“…Aided by single-crystal X-ray using CuK α radiation (CCDC-2121782, Figure 4), we clarified the absolute configuration of 2 as 4S,5R,8S,9S,10R,12S,16S and, accordingly, 2 was structurally elucidated unequivocally and named acrocalyene B. Through comparison of the present NMR spectra versus published data, the already-recognized compounds were elucidated respectively as agathic acid (3), [17] demethyl incisterol A 2 (4), [18] 23R-hydroxy-(20Z,24R)-ergosta-4,6,8 (14),20(22)-tetraen-3-one (5), [19] (22E,24S)-5,8-epidioxy-24-methylcholesta-6,9(11),22-trien-3-ol (6), [20] ganodermasides A (7) and B (8), [21] methyl dihydroferulate (9). [22] Cytotoxicity assessment was accomplished against such human carcinoma cells as RKO, HeLa and HCC-1806 for all the isolated compounds (Table 2).…”