ISSN: 0960-894X

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Bioorganic and Medicinal Chemistry Letters Q1 Unclaimed

Elsevier Ltd. United Kingdom

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Bioorganic and Medicinal Chemistry Letters is a journal indexed in SJR in Molecular Biology and Biochemistry with an H index of 141. It has an SJR impact factor of 0,64 and it has a best quartile of Q1. It is published in English.

Bioorganic and Medicinal Chemistry Letters focuses its scope in these topics and keywords: inhibitors, potent, derivatives, receptor, synthesis, evaluation, activity, selective, protein, d, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Pharmaceutical Science (Q1) Clinical Biochemistry (Q2) Clinical Biochemistry (Q2) Drug Discovery (Q2) Organic Chemistry (Q2) Biochemistry (Q3) Molecular Biology (Q3) Molecular Medicine (Q3)

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Green OA

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Metrics

Bioorganic and Medicinal Chemistry Letters

0,64

SJR Impact factor

141

H Index

609

Total Docs (Last Year)

2860

Total Docs (3 years)

19295

Total Refs

7487

Total Cites (3 years)

2828

Citable Docs (3 years)

2,64

Cites/Doc (2 years)

31,68

Ref/Doc

Other journals with similar parameters

Nature Structural and Molecular Biology Q1
Molecular Biology and Evolution Q1
Trends in Biochemical Sciences Q1
Nature Protocols Q1
Microbiology and Molecular Biology Reviews Q1

Aims and Scope

Best articles

2-(Anilinomethyl)imidazolines as a1-adrenoceptor agonists: the identification of a1A subtype selective 2'-carboxylic acid esters and amides

2-Aryl indole NK1 antagonists: optimisation of the amide substituent

2-Nitro analogues of adenosine and 1-deazaadenosine: synthesis and binding studies at the adenosine A1, A2A and A3 receptor subtypes

3-Aryl-4-aryloyl-1-(1H-imidazol-5-yl)methylpyrrole, a novel class of farnesyltransferase inhibitors

5-HETE congeners as modulators of cell proliferation

6-bicyclopiperazinyl-1-arylsulfonylindoles and 6-bicyclopiperidinyl-1-arylsulfonylindoles derivatives as novel, potent, and selective 5-HT6 receptor antagonists

7-Nitrobenzofurazan (NBD) derivatives of 5'-N-ethylcarboxamidoadenosine (NECA) as new fluorescent probes for human A3 adenosine receptors

A case study of combinatorial libraries: Endothelin receptor antagonist hexapeptides

A convenient synthesis of novel bifunctional prochelators for coupling to bioactive peptides for radiometal labelling

A new deprotection strategy for automated oligonucleotide synthesis using a novel silyl-linked solid support

A novel series of highly potent 5-lipoxygenase inhibitors; 2-aryldienylbenzoxazoles

A QSAR study investigating the effect of l-alanine ester variation on the anti-HIV activity of some phosphoramidate derivatives of d4T

SHOW MORE ARTICLES

A Unique Ring-Expanded Acyclic Nucleoside Analogue that Inhibits Both Adenosine Deaminase (ADA) and Guanine Deaminase (GDA; Guanase): Synthesis and Enzyme Inhibition Studies of 4,6-Diamino-8H-1-hydroxyethoxymethyl-8-iminoimidazo[4,5-e][1,3]diazepine

Amino acid phosphoramidate nucleosides: potential ADEPT/GDEPT substrates

Amino azoles and azolo-azines as potential hepatoprotectants: Part III

Anionic Cyclophanes as Potential Reversal Agents of Muscle Relaxants by Chemical Chelation

Assamicin I and II, Novel Triterpenoid Saponins with Insulin-Like Activity from Aesculus assamica Griff.

Biologically active oligodeoxyribonucleotides. Part 12:1 N2-Methylation of 2'-deoxyguanosines enhances stability of parallel G-quadruplex and anti-HIV-1 activity

Cellular solid-phase binding assay and mass spectrometry for screening of a4beta7 integrin antagonists

Computational binding studies of human pp60c-src SH2 domain with a series of nonpeptide, phosphophenyl-containing ligands

Conformationally-restricted ligands for the histamine H 1 receptor

Copper-Promoted overall transformation of 4- tert -butylphenol to its para -hydroxyquinonic derivative, 2-hydroxy-5- tert -butyl-1,4-benzoquinone. Biomimetic studies on the generation of topaquinone in copper amine oxidases

Corrigendum to "Amino acid derived sulfonamide hydroxamates as inhibitors of procollagen C-proteinase: solid-phase synthesis of ornithine analogues"[Bioorg. Med. Chem. Lett. 11 (2001) 2085]†

Corrigendum to "First pharmacophoric hypothesis for 5-HT7 antagonism"

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