Default: European Journal of Medicinal Chemistry

ISSN: 0223-5234

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European Journal of Medicinal Chemistry Q1 Unclaimed

Elsevier Masson SAS France
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European Journal of Medicinal Chemistry is a journal indexed in SJR in Medicine (miscellaneous) and Drug Discovery with an H index of 162. It has an SJR impact factor of 1,177 and it has a best quartile of Q1. It is published in English.

European Journal of Medicinal Chemistry focuses its scope in these topics and keywords: derivatives, evaluation, inhibitors, biological, activity, potent, synthesis, derivativessynthesis, discovery, agents, ...

Type: Journal

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Languages: English

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European Journal of Medicinal Chemistry


SJR Impact factor


H Index


Total Docs (Last Year)


Total Docs (3 years)


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Total Cites (3 years)


Citable Docs (3 years)


Cites/Doc (2 years)



Aims and Scope

derivatives, evaluation, inhibitors, biological, activity, potent, synthesis, derivativessynthesis, discovery, agents, anticancer, study, virus, structural, binding, hybrids, cancer, human, ii, interaction, properties, relationship, series, substituted, thioredoxin,

Best articles

"Synthesis and beta-adrenoceptor agonist properties of (±)-1-(3',4'-dihydroxyphenoxy)-3-(3"",4""-dimethoxyphenyl) ethylamino-2-propanol hydrochloride, (±)-RO363.HCl, and the (2S)-(-)-isomer"

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10-Aminomethylene-1,8-dihydroxy-9(10H)-anthracenones: Inhibitory action against 5-lipoxygenase and the growth of HaCaT cells

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2-Oxo-2-(phen-2-ylpyrrol-2-yl)acetamides as potential anxiolytic agents: Synthesis and affinity at the central benzodiazepine receptor

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5(10=>9)Abeo-ergoline derivatives: Synthesis, 5-HT1A-receptor affinity and selectivity

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6-Amino-2,4-lutidine carboxamides: a-aminoamide derivatives as systemic and topical inflammation inhibitors

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A CoMFA investigation of sigma receptor binding affinity: Reexamination of a spurious sigma ligand

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A model allowing the design of modified nucleosides as HIV-RT inhibitors

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A QSAR study confirming the heterogeneity of the HEPT derivative series regarding their interaction with HIV reverse transcriptase

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A rational approach to the design of flavones as xanthine oxidase inhibitors

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a-Methoxy-O-(N-arylcarbamoyl)oximes: synthesis and pharmacological activities

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Adenosine receptors: synthesis, structure-activity relationships and biological activity of new 6-amino purine derivatives

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Anthraquinone intercalators as carrier molecules for second-generation platinum anticancer drugs

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Antifungal estrogen-like imidazoles. Synthesis and antifungal activities of thienyl and 1H-pyrrolyl derivatives of 1-aryl-2-(1H-imidazol-1-yl)ethane

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Anxiolytic activity of analogues of 4-benzylamino-2-methyl-7H-pyrrolo[2,3-d]pyrimidines

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Benzofuran derivatives as ETA-selective, non-peptide endothelin antagonists

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beta1- and beta2-Adrenoceptor antagonist activity of a series of para-substituted N-isopropylphenoxypropanolamines

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Carbonic anhydrase inhibitors - Part 47: Quantum chemical quantitative structure-activity relationships for a group of sulfanilamide Schiff base inhibitors of carbonic anhydrase

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Competition between two metabolic pathways: oxidation and desulfuration in the thiobarbiturate series

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D1 Agonist and/or D2 antagonist dopamine receptor properties of a series of ergoline derivatives: a structure-activity study

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Design and synthesis of substituted compounds containing the 1,4-benzodioxin subunit. New potential calcium antagonists

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Dibenzo[1,6]naphthyridindiones as modified quinolone antibacterials

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Dihydropyridines bearing an imidazo[2,1-b]thiazole system

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DNA-binding properties of pyrrolo[2,1-c][1,4]benzodiazepine N10-C11 amidines

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Effect of lowered lipophilicity on the affinity of PCP analogues for the PCP receptor and the dopamine transporter

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