-
1
-
-
0028893480
-
Leukotrienes: Biosynthesis, metabolism, and pathophysiologic significance
-
Mayatepek, E.; Hoffmann, G. F. Leukotrienes: Biosynthesis, metabolism, and pathophysiologic significance. Pediatric Res. 1995, 37, 1-9.
-
(1995)
Pediatric Res.
, vol.37
, pp. 1-9
-
-
Mayatepek, E.1
Hoffmann, G.F.2
-
2
-
-
0029132046
-
Leukotriene receptor antagonists and biosynthesis inhibitors: Potential breakthrough in asthma therapy
-
Chung, K. F. Leukotriene receptor antagonists and biosynthesis inhibitors: Potential breakthrough in asthma therapy. Eur. Respir. J. 1995, 8, 1203-1213.
-
(1995)
Eur. Respir. J.
, vol.8
, pp. 1203-1213
-
-
Chung, K.F.1
-
4
-
-
0029162007
-
Cysteinyl leukotriene production in anaphylactic reactions
-
Denzlinger, C.; Haberl, C.; Wilmanns, W. Cysteinyl leukotriene production in anaphylactic reactions. Int. Arch. Allergy Immunol. 1995, 108, 158-164.
-
(1995)
Int. Arch. Allergy Immunol.
, vol.108
, pp. 158-164
-
-
Denzlinger, C.1
Haberl, C.2
Wilmanns, W.3
-
5
-
-
0027972565
-
Leukotrienes as a target in asthma therapy
-
Chanarin, N.; Johnston, S. L. Leukotrienes as a target in asthma therapy. Drugs 1994, 47, 12-24.
-
(1994)
Drugs
, vol.47
, pp. 12-24
-
-
Chanarin, N.1
Johnston, S.L.2
-
6
-
-
0029156140
-
Leukotrienes as therapeutic target in asthma
-
Pauwels, R. A.; Joos, G. F.; Kips, J. C. Leukotrienes as therapeutic target in asthma. Allergy 1995, 30, 615-622.
-
(1995)
Allergy
, vol.30
, pp. 615-622
-
-
Pauwels, R.A.1
Joos, G.F.2
Kips, J.C.3
-
7
-
-
0029152856
-
Cysteinyl leukotrienes in asthma: Old mediators up to new tricks
-
Hay, D. W. P.; Torphy, T. J.; Undem, B. J. Cysteinyl leukotrienes in asthma: Old mediators up to new tricks. Trends Pharmacol. Sci. 1995, 16, 304-309.
-
(1995)
Trends Pharmacol. Sci.
, vol.16
, pp. 304-309
-
-
Hay, D.W.P.1
Torphy, T.J.2
Undem, B.J.3
-
8
-
-
0028566488
-
The role of leukotrienes in inflammation
-
Henderson, J. W. R. The role of leukotrienes in inflammation. Ann. Intern. Med. 1994, 121, 684-697.
-
(1994)
Ann. Intern. Med.
, vol.121
, pp. 684-697
-
-
Henderson, J.W.R.1
-
9
-
-
0028838475
-
Leukotriene receptors
-
2 receptors. For a review of leukotriene receptors, see: Metters, K. M. Leukotriene receptors. J. Lipid Mediat. Cell Signal. 1995, 12, 413-427.
-
(1995)
J. Lipid Mediat. Cell Signal.
, vol.12
, pp. 413-427
-
-
Metters, K.M.1
-
10
-
-
0020597565
-
Leukotrienes: Mediators of immediate hyper-sensitivity reactions and inflammation
-
Samuelsson, B. Leukotrienes: Mediators of immediate hyper-sensitivity reactions and inflammation. Science 1983, 220, 568-575.
-
(1983)
Science
, vol.220
, pp. 568-575
-
-
Samuelsson, B.1
-
11
-
-
21144478185
-
Peptidoleukotriene antagonists: State of the art
-
Sprecher, V. A.; Beck, A.; Gerspacher, M.; Bray, M. A. Peptidoleukotriene antagonists: state of the art. Chimia 1992, 46, 304-311.
