Results 11 to 20 of about 21,898 (241)

Cytotoxic Effects of Diterpenoid Alkaloids Against Human Cancer Cells

open access: yesMolecules, 2019
Diterpenoid alkaloids are isolated from plants of the genera Aconitum, Delphinium, and Garrya (Ranunculaceae) and classified according to their chemical structures as C18-, C19- or C20-diterpenoid alkaloids. The extreme toxicity of certain compounds, e.g.
Koji Wada, Hiroshi Yamashita
doaj   +2 more sources

OsJAC1 Positively Regulates Brown Planthopper Resistance in Rice Through Priming of Diterpenoid Biosynthesis and Amplification of Jasmonic Acid Signaling [PDF]

open access: yesPlants
Brown planthopper (BPH) is a devastating rice pest worldwide, and enhancing intrinsic plant resistance represents a sustainable strategy for its control. Here, we report that OsJAC1, a gene encoding a protein harboring dirigent and jacalin-related lectin
Jie Wang   +8 more
doaj   +2 more sources

Structural Revisions of Diterpenoid Alkaloids [PDF]

open access: yes, 2020
Twelve diterpenoid alkaloids aconicarmichosides A–L (1–12) reported in the journals Chinese Chemical Letters (2017, 28, 1705–1710) and Acta Pharmaceutica Sinica B (2018, 8, 409–419) have been revised as their corresponding trifluoroacetates (1a–12a ...
Feng-Peng, Wang
core   +2 more sources

Defensive Molecules Momilactones A and B: Function, Biosynthesis, Induction and Occurrence

open access: yesToxins, 2023
Labdane-related diterpenoids, momilactones A and B were isolated and identified in rice husks in 1973 and later found in rice leaves, straws, roots, root exudate, other several Poaceae species and the moss species Calohypnum plumiforme.
Hisashi Kato-Noguchi
doaj   +1 more source

Antitumor and Antibacterial Derivatives of Oridonin: A Main Composition of Dong-Ling-Cao

open access: yesMolecules, 2016
Isodon rubescens has been used as a traditional green tea for more than 1000 years and many medicinal functions of I. rubescens are also very useful, such as its well-known antitumor and antibacterial activities.
Dahong Li   +9 more
doaj   +1 more source

Chemical Constituents from the Leaves of Annona reticulata and Their Inhibitory Effects on NO Production

open access: yesMolecules, 2013
In the present study, the chemical investigation of the leaves of Annona reticulata has resulted in the identification of nine compounds, including annonaretin A, (1), a new triterpenoid.
Ngo Xuan Luong   +7 more
doaj   +1 more source

Diterpenoids and C13 Nor-Isoprenoid Identified From the Leaves and Twigs of Croton yanhuii Activating Apoptosis and Pyroptosis

open access: yesFrontiers in Chemistry, 2022
Croton yanhuii (Family Euphorbiaceae) is an annual aromatic plant endemic to Yunnan Province, China, which yields an aromatic, spicy oil used as a flavoring and fragrance.
Yue-qian Li   +13 more
doaj   +1 more source

Cespitulones A and B, Cytotoxic Diterpenoids of a New Structure Class from the Soft Coral Cespitularia taeniata

open access: yesMarine Drugs, 2014
Two novel diterpenoids, cespitulones A (1) and B (2), were isolated from extracts of the soft coral Cespitularia taeniata. Both compounds possess an unprecedented bicyclo [10.3.1] ring system with C-C bond connections between C-10 and C-20, and between C-
Yu-Chi Lin   +4 more
doaj   +1 more source

Effusanin B Inhibits Lung Cancer by Prompting Apoptosis and Inhibiting Angiogenesis

open access: yesMolecules, 2023
Cancer is one of the deadliest human diseases, causing high rates of illness and death. Lung cancer has the highest mortality rate among all malignancies worldwide.
Jiantong Hou   +6 more
doaj   +1 more source

Total Syntheses of the C19 Diterpenoid Alkaloids (–)-Talatisamine, (–)-Liljestrandisine, and (–)-Liljestrandinine by a Fragment Coupling Approach [PDF]

open access: yes, 2021
The C19 aconitine-type diterpenoid alkaloids (–)-talatisamine, (–)-liljestrandisine, and (–)-liljestrandinine have been prepared in 31, 30, and 33 steps, respectively, from phenol. The synthetic approach features a 1,2-addition/semi-pinacol rearrangement
Jeff, Kerkovius   +5 more
core   +2 more sources

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