-
1
-
-
0025355448
-
Synthesis of some isoxazole analogues of retinoids: Biological effects toward tumor cell lines
-
Baraldi, P. G.; Guarneri, M.; Manfredini, S.; Simoni, D.; Aghazade Tabrizi, M.; Barbieri, R.; Gambari, R.; Nastruzzi, C. Synthesis of some isoxazole analogues of retinoids: Biological effects toward tumor cell lines. Eur. J. Med. Chem. 1990, 25, 279.
-
(1990)
Eur. J. Med. Chem.
, vol.25
, pp. 279
-
-
Baraldi, P.G.1
Guarneri, M.2
Manfredini, S.3
Simoni, D.4
Aghazade Tabrizi, M.5
Barbieri, R.6
Gambari, R.7
Nastruzzi, C.8
-
2
-
-
29244479188
-
Blocking tumor cell migration and invasion with biphenyl isoxazole derivative KRIBB3, a synthetic molecule that inhibits hsp27 phosphorylation
-
Shin, K. D.; Lee, M. Y.; Shin, D. S.; Lee, S.; Son, K. H.; Koh, Y. K.; Paik Kwon, B. M.; Han, D. C. Blocking tumor cell migration and invasion with biphenyl isoxazole derivative KRIBB3, a synthetic molecule that inhibits hsp27 phosphorylation. J. Biol. Chem. 2005, 280, 41439.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 41439
-
-
Shin, K.D.1
Lee, M.Y.2
Shin, D.S.3
Lee, S.4
Son, K.H.5
Koh, Y.K.6
Paik Kwon, B.M.7
Han, D.C.8
-
3
-
-
32944470419
-
Synthesis and anti-HIV activity of new alkenyldiarylmethane (ADAM) non-nucleoside reverse transcriptase inhibitors (NNRTIs) incorporating benzoxazolone and benzisoxazole rings
-
Deng, B. L.; Cullen, M. D.; Zhou, Z.; Hartman, T. L.; Buckheit Jr., R. W.; Pannecouque, C.; Declescq, E.; Fanwick, P. E.; Cushman, M. Synthesis and anti-HIV activity of new alkenyldiarylmethane (ADAM) non-nucleoside reverse transcriptase inhibitors (NNRTIs) incorporating benzoxazolone and benzisoxazole rings. Bioorg. Med. Chem. 2006, 14, 2366.
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 2366
-
-
Deng, B.L.1
Cullen, M.D.2
Zhou, Z.3
Hartman, T.L.4
Buckheit Jr., R.W.5
Pannecouque, C.6
Declescq, E.7
Fanwick, P.E.8
Cushman, M.9
-
4
-
-
19844363802
-
Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents
-
Bhat, B. A.; Dhar, K. L.; Purin, S. C.; Saxena, A. K.; Shanmugavel, M.; Qazi, G. N. Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents. Bioorg. Med. Chem. Lett. 2005, 15, 3177.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 3177
-
-
Bhat, B.A.1
Dhar, K.L.2
Purin, S.C.3
Saxena, A.K.4
Shanmugavel, M.5
Qazi, G.N.6
-
5
-
-
72249098737
-
3,4-Diaryl-isoxazoles and -imidazoles as potent dual inhibitors of p38r nitrogen activated protein kinase and casein kinase 1d
-
Peifer, C.; Abadleh, M.; Bischof, J.; Hauser, D.; Schattel, V.; Hirner, H.; Knippschild, U.; Laufer, S. 3,4-Diaryl-isoxazoles and -imidazoles as potent dual inhibitors of p38r nitrogen activated protein kinase and casein kinase 1d. J. Med. Chem. 2009, 52, 7618.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7618
-
-
Peifer, C.1
Abadleh, M.2
Bischof, J.3
Hauser, D.4
Schattel, V.5
Hirner, H.6
Knippschild, U.7
Laufer, S.8
-
6
-
-
0342368828
-
Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents
-
Gursoy, A.; Demirayak, S.; Capan, G.; Erol, K.; Vural, K. Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents. Eur. J. Med. Chem. 2000, 35, 359.
-
(2000)
Eur. J. Med. Chem.
, vol.35
, pp. 359
-
-
Gursoy, A.1
Demirayak, S.2
Capan, G.3
Erol, K.4
Vural, K.5
-
7
-
-
67651165037
-
Synthesis of some novel bioactive 4-oxy/ thio substituted-1H-pyrazol- 5(4H)-ones via efficient cross-Claisen condensation
-
Ragavan, R. V.; Vijayakumar, V.; Kumari, N. S. Synthesis of some novel bioactive 4-oxy/ thio substituted-1H-pyrazol-5(4H)-ones via efficient cross-Claisen condensation. Eur. J. Med. Chem. 2009, 44, 3852.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 3852
-
-
Ragavan, R.V.1
Vijayakumar, V.2
Kumari, N.S.3
-
8
-
-
19544366936
-
Novel pyrazole derivatives as potential promising anti-inflammatory antimicrobial agents
-
Bekhit, A. A.; Ashous, H. M.; Guemei, A. A. Novel pyrazole derivatives as potential promising anti-inflammatory antimicrobial agents, B. Arch. Pharm. 2005, 338, 167.
