-
1
-
-
0011197025
-
A fern constituent, fernene, a triterpenoid hydrocarbon of a new type
-
Ageta H., Iwata K., and Natori S. A fern constituent, fernene, a triterpenoid hydrocarbon of a new type. Tetrahedron Lett. (1963) 1447-1450
-
(1963)
Tetrahedron Lett.
, pp. 1447-1450
-
-
Ageta, H.1
Iwata, K.2
Natori, S.3
-
2
-
-
0002637359
-
Fern constituents: dryocrassol and dryocrassyl acetate isolated from the leaves of aspidiaceous fern
-
Ageta H., Shiojima K., Arai Y., Kasama T., and Kajii K. Fern constituents: dryocrassol and dryocrassyl acetate isolated from the leaves of aspidiaceous fern. Tetrahedron Lett. (1975) 3297-3298
-
(1975)
Tetrahedron Lett.
, pp. 3297-3298
-
-
Ageta, H.1
Shiojima, K.2
Arai, Y.3
Kasama, T.4
Kajii, K.5
-
3
-
-
0009557877
-
Chemotaxonomy of ferns
-
Ageta H., Aimi N., Ebizuka Y., Fujita T., and Honda G. (Eds), Elsevier Science B.V, Amsterdam
-
Ageta H., Shiojima K., Arai Y., and Masuda K. Chemotaxonomy of ferns. In: Ageta H., Aimi N., Ebizuka Y., Fujita T., and Honda G. (Eds). Towards Natural Medicine Research in the 21st Century (1998), Elsevier Science B.V, Amsterdam 3-13
-
(1998)
Towards Natural Medicine Research in the 21st Century
, pp. 3-13
-
-
Ageta, H.1
Shiojima, K.2
Arai, Y.3
Masuda, K.4
-
4
-
-
2442615925
-
Genome mining to identify new plant triterpenoids
-
Fazio G.C., Xu R., and Matsuda S.P.T. Genome mining to identify new plant triterpenoids. J. Am. Chem. Soc. 126 (2004) 5678-5679
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 5678-5679
-
-
Fazio, G.C.1
Xu, R.2
Matsuda, S.P.T.3
-
5
-
-
0040238197
-
Conserved Tyr residues determine functions of Alicyclobacillus acidocaldarius squalene-hopene cyclase
-
Füll C., and Poralla K. Conserved Tyr residues determine functions of Alicyclobacillus acidocaldarius squalene-hopene cyclase. FEMS Microbiol. Lett. 183 (2000) 221-224
-
(2000)
FEMS Microbiol. Lett.
, vol.183
, pp. 221-224
-
-
Füll, C.1
Poralla, K.2
-
6
-
-
0034696564
-
Unnatural natural triterpenes produced by altering isoleucine into alanine at position 261 in hopene synthase and the importance of having the appropriate bulk size at this position for directing the stereochemical destiny during the polycyclization cascade
-
Hoshino T., Abe T., and Kouda M. Unnatural natural triterpenes produced by altering isoleucine into alanine at position 261 in hopene synthase and the importance of having the appropriate bulk size at this position for directing the stereochemical destiny during the polycyclization cascade. Chem. Commun. (2000) 441-442
-
(2000)
Chem. Commun.
, pp. 441-442
-
-
Hoshino, T.1
Abe, T.2
Kouda, M.3
-
7
-
-
0037148784
-
Squalene-hopene cyclase: catalytic mechanism and substrate recognition
-
Hoshino T., and Sato T. Squalene-hopene cyclase: catalytic mechanism and substrate recognition. Chem. Commun. (2002) 291-301
-
(2002)
Chem. Commun.
, pp. 291-301
-
-
Hoshino, T.1
Sato, T.2
-
8
-
-
0036549820
-
Molecular cloning and functional expression of cDNAs encoding oxidosqualene cyclases from Costus speciosus
-
Kawano N., Ichinose K., and Ebizuka Y. Molecular cloning and functional expression of cDNAs encoding oxidosqualene cyclases from Costus speciosus. Biol. Pharm. Bull. 25 (2002) 477-482
-
(2002)
Biol. Pharm. Bull.
, vol.25
, pp. 477-482
-
-
Kawano, N.1
Ichinose, K.2
Ebizuka, Y.3
-
9
-
-
0000031325
-
Fern constituents: six tetracyclic triterpenoid hydrocarbons having different carbon skeletons, isolated from Lemmaphyllum microphyllum var Obovatum
-
Masuda K., Shiojima K., and Ageta H. Fern constituents: six tetracyclic triterpenoid hydrocarbons having different carbon skeletons, isolated from Lemmaphyllum microphyllum var Obovatum. Chem. Pharm. Bull. 31 (1983) 2530-2533
-
(1983)
Chem. Pharm. Bull.
