-
1
-
-
37049137150
-
Reaction of 2,3-epoxy-3-(2-nitrophenyl)propiophenone (2-nitrochalcone epoxide) with hydrogen chloride
-
Sword, I. P. Reaction of 2,3-epoxy-3-(2-nitrophenyl)propiophenone (2-nitrochalcone epoxide) with hydrogen chloride. J. Chem. Soc. Sect C., 1971, 5, 820-823.
-
(1971)
J. Chem. Soc. Sect C
, vol.5
, pp. 820-823
-
-
Sword, I.P.1
-
2
-
-
37049124111
-
Chemistry of nitro compounds. I. Acid-catalyzed ring-opening reactions of substituted (onitrophenyl) ethylene oxides involving participation by the nitro group
-
Spence, T. W. M.; Tennant, G. Chemistry of nitro compounds. I. Acid-catalyzed ring-opening reactions of substituted (onitrophenyl) ethylene oxides involving participation by the nitro group. J. Chem. Soc. Sect. C., 1971, 22, 3712-3719.
-
(1971)
J. Chem. Soc. Sect. C
, vol.22
, pp. 3712-3719
-
-
Spence, T.W.M.1
Tennant, G.2
-
3
-
-
70349117962
-
-
Venturella, P.; Bellino.A.; Piozzi, F.; Marino, M. L. Synthesis of quinoline alkaloids. VIII. The synthesis of japonine. Heterocycles, 1976, 4, 1089-1094.
-
Venturella, P.; Bellino.A.; Piozzi, F.; Marino, M. L. Synthesis of quinoline alkaloids. VIII. The synthesis of japonine. Heterocycles, 1976, 4, 1089-1094.
-
-
-
-
4
-
-
70349158973
-
A novel synthesis of 2-aryl-3-hydroxy(alkoxy)-4-quinolones by expanding the ring of 1-acetyl-2-(arylmethylene)-3-indolines
-
Velezheva V.S., Mel'man A.I., Pol'shakov V.I.; Asimova O.S. A novel synthesis of 2-aryl-3-hydroxy(alkoxy)-4-quinolones by expanding the ring of 1-acetyl-2-(arylmethylene)-3-indolines. Khim. Geter. Soed., 1992, 2, 279-280.
-
(1992)
Khim. Geter. Soed
, vol.2
, pp. 279-280
-
-
Velezheva, V.S.1
Mel'man, A.I.2
Pol'shakov, V.I.3
Asimova, O.S.4
-
5
-
-
13044310577
-
Conversion of 4-quinolones into 3-hydroxy-4-quinolones via the corresponding sulfates
-
Behrman J.E.; Kiser L.R.; Garas W.F.; Behrman E.C.; Pitt B.M. Conversion of 4-quinolones into 3-hydroxy-4-quinolones via the corresponding sulfates. J. Chem. Res., Synop., 1995, 5, 164-165.
-
(1995)
J. Chem. Res., Synop
, vol.5
, pp. 164-165
-
-
Behrman, J.E.1
Kiser, L.R.2
Garas, W.F.3
Behrman, E.C.4
Pitt, B.M.5
-
6
-
-
0142117622
-
Synthesis of 2-aryl-3-hydroxyquinolin-4(1H)-ones
-
Hradil, P.; Jirman, J. Synthesis of 2-aryl-3-hydroxyquinolin-4(1H)-ones. Collect. Czech. Chem. Commun., 1995, 60, 1357-1366.
-
(1995)
Collect. Czech. Chem. Commun
, vol.60
, pp. 1357-1366
-
-
Hradil, P.1
Jirman, J.2
-
7
-
-
0032930481
-
Preparation of 1,2-disubstituted-3-hydroxy-4(1H)-quinolinones and the influence of substitution on the course of cyclization
-
Hradil P., Hlaváĉ J., Lemr K.: Preparation of 1,2-disubstituted-3-hydroxy-4(1H)-quinolinones and the influence of substitution on the course of cyclization. J. Heterocyclic Chem., 1999, 36, 141-144.
-
(1999)
J. Heterocyclic Chem
, vol.36
, pp. 141-144
-
-
Hradil, P.1
Hlaváĉ, J.2
Lemr, K.3
-
8
-
-
33747397956
-
Synthesis of N-amino-3-hydroxy-2-phenyl-4(1H)-quinolinone
-
Spáĉilová L., Hlaváĉ J., Hradil P. Hajduch M., Krejĉí P. Synthesis of N-amino-3-hydroxy-2-phenyl-4(1H)-quinolinone. J. Heterocyclic. Chem., 2006, 43, 1065-1070.
