WebProtein target information for Camelliol C synthase (thale cress). Find diseases associated with this biological target and compounds tested against it in bioassay experiments. This … WebCAMELLIOL C SYNTHASE 1, CAMS1 Description Encodes a cyclase that generates predominantly a monocyclic triterpene alcohol. The product is 97% camelliol, 2% achilleol A and 0.2% beta-amyrin. Achilleol is an isomer of camelliol C with a 4-methylenecyclohexanol ring system. Other Gene Models AT1G78955.2 (splice variant) AT1G78955.3 (splice …
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WebCamelliol C is a triterpenoid that is 4,6,6-trimethylcyclohex-3-en-1-ol which is substituted at position 5 by a (3E,7E,11E)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraen-1-yl … WebNov 22, 2024 · Subsequently, (S)-2,3-epoxysqualene is converted to beta-amyrin and camelliol C in the presence of multifunctional (S)-2,3-epoxysqualene cyclase via beta …
WebJan 1, 2024 · For OSC1, OSC3, and OSC4, they are monofunctional enzymes responsible for biosynthesis of oleanane triterpenoids, sterol scaffold, and lupane triterpenoids, respectively. For OSC2, it is a multifunctional cyclase that generates precursors for ursane- and oleanane-type triterpenoids ( Srivastava et al., 2024 ). WebCAMS1 camelliol C synthase 1 [ (thale cress)] Gene ID: 844235, updated on 8-Nov-2024 Summary Encodes a cyclase that generates predominantly a monocyclic triterpene …
http://www.thegoodscentscompany.com/data/rw1833721.html WebNov 7, 2007 · CAMS1 is the first characterized cyclase that generates predominantly a monocyclic triterpene alcohol. Phylogenetic analysis shows that CAMS1 evolved from …
WebDec 1, 2024 · LsOSC2 encodes a multifunctional triterpene synthase that produces two triterpenes (baurenol and ψ- taraxasterol). LsOSC3, LsOSC4, and LsOSC5 encode a monofunctional β-amyrin synthase, taraxerol synthase, and lupeol synthase, respectively.
Webcamelliol C synthase-like. Gene provides a unified query environment for genes defined by sequence and/or in NCBI's Map Viewer. LOC104813625 camelliol C synthase-like [] Gene ID: 104813625, updated on 5-Sep-2024. Summary. Other designations. camelliol C synthase-like ... lampada design mangiarottiWebPredicted LC-MS/MS Spectrum - Camelliol C 40V, Positive-QTOF: splash10-0a5c-8911000000-096305b26ed959fea878: 2024-09-24: Wishart Lab: View Spectrum: NMR Spectra. Spectrum Type Description Deposition Date Source View; Predicted 1D NMR: 13 C NMR Spectrum (1D, 100 MHz, H 2 O, predicted) 2024-08-20: jesse aragonWebMay 3, 2007 · Arabidopsis Camelliol C Synthase Evolved from Enzymes That Make Pentacycles. Organic Letters 2007, 9 (25) , 5223-5226. DOI: 10.1021/ol702399g. Silvia Lodeiro,, Quanbo Xiong,, William K. Wilson,, Mariya D. Kolesnikova,, Carl S. Onak, and, Seiichi P. T. Matsuda. lampada design bambiniWebNov 1, 2000 · This yield is a result of an equilibrium between the ligase and a thioesterase also present in the crude enzyme preparation. The activity of caffeic acid 3-O-methyl … jesse and trini lopezWebCamelliol C synthase(EC5.4.99.38, CAMS1, LUP3 (gene)) is an enzymewith systematic name(3S)-2,3-epoxy-2,3-dihydrosqualene mutase (cyclizing, camelliol-C-forming).[1] This enzyme catalysesthe following chemical reaction (3S)-2,3-epoxy-2,3-dihydrosqualene ⇌{\displaystyle \rightleftharpoons }camelliol C The product is mainly camelliol. References jesse aracajuWebCamelliols A−C, Three Novel Incompletely Cyclized Triterpene Alcohols from Sasanqua Oil (Camellia sasanqua) Toshihiro Akihisa , Koichi Arai , Yumiko Kimura , Kazuo Koike , Wilhelmus C. M. C. Kokke , Tsuyoshi Shibata , and Tamotsu Nikaido View Author Information Cite this: J. Nat. Prod. 1999, 62, 2, 265–268 Publication Date: December 16, … jesse aranaWebNov 1, 2009 · This synthase makes one major product but produces over 20 minor products as byproducts through aborted cyclization, overcyclization, Grob fragmentation, … lampada design da tavolo