-
1
-
-
34447273560
-
Antiplasmodial activity of aryltetralone lignans from Holostylis reniformis
-
Andrade-Neto V.F., da Silva T., Lopes L.M.X., do Rosário V.E., Varotti F.P., and Krettli A.U. Antiplasmodial activity of aryltetralone lignans from Holostylis reniformis. Antimicrob. Agents Chemoth. 51 (2007) 2346-2350
-
(2007)
Antimicrob. Agents Chemoth.
, vol.51
, pp. 2346-2350
-
-
Andrade-Neto, V.F.1
da Silva, T.2
Lopes, L.M.X.3
do Rosário, V.E.4
Varotti, F.P.5
Krettli, A.U.6
-
2
-
-
0141523117
-
(+)-Larreatricin hydroxylase, an enantio-specific polyphenol oxidase from the creosote bush (Larrea tridentata)
-
Cho M.-H., Moinuddin S.G.A., Helms G.L., Hishiyama S., Eichinger D., Davin L.B., and Lewis N.G. (+)-Larreatricin hydroxylase, an enantio-specific polyphenol oxidase from the creosote bush (Larrea tridentata). Proc. Natl. Acad. Sci. USA 100 (2003) 10641-10646
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 10641-10646
-
-
Cho, M.-H.1
Moinuddin, S.G.A.2
Helms, G.L.3
Hishiyama, S.4
Eichinger, D.5
Davin, L.B.6
Lewis, N.G.7
-
3
-
-
1542375402
-
Aryltetralone lignans and 7,8-secolignans from Holostylis reniformis
-
da Silva T., and Lopes L.M.X. Aryltetralone lignans and 7,8-secolignans from Holostylis reniformis. Phytochemistry 65 (2004) 751-759
-
(2004)
Phytochemistry
, vol.65
, pp. 751-759
-
-
da Silva, T.1
Lopes, L.M.X.2
-
4
-
-
33646029406
-
Aryltetralol and aryltetralone lignans from Holostylis reniformis
-
da Silva T., and Lopes L.M.X. Aryltetralol and aryltetralone lignans from Holostylis reniformis. Phytochemistry 67 (2006) 929-937
-
(2006)
Phytochemistry
, vol.67
, pp. 929-937
-
-
da Silva, T.1
Lopes, L.M.X.2
-
5
-
-
64949186923
-
-
Patent PI0404986-1, 2004. Lignanas, lignanas ariltetralônicas, extratos, processos de obtenção de lignanas, processo de obtenção de extratos, uso de lignanas, uso de extratos e composição farmacêutica para prevenir e tratar malária. Rev. Prop. Ind. 2004, p. 1774
-
da Silva, T., Krettli, A.U., Andrade-Neto, V.F., Lopes, L.M.X., Patent PI0404986-1, 2004. Lignanas, lignanas ariltetralônicas, extratos, processos de obtenção de lignanas, processo de obtenção de extratos, uso de lignanas, uso de extratos e composição farmacêutica para prevenir e tratar malária. Rev. Prop. Ind. 2004, p. 1774.
-
-
-
da Silva, T.1
Krettli, A.U.2
Andrade-Neto, V.F.3
Lopes, L.M.X.4
-
6
-
-
16844377224
-
An historical perspective on lignan biosynthesis: monolignol, allylphenol and hydroxycinnamic acid coupling and downstream metabolism
-
Davin L.B., and Lewis N.G. An historical perspective on lignan biosynthesis: monolignol, allylphenol and hydroxycinnamic acid coupling and downstream metabolism. Phytochem. Rev. 2 (2003) 257-288
-
(2003)
Phytochem. Rev.
, vol.2
, pp. 257-288
-
-
Davin, L.B.1
Lewis, N.G.2
-
7
-
-
23444445169
-
Dirigent phenoxy radical coupling: advances and challenges
-
Davin L.B., and Lewis N.G. Dirigent phenoxy radical coupling: advances and challenges. Curr. Opin. Biotechnol. 16 (2005) 398-406
-
(2005)
Curr. Opin. Biotechnol.
, vol.16
, pp. 398-406
-
-
Davin, L.B.1
Lewis, N.G.2
-
8
-
-
0031031957
-
Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center
-
Davin L.B., Wang H.-B., Crowell A.L., Bedgar D.L., Martin D.M., Sarkanen S., and Lewis N.G. Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center. Science 275 (1997) 362-366
-
(1997)
Science
, vol.275
, pp. 362-366
-
-
Davin, L.B.1
Wang, H.-B.2
Crowell, A.L.3
Bedgar, D.L.4
Martin, D.M.5
Sarkanen, S.6
Lewis, N.G.7
-
9
-
-
20444385315
-
Lignans in plant cell and organ cultures: an overview
-
Fuss E. Lignans in plant cell and organ cultures: an overview. Phytochem. Rev. 2 (2003) 307-320
-
(2003)
Phytochem. Rev.
