-
1
-
-
34748876074
-
-
U.S. US 5,382,572, Prepration of alkyl and acyl substituted quinolinesas antiviral agents. Chem. Abstr, 122: 213949r
-
Afonso, A., J. Weinstein and M.J. Gentles, 1995. U.S. US 5,382,572, 1995; Prepration of alkyl and acyl substituted quinolinesas antiviral agents. Chem. Abstr., 122: 213949r.
-
(1995)
, pp. 1995
-
-
Afonso, A.1
Weinstein, J.2
Gentles, M.J.3
-
2
-
-
0035128467
-
An efficient and facile synthesis of 2-chloro-3- formylquinolines from acetanilides in miceller by Vilsmeier Haack cyclisation
-
Ali, M., M. Tasneem, K.C. Rajanna and P.K. Saiprakash, 2001. An efficient and facile synthesis of 2-chloro-3- formylquinolines from acetanilides in miceller by Vilsmeier Haack cyclisation. Synlet., 2: 251-253.
-
(2001)
Synlet
, vol.2
, pp. 251-253
-
-
Ali, M.1
Tasneem, M.2
Rajanna, K.C.3
Saiprakash, P.K.4
-
3
-
-
0029052166
-
Novel, potent and selective 5-HTZ receptor antagonists based on the piperizine skelton: Synthesis, structure biological activity and comparative molecular field analysis
-
Anzini, M., A. Cappelli, S. Vomero, G. Giorge, T. Langer, M. Hamoon, N. Merahi, B.M. Emerit, A. Cagnotto, M. Skorupska, T. Mennini and J.C. Pinto, 1995. Novel, potent and selective 5-HTZ receptor antagonists based on the piperizine skelton: Synthesis, structure biological activity and comparative molecular field analysis. J. Med. Chem., 38: 2692-2704.
-
(1995)
J. Med. Chem
, vol.38
, pp. 2692-2704
-
-
Anzini, M.1
Cappelli, A.2
Vomero, S.3
Giorge, G.4
Langer, T.5
Hamoon, M.6
Merahi, N.7
Emerit, B.M.8
Cagnotto, A.9
Skorupska, M.10
Mennini, T.11
Pinto, J.C.12
-
4
-
-
0035811449
-
Synthesis and antibacterial evaluation of certain quinolone derivatives
-
Chen, Y.L., K.C. Fang, J.Y. Sheu, S.L. Hsu and C.C. Tzeng, 2001. Synthesis and antibacterial evaluation of certain quinolone derivatives. J. Med. Chem., 44: 2374-2377.
-
(2001)
J. Med. Chem
, vol.44
, pp. 2374-2377
-
-
Chen, Y.L.1
Fang, K.C.2
Sheu, J.Y.3
Hsu, S.L.4
Tzeng, C.C.5
-
5
-
-
0030026595
-
-
Doses, P., J.M. Lepagnol, P. Morain, P. Lestage and A.A. Cordi, 1996. Structure-Activity relationship in a series of 2(1H)-quinolones bearing different acidic function in the 3-position: 6,7-dichloro-2(1 H) oxoquinoine-3-phosphonic acid, a new potent and selective AMPA/ Kainate Antagonist with Neuroprotective properties. J. Med. Chem., 39: 197-206.
-
Doses, P., J.M. Lepagnol, P. Morain, P. Lestage and A.A. Cordi, 1996. Structure-Activity relationship in a series of 2(1H)-quinolones bearing different acidic function in the 3-position: 6,7-dichloro-2(1 H) oxoquinoine-3-phosphonic acid, a new potent and selective AMPA/ Kainate Antagonist with Neuroprotective properties. J. Med. Chem., 39: 197-206.