-
(2005)
B. Arch. Pharm.
, vol.338
, pp. 167
-
-
Bekhit, A.A.1
Ashous, H.M.2
Guemei, A.A.3
-
9
-
-
33847411932
-
Synthesis and studies on antidepressant and anticonvulsant activities of some 3-(2-furyl)-pyrazoline derivatives
-
Ozdemir, Z.; Kandilei, H. B.; Gumusel, Calis, U.; Bilgin, A. A. Synthesis and studies on antidepressant and anticonvulsant activities of some 3-(2-furyl)-pyrazoline derivatives. Eur. J. Med. Chem. 2007, 42, 373.
-
(2007)
Eur. J. Med. Chem.
, vol.42
, pp. 373
-
-
Ozdemir, Z.1
Kandilei, H.B.2
Gumusel Calis, U.3
Bilgin, A.A.4
-
10
-
-
0030979729
-
Effects of a novel free radical scavenger, MCl-186, on ischemic brain damage in the rat distal middle cerebral artery occlusion model
-
Kawai, H.; Nakai, H.; Suga, M.; Yuki, S.; Watanabe, T.; Saito, K. I. Effects of a novel free radical scavenger, MCl-186, on ischemic brain damage in the rat distal middle cerebral artery occlusion model. J. Pharmacol. Exp. Ther. 1997, 281, 921.
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.281
, pp. 921
-
-
Kawai, H.1
Nakai, H.2
Suga, M.3
Yuki, S.4
Watanabe, T.5
Saito, K.I.6
-
11
-
-
0037183707
-
Myocardial protection of MCI-186 in rabbit ischemia-reperfusion
-
Wu, T. W.; Zeng, L. H.; Wu, J.; Fung, K. P. Myocardial protection of MCI-186 in rabbit ischemia-reperfusion. Life Sci. 2002, 71, 2249.
-
(2002)
Life Sci.
, vol.71
, pp. 2249
-
-
Wu, T.W.1
Zeng, L.H.2
Wu, J.3
Fung, K.P.4
-
13
-
-
0038825687
-
Anti-androgens with full antagonistic activity toward human prostate tumor LNCaP cells with mutated androgen receptor
-
Ishioka, T.; Tanatani, A.; Nagasawa, K.; Hashimoto, Y. Anti-androgens with full antagonistic activity toward human prostate tumor LNCaP cells with mutated androgen receptor. Bioorg. Med. Chem. 2003, 13, 2655.
-
(2003)
Bioorg. Med. Chem.
, vol.13
, pp. 2655
-
-
Ishioka, T.1
Tanatani, A.2
Nagasawa, K.3
Hashimoto, Y.4
-
14
-
-
0036186204
-
Novel non-steroidal/non-anilide type androgen antagonists with an isoxazolone moiety
-
Ishioka, T.; Kubo, A.; Koiso, Y.; Nagasawa, K.; Itai, A.; Hashimoto, Y. Novel non-steroidal/non-anilide type androgen antagonists with an isoxazolone moiety. Bioorg. Med. Chem. 2002, 10, 1555.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 1555
-
-
Ishioka, T.1
Kubo, A.2
Koiso, Y.3
Nagasawa, K.4
Itai, A.5
Hashimoto, Y.6
-
15
-
-
65149087208
-
Substituted isoxazole analogs of farnesoid X receptor (FXR) agonist GW4064
-
Bass, J. Y.; Caldwell, R. D.; Caravella, J. A.; Chen, L.; Creech, K. L.; Deaton, D. N.; Madauss, K. P.; Marr, H. B.; McFadyen, R. B.; Miller, A. B.; Parks, D. J.; Todd, D.; Williams, S. P.; Wisely, G. B. Substituted isoxazole analogs of farnesoid X receptor (FXR) agonist GW4064. Bioorg. Med. Chem. Lett. 2009, 19, 2969.
