptor in Astrocytes: Implications for Mitogen-Activated Protein Kinase Signaling

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1-Methyl-4-Phenylpyridinium Induces Autocrine Excitotoxicity, Protease Activation, and Neuronal Apoptosis

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8R-Lisuride Is a Potent Stereospecific Histamine H1-Receptor Partial Agonist

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A New and Simple Method for Delivering Clamped Nitric Oxide Concentrations in the Physiological Range: Application to Activation of Guanylyl Cyclase-Coupled Nitric Oxide Receptors

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A Novel Synthetic Cannabinoid Derivative Inhibits Inflammatory Liver Damage via Negative Cytokine Regulation

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A Tetratricopeptide Repeat Half-Site in the Aryl Hydrocarbon Receptor Is Important for DNA Binding andtrans-Activation Potential

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Acquired Cellular Resistance to Flavopiridol in a Human Colon Carcinoma Cell Line Involves Up-Regulation of the Telomerase Catalytic Subunit and Telomere Elongation. Sensitivity of Resistant Cells to Combination Treatment with a Telomerase Inhibitor

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Altered Striatal Function and Muscarinic Cholinergic Receptors in Acetylcholinesterase Knockout Mice

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An Apamin- and Scyllatoxin-Insensitive Isoform of the Human SK3 Channel

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An N-Terminal Histidine Is the Primary Determinant of a Subunit-Dependent Cu2+ Sensitivity of abeta3 gamma2L GABAA Receptors

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Aryl Hydrocarbon Receptor Splice Variants in the Dioxin-Resistant Rat: Tissue Expression and Transactivational Activity

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Aspartate Aminotransferase Generates Proagonists of the Aryl Hydrocarbon Receptor

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Barbiturates Directly Inhibit the Calmodulin/Calcineurin Complex: a Novel Mechanism of Inhibition of Nuclear Factor of Activated T Cells

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beta2-Adrenergic Signaling in Human Heart: Shift from the Cyclic AMP to the Arachidonic Acid Pathway

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c-Jun NH2-Terminal Kinase Inhibitor

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c-Myc Exerts a Protective Function through Ornithine Decarboxylase against Cellular Insults

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Caffeic Acid Esters Activate TREK-1 Potassium Channels and Inhibit Depolarization-Dependent Secretion

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Caffeine Regulates Neuronal Expression of the Dopamine 2 Receptor Gene

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CB1 Receptor Allosteric Modulators Display Both Agonist and Signaling Pathway Specificity

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Characterization of the Human Calcitonin Gene-Related Peptide Receptor Subtypes Associated with Receptor Activity-Modifying Proteins

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Combinatorial Interaction of Scorpion Toxins Lqh-2, Lqh-3, and LqhaIT with Sodium Channel Receptor Sites-3

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Covalent and Noncovalent Interactions Mediate Metabotropic Glutamate Receptor mGlu5Dimerization

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Cytochrome P4501A1 Promotes G1 Phase Cell Cycle Progression by Controlling Aryl Hydrocarbon Receptor Activity

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Defining the Propofol Binding Site Location on the GABAA Receptor

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