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OpenAlex topic

Synthesis and bioactivity of alkaloids

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 559 works 7 author topics

Works

559 works

  1. Cytotoxicity, antiviral and antimicrobial activities of alkaloids, flavonoids, and phenolic acids 2011
    OpenAlex top 10% OpenAlex 98.7%

    OBJECTIVE: Some natural products consisting of the alkaloids yohimbine and vincamine (indole-type), scopolamine and atropine (tropane-type), colchicine (tropolone-type), allantoin (imidazolidine-type), trigonelline (pyridine-type) as well as octopamine, synephrine, and capsaicin (exocyclic amine-type); the flavonoid d…

  2. Cytotoxicity antiviral and antimicrobial activities of alkaloids flavonoids and phenolic acids 2011
    YÖKSİS SJR Q2 JCR Q3 OpenAlex top 10% OpenAlex 98.7%

    OBJECTIVE: Some natural products consisting of the alkaloids yohimbine and vincamine (indole-type), scopolamine and atropine (tropane-type), colchicine (tropolone-type), allantoin (imidazolidine-type), trigonelline (pyridine-type) as well as octopamine, synephrine, and capsaicin (exocyclic amine-type); the flavonoid d…

  3. Cytotoxicity, antiviral and antimicrobial activities of alkaloids, flavonoids, and phenolic acids 2011
    YÖKSİS OpenAlex top 10% OpenAlex 98.7%

    OBJECTIVE: Some natural products consisting of the alkaloids yohimbine and vincamine (indole-type), scopolamine and atropine (tropane-type), colchicine (tropolone-type), allantoin (imidazolidine-type), trigonelline (pyridine-type) as well as octopamine, synephrine, and capsaicin (exocyclic amine-type); the flavonoid d…

  4. Luotonin A A Naturally Occurring Human DNA Topoisomerase I Poison 2003
    YÖKSİS SJR Q1 JCR Q1 OpenAlex top 10% OpenAlex 92.9%

    Luotonin A is a pyrroloquinazolinoquinoline alkaloid isolated from the Chinese herbal medicinal plant Peganum nigellastrum. Although previously shown to exhibit cytotoxicity against the murine leukemia P-388 cell line, the mechanism of action of luotonin A is unknown. Presently, we demonstrate that luotonin A stabiliz…

  5. HPLC method for the analysis of harmol, harmalol, harmine and harmaline in the seeds of Peganum harmala L. 2003
    OpenAlex 74.8%

    No abstract yet.

  6. HPLC Method for the Analysis of Harmol Harmalol Harmine and Harmaline in the Seeds of Peganum harmala L 2003
    YÖKSİS SJR Q1 JCR Q2 OpenAlex top 10% OpenAlex 90.9%

    No abstract yet.

  7. Some benzoxazoles and benzimidazoles as DNA topoisomerase I and II inhibitors 2008
    YÖKSİS SJR Q2 JCR Q3 OpenAlex 81.7%

    Some novel fused heterocyclic compounds of 2, 5-disubstituted-benzoxazole and benzimidazole derivatives, which were previously synthesized by our group, were investigated for their inhibitory activity on both eukaryotic DNA topoisomerase I and II in a cell free system. 2-Phenoxymethylbenzimidazole (17), 5-amino-2-(p-f…

  8. Some benzoxazoles and benzimidazoles as DNA topoisomerase I and II inhibitors 2008
    YÖKSİS SJR Q2 JCR Q3 OpenAlex 81.7%

    Some novel fused heterocyclic compounds of 2, 5-disubstituted-benzoxazole and benzimidazole derivatives, which were previously synthesized by our group, were investigated for their inhibitory activity on both eukaryotic DNA topoisomerase I and II in a cell free system. 2-Phenoxymethylbenzimidazole (17), 5-amino-2-(p-f…

  9. Some benzoxazoles and benzimidazoles as DNA topoisomerase I and II inhibitors 2008
    YÖKSİS SJR Q2 JCR Q3 OpenAlex 81.8%

    Some novel fused heterocyclic compounds of 2, 5-disubstituted-benzoxazole and benzimidazole derivatives, which were previously synthesized by our group, were investigated for their inhibitory activity on both eukaryotic DNA topoisomerase I and II in a cell free system. 2-Phenoxymethylbenzimidazole (17), 5-amino-2-(p-f…

  10. Some benzoxazoles and benzimidazoles as DNA topoisomerase I and II inhibitors 2008
    YÖKSİS SJR Q2 JCR Q3 OpenAlex 81.8%

    Some novel fused heterocyclic compounds of 2, 5-disubstituted-benzoxazole and benzimidazole derivatives, which were previously synthesized by our group, were investigated for their inhibitory activity on both eukaryotic DNA topoisomerase I and II in a cell free system. 2-Phenoxymethylbenzimidazole (17), 5-amino-2-(p-f…

  11. Some Fused Heterocyclic Compounds as Eukaryotic Topoisomerase II Inhibitors 2004
    YÖKSİS SJR Q1 JCR Q2 OpenAlex 83.1%

    No abstract yet.

  12. Some fused heterocyclic compounds as eukaryotic topoisomerase II inhibitors 2004
    YÖKSİS OpenAlex 83.1%

    No abstract yet.

Academicians

7 academicians