-
1
-
-
14944383798
-
The evolving role of natural products in dnig discovery
-
Koehn, F. E.; Carter, G. T. The evolving role of natural products in dnig discovery. Nat. Rev. Drug Discovery 2005, 4, 206-220.
-
(2005)
Nat. Rev. Drug Discovery
, vol.4
, pp. 206-220
-
-
Koehn, F.E.1
Carter, G.T.2
-
2
-
-
33745784158
-
Charting Biological and Chemical Space: PSSC and SCONP as guiding principles for the development of compound collections based on natural product scaffolds
-
Arve, L.; Voigt, T.; Waldmann, H. Charting Biological and Chemical Space: PSSC and SCONP as guiding principles for the development of compound collections based on natural product scaffolds. QSAR Comb. Sci. 2006, 25, 449-456.
-
(2006)
QSAR Comb. Sci
, vol.25
, pp. 449-456
-
-
Arve, L.1
Voigt, T.2
Waldmann, H.3
-
3
-
-
0037119336
-
From protein domains to drug candidates: Natural products as guiding principles in the design and synthesis of compound libraries
-
Breinbauer, R.; Vetter, I. R.; Waldmann, H. From protein domains to drug candidates: Natural products as guiding principles in the design and synthesis of compound libraries. Angew. Chem. Int. Ed. 2002, 41, 2879-2890.
-
(2002)
Angew. Chem. Int. Ed
, vol.41
, pp. 2879-2890
-
-
Breinbauer, R.1
Vetter, I.R.2
Waldmann, H.3
-
4
-
-
5644294669
-
Current progress in natural product-like libraries for discovery screening
-
Tan, D. S. Current progress in natural product-like libraries for discovery screening. Comb. Chem. High Throughput Screening 2004, 7, 631-643.
-
(2004)
Comb. Chem. High Throughput Screening
, vol.7
, pp. 631-643
-
-
Tan, D.S.1
-
5
-
-
2942590399
-
Libraries from natural product-like scaffolds
-
Boldi, A. M. Libraries from natural product-like scaffolds. Curr. Opin. Chem. Biol. 2004, 8, 281-286.
-
(2004)
Curr. Opin. Chem. Biol
, vol.8
, pp. 281-286
-
-
Boldi, A.M.1
-
6
-
-
0141988625
-
Diversity oriented synthesis and branching reaction pathway to generate natural product-like compounds
-
Liao, Y.; Hu, Y.; Wu, J.; Zhu, Q.; Donovan, M.; Fathi, R.; Yang, Z. Diversity oriented synthesis and branching reaction pathway to generate natural product-like compounds. Curr. Med. Chem. 2003, 10, 2285-2316.
-
(2003)
Curr. Med. Chem
, vol.10
, pp. 2285-2316
-
-
Liao, Y.1
Hu, Y.2
Wu, J.3
Zhu, Q.4
Donovan, M.5
Fathi, R.6
Yang, Z.7
-
7
-
-
0037208308
-
Property distributions: Differences between drugs, natural products, and molecules from combinatorial chemistry
-
Feher, M.; Schmidt, J. M. Property distributions: Differences between drugs, natural products, and molecules from combinatorial chemistry. J. Chem. Inf. Comput. Sci. 2003, 43, 218-227.
-
(2003)
J. Chem. Inf. Comput. Sci
, vol.43
, pp. 218-227
-
-
Feher, M.1
Schmidt, J.M.2
-
8
-
-
33846934752
-
Structural Simplification of Bioactive Natural Products with Multicomponent Synthesis: Dihydropyridopyrazole Analogues of Podophyllotoxin
-
Magedov, I. V.; Manpadi, M.; Rozhkova, E.; Przheval'skii, N. M.; Rogelj, S.; Shors, S. T.; Steelant, W. F. A.; Van Slambrouck, S.; Kornienko, A. Structural Simplification of Bioactive Natural Products with Multicomponent Synthesis: Dihydropyridopyrazole Analogues of Podophyllotoxin. Bioorg. Med. Chem. Lett. 2007, 17, 1381-1385.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 1381-1385
-
-
Magedov, I.V.1
Manpadi, M.2
Rozhkova, E.3
Przheval'skii, N.M.4
Rogelj, S.5
Shors, S.T.6
Steelant, W.F.A.7
Van Slambrouck, S.8
Kornienko, A.9
-
9
-
-
35348813795
-
Discovery and Investigation of Antiproliferative and Apoptosis-Inducing Properties of New Heterocyclic Podophyllotoxin Analogues Accessible by a One-Step Multicomponent Synthesis
-
Magedov, I. V.; Manpadi, M.; Van Slambrouck, S.; Steelant, W. F. A.; Rozhkova, E.; Przhevalískii, N. M.; Rogelj, S.; Kornienko, A. Discovery and Investigation of Antiproliferative and Apoptosis-Inducing Properties of New Heterocyclic Podophyllotoxin Analogues Accessible by a One-Step Multicomponent Synthesis. J. Med. Chem. 2007, 50, 5183-5192.
