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197 related items for PubMed ID: 26069216
21. Lord of the rings--the mechanism for oxidosqualene:lanosterol cyclase becomes crystal clear. Huff MW, Telford DE. Trends Pharmacol Sci; 2005 Jul; 26(7):335-40. PubMed ID: 15951028 [Abstract] [Full Text] [Related]
22. Squalene-hopene cyclase: final deprotonation reaction, conformational analysis for the cyclization of (3R,S)-2,3-oxidosqualene and further evidence for the requirement of an isopropylidene moiety both for initiation of the polycyclization cascade and for the formation of the 5-membered E-ring. Hoshino T, Nakano S, Kondo T, Sato T, Miyoshi A. Org Biomol Chem; 2004 May 21; 2(10):1456-70. PubMed ID: 15136801 [Abstract] [Full Text] [Related]
23. New cyclization mechanism for squalene: a ring-expansion step for the five-membered C-ring intermediate in hopene biosynthesis. Hoshino T, Kouda M, Abe T, Ohashi S. Biosci Biotechnol Biochem; 1999 Nov 21; 63(11):2038-41. PubMed ID: 10635573 [Abstract] [Full Text] [Related]
24. Ro 48-8.071, a new 2,3-oxidosqualene:lanosterol cyclase inhibitor lowering plasma cholesterol in hamsters, squirrel monkeys, and minipigs: comparison to simvastatin. Morand OH, Aebi JD, Dehmlow H, Ji YH, Gains N, Lengsfeld H, Himber J. J Lipid Res; 1997 Feb 21; 38(2):373-90. PubMed ID: 9162756 [Abstract] [Full Text] [Related]
25. A putative precursor of isomalabaricane triterpenoids from lanosterol synthase mutants. Lodeiro S, Wilson WK, Shan H, Matsuda SP. Org Lett; 2006 Feb 02; 8(3):439-42. PubMed ID: 16435854 [Abstract] [Full Text] [Related]
29. Histone deacetylase 3 down-regulates cholesterol synthesis through repression of lanosterol synthase gene expression. Villagra A, Ulloa N, Zhang X, Yuan Z, Sotomayor E, Seto E. J Biol Chem; 2007 Dec 07; 282(49):35457-70. PubMed ID: 17925399 [Abstract] [Full Text] [Related]
30. Conversion of squalene to the pentacarbocyclic hopene. Reinert DJ, Balliano G, Schulz GE. Chem Biol; 2004 Jan 07; 11(1):121-6. PubMed ID: 15113001 [Abstract] [Full Text] [Related]
31. Profound insights into squalene cyclization. Poralla K. Chem Biol; 2004 Jan 07; 11(1):12-4. PubMed ID: 15112988 [Abstract] [Full Text] [Related]
32. Importance of Saccharomyces cerevisiae oxidosqualene-lanosterol cyclase tyrosine 707 residue for chair-boat bicyclic ring formation and deprotonation reactions. Wu TK, Wang TT, Chang CH, Liu YT, Shie WS. Org Lett; 2008 Nov 06; 10(21):4959-62. PubMed ID: 18842050 [Abstract] [Full Text] [Related]
33. Rationally designed inhibitors as tools for comparing the mechanism of squalene-hopene cyclase with oxidosqualene cyclase. Viola F, Ceruti M, Cattel L, Milla P, Poralla K, Balliano G. Lipids; 2000 Mar 06; 35(3):297-303. PubMed ID: 10783007 [Abstract] [Full Text] [Related]
34. Analysis of the Catalytic Mechanism of Bifunctional Triterpene/Sesquarterpene Cyclase: Tyr167 Functions To Terminate Cyclization of Squalene at the Bicyclic Step. Tenkovskaia L, Murakami M, Okuno K, Ueda D, Sato T. Chembiochem; 2017 Oct 05; 18(19):1910-1913. PubMed ID: 28881085 [Abstract] [Full Text] [Related]
35. Nonenzymic polycyclization of analogues of oxidosqualene with a preformed C-ring. Winne JM, De Clercq PJ, Milanesio M, Pattison P, Viterbo D. Org Biomol Chem; 2008 Jun 07; 6(11):1918-25. PubMed ID: 18480904 [Abstract] [Full Text] [Related]
36. Formation of the C ring in the lanosterol biosynthesis from squalene. Hess BA. Org Lett; 2003 Jan 23; 5(2):165-7. PubMed ID: 12529131 [Abstract] [Full Text] [Related]
37. Inhibition of 2,3-oxidosqualene cyclase and sterol biosynthesis by 10- and 19-azasqualene derivatives. Viola F, Brusa P, Balliano G, Ceruti M, Boutaud O, Schuber F, Cattel L. Biochem Pharmacol; 1995 Sep 07; 50(6):787-96. PubMed ID: 7575639 [Abstract] [Full Text] [Related]
38. Compelling computational evidence for the concerted cyclization of the ABC rings of hopene from protonated squalene. Smentek L, Hess BA. J Am Chem Soc; 2010 Dec 08; 132(48):17111-7. PubMed ID: 21080653 [Abstract] [Full Text] [Related]
39. Phenylalanine 445 within oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae influences C-Ring cyclization and deprotonation reactions. Wu TK, Liu YT, Chiu FH, Chang CH. Org Lett; 2006 Oct 12; 8(21):4691-4. PubMed ID: 17020279 [Abstract] [Full Text] [Related]
40. Tryptophan 232 within oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae influences rearrangement and deprotonation but not cyclization reactions. Wu TK, Yu MT, Liu YT, Chang CH, Wang HJ, Diau EW. Org Lett; 2006 Mar 30; 8(7):1319-22. PubMed ID: 16562881 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]