oxidosqualene lanosterol cyclase Latest Research Papers

Protein engineering of oxidosqualene-lanosterol cyclase into triterpene monocyclase

Organic & Biomolecular Chemistry ◽

10.1039/c3ob40493e ◽

2013 ◽

Vol 11 (25) ◽

pp. 4214 ◽

Cited By ~ 18

Author(s):

Cheng-Hsiang Chang ◽

Hao-Yu Wen ◽

Wen-Shiang Shie ◽

Ching-Ting Lu ◽

Meng-Erh Li ◽

...

Keyword(s):

Protein Engineering ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

Catalytic Mechanism and Product Specificity of Oxidosqualene-Lanosterol Cyclase: A QM/MM Study

The Journal of Physical Chemistry B ◽

10.1021/jp3091396 ◽

2012 ◽

Vol 116 (47) ◽

pp. 13857-13862 ◽

Cited By ~ 16

Author(s):

Bo-Xue Tian ◽

Leif A. Eriksson

Keyword(s):

Catalytic Mechanism ◽

Product Specificity ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

The cysteine 703 to isoleucine or histidine mutation of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae generates an iridal-type triterpenoid

Biochimie ◽

10.1016/j.biochi.2012.06.014 ◽

2012 ◽

Vol 94 (11) ◽

pp. 2376-2381 ◽

Cited By ~ 11

Author(s):

Cheng-Hsiang Chang ◽

Yi-Chi Chen ◽

Sheng-Wei Tseng ◽

Yuan-Ting Liu ◽

Hao-Yu Wen ◽

...

Keyword(s):

Saccharomyces Cerevisiae ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

Protein Engineering of Saccharomyces cerevisiae Oxidosqualene-Lanosterol Cyclase into Parkeol Synthase

Organic Letters ◽

10.1021/ol302341h ◽

2012 ◽

Vol 14 (20) ◽

pp. 5222-5225 ◽

Cited By ~ 8

Author(s):

Yuan-Ting Liu ◽

Tain-Chang Hu ◽

Cheng-Hsiang Chang ◽

Wen-Shiang Shie ◽

Tung-Kung Wu

Keyword(s):

Saccharomyces Cerevisiae ◽

Protein Engineering ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

Mutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17α/β-exocyclic side chain stereochemistry

Organic & Biomolecular Chemistry ◽

10.1039/c0ob00582g ◽

2011 ◽

Vol 9 (4) ◽

pp. 1092-1097 ◽

Cited By ~ 12

Author(s):

Tung-Kung Wu ◽

Yi-Chun Chang ◽

Yuan-Ting Liu ◽

Cheng-Hsiang Chang ◽

Hao-Yu Wen ◽

...

Keyword(s):

Saccharomyces Cerevisiae ◽

Side Chain ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

ChemInform Abstract: Synthesis of Inhibitors of 2,3-Oxidosqualene-Lanosterol Cyclase. Part 2. Cyclocondensation of γ,δ-Unsaturated β-Keto Esters with Imines.

ChemInform ◽

10.1002/chin.199320212 ◽

2010 ◽

Vol 24 (20) ◽

pp. no-no

Author(s):

D. S. DODD ◽

A. C. OEHLSCHLAGER ◽

N. H. GEORGOPAPADAKOU ◽

A.-M. POLAK ◽

P. G. HARTMAN

Keyword(s):

Keto Esters ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

ChemInform Abstract: Synthesis of (6E)-8-Thia- and (14E)-13-Thia-2,3-oxidosqualene: Inhibitors of 2,3-Oxidosqualene-Lanosterol Cyclase.

ChemInform ◽

10.1002/chin.199514211 ◽

2010 ◽

Vol 26 (14) ◽

pp. no-no

Author(s):

Y. F. ZHENG ◽

A. C. OEHLSCHLAGER ◽

P. G. HARTMAN

Keyword(s):

Oxidosqualene Lanosterol Cyclase

Download Full-text

ChemInform Abstract: Substitution of the Methyl Groups with Ethyl Groups at C-10 and C-15 of 2,3-Oxidosqualene Halts the Enzymatic Reaction of Oxidosqualene- Lanosterol Cyclase at the Monocyclic Ring Stage.

ChemInform ◽

10.1002/chin.199618177 ◽

2010 ◽

Vol 27 (18) ◽

pp. no-no

Author(s):

T. HOSHINO ◽

E. ISHIBASHI ◽

K. KANEKO

Keyword(s):

Enzymatic Reaction ◽

Methyl Groups ◽

Ring Stage ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

ChemInform Abstract: Synthesis and Inhibition Studies of Sulfur-Substituted Squalene Oxide Analogues as Mechanism-Based Inhibitors of 2,3-Oxidosqualene- Lanosterol Cyclase.

