ISSN: 0968-0896

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Bioorganic and Medicinal Chemistry Q2 Unclaimed

Elsevier Ltd. United Kingdom

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Bioorganic and Medicinal Chemistry is a journal indexed in SJR in Molecular Biology and Biochemistry with an H index of 171. It has a price of 2917 €. It has an SJR impact factor of 0.598 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0.598.

Bioorganic and Medicinal Chemistry focuses its scope in these topics and keywords: evaluation, derivatives, activity, synthesis, biological, receptor, inhibitors, potential, binding, activities, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Drug Discovery (Q2) Organic Chemistry (Q2) Pharmaceutical Science (Q2) Biochemistry (Q3) Clinical Biochemistry (Q3) Clinical Biochemistry (Q3) Molecular Biology (Q3) Molecular Medicine (Q3)

Price

2917 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0.598

SJR Impact factor

171

H Index

439

Total Docs (Last Year)

1508

Total Docs (3 years)

21209

Total Refs

5372

Total Cites (3 years)

1498

Citable Docs (3 years)

3.4

Cites/Doc (2 years)

48.31

Ref/Doc

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Aims and Scope

Best articles by citations

Sequence-specific delivery of a quinone methide intermediate to the major groove of DNA

Exploration of the DTrp-NMeLys Motif in the Search for potent somatostatin antagonists

Synthesis and evaluation of microtubule assembly inhibition and cytotoxicity of prenylated derivatives of cyclo-l-Trp-l-Pro

Identification of preferred actinomycin-DNA binding sites by the combinatorial method REPSA

Testosterone delivery using glutamide-based complex high axial ratio microstructures

A Practical Synthesis and Biological Evaluation of 9-Halogenated PGF Analogues

Immunostimulatory activity of CpG oligonucleotides containing non-ionic methylphosphonate linkages

A practical synthesis of the serotonin 5-HT2a receptor antagonist mdl 100907, its enantiomer and their 3-phenolic derivatives as precursors for [11c]labeled pet ligands

Pentopyranosyl oligonucleotide systems. Part 11: systems with shortened backbones: (?)-beta-ribopyranosyl-(4'=>3')- and (?)-a-lyxopyranosyl-(4'=>3')-oligonucleotides

Inducible regulation of the S. cerevisiae cell cycle mediated by an RNA aptamer-ligand complex

Corrigendum to "Imidazole-containing amino acids as selective inhibitors of nitric oxide synthases"

Design and structure-activity relationship of thrombin inhibitors with an azaphenylalanine scaffold: potency and selectivity enhancements via P2 optimization

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Synthesis of pyridino[2,3- f ]indole-4,9-dione 6,7-disubstituted quinoline-5,8-dione derivatives and evaluation on their cytotoxic activity

alternative heterocycles for dna recognition: a 3-pyrazole/pyrrole pair specifies for g¬?c base pairs

Chemical Modification of the beta-Glucocerebrosidase Inhibitor N-Octyl-beta-valienamine: Synthesis and Biological Evaluation of 4-Epimeric and 4-O-(beta-?-Galactopyranosyl) Derivatives

Application of enzymatically stable dipeptides for enhancement of intestinal permeability. Synthesis and In vitro evaluation of dipeptide-Coupled compounds

Ethenesulfonamide and ethanesulfonamide derivatives, a novel class of orally active endothelin-A receptor antagonists

Modification of cell response to insulin by membrane-Acting agents in rat white adipocytes: analysis of structural features by computational simulation

Design and Synthesis of Novel Potent Antinociceptive Agents: Methyl-imidazolyl N-Acylhydrazone Derivatives

Structure-activity relationships and optimisation of the selective MDR modulator 2-(3,4-dimethoxyphenyl)-5-(9-fluorenylamino)-2-(methylethyl) pentanenitrile and its N-methyl derivative

Functionalized oligoanthranilamides: modular and conformationally controlled scaffolds

The Conformation and Activity Relationship of Benzofuran Type of Angiotensin II Receptor Antagonists

DNA Analogues: From Supramolecular Principles to Biological Properties

Synthesis of Feruloyl-myo-insitol derivatives and their inhibitory effects on phorbol ester-induced superoxide generation and esptein-barr virus activation