-
(2007)
J. Med. Chem
, vol.50
, pp. 5183-5192
-
-
Magedov, I.V.1
Manpadi, M.2
Van Slambrouck, S.3
Steelant, W.F.A.4
Rozhkova, E.5
Przhevalískii, N.M.6
Rogelj, S.7
Kornienko, A.8
-
10
-
-
8144222975
-
One-pot Synthesis and the Biological Activities of 4-Methylpyrano[3,2-c]-quinolin-2,5-[6H]-diones
-
Kumar, N. V.; Rajendran, S. P. One-pot Synthesis and the Biological Activities of 4-Methylpyrano[3,2-c]-quinolin-2,5-[6H]-diones. Asian J. Chem. 2004, 16, 1911-1914.
-
(2004)
Asian J. Chem
, vol.16
, pp. 1911-1914
-
-
Kumar, N.V.1
Rajendran, S.P.2
-
11
-
-
3042796046
-
Photo-activated DNA binding and antimicrobial activities of Furoquinoline and Pyranoquinolone alkaloids from Rutaceae
-
Ilanawa, F.; Fokialakis, N.; Skaltsounis, A. L. Photo-activated DNA binding and antimicrobial activities of Furoquinoline and Pyranoquinolone alkaloids from Rutaceae. Planta Med. 2004, 70, 531-535.
-
(2004)
Planta Med
, vol.70
, pp. 531-535
-
-
Ilanawa, F.1
Fokialakis, N.2
Skaltsounis, A.L.3
-
12
-
-
22444443937
-
The relative and absolute configuration of PF1140
-
Fujita, Y.; Oguri, H.; Oikawa, H. The relative and absolute configuration of PF1140. J. Antibiot. 2005, 58, 425-427.
-
(2005)
J. Antibiot
, vol.58
, pp. 425-427
-
-
Fujita, Y.1
Oguri, H.2
Oikawa, H.3
-
13
-
-
27144462057
-
Isolation and identification of antifungal and antialgal alkaloids from Haplophyllum sieversii
-
Cantrell, C. L.; Schrader, K. K.; Mamonov, L. K.; Sitpaeva, G. T.; Kustova, T. S.; Dunbar, C.; Wedge, D. E. Isolation and identification of antifungal and antialgal alkaloids from Haplophyllum sieversii. J. Agric. Food Chem. 2005, 53, 7741-7748.
-
(2005)
J. Agric. Food Chem
, vol.53
, pp. 7741-7748
-
-
Cantrell, C.L.1
Schrader, K.K.2
Mamonov, L.K.3
Sitpaeva, G.T.4
Kustova, T.S.5
Dunbar, C.6
Wedge, D.E.7
-
14
-
-
35348903158
-
New phenylpropenoids, bis(1-phenyletbyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integfifoliolum
-
Chen, J. J.; Chen, P. H.; Liao, C. H.; Huang, S. Y.; Chen, I. S. New phenylpropenoids, bis(1-phenyletbyl)phenols, bisquinolinone alkaloid, and anti-inflammatory constituents from Zanthoxylum integfifoliolum. J. Nat. Prod. 2007, 70, 1444-1448.
-
(2007)
J. Nat. Prod
, vol.70
, pp. 1444-1448
-
-
Chen, J.J.1
Chen, P.H.2
Liao, C.H.3
Huang, S.Y.4
Chen, I.S.5
-
15
-
-
0035854290
-
-
Isaka, M.; Tanticharoen, M.; Kongsaeree, P.; Thebtaranonth, Y. Structures of cordypyridones A-D. antimalarial N-hydroxy- and N-methoxy-2- pyridones from the insect pathogenic fungus Cordyceps nipponica. J. Org. Chem. 2001, 66, 4803-4808.
