Results 51 to 60 of about 1,077 (172)
New Lobane and Cembrane Diterpenes from Two Comorian Soft Corals
Marine Drugs, 2010 Preliminary biological investigation of a collection of Comorian soft corals resulted in the selection of two specimens, one of Sarcophyton and the other of Lobophytum, on the basis of their toxicity on larvae of the brine shrimp (Artemia salina) and ...
Maurice Aknin +4 more
doaj +1 more source
New Cembranoid Diterpenes from the Cultured Octocoral Nephthea columnaris
Molecules, 2015 Two new 15-hydroxycembranoid diterpenes, 2β-hydroxy-7β,8α-epoxynephthenol (1) and 2β-hydroxy-11α,12β-epoxynephthenol (2), were isolated from extracts of the octocoral Nephthea columnaris along with a new natural cembrane, epoxynephthenol (3) and a known ...
Ting-Hsi Hsiao +8 more
doaj +1 more source
Polyoxygenated cembrane-type diterpenes from the Hainan soft coral Lobophytum crassum as a promising source of anticancer agents with ErbB3 and ROR1 inhibitory potential. [PDF]
Acta Pharmacol SinShen SM +5 more
europepmc +3 more sources
A Great Barrier Reef <em>Sinularia</em> sp. Yields Two New Cytotoxic Diterpenes
Marine Drugs, 2012 The methanol extract of a <em>Sinularia </em>sp., collected from Bowden Reef, Queensland, Australia, yielded ten natural products. These included the new nitrogenous diterpene (4<em>R</em>*,5<em>R</em>*,9<em>S<
Cherie A. Motti +4 more
doaj +1 more source
The Plant Journal, Volume 104, Issue 3, Page 693-705, November 2020., 2020 SUMMARY Serrulatane diterpenoids are natural products found in plants from a subset of genera within the figwort family (Scrophulariaceae). Many of these compounds have been characterized as having anti‐microbial properties and share a common diterpene backbone.
Garret P. Miller +5 more
wiley +1 more source
Terpenoids from Octocorals of the Genus Pachyclavularia
Marine Drugs, 2017 In this paper, we reviewed natural compounds isolated from octocorals belonging to the genus Pachyclavularia, including 20 cembrane-, 39 briarane-, and eight briarellin-related diterpenoids, and one secosterol.
Yu-Chia Chang +3 more
doaj +1 more source
An Unexpected Transannular [4+2] Cycloaddition during the Total Synthesis of (+)‐Norcembrene 5
Angewandte Chemie International Edition, Volume 59, Issue 14, Page 5521-5525, March 27, 2020., 2020 They may look alike… During studies toward the total synthesis of the norditerpene natural product norcembrene 5, one diastereomer of a key intermediate (α‐OAc at C13) underwent clean and spontaneous Diels–Alder cycloaddition at room temperature (see scheme).
Michael Breunig, Po Yuan, Tanja Gaich
wiley +1 more source
EBC‐342: A Novel Tetrahydrofuran Moiety Containing Casbane from the Australian Rainforest
European Journal of Organic Chemistry, Volume 2020, Issue 8, Page 1042-1045, February 28, 2020., 2020 Although well known, the casbane family of natural products are not often isolated from either terrestrial or marine environments. The Australian Rainforest plant Croton insularis has provided a number of interesting casbanes, of which EBC‐342 described herein, is the first to contain a tetrahydrofuran ring.
Lidia A. Maslovskaya +9 more
wiley +1 more source
Marine Drugs, 2018 The ubiquitin-proteasome system (UPS) is a major proteolytic pathway that safeguards protein homeostasis. The main 26S proteasome consists of a 20S catalytic core proteasome and a 19S substrate recognition proteasome.
Xue-Hua Ling +4 more
doaj +1 more source
Terpenoids from the Octocorals Menella sp. (Plexauridae) and Lobophytum crassum (Alcyonacea)
Marine Drugs, 2012 A new germacrane-type sesquiterpenoid, menelloide E (1), and a new cembrane-type diterpenoid, lobocrassin F (2), were isolated from the octocorals Menella sp. and Lobophytum crassum, respectively.
Zhi-Hong Wen +8 more
doaj +1 more source