-
(1992)
Chimia
, vol.46
, pp. 304-311
-
-
Sprecher, V.A.1
Beck, A.2
Gerspacher, M.3
Bray, M.A.4
-
12
-
-
0029946682
-
Modulators of leukotriene biosynthesis and receptor activation
-
Brooks, C. D. W.; Summers, J. B. Modulators of leukotriene biosynthesis and receptor activation. J. Med. Chem. 1996, 39, 2629-2654.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2629-2654
-
-
Brooks, C.D.W.1
Summers, J.B.2
-
13
-
-
0028915887
-
Clinical activity of leukotriene inhibitors
-
Harris, R. R.; Carter, G. W.; Bell, R. L.; Moore, J. L.; Brooks, D. W. Clinical activity of leukotriene inhibitors. Int. J. Immunopharmacol. 1995, 17, 147-156.
-
(1995)
Int. J. Immunopharmacol.
, vol.17
, pp. 147-156
-
-
Harris, R.R.1
Carter, G.W.2
Bell, R.L.3
Moore, J.L.4
Brooks, D.W.5
-
14
-
-
0029049530
-
Treatment of chronic stable asthma with drugs active on the 5-lipoxygenase pathway
-
Drazen, J. M.; Israel, E. Treatment of chronic stable asthma with drugs active on the 5-lipoxygenase pathway. Int. Arch. Allergy Immunol. 1995, 707, 319-320.
-
(1995)
Int. Arch. Allergy Immunol.
, vol.707
, pp. 319-320
-
-
Drazen, J.M.1
Israel, E.2
-
15
-
-
0028918147
-
Clinical studies with agents active on the 5-lipoxy-genase pathway
-
Drazen, J. Clinical studies with agents active on the 5-lipoxy-genase pathway. Allergy 1995, 50, 22-26.
-
(1995)
Allergy
, vol.50
, pp. 22-26
-
-
Drazen, J.1
-
16
-
-
0023237296
-
The leukotrienes: Prospects for therapy against a unique family of pathophysiological mediators
-
Gillard, J. W.; Guindon, Y. The leukotrienes: Prospects for therapy against a unique family of pathophysiological mediators. Drugs Future 1987, 12, 453-474.
-
(1987)
Drugs Future
, vol.12
, pp. 453-474
-
-
Gillard, J.W.1
Guindon, Y.2
-
17
-
-
0029121449
-
Cysteinyl leukotrienes in asthma: Current state of therapeutic evaluation
-
Taylor, I. K. Cysteinyl leukotrienes in asthma: Current state of therapeutic evaluation. Thorax 1995, 50, 1005-1010.
-
(1995)
Thorax
, vol.50
, pp. 1005-1010
-
-
Taylor, I.K.1
-
18
-
-
0023183449
-
Leukotriene receptor antagonists 1. Synthesis and structure-activity relationships of alkoxyacetophenone derivatives
-
Marshall, W. S.; Goodson, T.; Cullinan, G. J.; Swanson-Bean, D.; Haisch, K. D.; Rinkema, L. E.; Fleisch, J. H. Leukotriene receptor antagonists 1. Synthesis and structure-activity relationships of alkoxyacetophenone derivatives. J. Med. Chem. 1987, 30, 682-689.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 682-689
-
-
Marshall, W.S.1
Goodson, T.2
Cullinan, G.J.3
Swanson-Bean, D.4
Haisch, K.D.5
Rinkema, L.E.6
Fleisch, J.H.7
-
19
-
-
0011388496
-
SK&F 104353 2(S)-Hydroxy-3(R)-(2-carboxyethylthio)-3-[2-(8-phenyloctyl)phenyl]propanoic acid
-
Hay, D. W. P. SK&F 104353 2(S)-Hydroxy-3(R)-(2-carboxyethylthio)-3-[2-(8-phenyloctyl)phenyl]propanoic acid. Drugs Future 1990, 15, 240-244.
