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Zheng, S; Ma, Z; Ye, J; Wang, G; Wang, R; Zhou, H; Zeng, S; Jiang, H (1 January 2014). "Determination of three triterpene alcohols in rat plasma after oral administration of pollen of
Brassica campestris based on the utilization of fetal bovine serum as surrogate matrix".
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Hartmann, MA; Perret, AM; Carde, JP; Cassagne, C; Moreau, P (8 August 2002). "Inhibition of the sterol pathway in leek seedlings impairs phosphatidylserine and glucosylceramide synthesis but triggers an accumulation of triacylglycerols".
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InChI=1S/C29H48O/c1-19(2)8-7-9-20(3)22-12-14-27(6)25-11-10-23-21(4)24(30)13-15-28(23)18-29(25,28)17-16-26(22,27)5/h8,20-25,30H,7,9-18H2,1-6H3/t20-,21+,22-,23+,24+,25+,26-,27+,28?,29?/m1/s1
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332:"Structural requirements for substrate recognition of Mycobacterium tuberculosis 14 alpha-demethylase: implications for sterol biosynthesis"
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Bayer, M; Proksch, P; Felsner, I; Brenden, H; Kohne, Z; Walli, R; Duong, TN; Götz, C; Krutmann, J; Grether-Beck, S (November 2011).
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373:"Photoprotection against UVAR: effective triterpenoids require a lipid raft stabilizing chemical structure"
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Journal of
Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
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zoology and botany are different in numbering of steroids side chain, 24 to 28, 24 to 29
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Bellamine, A; Mangla, AT; Dennis, AL; Nes, WD; Waterman, MR (January 2001).
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Biochimica et
Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
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Except where otherwise noted, data are given for materials in their
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249:. In the pathway, it is transformed from demethylation of
253:, then 9,19-cyclopropyl-ring opening reaction occurs to
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236:4α,14α-dimethyl-9β,19-cyclo-5α-cholest-24-en-3β-ol
38:4α,14α-dimethyl-9β,19-cyclo-5α-cholest-24-en-3β-ol
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457:"Rosa chinensis plant sterol biosynthesis II"
154:C12CC34(CC(4(CCC35C2(C5)CC1O)C)(C)CCC=C(C)C)C
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133:Key: XZEUYTKSAYNYPK-YETBRXCGSA-N
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390:10.1111/j.1600-0625.2011.01350.x
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212:(at 25 °C , 100 kPa).
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50:3D model (
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