, vol.31
, pp. 2530-2533
-
-
Masuda, K.1
Shiojima, K.2
Ageta, H.3
-
10
-
-
0001624650
-
Occurrence, structure and taxonomic implications of fern constituents
-
Herz W., Grisebach H., Kirby G.W., and Tamm Ch. (Eds), Springer-Verlag, New York
-
Murakami T., and Tanaka N. Occurrence, structure and taxonomic implications of fern constituents. In: Herz W., Grisebach H., Kirby G.W., and Tamm Ch. (Eds). Progress in the Chemistry of Organic Natural Products vol. 54 (1988), Springer-Verlag, New York
-
(1988)
Progress in the Chemistry of Organic Natural Products
, vol.54
-
-
Murakami, T.1
Tanaka, N.2
-
11
-
-
0026576348
-
Cloning, expression, and sequencing of squalene-hopene cyclase, a key enzyme in triterpenoid metabolism
-
Ochs D., Kaletta C., Entian K.-D., Beck-Sickinger A., and Poralla K. Cloning, expression, and sequencing of squalene-hopene cyclase, a key enzyme in triterpenoid metabolism. J. Bacteriol. 174 (1992) 298-302
-
(1992)
J. Bacteriol.
, vol.174
, pp. 298-302
-
-
Ochs, D.1
Kaletta, C.2
Entian, K.-D.3
Beck-Sickinger, A.4
Poralla, K.5
-
12
-
-
0000730062
-
Hopanoids. 2. Biohopanoids: a novel class of bacterial lipids
-
Ourisson G., and Rohmer M. Hopanoids. 2. Biohopanoids: a novel class of bacterial lipids. Acc. Chem. Res. 25 (1992) 403-408
-
(1992)
Acc. Chem. Res.
, vol.25
, pp. 403-408
-
-
Ourisson, G.1
Rohmer, M.2
-
13
-
-
0031709419
-
Occurrence of cationic intermediates and deficient control during the enzymatic cyclization of squalene to hopanoids
-
Pale-Grosdemange C., Feil C., Rohmer M., and Poralla K. Occurrence of cationic intermediates and deficient control during the enzymatic cyclization of squalene to hopanoids. Angew. Chem., Int. Ed. 37 (1998) 2237-2240
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 2237-2240
-
-
Pale-Grosdemange, C.1
Feil, C.2
Rohmer, M.3
Poralla, K.4
-
14
-
-
1842328052
-
Squalene-hopene cyclase from Bradyrhizobium japonicum: cloning, expression, sequence analysis and comparison to other triterpenoid cyclases
-
Perzl M., Müller P., Poralla K., and Kannenberg E.L. Squalene-hopene cyclase from Bradyrhizobium japonicum: cloning, expression, sequence analysis and comparison to other triterpenoid cyclases. Microbiology 143 (1997) 1235-1242
-
(1997)
Microbiology
, vol.143
, pp. 1235-1242
-
-
Perzl, M.1
Müller, P.2
Poralla, K.3
Kannenberg, E.L.4
-
16
-
-
0028817559
-
Zymomonas mobilis squalene-hopene cyclase gene (shc): cloning, DNA sequence analysis, and expression in Escherichia coli
-
Reipen I., Poralla K., Sahm H., and Sprenger G.A. Zymomonas mobilis squalene-hopene cyclase gene (shc): cloning, DNA sequence analysis, and expression in Escherichia coli. Microbiology 141 (1995) 155-161
-
(1995)
Microbiology
, vol.141
, pp. 155-161
-
-
Reipen, I.1
Poralla, K.2
Sahm, H.3
Sprenger, G.A.4
-
17
-
-
0033252974
-
Functional analysis of the DXDDTA motif in squalene-hopene cyclase by site-directed mutagenesis experiments: initiation site of the polycyclization reaction and stabilization site of the carbocation intermediate of the initially cyclized A-ring
-
Sato T., and Hoshino T. Functional analysis of the DXDDTA motif in squalene-hopene cyclase by site-directed mutagenesis experiments: initiation site of the polycyclization reaction and stabilization site of the carbocation intermediate of the initially cyclized A-ring. Biosci. Biotechnol. Biochem. 63 (1999) 2189-2198
-
(1999)
Biosci. Biotechnol. Biochem.
