Default: Journal of Medicinal Chemistry

ISSN: 0022-2623

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Journal of Medicinal Chemistry Q1 Unclaimed

American Chemical Society United States
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Journal of Medicinal Chemistry is a journal indexed in SJR in Drug Discovery and Molecular Medicine with an H index of 251. It has a price of 3678 €. It has an SJR impact factor of 2,093 and it has a best quartile of Q1. It is published in English.

Journal of Medicinal Chemistry focuses its scope in these topics and keywords: inhibitors, activity, synthesis, evaluation, derivatives, biological, receptor, potent, selective, agents, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -


3678 €

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Journal of Medicinal Chemistry


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, activity, synthesis, evaluation, derivatives, biological, receptor, potent, selective, agents, binding, structure, ligands, inhibitor, series, potential, acid, analogs, relationships, design, antitumor,

Best articles

2-[3-[2-[(2S)-2-Cyano-1-pyrrolidinyl]-2-oxoethylamino]-3-methyl-1-oxobutyl]- 1,2,3,4-tetrahydroisoquinoline: A Potent, Selective, and Orally Bioavailable Dipeptide-Derived Inhibitor of Dipeptidyl Peptidase IV

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4-(((4-Iodophenyl)methyl)-4H-1,2,4-triazol-4-ylamino)-benzonitrile: A Potential Imaging Agent for Aromatase

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A Cyclic Tetrapeptide ("Cyclodal") and Its Mirror-Image Isomer Are Both High-Affinity µ Opioid Receptor Antagonists

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A Novel Parkinson's Disease Drug Candidate with Potent Anti-neuroinflammatory Effects through the Src Signaling Pathway

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a-Methyl Polyamines: Efficient Synthesis and Tolerance Studies in Vivo and in Vitro. First Evidence for Dormant Stereospecificity of Polyamine Oxidase

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AnN,N-Bis(benzimidazolylpicolinoyl)piperazine (BT-11): A Novel Lanthionine Synthetase C-Like 2-Based Therapeutic for Inflammatory Bowel Disease

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Antibacterial and Antibiofilm Activity of Cationic Small Molecules with Spatial Positioning of Hydrophobicity: An in Vitro and in Vivo Evaluation

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Antitumoral Activity of Non-Platinum Xanthate Complexes

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Antiviral activity of C-alkylated purine nucleosides obtained by cross-coupling with tetraalkyltin reagents

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Antivirulence C-Mannosides as Antibiotic-Sparing, Oral Therapeutics for Urinary Tract Infections

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beta-Sulfonamido Functionalized Aspartate Analogues as Excitatory Amino Acid Transporter Inhibitors: Distinct Subtype Selectivity Profiles Arising from Subtle Structural Differences

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Biophysical Characterization of Zinc Ejection from HIV Nucleocapsid Protein by Anti-HIV 2,2'-Dithiobis[benzamides] and Benzisothiazolones

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Biphenyl Pyridazinone Derivatives as Inhaled PDE4 Inhibitors: Structural Biology and Structure-Activity Relationships

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Bis-Michael Acceptors as Novel Probes to Study the Keap1/Nrf2/ARE Pathway

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Crystallographic Investigation of the Inhibition Mode of a VIM-2 Metallo-beta-lactamase fromPseudomonas aeruginosaby a Mercaptocarboxylate Inhibitor

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Design and Synthesis of Potent Quinazolines as Selective beta-Glucocerebrosidase Modulators

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Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) Inhibitors

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Design of Potent and Druglike Nonphenolic Inhibitors for Catechol O-Methyltransferase Derived from a Fragment Screening Approach Targeting the S-Adenosyl-l-methionine Pocket

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Design, Synthesis, and Binding Affinities of Potential Positron Emission Tomography (PET) Ligands for Visualization of Brain Dopamine D3Receptors

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Design, Synthesis, and Biological Evaluation of a Series of 2-Hydroxyisoquinoline-1,3(2H,4H)-diones as Dual Inhibitors of Human Immunodeficiency Virus Type 1 Integrase and the Reverse Transcriptase RNase H Domain

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Design, Synthesis, and Biological Evaluation of Novel Tetrahydroprotoberberine Derivatives (THPBs) as Selective a1A-Adrenoceptor Antagonists

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Design, Synthesis, and Structure-Activity Relationships of 1-,3-,8-, and 9-Substituted-9-deazaxanthines at the Human A2BAdenosine Receptor

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Design, Synthesis, Protein-Ligand X-ray Structure, and Biological Evaluation of a Series of Novel Macrocyclic Human Immunodeficiency Virus-1 Protease Inhibitors to Combat Drug Resistance

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Development and Characterization of a Fluorescent Probe for GLS1 and the Application for High-Throughput Screening of Allosteric Inhibitors

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