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新型抗疟药伊罗霉素类似物由链霉菌 RBL-0292 产生。

New antimalarial iromycin analogs produced by Streptomyces sp. RBL-0292.

机构信息

Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

Ōmura Satoshi Memorial Institute, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

出版信息

J Antibiot (Tokyo). 2024 May;77(5):272-277. doi: 10.1038/s41429-024-00707-5. Epub 2024 Mar 4.

DOI:10.1038/s41429-024-00707-5
PMID:38438501
Abstract

Two new antimalarial compounds, named prenylpyridones A (1) and B (2), were discovered from the actinomycete cultured material of Streptomyces sp. RBL-0292 isolated from the soil on Hamahiga Island in Okinawa prefecture. The structures of 1 and 2 were elucidated as new iromycin analogs having α-pyridone ring by MS and NMR analyses. Compounds 1 and 2 showed moderate in vitro antimalarial activity against chloroquine-sensitive and chloroquine-resistant Plasmodium falciparum strains, with IC values ranging from 80.7 to 106.7 µM.

摘要

从冲绳县滨比嘉岛上的土壤中分离到的链霉菌属 RBL-0292 的放线菌培养物中发现了两种新型抗疟化合物,命名为烯丙基吡啶酮 A(1)和 B(2)。通过 MS 和 NMR 分析,确定了 1 和 2 的结构为具有α-吡啶酮环的新型伊罗米辛类似物。化合物 1 和 2 对氯喹敏感和氯喹耐药的恶性疟原虫株表现出中等体外抗疟活性,IC 值范围为 80.7 至 106.7 μM。

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PLoS One. 2019 Apr 9;14(4):e0214023. doi: 10.1371/journal.pone.0214023. eCollection 2019.
3
Kozupeptins, Antimalarial Agents Produced by Paracamarosporium Species: Isolation, Structural Elucidation, Total Synthesis, and Bioactivity.
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Org Lett. 2019 Apr 5;21(7):2180-2184. doi: 10.1021/acs.orglett.9b00483. Epub 2019 Mar 12.
4
Malaria.疟疾。
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6
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7
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