, vol.63
, pp. 2189-2198
-
-
Sato, T.1
Hoshino, T.2
-
18
-
-
33846786872
-
Origin of structural diversity in natural triterpenes: direct synthesis of seco-triterpene skeletons by oxidosqualene cyclase
-
Shibuya M., Xiang T., Katsube Y., Otsuka M., Zhang H., and Ebizuka Y. Origin of structural diversity in natural triterpenes: direct synthesis of seco-triterpene skeletons by oxidosqualene cyclase. J. Am. Chem. Soc. 129 (2007) 1450-1455
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 1450-1455
-
-
Shibuya, M.1
Xiang, T.2
Katsube, Y.3
Otsuka, M.4
Zhang, H.5
Ebizuka, Y.6
-
19
-
-
38049088826
-
Squalene cyclase and oxidosqualene cyclase from a fern
-
Shinozaki J., Shibuya M., Masuda K., and Ebizuka Y. Squalene cyclase and oxidosqualene cyclase from a fern. FEBS Lett. 582 (2008) 310-318
-
(2008)
FEBS Lett.
, vol.582
, pp. 310-318
-
-
Shinozaki, J.1
Shibuya, M.2
Masuda, K.3
Ebizuka, Y.4
-
20
-
-
0009934985
-
Seasonal fluctuation of triterpenoid constituents from dried leaflets of Dryopteris crassirhizoma
-
Shiojima K., Arai Y., and Ageta H. Seasonal fluctuation of triterpenoid constituents from dried leaflets of Dryopteris crassirhizoma. Phytochemistry 29 (1990) 1079-1082
-
(1990)
Phytochemistry
, vol.29
, pp. 1079-1082
-
-
Shiojima, K.1
Arai, Y.2
Ageta, H.3
-
21
-
-
0028355599
-
Fern constituent: a new triterpenoid hydrocarbon, trisnorhopane, isolated from the leaves of Dryopteris crassirhizoma and Gleichenia japonica
-
Shiojima K., Suzuki M., Matsumura T., and Ageta H. Fern constituent: a new triterpenoid hydrocarbon, trisnorhopane, isolated from the leaves of Dryopteris crassirhizoma and Gleichenia japonica. Chem. Pharm. Bull. 42 (1994) 377-378
-
(1994)
Chem. Pharm. Bull.
, vol.42
, pp. 377-378
-
-
Shiojima, K.1
Suzuki, M.2
Matsumura, T.3
Ageta, H.4
-
22
-
-
0032579970
-
Squalene-hopene cyclase from Methylococcus capsulatus (Bath): a bacterium producing hopanoids and steroids
-
Tippelt A., Jahnke L., and Poralla K. Squalene-hopene cyclase from Methylococcus capsulatus (Bath): a bacterium producing hopanoids and steroids. Biochim. Biophys. Acta 1391 (1998) 223-232
-
(1998)
Biochim. Biophys. Acta
, vol.1391
, pp. 223-232
-
-
Tippelt, A.1
Jahnke, L.2
Poralla, K.3
-
23
-
-
0030769202
-
Structure and function of a squalene cyclase
-
Wendt K.U., Poralla K., and Schulz G.E. Structure and function of a squalene cyclase. Science 277 (1997) 1811-1815
-
(1997)
Science
, vol.277
, pp. 1811-1815
-
-
Wendt, K.U.1
Poralla, K.2
Schulz, G.E.3
-
24
-
-
33746153480
-
A new triterpene synthase from Arabidopsis thaliana produces a tricyclic triterpene with two hydroxyl groups
-
Xiang T., Shibuya M., Katsube Y., Tsutsumi T., Otsuka M., Zhang H., Masuda K., and Ebizuka Y. A new triterpene synthase from Arabidopsis thaliana produces a tricyclic triterpene with two hydroxyl groups. Org. Lett. 8 (2006) 2835-2838
-
(2006)
Org. Lett.
, vol.8
, pp. 2835-2838
-
-
Xiang, T.1
Shibuya, M.2
Katsube, Y.3
Tsutsumi, T.4
Otsuka, M.5
Zhang, H.6
Masuda, K.7
Ebizuka, Y.8
-
25
-
-
33646124608
-
An Arabidopsis oxidosqualene cyclase catalyzes iridal skeleton formation by Grob fragmentation
-
Xiong Q., Wilson W.K., and Matsuda S.P.T. An Arabidopsis oxidosqualene cyclase catalyzes iridal skeleton formation by Grob fragmentation. Angew. Chem., Int. Ed. 45 (2006) 1285-1288
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 1285-1288
-
-
Xiong, Q.1
Wilson, W.K.2
Matsuda, S.P.T.3
-
26
-
-
0032417355
-
Dammarane triterpenoids from rhizomes of Pyrrosia lingua
-
Yamashita H., Masuda K., Kobayashi T., Ageta H., and Shiojima K. Dammarane triterpenoids from rhizomes of Pyrrosia lingua. Phytochemistry 49 (1998) 2461-2466
-
(1998)
Phytochemistry
, vol.49
, pp. 2461-2466
-
-
Yamashita, H.1
Masuda, K.2
Kobayashi, T.3
Ageta, H.4
Shiojima, K.5
|