Перейти к основному содержанию
AkademIndex

Продукты

Для разработчиков

AkademBaseОткрытый API экосистемы
← Назад к работе

Работы, цитирующие эту работу

Работ: 6

Работа: Novel deoxyvasicinone derivatives as potent multitarget-directed ligands for the treatment of Alzheimer's disease: Design, synthesis, and biological evaluation

  1. Design, combinatorial synthesis and cytotoxic activity of 2-substituted furo[2,3-d]pyrimidinone and pyrrolo[2,3-d]pyrimidinone library

    Buer Song, Lifei Nie, Khurshed Bozorov +3

    СтатьяSynthesis and Biological EvaluationMolecular Diversity2022Цитирований: 19
    ABI

  2. Design, synthesis, in vitro evaluation of a new pyrrolo[1,2‐<i>a</i>]thiazolo[5,4‐<i>d</i>]pyrimidinone derivatives as cholinesterase inhibitors against Alzheimer's disease

    Yan Zeng, Lifei Nie, Liu Liu +6

    СтатьяCholinesterase and Neurodegenerative DiseasesJournal of Heterocyclic Chemistry2022Цитирований: 17
    ABI

  3. 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

    Davron Turgunov, Lifei Nie, Azizbek Nasrullaev +7

    СтатьяCholinesterase and Neurodegenerative DiseasesMolecules2025Цитирований: 5
    ABI

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

    Yan Zeng, Lifei Nie, Liu Liu +2

    СтатьяCholinesterase and Neurodegenerative DiseasesJournal of Heterocyclic Chemistry2024Цитирований: 3
    ABI

  5. New Tricyclic Aryl Quinazoline Derivatives by Suzuki‐Miyaura Cross‐Coupling

    Burkhon Elmuradov, R. Ya. Okmanov, Bakhromjon B. Juraev +2

    СтатьяQuinazolinone synthesis and applicationsChemistryOpen2024Цитирований: 0
    ABI

  6. Scaffold-Hopping Design and Synthesis of Thieno[3,2-d]pyrimidines: Anticancer Activity, Apoptosis Induction, and In Silico Inhibition of CDKs

    Zukela Ruzi, Anvarjon Buronov, Lifei Nie +7

    СтатьяSynthesis and biological activityInternational Journal of Molecular Sciences2025Цитирований: 0
    ABI