Default: Journal of Medicinal Chemistry

ISSN: 0022-2623

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Journal of Medicinal Chemistry Q1 Unclaimed

American Chemical Society United States
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

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.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Price

3678 €

Gold OA

-

Green OA

0 €

Non OA

Metrics

Journal of Medicinal Chemistry

2,093

SJR Impact factor

251

H Index

744

Total Docs (Last Year)

2247

Total Docs (3 years)

44215

Total Refs

14305

Total Cites (3 years)

2163

Citable Docs (3 years)

6,34

Cites/Doc (2 years)

59,43

Ref/Doc


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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