-
Isaka, M.; Tanticharoen, M.; Kongsaeree, P.; Thebtaranonth, Y. Structures of cordypyridones A-D. antimalarial N-hydroxy- and N-methoxy-2- pyridones from the insect pathogenic fungus Cordyceps nipponica. J. Org. Chem. 2001, 66, 4803-4808.
-
-
-
-
16
-
-
38449101721
-
YCM1008A, a novel Ca2+ signaling inhibitor, produced by Fusarium sp. YCM1008
-
Koizumi, F.; Fukumitsu, N.; Zhao, J.; Chanklan, R.; Miyakawa, T.; Kawahara, S.; Iwamoto, S.; Suzuki, M.; Kakita, S.; Rahayu, E. S.; Hosokawa, S.; Tatsula, K.; Ichimura, M. YCM1008A, a novel Ca2+ signaling inhibitor, produced by Fusarium sp. YCM1008. J. Antibiot. 2007, 60, 455-458.
-
(2007)
J. Antibiot
, vol.60
, pp. 455-458
-
-
Koizumi, F.1
Fukumitsu, N.2
Zhao, J.3
Chanklan, R.4
Miyakawa, T.5
Kawahara, S.6
Iwamoto, S.7
Suzuki, M.8
Kakita, S.9
Rahayu, E.S.10
Hosokawa, S.11
Tatsula, K.12
Ichimura, M.13
-
17
-
-
0030772641
-
Pyranoquinoline alkaloids from Zanthoxylum simulans
-
Chen, I. S.; Tsai, I. W.; Teng, C. M.; Chen, J. J.; Chang, Y. L.; Ko, P. N.; Lu, M. C.; Pezzuto, J. M. Pyranoquinoline alkaloids from Zanthoxylum simulans. Phytochemistry 1997, 46, 525-529.
-
(1997)
Phytochemistry
, vol.46
, pp. 525-529
-
-
Chen, I.S.1
Tsai, I.W.2
Teng, C.M.3
Chen, J.J.4
Chang, Y.L.5
Ko, P.N.6
Lu, M.C.7
Pezzuto, J.M.8
-
18
-
-
10044281491
-
Quinolone alkaloids with nitric oxide production inhibitory activity from Orixa japonica
-
Ito, C.; Itoigawa, M.; Furukawa, A.; Hirano, T.; Murata, T.; Kaneda, N.; Hisada, Y.; Okuda, K.; Furukawa, H. Quinolone alkaloids with nitric oxide production inhibitory activity from Orixa japonica. J. Nut. Prod. 2004, 67, 1800-1803.
-
(2004)
J. Nut. Prod
, vol.67
, pp. 1800-1803
-
-
Ito, C.1
Itoigawa, M.2
Furukawa, A.3
Hirano, T.4
Murata, T.5
Kaneda, N.6
Hisada, Y.7
Okuda, K.8
Furukawa, H.9
-
19
-
-
12644299592
-
-
McBrien, K. D.; Gao, Q.; Huang, S.; Klohr, S. E.; Wang, R. R.; Pirnik, D. M.; Neddermann, K. M.; Bursuker, I.; Kadow, K. F.; Leet, J. F. Fusaricide, a new cytotoxic N-hydroxypyridone from Fusarium sp. J. Nat. Prod. 1996, 59, 1151-1153.
-
McBrien, K. D.; Gao, Q.; Huang, S.; Klohr, S. E.; Wang, R. R.; Pirnik, D. M.; Neddermann, K. M.; Bursuker, I.; Kadow, K. F.; Leet, J. F. Fusaricide, a new cytotoxic N-hydroxypyridone from Fusarium sp. J. Nat. Prod. 1996, 59, 1151-1153.
-
-
-
-
20
-
-
0345491026
-
Bisquinolinone alkaloids from Melicope ptelefolia
-
Kamperdick, C.; Van, N. H.; Van Sung, T.; Adam, G. Bisquinolinone alkaloids from Melicope ptelefolia. Phytochemistry 1999, 50, 177-181.
