5β-Hydroxy-ecdysones and a revision of the structure of ponasterone C
Abstract
Some of the spectral properties characteristic of the 5β-hydroxy-ecdysones are described and the structure of ponasterone C has been revised to (V); ponasterone B (I) is the only ecdysone having 2α,3α-dihydroxy-groups.
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Two early reports also identified close analogues: ponasterone A, ponasterone B, ponasterone C and inokosterone.
“two reports also identified close analogues-ponasterone A (25-deoxy-20-hydroxyecdysone; ponA), which is amongst the most biologically active ecdysteroids in arthropod systems, ponasterone B (2,3-di-epi-ponA), ponasterone C (5β,24S-dihydroxyponA) [18,25,26] and inokosterone [19].”
From Ecdysteroids (2021) · cites this paper as [25]
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- Authors
- Koreeda, M., & Nakanishi, K.
- ORCID
- Nakanishi, Koji
- Venue
- J. Chem. Soc. D
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 1970
- Volume
- 0
- Issue
- 6
- Pages
- 351-352
- ISSN
- 0577-6171 (ISSN-L)
- OpenAlex
- W2140429647
- Cited by
- 24
- References
- 0
- Citations by year
- 2026: 1 · 2021: 1 · 2012: 1
- FWCI
- 1.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the Chemical Society D Chemical Communications (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Steroid Chemistry and Biochemistry
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phytochemical Studies and Bioactivities
- Physical Sciences › Materials Science › Biomaterials › Phytochemistry and Bioactive Compounds
- Keywords
- ecdysteroids, structure revision, spectral properties
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