Default: Bioorganic and Medicinal Chemistry Letters

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: -


Bioorganic and Medicinal Chemistry Letters


SJR Impact factor


H Index


Total Docs (Last Year)


Total Docs (3 years)


Total Refs


Total Cites (3 years)


Citable Docs (3 years)


Cites/Doc (2 years)



Aims and Scope

inhibitors, potent, derivatives, receptor, synthesis, evaluation, activity, selective, protein, d, kinase, biological, based, human, part, relationship, series, relationships, analogs, discovery, tyrosine, potential, sar, type,

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

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

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

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

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5-HETE congeners as modulators of cell proliferation

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

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

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A case study of combinatorial libraries: Endothelin receptor antagonist hexapeptides

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

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

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

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

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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

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Amino acid phosphoramidate nucleosides: potential ADEPT/GDEPT substrates

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

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

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

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

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

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

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Conformationally-restricted ligands for the histamine H 1 receptor

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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

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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]†

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

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