-
1
-
-
0033635776
-
Potassium channels molecular defects diseases therapeutic opportunities
-
Shieh, C.-C.; Coghlan, M.J.; Sullivan, J.P.; Gopalakrishnan, M. Potassium channels, molecular defects, diseases, and therapeutic opportunities. Pharmacol. Rev. 2000, 52, 557-593.
-
(2000)
Pharmacol. Rev.
, vol.52
, pp. 557-593
-
-
Shieh, C.-C.1
Coghlan, M.J.2
Sullivan, J.P.3
Gopalakrishnan, M.4
-
2
-
-
0036240546
-
Potassium channels gene family therapeutic relevance high-throughput screening technologies drug discovery
-
Ford, J.W.; Stevens, E.B.; Treherne, J.M.; Packer, J.; Bushfield, M. Potassium channels, gene family, therapeutic relevance, high-throughput screening technologies and drug discovery. Progr. Drug Res. 2002, 58, 133-168.
-
(2002)
Progr. Drug Res.
, vol.58
, pp. 133-168
-
-
Ford, J.W.1
Stevens, E.B.2
Treherne, J.M.3
Packer, J.4
Bushfield, M.5
-
3
-
-
0035942510
-
Recent developments in the biology medicinal chemistry of potassium channel modulators update from a decade of progress
-
Coghlan, M.J.; Carroll, W.A.; Gopalakrishnan, M. Recent developments in the biology and medicinal chemistry of potassium channel modulators, update from a decade of progress. J. Med. Chem. 2001, 44, 1627-1653.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 1627-1653
-
-
Coghlan, M.J.1
Carroll, W.A.2
Gopalakrishnan, M.3
-
5
-
-
0026731038
-
Modulation of potassium channels by organic molecules
-
Atwal, K. Modulation of potassium channels by organic molecules. Med. Res. Rev. 1992, 6, 569-591.
-
(1992)
Med. Res. Rev.
, vol.6
, pp. 569-591
-
-
Atwal, K.1
-
6
-
-
0028313317
-
Potassium channel activators, pharmacological methods, models, and structure-activity relationships
-
Evans, J.M.; Taylor, S.G. Potassium channel activators, pharmacological methods, models, and structure-activity relationships. Progr. Med. Chem. 1994, 31, 412-446.
-
(1994)
Progr. Med. Chem.
, vol.31
, pp. 412-446
-
-
Evans, J.M.1
Taylor, S.G.2
-
8
-
-
0041889629
-
Conformational analysis of potassium channel activators
-
Evans, J.M.; Hamilton, T.C.; Longman, S.D.; Stemp, G.; Eds.; Taylor & Francis: London
-
Edge, C.M. Conformational analysis of potassium channel activators. In Potassium channels and their modulators. Evans, J.M.; Hamilton, T.C.; Longman, S.D.; Stemp, G.; Eds.; Taylor & Francis: London, 1996; pp. 79-97.
-
(1996)
Potassium Channels and Their Modulators
, pp. 79-97
-
-
Edge, C.M.1
-
9
-
-
0023030013
-
Synthesis antihypertensive activity of 4-(cyclic amido)-2H-1-benzopyrans
-
Ashwood, V.A.; Buckingham, R.E.; Cassidy, F.; Evans, J.M.; Faruk, E.A.; Hamilton, T.C.; Nash, D.J.; Stemp, G.; Willcocks, K. Synthesis and antihypertensive activity of 4-(cyclic amido)-2H-1-benzopyrans. J. Med. Chem. 1986, 29, 2194-2201.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 2194-2201
-
-
Ashwood, V.A.1
Buckingham, R.E.2
Cassidy, F.3
Evans, J.M.4
Faruk, E.A.5
Hamilton, T.C.6
Nash, D.J.7
Stemp, G.8
Willcocks, K.9
-
10
-
-
0007873287
-
Discovery and development of cromakalim and related potassium channel activators
-
Ganellin, C.R.; Roberts, S.M.; Eds; Academic Press: London
-
Stemp G, Evans JM. Discovery and development of cromakalim and related potassium channel activators. In Medicinal Chemistry. The role of organic chemistty in drug research. Ganellin, C.R.; Roberts, S.M.; Eds; Academic Press: London, 1993; pp. 141-162.
-
(1993)
Medicinal Chemistry. The Role of Organic Chemistry in Drug Research
, pp. 141-162
-
-
Stemp, G.1
Evans, J.M.2
-
11
-
-
0004890494
-
Structure-activity relationships of benzopyran based potassium channel activators
-
Evans J.M.; Hamilton T.C.; Longman S.D.; Stemp G. Eds.; Taylor Francis: London
-
Evans, J.M.; Stemp, G. Structure-activity relationships of benzopyran based potassium channel activators. In Potassium channels and their modulators. Evans, J.M.; Hamilton, T.C.; Longman, S.D.; Stemp, G., Eds.; Taylor & Francis: London, 1996; pp. 27-55.
-
(1996)
Potassium Channels Their Modulators
, pp. 27-55
-
-
Evans, J.M.1
Stemp, G.2
-
12
-
-
0025048803
-
Relaxant activity of 4-amido-3,4-dihydro-2H-1-benzopyran-3-ols and 4-amido-2H-1-benzopyrans on guinea pig isolated trachealis
-
Buckle; D.R.; Arch, J.R.S.; Fenwick, A.E.; Houge-Frydrych, C.S.V.; Pinto, I.L.; Smith, D.G.; Taylor, S.G.; Tedder, J.M. Relaxant activity of 4-amido-3,4-dihydro-2H-1-benzopyran-3-ols and 4-amido-2H-1-benzopyrans on guinea pig isolated trachealis. J. Med. Chem. 1990, 33, 3028-3034.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 3028-3034
-
-
Buckle, D.R.1
Arch, J.R.S.2
Fenwick, A.E.3
Houge-Frydrych, C.S.V.4
Pinto, I.L.5
Smith, D.G.6
Taylor, S.G.7
Tedder, J.M.8
-
13
-
-
0025015260
-
Synthesis antihypertensive activity of 4-(12-dihydro-2-oxo-1-pyridyl)-2 H-1- benzopyrans related compounds new potassium channel activators
-
Bergmann, R.; Gericke, R. Synthesis and antihypertensive activity of 4-(1,2-dihydro-2-oxo-1-pyridyl)-2 H-1- benzopyrans and related compounds, new potassium channel activators. J. Med. Chem. 1990, 33, 492-504.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 492-504
-
-
Bergmann, R.1
Gericke, R.2
-
14
-
-
0027230173
-
Synthesis biological activity of spirocyclic benzopyran imidazolone potassium channel openers
-
Gadwood, R.C.; Kamdar, B.V.; Cipkus Dubray, L.A.; Wolfe, M.L.; Smith, M.P.; Watt, W.; Mizsak, S.A.; Groppi, V.E. Synthesis and biological activity of spirocyclic benzopyran imidazolone potassium channel openers. J. Med. Chem. 1993, 36, 1480-1487.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 1480-1487
-
-
Gadwood, R.C.1
Kamdar, B.V.2
Cipkus Dubray, L.A.3
Wolfe, M.L.4
Smith, M.P.5
Watt, W.6
Mizsak, S.A.7
Groppi, V.E.8
-
15
-
-
0029165118
-
Chiral spirocyclic benzopyran potassium channel openers evidence for the active conformation of levcromakalim
-
Gadwood, R.C.; Thomasco, L.M.; Groppi, V.E.; Burnett, B.A.; Smith, M.P.; Watt, W. Chiral spirocyclic benzopyran potassium channel openers, evidence for the active conformation of levcromakalim. Bioorg. Med. Chem. Lett. 1995, 5, 2101-2104.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2101-2104
-
-
Gadwood, R.C.1
Thomasco, L.M.2
Groppi, V.E.3
Burnett, B.A.4
Smith, M.P.5
Watt, W.6
-
16
-
-
0025113459
-
4-Heterocyclyloxy-2H-1-benzopyran potassium channel activators
-
Bergmann, R.; Eiermann, V.; Gericke, R. 4-Heterocyclyloxy-2H-1-benzopyran potassium channel activators. J. Med. Chem. 1990, 33, 2759-2767.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 2759-2767
-
-
Bergmann, R.1
Eiermann, V.2
Gericke, R.3
-
17
-
-
0025983673
-
3-Methyl-2H-1-benzopyran potassium channel activators
-
Gericke, R.; Harting, J.; Lues, I.; Schittenhelm, C. 3-Methyl-2H-1-benzopyran potassium channel activators. J. Med. Chem. 1991, 34, 3074-3085.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 3074-3085
-
-
Gericke, R.1
Harting, J.2
Lues, I.3
Schittenhelm, C.4
-
18
-
-
0028276279
-
Benzopyran potassium channel activators related to cromakalim - Heterocyclic amide replacements at position 4
-
Burrell, G., Evans, J.M.; Hadley, M.S.; Hicks, F.; Stemp, G. Benzopyran potassium channel activators related to cromakalim - heterocyclic amide replacements at position 4. Bioorg. Med. Chem. Lett. 1994, 4, 1285-1290.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, pp. 1285-1290
-
-
Burrell, G.1
Evans, J.M.2
Hadley, M.S.3
Hicks, F.4
Stemp, G.5
-
20
-
-
0027370493
-
+ channel opener with long duration of action less tachycardia
-
+ channel opener with long duration of action and less tachycardia. Bioorg. Med. Chem. Letters 1993, 3, 2005-2010.
