-
1
-
-
33749034730
-
Topoisomerase 1 inhibitors: Camptothecins and beyond
-
Pommier, Y. Topoisomerase 1 inhibitors: camptothecins and beyond. Nat. Rev. Cancer. 2006, 6, 789-802.
-
(2006)
Nat. Rev. Cancer
, vol.6
, pp. 789-802
-
-
Pommier, Y.1
-
2
-
-
0036085460
-
Cellular roles of DNA topoisomerases: A molecular perspective
-
Wang, J. C. Cellular roles of DNA topoisomerases: a molecular perspective. Nat. Rev. Mol. Cell Biol. 2002, 3, 430-440.
-
(2002)
Nat. Rev. Mol. Cell Biol
, vol.3
, pp. 430-440
-
-
Wang, J.C.1
-
3
-
-
0028998076
-
Synthesis and antitumor activity of novel water soluble derivatives of camptothecin as specific inhibitors of topoisomerase I
-
Luzzio, M. J.; Besterman, J. M.; Emerson, D. L.; Evans, M. G.; Lackey, K.; Leitner, P. L.; McIntyre, G.; Morton, B.; Myers, P. L.; Peel, M.; Sisco, J. M.; Sternbach, D. D.; Tong, W.; Traesdale, A.; Uehling, D. E.; Vuong, A.; Yates, J. Synthesis and antitumor activity of novel water soluble derivatives of camptothecin as specific inhibitors of topoisomerase I. J. Med. Chem. 1995, 38, 395-401.
-
(1995)
J. Med. Chem
, vol.38
, pp. 395-401
-
-
Luzzio, M.J.1
Besterman, J.M.2
Emerson, D.L.3
Evans, M.G.4
Lackey, K.5
Leitner, P.L.6
McIntyre, G.7
Morton, B.8
Myers, P.L.9
Peel, M.10
Sisco, J.M.11
Sternbach, D.D.12
Tong, W.13
Traesdale, A.14
Uehling, D.E.15
Vuong, A.16
Yates, J.17
-
4
-
-
0028006314
-
Elevation of topoisomerase I messenger RNA, protein, and catalytic activity in human tumors: Demonstration of tumor-type specficity and implications for cancer chemotherapy
-
Husain, I.; Mohler, J. L.; Seigler, H. F.; and Besterman, J. M. Elevation of topoisomerase I messenger RNA, protein, and catalytic activity in human tumors: demonstration of tumor-type specficity and implications for cancer chemotherapy. Cancer. Res. 1994, 54 (2), 539-546.
-
(1994)
Cancer. Res
, vol.54
, Issue.2
, pp. 539-546
-
-
Husain, I.1
Mohler, J.L.2
Seigler, H.F.3
Besterman, J.M.4
-
5
-
-
1542507062
-
Camptothecin: Current perspectives
-
Thomas, C. J.; Rahier, N. J.; Hecht, S. M. Camptothecin: current perspectives. Bioorg. Med. Chem. 2004, 12, 1585-1604.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 1585-1604
-
-
Thomas, C.J.1
Rahier, N.J.2
Hecht, S.M.3
-
6
-
-
0038207882
-
Non-camptothecin DNA topoisomerase I inhibitors in cancer chemotherapy
-
Meng, L.-H.; Liao, Y.-Z.; Pommier, Y. Non-camptothecin DNA topoisomerase I inhibitors in cancer chemotherapy. Curr. Top. Med. Chem. 2003, 3, 305-320.
-
(2003)
Curr. Top. Med. Chem
, vol.3
, pp. 305-320
-
-
Meng, L.-H.1
Liao, Y.-Z.2
Pommier, Y.3
-
7
-
-
0034040082
-
-
Bailly, C. Topoisomerase I poisons and suppressors as anticancer drugs. Curr. Med. Chem. 2000, 7, 39-58.
-
Bailly, C. Topoisomerase I poisons and suppressors as anticancer drugs. Curr. Med. Chem. 2000, 7, 39-58.
-
-
-
-
8
-
-
7144248725
-
The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminata
-
Wall, M. E.; Wani, M. C.; Cook, C. E.; Palmer, K. H.; McPhail, A. T.; Sim, G. A. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminata. J. Am. Chem. Soc. 1966, 88, 3888-3890.
-
(1966)
J. Am. Chem. Soc
, vol.88
, pp. 3888-3890
-
-
Wall, M.E.1
Wani, M.C.2
Cook, C.E.3
Palmer, K.H.4
McPhail, A.T.5
Sim, G.A.6
-
9
-
-
0037180432
-
The mechanism of topoisomerase I poisoning by a camptothecin analog
-
Staker, B. L.; Hjerrild, K.; Feese, M. D.; Behnke, C. A.; Burgin, A. B.; Stewart, L. The mechanism of topoisomerase I poisoning by a camptothecin analog. Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 15387-15392.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A
, vol.99
, pp. 15387-15392
-
-
Staker, B.L.1
Hjerrild, K.2
Feese, M.D.3
Behnke, C.A.4
Burgin, A.B.5
Stewart, L.6
-
10
-
-
17144371295
-
Structures of three classes of anticancer agents bound to the human topoisomerase I - DNA covalent complex
-
Staker, B. L.; Feese, M. D.; Cushman, M.; Pommier, Y.; Zembower, D.; Stewart, L.; Burgin, A. Structures of three classes of anticancer agents bound to the human topoisomerase I - DNA covalent complex. J. Med. Chem. 2005, 48, 2336-2345.
