-
1
-
-
0012473279
-
The nuclear receptor superfamily: The second decade
-
Mangelsdorf, D. J.; Thummel, C.; Beato, M.; Herrlich, P.; Schutz, G.; Umesono, K.; Blumberg, B.; Kastner, P.; Mark, M.; Chambon, P.; Evans, R. M. The nuclear receptor superfamily: The second decade. Cell 1995, 83, 835-839.
-
(1995)
Cell
, vol.83
, pp. 835-839
-
-
Mangelsdorf, D.J.1
Thummel, C.2
Beato, M.3
Herrlich, P.4
Schutz, G.5
Umesono, K.6
Blumberg, B.7
Kastner, P.8
Mark, M.9
Chambon, P.10
Evans, R.M.11
-
2
-
-
0035798402
-
Fungal metabolities, PF 1092 compounds and their derivatives, are nonsteroidal and selective progesterone receptor modulators
-
Tabata, Y.; Iizuka, Y.; Kashiwa, J.; Masuda, N. T.; Shinei, R.; Kurihara, K.; Okonogi, T.; Hoshiko, S.; Kurata, Y. Fungal metabolities, PF 1092 compounds and their derivatives, are nonsteroidal and selective progesterone receptor modulators. Eur. J. Pharmacol. 2001, 430, 159-165.
-
(2001)
Eur. J. Pharmacol.
, vol.430
, pp. 159-165
-
-
Tabata, Y.1
Iizuka, Y.2
Kashiwa, J.3
Masuda, N.T.4
Shinei, R.5
Kurihara, K.6
Okonogi, T.7
Hoshiko, S.8
Kurata, Y.9
-
3
-
-
0034484857
-
Nonsteriodal progesterone receptor ligands with unprecedented receptor ligands with unprecedented receptor selectivity
-
Palmer, S.; Campen, C. A.; Allan, G. F.; Rybczynski, P.; Haynes-Johnson, D.; Hutchins, A.; Kraft, P.; Kiddoe, M.; Lai, M.-T.; Lombardi, E.; Pedersen, P.; Hodgen, G.; Combs, D. W. Nonsteriodal progesterone receptor ligands with unprecedented receptor ligands with unprecedented receptor selectivity. J. Steriod Biochem. Mol. Biol. 2001, 75, 33-42.
-
(2001)
J. Steriod Biochem. Mol. Biol.
, vol.75
, pp. 33-42
-
-
Palmer, S.1
Campen, C.A.2
Allan, G.F.3
Rybczynski, P.4
Haynes-Johnson, D.5
Hutchins, A.6
Kraft, P.7
Kiddoe, M.8
Lai, M.-T.9
Lombardi, E.10
Pedersen, P.11
Hodgen, G.12
Combs, D.W.13
-
4
-
-
0032491268
-
Nonsteroidal progesterone receptor antagonists based on a conformationally restricted subseries of 6-aryl-1,2-dihydro-2,2,4- trimethylquinolines
-
Hamann, L. G.; Winn, D. T.; Pooley, C. L.F.; Tegley, C. M.; West, S. J.; Farmer, L. J.; Zhi, L.; Edwards, J. P.; Marschke, K. B.; Mais, D. E.; Goldman, M. E.; Jones, T. K. Nonsteroidal progesterone receptor antagonists based on a conformationally restricted subseries of 6-aryl-1,2-dihydro-2,2,4- trimethylquinolines. Bioorg. Med. Chem. Lett. 1998, 8, 2731-2736.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2731-2736
-
-
Hamann, L.G.1
Winn, D.T.2
Pooley, C.L.F.3
Tegley, C.M.4
West, S.J.5
Farmer, L.J.6
Zhi, L.7
Edwards, J.P.8
Marschke, K.B.9
Mais, D.E.10
Goldman, M.E.11
Jones, T.K.12
-
5
-
-
0034611152
-
Nonsteroidal progesterone receptor antagonists based on 6-thiophenylhydroquinolines
-
Zhi, L.; Tegley, C. M.; Pio, B.; West, S. J.; MarSchke, K. B.; Mais, D. E.; Jones, T. K. Nonsteroidal progesterone receptor antagonists based on 6-thiophenylhydroquinolines. Bioorg. Med. Chem. Lett. 2000, 10, 415-418.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 415-418
-
-
Zhi, L.1
Tegley, C.M.2
Pio, B.3
West, S.J.4
Marschke, K.B.5
Mais, D.E.6
Jones, T.K.7
-
6
-
-
0029916422
-
Synthesis and biological activity of novel nonsteroidal progesterone receptors antagonists based on cyclocymopol monomethyl ether
-
Hamann, L. G.; Farmer, L. J.; Johson, M. G.; Bender, S. L.; Mais, D. E.; Wang, M.-W.; Crombie, D.; Goldman, M. E.; Jones, T. K. Synthesis and biological activity of novel nonsteroidal progesterone receptors antagonists based on cyclocymopol monomethyl ether. J. Med. Chem. 1996, 39, 1778-1789.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 1778-1789
-
-
Hamann, L.G.1
Farmer, L.J.2
Johson, M.G.3
Bender, S.L.4
Mais, D.E.5
Wang, M.-W.6
Crombie, D.7
Goldman, M.E.8
Jones, T.K.9
-
7
-
-
0032572837
-
Discovery and preliminary SAR studies of a novel, nonsteroidal progesterone receptor antagonist pharmacophore
-
Pooley, C. L. F.; Edwards, J. P.; Goldman, M. E.; Wang, M.-W.; Marschke, K. B.; Crombie, D. L.; Jones, T. K. Discovery and preliminary SAR studies of a novel, nonsteroidal progesterone receptor antagonist pharmacophore. J. Med. Chem. 1996, 41, 3461-3466.