-
(1993)
Bioorg. Med. Chem. Letters
, vol.3
, pp. 2005-2010
-
-
Koga, H.1
Sato, H.2
Imagawa, J.3
Ishizawa, T.4
Yoshida, S.5
Sugo, I.6
Taka, N.7
Takahashi, T.8
Nabata, H.9
-
22
-
-
0027430212
-
The effect of a novel benzopyran derivative KC 399 on the isolated guinea-pig trachealis human bronchi
-
Imagawa, J.; Yoshida, S.; Koga, T.; Kamei, K.; Nabata, H. The effect of a novel benzopyran derivative, KC 399, on the isolated guinea-pig trachealis and human bronchi. Gen. Pharmacol 1993, 24, 1505-1512.
-
(1993)
Gen. Pharmacol.
, vol.24
, pp. 1505-1512
-
-
Imagawa, J.1
Yoshida, S.2
Koga, T.3
Kamei, K.4
Nabata, H.5
-
23
-
-
0034131290
-
+ channel openers
-
+ channel openers. Bioorg. Med. Chem. 2000, 8, 1393-1405.
-
(2000)
Bioorg. Med. Chem.
, vol.8
, pp. 1393-1405
-
-
Taka, N.1
Koga, H.2
Sato, H.3
Ishizawa, T.4
Takahashi, T.5
Imagawa, J.6
-
24
-
-
0028596520
-
Comparative molecular field analysis of benzopyran-4-carbothioamide potassium channel openers
-
Ohta, M.; Koga, H.; Sato, H.; Ishizawa, T. Comparative molecular field analysis of benzopyran-4-carbothioamide potassium channel openers. Bioorg. Med Chem. Lett. 1994, 4, 2903-2906.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, pp. 2903-2906
-
-
Ohta, M.1
Koga, H.2
Sato, H.3
Ishizawa, T.4
-
25
-
-
0027290769
-
Structure-activity relationships of 6-substituted benzopyran-4-carbothioamide potassium channel openers
-
Ishizawa, T.; Koga, H.; Ohta, M.; Sato, H.; Makino, T.; Kuromaru, K.; Taka, N.; Takahashi, T.; Sato, T.; Nabata, H. Structure-activity relationships of 6-substituted benzopyran-4-carbothioamide potassium channel openers. Bioorg. Med. Chem. Lett. 1993, 3, 1659-1662.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 1659-1662
-
-
Ishizawa, T.1
Koga, H.2
Ohta, M.3
Sato, H.4
Makino, T.5
Kuromaru, K.6
Taka, N.7
Takahashi, T.8
Sato, T.9
Nabata, H.10
-
26
-
-
0027729074
-
+ channel openers
-
+ channel openers. Bioorg. Med. Chem. Lett. 1993, 3, 2627-2630.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 2627-2630
-
-
Sato, H.1
Koga, H.2
Ishizawa, T.3
Makino, T.4
Kuromaru, K.5
Taka, N.6
Takahashi, T.7
Sato, T.8
Nabata, H.9
-
27
-
-
0026672177
-
Synthesis of homochiral potassium channel openers role of the benzopyranyl 3-hydroxyl group in cromkalim pyridine N-oxides in determining the biological activities of enantiomers
-
Attwood, M.R.; Brown, B.S.; Dunsdon, R.M.; Hurst, D.N.; Jones, P.S.; Kay, P.B. Synthesis of homochiral potassium channel openers, role of the benzopyranyl 3-hydroxyl group in cromkalim and pyridine N-oxides in determining the biological activities of enantiomers. Bioorg. Med. Chem. Lett. 1992, 2, 229-234.
-
(1992)
Bioorg. Med. Chem. Lett.
, vol.2
, pp. 229-234
-
-
Attwood, M.R.1
Brown, B.S.2
Dunsdon, R.M.3
Hurst, D.N.4
Jones, P.S.5
Kay, P.B.6
-
28
-
-
37049080235
-
Conformational steric modifications of the pyran ring of the potassium-channel activator cromakalim
-
Buckle, D.R.; Eggleston, D.S.; Houge-Frydrych, C.S.V.; Pinto, I.L.; Readshaw, S.A.; Smith, D.G.; Webster, R.A.B. Conformational and steric modifications of the pyran ring of the potassium-channel activator cromakalim. J. Chem. Soc. Perkin Trans. I 1991, 1, 2763-2771.