-
(1999)
Phytochemistry
, vol.50
, pp. 177-181
-
-
Kamperdick, C.1
Van, N.H.2
Van Sung, T.3
Adam, G.4
-
21
-
-
0028004138
-
Chemical and Bioactive Constituents from Zanthoxylum Simulans
-
Chen, I. S.; Wu, S. J.; Tsai, I. L.; Wu, T. S.; Pezzuto, J. M.; Lu, M. C.; Chai, H.; Suh, N.; Teng, C. M. Chemical and Bioactive Constituents from Zanthoxylum Simulans. J. Nat. Prod. 1994, 57, 1206-1211.
-
(1994)
J. Nat. Prod
, vol.57
, pp. 1206-1211
-
-
Chen, I.S.1
Wu, S.J.2
Tsai, I.L.3
Wu, T.S.4
Pezzuto, J.M.5
Lu, M.C.6
Chai, H.7
Suh, N.8
Teng, C.M.9
-
22
-
-
33746596592
-
Substituted 4-(3-cyanopyridin-2-yhhio)acetoacetates: New convenient reagents for the synthesis of heterocycles
-
(a) Rodinovskaya, L. A.; Shestopalov, A. M.; Gromova, A. V.; Shestopalov, A. A. Substituted 4-(3-cyanopyridin-2-yhhio)acetoacetates: new convenient reagents for the synthesis of heterocycles. Synthesis 2006, 2357-2370.
-
(2006)
Synthesis
, pp. 2357-2370
-
-
Rodinovskaya, L.A.1
Shestopalov, A.M.2
Gromova, A.V.3
Shestopalov, A.A.4
-
23
-
-
3843077397
-
4-(3-Cyanopyridin-2-ylthio)acetoacetates in synthesis of heterocycles
-
(b) Rodinovskaya, L. A.; Shestopalov, A. M.; Gromova, A. V. 4-(3-Cyanopyridin-2-ylthio)acetoacetates in synthesis of heterocycles. Russ. Chem. Bull., Int. Ed. 2003, 52, 2185-2196.
-
(2003)
Russ. Chem. Bull., Int. Ed
, vol.52
, pp. 2185-2196
-
-
Rodinovskaya, L.A.1
Shestopalov, A.M.2
Gromova, A.V.3
-
24
-
-
4544298187
-
-
Wang, X. S.; Zeng, Z. S.; Shi, D. Q.; Wei, X. Y.; Zong, Z. M. One-step synthesis of 2-amino-3-cyano-4-aryl-1,4,5,6-tetrahydropyrano[3,2-c]quinolin-5-one derivatives using KF-A12O3 as catalyst. Synth. Commun. 2004, 34, 3021-3027.
-
(c) Wang, X. S.; Zeng, Z. S.; Shi, D. Q.; Wei, X. Y.; Zong, Z. M. One-step synthesis of 2-amino-3-cyano-4-aryl-1,4,5,6-tetrahydropyrano[3,2-c]quinolin-5-one derivatives using KF-A12O3 as catalyst. Synth. Commun. 2004, 34, 3021-3027.
-
-
-
-
25
-
-
0034553666
-
New heterocycles from substituted 2-amino-5-oxo-4-phenyl-6-hydro-4H-pyrano[3,2-c] quinoline-3-carbonitriles
-
For recent examples, see
-
(a) For recent examples, see Dodia, N.; Shah, A. New heterocycles from substituted 2-amino-5-oxo-4-phenyl-6-hydro-4H-pyrano[3,2-c] quinoline-3-carbonitriles. Indian J. Heterocycl. Chem. 2000, 10, 155-156.
-
(2000)
Indian J. Heterocycl. Chem
, vol.10
, pp. 155-156
-
-
Dodia, N.1
Shah, A.2
-
26
-
-
0002116611
-
General method for the preparation of substituted 2-amino-4H,5H-pyrano[4,3-b]pyran-5-ones and 2-amino-4H-pyrano[3,2-c]pyridine-5-ones
-
(b) Stoyanov, E. V.; Ivanov, I. C.; Heber, D. General method for the preparation of substituted 2-amino-4H,5H-pyrano[4,3-b]pyran-5-ones and 2-amino-4H-pyrano[3,2-c]pyridine-5-ones. Molecules 2000, 5, 19-32.
