-
1
-
-
3242797370
-
Structural studies on bioactive compounds. 39. Biological consequences of the structural modification of DHFR-inhibitory 2,4-diamino-6-(4-substituted- benzylamino-3-nitrophenyl)-6-ethylpyrimidines ('benzoprims')
-
Part 39: Richardson, M. L.; Croughton, K. A.; Matthews, C. S.; Stevens, M. F. G. Structural studies on bioactive compounds. 39. Biological consequences of the structural modification of DHFR-inhibitory 2,4-diamino-6-(4-substituted- benzylamino-3-nitrophenyl)-6-ethylpyrimidines ('benzoprims'). J. Med. Chem. 2004, 47, 4105-4108.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 4105-4108
-
-
Richardson, M.L.1
Croughton, K.A.2
Matthews, C.S.3
Stevens, M.F.G.4
-
2
-
-
0034736046
-
Advances in flavanoid research since 1992
-
Harborne, J. B.; Williams, C. A. Advances in flavanoid research since 1992. Phytochemistry 2000, 55, 481-504.
-
(2000)
Phytochemistry
, vol.55
, pp. 481-504
-
-
Harborne, J.B.1
Williams, C.A.2
-
3
-
-
0033637140
-
The effects of plant flavonoids on mammalian cells: Implications for inflammation, heart disease and cancer
-
Middleton, E.; Kandaswami, C.; Theoharides, T. C. The effects of plant flavonoids on mammalian cells: implications for inflammation, heart disease and cancer. Pharmacol. Rev. 2000, 52, 673-751.
-
(2000)
Pharmacol. Rev.
, vol.52
, pp. 673-751
-
-
Middleton, E.1
Kandaswami, C.2
Theoharides, T.C.3
-
4
-
-
0034807826
-
Dietary agents in cancer prevention: Flavonoids and isoflavonoids
-
Birt, D. F.; Hendrich, S.; Wang, W. Dietary agents in cancer prevention: flavonoids and isoflavonoids. Pharmacol. Ther. 2001, 90, 157-177.
-
(2001)
Pharmacol. Ther.
, vol.90
, pp. 157-177
-
-
Birt, D.F.1
Hendrich, S.2
Wang, W.3
-
5
-
-
20944451921
-
Effects of flavonoids on cell proliferation and caspase activation in a human colonic cell line HT29: An SAR study
-
Daskiewicz, J.-P.; Depeint, F.; Vionery, L.; Bayet, C.; Comte-Sarrazin, G.; Comte, G.; Gee, J. M.; Johnson, I. T.; Ndjoko, K.; Hostettmann, K.; Barron, D. Effects of flavonoids on cell proliferation and caspase activation in a human colonic cell line HT29: An SAR study. J. Med. Chem. 2005, 48, 2790-2804.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 2790-2804
-
-
Daskiewicz, J.-P.1
Depeint, F.2
Vionery, L.3
Bayet, C.4
Comte-Sarrazin, G.5
Comte, G.6
Gee, J.M.7
Johnson, I.T.8
Ndjoko, K.9
Hostettmann, K.10
Barron, D.11
-
6
-
-
23044498269
-
Inactivation of nuclear factor κB by soy isoflavone genistein contributes to increased apoptosis induced by chemotherapeutic agents in human cancer cells
-
Li, Y. W.; Ahmed, F.; Ali, S.; Philip, P. A.; Kucuk, O.; Sarkar, F. H. Inactivation of nuclear factor κB by soy isoflavone genistein contributes to increased apoptosis induced by chemotherapeutic agents in human cancer cells. Cancer Res. 2005, 65, 6934-6942.
-
(2005)
Cancer Res.
, vol.65
, pp. 6934-6942
-
-
Li, Y.W.1
Ahmed, F.2
Ali, S.3
Philip, P.A.4
Kucuk, O.5
Sarkar, F.H.6
-
7
-
-
17144398060
-
Dietary genistein reduces metastasis in a postsurgical orthotopic breast cancer model
-
Van tyghem, S. A.; Wilson, S. M.; Postenka, C. O.; Al-Katib, W.; Tuck, A. B.; Chambers, A. F. Dietary genistein reduces metastasis in a postsurgical orthotopic breast cancer model. Cancer Res. 2005, 65, 3396-3403.
-
(2005)
Cancer Res.