-
(1991)
J. Chem. Soc. Perkin Trans. I
, vol.1
, pp. 2763-2771
-
-
Buckle, D.R.1
Eggleston, D.S.2
Houge-Frydrych, C.S.V.3
Pinto, I.L.4
Readshaw, S.A.5
Smith, D.G.6
Webster, R.A.B.7
-
29
-
-
0025012188
-
Variation in the aromatic ring of cromakalim antihypertensive activity of pyranopyridines 6-alky1-2H-1-benzopyrans
-
Burrell, G.; Cassidy, F.; Evans, J.M.; Lightowler, D.; Stemp, G. Variation in the aromatic ring of cromakalim, antihypertensive activity of pyranopyridines and 6-alky1-2H-1-benzopyrans, J. Med. Chem. 1990, 33, 3023-3027.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 3023-3027
-
-
Burrell, G.1
Cassidy, F.2
Evans, J.M.3
Lightowler, D.4
Stemp, G.5
-
31
-
-
0033602529
-
6-varied benzopyrans as potassium channel activators synthesis vasodilator properties multivariate analysis
-
Mannhold, R.; Cruciani, G.; Weber, H.; Lemoine, H.; Derix, A.; Weichel, C.; Clementi, M. 6-varied benzopyrans as potassium channel activators, synthesis, vasodilator properties and multivariate analysis. J. Med. Chem. 1999, 42, 981-991.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 981-991
-
-
Mannhold, R.1
Cruciani, G.2
Weber, H.3
Lemoine, H.4
Derix, A.5
Weichel, C.6
Clementi, M.7
-
33
-
-
0027155104
-
Thiophene systems. 15. Synthesis antihypertensive activity of 7-(subsituted benzamido)-6-hydroxythieno[32-b]pyrans as new potassium channel activitors
-
Sanfilippo, P.J.; McNally, J.J.; Press, J.B.; Falotico, R.; Giardino, E.; Katz, L.B. Thiophene systems. 15. Synthesis and antihypertensive activity of 7-(subsituted benzamido)-6-hydroxythieno[3,2,-b]pyrans as new potassium channel activitors. Bioorg. Med. Chem. Lett. 1993, 3, 1385-1388.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 1385-1388
-
-
Sanfilippo, P.J.1
McNally, J.J.2
Press, J.B.3
Falotico, R.4
Giardino, E.5
Katz, L.B.6
-
34
-
-
0026494945
-
Thiophene systems. 14. Synthesis antihypertensive activity of novel 7-(cyclic amido)-6-hydroxythieno [32-b]pyrans related compounds as new potassium channel activators
-
Sanfilippo, P.J.; McNally, J.J.; Press, J.B.; Fitzpatrick, L.J.; Urbanski, M.J.; Katz, L.B.; Giardino, E.; Falotico, R.; Salata, J.; Moore Jr, J.B.; Miller, W. Thiophene systems. 14. Synthesis and antihypertensive activity of novel 7-(cyclic amido)-6-hydroxythieno [3,2-b]pyrans and related compounds as new potassium channel activators. J. Med. Chem. 1992, 35, 4425-4433.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 4425-4433
-
-
Sanfilippo, P.J.1
McNally, J.J.2
Press, J.B.3
Fitzpatrick, L.J.4
Urbanski, M.J.5
Katz, L.B.6
Giardino, E.7
Falotico, R.8
Salata, J.9
Moore Jr., J.B.10
Miller, W.11
-
35
-
-
37049088249
-
4-Amido-3,4-dihydro-2H-1-benzothiopyran-3-ols and their sulphoxide and sulphone derivatives - Cromakalim analogs
-
Smith, D.G. 4-Amido-3,4-dihydro-2H-1-benzothiopyran-3-ols and their sulphoxide and sulphone derivatives - cromakalim analogs. J. Chem. Soc. Perkin Trans. I 1990, 3187-3191.
-
(1990)
J. Chem. Soc. Perkin Trans. I
, pp. 3187-3191
-
-
Smith, D.G.1
-
36
-
-
0027237834
-
22-Dialkylnaphthalen-1-ones as new potassium channel activators
-
Almansa, C.;, Gómez, L.A.; Cavalcanti, F.L.; Rodríguez, R.; Carceller, E.; Bartroli, J.; García-Rafanell, J.; Forn, J. 2,2-Dialkylnaphthalen-1-ones as new potassium channel activators. J. Med. Chem. 1993, 36, 2121-2133.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 2121-2133
-
-
Almansa, C.1
Gómez, L.A.2
Cavalcanti, F.L.3
Rodríguez, R.4
Carceller, E.5
Bartroli, J.6
García-Rafanell, J.7
Forn, J.8
-
37
-
-
0027765713
-
+ channels in cardiac myocytes
-
+ channels in cardiac myocytes. J. Pharmacol Exp. Ther. 1993, 267, 1544-1549.
-
(1993)
J. Pharmacol. Exp. Ther.
, vol.267
, pp. 1544-1549
-
-
Yamada, M.1
Terzic, A.2
Findlay, I.3
Jahangir, A.4
Shen, W.K.5
Kurachi, Y.6
-
38
-
-
0028123486
-
Pharmacologic profiles of YM934 a novel potassium channel opener
-
Uchida, W.; Masuda, N.; Taguchi, T.; Shibasaki, K.; Shirai, Y.; Asano, M.; Matsumoto, Y.; Tsuzuki, R.; Fujikura, T.; Takenaka, T. Pharmacologic profiles of YM934, a novel potassium channel opener. J. Cardiovasc. Pharmacol. 1994, 23, 180-187.
-
(1994)
J. Cardiovasc. Pharmacol.
, vol.23
, pp. 180-187
-
-
Uchida, W.1
Masuda, N.2
Taguchi, T.3
Shibasaki, K.4
Shirai, Y.5
Asano, M.6
Matsumoto, Y.7
Tsuzuki, R.8
Fujikura, T.9
Takenaka, T.10
-
39
-
-
0033999086
-
Novel potassium channel openers. Part 4 Transformation of the 14-benzoxazine skeleton into 14-benzothiazine 1234-tetrahydroquinoline 1234-tetrahydroquinoxaline indoline 15-benzoxazepine
-
Matsumoto, Y.; Tsuzuki, R.; Matsuhisa, A.; Yoden, T.; Yamagiwa, Y.; Yanagisawa, I.; Shibanuma, T.; Nohira, H. Novel potassium channel openers. Part 4, Transformation of the 1,4-benzoxazine skeleton into 1,4-benzothiazine, 1,2,3,4-tetrahydroquinoline, 1,2,3,4-tetrahydroquinoxaline, indoline and 1,5-benzoxazepine. Bioorg. Med. Chem. 2000, 8, 393-404.
-
(2000)
Bioorg. Med. Chem.
, vol.8
, pp. 393-404
-
-
Matsumoto, Y.1
Tsuzuki, R.2
Matsuhisa, A.3
Yoden, T.4
Yamagiwa, Y.5
Yanagisawa, I.6
Shibanuma, T.7
Nohira, H.8
-
40
-
-
0041731570
-
ATP channel openers
-
ATP channel openers. J. Med. Chem. 2003, 46, 3670-3679.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3670-3679
-
-
Cecchetti, V.1
Calderone, V.2
Tabarrini, O.3
Sabatini, S.4
Filipponi, E.5
Testai, L.6
Fravolini, A.7
-
41
-
-
0027965438
-
Substituent effects of benzopyran-4-(N-cyano)-carboxamidine potassium channel openers for selectivity to guinea pig trachealis
-
Ishizawa, T.; Koga, H.; Sato, H.; Makino, T.; Taka, N.; Takahashi, T.; Sato, T.; Nabata, H. Substituent effects of benzopyran-4-(N-cyano)-carboxamidine potassium channel openers for selectivity to guinea pig trachealis. Bioorg. Med Chem. Lett. 1994, 4, 1995-1998.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, pp. 1995-1998
-
-
Ishizawa, T.1
Koga, H.2
Sato, H.3
Makino, T.4
Taka, N.5
Takahashi, T.6
Sato, T.7
Nabata, H.8
-
42
-
-
0027255629
-
NN-disubstituted benzopyran-4-(N′-cyano)-carboxamidines cromakalim analogs with selective activity for guinea pig trachealis
-
Koga, H.; Sato, H.; Ishizawa, T.; Kuromaru, K.; Nabata, H.; Imagawa, J.; Yoshida, S.; Sugo, I. N,N-disubstituted benzopyran-4-(N′-cyano)-carboxamidines, cromakalim analogs with selective activity for guinea pig trachealis. Bioorg. Med. Chem. Lett. 1993, 3, 1111-1114.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 1111-1114
-
-
Koga, H.1
Sato, H.2
Ishizawa, T.3
Kuromaru, K.4
Nabata, H.5
Imagawa, J.6
Yoshida, S.7
Sugo, I.8
-
43
-
-
0027284153
-
Comparison of the airways relaxant hypotensive potencies of the potassium channel activators BRL 55834 levcromakalim (BRL 38227) in vivo in guinea-pigs rats
-
Bowring, N.E.; Arch, J.R.S.; Buckle, D.R.; Taylor, J.F. Comparison of the airways relaxant and hypotensive potencies of the potassium channel activators BRL 55834 and levcromakalim (BRL 38227) in vivo in guinea-pigs and rats. Br. J. Pharmacol. 1993, 109, 1133-1139.
