-
1
-
-
0037393246
-
-
For botanical classification see: An update of the angiosperm phylogeny group classification for the orders and families of flowering plants, APG II. Bot J Linn Soc 2003; 141: 399-436.
-
For botanical classification see: An update of the angiosperm phylogeny group classification for the orders and families of flowering plants, APG II. Bot J Linn Soc 2003; 141: 399-436.
-
-
-
-
2
-
-
0345443217
-
-
For a historical summary see:, Weinheim: Wiley-VCH;
-
For a historical summary see: Hesse M. Alkaloids, nature's curse or blessing. Weinheim: Wiley-VCH; 2002: 41-55.
-
(2002)
Alkaloids, nature's curse or blessing
, pp. 41-55
-
-
Hesse, M.1
-
4
-
-
0037355914
-
Activity of Zanthoxylum clava-herculis extracts against multi-drug resistant methicillin-resistant Staphylococcus aureus
-
Gibbons S, Leimkugel J, Oluwatuyi M, Heinrich M. Activity of Zanthoxylum clava-herculis extracts against multi-drug resistant methicillin-resistant Staphylococcus aureus. Phytother Res 2003; 17: 274-5.
-
(2003)
Phytother Res
, vol.17
, pp. 274-275
-
-
Gibbons, S.1
Leimkugel, J.2
Oluwatuyi, M.3
Heinrich, M.4
-
5
-
-
1942502195
-
Anti-staphylococcal plant natural products
-
Gibbons S. Anti-staphylococcal plant natural products. Nat Prod Rep 2004; 21: 263-77.
-
(2004)
Nat Prod Rep
, vol.21
, pp. 263-277
-
-
Gibbons, S.1
-
6
-
-
0034652383
-
Synergy in a medicinal plant: Antimicrobial action of berberine potentiated by 5′-methoxyhydnocarpin, a multidrug pump inhibitor
-
Stermitz FR, Lorenz P, Tawara JN, Zenewicz LA, Lewis K. Synergy in a medicinal plant: Antimicrobial action of berberine potentiated by 5′-methoxyhydnocarpin, a multidrug pump inhibitor. Proc Natl Acad Sci USA 2000; 97: 1433-7.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 1433-1437
-
-
Stermitz, F.R.1
Lorenz, P.2
Tawara, J.N.3
Zenewicz, L.A.4
Lewis, K.5
-
7
-
-
0033860361
-
5′-Methoxyhydnocarpin-D and pheophorbide A: Berberis species components that potentiate berberine growth inhibition of resistant Staphylococcus aureus
-
Stermitz FR, Tawara-Matsuda J, Lorenz P, Mueller P, Zenewicz L, Lewis K. 5′-Methoxyhydnocarpin-D and pheophorbide A: Berberis species components that potentiate berberine growth inhibition of resistant Staphylococcus aureus. J Nat Prod 2000; 63: 1146-9.
-
(2000)
J Nat Prod
, vol.63
, pp. 1146-1149
-
-
Stermitz, F.R.1
Tawara-Matsuda, J.2
Lorenz, P.3
Mueller, P.4
Zenewicz, L.5
Lewis, K.6
-
8
-
-
15444350123
-
Antitubercular natural products: Berberine from the roots of commercial Hydrastis canadensis powder
-
Gentry EJ, Jampani HB, Keshavarz-Shokri A, Morton MD, Vander Velde D, Telikepalli H et al. Antitubercular natural products: Berberine from the roots of commercial Hydrastis canadensis powder. J Nat Prod 1998; 61: 1187-93.
-
(1998)
J Nat Prod
, vol.61
, pp. 1187-1193
-
-
Gentry, E.J.1
Jampani, H.B.2
Keshavarz-Shokri, A.3
Morton, M.D.4
Vander Velde, D.5
Telikepalli, H.6
-
9
-
-
0344406943
-
In vitro susceptibility of Heliobacter pylori to isoquinoline alkaloids from Sanguinara canadensis and Hydrastis canadensis
-
Ahady GB, Pendland SL, Stoia A, Chadwick LR. In vitro susceptibility of Heliobacter pylori to isoquinoline alkaloids from Sanguinara canadensis and Hydrastis canadensis. Phytother Res 2003; 17: 217-21.