, vol.65
, pp. 3396-3403
-
-
Van Tyghem, S.A.1
Wilson, S.M.2
Postenka, C.O.3
Al-Katib, W.4
Tuck, A.B.5
Chambers, A.F.6
-
8
-
-
0036569703
-
Dietary genistein negates the inhibitory effect of tamoxifen on growth of estrogen-dependent human breast cancer (MCF-7) tumors in a dose-dependent manner
-
Ju, Y. H.; Doerge, D. R.; Allred, K. F.; Allred, C. D.; Helferich, W. G. Dietary genistein negates the inhibitory effect of tamoxifen on growth of estrogen-dependent human breast cancer (MCF-7) tumors in a dose-dependent manner. Cancer Res. 2002, 62, 2474-2477.
-
(2002)
Cancer Res.
, vol.62
, pp. 2474-2477
-
-
Ju, Y.H.1
Doerge, D.R.2
Allred, K.F.3
Allred, C.D.4
Helferich, W.G.5
-
9
-
-
0033869533
-
Decreased ovarian hormones during a soya diet: Implications for breast cancer prevention
-
Lu, L. J. W.; Anderson, K. E.; Grady, J. J.; Kohen, F.; Nagamani, M. Decreased ovarian hormones during a soya diet: implications for breast cancer prevention. Cancer Res. 2000, 60, 4112-4121.
-
(2000)
Cancer Res.
, vol.60
, pp. 4112-4121
-
-
Lu, L.J.W.1
Anderson, K.E.2
Grady, J.J.3
Kohen, F.4
Nagamani, M.5
-
10
-
-
0028241286
-
Structural studies on bioactive compounds. 23. Synthesis of polyhydroxylated 2-phenylbenzothiazoles and a comparison of their cytotoxicities and pharmacological properties with genistein and quercetin
-
Stevens, M. F. G.; McCall, C. J.; Lelieveld, P.; Alexander, P.; Richter, A.; Davies, D. E. Structural studies on bioactive compounds. 23. Synthesis of polyhydroxylated 2-phenylbenzothiazoles and a comparison of their cytotoxicities and pharmacological properties with genistein and quercetin. J. Med. Chem. 1994, 37, 1689-1695.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1689-1695
-
-
Stevens, M.F.G.1
McCall, C.J.2
Lelieveld, P.3
Alexander, P.4
Richter, A.5
Davies, D.E.6
-
11
-
-
0036140930
-
The aryl hydrocarbon receptor mediates sensitivity of MCF-7 breast cancer cells to the antitumor agent 2-(4-amino-3-methylphenyl)benzothiazole
-
Loaiza-Pérez, A. L.; Trapani, V.; Hose, C.; Singh, S. S.; Trepel, J.; Stevens, M. F. G.; Bradshaw, T. D.; Sausville, E. A. The aryl hydrocarbon receptor mediates sensitivity of MCF-7 breast cancer cells to the antitumor agent 2-(4-amino-3-methylphenyl)benzothiazole. Mol. Pharmacol. 2002, 61, 13-19.
-
(2002)
Mol. Pharmacol.
, vol.61
, pp. 13-19
-
-
Loaiza-Pérez, A.L.1
Trapani, V.2
Hose, C.3
Singh, S.S.4
Trepel, J.5
Stevens, M.F.G.6
Bradshaw, T.D.7
Sausville, E.A.8
-
12
-
-
0037463319
-
DNA damage and cell cycle arrest induced by 2-(4-amino-3-methylphenyl)-5- fluorobenzothiazole (5F 203, NSC 703786) is attenuated in aryl hydrocarbon receptor deficient MCF-7 cells
-
Trapani, V.; Patel, V.; Ciolino, H. P.; Yeh, G. C.; Hose, C.; Trepel, J. B.; Stevens, M. F. G.; Sausville, E. A.; Loaiza-Pérez, A. L. DNA damage and cell cycle arrest induced by 2-(4-amino-3-methylphenyl)-5- fluorobenzothiazole (5F 203, NSC 703786) is attenuated in aryl hydrocarbon receptor deficient MCF-7 cells. Br. J. Cancer 2003, 88, 599-605.