-
(1993)
Br. J. Pharmacol.
, vol.109
, pp. 1133-1139
-
-
Bowring, N.E.1
Arch, J.R.S.2
Buckle, D.R.3
Taylor, J.F.4
-
44
-
-
0033106499
-
ATP channel openers for the treatment of airways hyperreactivity
-
ATP channel openers for the treatment of airways hyperreactivity. Pulm. Pharmacol. Ther. 1999, 12, 103-105.
-
(1999)
Pulm. Pharmacol. Ther.
, vol.12
, pp. 103-105
-
-
Buchheit, K.H.1
Fozard, J.R.2
-
45
-
-
0036197263
-
ATP) channels which suppresses airways hyperreactivity at doses devoid of cardiovascular effects
-
ATP) channels which suppresses airways hyperreactivity at doses devoid of cardiovascular effects. Naunyn-Schmiedeberg's Arch. Pharmacol. 2002, 365, 220-230
-
(2002)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.365
, pp. 220-230
-
-
Buchheit, K.H.1
Manley, P.W.2
Quast, U.3
Russ, U.4
Mazzoni, L.5
Fozard, J.R.6
-
46
-
-
0032478059
-
Synthesis of 234a11b-tetrahydro-oxazino[23-c] benzopyran-9-carbonitriles as ATP-sensitive potassium channel openers
-
Cheng, C.-Y.; Chiu, H.-I.; Chang, M.-J.; Lin, Y.-C.; Tsai, M.-C.; Yu, H.-C. Synthesis of 2,3,4a,11b-tetrahydro-oxazino[2,3-c] benzopyran-9-carbonitriles as ATP-sensitive potassium channel openers. Bioorg. Med. Chem. Lett. 1998, 8, 463-468.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 463-468
-
-
Cheng, C.-Y.1
Chiu, H.-I.2
Chang, M.-J.3
Lin, Y.-C.4
Tsai, M.-C.5
Yu, H.-C.6
-
47
-
-
0035081616
-
N-Acyl-1 234a510b-hexahydro-[1]benzopyrano-[34b][14]oxacine -9-carbonitriles as bladder-selective potassium channel openers
-
Chiu, H.-I.; Lin, Y.-C.; Cheng, C.-Y.; Tsai, M.-C.; Yu, H.-C. N-Acyl-1, 2,3,4a,5,10b-hexahydro-[1]benzopyrano-[3,4b][1,4]oxacine -9-carbonitriles as bladder-selective potassium channel openers. Bioorg. Med. Chem. 2001, 9, 383-393.
-
(2001)
Bioorg. Med. Chem.
, vol.9
, pp. 383-393
-
-
Chiu, H.-I.1
Lin, Y.-C.2
Cheng, C.-Y.3
Tsai, M.-C.4
Yu, H.-C.5
-
48
-
-
0027143194
-
Cardioselective Anti-ischemic ATP-Sensitive Potassium Channel Openers
-
Atwal, K.S.; Grover, G.J.; Ahmed, S.Z.; Ferrara, F.N.; Harper, T.W.; Kim, K.S.; Sleph, P.G.; Dzwonczyk, S.; Russell, A.D.; Moreland, S.; McCullough, J.R.; Normandin, D.E. Cardioselective Anti-ischemic ATP-Sensitive Potassium Channel Openers. J. Med. Chem. 1993, 36, 3971-3974.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3971-3974
-
-
Atwal, K.S.1
Grover, G.J.2
Ahmed, S.Z.3
Ferrara, F.N.4
Harper, T.W.5
Kim, K.S.6
Sleph, P.G.7
Dzwonczyk, S.8
Russell, A.D.9
Moreland, S.10
McCullough, J.R.11
Normandin, D.E.12
-
49
-
-
0029003207
-
Cardioselective antiischemic ATP-sensitive potassium channel openers. 2. Structure-activity studies on benzopyranylcyanoguanidines Modification of the benzopyran ring
-
Atwal, K.S.; Grover, G.J.; Ferrara, F.N.; Ahmed, S.Z.; Sleph, P.G.; Dzwonczyk, S.; Normandin, D.E. Cardioselective antiischemic ATP-sensitive potassium channel openers. 2. Structure-activity studies on benzopyranylcyanoguanidines, Modification of the benzopyran ring. J. Med. Chem. 1995, 38, 1966-1973.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1966-1973
-
-
Atwal, K.S.1
Grover, G.J.2
Ferrara, F.N.3
Ahmed, S.Z.4
Sleph, P.G.5
Dzwonczyk, S.6
Normandin, D.E.7
-
50
-
-
0029166716
-
Cardioselective antiischemic ATP-sensitive potassium channel openers. 3. Structure-activity studies on benzopyranyl cyanoguanidines Modification of the cyanoguanidine portion
-
Atwal, K.S.; Grover, G.J.; Ahmed, S.Z.; Sleph, P.G.; Dzwonczyk, S.; Baird, A.J.; Normandin, D.E. Cardioselective antiischemic ATP-sensitive potassium channel openers. 3. Structure-activity studies on benzopyranyl cyanoguanidines, Modification of the cyanoguanidine portion. J. Med. Chem. 1995, 38, 3236-3245.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 3236-3245
-
-
Atwal, K.S.1
Grover, G.J.2
Ahmed, S.Z.3
Sleph, P.G.4
Dzwonczyk, S.5
Baird, A.J.6
Normandin, D.E.7
-
51
-
-
0030068857
-
Cardioselective antiischemic ATP-sensitive potassium channel openers. 4. Structure-activity studies on benzopyranyl cyanoguanidines Replacement of the benzopyran portion
-
Atwal, K.S.; Ferrara, F.N.; Ding, CZ; Grover, G.J.; Sleph, P.G.; Dzwonczyk, S.; Baird, A.J.; Normandin, D.E. Cardioselective antiischemic ATP-sensitive potassium channel openers. 4. Structure-activity studies on benzopyranyl cyanoguanidines, Replacement of the benzopyran portion. J. Med. Chem. 1996, 39, 304-313.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 304-313
-
-
Atwal, K.S.1
Ferrara, F.N.2
Ding, C.Z.3
Grover, G.J.4
Sleph, P.G.5
Dzwonczyk, S.6
Baird, A.J.7
Normandin, D.E.8
-
52
-
-
8044260833
-
ATP) openers. 5. Identification of 4-(N-aryl)-substituted benzopyran derivatives with high selectivity
-
ATP) openers. 5. Identification of 4-(N-aryl)-substituted benzopyran derivatives with high selectivity. J. Med. Chem. 1997, 40, 24-34.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 24-34
-
-
Rovnyak, G.C.1
Ahmed, S.Z.2
Ding, C.Z.3
Dzwonczyk, S.4
Ferrara, F.N.5
Humphreys, L.G.6
Grover, G.J.7
Santafianos, D.8
Atwal, K.S.9
Baird, A.J.10
McLaughlin, L.G.11
Normandin, D.E.12
Sleph, P.G.13
Traeger, S.C.14
-
53
-
-
0033539130
-
ATP) openers. 6. Effect of modifications at C6 of benzopyranyl cyanoguanidines
-
ATP) openers. 6. Effect of modifications at C6 of benzopyranyl cyanoguanidines. J. Med. Chem. 1999, 42, 3711-3717.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 3711-3717
-
-
Ding, C.Z.1
Rovnyak, G.C.2
Misra, R.N.3
Grover, G.J.4
Miller, A.V.5
Ahmed, S.Z.6
Kelly, Y.7
Normandin, D.E.8
Sleph, P.G.9
Atwal, K.S.10
-
54
-
-
0018098215
-
Synthesis hypotensive activity of N-alkyl-N″-cyano-N′-pyridylguanidines
-
Petersen, H.J.; Nielsen, C.K.; Arrigoni-Martelli, E. Synthesis and hypotensive activity of N-alkyl-N″-cyano-N′-pyridylguanidines. J. Med. Chem. 1978, 21, 773-781.