ChemInform ◽

10.1002/chin.199718222 ◽

2010 ◽

Vol 28 (18) ◽

pp. no-no

Author(s):

D. STACH ◽

Y. F. ZHENG ◽

A. L. PEREZ ◽

A. C. OEHLSCHLAGER ◽

I. ABE ◽

...

Keyword(s):

Oxidosqualene Lanosterol Cyclase ◽

Inhibition Studies

Download Full-text

ChemInform Abstract: Further Evidence that the Polycyclization Reaction by Oxidosqualene-Lanosterol Cyclase Proceeds via a Ring Expansion of the 5-Membered C-Ring Formed by Markovnikov Closure. Enzymatic Products of the Oxidosqualene Analogue Having an Et

ChemInform ◽

10.1002/chin.199848207 ◽

2010 ◽

Vol 29 (48) ◽

pp. no-no

Author(s):

T. HOSHINO ◽

Y. SAKAI

Keyword(s):

Ring Expansion ◽

Oxidosqualene Lanosterol Cyclase

Download Full-text

oxidosqualene lanosterol cyclase
Recently Published Documents

TOTAL DOCUMENTS

H-INDEX

Protein engineering of oxidosqualene-lanosterol cyclase into triterpene monocyclase

Catalytic Mechanism and Product Specificity of Oxidosqualene-Lanosterol Cyclase: A QM/MM Study

The cysteine 703 to isoleucine or histidine mutation of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae generates an iridal-type triterpenoid

Protein Engineering of Saccharomyces cerevisiae Oxidosqualene-Lanosterol Cyclase into Parkeol Synthase

Mutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17α/β-exocyclic side chain stereochemistry

ChemInform Abstract: Synthesis of Inhibitors of 2,3-Oxidosqualene-Lanosterol Cyclase. Part 2. Cyclocondensation of γ,δ-Unsaturated β-Keto Esters with Imines.

ChemInform Abstract: Synthesis of (6E)-8-Thia- and (14E)-13-Thia-2,3-oxidosqualene: Inhibitors of 2,3-Oxidosqualene-Lanosterol Cyclase.

ChemInform Abstract: Substitution of the Methyl Groups with Ethyl Groups at C-10 and C-15 of 2,3-Oxidosqualene Halts the Enzymatic Reaction of Oxidosqualene- Lanosterol Cyclase at the Monocyclic Ring Stage.

ChemInform Abstract: Synthesis and Inhibition Studies of Sulfur-Substituted Squalene Oxide Analogues as Mechanism-Based Inhibitors of 2,3-Oxidosqualene- Lanosterol Cyclase.

ChemInform Abstract: Further Evidence that the Polycyclization Reaction by Oxidosqualene-Lanosterol Cyclase Proceeds via a Ring Expansion of the 5-Membered C-Ring Formed by Markovnikov Closure. Enzymatic Products of the Oxidosqualene Analogue Having an Et

Export Citation Format

oxidosqualene lanosterol cyclaseRecently Published Documents

TOTAL DOCUMENTS

H-INDEX

Protein engineering of oxidosqualene-lanosterol cyclase into triterpene monocyclase

Catalytic Mechanism and Product Specificity of Oxidosqualene-Lanosterol Cyclase: A QM/MM Study

The cysteine 703 to isoleucine or histidine mutation of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae generates an iridal-type triterpenoid

Protein Engineering of Saccharomyces cerevisiae Oxidosqualene-Lanosterol Cyclase into Parkeol Synthase

Mutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17α/β-exocyclic side chain stereochemistry

ChemInform Abstract: Synthesis of Inhibitors of 2,3-Oxidosqualene-Lanosterol Cyclase. Part 2. Cyclocondensation of γ,δ-Unsaturated β-Keto Esters with Imines.

ChemInform Abstract: Synthesis of (6E)-8-Thia- and (14E)-13-Thia-2,3-oxidosqualene: Inhibitors of 2,3-Oxidosqualene-Lanosterol Cyclase.

ChemInform Abstract: Substitution of the Methyl Groups with Ethyl Groups at C-10 and C-15 of 2,3-Oxidosqualene Halts the Enzymatic Reaction of Oxidosqualene- Lanosterol Cyclase at the Monocyclic Ring Stage.

ChemInform Abstract: Synthesis and Inhibition Studies of Sulfur-Substituted Squalene Oxide Analogues as Mechanism-Based Inhibitors of 2,3-Oxidosqualene- Lanosterol Cyclase.

ChemInform Abstract: Further Evidence that the Polycyclization Reaction by Oxidosqualene-Lanosterol Cyclase Proceeds via a Ring Expansion of the 5-Membered C-Ring Formed by Markovnikov Closure. Enzymatic Products of the Oxidosqualene Analogue Having an Et

oxidosqualene lanosterol cyclase
Recently Published Documents