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69 та иш

Иш: Synthesis of Novel 7-Phenyl-2,3-Dihydropyrrolo[2,1-b]Quinazolin-9(1H)-ones as Cholinesterase Inhibitors Targeting Alzheimer’s Disease Through Suzuki–Miyaura Cross-Coupling Reaction

  1. Nootropic and Anti-Alzheimer’s Actions of Medicinal Plants: Molecular Insight into Therapeutic Potential to Alleviate Alzheimer’s Neuropathology

    Md. Sahab Uddin, Abdullah Al Mamun, Md. Tanvir Kabir +4

    Шарҳ мақола20183 иқтибос
    ABI

  2. Design, synthesis, biological evaluation of a new tricyclicthiazolopy‐rimidinone derivatives as acetylcholinesterase inhibitors

    Yan Zeng, Lifei Nie, Liu Liu +2

    МақолаCholinesterase and Neurodegenerative DiseasesJournal of Heterocyclic Chemistry20243 иқтибос
    ABI

  3. [Radius of gyration is indicator of compactness of protein structure].

    M Iu Lobanov, Natalya S. Bogatyreva, Galzitskaia Ov

    Мақола20082 иқтибос
    ABI

  4. The amyloid hypothesis for Alzheimer’s disease: a critical reappraisal

    John Hardy

    Шарҳ мақола20092 иқтибос
    ABI

  5. Acetylcholinesterase inhibitors as Alzheimer therapy: From nerve toxins to neuroprotection

    Manjinder Singh, Maninder Kaur, Hitesh Kukreja +3

    Шарҳ мақола20132 иқтибос
    ABI

  6. Neuroprotective Tri- and Tetracyclic BChE Inhibitors Releasing Reversible Inhibitors upon Carbamate Transfer

    Fouad H. Darras, Beata Kling, Jörg Heilmann +1

    Мақола20122 иқтибос
    ABI

  7. Quaternary ligand binding to aromatic residues in the active-site gorge of acetylcholinesterase.

    Michal Harel, Isabelle J. Schalk, Laurence Ehret‐Sabatier +6

    Мақола19932 иқтибос
    ABI

  8. Synthesis, Biological Evaluation, and Computational Studies of Tri- and Tetracyclic Nitrogen-Bridgehead Compounds as Potent Dual-Acting AChE Inhibitors and<i>h</i>H<sub>3</sub>Receptor Antagonists

    Fouad H. Darras, Steffen Pockes, Guozheng Huang +6

    Мақола20142 иқтибос
    ABI

  9. Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology.

    Inge Grundke‐Iqbal, Khurshid Iqbal, Y C Tung +3

    Мақола19862 иқтибос
    ABI

  10. Acetylcholinesterase in Alzheimer's disease

    Vincenzo Nicola Talesa

    Шарҳ мақола20012 иқтибос
    ABI

  11. Alzheimer's disease, enzyme targets and drug discovery struggles: From natural products to drug prototypes

    Tiago Silva, Joana Reis, José Teixeira +1

    Шарҳ мақола20142 иқтибос
    ABI

  12. Discovery and Biological Evaluation of a Novel Highly Potent Selective Butyrylcholinsterase Inhibitor

    Qi Li, Shuaishuai Xing, Ying Chen +11

    Мақола20202 иқтибос
    ABI

  13. SARS-CoV-2 vaccines in development

    Florian Krammer

    Шарҳ мақола20202 иқтибос
    ABI

  14. Computer-Aided Drug Design

    Dev Bukhsh Singh

    Китоб20202 иқтибос
    ABI

  15. A retrospective-prospective review of Suzuki–Miyaura reaction: From cross-coupling reaction to pharmaceutical industry applications

    Mehran Farhang, Ali Reza Akbarzadeh, Mahboubeh Rabbani +1

    Шарҳ мақола20222 иқтибос
    ABI

  16. Synthesis and Cytotoxic Activity of a New Derivative of Rupestonic Acid

    Paruke Aibibula, Haji Akber Aisa, Khurshed Bozorov +1

    МақолаMarine Sponges and Natural ProductsChemistry of Natural Compounds20232 иқтибос
    ABI

  17. Сарлавҳасиз

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