-
(1978)
J. Med. Chem.
, vol.21
, pp. 773-781
-
-
Petersen, H.J.1
Nielsen, C.K.2
Arrigoni-Martelli, E.3
-
55
-
-
0026628740
-
Structure-activity studies of potassium channel opening in pinacidil-type cyanoguanidines nitroethene-diamines thioureas ureas
-
Manley, P.W.; Quasi, U. Structure-activity studies of potassium channel opening in pinacidil-type cyanoguanidines, nitroethene-diamines, thioureas, and ureas. J. Med. Chem. 1992, 35, 2327-2340.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 2327-2340
-
-
Manley, P.W.1
Quasi, U.2
-
56
-
-
0028036267
-
Novel potassium channel openers synthesis pharmacological evaluation of new N-(substituted-3-pyridyl)-N′-alkylthioureas related compounds
-
Takemoto, T.; Eda, M.; Okada, T.; Sakashita, H.; Matzno, S.; Gohda, M.; Ebisu, H.; Nakamura, N.; Fukaya, C.; Hihara, M.; Eiraku, M.; Yamanouchi, K.; Yokoyama, K. Novel potassium channel openers, synthesis and pharmacological evaluation of new N-(substituted-3-pyridyl)-N′-alkylthioureas and related compounds. J. Med. Chem. 1994, 37, 18-25.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 18-25
-
-
Takemoto, T.1
Eda, M.2
Okada, T.3
Sakashita, H.4
Matzno, S.5
Gohda, M.6
Ebisu, H.7
Nakamura, N.8
Fukaya, C.9
Hihara, M.10
Eiraku, M.11
Yamanouchi, K.12
Yokoyama, K.13
-
57
-
-
0027934843
-
Novel potassium channel openers preparation pharmacological evaluation of racemic optically active N-(6-amino-3-pyridyl)-N′-bicyclo-alkyl- N″-cyanoguanidine derivatives
-
Eda, M.; Takemoto, T.; Ono, S.; Okada, T.; Kosaka, K.; Gohda, M.; Matzno, S.; Nakamura, N.; Fukaya, C. Novel potassium channel openers, preparation and pharmacological evaluation of racemic and optically active N-(6-amino-3-pyridyl-N″-bicyclo-alkyl-N″-cyanoguanidine derivatives. J. Med. Chem. 1994, 37, 1983-1990.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1983-1990
-
-
Eda, M.1
Takemoto, T.2
Ono, S.3
Okada, T.4
Kosaka, K.5
Gohda, M.6
Matzno, S.7
Nakamura, N.8
Fukaya, C.9
-
58
-
-
0029857426
-
Synthesis structure-activity relationships of novel phenylcyanoguanidine derivatives as potassium channel openers
-
Yoshiizumi, K.; Ikeda, S.; Goto, K.; Morita, T.; Nishimura, N.; Sukamoto,T.; Yoshino, K. Synthesis and structure-activity relationships of novel phenylcyanoguanidine derivatives as potassium channel openers. Chem. Pharm. Bull. 1996, 44, 2042-2050.
-
(1996)
Chem. Pharm. Bull.
, vol.44
, pp. 2042-2050
-
-
Yoshiizumi, K.1
Ikeda, S.2
Goto, K.3
Morita, T.4
Nishimura, N.5
Sukamoto, T.6
Yoshino, K.7
-
59
-
-
0034613561
-
NMR analysis of tautomerisms of active pinacidil-type potassium channel openers a less active one
-
Yoshiizumi, K.; Nakajima, F.; Kiyoi, T.; Kondo, H. NMR analysis of tautomerisms of active pinacidil-type potassium channel openers and a less active one. Bioorg, Med. Chem. Lett. 2000, 10, 2463-2466.
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2463-2466
-
-
Yoshiizumi, K.1
Nakajima, F.2
Kiyoi, T.3
Kondo, H.4
-
60
-
-
0025696420
-
2-(3-pyridyl)-tetrahydrothiopyran-2-carbothioamide derivatives analogues a novel family of potent potassium channel openers
-
Aloup, J.C.; Farge, D.; James, C.; Mondot, S.; Cavero, I. 2-(3-pyridyl)-tetrahydrothiopyran-2-carbothioamide derivatives and analogues, a novel family of potent potassium channel openers. Drugs Fut. 1990, 15, 1097-1108.
-
(1990)
Drugs Fut.
, vol.15
, pp. 1097-1108
-
-
Aloup, J.C.1
Farge, D.2
James, C.3
Mondot, S.4
Cavero, I.5
-
61
-
-
1242266021
-
RP 49356 a vasorelaxant agent with potassium channel activating properties
-
Mondot, S.; Mestre, M.; Caillard, C.G.; Cavern, I. RP 49356, a vasorelaxant agent with potassium channel activating properties. Br. J. Pharmacol. 1988, 95(Suppl), 813P.
-
(1988)
Br. J. Pharmacol.
, vol.95
, Issue.SUPPL.
-
-
Mondot, S.1
Mestre, M.2
Caillard, C.G.3
Cavern, I.4
-
62
-
-
0026686540
-
Synthesis biological activity of trans-(±) N-methyl-2-(3-pyridyl)- 2-tetrahydrothiopyrancarbothioamide 1-oxide (RP 49356) analogues a new class of potassium channel opener
-
Brown, Th.J.; Chapman, R.F.; Cook, D.C.; Hart, T.W.; McLay, I.M.; Jordan, R.; Mason, J.S.; Palfreyman, M.N.; Walsh, R.J.A.; Withnall, M.T.; Aloup, J.C.; Cavero, I.; Farge, D.; James, C.; Mondot, S. Synthesis and biological activity of trans-(±) N-methyl-2-(3-pyridyl)-2-tetrahydrothiopyrancarbothioamide 1-oxide (RP 49356) and analogues, a new class of potassium channel opener. J. Med. Chem. 1992, 35, 3613-3624.
-
(1992)
J. Med. Chem.
, vol.35
, pp. 3613-3624
-
-
Brown, Th.J.1
Chapman, R.F.2
Cook, D.C.3
Hart, T.W.4
McLay, I.M.5
Jordan, R.6
Mason, J.S.7
Palfreyman, M.N.8
Walsh, R.J.A.9
Withnall, M.T.10
Aloup, J.C.11
Cavero, I.12
Farge, D.13
James, C.14
Mondot, S.15
-
63
-
-
1242311051
-
Syntheses and structure-activity relationships of pyridine based potassium channel activators
-
Evans, J.M.; Hamilton, T.C.; Longman, S.D.; Stemp, G.; Eds; Taylor & Francis: London
-
Palfreyman, M.N. Syntheses and structure-activity relationships of pyridine based potassium channel activators. In Potassium channels and their modulators. Evans, J.M.; Hamilton, T.C.; Longman, S.D.; Stemp, G.; Eds; Taylor & Francis: London, 1996, pp. 57-77.