-
-
-
-
6
-
-
17544392459
-
Quinolines as potent 5-lipoxygenase inhibitor: Synthesis andbiological profile
-
Dube, D.M. Bloun, C. Brideau, C. Chan, S. Desmarais, D. Eithier, J.P. Falgueyeret, R.W. Friesen, M. Girad, Y. Girad, J. Guay, P. Tagri and R.N. Yong, 1998. Quinolines as potent 5-lipoxygenase inhibitor: Synthesis andbiological profile. Bioorg. Med. Chem. Lett., 8: 1255-1260.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 1255-1260
-
-
Dube1
Bloun, D.M.2
Brideau, C.3
Chan, C.4
Desmarais, S.5
Eithier, D.6
Falgueyeret, J.P.7
Friesen, R.W.8
Girad, M.9
Girad, Y.10
Guay, J.11
Tagri, P.12
Yong, R.N.13
-
7
-
-
0029899203
-
Isolation of E-1-(4-hydroxy phenyl)-but-1-en-3-one from Scutellaria barbata
-
Ducki, S., J.A. Hadfield, N.J. Lawerence and X. Zhang, 1996. Isolation of E-1-(4-hydroxy phenyl)-but-1-en-3-one from Scutellaria barbata. Planta Medica, 62: 185-186.
-
(1996)
Planta Medica
, vol.62
, pp. 185-186
-
-
Ducki, S.1
Hadfield, J.A.2
Lawerence, N.J.3
Zhang, X.4
-
8
-
-
0029798679
-
Evaluation of Anchorage-Indepdent proliferation in Tumorigenic cells using the redox dye alamar blue
-
Gray, G.D. and E. Wickstrom, 1996. Evaluation of Anchorage-Indepdent proliferation in Tumorigenic cells using the redox dye alamar blue. Biotechniques, 21: 780-782.
-
(1996)
Biotechniques
, vol.21
, pp. 780-782
-
-
Gray, G.D.1
Wickstrom, E.2
-
9
-
-
28444491228
-
Jpn. Tokkyo Koho JP 02 32,086[9032,086], 1990. Platinium compound and agent for treating malignant tumor
-
Hasegawa, S., K. Masunaga, M. Muto and S. Hanada, 1991. Jpn. Tokkyo Koho JP 02 32,086[9032,086], 1990. Platinium compound and agent for treating malignant tumor. Chem. Abstr., 114: 34897k.
-
(1991)
Chem. Abstr
, vol.114
-
-
Hasegawa, S.1
Masunaga, K.2
Muto, M.3
Hanada, S.4
-
10
-
-
0033585872
-
Evaluation of glycine site antagonists vof the NMDA receptor in global cerebral ischaemia
-
Hicks, C.A., M.A. Ward, N. Ragumorthy, S.A. Amber, C.P. Dell, D. Dobson, J.M. O'Neil, 1999. Evaluation of glycine site antagonists vof the NMDA receptor in global cerebral ischaemia. Brain Res., 819: 65-74.
-
(1999)
Brain Res
, vol.819
, pp. 65-74
-
-
Hicks, C.A.1
Ward, M.A.2
Ragumorthy, N.3
Amber, S.A.4
Dell, C.P.5
Dobson, D.6
O'Neil, J.M.7
-
11
-
-
84886760499
-
3-Acryolyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxo quinoline derivatives and their behaviour towards some nucleophiles
-
Ibrahim, S.S., H.A. Allimony and E.S. Othman, 1996. 3-Acryolyl-1,2-dihydro-4-hydroxy-1-methyl-2-oxo quinoline derivatives and their behaviour towards some nucleophiles. Chem. Papers, 51: 3342.
-
(1996)
Chem. Papers
, vol.51
, pp. 3342
-
-
Ibrahim, S.S.1
Allimony, H.A.2
Othman, E.S.3
-
12
-
-
84986928010
-
-
Kappe, T., R. Aiger, P. Hohengassner and W. Stadlbauer, 1994. Synthesis of 3-Acyl-4-hydroxy-2(1H) quinolones. J. Parkat. Chem., 336: 596-601.
-
Kappe, T., R. Aiger, P. Hohengassner and W. Stadlbauer, 1994. Synthesis of 3-Acyl-4-hydroxy-2(1H) quinolones. J. Parkat. Chem., 336: 596-601.
-
-
-
-
13
-
-
0037375084
-
Antimicrobial activity of aqueous and methanol extracts of Junipreus oxycedrus L
-
Karaman, I., F. Sahin, M. Gulluce, H. Ogutcu, M. Sengul and Adiguzel, 2003. Antimicrobial activity of aqueous and methanol extracts of Junipreus oxycedrus L. J. Ethnopharmacol., 85: 231-235.