-
(1990)
Drugs Future
, vol.15
, pp. 240-244
-
-
Hay, D.W.P.1
-
20
-
-
0023259921
-
High-affinity leukotriene receptor antagonists. Synthesis and pharmacological characterization of 2-hydroxy-3-[(2-carboxyethyl)thio]-3-[2-(8-phenyloctyl)phenyl]propanoic acid
-
Gleason, J. G.; Hall, R. F.; Perchonock, C. D.; Erhard, K. F.; Frazee, J. S.; Ku, T. W.; Kondrad, K.; McCarthy, M. E.; Mong, S.; Crooke, S. T.; Chi-Rosso, G.; Wasserman, M. A.; Torphy, T. J.; Muccitelli, R. M.; Hay, D. W.; Tucker, S. S.; Vickery-Clark, L. High-affinity leukotriene receptor antagonists. Synthesis and pharmacological characterization of 2-hydroxy-3-[(2-carboxyethyl)thio]-3-[2-(8-phenyloctyl)phenyl]propanoic acid. J. Med. Chem. 1987, 30, 959-961.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 959-961
-
-
Gleason, J.G.1
Hall, R.F.2
Perchonock, C.D.3
Erhard, K.F.4
Frazee, J.S.5
Ku, T.W.6
Kondrad, K.7
McCarthy, M.E.8
Mong, S.9
Crooke, S.T.10
Chi-Rosso, G.11
Wasserman, M.A.12
Torphy, T.J.13
Muccitelli, R.M.14
Hay, D.W.15
Tucker, S.S.16
Vickery-Clark, L.17
-
21
-
-
0022504988
-
Synthesis and structure-activity relationship studies of a series of 5-aryl-4,6-dithianonanedioic acids and related compounds: A novel class of leukotriene antagonists
-
Perchonock, C. D.; Uzinskas, I.; McCarthy, M. E.; Erhard, K. F.; Gleason, J. G.; Wasserman, M. A.; Muccitelli, R. M.; DeVan, J. F.; Tucker, S. S.; Vickery, L. M.; Kirchner, T.; Weichman, B. M.; Mong, S.; Scott, M. O.; Chi-Rosso, G.; Wu, H. J.; Crooke, S. T.; Newton, J. F. Synthesis and structure-activity relationship studies of a series of 5-aryl-4,6-dithianonanedioic acids and related compounds: A novel class of leukotriene antagonists. J. Med. Chem. 1986, 29, 1442-1452.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1442-1452
-
-
Perchonock, C.D.1
Uzinskas, I.2
McCarthy, M.E.3
Erhard, K.F.4
Gleason, J.G.5
Wasserman, M.A.6
Muccitelli, R.M.7
Devan, J.F.8
Tucker, S.S.9
Vickery, L.M.10
Kirchner, T.11
Weichman, B.M.12
Mong, S.13
Scott, M.O.14
Chi-Rosso, G.15
Wu, H.J.16
Crooke, S.T.17
Newton, J.F.18
-
22
-
-
0026632349
-
4) receptor antagonists
-
4) receptor antagonists. J. Med. Chem. 1992, 35, 1191-1200.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1191-1200
-
-
Harper, R.W.1
Herron, D.K.2
Bollinger, N.G.3
Sawyer, J.S.4
Baldwin, R.F.5
Roman, C.R.6
Rinkema, L.E.7
Fleisch, J.H.8
-
23
-
-
0025810619
-
Sulukast (LY-170680): Leukotriene D4/E4 antagonist
-
Baker, S. R.; Boot, J. R.; Wishart, G. Sulukast (LY-170680): Leukotriene D4/E4 antagonist. Drugs Future 1991, 16, 432-436.
-
(1991)
Drugs Future
, vol.16
, pp. 432-436
-
-
Baker, S.R.1
Boot, J.R.2
Wishart, G.3
-
24
-
-
0027171068
-
A new structural analogue antagonist of peptide leukotrienes. the discovery of BAY x7195
-
Abram, T. S.; Boshagen, H.; Futler, J. E.; Cuthbert, N. J.; Francis, H. P.; Gardiner, P. F.; Hartwig, W.; Kluender, H. C.; Norman, P.; Meier, H.; Rosentreter, U.; Schlemmer, K. H.; Tudhope, S. R.; Taylor, W. A. A new structural analogue antagonist of peptide leukotrienes. The discovery of BAY x7195. Bioorg. Med. Chem. Lett. 1993, 3, 1517-1522.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 1517-1522
-
-
Abram, T.S.1
Boshagen, H.2
Futler, J.E.3
Cuthbert, N.J.4
Francis, H.P.5
Gardiner, P.F.6
Hartwig, W.7
Kluender, H.C.8
Norman, P.9
Meier, H.10
Rosentreter, U.11
Schlemmer, K.H.12
Tudhope, S.R.13
Taylor, W.A.14
-
25
-
-
0025195923
-
4 antagonist activity of bicyclic and monocyclic cyclopentylurethane and cyclopentylacetamide N-arylsulfonyl amides
-