-
(1996)
Potassium Channels and Their Modulators
, pp. 57-77
-
-
Palfreyman, M.N.1
-
64
-
-
0027232905
-
Syntheses biological activities of potent potassium channel openers derived from (±)-2-oxo-1-pyridin-3-yl-cyclohexanecarbothioic acid methylamide new potassium channel openers
-
Brown, Th.J.; Chapman, R.F.; Mason, J.S.; Palfreyman, M.N.; Vicker, N.; Walsh, R.J.A. Syntheses and biological activities of potent potassium channel openers derived from (±)-2-oxo-1-pyridin-3-yl-cyclohexanecarbothioic acid methylamide, new potassium channel openers. J. Med. Chem. 1993, 36, 1604-1612.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 1604-1612
-
-
Brown, Th.J.1
Chapman, R.F.2
Mason, J.S.3
Palfreyman, M.N.4
Vicker, N.5
Walsh, R.J.A.6
-
65
-
-
0003893293
-
Characterization of vasorelaxant action of MCC-134 a novel benzenepropanethioamide derivative
-
Seino, A.; Bessho, H.; Ishibashi, A.; Nagano, T.; Shinpuku, T.; Tsutsui, M.; Okushima, H.; Narimatsu, A. Characterization of vasorelaxant action of MCC-134, a novel benzenepropanethioamide derivative. Jpn. J. Pharmacol. 1996, 71(Suppl.), 141P.
-
(1996)
Jpn. J. Pharmacol.
, vol.71
, Issue.SUPPL.
-
-
Seino, A.1
Bessho, H.2
Ishibashi, A.3
Nagano, T.4
Shinpuku, T.5
Tsutsui, M.6
Okushima, H.7
Narimatsu, A.8
-
66
-
-
0024354763
-
+ channel openers diazoxide cromakalim their inhibition by glibenclamide
-
+ channel openers, diazoxide and cromakalim, and their inhibition by glibenclamide. J. Pharmacol. Exp. Ther. 1989, 250, 261-271.
-
(1989)
J. Pharmacol. Exp. Ther.
, vol.250
, pp. 261-271
-
-
Quast, U.1
Cook, N.S.2
-
67
-
-
0027469677
-
3H]P1075 in rat isolated aorta relationship to functional effects of openers blockers
-
3H]P1075 in rat isolated aorta, relationship to functional effects of openers and blockers. Mol. Pharmacol. 1993, 43, 474-481.
-
(1993)
Mol. Pharmacol.
, vol.43
, pp. 474-481
-
-
Quast, U.1
Bray, K.M.2
Andres, H.3
Manley, P.W.4
Baumlin, Y.5
Dosogne, J.6
-
69
-
-
0026740899
-
Mechanical ionic response of rat aorta to diazoxide
-
Antoine, M.-H.; Berkenboom, G.; Fang, Z.-Y.; Fontaine, J.; Herchuelz, A.; Lebrun, P. Mechanical and ionic response of rat aorta to diazoxide. Eur. J. Pharmacol. 1992, 216, 299-306.
-
(1992)
Eur. J. Pharmacol.
, vol.216
, pp. 299-306
-
-
Antoine, M.-H.1
Berkenboom, G.2
Fang, Z.-Y.3
Fontaine, J.4
Herchuelz, A.5
Lebrun, P.6
-
70
-
-
0027359857
-
3-(Alkylamino)-4H-pyrido[43-e]-124-thiadiazine-11-dioxides as powerful inhibitors of insulin release from rat pancreatic b-cells a new class of potassium channel openers?
-
Pirotte, B.; de Tullio, P.; Lebrun, P.; Antoine, M.-H.; Fontaine, J.; Masereel, B.; Schynts, M.; Dupont; L.; Herchuelz, A.; Delarge, J. 3-(Alkylamino)-4H-pyrido[4,3-e]-1,2,4-thiadiazine-1,1-dioxides as powerful inhibitors of insulin release from rat pancreatic b-cells, a new class of potassium channel openers? J. Med Chem. 1993, 36, 3211-3213.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3211-3213
-
-
Pirotte, B.1
de Tullio, P.2
Lebrun, P.3
Antoine, M.-H.4
Fontaine, J.5
Masereel, B.6
Schynts, M.7
Dupont, L.8
Herchuelz, A.9
Delarge, J.10
-
71
-
-
0030051553
-
3- 4-substituted 4H-pyrido [43-e]-124-thiadiazine 11-dioxides as potassium channel openers synthesis pharmacological evaluation structure-activity relationships
-
deTullio, P.; Pirotte, B.; Lebrun, P.; Fontaine, J.; Dupont, L.; Antoine, M.-H.; Ouedraogo, R; Khelili, S.; Maggetto, C.; Masereel, B.; Diouf, O., Podona, T.; Delarge, J. 3- and 4-substituted 4H-pyrido [4,3-e]-1,2,4-thiadiazine 1,1-dioxides as potassium channel openers, synthesis, pharmacological evaluation, and structure-activity relationships. J. Med. Chem. 1996, 39, 937-948.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 937-948
-
-
deTullio, P.1
Pirotte, B.2
Lebrun, P.3
Fontaine, J.4
Dupont, L.5
Antoine, M.-H.6
Ouedraogo, R.7
Khelili, S.8
Maggetto, C.9
Masereel, B.10
Diouf, O.11
Podona, T.12
Delarge, J.13
-
72
-
-
0032792738
-
Preparation pharmacological evaluation of the R- S-enantiomers of 3-(2′-butylamino)-4H- 3-(3′-methyl-2′-butylamino)-4H- pyrido [43-e]-124-thiadiazine 11-dioxide two tissue selective ATP-sensitive potassium channel openers
-
Khelili, S.; deTullio, P.; Lebrun, P.; Fillet, M.; Antoine, M.-H.; Ouedraogo, R.; Dupont, L.; Fontaine, J.; Felekidis, A.; Leclerc, G.; Delarge, J.; Pirotte, B. Preparation and pharmacological evaluation of the R- and S-enantiomers of 3-(2′-butylamino)-4H- and 3-(3′-methyl-2′-butylamino)-4H-pyrido [4,3-e]-1,2,4-thiadiazine 1,1-dioxide, two tissue selective ATP-sensitive potassium channel openers. Bioorg. Med. Chem. 1999, 7, 1513-1520.
-
(1999)
Bioorg. Med. Chem.
, vol.7
, pp. 1513-1520
-
-
Khelili, S.1
deTullio, P.2
Lebrun, P.3
Fillet, M.4
Antoine, M.-H.5
Ouedraogo, R.6
Dupont, L.7
Fontaine, J.8
Felekidis, A.9
Leclerc, G.10
Delarge, J.11
Pirotte, B.12
-
73
-
-
18144437525
-
3-Alkylamino-4H-pyrido [23-e]-124-thiadiazine 11-dioxides structurally related to diazoxide pinacidil as potassium channel openers acting on vascular smooth muscle cells design synthesis pharmacological evaluation
-
Pirotte, B.; Ouedraogo, R.; deTullio, P.; Khelili, S.; Somers, F.; Boverie, S.; Dupont, L.; Fontaine, J.; Damas, J.; Lebrun, P. 3-Alkylamino-4H-pyrido [2,3-e]-1,2,4-thiadiazine 1,1-dioxides structurally related to diazoxide and pinacidil as potassium channel openers acting on vascular smooth muscle cells, design, synthesis, and pharmacological evaluation. J. Med. Chem. 2000, 43, 1456-1466.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1456-1466
-
-
Pirotte, B.1
Ouedraogo, R.2
deTullio, P.3
Khelili, S.4
Somers, F.5
Boverie, S.6
Dupont, L.7
Fontaine, J.8
Damas, J.9
Lebrun, P.10
-
74
-
-
0037479902
-
ATP channel openers belonging to 3-alkylamino-7-halo-4H-1 24-benzothiadiazine 11-dioxides
-
ATP channel openers belonging to 3-alkylamino-7-halo-4H-1, 2,4-benzothiadiazine 1,1-dioxides. J. Med. Chem. 2003, 46, 3342-3353.