-
(2003)
Br. J. Cancer
, vol.88
, pp. 599-605
-
-
Trapani, V.1
Patel, V.2
Ciolino, H.P.3
Yeh, G.C.4
Hose, C.5
Trepel, J.B.6
Stevens, M.F.G.7
Sausville, E.A.8
Loaiza-Pérez, A.L.9
-
13
-
-
12344263872
-
In vitro, in vivo, and in silico analyses of the antitumor activity of 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazoles
-
Leong, C. O.; Suggitt, M.; Swaine, D. J.; Bibby, M. C.; Stevens, M. F. G.; Bradshaw, T. D. In vitro, in vivo, and in silico analyses of the antitumor activity of 2-(4-amino-3-methylphenyl)-5-fluorobenzothiazoles. Mol. Cancer Ther. 2004, 3, 1565-1575.
-
(2004)
Mol. Cancer Ther.
, vol.3
, pp. 1565-1575
-
-
Leong, C.O.1
Suggitt, M.2
Swaine, D.J.3
Bibby, M.C.4
Stevens, M.F.G.5
Bradshaw, T.D.6
-
14
-
-
4544294382
-
The experimental antitumor agents Phortress and doxorubicin are equiactive against human-derived breast carcinoma xenograft models
-
Fichtner, I.; Monks, A.; Hose, C.; Stevens, M. F. G.; Bradshaw, T. D. The experimental antitumor agents Phortress and doxorubicin are equiactive against human-derived breast carcinoma xenograft models. Breast Cancer Res. Treat. 2004, 87, 97-107.
-
(2004)
Breast Cancer Res. Treat.
, vol.87
, pp. 97-107
-
-
Fichtner, I.1
Monks, A.2
Hose, C.3
Stevens, M.F.G.4
Bradshaw, T.D.5
-
15
-
-
1842484230
-
The development of the antitumour benzothiazole prodrug, Phortress, as a clinical candidate
-
Bradshaw, T. D.; Westwell, A. D. The development of the antitumour benzothiazole prodrug, Phortress, as a clinical candidate. Curr. Med. Chem. 2004, 11, 1241-1253.
-
(2004)
Curr. Med. Chem.
, vol.11
, pp. 1241-1253
-
-
Bradshaw, T.D.1
Westwell, A.D.2
-
16
-
-
30444437324
-
Antitumor benzothiazoles. 26. 2-(3,4-Dimethoxyphenyl)-5- fluorobenzothiazole (GW 610; NSC 721648), a simple fluorinated 2-arylbenzothiazole, shows potent and selective inhibitory activity against lung, colon and breast cancer cell lines
-
Mortimer, C. G.; Wells, G.; Crochard, J.-P.; Stone, E. L.; Bradshaw, T. D.; Stevens, M. F. G.; Westwell, A. D. Antitumor benzothiazoles. 26. 2-(3,4-Dimethoxyphenyl)-5-fluorobenzothiazole (GW 610; NSC 721648), a simple fluorinated 2-arylbenzothiazole, shows potent and selective inhibitory activity against lung, colon and breast cancer cell lines. J. Med. Chem. 2006, 49, 179-185.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 179-185
-
-
Mortimer, C.G.1
Wells, G.2
Crochard, J.-P.3
Stone, E.L.4
Bradshaw, T.D.5
Stevens, M.F.G.6
Westwell, A.D.7
-
17
-
-
85008284347
-
Facile synthesis of isoflavones by the cross-coupling reaction of 3-iodochromone with arylboronic acids
-
Yokoe, I.; Sugita, Y.; Shirataki, Y. Facile synthesis of isoflavones by the cross-coupling reaction of 3-iodochromone with arylboronic acids. Chem. Pharm. Bull. 1989, 37, 529-530.
-
(1989)
Chem. Pharm. Bull.
, vol.37
, pp. 529-530
-
-
Yokoe, I.1
Sugita, Y.2
Shirataki, Y.3
-
18
-
-
0035830512
-
Synthesis of homochiral 5- and 8-substituted 2-[((2-(2,6- dimethoxyphenoxy)ethyl)-amino)methyl]-1,4-benzodioxanes and electrophoretic determination of their enantiomeric excess
-
Valoti, E.; Pallavicini, M.; Villa, L.; Pezzetta, D. Synthesis of homochiral 5- and 8-substituted 2-[((2-(2,6-dimethoxyphenoxy)ethyl)-amino) methyl]-1,4-benzodioxanes and electrophoretic determination of their enantiomeric excess. J. Org. Chem. 2001, 66, 1018-1025.