-
(2006)
J. Heterocyclic. Chem
, vol.43
, pp. 1065-1070
-
-
Spáĉilová, L.1
Hlaváĉ, J.2
Hradil, P.3
Hajduch, M.4
Krejĉí, P.5
-
9
-
-
70349109492
-
-
Yeleswarapu, K.R.; Manojit, P.; Vedula M.S.; Akella, V.; Pillarisetti, S.; Padakanti, S.; Kalleda, S.R. Preparation of heterocyclic compounds including chromenones, quinazolinones, quinolinones and pyrazolopyrimidinone that block the effects of advanced glycation end products. WO2005040163 (Reddy's Laboratories Ltd., India). CAS: 142:447230.
-
Yeleswarapu, K.R.; Manojit, P.; Vedula M.S.; Akella, V.; Pillarisetti, S.; Padakanti, S.; Kalleda, S.R. Preparation of heterocyclic compounds including chromenones, quinazolinones, quinolinones and pyrazolopyrimidinone that block the effects of advanced glycation end products. WO2005040163 (Reddy's Laboratories Ltd., India). CAS: 142:447230.
-
-
-
-
10
-
-
30344458827
-
Synthesis and fluorescence properties of 2-aryl-3-hydroxyquinolones, a new class of dyes displaying dual fluorescence
-
Yushchenko, D.A.; Bilokin', M.D.; Pyvovarenko, O. V.; Duportail, G.; Mely, Y.; Pivovarenko, V.G. Synthesis and fluorescence properties of 2-aryl-3-hydroxyquinolones, a new class of dyes displaying dual fluorescence. Tetrahedron Lett., 2006, 47, 905-908.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 905-908
-
-
Yushchenko, D.A.1
Bilokin', M.D.2
Pyvovarenko, O.V.3
Duportail, G.4
Mely, Y.5
Pivovarenko, V.G.6
-
11
-
-
33646449777
-
Solid-state induced heterocyclization under microwave irradiation: Synthesis of 2-phenyl-3-hydroxyquinolin-4(1H)-one
-
Heravi, M.M.; Oskooie, H.A.; Bahrami, L.; Ghassemzadeh, M. Solid-state induced heterocyclization under microwave irradiation: synthesis of 2-phenyl-3-hydroxyquinolin-4(1H)-one. Indian J. Chem., Sect. B, 2006, 45B, 779-781.
-
(2006)
Indian J. Chem., Sect. B
, vol.45 B
, pp. 779-781
-
-
Heravi, M.M.1
Oskooie, H.A.2
Bahrami, L.3
Ghassemzadeh, M.4
-
12
-
-
34948818778
-
Efficient Solid-Phase Synthesis of 2-Substituted-3-Hydroxy-4(1H)-Quinolinone-7-Carboxamides with Two Diversity Positions
-
Soural, M.; Krchnak, V. Efficient Solid-Phase Synthesis of 2-Substituted-3-Hydroxy-4(1H)-Quinolinone-7-Carboxamides with Two Diversity Positions. J. Comb. Chem., 2007, 9, 793-796.
-
(2007)
J. Comb. Chem
, vol.9
, pp. 793-796
-
-
Soural, M.1
Krchnak, V.2
-
13
-
-
70349128016
-
-
Rao, Y.K.; Pal, M.; Sharma, V.M.; Venkateswarlu, A.; Pillarisetti, R. Preparation of chromenones, quinolones, and related compounds as modulators of inflammatory responses such as those resulting from AGE and glycated protein accumulation. WO2005042712 (Reddy US Therapeutics, Inc., USA). CAS: 142:463715.
-
Rao, Y.K.; Pal, M.; Sharma, V.M.; Venkateswarlu, A.; Pillarisetti, R. Preparation of chromenones, quinolones, and related compounds as modulators of inflammatory responses such as those resulting from AGE and glycated protein accumulation. WO2005042712 (Reddy US Therapeutics, Inc., USA). CAS: 142:463715.
-
-
-
-
14
-
-
70349110368
-
-
Tamura, T.; Kuriyama, H.; Agoh, M.; Agoh, Y.; Soga, M.; Mori, T. Preparation of 1,2-disubstituted 1,4-dihydro-4-oxoquinoline compounds as antiviral agents. EP1380575 (Maruishi Pharmaceutical Co., Ltd., Japan); CAS: 140:93939.
-
Tamura, T.; Kuriyama, H.; Agoh, M.; Agoh, Y.; Soga, M.; Mori, T. Preparation of 1,2-disubstituted 1,4-dihydro-4-oxoquinoline compounds as antiviral agents. EP1380575 (Maruishi Pharmaceutical Co., Ltd., Japan); CAS: 140:93939.