-
(2003)
J. Med. Chem.
, vol.46
, pp. 3342-3353
-
-
deTullio, P.1
Becker, B.2
Boverie, S.3
Dabrowski, M.4
Wahl, P.5
Antoine, M.-H.6
Somers, F.7
Sebille, S.8
Ouedraogo, R.9
Hansen, J.B.10
Lebrun, P.11
Pirotte, B.12
-
75
-
-
9644255738
-
Synthesis pharmacological evaluation of 4H-14-benzothiazine-2-carbonitrile 11-dioxides N-(2-cyanomethyl-sulfonylphenyl) acylamide derivatives as potential activators of ATP sensitive potassium chanels
-
Schou, S.C.; Hansen, H.C.; Tagmose, T.M.; Boonen, H.C.M.; Worsaae, A.; Dabrowski, M.; Wahl, P.; Arkhammar, P.O.G.; Bodvarsdottir, T.B.; Antoine, M.-H.; Lebrun, P, Hansen J.B. Synthesis and pharmacological evaluation of 4H-1,4-benzothiazine-2-carbonitrile 1,1-dioxides and N-(2-cyanomethyl-sulfonylphenyl) acylamide derivatives as potential activators of ATP sensitive potassium chanels. Bioorg. Med. Chem. 2005, 13, 141-155.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 141-155
-
-
Schou, S.C.1
Hansen, H.C.2
Tagmose, T.M.3
Boonen, H.C.M.4
Worsaae, A.5
Dabrowski, M.6
Wahl, P.7
Arkhammar, P.O.G.8
Bodvarsdottir, T.B.9
Antoine, M.-H.10
Lebrun, P.11
Hansen, J.B.12
-
76
-
-
0037068466
-
6-chloro-3-alkylamino-4H-thieno [32-e]-124-thiadiazine 11-dioxide derivatives potently selectively activate ATP sensitive potassium channels of pancreatic β-cells
-
Nielsen, F.E.; Bodvarsdottir, T.B.; Worsaae, A.; MacKay, P.; Stidsen, C.E.; Boonen, H.C.M.; Pridal, L.; Arkhammar, P.O.G.; Wahl, P.; Ynddal, L.; Junager, F.; Dragsted, N.; Tagmose, T.M.; Mogensen, J.P.; Koch, A.; Treppendahl, S.P.; Hansen, J.B. 6-chloro-3-alkylamino-4H-thieno [3,2-e]-1,2,4-thiadiazine 1,1-dioxide derivatives potently and selectively activate ATP sensitive potassium channels of pancreatic β-cells. J. Med. Chem. 2002, 45, 4171-4187.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 4171-4187
-
-
Nielsen, F.E.1
Bodvarsdottir, T.B.2
Worsaae, A.3
MacKay, P.4
Stidsen, C.E.5
Boonen, H.C.M.6
Pridal, L.7
Arkhammar, P.O.G.8
Wahl, P.9
Ynddal, L.10
Junager, F.11
Dragsted, N.12
Tagmose, T.M.13
Mogensen, J.P.14
Koch, A.15
Treppendahl, S.P.16
Hansen, J.B.17
-
77
-
-
2542574087
-
ATP channels inhibitors of insulin release
-
ATP channels and inhibitors of insulin release. J. Med. Chem. 2004, 47, 3202-3211.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 3202-3211
-
-
Tagmose, T.M.1
Schou, S.C.2
Mogensen, J.P.3
Nielsen, F.E.4
Arkhammar, P.O.G.5
Wahl, P.6
Hansen, B.S.7
Worsaae, A.8
Boonen, H.C.M.9
Antoine, M.-H.10
Lebrun, P.11
Hansen, J.B.12
-
78
-
-
7044247605
-
ATP channels
-
ATP channels. Bioorg. Med. Chem Lett. 2004, 14, 5727-5730.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 5727-5730
-
-
Nielsen, F.E.1
Jacobsen, P.2
Worsaae, A.3
Arkhammar, P.O.G.4
Wahl, P.5
Hansen, J.B.6
-
79
-
-
1642575087
-
ATP channel agonists
-
ATP channel agonists. Bioorg. Med. Chem. Letters 2004, 14, 813-816.
-
(2004)
Bioorg. Med. Chem. Letters
, vol.14
, pp. 813-816
-
-
Peat, A.J.1
Townsend, C.2
Craig, M.M.3
Garrido, D.4
Terry, C.M.5
Wilson, J.L.6
Thomson, S.A.7
-
80
-
-
17144465234
-
Design SAR of novel potassium channel openers targeted for urge urinary incontinence I. N-Cyanoguanidine bioisosteres possessing in vivo bladder selectivity
-
Butera, J.A.; Antane, M.M.; Antane, S.A.; Argentieri, T.M.; Freeden, C.; Graceffa, R.F.; Hirth, B.H.; Jenkins, D.; Lennox, J.R.; Matelan, E.; Norton, N.W.; Quagliato, D.; Sheldon, J.H.; Spinelli, W.; Warga, D.; Wojdan, A.; Woods, M. Design and SAR of novel potassium channel openers targeted for urge urinary incontinence I. N-Cyanoguanidine bioisosteres possessing in vivo bladder selectivity. J. Med. Chem. 2000, 43, 1187-1202.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1187-1202
-
-
Butera, J.A.1
Antane, M.M.2
Antane, S.A.3
Argentieri, T.M.4
Freeden, C.5
Graceffa, R.F.6
Hirth, B.H.7
Jenkins, D.8
Lennox, J.R.9
Matelan, E.10
Norton, N.W.11
Quagliato, D.12
Sheldon, J.H.13
Spinelli, W.14
Warga, D.15
Wojdan, A.16
Woods, M.17
-
81
-
-
17144468785
-
Design SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective potent benzylamino cyclobutenediones
-
Gilbert, A.M.; Antane, M.M.; Argentieri, T.M.; Butera, J.A.; Francisco, G.D.; Freeden, C.; Gundersen, E.G.; Graceffa, R.F.; Herbst, D., Hirth, B.H.; Lennox, J.R.; McFarlane, G.; Norton, N.W.; Quagliato, D.; Sheldon, J.H.; Warga, D.; Wojdan, A.; Woods, M. Design and SAR of novel potassium channel openers targeted for urge urinary incontinence. 2. Selective and potent benzylamino cyclobutenediones. J. Med Chem. 2000, 43, 1203-1214.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 1203-1214
-
-
Gilbert, A.M.1
Antane, M.M.2
Argentieri, T.M.3
Butera, J.A.4
Francisco, G.D.5
Freeden, C.6
Gundersen, E.G.7
Graceffa, R.F.8
Herbst, D.9
Hirth, B.H.10
Lennox, J.R.11
McFarlane, G.12
Norton, N.W.13
Quagliato, D.14
Sheldon, J.H.15
Warga, D.16
Wojdan, A.17
Woods, M.18
-
82
-
-
0024491553
-
Pharmacological modulation of calcium potassium channels in isolated vascular smooth muscle cells
-
Klöckner, U.; Trieschmann, U.; Isenberg, G. Pharmacological modulation of calcium and potassium channels in isolated vascular smooth muscle cells. Arzneim. Forsch. Drug Res. 1989, 39, 120-126.
-
(1989)
Arzneim. Forsch. Drug Res.
, vol.39
, pp. 120-126
-
-
Klöckner, U.1
Trieschmann, U.2
Isenberg, G.3
-
83
-
-
0029018413
-
3H-P1075 binding in urinary bladder smooth muscle
-
3H-P1075 binding in urinary bladder smooth muscle. Res. Commun. Mol. Pathol. Pharmacol. 1995, 88, 137-51.
-
(1995)
Res. Commun. Mol. Pathol. Pharmacol.
, vol.88
, pp. 137-151
-
-
Trivedi, S.1
Potter-Lee, L.2
McConville, M.W.3
Li, J.H.4
Ohnmacht, C.J.5
Trainor, D.A.6
Kau, S.T.7
-
84
-
-
0031467256
-
ATP channel activator
-
ATP channel activator. Cardiovasc. Drug Rev. 1997, 15, 220-231.