-
(2001)
J. Org. Chem.
, vol.66
, pp. 1018-1025
-
-
Valoti, E.1
Pallavicini, M.2
Villa, L.3
Pezzetta, D.4
-
19
-
-
2742589324
-
Synthesis of naturally occurring pratensein and 6,8-di-C-prenylpratensein
-
Jain, A. C.; Bambah, P. K. Synthesis of naturally occurring pratensein and 6,8-di-C-prenylpratensein. Indian J. Chem. 1987, 26, 488-490.
-
(1987)
Indian J. Chem.
, vol.26
, pp. 488-490
-
-
Jain, A.C.1
Bambah, P.K.2
-
20
-
-
70449367182
-
A new efficient synthesis of 3-halogenated 4H-1-benzopyran-4-ones
-
Gammill, R. B. A new efficient synthesis of 3-halogenated 4H-1-benzopyran-4-ones. Synthesis 1979, 901-903.
-
(1979)
Synthesis
, pp. 901-903
-
-
Gammill, R.B.1
-
21
-
-
0001766644
-
Novel palladium(0)-catalysed coupling reactions of dialkoxyborane with aryl halides: Convenient synthetic route to arylboronates
-
Murata, M.; Watanabe, S.; Masuda, Y. Novel palladium(0)-catalysed coupling reactions of dialkoxyborane with aryl halides: convenient synthetic route to arylboronates. J. Org. Chem. 1997, 62, 6458-6459.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6458-6459
-
-
Murata, M.1
Watanabe, S.2
Masuda, Y.3
-
22
-
-
0033958547
-
Palladium-catalysed borylation of aryl halides or inflates with dialkoxyborane: A novel and facile synthetic route to arylboronates
-
Murata, M.; Oyama, T.; Watanabe, S.; Masuda, Y. Palladium-catalysed borylation of aryl halides or inflates with dialkoxyborane: a novel and facile synthetic route to arylboronates. J. Org. Chem. 2000, 65, 164-168.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 164-168
-
-
Murata, M.1
Oyama, T.2
Watanabe, S.3
Masuda, Y.4
-
23
-
-
0026699017
-
Palladium-catalysed reactions of organotin compounds
-
Mitchell, T. M. Palladium-catalysed reactions of organotin compounds. Synthesis 1992, 803-815.
-
(1992)
Synthesis
, pp. 803-815
-
-
Mitchell, T.M.1
-
24
-
-
0002701426
-
Preparation and palladium mediated cross-coupling reactions of cis-2,3-disubstituted 5-halodihydropyran-4-ones
-
Evans, P. A.; Nelson, J. D.; Mannanagan, T. Preparation and palladium mediated cross-coupling reactions of cis-2,3-disubstituted 5-halodihydropyran-4- ones. Synlett 1997, 968-970.
-
(1997)
Synlett
, pp. 968-970
-
-
Evans, P.A.1
Nelson, J.D.2
Mannanagan, T.3
-
25
-
-
0028906786
-
Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen
-
Boyd, M. R.; Paull, K. D. Some practical considerations and applications of the National Cancer Institute in vitro anticancer drug discovery screen. Drug Dev. Res. 1995, 34, 91-104.
-
(1995)
Drug Dev. Res.
, vol.34
, pp. 91-104
-
-
Boyd, M.R.1
Paull, K.D.2
-
26
-
-
0031035181
-
An information-intensive approach to the molecular pharmacology of cancer
-
Weinstein, J. N.; Myers, T. G.; O'Connor, P. M.; Friend, S. H.; Fornace, A. J.; Kohn, K. W.; Fojo, T.; Bates, S. E.; Rubinstein, L. V.; Anderson, N. L.; Buolamwini, J. K.; van Osdol, W. W.; Monks, A. P.; Scudiero, D. A.; Sausville, E. A.; Zaharevitz, D. W.; Bunow, B.; Viswanadhan, V. N.; Johnson, G. S.; Wittes, R. E.; Paull, K. D. An information-intensive approach to the molecular pharmacology of cancer. Science 1997, 275, 343-349.