-
(2000)
Molecules
, vol.5
, pp. 19-32
-
-
Stoyanov, E.V.1
Ivanov, I.C.2
Heber, D.3
-
27
-
-
0035622253
-
Synthesis of some tricyclic and tetracyclic ring systems built on 4-hydroxy-2-quinolones
-
(c) Dodia, N.; Shah, A. Synthesis of some tricyclic and tetracyclic ring systems built on 4-hydroxy-2-quinolones. Heterocycl. Commun. 2001, 7, 289-294.
-
(2001)
Heterocycl. Commun
, vol.7
, pp. 289-294
-
-
Dodia, N.1
Shah, A.2
-
28
-
-
10044273148
-
Malonates in cyclocondensation reactions
-
(d) Stadlbauer, W.; Badawey, E. S.; Hojas, G.; Roschger, P.; Kappe, T. Malonates in cyclocondensation reactions. Molecules 2001, 6, 338-352.
-
(2001)
Molecules
, vol.6
, pp. 338-352
-
-
Stadlbauer, W.1
Badawey, E.S.2
Hojas, G.3
Roschger, P.4
Kappe, T.5
-
29
-
-
0036661517
-
One-pot synthesis of novel spiro pyranoquinolones
-
(e) Mulwad, V. V.; Lobar, M. V. One-pot synthesis of novel spiro pyranoquinolones. Indian J. Heterocycl. Chem. 2002, 12, 57-60.
-
(2002)
Indian J. Heterocycl. Chem
, vol.12
, pp. 57-60
-
-
Mulwad, V.V.1
Lobar, M.V.2
-
30
-
-
27144521964
-
Cross reactions of cyanoacetic acid derivatives with carbonyl compounds 3. One-step synthesis of substituted 2-amino-5-oxo-4,5- dihydropyrano[3,2-c]chromenes
-
(f) Rodinovskaya, L. A.; Shestopalov, A. M.; Shestopalov, A. A.; Litvinov, V. P. Cross reactions of cyanoacetic acid derivatives with carbonyl compounds 3. One-step synthesis of substituted 2-amino-5-oxo-4,5- dihydropyrano[3,2-c]chromenes. Russ. Chem. Bull., Int. Ed. 2005, 54, 992-996.
-
(2005)
Russ. Chem. Bull., Int. Ed
, vol.54
, pp. 992-996
-
-
Rodinovskaya, L.A.1
Shestopalov, A.M.2
Shestopalov, A.A.3
Litvinov, V.P.4
-
31
-
-
22244439822
-
Studies with quinolines: New synthetic routes to 4H,5H,6H,9H-benzo[ij]pyrano[2,3-b]quinolizine-8- one. 4H-pyrano[2,3-b]pyridine. 2H-pyran-2-one and pyranopyridoquinoline derivatives
-
(g) El-Taweel, F. M. A. A. Studies with quinolines: New synthetic routes to 4H,5H,6H,9H-benzo[ij]pyrano[2,3-b]quinolizine-8- one. 4H-pyrano[2,3-b]pyridine. 2H-pyran-2-one and pyranopyridoquinoline derivatives. J. Heterocycl. Chem. 2005, 42, 943-946.
-
(2005)
J. Heterocycl. Chem
, vol.42
, pp. 943-946
-
-
El-Taweel, F.M.A.A.1
-
32
-
-
0344391912
-
Synthesis of biologically active 3,8-dioxo-10-hydroxypyrano[2,3-f]quinoline and its reactions
-
(a) Choudhari, B. P.; Mulwad, V. V. Synthesis of biologically active 3,8-dioxo-10-hydroxypyrano[2,3-f]quinoline and its reactions. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2003, 42, 2080-2085.
-
(2003)
Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem
, vol.42
, pp. 2080-2085
-
-
Choudhari, B.P.1
Mulwad, V.V.2
-
33
-
-
2842594783
-
Synthesis and biological activity of novel pyranobisbenzopyrans and benzopyranopyranoquinolines
-
(b) Balasubramanian, C.; Sekur, M.; Mohan, P. S. Synthesis and biological activity of novel pyranobisbenzopyrans and benzopyranopyranoquinolines. Indian J. Chem., Sect B: Org. Chem. Incl. Med. Chem. 1996, 35, 1225-1227.