-
(2003)
Phytother Res
, vol.17
, pp. 217-221
-
-
Ahady, G.B.1
Pendland, S.L.2
Stoia, A.3
Chadwick, L.R.4
-
10
-
-
38149062947
-
Alkaloids of fumaraceous plants, Adlumia fungosa
-
Manske RHF. Alkaloids of fumaraceous plants, Adlumia fungosa. Can J Res 1933; 8: 210-6.
-
(1933)
Can J Res
, vol.8
, pp. 210-216
-
-
Manske, R.H.F.1
-
11
-
-
34547836094
-
The alkaloids of fumariaceous plants, Corydalis solida
-
Manske RHF. The alkaloids of fumariaceous plants, Corydalis solida. Can J Chem 1956; 34: 1-3.
-
(1956)
Can J Chem
, vol.34
, pp. 1-3
-
-
Manske, R.H.F.1
-
12
-
-
38149099435
-
-
Manske RHF, Rodrigo R, Holland HL, Hughes DW, MacLean DB, Saunders JK. Solidaline. A modified protoberberine alkaloid from Corydalis solida. Can J Chem 1978; 56: 383-6.
-
Manske RHF, Rodrigo R, Holland HL, Hughes DW, MacLean DB, Saunders JK. Solidaline. A modified protoberberine alkaloid from Corydalis solida. Can J Chem 1978; 56: 383-6.
-
-
-
-
13
-
-
0037315119
-
Chemical studies on plant leaf movement controlled by a biological clock
-
Ueda M, Sugimoto T, Sawai Y, Ohnuki T, Yamamura S. Chemical studies on plant leaf movement controlled by a biological clock. Pure Appl Chem 2003; 75: 353-8.
-
(2003)
Pure Appl Chem
, vol.75
, pp. 353-358
-
-
Ueda, M.1
Sugimoto, T.2
Sawai, Y.3
Ohnuki, T.4
Yamamura, S.5
-
14
-
-
0017822088
-
The constituent of the vines of Menispermum dauricum DC
-
Takahashi K, Matsuzawa S, Takani M. The constituent of the vines of Menispermum dauricum DC. Chem Pharm Bull 1978; 26: 1677-81.
-
(1978)
Chem Pharm Bull
, vol.26
, pp. 1677-1681
-
-
Takahashi, K.1
Matsuzawa, S.2
Takani, M.3
-
15
-
-
3543022404
-
A butenolide of the Ranunculaceae: Aquilegiolide from Aquilegia atrata
-
Guerriero A, Pietra F. A butenolide of the Ranunculaceae: aquilegiolide from Aquilegia atrata. Phytochemistry 1984; 23: 2394-6.
-
(1984)
Phytochemistry
, vol.23
, pp. 2394-2396
-
-
Guerriero, A.1
Pietra, F.2
-
16
-
-
0025265529
-
-
Yogo M, Ishiguro S, Murata H, Furukawa H. Coclauril, a nonglucosidic 2-cyclohexen-1-ylideneacetonitrile, from Cocculus lauriforius DC. Chem Pharm Bull 1990; 38: 225-6.
-
Yogo M, Ishiguro S, Murata H, Furukawa H. Coclauril, a nonglucosidic 2-cyclohexen-1-ylideneacetonitrile, from Cocculus lauriforius DC. Chem Pharm Bull 1990; 38: 225-6.
-
-
-
-
19
-
-
0000467594
-
Butenolides from Sinomenium acutum
-
Otsuka H, Ito A, Fujioka N, Kawamata KI, Kasai R, Yamasaki K et al. Butenolides from Sinomenium acutum. Phytochemistry 1993; 33: 389-92.