-
(1997)
Science
, vol.275
, pp. 343-349
-
-
Weinstein, J.N.1
Myers, T.G.2
O'Connor, P.M.3
Friend, S.H.4
Fornace, A.J.5
Kohn, K.W.6
Fojo, T.7
Bates, S.E.8
Rubinstein, L.V.9
Anderson, N.L.10
Buolamwini, J.K.11
Van Osdol, W.W.12
Monks, A.P.13
Scudiero, D.A.14
Sausville, E.A.15
Zaharevitz, D.W.16
Bunow, B.17
Viswanadhan, V.N.18
Johnson, G.S.19
Wittes, R.E.20
Paull, K.D.21
more..
-
27
-
-
0034665390
-
Role of CYP1A1 in modulation of antitumor properties of the novel agent 2-(4-amino-3-methylphenyl)benzothiazole (DF 203, NSC 674495) in human breast cancer cells
-
Chua, M. S.; Kashiyama, E.; Bradshaw, T. D.; Stinson, S. F.; Brantley, E.; Sausville, E. A.; Stevens, M. F. G. Role of CYP1A1 in modulation of antitumor properties of the novel agent 2-(4-amino-3-methylphenyl)benzothiazole (DF 203, NSC 674495) in human breast cancer cells. Cancer Res. 2000, 60, 5196-5203.
-
(2000)
Cancer Res.
, vol.60
, pp. 5196-5203
-
-
Chua, M.S.1
Kashiyama, E.2
Bradshaw, T.D.3
Stinson, S.F.4
Brantley, E.5
Sausville, E.A.6
Stevens, M.F.G.7
-
28
-
-
0033533836
-
Antitumor benzothiazoles. 14. Synthesis and in vitro biological properties of fluorinated 2-(4-aminophenyl)benzothiazoles
-
Hutchinson, I.; Chua, M.-S.; Browne, H. L.; Trapani, V.; Bradshaw, T. D.; Westwell, A. D.; Stevens, M. F. G. Antitumor benzothiazoles. 14. Synthesis and in vitro biological properties of fluorinated 2-(4-aminophenyl)benzothiazoles. J. Med. Chem. 2001, 42, 4172-4184.
-
(2001)
J. Med. Chem.
, vol.42
, pp. 4172-4184
-
-
Hutchinson, I.1
Chua, M.-S.2
Browne, H.L.3
Trapani, V.4
Bradshaw, T.D.5
Westwell, A.D.6
Stevens, M.F.G.7
-
29
-
-
0033533836
-
Antitumor benzothiazoles. 8. Synthesis, metabolic formation and biological properties of the C- and N-oxidation products of antitumor 2-(4-aminophenyl)benzothiazoles
-
Kashiyama, E.; Hutchinson, I.; Chua, M.-S.; Stinson, S. F.; Phillips, L. R.; Kaur, G.; Sausville, E. A.; Bradshaw, T. D.; Westwell, A. D.; Stevens, M. F. G. Antitumor benzothiazoles. 8. Synthesis, metabolic formation and biological properties of the C- and N-oxidation products of antitumor 2-(4-aminophenyl) benzothiazoles. J. Med. Chem. 1999, 42, 4172-4184.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4172-4184
-
-
Kashiyama, E.1
Hutchinson, I.2
Chua, M.-S.3
Stinson, S.F.4
Phillips, L.R.5
Kaur, G.6
Sausville, E.A.7
Bradshaw, T.D.8
Westwell, A.D.9
Stevens, M.F.G.10
-
30
-
-
0032482377
-
Structure-activity relationships of the 7-substituents of 5,4′-diamino-6,8,3-trifluoroflavone, a potent antitumor agent
-
Akama, T.; Ishida, H.; Kimura, U.; Gomi, K.; Saito, H. Structure-activity relationships of the 7-substituents of 5,4′-diamino-6,8,3- trifluoroflavone, a potent antitumor agent. J. Med. Chem. 1998, 41, 2056-2067.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2056-2067
-
-
Akama, T.1
Ishida, H.2
Kimura, U.3
Gomi, K.4
Saito, H.5
-
31
-
-
0028226507
-
A comparative study of constituitive and induced alkoxyresorufin O-dealkylation and individual cytochrome P450 forms in cynomolgus monkey (macaca fascicularis), human, mouse, rat and hamster liver microsomes
-
Weaver, R. J.; Thompson, S.; Smith, G.; Dickins, M.; Elcombe, C. R.; Mayer, R. T.; Burke, M. D. A comparative study of constituitive and induced alkoxyresorufin O-dealkylation and individual cytochrome P450 forms in cynomolgus monkey (macaca fascicularis), human, mouse, rat and hamster liver microsomes. Biochem. Pharmacol. 1994, 47, 763-773.