-
(2005)
J. Med. Chem
, vol.48
, pp. 2336-2345
-
-
Staker, B.L.1
Feese, M.D.2
Cushman, M.3
Pommier, Y.4
Zembower, D.5
Stewart, L.6
Burgin, A.7
-
11
-
-
0034513226
-
Molecular and biological determinants of the cytotoxic actions of camptothecins. Perspective for the development of new topoisomerase I inhibitors
-
Kohn, K. W.; Pommier, Y. Molecular and biological determinants of the cytotoxic actions of camptothecins. Perspective for the development of new topoisomerase I inhibitors. Ann. N. Y. Acad. Sci. 2000, 922, 11-26.
-
(2000)
Ann. N. Y. Acad. Sci
, vol.922
, pp. 11-26
-
-
Kohn, K.W.1
Pommier, Y.2
-
12
-
-
0032189683
-
Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme
-
Pommier, Y.; Pourquier, P.; Fan, Y.; Strumberg, D. Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme. Biochim. Biophys. Acta 1998, 1400, 83-106.
-
(1998)
Biochim. Biophys. Acta
, vol.1400
, pp. 83-106
-
-
Pommier, Y.1
Pourquier, P.2
Fan, Y.3
Strumberg, D.4
-
13
-
-
0027435043
-
Plant Antitumor Agents. 30. Synthesis and structure activity of novel camptothecin analogs
-
Wall, M. E.; Wani, M. C.; Nicholas, A. W.; Manikumar, G.; Tele, C.; Moore, L.; Truesdale, A.; Leitner, P.; Besterman, J. M. Plant Antitumor Agents. 30. Synthesis and structure activity of novel camptothecin analogs. J. Med. Chem. 1993, 36, 2689-2700.
-
(1993)
J. Med. Chem
, vol.36
, pp. 2689-2700
-
-
Wall, M.E.1
Wani, M.C.2
Nicholas, A.W.3
Manikumar, G.4
Tele, C.5
Moore, L.6
Truesdale, A.7
Leitner, P.8
Besterman, J.M.9
-
14
-
-
0028856206
-
Convergent approach to water-soluble camptothecin derivatives
-
Xie, Z.; Ootsu, K.; and Akimoto, H. Convergent approach to water-soluble camptothecin derivatives. Bioorg. Med. Chem. Lett. 1995, 5 (19), 2189-2194.
-
(1995)
Bioorg. Med. Chem. Lett
, vol.5
, Issue.19
, pp. 2189-2194
-
-
Xie, Z.1
Ootsu, K.2
Akimoto, H.3
-
15
-
-
0023034927
-
Plant antitumor agents. 23. Synthesis and antileukemic activity of camptothecin analogues
-
Wani, M. C.; Nicholas, A. W.; Wall, M. E. Plant antitumor agents. 23. Synthesis and antileukemic activity of camptothecin analogues. J. Med. Chem. 1986, 29, 2358-2363.
-
(1986)
J. Med. Chem
, vol.29
, pp. 2358-2363
-
-
Wani, M.C.1
Nicholas, A.W.2
Wall, M.E.3
-
16
-
-
0032555250
-
Synthesis and in vitro cytotoxicity of C(20)(RS)- camptothecin analogues modified at both B (or A) and E ring
-
Jew, S.-S.; Kim, M. G.; Kim, H.-J.; Rho, E.-Y.; Park, H.-G.; Kim, J.-K.; Han, H.-J.; Lee, H. Synthesis and in vitro cytotoxicity of C(20)(RS)- camptothecin analogues modified at both B (or A) and E ring. Bioorg. Med. Chem. Lett. 1998, 8, 1797-1800.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 1797-1800
-
-
Jew, S.-S.1
Kim, M.G.2
Kim, H.-J.3
Rho, E.-Y.4
Park, H.-G.5
Kim, J.-K.6
Han, H.-J.7
Lee, H.8
-
17
-
-
0033756761
-
Practical synthesis of (S)-7-(2-isopropylamino)ethylcamptothecin hydrochloride, potent topoisomerase I inhibitor
-
Sep-Oct
-
Ahn, S. K.; Choi, N. S.; Jeong, B. S.; Kim, K. K.; Journ, D. J.; Kim, J. K.; Lee, S. J.; Kim, J. W.; Hong, C. I.; Jew, S. Practical synthesis of (S)-7-(2-isopropylamino)ethylcamptothecin hydrochloride, potent topoisomerase I inhibitor. J. Heterocycl. Chem 2000, (Sep-Oct), 1141.