-
(1993)
Phytochemistry
, vol.33
, pp. 389-392
-
-
Otsuka, H.1
Ito, A.2
Fujioka, N.3
Kawamata, K.I.4
Kasai, R.5
Yamasaki, K.6
-
20
-
-
19244373523
-
Cyclohexenyl butenolides from Phyllanthus klotzschianus
-
Kuster RM, Mors WB, Wagner H. Cyclohexenyl butenolides from Phyllanthus klotzschianus. Biochem Syst Ecol 1997; 25: 675.
-
(1997)
Biochem Syst Ecol
, vol.25
, pp. 675
-
-
Kuster, R.M.1
Mors, W.B.2
Wagner, H.3
-
21
-
-
38149100201
-
-
The heats of formation of compounds 1, 88.48 kcal/mol, 2, 87.68, and 3, 78.86 were obtained with HyperChem (Release 7.03 for Windows, Hypercube, Inc, 1115 NW 4th Street, Gainesville, Florida 32 601, USA) using the PM3 forcefield. Optimized geometries were obtained using the Polak-Rebiere algorithm with the RMSG (root mean square gradient) set at 0.001 kcal/(Å mol) and used in single-point heat of formation calculations at the same RMSG. frequency analyses, no imaginary frequencies were found, confirmed that the optimized geometries of 1, 2, and 3 were minima on the potential energy surface
-
The heats of formation of compounds 1 (-88.48 kcal/mol), 2 (-87.68), and 3 (-78.86) were obtained with HyperChem (Release 7.03 for Windows, Hypercube, Inc., 1115 NW 4th Street, Gainesville, Florida 32 601, USA) using the PM3 forcefield. Optimized geometries were obtained using the Polak-Rebiere algorithm with the RMSG (root mean square gradient) set at 0.001 kcal/(Å mol) and used in single-point heat of formation calculations at the same RMSG. frequency analyses - no imaginary frequencies were found - confirmed that the optimized geometries of 1, 2, and 3 were minima on the potential energy surface.
-
-
-
-
22
-
-
0031023084
-
Synthesis and absolute configuration of phyllanthurinolactone, the leaf-closing factor of a nyctinastic plant
-
Mori K, Audran G, Nakahara Y, Bando M, Kido M. Synthesis and absolute configuration of phyllanthurinolactone, the leaf-closing factor of a nyctinastic plant. Tetrahedron Lett 1997; 38: 575-8.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 575-578
-
-
Mori, K.1
Audran, G.2
Nakahara, Y.3
Bando, M.4
Kido, M.5
-
23
-
-
0008793589
-
Synthesis of phyllanthurinolactone, the leaf-closing factor of Phyllanthus urinaria L., and its three stereoisomers
-
Audran G, Mori K. Synthesis of phyllanthurinolactone, the leaf-closing factor of Phyllanthus urinaria L., and its three stereoisomers. Eur J Org Chem; 1998: 57-62
-
(1998)
Eur J Org Chem
, pp. 57-62
-
-
Audran, G.1
Mori, K.2
-
24
-
-
0037023444
-
First synthesis of (+)-rengylone and (+)- and (-)-menisdaurilide
-
Canto M, de March P, Figueredo M, Font J, Rodriguez S, Alvarez-Larana A et al. First synthesis of (+)-rengylone and (+)- and (-)-menisdaurilide. Tetrahedron: Asymmetry 2002; 13: 455-9.
-
(2002)
Tetrahedron: Asymmetry
, vol.13
, pp. 455-459
-
-
Canto, M.1
de March, P.2
Figueredo, M.3
Font, J.4
Rodriguez, S.5
Alvarez-Larana, A.6
-
25
-
-
0037016964
-
A synthesis of cyclohexanoid butenolides isolated from Sinomenium acutum
-
Honzumi M, Ogasawara K. A synthesis of cyclohexanoid butenolides isolated from Sinomenium acutum. Tetrahedron Lett 2002; 43: 1047-9.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 1047-1049
-
-
Honzumi, M.1
Ogasawara, K.2
-
26
-
-
0037484718
-
From p-benzoquinone to cyclohexane chirons: First asymmetric synthesis of (+)-rengylone and (-)-menisdaurilide
-
Busque F, Canto M, de March P, Figueredo M, Font J, Rodriguez S. From p-benzoquinone to cyclohexane chirons: first asymmetric synthesis of (+)-rengylone and (-)-menisdaurilide. Tetrahedron: Asymmetry 2003; 14: 2021-32.
