Hypoglaucines A−D, Unusual Isoquinoline Dimers from the Roots of Cyclea hypoglauca
Abstract Hypoglaucines A−D (1−4), four unusual isoquinoline dimers, were isolated from the roots of Cyclea hypoglauca. Compound 1 features p-tolylmethanol and 4-(hydroxymethyl)phenol linkages that join two isoquinoline monomers into a 19-membered macrocyclic ring. Compounds 2−4 are bisbenzylisoquinoline derivatives containing a benzoyl unit. The structures of 1−4, including their absolute configurations, were determined by spectroscopic, computational, and single-crystal X-ray diffraction methods. Compound 1 potently inhibited the proliferation of NCI-H1975 cells with an IC50 of 1.43 ± 0.15 μM by inducing G0/G1 phase arrest.
Authors
- Fang-Yu Yuan
- Long Jiang (ORCID: https://orcid.org/0000-0002-3230-4522)
- Dong Huang (ORCID: https://orcid.org/0000-0002-4207-6105)
- Jia-Luo Huang (ORCID: https://orcid.org/0009-0008-5616-9661)
- G.H. Tang (ORCID: https://orcid.org/0000-0002-7881-2573)
- Sheng Yin (ORCID: https://orcid.org/0000-0002-5678-6634)
- Lei Li (ORCID: https://orcid.org/0000-0002-4485-1937)
- Lu Gan (ORCID: https://orcid.org/0000-0003-4641-9336)
- Nan An
- Zhan-Tao Zhao
- Wei-Ye Wu
Institutions
- Sun Yat-sen University (CN)
Publication Details
- Journal
- Journal of Natural Products
- Published
- 2026-10-03
- DOI
- https://doi.org/10.1021/acs.jnatprod.6c00943
- Primary Topic
- Traditional and Medicinal Uses of Annonaceae
- Type
- article
- Field-Weighted Citation Impact
- 0.00