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European journal of medicinal chemistry

European journal of medicinal chemistry
紙記録メディア雑誌
Elsevier<Z53-V266>
国立国会図書館全国の図書館
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Exploration of LPS2 agonist binding modes using the combination of a new hydrophobic scaffold and homology modeling

Exploration of LPS2 agonist binding modes using the combination of a new hydrophobic scaffold and homology modeling
デジタル記事
2023-04European Journal of Medicinal Chemistry252p.115271-
全国の図書館
  • 掲載誌（ISSN）02235234

5-Fluorouracil nano-delivery systems as a cutting-edge for cancer therapy

5-Fluorouracil nano-delivery systems as a cutting-edge for cancer therapy
デジタル記事
2023-01European Journal of Medicinal Chemistry246p.114995-
全国の図書館
  • 掲載誌（ISSN）02235234

Natural quinazolinones: From a treasure house to promising anticancer leads

Natural quinazolinones: From a treasure house to promising anticancer leads
デジタル記事
2023-01European Journal of Medicinal Chemistry245p.114915-
全国の図書館
  • 掲載誌（ISSN）02235234

The current strategies of optimization of oseltamivir against mutant neuraminidases of influenza A：A review

The current strategies of optimization of oseltamivir against mutant neuraminidases of influenza A：A review
デジタル記事
2022-12European Journal of Medicinal Chemistry243p.114711-
全国の図書館
  • 掲載誌（ISSN）02235234

Discovery of pimozide derivatives as novel T-type calcium channel inhibitors with little binding affinity to dopamine D2 receptors for treatment of somatic and visceral pain

Discovery of pimozide derivatives as novel T-type calcium channel inhibitors with little binding affinity to dopamine D2 receptors for treatment of somatic and visceral pain
デジタル記事
2022-12European Journal of Medicinal Chemistry243p.114716-
全国の図書館
  • 掲載誌（ISSN）02235234

C-6 fluorinated casuarines as highly potent and selective amyloglucosidase inhibitors: Synthesis and structure-activity relationship study

C-6 fluorinated casuarines as highly potent and selective amyloglucosidase inhibitors: Synthesis and structure-activity relationship study
デジタル記事
2022-12European Journal of Medicinal Chemistry244p.114852-
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  • 掲載誌（ISSN）02235234

Development of fluorizoline analogues as prohibitin ligands that modulate C-RAF signaling, p21 expression and melanogenesis

Development of fluorizoline analogues as prohibitin ligands that modulate C-RAF signaling, p21 expression and melanogenesis
デジタル記事
2022-11European Journal of Medicinal Chemistry242p.114635-
全国の図書館
  • 掲載誌（ISSN）02235234

Discovery of novel orexin receptor antagonists using a 1,3,5-trioxazatriquinane bearing multiple effective residues (TriMER) library

Discovery of novel orexin receptor antagonists using a 1,3,5-trioxazatriquinane bearing multiple effective residues (TriMER) library
デジタル記事
2022-10European Journal of Medicinal Chemistry240p.114505-
インターネットで読める全国の図書館
  • 掲載誌（ISSN）02235234

A multi-pronged evaluation of aldehyde-based tripeptidyl main protease inhibitors as SARS-CoV-2 antivirals

A multi-pronged evaluation of aldehyde-based tripeptidyl main protease inhibitors as SARS-CoV-2 antivirals
デジタル記事
2022-10European Journal of Medicinal Chemistry240p.114570-
全国の図書館
  • 掲載誌（ISSN）02235234

Design and synthesis of aryl-piperidine derivatives as potent and selective PET tracers for cholesterol 24-hydroxylase (CH24H)

Design and synthesis of aryl-piperidine derivatives as potent and selective PET tracers for cholesterol 24-hydroxylase (CH24H)
デジタル記事
2022-10European Journal of Medicinal Chemistry240p.114612-
全国の図書館
  • 掲載誌（ISSN）02235234

Computational method for the systematic alignment of analogue series with structure-activity relationship transfer potential across different targets

Computational method for the systematic alignment of analogue series with structure-activity relationship transfer potential across different targets
デジタル記事
2022-09European Journal of Medicinal Chemistry239p.114558-
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Design, synthesis, and structure–activity relationship of TAK-418 and its derivatives as a novel series of LSD1 inhibitors with lowered risk of hematological side effects

Design, synthesis, and structure–activity relationship of TAK-418 and its derivatives as a novel series of LSD1 inhibitors with lowered risk of hematological side effects
デジタル記事
2022-09European Journal of Medicinal Chemistry239p.114522-
全国の図書館
  • 掲載誌（ISSN）02235234

Novel flavonoid hybrids as potent antiviral agents against hepatitis A: Design, synthesis and biological evaluation

Novel flavonoid hybrids as potent antiviral agents against hepatitis A: Design, synthesis and biological evaluation
デジタル記事
2022-08European Journal of Medicinal Chemistry238p.114452-
全国の図書館
  • 掲載誌（ISSN）02235234

Novel bifluorescent Zn(II)–cryptolepine–cyclen complexes trigger apoptosis induced by nuclear and mitochondrial DNA damage in cisplatin-resistant lung tumor cells

Novel bifluorescent Zn(II)–cryptolepine–cyclen complexes trigger apoptosis induced by nuclear and mitochondrial DNA damage in cisplatin-resistant lung tumor cells
デジタル記事
2022-08European Journal of Medicinal Chemistry238p.114418-
全国の図書館
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trans, trans-2-C-Aryl-3,4-dihydroxypyrrolidines as potent and selective β-glucosidase inhibitors: Pharmacological chaperones for Gaucher disease

trans, trans-2-C-Aryl-3,4-dihydroxypyrrolidines as potent and selective β-glucosidase inhibitors: Pharmacological chaperones for Gaucher disease
デジタル記事
2022-08European Journal of Medicinal Chemistry238p.114499-
全国の図書館
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The structure-based design of peptidomimetic inhibitors against SARS-CoV-2 3C like protease as Potent anti-viral drug candidate

The structure-based design of peptidomimetic inhibitors against SARS-CoV-2 3C like protease as Potent anti-viral drug candidate
デジタル記事
2022-08European Journal of Medicinal Chemistry238p.114458-
全国の図書館
  • 掲載誌（ISSN）02235234

The azulene scaffold from a medicinal chemist's perspective: Physicochemical and in vitro parameters relevant for drug discovery

The azulene scaffold from a medicinal chemist's perspective: Physicochemical and in vitro parameters relevant for drug discovery
デジタル記事
2022-07European Journal of Medicinal Chemistry237p.114374-
全国の図書館
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Synthesis of heterocyclic ring-fused analogs of HMG499 as novel degraders of HMG-CoA reductase that lower cholesterol

Synthesis of heterocyclic ring-fused analogs of HMG499 as novel degraders of HMG-CoA reductase that lower cholesterol
デジタル記事
2022-06European Journal of Medicinal Chemistry236p.114323-
全国の図書館
  • 掲載誌（ISSN）02235234

Design, synthesis, and in vitro and in vivo characterization of new memantine analogs for Alzheimer's disease

Design, synthesis, and in vitro and in vivo characterization of new memantine analogs for Alzheimer's disease
デジタル記事
2022-06European Journal of Medicinal Chemistry236p.114354-
全国の図書館
  • 掲載誌（ISSN）02235234