, vol.2
, pp. 307-320
-
-
Fuss, E.1
-
11
-
-
33745601102
-
Eugenol and isoeugenol, characteristic aromatic constituents of spices, are biosynthesized via reduction of a coniferyl alcohol ester
-
Koeduka T., Fridman E., Gang D.R., Vassão D.G., Jackson B.L., Kish C.M., Orlova I., Spassova S.M., Lewis N.G., Noel J.P., Baiga T.J., Dudareva N., and Pichersky E. Eugenol and isoeugenol, characteristic aromatic constituents of spices, are biosynthesized via reduction of a coniferyl alcohol ester. Proc. Natl. Acad. Sci. USA 103 (2006) 10128-10133
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 10128-10133
-
-
Koeduka, T.1
Fridman, E.2
Gang, D.R.3
Vassão, D.G.4
Jackson, B.L.5
Kish, C.M.6
Orlova, I.7
Spassova, S.M.8
Lewis, N.G.9
Noel, J.P.10
Baiga, T.J.11
Dudareva, N.12
Pichersky, E.13
-
12
-
-
1842817423
-
O-Methylation of benzaldehyde derivatives by "lignin specific" caffeic acid 3-O-methyltransferase
-
Kota P., Guo D., Zubieta C., Noel J., and Dixon R.A. O-Methylation of benzaldehyde derivatives by "lignin specific" caffeic acid 3-O-methyltransferase. Phytochemistry 65 (2004) 837-846
-
(2004)
Phytochemistry
, vol.65
, pp. 837-846
-
-
Kota, P.1
Guo, D.2
Zubieta, C.3
Noel, J.4
Dixon, R.A.5
-
13
-
-
0034583327
-
Nomenclature of lignans and neolignans
-
Moss G.P. Nomenclature of lignans and neolignans. Pure Appl. Chem. 72 (2000) 1493-1523
-
(2000)
Pure Appl. Chem.
, vol.72
, pp. 1493-1523
-
-
Moss, G.P.1
-
14
-
-
0034680716
-
Stereoselective synthesis of 8,9-licarinediols
-
Nascimento I.R., Lopes L.M.X., Davin L.B., and Lewis N.G. Stereoselective synthesis of 8,9-licarinediols. Tetrahedron 56 (2000) 9181-9193
-
(2000)
Tetrahedron
, vol.56
, pp. 9181-9193
-
-
Nascimento, I.R.1
Lopes, L.M.X.2
Davin, L.B.3
Lewis, N.G.4
-
15
-
-
0028227564
-
(+)-Pinoresinol synthase: a stereoselective oxidase catalyzing 8,8′-lignan formation in Forsythia intermedia
-
Paré P.W., Wang H.-B., Davin L.B., and Lewis N.G. (+)-Pinoresinol synthase: a stereoselective oxidase catalyzing 8,8′-lignan formation in Forsythia intermedia. Tetrahedron Lett. 27 (1994) 4731-4734
-
(1994)
Tetrahedron Lett.
, vol.27
, pp. 4731-4734
-
-
Paré, P.W.1
Wang, H.-B.2
Davin, L.B.3
Lewis, N.G.4
-
16
-
-
0000191645
-
Further studies on the biosynthesis of pseudoisoeugenols in tissue cultures of Pimpinella anisum
-
Reichling J., and Martin R. Further studies on the biosynthesis of pseudoisoeugenols in tissue cultures of Pimpinella anisum. Z. Naturforsch. 45c (1990) 942-948
-
(1990)
Z. Naturforsch.
, vol.45 c
, pp. 942-948
-
-
Reichling, J.1
Martin, R.2
-
17
-
-
29844454699
-
Reactivity of 4-vinylphenol radical cations in solution: implications for the biosynthesis of lignans
-
Rodríguez-Evora Y., and Schepp N.P. Reactivity of 4-vinylphenol radical cations in solution: implications for the biosynthesis of lignans. Org. Biomol. Chem. 3 (2005) 4444-4449
-
(2005)
Org. Biomol. Chem.
, vol.3
, pp. 4444-4449
-
-
Rodríguez-Evora, Y.1
Schepp, N.P.2
-
18
-
-
0347926550
-
Biosynthesis of podophyllotoxin in Linum album cell cultures
-
Seidel V., Windhövel J., Eaton G., Alfermann A.W., Arroo R.R.J., Medarde M., Petersen M., and Woolley J.G. Biosynthesis of podophyllotoxin in Linum album cell cultures. Planta 215 (2002) 1031-1039
-
(2002)
Planta
, vol.215
, pp. 1031-1039
-
-
Seidel, V.1
Windhövel, J.2
Eaton, G.3
Alfermann, A.W.4
Arroo, R.R.J.5
Medarde, M.6
Petersen, M.7
Woolley, J.G.8
-
19
-
-
16844385289
-
Diversity in lignan biosynthesis
-
Umezawa T. Diversity in lignan biosynthesis. Phytochem. Rev. 2 (2003) 371-390
-
(2003)
Phytochem. Rev.
, vol.2
, pp. 371-390
-
-
Umezawa, T.1
-
20
-
-
33745912517
-
Chavicol formation in sweet basil (Ocimum basilicum): cleavage of an esterified C9 hydroxyl group with NAD(P)H-dependent reduction
-
Vassão D.G., Gang D.R., Koeduka T., Jackson B., Pichersky E., Davin L.B., and Lewis N.G. Chavicol formation in sweet basil (Ocimum basilicum): cleavage of an esterified C9 hydroxyl group with NAD(P)H-dependent reduction. Org. Biomol. Chem. 4 (2006) 2733-2744
-
(2006)
Org. Biomol. Chem.
, vol.4
, pp. 2733-2744
-
-
Vassão, D.G.1
Gang, D.R.2
Koeduka, T.3
Jackson, B.4
Pichersky, E.5
Davin, L.B.6
Lewis, N.G.7
-
21
-
-
34548009392
-
A pinoresinol-lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/isoeugenol
-
Vassão D.G., Kim S.-J., Milhollan J.K., Eichinger D., Davin L.B., and Lewis N.G. A pinoresinol-lariciresinol reductase homologue from the creosote bush (Larrea tridentata) catalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/isoeugenol. Arch. Biochem. Biophys. 465 (2007) 209-218
-
(2007)
Arch. Biochem. Biophys.
, vol.465
, pp. 209-218
-
-
Vassão, D.G.1
Kim, S.-J.2
Milhollan, J.K.3
Eichinger, D.4
Davin, L.B.5
Lewis, N.G.6
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