-
-
-
-
15
-
-
0000647729
-
Ring closing and photooxidation in nitrogen analogs of 3-hydroxyflavone
-
Gao, F.; Johnson K.F.; Schlenoff J.B. Ring closing and photooxidation in nitrogen analogs of 3-hydroxyflavone. J. Chem. Soc., Perkin Trans., 2, 1996, 269-273.
-
(1996)
J. Chem. Soc., Perkin Trans., 2
, pp. 269-273
-
-
Gao, F.1
Johnson, K.F.2
Schlenoff, J.B.3
-
16
-
-
0032750748
-
Synthesis and topoisomerase inhibitory activities of novel aza-analogues of flavones
-
Sui Z. Nguyen, V.N.; Altom, J.; Fernandez, J.; Hilliard, J.J.; Bernstein, J.I.; Barrett, J.F.; Ohemeng, K.A. Synthesis and topoisomerase inhibitory activities of novel aza-analogues of flavones. Eur. J. Med. Chem. 1999, 34, 381-387.
-
(1999)
Eur. J. Med. Chem
, vol.34
, pp. 381-387
-
-
Sui, Z.1
Nguyen, V.N.2
Altom, J.3
Fernandez, J.4
Hilliard, J.J.5
Bernstein, J.I.6
Barrett, J.F.7
Ohemeng, K.A.8
-
17
-
-
0033786974
-
-
Hradil, P.; Kvapil, L.; Hlaváĉ, J.; Weidlich T.; Lyĉka, A. Preparation of 2-phenyl-2-hydroxymethyl-4-oxo-1,2,3,4-tetrahydroquinazoline and 2-methyl-4-oxo-3,4-dihydroquinazoline derivatives. J. Heterocyclic Chem., 2000, 37, 831-837.
-
Hradil, P.; Kvapil, L.; Hlaváĉ, J.; Weidlich T.; Lyĉka, A. Preparation of 2-phenyl-2-hydroxymethyl-4-oxo-1,2,3,4-tetrahydroquinazoline and 2-methyl-4-oxo-3,4-dihydroquinazoline derivatives. J. Heterocyclic Chem., 2000, 37, 831-837.
-
-
-
-
18
-
-
0008942193
-
-
Ulubelen, A.; Terem, B.; Tuzlaci, E.; Cheng, K. F.; Kong, Y. C. Phytochemistry, 1986, 25, 2692-2693.
-
(1986)
Phytochemistry
, vol.25
, pp. 2692-2693
-
-
Ulubelen, A.1
Terem, B.2
Tuzlaci, E.3
Cheng, K.F.4
Kong, Y.C.5
-
19
-
-
0036967106
-
In vitro chemoresistance profile and expression/function of MDR associated proteins in resistant cell lines derived from CCRF-CEM, K562, A549 and MDA MB 231 parental cells
-
Noskova, V.; Dzubak, P.; Kuzmina, G.; Ludkova, A.; Stehlik, D.; Trojanec, R.; Janostakova, A.; Korinkova, G.; Mihal, V.; Hajduch, M. In vitro chemoresistance profile and expression/function of MDR associated proteins in resistant cell lines derived from CCRF-CEM, K562, A549 and MDA MB 231 parental cells. Neoplasma, 2002, 49, 418-425;
-
(2002)
Neoplasma
, vol.49
, pp. 418-425
-
-
Noskova, V.1
Dzubak, P.2
Kuzmina, G.3
Ludkova, A.4
Stehlik, D.5
Trojanec, R.6
Janostakova, A.7
Korinkova, G.8
Mihal, V.9
Hajduch, M.10
-
20
-
-
10744224623
-
-
Sarek, J.; Klinot, J.; Dzubak, P.; Klinotova, E.; Noskova, V.; Krecek, V.; Korinkova, G.; Thomson, J. O.; Janost'akova, A.; Wang, S.; Parsons, S.; Fischer, P.M; Zhelev, N.Z; Hajduch, M. New lupane derived compounds with pro-apoptotic activity in cancer cells: synthesis and structureactivity relationships. J. Med. Chem., 2003, 46, 5402-5415;
-
b) Sarek, J.; Klinot, J.; Dzubak, P.; Klinotova, E.; Noskova, V.; Krecek, V.; Korinkova, G.; Thomson, J. O.; Janost'akova, A.; Wang, S.; Parsons, S.; Fischer, P.M; Zhelev, N.Z; Hajduch, M. New lupane derived compounds with pro-apoptotic activity in cancer cells: synthesis and structureactivity relationships. J. Med. Chem., 2003, 46, 5402-5415;
-
-
-
-
21
-
-
33744906765
-
Pharmacological activities of natural triterpenoids and their therapeutic implications
-
c) Dzubak, P.; Hajduch, M.; Vydra, D.; Hustova, A.; Kvasnica, M.; Biedermann, D.; Markova, L.; Urban, M.; Sarek, J. Pharmacological activities of natural triterpenoids and their therapeutic implications. Nat. Prod. Rep., 2006, 23, 394-411.