-
(2003)
J. Ethnopharmacol
, vol.85
, pp. 231-235
-
-
Karaman, I.1
Sahin, F.2
Gulluce, M.3
Ogutcu, H.4
Sengul, M.5
Adiguzel6
-
14
-
-
0003607021
-
-
Rees, C.W, Ed, Pergamon Press, Oxford
-
Katritzky, A.R., 1984. Comprehensive Hetrocyclic Chemistry. Rees, C.W. (Ed.), Vol. 2. Pergamon Press, Oxford.
-
(1984)
Comprehensive Hetrocyclic Chemistry
, vol.2
-
-
Katritzky, A.R.1
-
15
-
-
15844376844
-
Practicalroute toa new class of LTD, Receptor Antagonists
-
Larsen, R.D., E.G. Corley, A.O. King, J.D. Carrol, P. Davis, T.R. Verhoeven, P.J. Reider, M. Labelle, J.Y. Gauthier, Y.B. Xiang and R. Zamboni, 1996. Practicalroute toa new class of LTD, Receptor Antagonists. J. Org. Chem., 61: 3398-3405.
-
(1996)
J. Org. Chem
, vol.61
, pp. 3398-3405
-
-
Larsen, R.D.1
Corley, E.G.2
King, A.O.3
Carrol, J.D.4
Davis, P.5
Verhoeven, T.R.6
Reider, P.J.7
Labelle, M.8
Gauthier, J.Y.9
Xiang, Y.B.10
Zamboni, R.11
-
16
-
-
0036776442
-
Improved synthesis of chalcones under ultrasonic irradiation
-
Li, J.T., W.Z. Yang, S.X, Wang, S.H. Li and T.S. Li, 2002. Improved synthesis of chalcones under ultrasonic irradiation. Ultrason Sonochem., 9: 237-239.
-
(2002)
Ultrason Sonochem
, vol.9
, pp. 237-239
-
-
Li, J.T.1
Yang, W.Z.2
Wang, S.X.3
Li, S.H.4
Li, T.S.5
-
17
-
-
0030793673
-
1,4-Diaryl-2-oxo- 1,2-dihydroquinolin-3-carboxylic acid as endothelin receptor antagonists
-
Mederski, W.W., M. Oswald, D. Dorsch, M. Christlader, C.J. Schmitges and C. Wilm, 1997. 1,4-Diaryl-2-oxo- 1,2-dihydroquinolin-3-carboxylic acid as endothelin receptor antagonists. Bioorg. Med. Chem. Lett., 7: 1883-1886.
-
(1997)
Bioorg. Med. Chem. Lett
, vol.7
, pp. 1883-1886
-
-
Mederski, W.W.1
Oswald, M.2
Dorsch, D.3
Christlader, M.4
Schmitges, C.J.5
Wilm, C.6
-
18
-
-
0000525422
-
A versatile new synthesis of quinolines, thiopyrimidines and related fused pyridines
-
Meth-Cohn, O. and B. Narine, 1978. A versatile new synthesis of quinolines, thiopyrimidines and related fused pyridines. Tetrahedron Lett., 23: 2045-2048.
-
(1978)
Tetrahedron Lett
, vol.23
, pp. 2045-2048
-
-
Meth-Cohn, O.1
Narine, B.2
-
19
-
-
0000548138
-
Synthesis of some multiazaheterocycles as substituents to quinolone moiety of specific biological activity
-
Mohamed, E.A., M.M. Ismil, Y. Gabr and M. Abass, 1994. Synthesis of some multiazaheterocycles as substituents to quinolone moiety of specific biological activity. Chem. Papers, 48: 285-292.