-
(1996)
J. Med. Chem.
, vol.41
, pp. 3461-3466
-
-
Pooley, C.L.F.1
Edwards, J.P.2
Goldman, M.E.3
Wang, M.-W.4
Marschke, K.B.5
Crombie, D.L.6
Jones, T.K.7
-
8
-
-
0035935207
-
Synthesis and progesterone receptor antagonist activities of 6-aryl benzimidazolones and benzothiazolones
-
Zhang, P.; Terefenko, E. A.; Wrobel, J.; Zhang, Z.; Zhu, Y.; Cohen, J.; Marschke, K. B.; Mais, D. Synthesis and progesterone receptor antagonist activities of 6-aryl benzimidazolones and benzothiazolones. Bioorg. Med. Chem. Lett. 2001, 11, 2747-2750.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2747-2750
-
-
Zhang, P.1
Terefenko, E.A.2
Wrobel, J.3
Zhang, Z.4
Zhu, Y.5
Cohen, J.6
Marschke, K.B.7
Mais, D.8
-
9
-
-
0037060909
-
Potent nonsteroidal progesterone receptor agonists: Synthesis and SAR study of 6-aryl benzoxazines
-
Zhang, P.; Terefenko, E. A.; Fensome, A.; Zhang, Z.; Zhu, Y.; Cohen, J.; Winneker, R.; Wrobel, J.; Yardley, J. Potent nonsteroidal progesterone receptor agonists: Synthesis and SAR study of 6-aryl benzoxazines. Bioorg. Med. Chem. Lett. 2002, 12, 787-790.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 787-790
-
-
Zhang, P.1
Terefenko, E.A.2
Fensome, A.3
Zhang, Z.4
Zhu, Y.5
Cohen, J.6
Winneker, R.7
Wrobel, J.8
Yardley, J.9
-
10
-
-
0037179638
-
6-Aryl-1,4-dihydro-benzo[d][1,3]oxazin-2-ones: A novel class of potent, selective, and orally active nonstereodal pogesterone receptor antagonists
-
Zhang, P.; Terefenko, E. A.; Fensome, A.; Wrobel, J.; Winneker, R.; Lundeen, S.; Marschke, K. B.; Zhang, Z. 6-Aryl-1,4-dihydro-benzo[d][1,3]oxazin- 2-ones: A novel class of potent, selective, and orally active nonstereodal pogesterone receptor antagonists. J. Med. Chem. 2002, 45, 4379-4382.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4379-4382
-
-
Zhang, P.1
Terefenko, E.A.2
Fensome, A.3
Wrobel, J.4
Winneker, R.5
Lundeen, S.6
Marschke, K.B.7
Zhang, Z.8
-
11
-
-
0034727865
-
Synthesis and biological activity of a novel, highly potent progesterone receptor antagonist
-
Fuhrmann, U.; Hess-Stump, H.; Cleve, A.; Neef, G.; Schwede, W.; Hoffmann, J.; FritzeMeir, K.-H.; Chwalisz, K. Synthesis and biological activity of a novel, highly potent progesterone receptor antagonist. J. Med. Chem. 2000, 43, 5010-5016.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 5010-5016
-
-
Fuhrmann, U.1
Hess-Stump, H.2
Cleve, A.3
Neef, G.4
Schwede, W.5
Hoffmann, J.6
Fritzemeir, K.-H.7
Chwalisz, K.8
-
12
-
-
0029073473
-
Pharmacological properties of a new selective antiprogestagen: Org 33628
-
Kloosterboer, H. J.; Deckers, G. H.; de Gooyer, M. E.; Dijkema, R.; Orlemans, E. O. M.; Schoonen, W. G. E. J. Pharmacological properties of a new selective antiprogestagen: Org 33628. Ann. N. Y. Acad. Sci. 1995, 761, 192-201.
-
(1995)
Ann. N. Y. Acad. Sci.
, vol.761
, pp. 192-201
-
-
Kloosterboer, H.J.1
Deckers, G.H.2
De Gooyer, M.E.3
Dijkema, R.4
Orlemans, E.O.M.5
Schoonen, W.G.E.J.6
-
13
-
-
0033645769
-
Preclinical experience with two selective progesterone receptor modulators on breast and endometrium
-
Kloosterboer, H. J.; Deckers, G. H.; Schoonen, W. G. E. J.; Hanssen, R. G. J. M.; Rose, U. M.; Verbost, P. M.; Hsiu, J. G.; Williams, R. F.; Hodgen, G. D. Preclinical experience with two selective progesterone receptor modulators on breast and endometrium. Steriods 2000, 65, 733-740.
-
(2000)
Steriods
, vol.65
, pp. 733-740
-
-
Kloosterboer, H.J.1
Deckers, G.H.2
Schoonen, W.G.E.J.3
Hanssen, R.G.J.M.4
Rose, U.M.5
Verbost, P.M.6
Hsiu, J.G.7
Williams, R.F.8
Hodgen, G.D.9
-
14
-
-
0038627551
-
Enhanced stereoselectivity in internucleotide bond formation by the use of the chiral ribose moiety of thymidine
-
Seio, K.; Kumura, K.; Bologna, J. C.; Sekine, M. Enhanced stereoselectivity in internucleotide bond formation by the use of the chiral ribose moiety of thymidine. J. Org. Chem. 2003, 68, 3849-3859.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 3849-3859
-
-
Seio, K.1
Kumura, K.2
Bologna, J.C.3
Sekine, M.4
|