4 antagonist activity of bicyclic and monocyclic cyclopentylurethane and cyclopentylacetamide N-arylsulfonyl amides. J. Med. Chem. 1990, 33, 2621-2629.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2621-2629
-
-
Matassa, V.G.1
Brown, F.J.2
Bernstein, P.R.3
Shapiro, H.S.4
Maduskuie, J.T.P.5
Cronk, L.A.6
Vacek, E.P.7
Yee, Y.K.8
Snyder, D.W.9
Krell, R.D.10
Lerman, C.L.11
Maloney, J.J.12
-
26
-
-
0025099864
-
A novel series of selective leukotriene antagonists: Exploration and optimization of the acidic region in 1,6-disubstituted indoles and indazoles
-
Yee, Y. K.; Bernstein, P. R.; Adams, E. J.; Brown, F. J.; Cronk, L. A.; Hebbel, K. C.; Vacek, E. P.; Krell, R. D.; Snyder, D. W. A novel series of selective leukotriene antagonists: Exploration and optimization of the acidic region in 1,6-disubstituted indoles and indazoles. J. Med. Chem. 1990, 33, 2437-2451.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2437-2451
-
-
Yee, Y.K.1
Bernstein, P.R.2
Adams, E.J.3
Brown, F.J.4
Cronk, L.A.5
Hebbel, K.C.6
Vacek, E.P.7
Krell, R.D.8
Snyder, D.W.9
-
27
-
-
0025302763
-
Evolution of a series of peptidoleukotriene antagonists: Synthesis and structure-activity relationships of 1,6-disubstituted indoles and indazoles
-
Brown, F. J.; Yee, Y. K.; Cronk, L. A.; Hebbel, K. C.; Krell, R. D.; Snyder, D. W. Evolution of a series of peptidoleukotriene antagonists: Synthesis and structure-activity relationships of 1,6-disubstituted indoles and indazoles. J. Med. Chem. 1990, 33, 1771-1781.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 1771-1781
-
-
Brown, F.J.1
Yee, Y.K.2
Cronk, L.A.3
Hebbel, K.C.4
Krell, R.D.5
Snyder, D.W.6
-
28
-
-
0027536862
-
Substituted 3-(Phenylmethyl)-lH-indole-5-carboxamides and l-(Phenylmethyl)indole-6-carboxamides as potent, selective, orally active antagonists of the peptidoleukotrienes
-
Jacobs, R. T.; Brown, F. J.; Cronk, L. A.; Aharony, D.; Buckner, C. K.; Kusner, E. J.; Kirkland, K. M.; Neilson, K. L. Substituted 3-(Phenylmethyl)-lH-indole-5-carboxamides and l-(Phenylmethyl)indole-6-carboxamides as potent, selective, orally active antagonists of the peptidoleukotrienes. J. Med. Chem. 1993, 36, 394-409.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 394-409
-
-
Jacobs, R.T.1
Brown, F.J.2
Cronk, L.A.3
Aharony, D.4
Buckner, C.K.5
Kusner, E.J.6
Kirkland, K.M.7
Neilson, K.L.8
-
29
-
-
0010641260
-
-
Merluzi, V. J., Adams, J., Eds.; Birkhauser: Boston
-
Brown, F. J. In The Search for Antiinflammatory Drugs. Case Histories from Concept to Clinic; Merluzi, V. J., Adams, J., Eds.; Birkhauser: Boston, 1995; pp 161-189.
-
(1995)
The Search for Antiinflammatory Drugs. Case Histories from Concept to Clinic
, pp. 161-189
-
-
Brown, F.J.1
-
30
-
-
8544274756
-
A potent antagonist of the slow-reacting substance of anaphylaxis
-
Toda, M.; Nakai, H.; Kosuge, S.; Konno, M.; Arai, Y.; Miyamoto, T.; Obata, T.; Katsube, N.; Kawasaki, A. A potent antagonist of the slow-reacting substance of anaphylaxis. Adv. Prostaglandin Thromboxane Leukotriene Res. 1985, 15, 307-308.
-
(1985)
Adv. Prostaglandin Thromboxane Leukotriene Res.
, vol.15
, pp. 307-308
-
-
Toda, M.1
Nakai, H.2
Kosuge, S.3
Konno, M.4
Arai, Y.5
Miyamoto, T.6
Obata, T.7
Katsube, N.8
Kawasaki, A.9
-
31
-
-
0023848175
-
New potent antagonists of leukotrienes C4 and D4. 1. Synthesis and structure-activity relationships
-
Nakai, H.; Konno, M.; Kosuge, S.; Sakuyama, S.; Toda, M.; Arai, Y.; Obata, T.; Katsube, N.; Miyamoto, T.; Okegawa, T.; Kawasaki, A. New potent antagonists of leukotrienes C4 and D4. 1. Synthesis and structure-activity relationships. J. Med. Chem. 1988, 31, 84-91.