-
(1997)
Cardiovasc. Drug Rev.
, vol.15
, pp. 220-231
-
-
Li, J.H.1
-
86
-
-
0036785473
-
(-)-(9S)-9-(3-bromo-4-fluorophenyl)-235679-hexahydrothieno [32-b]quinolin-8(4H)-one 11-dioxide (A-278637) A novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. I. In vitro characterization
-
Gopalakrishnan, M.; Buckner, S.A.; Whiteaker, K.L.; Shieh, C.-C.; Molinari, E.J.; Milicic, I.; Daza, A.V.; Davis-Taber, R.; Scott, V.E.; Sellers, D.; Chess-Williams, R.; Chapple, C.R.; Liu, Y.; Liu, D.; Brioni, J.D.; Sullivan, J.P.; Williams, M.; Carroll, W.A.; Coghlan, M.J. (-)-(9S)-9-(3-bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno [3,2-b]quinolin-8(4,H)-one 1,1-dioxide (A-278637), A novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. I. In vitro characterization. J. Pharmacol. Exp. Ther. 2002, 303, 379-386.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.303
, pp. 379-386
-
-
Gopalakrishnan, M.1
Buckner, S.A.2
Whiteaker, K.L.3
Shieh, C.-C.4
Molinari, E.J.5
Milicic, I.6
Daza, A.V.7
Davis-Taber, R.8
Scott, V.E.9
Sellers, D.10
Chess-Williams, R.11
Chapple, C.R.12
Liu, Y.13
Liu, D.14
Brioni, J.D.15
Sullivan, J.P.16
Williams, M.17
Carroll, W.A.18
Coghlan, M.J.19
-
87
-
-
0036784510
-
(-)-(9S)-9-(3-bromo-4-fluorophenyl)-2 35679-hexahydrothieno[32-b]quinolin-8(4H)-one 11-dioxide (A-278637) A novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. In vivo characterization
-
Brune, M.E.; Fey, T.A.; Brioni, J.D.; Sullivan, J.P.; Williams, M.; Carroll, W.A.; Coghlan, M.J.; Gopalakrishnan, M. (-)-(9S)-9-(3-bromo-4-fluorophenyl)-2, 3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637), A novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. In vivo characterization. J. Pharmacol. Exp. Ther. 2002, 303, 387-394.
-
(2002)
J. Pharmacol. Exp. Ther.
, vol.303
, pp. 387-394
-
-
Brune, M.E.1
Fey, T.A.2
Brioni, J.D.3
Sullivan, J.P.4
Williams, M.5
Carroll, W.A.6
Coghlan, M.J.7
Gopalakrishnan, M.8
-
88
-
-
0037013429
-
ATP channel openers (KCOs)
-
ATP channel openers (KCOs). Bioorg, Med. Chem. Lett. 2002, 12, 1481-1484.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1481-1484
-
-
Drizin, I.1
Holladay, M.W.2
Yi, L.3
Zhang, H.Q.4
Gopalakrishnan, S.5
Gopalakrishnan, M.6
Whiteaker, K.L.7
Buckner, S.A.8
Sullivan, J.P.9
Carroll, W.A.10
-
89
-
-
0026073112
-
Non-steroidal antiandrogens. Design of novel compounds based on infrared study of the dominant conformation hydrogen-bonding properties of a series of anilide antiandrogens
-
Morris, J.J.; Hughes, L.R.; Glen, A.T.; Taylor, P.J. Non-steroidal antiandrogens. Design of novel compounds based on infrared study of the dominant conformation and hydrogen-bonding properties of a series of anilide antiandrogens. J. Med. Chem. 1991, 34, 447-455
-
(1991)
J. Med. Chem.
, vol.34
, pp. 447-455
-
-
Morris, J.J.1
Hughes, L.R.2
Glen, A.T.3
Taylor, P.J.4
-
91
-
-
0029068306
-
3H-P1075 binding in bladder smooth muscle
-
3H-P1075 binding in bladder smooth muscle. Pharmacol. 1995, 50, 388-397.
-
(1995)
Pharmacol.
, vol.50
, pp. 388-397
-
-
Trivedi, S.1
Stetz, S.L.2
Potter-Lee, L.3
McConville, M.4
Li, J.H.5
Empfield, J.R.6
Ohnmacht, C.J.7
Russell, K.8
Brown, F.J.9
Trainor, D.A.10
Kau, S.T.11
-
92
-
-
0027771659
-
Anilide tertiary carbinols a new structural class of potent potassium channel openers
-
Grant, T.L.; Frank, C.A.; Kau, S.T.; Li, J.H.; McLaren, F.M.; Ohnmacht C.J.; Russell, K.; Shapiro, H.S.; Trivedi, S. Anilide tertiary carbinols, a new structural class of potent potassium channel openers. Bioorg, Med. Chem. Lett. 1993, 3, 2723-2724.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 2723-2724
-
-
Grant, T.L.1
Frank, C.A.2
Kau, S.T.3
Li, J.H.4
McLaren, F.M.5
Ohnmacht, C.J.6
Russell, K.7
Shapiro, H.S.8
Trivedi, S.9
-
93
-
-
10544224541
-
ATP potassium channel openers. Modifications on the western region
-
ATP potassium channel openers. Modifications on the western region. J. Med Chem. 1996, 39, 4592-4601.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 4592-4601
-
-
Ohnmacht, C.J.1
Russell, K.2
Empfield, J.R.3
Frank, C.A.4
Gibson, K.H.5
Mayhugh, D.R.6
McLaren, F.M.7
Shapiro, H.S.8
Brown, F.J.9
Trainor, D.A.10
Ceccarelli, C.11
Lin, M.M.12
Masek, B.B.13
Forst, J.M.14
Harris, R.J.15
Hulsizer, J.M.16
Lewis, J.J.17
Silverman, S.M.18
Smith, R.W.19
Warwick, P.J.20
Kau, S.T.21
Chun, A.L.22
Grant, T.L.23
Howe, B.B.24
Neilson, K.L.25
more..
-
95
-
-
0029161646
-
ATP channel opener with in vivo selectivity for urinary bladder
-
ATP channel opener with in vivo selectivity for urinary bladder. J. Pharmacol. Exp. Ther. 1995, 274, 884-890.
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.274
, pp. 884-890
-
-
Howe, B.B.1
Halterman, T.J.2
Yochim, C.L.3
Do, M.L.4
Pettinger, S.J.5
Stow, R.B.6
Ohnmacht, C.J.7
Russell, K.8
Empfield, J.R.9
Trainor, D.A.10
Brown, F.J.11
Kau, S.T.12
-
96
-
-
0036336809
-
N-arylated pyrrolidin-2-ones morpholin-3-ones as potassium channel openers
-
Liang, P.-H., Hsin, L.-W., Cheng, C.-Y. N-arylated pyrrolidin-2-ones and morpholin-3-ones as potassium channel openers. Bioorg. Med. Chem. 2002, 10, 3267-3276.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 3267-3276
-
-
Liang, P.-H.1
Hsin, L.-W.2
Cheng, C.-Y.3
-
97
-
-
26944455708
-
ATP channel opener
-
Barcelona, Drugs Fut
-
ATP channel opener. XVIIth Int Symp Med Chem, Barcelona, Drugs Fut. 27(Suppl A),C47.
-
XVIIth Int Symp Med Chem
, vol.27
, Issue.SUPPL. A
-
-
Turner, S.C.1
Carroll, W.A.2
White, T.K.3
Brune, M.E.4
Buckner, S.A.5
Gopalakrishnan, M.6
Fey, T.A.7
Coghlan, M.J.8
Castle, N.A.9
Scott, V.E.10
Whiteaker, K.L.11
Daza, A.V.12
Milicic, I.13
Sullivan, J.P.14
|