“…86 All of the p-terphenyl compounds obtained from T. aurantiotincta and H. caeruleum possess two free hydroxyl groups at para position. In contrary, Japanese Thelephora terrestris elaborated p-terphenyl derivatives with two substitution groups at ortho position to each other, terrestrins A ¶G (96)(97)(98)(99)(100)(101)(102), together with three known related compounds ganbajunin B (103), 79 thelephantin F (81), and thelephantin H (83). 88 Further fractionation of the methanolic extract of T. terrestris has led to the isolation and characterization of two unusual new pregnanetype steroids, 2β,3α-dihydroxypregna-4,7,16-trien-12,20-dione (104) and 1α,2β,3α-trihydroxypregna-4,7,16-trien-12, 20-dione (105), which are named terresterones A and B (104, 105), as well as the previously known compound stizophyllin, 90 now assigned as 2β,3α,12β-trihydroxypregna-4,7,16-trien-20-one (106) (Fig.…”