Web18 feb 2011 · A new hirsutane sesquiterpenoid, hirsutanol E (1), together with the known compounds hirsutanol A (2) and hirsutanol F (3; gloeosteretriol) were obtained from … WebCytotoxic alkaloids from the marine shellfish-associated fungus Aspergillus sp. XBB-4 induced by an amino acid-directed strategy†. Yi Qiu a, Qi Guo a, Yan-Qin Ran b, Wen-Jian Lan c, Chi-Keung Lam a, Gong-Kan Feng d, Rong Deng d, Xiao-Feng Zhu d, Hou-Jin Li * a and Liu-Ping Chen * a a School of Chemistry, Sun Yat-sen University, Guangzhou …
Hirsutane Sesquiterpenoids from the Marine‐Derived Fungus ...
Web21 ago 2024 · Linear triquinane sesquiterpenoids represent an important class of natural products. Most of these compounds were isolated from fungi, sponges, and soft corals, and many of them displayed a wide range of biological activities. On account of their structural diversity and complexity, linear triquinane sesquiterpenoids present new challenges … WebHirsutane-Type Sesquiterpenes with Inhibitory Activity of Microglial Nitric Oxide Production from the Red Alga-Derived Fungus Chondrostereum sp. NTOU4196 maplestory 228
Cytotoxic alkaloids from the marine shellfish-associated fungus
Web25 giu 1998 · Hirsutanol A (6) and ent-gloeosteretriol (10) were found to be anti-microbial (Bacillus subtilus) active. All structures were elucidated by spectroscopic methods. Five … Web31 ago 2011 · Because both optical rotations of 1 and hirsutanol A, a major component from an unidentified fungus, 4 are negative and the 13 C NMR data of 1 are in accord … WebFigure 1. Chemical structures of compounds 1. 4, hirsutanol A, incarnal, and chondrosterins A and J. 2. Results and Discussion 2.1. Structure Elucidation Chondrosterin K (1) was isolated as a colorless oil. The HR-EI-MS data at m/z 250.1568 [M]+ (Supplementary Figure S1), along with the NMR data (Tables 1 and 2, Supplementary … maplestory 2 2021