-
(1988)
J. Med. Chem.
, vol.31
, pp. 84-91
-
-
Nakai, H.1
Konno, M.2
Kosuge, S.3
Sakuyama, S.4
Toda, M.5
Arai, Y.6
Obata, T.7
Katsube, N.8
Miyamoto, T.9
Okegawa, T.10
Kawasaki, A.11
-
32
-
-
0028237854
-
Pharmacological profile of the novel, potent and selective peptide leukotriene antagonist (E)-2,2-Diethyl-3′-[2-[2-4-isopropyl;thiazolyl]ethenyl]siccinanilic acid
-
Yamada, N.; Yamada, K.; Takahashi, K.; Nakao, E.; Kadowaki, S.; Umezu, K. Pharmacological profile of the novel, potent and selective peptide leukotriene antagonist (E)-2,2-Diethyl-3′-[2-[2-(4-isopropyl;thiazolyl]ethenyl]siccinanilic acid. Arzneim.-Forsch. / Drug Res. 1994, 44, 749-753.
-
(1994)
Arzneim.-Forsch. / Drug Res.
, vol.44
, pp. 749-753
-
-
Yamada, N.1
Yamada, K.2
Takahashi, K.3
Nakao, E.4
Kadowaki, S.5
Umezu, K.6
-
34
-
-
0025879330
-
4 receptor binding affinity
-
4 receptor binding affinity. J. Med. Chem. 1991, 34, 1704-1707.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1704-1707
-
-
Huang, F.C.1
Galemmo, J.R.A.2
Poli, G.B.3
Learn, K.S.4
Morrissette, M.M.5
Johnson, J.W.H.6
Dankulich, W.P.7
Campbell, H.F.8
Carnathan, G.W.9
Vaninwegen, R.G.10
-
35
-
-
0028888059
-
4 receptor antagonist devoid of peroxisomal enzyme induction
-
4 receptor antagonist devoid of peroxisomal enzyme induction. Bioorg. Med. Chem. Lett. 1995, 5, 283-288.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 283-288
-
-
Labelle, M.1
Belley, M.2
Gareau, Y.3
Gauthier, J.Y.4
Guay, D.5
Gordon, R.6
Grossman, S.G.7
Jones, T.R.8
Leblanc, Y.9
McAuliffe, M.10
McFarlane, C.11
Masson, P.12
Metters, K.M.13
Oiumet, N.14
Patrick, D.H.15
Piechuta, H.16
Rochette, C.17
Sawyer, N.18
Xiang, Y.B.19
Pickett, C.B.20
Ford-Hutchinson, A.W.21
Zamboni, R.J.22
Young, R.N.23
more..
-
36
-
-
0027005062
-
Strategies in the design of peptidoleukotriene antagonists
-
Sprecher, V. A.; Beck, A.; Gerspacher, M.; Sallmann, A.; Anderson, G. P.; Subramanian, N.; Niederhauser, U.; Bray, M. A. Strategies in the design of peptidoleukotriene antagonists. J. Lipid Mediators 1993, 6, 265-273.
-
(1993)
J. Lipid Mediators
, vol.6
, pp. 265-273
-
-
Sprecher, V.A.1
Beck, A.2
Gerspacher, M.3
Sallmann, A.4
Anderson, G.P.5
Subramanian, N.6
Niederhauser, U.7
Bray, M.A.8
-
37
-
-
0023790375
-
4 antagonists
-
4 antagonists. Drugs Future 1988, 13, 745-759.
-
(1988)
Drugs Future
, vol.13
, pp. 745-759
-
-
Young, R.N.1
-
38
-
-
77957032892
-
-
Fujita, T., Ed.
-
Terada, H.; Goto, S.; Hori, H.; Taira, Z. In QSAR and Drug Design - New Developments and Applications; Fujita, T., Ed.; 1995; pp 341-367.
