ISSN: 0960-894X
Journal Home
Journal Guideline
Bioorganic and Medicinal Chemistry Letters Q2 Unclaimed
Bioorganic and Medicinal Chemistry Letters is a journal indexed in SJR in Molecular Biology and Biochemistry with an H index of 172. It has an SJR impact factor of 0,472 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,472.
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: -


- €
Inmediate OANPD
Embargoed OA0 €
Non OAMetrics
0,472
SJR Impact factor172
H Index285
Total Docs (Last Year)1213
Total Docs (3 years)9636
Total Refs2992
Total Cites (3 years)1213
Citable Docs (3 years)2.19
Cites/Doc (2 years)33.81
Ref/DocOther journals with similar parameters
Frontiers in Molecular Neuroscience Q2
Molecular Biology of the Cell Q2
Mitochondrion Q2
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids Q2
Molecular Brain Q2
Compare this journals
Aims and Scope
Best articles by citations
Synthesis and PKC isozyme surrogate binding of indothiolactam-V, a new thioamide analogue of tumor promoting indolactam-V
View moreNonbenzamidine compounds as selective factor xa inhibitors
View moreA QSAR study investigating the effect of l-alanine ester variation on the anti-HIV activity of some phosphoramidate derivatives of d4T
View morePeptidyl aldehyde derivatives as potent and selective inhibitors of cathepsin L
View moreEnzymatic synthesis of (6R)- and (6S)-fluoroshikimic acids
View moreCorrigendum to "First pharmacophoric hypothesis for 5-HT7 antagonism"
View moreThe binding of cocaine to cyclodextrins
View moreImmunostimulatory activity of CpG containing phosphorothioate oligodeoxynucleotide is modulated by modification of a single deoxynucleoside
View moreA 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
View moreThe Synthesis and Selective IL-2 Inhibitory Activity of Bis Piperazine-Phenol Mannich Adducts
View moreDiscovery of selective metal-binding peptoids using 19F encoded combinatorial libraries
View moreCellular solid-phase binding assay and mass spectrometry for screening of a4beta7 integrin antagonists
View moreMechanistic studies on prolyl-4-hydroxylase: the vitamin c requiring uncoupled oxidation
View moreSynthesis of a water-soluble prodrug of entacapone
View moreDesign and synthesis of a conformationally constrained analog of the bis(heteroaryl)piperazine (BHAP) HIV-1 reverse transcriptase inhibitor atevirdine
View moreDesign and synthesis of a novel class of histone deacetylase inhibitors
View moreThe Synthesis of 4-Arylsulfanyl-substituted Kainoid Analogues from trans-4-Hydroxy-l-proline
View moreComputational binding studies of human pp60c-src SH2 domain with a series of nonpeptide, phosphophenyl-containing ligands
View moreStereo-random synthesis of highly functionalized proline analogues by azomethine cycloaddition
View moreDesign and synthesis of novel pyrrolobenzodiazepine (PBD) prodrugs for ADEPT and GDEPT
View moreWin 70197: a novel liver-targeted magnetic resonance imaging contrast agent
View morePolyhydroxylated 3-(N-phenyl) carbamoyl-2-iminochromene derivatives as potent inhibitors of tyrosine kinase p60c-src
View moreUnprecedented sugar-dependent in vivo antitumor activity of carbohydrate-pendant cis-diamminedichloroplatinum(II) complexes
View moreDesign and synthesis of potent thiol-based inhibitors of endothelin converting enzyme-1
View more
Comments