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  1. Article ; Online: Novel benzo chromene derivatives: design, synthesis, molecular docking, cell cycle arrest, and apoptosis induction in human acute myeloid leukemia HL-60 cells.

    Abd El-Hameed, Rania H / Mohamed, Mosaad S / Awad, Samir M / Hassan, Bardes B / Khodair, Marwa Abd El-Fattah / Mansour, Yara E

    Journal of enzyme inhibition and medicinal chemistry

    2022  Volume 38, Issue 1, Page(s) 405–422

    Abstract: A series of benzo[ ...

    Abstract A series of benzo[
    MeSH term(s) Humans ; HL-60 Cells ; Benzopyrans/pharmacology ; Molecular Docking Simulation ; Caspase 8 ; Caspase 3 ; Cell Cycle Checkpoints ; Leukemia, Myeloid, Acute ; Proto-Oncogene Proteins c-bcl-2 ; Apoptosis
    Chemical Substances Benzopyrans ; Caspase 8 (EC 3.4.22.-) ; Caspase 3 (EC 3.4.22.-) ; Proto-Oncogene Proteins c-bcl-2
    Language English
    Publishing date 2022-09-30
    Publishing country England
    Document type Journal Article
    ZDB-ID 2082578-X
    ISSN 1475-6374 ; 1475-6366
    ISSN (online) 1475-6374
    ISSN 1475-6366
    DOI 10.1080/14756366.2022.2151592
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Synthesis and Evaluation of Cytotoxic Activity of Certain Benzo[h]chromene Derivatives.

    Awad, Samir M / Mohamed, Mosaad S / Khodair, Marwa Abd El-Fattah / El-Hameed, Rania H Abd

    Anti-cancer agents in medicinal chemistry

    2020  Volume 21, Issue 8, Page(s) 963–986

    Abstract: Background: Benzo[h]chromenes attracted great attention because of their widespread biological activities, including anti-proliferate activity, and the discovery of novel effective anti-cancer agents is imperative.: Objective: The main objective was ... ...

    Abstract Background: Benzo[h]chromenes attracted great attention because of their widespread biological activities, including anti-proliferate activity, and the discovery of novel effective anti-cancer agents is imperative.
    Objective: The main objective was to synthesize new benzo[h]chromene derivatives and some reported derivatives, and then test all of them for their anti-cancer activities.
    Methods: The structures of the newly synthesized derivatives were confirmed by elemental and spectral analysis (IR, Mass,
    Results: Compounds 1a, 1c and 2b have the highest activities among all 35 tested compounds especially compound 1c.
    Conclusion: compound 1c has promising anti-cancer activities compared to the used standards and may need further modification and investigations.
    MeSH term(s) Antineoplastic Agents/chemical synthesis ; Antineoplastic Agents/pharmacology ; Benzopyrans/chemical synthesis ; Benzopyrans/pharmacology ; Cell Proliferation/drug effects ; Cell Survival/drug effects ; Colchicine/analogs & derivatives ; Colchicine/pharmacology ; Colchicine/standards ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; ErbB Receptors/antagonists & inhibitors ; Humans ; Molecular Docking Simulation ; Molecular Structure ; Protein Kinase Inhibitors/chemical synthesis ; Protein Kinase Inhibitors/pharmacology ; Sorafenib/pharmacology ; Sorafenib/standards ; Structure-Activity Relationship ; Tubulin Modulators/chemical synthesis ; Tubulin Modulators/pharmacology
    Chemical Substances Antineoplastic Agents ; Benzopyrans ; Protein Kinase Inhibitors ; Tubulin Modulators ; colchicone ; Sorafenib (9ZOQ3TZI87) ; ErbB Receptors (EC 2.7.10.1) ; Colchicine (SML2Y3J35T)
    Language English
    Publishing date 2020-09-27
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2217610-X
    ISSN 1875-5992 ; 1871-5206
    ISSN (online) 1875-5992
    ISSN 1871-5206
    DOI 10.2174/1871520620666200925103742
    Database MEDical Literature Analysis and Retrieval System OnLINE

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