-
(1995)
QSAR and Drug Design - New Developments and Applications
, pp. 341-367
-
-
Terada, H.1
Goto, S.2
Hori, H.3
Taira, Z.4
-
39
-
-
0005385473
-
-
Sanz, F., Giraldo, J., Manaut, F., Eds.; Prous Science Publishers: Barcelona
-
Palomer, A.; Giolitti, A.; Garcia, M. L.; Fos, E.; Cabre, F.; Mauleon, D.; Carganico, G. In QSAR and Molecular Modelling: Concepts, Computational Tools and Biological Applications; Sanz, F., Giraldo, J., Manaut, F., Eds.; Prous Science Publishers: Barcelona, 1995; pp 444-450.
-
(1995)
QSAR and Molecular Modelling: Concepts, Computational Tools and Biological Applications
, pp. 444-450
-
-
Palomer, A.1
Giolitti, A.2
Garcia, M.L.3
Fos, E.4
Cabre, F.5
Mauleon, D.6
Carganico, G.7
-
40
-
-
0026298527
-
OVID and SUPER: Two overlap programs for drug design
-
Hermann, R. B.; Herron, D. K. OVID and SUPER: Two overlap programs for drug design. J. Comput. -Aided. Mol. Des. 1991, 5, 511-524.
-
(1991)
J. Comput. -Aided. Mol. Des.
, vol.5
, pp. 511-524
-
-
Hermann, R.B.1
Herron, D.K.2
-
43
-
-
0030996616
-
1 (LTD4) receptor antagonists
-
1 (LTD4) receptor antagonists. J. Med. Chem. 1997, 40, 1075-1089.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1075-1089
-
-
Zwaagstra, M.E.1
Timmerman, H.2
Tamura, M.3
Tohma, T.4
Wada, Y.5
Onogi, K.6
Zhang, M.Q.7
-
46
-
-
0020509304
-
Synthesis of 6- And 8-phenyl-substituted flavonoids
-
Matsumura, H.; Tsuchiya, T.; Takeda, T.; Imafuku, K. Synthesis of 6- and 8-phenyl-substituted flavonoids. Bull. Chem. Soc. Jpn. 1983, 56, 2037-2043.
-
(1983)
Bull. Chem. Soc. Jpn.
, vol.56
, pp. 2037-2043
-
-
Matsumura, H.1
Tsuchiya, T.2
Takeda, T.3
Imafuku, K.4
-
47
-
-
0001469447
-
Studies on 3-acylcatechols. II. A new synthesis of 8-hydroxyflavone
-
Awad, W. I.; El-Neweihy, M. F.; Selim, S. F. Studies on 3-acylcatechols. II. A new synthesis of 8-hydroxyflavone. Chem. Ind. 1960, 25, 1333-1336.
-
(1960)
Chem. Ind.
, vol.25
, pp. 1333-1336
-
-
Awad, W.I.1
El-Neweihy, M.F.2
Selim, S.F.3
-
48
-
-
0008300465
-
An efficient procedure for cyclisation of 2′-hydroxychalcones into flavones
-
Makrandi, J. K. An efficient procedure for cyclisation of 2′-hydroxychalcones into flavones. Chem. Ind. 1989, 607.
-
(1989)
Chem. Ind.
, pp. 607
-
-
Makrandi, J.K.1
-
49
-
-
15644380916
-
Synthesis of 2-(2-quinoxalyl) chromone derivatives
-
Hsu, K. K.; Chang, S. F. Synthesis of 2-(2-quinoxalyl) chromone derivatives. Taiwan K'o Hsuch 1976, 30, 146-52.
-
(1976)
Taiwan K'o Hsuch
, vol.30
, pp. 146-152
-
-
Hsu, K.K.1
Chang, S.F.2
-
50
-
-
85077848579
-
Dehydrogenation of chromanones and flavanones by DDQ: A facile method for the synthesis of chromones and flavones
-
Shanker, C. G.; Mallaiah, B. V.; Srimannarayana, G. Dehydrogenation of chromanones and flavanones by DDQ: A facile method for the synthesis of chromones and flavones. Synthesis 1983, 310-311.
-
(1983)
Synthesis
, pp. 310-311
-
-
Shanker, C.G.1
Mallaiah, B.V.2
Srimannarayana, G.3
-
51
-
-
0008341762
-
Cyclodehydrogenation of 2′-hydroxychalcones with DDQ: A simple route for flavones and aurones
-
Imafuku, K.; Honda, M.; McOmie, J. F. W. Cyclodehydrogenation of 2′-hydroxychalcones with DDQ: A simple route for flavones and aurones. Synthesis 1987, 199-201.