-
(1996)
Indian J. Chem., Sect B: Org. Chem. Incl. Med. Chem
, vol.35
, pp. 1225-1227
-
-
Balasubramanian, C.1
Sekur, M.2
Mohan, P.S.3
-
34
-
-
25144441808
-
-
Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Zhao, J.; Jia, S.; Xu, L.; Crogan-Grundy, C.; Denis, R.; Barriault, N.; Vaillancourt, L.; Charron, S.; Dodd, J.; Attardo, G.; Labrecque, D.; Lamothe, S.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cui, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure - activity relationships of the 7- and 5-, 6-, 8-positions. Bioorg. Med. Chem. Lett. 2005, 15, 4745-4751.
-
(a) Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Zhao, J.; Jia, S.; Xu, L.; Crogan-Grundy, C.; Denis, R.; Barriault, N.; Vaillancourt, L.; Charron, S.; Dodd, J.; Attardo, G.; Labrecque, D.; Lamothe, S.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cui, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure - activity relationships of the 7- and 5-, 6-, 8-positions. Bioorg. Med. Chem. Lett. 2005, 15, 4745-4751.
-
-
-
-
35
-
-
9444265410
-
Antivascular and antitumor evaluation of 2-amino-4-(3-bromo-4,5-dimethoxy-phenyl)-3-cyano-4H-chromenes, a novel series of anticancer agents
-
(b) Gourdeau, H.; Leblond, L.; Hamelin, B.; Desputeau, C.; Dong, K.; Kianicka, I.; Custeau, D.; Boudreau, C.; Geerts, L.; Cai, S.-X.; Drewe, J.; Labrecque, D.; Kasibhatla, S.; Tseng, B. Antivascular and antitumor evaluation of 2-amino-4-(3-bromo-4,5-dimethoxy-phenyl)-3-cyano-4H-chromenes, a novel series of anticancer agents. Mol. Cancer Ther. 2004, 3, 1375-1383.
-
(2004)
Mol. Cancer Ther
, vol.3
, pp. 1375-1383
-
-
Gourdeau, H.1
Leblond, L.2
Hamelin, B.3
Desputeau, C.4
Dong, K.5
Kianicka, I.6
Custeau, D.7
Boudreau, C.8
Geerts, L.9
Cai, S.-X.10
Drewe, J.11
Labrecque, D.12
Kasibhatla, S.13
Tseng, B.14
-
36
-
-
9444289388
-
Discovery and mechanism of action of a novel series of apoptosis inducers with potential vascular targeting activity
-
(c) Kasibhatla, S.; Gourdeau, H.; Meerovitch, K.; Drewe, J.; Reddy, S.; Qiu, L.; Zhang, H.; Bergeron, F.; Bouffard, D.; Yang, Q.; Herich, J.; Lamothe, S.; Cai, S. X.; Tseng, B. Discovery and mechanism of action of a novel series of apoptosis inducers with potential vascular targeting activity. Mol. Cancer Ther. 2004, 3, 1365-1373.
-
(2004)
Mol. Cancer Ther
, vol.3
, pp. 1365-1373
-
-
Kasibhatla, S.1
Gourdeau, H.2
Meerovitch, K.3
Drewe, J.4
Reddy, S.5
Qiu, L.6
Zhang, H.7
Bergeron, F.8
Bouffard, D.9
Yang, Q.10
Herich, J.11
Lamothe, S.12
Cai, S.X.13
Tseng, B.14
-
37
-
-
9744248288
-
-
Kemnitzer, W.; Drewe, J.; Jiang, S.; Zhang, H.; Wang, Y.; Zhao, J.; Jia, S.; Herich, J.; Labreque, D.; Storer, R.; Meerovitch, K.; Bouffard, D.; Rej, R.; Denis, R.; Blais, C.; Lamothe, S.; Attardo, G.; Gourdeau, H.; Tseng, B.; Kasibhatla, S.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. I. Structure-activity relationships of the 4-aryl group. J. Med. Chem. 2004, 47, 6299-6310.
