-
2
-
-
13844269721
-
-
S. Gafner, S.K. Lee, M. Cuendet, S. Barthelemy, L. Vergnes, S. Labidalle, R.G. Mehta, C.W. Boone, and J.M. Pezzuto Phytochemistry 65 2004 2849
-
(2004)
Phytochemistry
, vol.65
, pp. 2849
-
-
Gafner, S.1
Lee, S.K.2
Cuendet, M.3
Barthelemy, S.4
Vergnes, L.5
Labidalle, S.6
Mehta, R.G.7
Boone, C.W.8
Pezzuto, J.M.9
-
4
-
-
0032479574
-
-
A. Simon, D.P. Allais, J.L. Duroux, J.P. Basly, S. Durand-Fontanier, and C. Delage Cancer Lett. 129 1998 111
-
(1998)
Cancer Lett.
, vol.129
, pp. 111
-
-
Simon, A.1
Allais, D.P.2
Duroux, J.L.3
Basly, J.P.4
Durand-Fontanier, S.5
Delage, C.6
-
5
-
-
0031860081
-
-
G. Shoba, D. Joy, T. Joseph, M. Majeed, R. Rajendran, and P.S. Srinivas Planta Med. 64 1998 353
-
(1998)
Planta Med.
, vol.64
, pp. 353
-
-
Shoba, G.1
Joy, D.2
Joseph, T.3
Majeed, M.4
Rajendran, R.5
Srinivas, P.S.6
-
6
-
-
0030839940
-
-
Y.J. Wang, M.H. Pan, A.L. Cheng, L. Lin, Y.S. Ho, and C.Y. Hsieh J. Pharm. Biomed. Anal. 15 1997 1867
-
(1997)
J. Pharm. Biomed. Anal.
, vol.15
, pp. 1867
-
-
Wang, Y.J.1
Pan, M.H.2
Cheng, A.L.3
Lin, L.4
Ho, Y.S.5
Hsieh, C.Y.6
-
7
-
-
2942726181
-
-
B.K. Adams, E.M. Ferstl, M.C. Davis, M. Herold, S. Kurtkaya, R.F. Camalier, M.G. Hollingshead, G. Kaur, E.A. Sausville, F.R. Rickles, J.P. Snyder, D.C. Liotta, and M. Shoji Bioorg. Med. Chem. 12 2004 3871
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 3871
-
-
Adams, B.K.1
Ferstl, E.M.2
Davis, M.C.3
Herold, M.4
Kurtkaya, S.5
Camalier, R.F.6
Hollingshead, M.G.7
Kaur, G.8
Sausville, E.A.9
Rickles, F.R.10
Snyder, J.P.11
Liotta, D.C.12
Shoji, M.13
-
8
-
-
61849139127
-
-
J.R. Fuchs, B. Pandit, D. Bhasin, J.P. Etter, N. Regan, D. Abdelhamid, C. Li, J. Lin, and P.K. Li Bioorg. Med. Chem. Lett. 19 2009 2065
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2065
-
-
Fuchs, J.R.1
Pandit, B.2
Bhasin, D.3
Etter, J.P.4
Regan, N.5
Abdelhamid, D.6
Li, C.7
Lin, J.8
Li, P.K.9
-
9
-
-
39149142812
-
-
Q. Zhang, Y. Fu, H.W. Wang, T. Gong, Y. Qin, and Z.R. Zhang Chin. Chem. Lett. 19 2008 281
-
(2008)
Chin. Chem. Lett.
, vol.19
, pp. 281
-
-
Zhang, Q.1
Fu, Y.2
Wang, H.W.3
Gong, T.4
Qin, Y.5
Zhang, Z.R.6
-
12
-
-
0033020351
-
-
J.O. Hill, J. Hauptman, J.W. Anderson, K. Fujioka, P.M. O'Neil, D.K. Smith, and J.H. Zavoral Am. J. Clin. Nutr. 69 1999 1108
-
(1999)
Am. J. Clin. Nutr.
, vol.69
, pp. 1108
-
-
Hill, J.O.1
Hauptman, J.2
Anderson, J.W.3
Fujioka, K.4
O'Neil, P.M.5
Smith, D.K.6
Zavoral, J.H.7
-
13
-
-
1642603546
-
-
K. Ninomiya, H. Matsuda, H. Shimoda, N. Nishida, N. Kasajima, T. Yoshino, T. Morikawa, and M. Yoshikawa Bioorg. Med. Chem. Lett. 14 2004 1943
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 1943
-
-
Ninomiya, K.1
Matsuda, H.2
Shimoda, H.3
Nishida, N.4
Kasajima, N.5
Yoshino, T.6
Morikawa, T.7
Yoshikawa, M.8
-
14
-
-
0036303006
-
-
M. Yoshikawa, H. Shimoda, N. Nishida, M. Takada, and H. Matsuda J. Nutr. 132 2002 1819
-
(2002)
J. Nutr.
, vol.132
, pp. 1819
-
-
Yoshikawa, M.1
Shimoda, H.2
Nishida, N.3
Takada, M.4
Matsuda, H.5
-
15
-
-
20744445815
-
-
M. Nakai, Y. Fukui, S. Asami, Y. Toyoda-Ono, T. Iwashita, H. Shibata, T. Mitsunaga, F. Hashimoto, and Y. Kiso J. Agric. Food. Chem. 53 2005 4593
-
(2005)
J. Agric. Food. Chem.
, vol.53
, pp. 4593
-
-
Nakai, M.1
Fukui, Y.2
Asami, S.3
Toyoda-Ono, Y.4
Iwashita, T.5
Shibata, H.6
Mitsunaga, T.7
Hashimoto, F.8
Kiso, Y.9
-
16
-
-
0041317714
-
-
A. Marfak, P. Trouillas, D.P. Allais, C.A. Calliste, J. Cook-Moreau, and J.L. Duroux Radiat. Res. 160 2003 355
-
(2003)
Radiat. Res.