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 2021-2032
-
-
Busque, F.1
Canto, M.2
de March, P.3
Figueredo, M.4
Font, J.5
Rodriguez, S.6
-
27
-
-
3242761382
-
Enantioselective synthesis of phyllanthurinolactone, a leaf-closing substance of Phyllanthus urinara L., and its analogs toward the development of molecular probes
-
Urakawa Y, Sugimoto T, Sato H, Ueda M. Enantioselective synthesis of phyllanthurinolactone, a leaf-closing substance of Phyllanthus urinara L., and its analogs toward the development of molecular probes. Tetrahedron Lett 2004; 45: 5885-8.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 5885-5888
-
-
Urakawa, Y.1
Sugimoto, T.2
Sato, H.3
Ueda, M.4
-
29
-
-
0031985647
-
-
Engeland M van, Nieland LJ, Ramaekers FC, Schutte B, Reutelingsperger CP. Annexin V-affinity assay: a review on an apoptosis detection system based on phosphatidylserine exposure. Cytometry 1998; 31: 1-9
-
Engeland M van, Nieland LJ, Ramaekers FC, Schutte B, Reutelingsperger CP. Annexin V-affinity assay: a review on an apoptosis detection system based on phosphatidylserine exposure. Cytometry 1998; 31: 1-9
-
-
-
-
30
-
-
32844472006
-
Apoptosis-inducing effect of epolactaene derivatives on BALL-1 cells
-
Kuramochi K, Matsui R, Matsubara Y, Nakai J, Sunoki T, Arai S et al. Apoptosis-inducing effect of epolactaene derivatives on BALL-1 cells. Bioorg Med Chem 2006; 14: 2151-61.
-
(2006)
Bioorg Med Chem
, vol.14
, pp. 2151-2161
-
-
Kuramochi, K.1
Matsui, R.2
Matsubara, Y.3
Nakai, J.4
Sunoki, T.5
Arai, S.6
-
31
-
-
21244439798
-
Pancratistatin causes early activation of caspase-3 and the flipping of phosphatidyl serine followed by rapid apoptosis specifically in human lymphoma cells
-
Kekre N, Griffin C, McNulty J, Pandey S. Pancratistatin causes early activation of caspase-3 and the flipping of phosphatidyl serine followed by rapid apoptosis specifically in human lymphoma cells. Cancer Chemother Pharmacol 2005; 56: 29-38.
-
(2005)
Cancer Chemother Pharmacol
, vol.56
, pp. 29-38
-
-
Kekre, N.1
Griffin, C.2
McNulty, J.3
Pandey, S.4
-
32
-
-
21244484687
-
Pancratistatin: A natural anti-cancer compound that targets mitochondria specifically in cancer cells to induce apoptosis
-
McLachlan A, Kekre N, McNulty J, Pandey S. Pancratistatin: a natural anti-cancer compound that targets mitochondria specifically in cancer cells to induce apoptosis. Apoptosis 2005; 10: 619-30.
-
(2005)
Apoptosis
, vol.10
, pp. 619-630
-
-
McLachlan, A.1
Kekre, N.2
McNulty, J.3
Pandey, S.4
-
34
-
-
33644996863
-
Antiproliferative and apoptotic effects of butyrolactone lignans from Arctium lappa on leukemic cells
-
Matsumoto T, Hosono-Nishiyama K, Yamada H. Antiproliferative and apoptotic effects of butyrolactone lignans from Arctium lappa on leukemic cells. Planta Med 2006; 72: 276-8.
-
(2006)
Planta Med
, vol.72
, pp. 276-278
-
-
Matsumoto, T.1
Hosono-Nishiyama, K.2
Yamada, H.3
|