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- Synthesis of obtusifoliol and analogues as CYP51 substrates. Luke R. Churchman, Lauren J. Salisbury, James J. De Voss
, Org. Biomol. Chem.
, 2022
, 20
, 7316
- In vitro incorporation of 2H at the C-10 methyl group of obtusifoliol during the enzymatic cleavage of the 9β,19β-cyclopropane ring of cycloeucalenol. Alain Rahier, Pierre Benveniste, Luigi Cattel
, J. Chem. Soc., Chem. Commun.
, 1976
, 287
- Inversion of the 4β-hydrogen during the conversion of the sterol obtusifoliol into poriferasterol by Ochromonas malhamensis. Furn F. Knapp, L. John Goad, Trevor W. Goodwin
, J. Chem. Soc., Chem. Commun.
, 1973
, 149
- Investigations on the biosynthesis of steroids and terpenoids. Part II. Role of 24-methylene derivatives in the biosynthesis of steroids and terpenoids. D. H. R. Barton, D. M. Harrison, G. P. Moss, D. A. Widdowson
, J. Chem. Soc. C
, 1970
, 775
- Variations on a (t)heme—novel mechanisms, redox partners and catalytic functions in the cytochrome P450 superfamily. Andrew W. Munro, Hazel M. Girvan, Kirsty J. McLean
, Nat. Prod. Rep.
, 2007
, 24
, 585
- The biosynthesis of triterpenoids, steroids, and carotenoids. D. M. Harrison
, Nat. Prod. Rep.
, 1988
, 5
, 387
- The biosynthesis of triterpenoids, steroids, and carotenoids. D. M. Harrison
, Nat. Prod. Rep.
, 1990
, 7
, 459
- 4α-Methyl-5α,14β-ergosta-8,24(241)-dien-3β-ol (“triticusterol”): the first naturally occurring 14β(H)-steroid. Toshihiro Akihisa, Wilhelmus C. M. C. Kokke, Kazuo Koike, Yumiko Kimura, Chiyo Mizukami, Aya Sadaie, Takenori Maruyama, Tamotsu Nikaido
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 497
- Structure-based virtual screening and ADME/T-based prediction analysis for the discovery of novel antifungal CYP51 inhibitors. Bin Sun, Hong Zhang, Min Liu, Zhuang Hou, Xinyong Liu
, Med. Chem. Commun.
, 2018
, 9
, 1178
- The biosynthesis of triterpenoids and steroids. D. M. Harrison
, Nat. Prod. Rep.
, 1985
, 2
, 525