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parkeol
Known as:
lanost-9(11)-en-3 beta-ol
, lanost-9(11)-en-3-ol
National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Lanosterol
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Investigations of the Specificity of Oxidosqualene Cyclization: Errors are the Rule, Not the Exception
Paul Gregory Bodager
2014
Corpus ID: 89722003
Investigations of the Specificity of Oxidosqualene Cyclization: Errors are the Rule, not the Exception By Paul G. Bodager This…
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2012
2012
Protein engineering of Saccharomyces cerevisiae oxidosqualene-lanosterol cyclase into parkeol synthase.
Yuanlian Liu
,
T. Hu
,
Cheng-Hsiang Chang
,
Wen-Shiang Shie
,
Tung-Kung Wu
Organic Letters
2012
Corpus ID: 31877476
A Saccharomyces cerevisiae oxidosqualene-lanosterol cyclase mutant, ERG7(T384Y/Q450H/V454I), produced parkeol but not lanosterol…
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2005
2005
Histidine Residue at Position 234 of Oxidosqualene‐Lanosterol Cyclase from Saccharomyces cerevisiae Simultaneously Influences Cyclization, Rearrangement, and Deprotonation Reactions
Tung-Kung Wu
,
Yuanlian Liu
,
Cheng-Hsian Chang
ChemBioChem
2005
Corpus ID: 102492
Oxidosqualene cyclases catalyze the biotransformation of acyclic (3S)-2,3-oxidosqualene (OS) to a variety of polycyclic sterols…
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2002
2002
Directed evolution experiments reveal mutations at cycloartenol synthase residue His477 that dramatically alter catalysis.
Michael J. R. Segura
,
Silvia Lodeiro
,
M. Meyer
,
Akash J. Patel
,
S. Matsuda
Organic Letters
2002
Corpus ID: 3002390
[reaction: see text] Cycloartenol synthase cyclizes and rearranges oxidosqualene to the protosteryl cation and then specifically…
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2000
2000
Steric bulk at cycloartenol synthase position 481 influences cyclization and deprotonation.
Seiichi P. T. Matsuda
,
Lisa B. Darr
,
+5 authors
Hala G. Schepmann
Organic Letters
2000
Corpus ID: 13509519
Cycloartenol synthase converts oxidosqualene to the pentacyclic sterol precursor cycloartenol. An Arabidopsis thaliana…
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1974
1974
Sterols, methylsterols, and triterpene alcohols in threeTheaceae and some other vegetable oils
T. Itoh
,
T. Tamura
,
Taro Matsumoto
Lipids
1974
Corpus ID: 3988704
The unsaponifiables from threeTheaceae (Camellia japonica L.,Camellia Sasanqua Thunb., andThea sinensis L.) oils and alfalfa…
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1972
1972
Biogenetic-type total synthesis. 24,25-Dihydrolanosterol, 24,25-dihydro- 13(17) -protosterol, isoeuphenol, (-)-isotirucallol, and parkeol.
E. E. van Tamelen
,
R. J. Anderson
Journal of the American Chemical Society
1972
Corpus ID: 43164126
1970
1970
The conversion of parkeol into its 24,25-epoxide by tissue cultures of Nicotiana tabacum.
Phillip C. Schaefer
,
François De Reinach
,
Guy Ourisson
European Journal of Biochemistry
1970
Corpus ID: 37494698
Tissue cultures of Nicotiana tabacum were incubated with [25-14C]parkeol. The resulting sterols, 4-methylsterols and 9,19-cyclo…
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1970
1970
[Synthesis of labeled tetracyclic triterpenes. I. Lanosterol, cycloartenol, parkeol and 31-norcycloartenol(25-14C) or (26,27-D). II. Lanosterol and cycloartenol (2-T)].
U. Wrzeciono
,
C. Murphy
,
+4 authors
G. Teller
Societe Chimique de France. Bulletin
1970
Corpus ID: 34917559
Highly Cited
1968
Highly Cited
1968
Studies in phytosterol biosynthesis. Mechanism of biosynthesis of cycloartenol.
H. Rees
,
L. Goad
,
T. Goodwin
Biochemical Journal
1968
Corpus ID: 24296803
1. The mechanism of cycloartenol biosynthesis in leaves of Solanum tuberosum was investigated with the use of [2-(14)C,(4R)-4-(3…
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