-
(1994)
Biochem. Pharmacol.
, vol.47
, pp. 763-773
-
-
Weaver, R.J.1
Thompson, S.2
Smith, G.3
Dickins, M.4
Elcombe, C.R.5
Mayer, R.T.6
Burke, M.D.7
-
32
-
-
0031260094
-
Aryl hydrocarbon (Ah) nonresponsiveness in estrogen-receptor negative MDA-MB-231 cells is associated with expression of a variant Arnt protein
-
Wilson, C. L.; Thomsen, J.; Hoivik, D. J.; Wormke, M. T.; Stanker, L.; Holtzapple, C.; Safe, S. H. Aryl hydrocarbon (Ah) nonresponsiveness in estrogen-receptor negative MDA-MB-231 cells is associated with expression of a variant Arnt protein. Arch. Biochem. Biophys. 1997, 346, 65-73.
-
(1997)
Arch. Biochem. Biophys.
, vol.346
, pp. 65-73
-
-
Wilson, C.L.1
Thomsen, J.2
Hoivik, D.J.3
Wormke, M.T.4
Stanker, L.5
Holtzapple, C.6
Safe, S.H.7
-
33
-
-
7744225987
-
Lack of antagonism of 2,3,7,8-tetrachlorodibenzo-p-dioxin's (TCDDs) induction of cytochrome P4501A1 (CYP1A1) by the putative selective aryl hydrocarbon receptor modulator 6-alkyl-1,3,8-trichlorodibenzofuran (6-MCDF) in the mouse hepatoma cell line Hepa-1c1c7
-
Fretland, A. J.; Safe, S.; Hankinson, O. Lack of antagonism of 2,3,7,8-tetrachlorodibenzo-p-dioxin's (TCDDs) induction of cytochrome P4501A1 (CYP1A1) by the putative selective aryl hydrocarbon receptor modulator 6-alkyl-1,3,8-trichlorodibenzofuran (6-MCDF) in the mouse hepatoma cell line Hepa-1c1c7. Chem.-Biol. Interact. 2004, 150, 161-170.
-
(2004)
Chem.-Biol. Interact.
, vol.150
, pp. 161-170
-
-
Fretland, A.J.1
Safe, S.2
Hankinson, O.3
-
34
-
-
37049086879
-
Oxidation of flavanones using thallium(III) salts: A new route for the synthesis of flavones and isoflavones
-
Kanna, M. S.; Singh, O. M.; Gag, C. P.; Kapoor, R. P. Oxidation of flavanones using thallium(III) salts: a new route for the synthesis of flavones and isoflavones. J. Chem. Soc., Perkin Trans. 1 1992, 2565-2568.
-
(1992)
J. Chem. Soc., Perkin Trans. 1
, pp. 2565-2568
-
-
Kanna, M.S.1
Singh, O.M.2
Gag, C.P.3
Kapoor, R.P.4
-
35
-
-
76949099394
-
A novel synthesis of isoflavones by the palladium-catalysed cross-coupling reaction of 3-bromochromones with arylboronic acids or its esters
-
Hoshino, Y.; Miyaura, N.; Suzuki, A. A novel synthesis of isoflavones by the palladium-catalysed cross-coupling reaction of 3-bromochromones with arylboronic acids or its esters. Bull. Chem. Soc. Jpn. 1988, 61, 3008-3010.
-
(1988)
Bull. Chem. Soc. Jpn.
, vol.61
, pp. 3008-3010
-
-
Hoshino, Y.1
Miyaura, N.2
Suzuki, A.3
-
36
-
-
0017184389
-
Rapid and sensitive method for quantitation of microgram quantities of protein utilizing principle of protein-dye binding
-
Bradford, M. M. Rapid and sensitive method for quantitation of microgram quantities of protein utilizing principle of protein-dye binding. Anal. Biochem. 1976, 72, 248-254.
-
(1976)
Anal. Biochem.
, vol.72
, pp. 248-254
-
-
Bradford, M.M.1
|