Sürdürülebilir Kalkınma Amaçları

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  • MakaleAçık Erişim2019Scopus SJRQ2
    Paenidigyamycin A, potent antiparasitic imidazole alkaloid from the ghanaian Paenibacillus sp. De2Sh

    Osei, Enoch; Kwain, Samuel; Mawuli, Gilbert Tetevi; Anang, Abraham Kwabena; Owusu, Kofi Baffour-Awuah; Camas, Mustafa; Camas, Anil Sazak; Ohashi, Mitsuko; Alexandru-Crivac, Cristina-Nicoleta; Deng, Hai

    A new alkaloid paenidigyamycin A (1) was obtained from the novel Ghanaian Paenibacillus sp. isolated from the mangrove rhizosphere soils of the Pterocarpus santalinoides tree growing in the wetlands of the Digya National Park, Ghana. Compound 1 was isolated on HPLC at tR = 37.0 min and its structure determined by MS, 1D, and 2D-NMR data. When tested against L. major, 1 (IC50 0.75 µM) was just as effective as amphotericin B (IC50 0.31 µM). Against L. donovani, 1 (IC50 7.02 µM) was twenty-two times less active than amphotericin B (IC50 0.32 µM), reinforcing the unique effectiveness of 1 against L. major. For T. brucei brucei, 1 (IC50 0.78 µM) was ten times more active than the laboratory standard Coptis japonica (IC50 8.20 µM). The IC50 of 9.08 µM for 1 against P. falciparum 3d7 compared to artesunate (IC50 36 nM) was not strong, but this result suggests the possibility of using the paenidigyamycin scaffold for the development of potent antimalarial drugs. Against cercariae, 1 showed high anticercaricidal activity compared to artesunate. The minimal lethal concentration (MLC) and minimal effective concentration (MEC) of the compound were 25 and 6.25 µM, respectively, while artesunate was needed in higher quantities to produce such results. However, 1 (IC50 > 100 µM) was not active against T. mobilensis.

    • SDG 3 · Sağlık ve Kaliteli Yaşam
    AtıfScopus32OpenAlex32
    ScopusWeb of SciencePubMedİncele
  • MakaleAçık Erişim2014Scopus SJRQ2
    Butrepyrazinone, a New Pyrazinone with an Unusual Methylation Pattern from a Ghanaian Verrucosispora sp K51G

    Kyeremeh, Kwaku; Acquah, Kojo Sekyi; Camas, Mustafa; Tabudravu, Jioji; Houssen, Wael; Deng, Hai; Jaspars, Marcel

    AtıfOpenAlex26
    Web of SciencePubMedİncele
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AlanDeğerDil
creativeworkseries.issn1660-3397
dc.date.accessioned2026-10-28T14:56:24.908769409Z
dc.date.available2026-10-28T14:56:24.908769409Z
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/3269
dc.publisherMDPI AG
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleMarine Drugs