Articles & Issues. European Journal of Medicinal Chemistry. CiteScore values are based on citation counts in a range of four years (e.g. Submit your article Guide for Authors. Copyright © 2020 Elsevier B.V. or its licensors or contributors. European Journal of Medicinal Chemistry 139 (2017) 153e167. 8.3 CiteScore. Majumdar, Sudipta Ponra, Tapas Ghosh, Ratan Sadhukhan, Utpal Ghosh, https://doi.org/10.1016/j.ejmech.2013.10.056, B. Chandrakantha, Arun M. Isloor, Prakash Shetty, Hoong Kun Fun, Gurumurthy Hegde, https://doi.org/10.1016/j.ejmech.2013.10.055, Narva Suresh, Hunsur Nagendra Nagesh, Janupally Renuka, Vikrant Rajput, ... Chandra Sekhar Kondapalli Venkata Gowri, https://doi.org/10.1016/j.ejmech.2013.10.076, Y.M. Synthesis, and molecular structure of novel series, select article Synthesis and biological evaluation of α-triazolyl chalcones as a new type of potential antimicrobial agents and their interaction with calf thymus DNA and human serum albumin, Synthesis and biological evaluation of α-triazolyl chalcones as a new type of potential antimicrobial agents and their interaction with calf thymus DNA and human serum albumin, select article Rational design and synthesis of novel dibenzo[b,d]furan-1,2,3-triazole conjugates as potent inhibitors of Mycobacterium tuberculosis, Rational design and synthesis of novel dibenzo[, select article 2-(1H-Pyrazol-1-yl)acetic acids as chemoattractant receptor-homologous molecule expressed on Th2 lymphocytes (CRTh2) antagonists, select article 1,2,4-Triazole/oxime hybrids as new strategy for nitric oxide donors: Synthesis, anti-inflammatory, ulceroginicity and antiproliferative activities, 1,2,4-Triazole/oxime hybrids as new strategy for nitric oxide donors: Synthesis, anti-inflammatory, ulceroginicity and antiproliferative activities, select article Design, synthesis, molecular docking and 3D-QSAR studies of potent inhibitors of enoyl-acyl carrier protein reductase as potential antimycobacterial agents, Design, synthesis, molecular docking and 3D-QSAR studies of potent inhibitors of enoyl-acyl carrier protein reductase as potential antimycobacterial agents, select article Synthesis and tumor cell growth inhibitory activity of biotinylated annonaceous acetogenins, Synthesis and tumor cell growth inhibitory activity of biotinylated annonaceous acetogenins, select article Synthesis and biological evaluation of a series of aminoalkyl-tetralones and tetralols as dual dopamine/serotonin ligands, Synthesis and biological evaluation of a series of aminoalkyl-tetralones and tetralols as dual dopamine/serotonin ligands, select article Discovery of a benzimidazole series of ADAMTS-5 (aggrecanase-2) inhibitors by scaffold hopping, Discovery of a benzimidazole series of ADAMTS-5 (aggrecanase-2) inhibitors by scaffold hopping, select article Design, synthesis, and biological evaluation of novel piperidine-4-carboxamide derivatives as potent CCR5 inhibitors, Design, synthesis, and biological evaluation of novel piperidine-4-carboxamide derivatives as potent CCR5 inhibitors, select article Anilides and quinolones with nitrogen-bearing substituents from benzothiophene and thienothiophene series: Synthesis, photochemical synthesis, cytostatic evaluation, 3D-derived QSAR analysis and DNA-binding properties, Anilides and quinolones with nitrogen-bearing substituents from benzothiophene and thienothiophene series: Synthesis, photochemical synthesis, cytostatic evaluation, 3D-derived QSAR analysis and DNA-binding properties, select article A novel tamoxifen derivative, ridaifen-F, is a nonpeptidic small-molecule proteasome inhibitor, A novel tamoxifen derivative, ridaifen-F, is a nonpeptidic small-molecule proteasome inhibitor, select article Synthesis of novel pyrano[3,2-f]quinoline, phenanthroline derivatives and studies of their interactions with proteins: An application in mammalian cell imaging, select article Synthesis and biological evaluation of novel substituted 1,3,4-thiadiazole and 2,6-di aryl substituted imidazo [2,1-b] [1,3,4] thiadiazole derivatives, Synthesis and biological evaluation of novel substituted 1,3,4-thiadiazole and 2,6-di aryl substituted imidazo [2,1-, select article Synthesis and evaluation of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-(2-(4-substitutedpiperazin-1-yl)acetyl)piperazin-1-yl)quinoline-3-carboxylic acid derivatives as anti-tubercular and antibacterial agents, Synthesis and evaluation of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-(2-(4-substitutedpiperazin-1-yl)acetyl)piperazin-1-yl)quinoline-3-carboxylic acid derivatives as anti-tubercular and antibacterial agents, select article Synthesis and antiproliferative action of a novel series of maprotiline analogues, Synthesis and antiproliferative action of a novel series of maprotiline analogues, select article Synthesis and characterization of new N-(4-(4-chloro-1H-imidazol-1-yl)-3-methoxyphenyl)amide/sulfonamide derivatives as possible antimicrobial and antitubercular agents, select article Platinated benzonaphthyridone is a stronger inhibitor of poly(ADP-ribose) polymerase-1 and a more potent anticancer agent than is the parent inhibitor, Platinated benzonaphthyridone is a stronger inhibitor of poly(ADP-ribose) polymerase-1 and a more potent anticancer agent than is the parent inhibitor, select article Development and biological evaluation of 99mTc-sulfonamide derivatives for in vivo visualization of CA IX as surrogate tumor hypoxia markers, select article Access to a new class of biologically active quinoline based 1,2,4-triazoles, Access to a new class of biologically active quinoline based 1,2,4-triazoles, select article Antimicrobial activity of de novo designed cationic peptides against multi-resistant clinical isolates, select article Urea/oxalamide tethered β-lactam-7-chloroquinoline conjugates: Synthesis and in vitro antimalarial evaluation, Urea/oxalamide tethered β-lactam-7-chloroquinoline conjugates: Synthesis and, select article Synthesis, characterization and anticancer screening of some novel piperonyl–tetrazole derivatives, Synthesis, characterization and anticancer screening of some novel piperonyl–tetrazole derivatives, select article Synthesis and evaluation of the antiparasitic activity of bis-(arylmethylidene) cycloalkanones, Synthesis and evaluation of the antiparasitic activity of bis-(arylmethylidene) cycloalkanones. Therefore, manuscripts should contain new work on the synthesis of new compounds and their biological evaluation. CiteScore: 8.3 ℹ CiteScore: 2019: 8.3 CiteScore measures the average citations received per peer-reviewed document published in this title. Log In; Automatic login IP; PUBLISHERS' AREA DISCOVER ISSN SERVICES SEARCH OPEN ACCESS RESOURCES KEEPERS REGISTRY ISSN INTERNATIONAL CENTER. Articles & Issues. Username or e-mail * Password * Forgot Password. We use cookies to help provide and enhance our service and tailor content and ads. Note: the citation style and format (paragraph spacing, line numbers, etc.)

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