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 2969
-
-
Bass, J.Y.1
Caldwell, R.D.2
Caravella, J.A.3
Chen, L.4
Creech, K.L.5
Deaton, D.N.6
Madauss, K.P.7
Marr, H.B.8
McFadyen, R.B.9
Miller, A.B.10
Parks, D.J.11
Todd, D.12
Williams, S.P.13
Wisely, G.B.14
-
16
-
-
70349911565
-
Synthesis of new 4-isopropylthiazole hydrazide analogs and some derived clubbed triazole, oxadiazole ring systems-A novel class of potential antibacterial, antifungal and antitubercular agents
-
Mallikarjuna, B. P.; Sastry, B. S.; Suresh Kumar, G. V.; Rajendraprasad, Y.; Chandrashekar, S. M.; Sathisha, K. Synthesis of new 4-isopropylthiazole hydrazide analogs and some derived clubbed triazole, oxadiazole ring systems-A novel class of potential antibacterial, antifungal and antitubercular agents. Eur. J. Med. Chem. 2009, 44, 4739.
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 4739
-
-
Mallikarjuna, B.P.1
Sastry, B.S.2
Suresh Kumar, G.V.3
Rajendraprasad, Y.4
Chandrashekar, S.M.5
Sathisha, K.6
-
20
-
-
13444292181
-
Pd-catalyzed one-pot multicomponent coupling reaction for the highly regioselective synthesis of polysubstituted benzenes
-
Xi, C.; Chen, C.; Lin, J.; Hong, X. Pd-catalyzed one-pot multicomponent coupling reaction for the highly regioselective synthesis of polysubstituted benzenes. Org. Lett. 2005, 7, 347.
-
(2005)
Org. Lett.
, vol.7
, pp. 347
-
-
Xi, C.1
Chen, C.2
Lin, J.3
Hong, X.4
-
21
-
-
0036188180
-
Convenient one-pot synthesis and antimicrobial activity of pyrimido[1,2-b][1,2,4,5]tetrazines
-
Shawali, A. S.; Abdallah, M. A.; Zayed, M. M. A. Convenient one-pot synthesis and antimicrobial activity of pyrimido[1,2-b][1,2,4,5]tetrazines. J. Heterocycl. Chem. 2002, 39, 45.
-
(2002)
J. Heterocycl. Chem.
, vol.39
, pp. 45
-
-
Shawali, A.S.1
Abdallah, M.A.2
Zayed, M.M.A.3
-
22
-
-
20344388819
-
"On water": Unique reactivity of organic compounds in aqueous suspension
-
Narayan, S.; Fokin, M. G.; Kolb, H. C.; Sharpless, K. B. "On water": Unique reactivity of organic compounds in aqueous suspension. Angew. Chem., Int. Ed. 2005, 44, 3275.
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 3275
-
-
Narayan, S.1
Fokin, M.G.2
Kolb, H.C.3
Sharpless, K.B.4
-
23
-
-
34047119658
-
Synthesis of bi- and tricyclic b-lactam libraries in aqueous medium
-
Kanizsai, I.; Gyónfalvi, S.; Szadonyi, Z.; Sillanpää, R.; Fülo2 p, F. Synthesis of bi- and tricyclic b-lactam libraries in aqueous medium. Green Chem. 2007, 9, 357.
-
(2007)
Green Chem.
, vol.9
, pp. 357
-
-
Kanizsai, I.1
Gyónfalvi, S.2
Szadonyi, Z.3
Sillanpää, R.4
Fülop, F.5
-
24
-
-
34447131678
-
Reactions of CH bonds in water
-
Herrerias, C. I.; Yao, X.; Li, Z.; Li, C. Reactions of CH bonds in water. Chem. Rev. 2007, 107, 2546.
-
(2007)
Chem. Rev.
, vol.107
, pp. 2546
-
-
Herrerias, C.I.1
Yao, X.2
Li, Z.3
Li, C.4
-
25
-
-
77956421360
-
Ultrasound-assisted one-pot, four component synthesis of 4-aryl 3,4-dihydropyridone derivatives
-
Ruiz, E.; Rodríguez, H.; Coro, J.; Salfrán, E.; Suárez, M.; Marti?nez-Alvarez, R.; Marti?n, N. Ultrasound-assisted one-pot, four component synthesis of 4-aryl 3,4-dihydropyridone derivatives. Ultrason. Sonochem. 2011, 18, 32.
-
(2011)
Ultrason. Sonochem.
, vol.18
, pp. 32
-
-
Ruiz, E.1
Rodríguez, H.2
Coro, J.3
Salfrán, E.4
Suárez, M.5
Martinez-Alvarez, R.6
Martin, N.7
-
26
-
-
60749129757
-
Ultrasound in heterocycles chemistry
-
Cella, R.; Stefani, H. Ultrasound in heterocycles chemistry. Tetrahedron 2009, 65, 2619.
-
(2009)
Tetrahedron
, vol.65
, pp. 2619
-
-
Cella, R.1
Stefani, H.2
|