-
(1994)
Chem. Papers
, vol.48
, pp. 285-292
-
-
Mohamed, E.A.1
Ismil, M.M.2
Gabr, Y.3
Abass, M.4
-
20
-
-
0035939374
-
Synthesis and evaluation of novel quinolines as HIV-reverse transcriptase inhibitors
-
Patel, M., R.J. Mc Hugh, B.C. Cordova, R.M. Klabe, L.T. Bachler, S. Erikson-Viitanen and J.D. Rodgers, 2001. Synthesis and evaluation of novel quinolines as HIV-reverse transcriptase inhibitors. Bioorg. Med. Chem. Lett., 11: 1943-1945.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 1943-1945
-
-
Patel, M.1
Mc Hugh, R.J.2
Cordova, B.C.3
Klabe, R.M.4
Bachler, L.T.5
Erikson-Viitanen, S.6
Rodgers, J.D.7
-
21
-
-
29144520126
-
Synthesis of some quinolinyl aryl unsaturated ketones
-
Rezig, R., M. Chebah, S. Rhouati, S. Ducki and N.J. Lawrence, 2000. Synthesis of some quinolinyl aryl unsaturated ketones. J. Soc. Alger. Chim., 10: 111-120.
-
(2000)
J. Soc. Alger. Chim
, vol.10
, pp. 111-120
-
-
Rezig, R.1
Chebah, M.2
Rhouati, S.3
Ducki, S.4
Lawrence, N.J.5
-
22
-
-
0027331480
-
-
Rowley, M., P.D. Leeson, G.I. Stevenson, A.M. Moseley, I. Stansfield, I. Sanderson, L. Robinson, R. Baker, J.A. Kemp, Marshell, A.C. Foster, S. Grimwood, M.D. Tricklebank and K.L. Saywell, 1993. 3-acyl-4- hydroxyquinolin-2(1H)-ones.- Systematically active anticonvulsants action by antagonism at the glycine site of N-methyl-D-asparate receptor complex. J. Med. Chem., 36: 3386-3396.
-
Rowley, M., P.D. Leeson, G.I. Stevenson, A.M. Moseley, I. Stansfield, I. Sanderson, L. Robinson, R. Baker, J.A. Kemp, Marshell, A.C. Foster, S. Grimwood, M.D. Tricklebank and K.L. Saywell, 1993. 3-acyl-4- hydroxyquinolin-2(1H)-ones.- Systematically active anticonvulsants action by antagonism at the glycine site of N-methyl-D-asparate receptor complex. J. Med. Chem., 36: 3386-3396.
-
-
-
-
23
-
-
0005702609
-
The behaviour of some 3-substituted 4- hydroxy-1-alkyl (or phenyl) carbostyrils towards amines and hydrazines
-
Sayed, A.A., S.M. Sami, A. Elfayoumi and E.A. Mohamed, 1976. The behaviour of some 3-substituted 4- hydroxy-1-alkyl (or phenyl) carbostyrils towards amines and hydrazines. Egypt J. Chem., 19: 811-826.
-
(1976)
Egypt J. Chem
, vol.19
, pp. 811-826
-
-
Sayed, A.A.1
Sami, S.M.2
Elfayoumi, A.3
Mohamed, E.A.4
-
24
-
-
6344269067
-
Ring closure reactions of 3-arylhydrazonalkyl-quinolin-2-ones to 1- arylpyrazolo[4,3-C]quinolin-2-ones
-
Stadlbauer, W. and G. Hojas, 2004. Ring closure reactions of 3-arylhydrazonalkyl-quinolin-2-ones to 1- arylpyrazolo[4,3-C]quinolin-2-ones. J. Heterocyclic Chem., 41: 681-690.
-
(2004)
J. Heterocyclic Chem
, vol.41
, pp. 681-690
-
-
Stadlbauer, W.1
Hojas, G.2
-
25
-
-
4243456595
-
4-Hydroxy-2-quinolones. 31. 3- amino-IR-2-oxop-4=hydroxyquinolines and their acyl derivatives
-
Ukrainets, I.V., S.G. Taran, L.V. Sidorenko, O.V. Gorokhova, A.A. Ogirenko, A.V. Turov and N.I. Filimonova, 1996. 4-Hydroxy-2-quinolones. 31. 3- amino-IR-2-oxop-4=hydroxyquinolines and their acyl derivatives. Khim. Geterotsikl. Soedin., 8: 1113-1123.
-
(1996)
Khim. Geterotsikl. Soedin
, vol.8
, pp. 1113-1123
-
-
Ukrainets, I.V.1
Taran, S.G.2
Sidorenko, L.V.3
Gorokhova, O.V.4
Ogirenko, A.A.5
Turov, A.V.6
Filimonova, N.I.7
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