-
(1987)
Synthesis
, pp. 199-201
-
-
Imafuku, K.1
Honda, M.2
McOmie, J.F.W.3
-
52
-
-
33748899925
-
Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones
-
Baker, W. Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones. J. Chem. Soc. 1933, 1381-1389.
-
(1933)
J. Chem. Soc.
, pp. 1381-1389
-
-
Baker, W.1
-
53
-
-
0024557407
-
Flavones. 2. Synthesis and structure-activity relationship of flavodilol and its analogues, a novel class of antihypertensive agents with catecholamine depleting properties
-
Wu, E. S. C.; Cole, T. E.; Davidson, T. A.; Dailey, M. A.; Doring, K. G.; Fedorchuk, M.; Loch, J. T.; Thomas, T. L.; Blosser, F. C.; Borrelli, A. R.; Kinsolving, C. R.; Parker, R. B.; Strand, J. C.; Watkins, B. E. Flavones. 2. Synthesis and structure-activity relationship of flavodilol and its analogues, a novel class of antihypertensive agents with catecholamine depleting properties. J. Med. Chem. 1989, 32, 183-192.
-
(1989)
J. Med. Chem.
, vol.32
, pp. 183-192
-
-
Wu, E.S.C.1
Cole, T.E.2
Davidson, T.A.3
Dailey, M.A.4
Doring, K.G.5
Fedorchuk, M.6
Loch, J.T.7
Thomas, T.L.8
Blosser, F.C.9
Borrelli, A.R.10
Kinsolving, C.R.11
Parker, R.B.12
Strand, J.C.13
Watkins, B.E.14
-
54
-
-
0026668233
-
(Aminoalkoxy)chromones. Selective s-receptor ligands
-
Erickson, R. H.; Natalie, K. J., Jr.; Bock, W.; Lu, Z.; Farzin, F.; Sherill, R. G.; Meloni, D. J.; Patch, R. J.; Rzesotarski, W. J.; Clifton, J.; Pontecorvo, M. J.; Bailey, M. A.; Naper, K.; Karbon, W. (Aminoalkoxy)chromones. Selective s-receptor ligands. J. Med. Chem. 1992, 35, 1526-1535.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1526-1535
-
-
Erickson, R.H.1
Natalie Jr., K.J.2
Bock, W.3
Lu, Z.4
Farzin, F.5
Sherill, R.G.6
Meloni, D.J.7
Patch, R.J.8
Rzesotarski, W.J.9
Clifton, J.10
Pontecorvo, M.J.11
Bailey, M.A.12
Naper, K.13
Karbon, W.14
-
55
-
-
0027716069
-
A convenient large-scale synthesis of 5-methoxyflavone and its application to analog preparation
-
Ares, J. J.; Outt, P. E.; Kakodkar, S. V.; Buss, R. C.; Geiger, J. C. A convenient large-scale synthesis of 5-methoxyflavone and its application to analog preparation. J. Org. Chem. 1993, 58, 7903-7905.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 7903-7905
-
-
Ares, J.J.1
Outt, P.E.2
Kakodkar, S.V.3
Buss, R.C.4
Geiger, J.C.5
-
56
-
-
0017874849
-
Antiallergic agents. I. Substituted 4-oxo-4H-1-benzopyran-6-carboxylic acids
-
Doria, G.; Romeo, C.; Giraldi, P.; Lauria, F.; Sberze, P.; Tibolla, M.; Corno, M. L.; Cadelli, G.; Montoro, C. Antiallergic agents. I. Substituted 4-oxo-4H-1-benzopyran-6-carboxylic acids. Ear. J. Med. Chem.-Chim. Ther. 1978, 13, 33-39.
-
(1978)
Ear. J. Med. Chem.-Chim. Ther.
, vol.13
, pp. 33-39
-
-
Doria, G.1
Romeo, C.2
Giraldi, P.3
Lauria, F.4
Sberze, P.5
Tibolla, M.6
Corno, M.L.7
Cadelli, G.8
Montoro, C.9
-
57
-
-
0032559886
-
4) antagonist model with an incorporated amino acid residue from the receptor
-
4) antagonist model with an incorporated amino acid residue from the receptor. J. Med. Chem. 1998, 41, 1439-1445.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1439-1445
-
-
Zwaagstra, M.E.1
Schoenmakers, S.H.H.F.2
Nederkoorn, P.H.J.3
Gelens, E.4
Timmerman, H.5
Zhang, M.-Q.6
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