verified SJR 1,052 · Q1 • database Scopus / SJR & Web of Science indexed

United States · Elsevier Inc.

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Molecular Pharmacology

Molecular Pharmacology is a journal indexed in SJR in Pharmacology and Molecular Medicine with an H index of 215. It has an SJR impact factor of 1,052 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 1,052.

Molecular Pharmacology focuses its scope in these topics and keywords: receptor, species, human, inhibitor, characterization, acetylcholine, drug, g, cells, inhibitors, ...

ISSN: 0026-895X

Editorial: Elsevier Inc.

Category: Pharmacology

Indexation: verifiedScopus / SJR verifiedWeb of Science

Unclaimed profile — some fields may be incomplete.

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SJR Impact Factor trending_up

1,052 Q1

H-index 215

Tasa de Aceptación pie_chart

19% Selectiva

Fuente Acceptance_Rate

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Metrics

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Scopus / SJR Web of Science

SJR Impact

1,052

H-index

215

Docs (year)

Docs 3y

215

Total refs

4581

Cites 3y

574

Citable 3y

211

Cites/Doc 2y

2.53

Ref/Doc

69.41

Immediate OA

—

Embargoed OA

NPD

Non OA / Submission

—

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Best articles by citations

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

Voltage-Gated Sodium Channels Regulating Action Potential Generation in Itch-, Nociceptive-, and Low-Threshold Mechanosensitive Cutaneous C-Fibers

Defining the Propofol Binding Site Location on the GABAA Receptor

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

Covalent and Noncovalent Interactions Mediate Metabotropic Glutamate Receptor mGlu5Dimerization

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

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

CB1 Receptor Allosteric Modulators Display Both Agonist and Signaling Pathway Specificity

Caffeine Regulates Neuronal Expression of the Dopamine 2 Receptor Gene

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

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

c-Jun NH2-Terminal Kinase Inhibitor

SHOW MORE ARTICLES

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

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

Aspartate Aminotransferase Generates Proagonists of the Aryl Hydrocarbon Receptor

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

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

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

Altered Striatal Function and Muscarinic Cholinergic Receptors in Acetylcholinesterase Knockout Mice

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

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

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

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

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

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