-
(2006)
Nat. Prod. Rep
, vol.23
, pp. 394-411
-
-
Dzubak, P.1
Hajduch, M.2
Vydra, D.3
Hustova, A.4
Kvasnica, M.5
Biedermann, D.6
Markova, L.7
Urban, M.8
Sarek, J.9
-
22
-
-
33646470165
-
Synthesis and cytotoxic activity of substituted 2-phenyl-3-hydroxy-4(1H)-quinolinones-7-carboxylic acids and their phenacyl esters
-
Soural, M.; Hlaváĉ, J.; Hradil, P.; Fryŝová, I.; Hajdúch, M.; Bertolasi, V.; Malon̂, M. Synthesis and cytotoxic activity of substituted 2-phenyl-3-hydroxy-4(1H)-quinolinones-7-carboxylic acids and their phenacyl esters. Eur. J. Med. Chem., 2006, 41, 467-474.
-
(2006)
Eur. J. Med. Chem
, vol.41
, pp. 467-474
-
-
Soural, M.1
Hlaváĉ, J.2
Hradil, P.3
Fryŝová, I.4
Hajdúch, M.5
Bertolasi, V.6
Malon̂, M.7
-
23
-
-
70349111705
-
Preparation of 2-phenyl-3-hydroxyquinolin-4(1H)-ones for treatment of immune system and proliferative disorders
-
CAS
-
Krejĉí P.; Hradil P.; Hlaváĉ J.; Hajdúch M. Preparation of 2-phenyl-3-hydroxyquinolin-4(1H)-ones for treatment of immune system and proliferative disorders. WO2008028427 (University of Palacky); CAS: 148:331570.
-
WO2008028427 (University of Palacky)
, vol.148
, pp. 331570
-
-
Krejĉí, P.1
Hradil, P.2
Hlaváĉ, J.3
Hajdúch, M.4
-
24
-
-
12844278089
-
Understanding topoisomerase I and II in terms of QSAR
-
Rajeshwar P. V. Understanding topoisomerase I and II in terms of QSAR. Bioorg. Med. Chem., 2005, 13, 1059-1067.
-
(2005)
Bioorg. Med. Chem
, vol.13
, pp. 1059-1067
-
-
Rajeshwar, P.V.1
-
25
-
-
70349111319
-
-
Iwanowicz, E.J.; Watterson, S.H.; Dhar, T. G. M.; Pitts, W. J.; Gu, H. H. Preparation of 6-(5-oxazolyl)-4(1H)-quinolinones as inhibitors of IMPDH enzyme. WO2001081340 (Bristol-Myers Squibb Company, USA); CAS: 135:344472.
-
Iwanowicz, E.J.; Watterson, S.H.; Dhar, T. G. M.; Pitts, W. J.; Gu, H. H. Preparation of 6-(5-oxazolyl)-4(1H)-quinolinones as inhibitors of IMPDH enzyme. WO2001081340 (Bristol-Myers Squibb Company, USA); CAS: 135:344472.
-
-
-
-
26
-
-
0000360075
-
The zoochrome of the sponge Verongia aerophoba ("uranidine")
-
Cimino, G.; De Rosa, S.; De Stefano, S.; Spinella, A.; Sodano, G. The zoochrome of the sponge Verongia aerophoba ("uranidine"). Tetrahedron Lett., 1984, 25, 2925-2928.
-
(1984)
Tetrahedron Lett
, vol.25
, pp. 2925-2928
-
-
Cimino, G.1
De Rosa, S.2
De Stefano, S.3
Spinella, A.4
Sodano, G.5
-
27
-
-
0028180077
-
3,5,8-Trihydroxy-4-quinolone, a novel natural inhibitor of the reverse transcriptases of human immunodeficiency viruses type 1 and type 2
-
Loya, S.; Rudi, A.; Tal, R.; Kashman, Y.; Loya, Y.; Hizi, A. 3,5,8-Trihydroxy-4-quinolone, a novel natural inhibitor of the reverse transcriptases of human immunodeficiency viruses type 1 and type 2. Arch. Biochem. Biophys., 1994, 309, 315-322.
-
(1994)
Arch. Biochem. Biophys
, vol.309
, pp. 315-322
-
-
Loya, S.1
Rudi, A.2
Tal, R.3
Kashman, Y.4
Loya, Y.5
Hizi, A.6
|