Naturally occurring physalins from the genus Physalis: A review. (November 2021)
- Record Type:
- Journal Article
- Title:
- Naturally occurring physalins from the genus Physalis: A review. (November 2021)
- Main Title:
- Naturally occurring physalins from the genus Physalis: A review
- Authors:
- Wu, Jiangping
Zhao, Jianping
Zhang, Tao
Gu, Yucheng
Khan, Ikhlas A.
Zou, Zhongmei
Xu, Qiongming - Abstract:
- Abstract: Physalins, including physalins and neophysalins, are a class of highly oxygenated ergostane-type steroids. They are commonly known by the name of 16, 24- cyclo -13, 14- seco steroids, in which the disconnection of C-13 and C-14 produces an eight or nine-membered ring and the carbocyclization of C-16 and C-24 generates a new six-membered ring. Meanwhile, the oxidation of C-18 methyl to carboxyl group forms a 18, 20-lactone, and the oxidation of C-14 and C-17 gets a heterocyclic oxygen acrossing rings C and D. Additionly, physalins frequently form an oxygen bridge to connect C-14 to C-27. Physalins are a kind of characteristic constituents from the species of the genus Physalis (Solanaceae), which are reported with a wide array of pharmacological activities, including anticancer, anti-inflammatory, immunoregulatory, antimicrobial, trypanocidal and leishmanicidal, antinociceptive, antidiabetic and some other activities. Herein, the research progress of physalins from the genus Physalis during the decade from 1970 to 2021 on phytochemistry, pharmacology, pharmacokinetics and application in China are systematically presented and discussed for the first time. Graphical abstract: Image 1 Highlights: Physalins act as the primary chemical constituents of the genus Physalis. A total of 78 physalins with extensive pharmacological activities have been isolated from genus Physalis until now. The research progress of physalins from the genus Physalis during the decade from 1970Abstract: Physalins, including physalins and neophysalins, are a class of highly oxygenated ergostane-type steroids. They are commonly known by the name of 16, 24- cyclo -13, 14- seco steroids, in which the disconnection of C-13 and C-14 produces an eight or nine-membered ring and the carbocyclization of C-16 and C-24 generates a new six-membered ring. Meanwhile, the oxidation of C-18 methyl to carboxyl group forms a 18, 20-lactone, and the oxidation of C-14 and C-17 gets a heterocyclic oxygen acrossing rings C and D. Additionly, physalins frequently form an oxygen bridge to connect C-14 to C-27. Physalins are a kind of characteristic constituents from the species of the genus Physalis (Solanaceae), which are reported with a wide array of pharmacological activities, including anticancer, anti-inflammatory, immunoregulatory, antimicrobial, trypanocidal and leishmanicidal, antinociceptive, antidiabetic and some other activities. Herein, the research progress of physalins from the genus Physalis during the decade from 1970 to 2021 on phytochemistry, pharmacology, pharmacokinetics and application in China are systematically presented and discussed for the first time. Graphical abstract: Image 1 Highlights: Physalins act as the primary chemical constituents of the genus Physalis. A total of 78 physalins with extensive pharmacological activities have been isolated from genus Physalis until now. The research progress of physalins from the genus Physalis during the decade from 1970 to 2021 are summarized. … (more)
- Is Part Of:
- Phytochemistry. Volume 191(2021)
- Journal:
- Phytochemistry
- Issue:
- Volume 191(2021)
- Issue Display:
- Volume 191, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 191
- Issue:
- 2021
- Issue Sort Value:
- 2021-0191-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-11
- Subjects:
- Physalis -- Solanaceae -- Physalins -- Phytochemistry -- Pharmacology -- Pharmacokinetics -- Application
Botanical chemistry -- Periodicals
Biochemistry -- Periodicals
Botany -- Periodicals
Chimie végétale -- Périodiques
572.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00319422 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.phytochem.2021.112925 ↗
- Languages:
- English
- ISSNs:
- 0031-9422
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6489.800000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18648.xml