ChemMedChem
ChemMedChem is a journal indexed in SJR in Biochemistry and Drug Discovery with an H index of 123. It has a price of 2040 €. It has an SJR impact factor of 0,717 and it has a best quartile of Q1. It has an SJR impact factor of 0,717.
ChemMedChem focuses its scope in these topics and keywords: inhibitors, drug, chemmedchem, chemistry, activity, analogues, human, molecules, medicinal, ligands, ...
Unclaimed profile — some fields may be incomplete.
Metrics
Campos Scimago / CoP — sin series inventadas
SJR Impact
0,717
H-index
123
Docs (year)
313
Docs 3y
810
Total refs
20699
Cites 3y
2849
Citable 3y
801
Cites/Doc 2y
3.31
Ref/Doc
66.13
Immediate OA
2040 €
Embargoed OA
NPD
Non OA / Submission
0 €
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Researcher reviews
Best articles by citations
Cationic Branched Polyethylenimine (BPEI) Disables Antibiotic Resistance in Methicillin-Resistant Staphylococcus epidermidis
View moreWhy Hydroxamates May Not Be the Best Histone Deacetylase Inhibitors-What Some May Have Forgotten or Would Rather Forget?
View moreDesign and Synthesis of Novel Cyclooxygenase-1 Inhibitors as Analgesics: 5-Amino-2-ethoxy-N-(substituted-phenyl)benzamides
View moreDesign and Synthesis of N-Acylated Aza-Goniothalamin Derivatives and Evaluation of Their in vitro and in vivo Antitumor Activity
View moreDesign and Synthesis of 4-(2,4,5-Trifluorophenyl)butane-1,3-diamines as Dipeptidyl Peptidase IV Inhibitors
View moreCu
View moreCover Picture: Molecular Assembly of Multifunctional 99mTc Radiopharmaceuticals Using "Clickable" Amino Acid Derivatives (ChemMedChem 12/2010)
View moreCover Picture: Characterization of C-Alkyl Amidines as Bioavailable Covalent Reversible Inhibitors of Human DDAH-1 (ChemMedChem 1/2011)
View moreConjugation of ATIII-Binding Pentasaccharides to Extend the Half-Life of Proteins: Long-Acting Insulin
View moreComparative Molecular Profiling of the PPARa/ gamma Activator Aleglitazar: PPAR Selectivity, Activity and Interaction with Cofactors
View moreCombating Cystic Fibrosis: In Search for CF Transmembrane Conductance Regulator (CFTR) Modulators
View moreChemistry, Biology, and QSAR Studies of Substituted Biaryl Hydroxamates and Mercaptoacetamides as HDAC Inhibitors - Nanomolar-Potency Inhibitors of Pancreatic Cancer Cell Growth
View moreChemical Synthesis and Biological Evaluation of the Englerin Analogues
View more(2,2-Diphenyl-[1,3]oxathiolan-5-ylmethyl)-(3-phenyl-propyl)-amine: a Potent and Selective 5-HT1AReceptor Agonist
View moreAuthors Profile
View moreAsymmetric Synthesis and Conformational Analysis by NMR Spectroscopy and MD of Aba- and a-MeAba-Containing Dermorphin Analogues
View moreAssessment of Bromodomain Target Engagement by a Series of BI2536 Analogues with Miniaturized BET-BRET
View moreAntiproliferative Effects of Ester- and Amide-Functionalized Rhizoxin Derivatives
View moreAnticancer Gold(III) Peptidomimetics: From Synthesis to in vitro and ex vivo Biological Evaluations
View moreAn Efficient Bioorthogonal Strategy Using CuAAC Click Chemistry for Radiofluorinations of SNEW Peptides and the Role of Copper Depletion
View moreAllosteric Inhibitor Development Targeting HIV-1 Integrase
View moreA Versatile and Practical Synthesis toward the Development of Novel HIV-1 Integrase Inhibitors
View moreA Synthetic C34 Trimer of HIV-1 gp41 Shows Significant Increase in Inhibition Potency
View moreA Potent Integrin Antagonist from a Small Library of Cyclic RGD Pentapeptide Mimics Including Benzyl-Substituted Azabicycloalkane Amino Acids
View more