-
(d) Kemnitzer, W.; Drewe, J.; Jiang, S.; Zhang, H.; Wang, Y.; Zhao, J.; Jia, S.; Herich, J.; Labreque, D.; Storer, R.; Meerovitch, K.; Bouffard, D.; Rej, R.; Denis, R.; Blais, C.; Lamothe, S.; Attardo, G.; Gourdeau, H.; Tseng, B.; Kasibhatla, S.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. I. Structure-activity relationships of the 4-aryl group. J. Med. Chem. 2004, 47, 6299-6310.
-
-
-
-
38
-
-
34250904254
-
Discovery of 4-Aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 3. Structure-activity relationships of fused rings at the 7,8-positions
-
(e) Kemnitzer, W.; Drewe, J.; Jiang, S. C.; Zhang, H.; Zhao, J. H.; Crogan-Grundy, C.; Xu, L. F.; Lamothe, S.; Gourdeau, H.; Denis, R.; Tseng, B.; Kasibhatla, S.; Cai, S. X. Discovery of 4-Aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 3. Structure-activity relationships of fused rings at the 7,8-positions. J. Med. Chem. 2007, 50, 2858-2864.
-
(2007)
J. Med. Chem
, vol.50
, pp. 2858-2864
-
-
Kemnitzer, W.1
Drewe, J.2
Jiang, S.C.3
Zhang, H.4
Zhao, J.H.5
Crogan-Grundy, C.6
Xu, L.F.7
Lamothe, S.8
Gourdeau, H.9
Denis, R.10
Tseng, B.11
Kasibhatla, S.12
Cai, S.X.13
-
39
-
-
43049104755
-
-
PCT Int. Appl. WO 2003097806 A2 20031127
-
(f) Cai, S. X.; Jiang, S.; Kemnitzer, W. E.; Zhang, H.; Attardo, G.; Denis, R. PCT Int. Appl. WO 2003097806 A2 20031127, 2004.
-
(2004)
-
-
Cai, S.X.1
Jiang, S.2
Kemnitzer, W.E.3
Zhang, H.4
Attardo, G.5
Denis, R.6
-
40
-
-
43049110696
-
-
PCT Int. Appl. WO 2003096982 A2 20031127
-
(g) Cai, S. X.; Jiang, S.; Attardo, G.; Denis, R.; Storer, R.; Rej, R. PCT Int. Appl. WO 2003096982 A2 20031127, 2003.
-
(2003)
-
-
Cai, S.X.1
Jiang, S.2
Attardo, G.3
Denis, R.4
Storer, R.5
Rej, R.6
-
43
-
-
43049105128
-
-
PCT Int. Appl. WO 2002092076 A1 20021121
-
(j) Cai, S. X.; Zhang, H.; Kemmitzer, W. E.; Jiang, S.; Drewe, J. A.; Storer, R. PCT Int. Appl. WO 2002092076 A1 20021121, 2002.
-
(2002)
-
-
Cai, S.X.1
Zhang, H.2
Kemmitzer, W.E.3
Jiang, S.4
Drewe, J.A.5
Storer, R.6
-
44
-
-
43049114311
-
-
PCT Int. Appl. WO 2001034591 A2 20010517
-
(k) Drewe, J. A.; Cai, S. X.; Wang, Y. PCT Int. Appl. WO 2001034591 A2 20010517, 2001.
-
(2001)
-
-
Drewe, J.A.1
Cai, S.X.2
Wang, Y.3
-
45
-
-
34250334153
-
Antiproliferative and apoptosis inducing properties of pyrano[3,2-c] pyridones accessible by a one-step multi-component synthesis
-
For preliminary communication describing part of this work, see
-
For preliminary communication describing part of this work, see Magedov, I. V.; Manpadi, M.; Evdokimov, N. M.; Elias, E. M.; Rozhkova, E.; Ogasawara, M. A.; Bettale, J. D.; Przeval'skii, N. M.; Rogelj, S.; Kornienko, A. Antiproliferative and apoptosis inducing properties of pyrano[3,2-c] pyridones accessible by a one-step multi-component synthesis. Bioorg. Med. Chem. Lett. 2007, 17, 3872-3876.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 3872-3876
-
-
Magedov, I.V.1
Manpadi, M.2
Evdokimov, N.M.3
Elias, E.M.4
Rozhkova, E.5
Ogasawara, M.A.6
Bettale, J.D.7
Przeval'skii, N.M.8
Rogelj, S.9
Kornienko, A.10
-
46
-
-
0343265614
-
Reaction of 4-hydroxy-6-methyl-2- pyrone with various primary amines: Synthesis of N-substituted 2-pyridones and aliphatic intermediates
-
Castillo, S.; Ouadahi, H.; Herault, V. Reaction of 4-hydroxy-6-methyl-2- pyrone with various primary amines: synthesis of N-substituted 2-pyridones and aliphatic intermediates. Bull. Soc. Chim. Fr. 1982, 257-261.