, vol.160
, pp. 355
-
-
Marfak, A.1
Trouillas, P.2
Allais, D.P.3
Calliste, C.A.4
Cook-Moreau, J.5
Duroux, J.L.6
-
17
-
-
0037077366
-
-
A. Marfak, P. Trouillas, D.P. Allais, Y. Champavier, C.A. Calliste, and J.L. Duroux J. Agric. Food. Chem. 50 2002 4827
-
(2002)
J. Agric. Food. Chem.
, vol.50
, pp. 4827
-
-
Marfak, A.1
Trouillas, P.2
Allais, D.P.3
Champavier, Y.4
Calliste, C.A.5
Duroux, J.L.6
-
19
-
-
79951720509
-
-
Irradiation was carried out at ambient temperature, using a cobalt-60 irradiator (point source AECL, IR-79, MDS Nordion International Co. Ltd, Ottawa, ON, Canada) in the Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (Jeongup, Korea). The source strength was approximately 320 kCi, with dose rate at the location of the sample of 10 kGy/h. Dosimetry was performed using 5 mm diameter alanine dosimeters (Bruker Instruments, Rheinstetten, Germany). The dosimeters were calibrated against an International Standard Set by the International Atomic Energy Agency (Vienna, Austria). Sample solution (2 g curcumin in 200 mL MeOH) in chapped vials were irradiated with 30 kGy (absorbed dose). The irradiated methanolic solution was immediately evaporated to remove the solvent and lyophilized
-
Irradiation was carried out at ambient temperature, using a cobalt-60 irradiator (point source AECL, IR-79, MDS Nordion International Co. Ltd, Ottawa, ON, Canada) in the Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute (Jeongup, Korea). The source strength was approximately 320 kCi, with dose rate at the location of the sample of 10 kGy/h. Dosimetry was performed using 5 mm diameter alanine dosimeters (Bruker Instruments, Rheinstetten, Germany). The dosimeters were calibrated against an International Standard Set by the International Atomic Energy Agency (Vienna, Austria). Sample solution (2 g curcumin in 200 mL MeOH) in chapped vials were irradiated with 30 kGy (absorbed dose). The irradiated methanolic solution was immediately evaporated to remove the solvent and lyophilized.
-
-
-
-
20
-
-
79951721836
-
-
4/MeCN (4.3:4.3:1.4, flow rate: 1.0/min, detection: 280 nm)
-
4/MeCN (4.3:4.3:1.4, flow rate: 1.0/min, detection: 280 nm).
-
-
-
-
21
-
-
12344279210
-
-
K. Peng, F. Chen, X. She, C. Yang, Y. Cui, and X. Pan Tetrahedron Lett. 46 2005 1217
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 1217
-
-
Peng, K.1
Chen, F.2
She, X.3
Yang, C.4
Cui, Y.5
Pan, X.6
-
25
-
-
79951723746
-
-
note
-
4, 222.0892).
-
-
-
-
27
-
-
79951724537
-
-
note
-
4, 222.0892).
-
-
-
-
28
-
-
33748414170
-
-
A. Delazar, F. Biglari, H. nazemiyeh, A.H. Talebpour, L. Nahar, and S.D. Sarker Phytochemistry 67 2006 2176
-
(2006)
Phytochemistry
, vol.67
, pp. 2176
-
-
Delazar, A.1
Biglari, F.2
Nazemiyeh, H.3
Talebpour, A.H.4
Nahar, L.5
Sarker, S.D.6
-
30
-
-
79951720808
-
-
note
-
4, 198.0892).
-
-
-
-
31
-
-
35448934436
-
-
2, pH 7.0). Then, 100 μL of the compounds at the test concentration or orlistat (Roche, Basel, Switzerland) was mixed with 880 μL of the enzyme-buffer, and incubated for 15 min at 37 °C, with 20 μL of the substrate solution [10 mM p-NPB (p-nitrophenylbutyrate) in dimethyl formamide] added and the enzymatic reactions allowed to proceed for 15 min at 37 °C. The pancreatic lipase activity was determined by measuring the hydrolysis of p-NPB to p-nitrophenol at 405 nm using an ELISA reader (Tecan, Infinite F200, Austria). Inhibition of the lipase activity was expressed as the percentage decrease in the OD when porcine pancreatic lipase was incubated with the test compounds.
-
(2007)
FEMS Microbiol. Lett.
, pp. 276
-
-
Kim, J.H.1
Kim, H.J.2
Park, H.W.3
Youn, S.H.4
Choi, D.Y.5
Shin, C.S.6
-
33
-
-
38849154619
-
-
G. Liang, S. Yang, L. Jiang, Y. Zhao, L. Shao, J. Xiao, F. Ye, Y. Li, and X. Li Chem. Pharm. Bull. 56 2008 162
-
(2008)
Chem. Pharm. Bull.
, vol.56
, pp. 162
-
-
Liang, G.1
Yang, S.2
Jiang, L.3
Zhao, Y.4
Shao, L.5
Xiao, J.6
Ye, F.7
Li, Y.8
Li, X.9
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