Default: European Journal of Medicinal Chemistry

ISSN: 0223-5234

Journal Home

Journal Guideline

European Journal of Medicinal Chemistry Q1 Unclaimed

Elsevier Masson SAS France
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

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. It has an SJR impact factor of 1,177.

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

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

European Journal of Medicinal Chemistry

1,177

SJR Impact factor

162

H Index

838

Total Docs (Last Year)

2853

Total Docs (3 years)

56099

Total Refs

17278

Total Cites (3 years)

2851

Citable Docs (3 years)

6,18

Cites/Doc (2 years)

66,94

Ref/Doc

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 by citations

Synthesis and antibacterial activity of 7-hydrazinoquinolones

View more

Evidence for new non-steroidal human aromatase inhibitors and comparison with equine aromatase inhibition for an understanding of the mammalian active site

View more

Synthesis and potential antiallergic activity of new pteridinones and related compounds

View more

Synthesis and potential coanthracyclinic activity of pyridylmethylene and indolylmethylene lactams

View more

Pyrroloquinolones and pyrazoloquinolones as potential antibacterial agents. Synthesis and antibacterial activity

View more

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

View more

Quantitative structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. Analysis of serotonin 5-HT1A effects in vivo and in vitro via partial least squares regression

View more

Sensitivity of the PCP receptor and the dopamine transporter to ligands bearing multiple asymmetric centres

View more

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

View more

Research on heterocyclic compounds. Part XXXVI. Imidazo[1,2-a]pyrimidine2-acetic derivatives: synthesis and antiinflammatory activity

View more

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

View more

Partial resistance of E. coli mutants against 2,4-diamino-5-benzylpyrimidines by interactions with bacterial membrane lipopolysaccharides. Derivation of quantitative structure-binding relationships

View more
SHOW MORE ARTICLES

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

View more

Synthesis and antimicrobial activities of monoindolyl- and bisindolyloximes

View more

Plasma stability and cytotoxicity of lipophilic daunorubicin derivatives incorporated into low density lipoproteins

View more

The influence of the lipophilicity of 7-oxoacyl-l-alanyl-d-isoglutamines on their immunorestoration activity in vivo

View more

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

View more

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

View more

Isoquinuclidine-based expectorants. Synthesis and biological activities of N-alkoxybenzylisoquinuclidines

View more

Synthesis and antineoplastic activity of cyclolignan aldehydes

View more

New indole derivatives as ACAT inhibitors: synthesis and structure-activity relationships

View more

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

View more

Synthesis and in vitro anti-HIV activities of amphiphilic heterodinucleoside phosphate derivatives containing the 2',3'-dideoxynucleosides ddC, AZT and ddI

View more

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

View more

Comments

No comments ... Be the first to comment!

FAQS