1. Chemical constituents and their cytotoxicities from mushroom Tricholoma imbricatum
- Author
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Xing Wu, Ji-Kai Liu, Hui-Xiang Yang, Tao Feng, Zheng-Hui Li, Fa-Lei Zhang, Jia-Yi Li, Juan He, and Shi-Qin Wang
- Subjects
0106 biological sciences ,Stereochemistry ,medicine.medical_treatment ,Plant Science ,Horticulture ,01 natural sciences ,Biochemistry ,Steroid ,Tricholomataceae ,Terpene ,chemistry.chemical_compound ,Ascomycota ,medicine ,Humans ,Cytotoxicity ,Molecular Biology ,Ergosterol ,Mushroom ,biology ,Molecular Structure ,010405 organic chemistry ,Tricholoma ,General Medicine ,biology.organism_classification ,Triterpenes ,0104 chemical sciences ,chemistry ,Rhodophyta ,Steroids ,Tricholoma imbricatum ,Derivative (chemistry) ,010606 plant biology & botany - Abstract
Two undescribed triterpenes, tricholimbrins A and B, three undescribed steroids, tricholimbrins C‒E, one undescribed 4-chromanone derivative, along with 27 known compounds were isolated from fruiting bodies of the mushroom Tricholoma imbricatum. Tricholimbrins A and B are two polycyclic triterpenoids with a carbon degradation, while tricholimbrin C is a ring-rearranged steroid containing an aromatic moiety that might be derived from an ergosterol. Isocyathisterol, 3β,15α-dihydroxyl-(22E,24R)-ergosta-5,8(14),22-trien-7-one, demethylincisterol A3, and volemolide showed cytotoxicities to six human cancer cell lines. 3β-Hydroxyl-(22E,24R)-ergosta-5,8,22-trien-7,15-dione and 3β-hydroxyl-(22E,24R)-ergosta-5,8,22-trien-7-one showed preferable cytotoxicities against HL-60 while chaxine C and volemolide showed preferable cytotoxicities against A-549, with IC50 values less than 10 μM.
- Published
- 2020