-
(1982)
Bull. Soc. Chim. Fr
, pp. 257-261
-
-
Castillo, S.1
Ouadahi, H.2
Herault, V.3
-
47
-
-
43049139270
-
-
X-ray data for compound 15 is available in the Supporting Information.
-
X-ray data for compound 15 is available in the Supporting Information.
-
-
-
-
48
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65, 55-63.
-
(1983)
J. Immunol. Methods
, vol.65
, pp. 55-63
-
-
Mosmann, T.1
-
49
-
-
0031080192
-
Study of the apoptosis induced in vitro by antitumoral drugs on leukaemic cells
-
See, for example
-
See, for example Vial, J. P.; Belloc, F.; Dumain, P.; Besnard, S.; Lacombe, F.; Boisseau, M. R.; Reiffers, J.; Bernard, P. Study of the apoptosis induced in vitro by antitumoral drugs on leukaemic cells. Leukemia Res. 1997, 21, 163-172.
-
(1997)
Leukemia Res
, vol.21
, pp. 163-172
-
-
Vial, J.P.1
Belloc, F.2
Dumain, P.3
Besnard, S.4
Lacombe, F.5
Boisseau, M.R.6
Reiffers, J.7
Bernard, P.8
-
50
-
-
0029043888
-
A novel assay for apoptosis: How cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein-labeled annexin-V
-
(a) Vermes, I.; Haanen, C.; Steffens-Nakken, H.; Reutelingsperger, C. A novel assay for apoptosis: How cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein-labeled annexin-V. J. Immunol. Methods 1995, 184, 39-51.
-
(1995)
J. Immunol. Methods
, vol.184
, pp. 39-51
-
-
Vermes, I.1
Haanen, C.2
Steffens-Nakken, H.3
Reutelingsperger, C.4
-
51
-
-
0026508561
-
Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages
-
(b) Fadok, V. A.; Voelkler, D. R.; Campbell, P. A.; Cohen, J. J.; Bratton, D. L.; Henson, P. M. Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J. Immunol. 1992, 148, 2207-2216.
-
(1992)
J. Immunol
, vol.148
, pp. 2207-2216
-
-
Fadok, V.A.1
Voelkler, D.R.2
Campbell, P.A.3
Cohen, J.J.4
Bratton, D.L.5
Henson, P.M.6
-
52
-
-
0142036683
-
Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin
-
Hamel, E. Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin. Cell Biochem. Biophys. 2003, 38, 1-21.
-
(2003)
Cell Biochem. Biophys
, vol.38
, pp. 1-21
-
-
Hamel, E.1
-
53
-
-
33846523617
-
Targeted anti-mitotic therapies: Can we improve on tubulin agents?
-
Jackson, J. R.; Patrick, D. R.; Dar, M. M.; Huang, P. S. Targeted anti-mitotic therapies: can we improve on tubulin agents? Nat. Rev. Cancer 2007, 7, 107-117.
-
(2007)
Nat. Rev. Cancer
, vol.7
, pp. 107-117
-
-
Jackson, J.R.1
Patrick, D.R.2
Dar, M.M.3
Huang, P.S.4
-
54
-
-
35748981525
-
Angiogenesis inhibitors. Drug selectivity and target specificity
-
Kesisis, G.; Broxterman, H.; Giaccone, G. Angiogenesis inhibitors. Drug selectivity and target specificity. Curr. Pharm. Des. 2007, 13, 2795-2809.
-
(2007)
Curr. Pharm. Des
, vol.13
, pp. 2795-2809
-
-
Kesisis, G.1
Broxterman, H.2
Giaccone, G.3
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