-
(2000)
J. Heterocycl. Chem
, pp. 1141
-
-
Ahn, S.K.1
Choi, N.S.2
Jeong, B.S.3
Kim, K.K.4
Journ, D.J.5
Kim, J.K.6
Lee, S.J.7
Kim, J.W.8
Hong, C.I.9
Jew, S.10
-
18
-
-
0018901322
-
Plant antitumor agents. 18. Synthesis and biological activity of camptothecin analogues
-
Wani, M. C.; Ronman, P. E.; Lindley, J. T.; Wall, M. E. Plant antitumor agents. 18. Synthesis and biological activity of camptothecin analogues. J. Med. Chem. 1980, 23, 554-560.
-
(1980)
J. Med. Chem
, vol.23
, pp. 554-560
-
-
Wani, M.C.1
Ronman, P.E.2
Lindley, J.T.3
Wall, M.E.4
-
19
-
-
0015292126
-
Treatment of malignant melanoma with camptochecin (NSC-100880)
-
Gottlieb, J. A.; Luce, J. K. Treatment of malignant melanoma with camptochecin (NSC-100880). Cancer Chemother. Rep. 1972, 56, 103-105.
-
(1972)
Cancer Chemother. Rep
, vol.56
, pp. 103-105
-
-
Gottlieb, J.A.1
Luce, J.K.2
-
20
-
-
0024560495
-
Structure-activity study of the actions of camptothecin derivatives on mammalian topoisomerase I: Evidence for a specific receptor site and a relation to antitumor activity
-
Jaxel, C.; Kohn, K. W.; Wani, M. C.; Wall, M. E.; Pommier, Y. Structure-activity study of the actions of camptothecin derivatives on mammalian topoisomerase I: evidence for a specific receptor site and a relation to antitumor activity. Cancer Res. 1989, 49, 1465-1469.
-
(1989)
Cancer Res
, vol.49
, pp. 1465-1469
-
-
Jaxel, C.1
Kohn, K.W.2
Wani, M.C.3
Wall, M.E.4
Pommier, Y.5
-
21
-
-
0010267346
-
Phase-I pharmacokinetic study of topotecan by 24-h continuous-infusion weekly
-
Haas, N. B.; LaCreta, F. P.; Walczak, J.; Hudes, G. R.; Brennan, J. M.; Ozols, R. F.; O'Dwyer, P. J. Phase-I pharmacokinetic study of topotecan by 24-h continuous-infusion weekly. Cancer Res. 1994, 54 (5), 1220-1226.
-
(1994)
Cancer Res
, vol.54
, Issue.5
, pp. 1220-1226
-
-
Haas, N.B.1
LaCreta, F.P.2
Walczak, J.3
Hudes, G.R.4
Brennan, J.M.5
Ozols, R.F.6
O'Dwyer, P.J.7
-
22
-
-
0031815336
-
Protein-linked DNA strand breaks induced by NSC 314622, a novel noncamptothecin topoisomerase I poison
-
Kohlhagen, G.; Pauli, K. D.; Cushman, M.; Nagafuji, P.; and Pommier, Y. Protein-linked DNA strand breaks induced by NSC 314622, a novel noncamptothecin topoisomerase I poison. Mol. Pharm. 1998, 54, 50-58.
-
(1998)
Mol. Pharm
, vol.54
, pp. 50-58
-
-
Kohlhagen, G.1
Pauli, K.D.2
Cushman, M.3
Nagafuji, P.4
Pommier, Y.5
-
23
-
-
7444233119
-
Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic rings
-
Nagarajan, M.; Morrell, A.; Fort, B. C.; Meckley, M. R.; Antony, S.; Kohlhagen, G.; Pommier, Y.; Cushman, M. Synthesis and anticancer activity of simplified indenoisoquinoline topoisomerase I inhibitors lacking substituents on the aromatic rings. J. Med. Chem. 2004, 47 (23), 5651-5661.
-
(2004)
J. Med. Chem
, vol.47
, Issue.23
, pp. 5651-5661
-
-
Nagarajan, M.1
Morrell, A.2
Fort, B.C.3
Meckley, M.R.4
Antony, S.5
Kohlhagen, G.6
Pommier, Y.7
Cushman, M.8
-
24
-
-
34548504314
-
Optimization of the indenonone ring of indenoisoquinoline topoisomerase I inhibitors
-
Morrell, A.; Placzek, M.; Parmley, S.; Grella, B.; Antony, S.; Pommier, Y.; Cushman, M. Optimization of the indenonone ring of indenoisoquinoline topoisomerase I inhibitors. J. Med. Chem. 2007, 50, 4388-4404.
-
(2007)
J. Med. Chem
, vol.50
, pp. 4388-4404
-
-
Morrell, A.1
Placzek, M.2
Parmley, S.3
Grella, B.4
Antony, S.5
Pommier, Y.6
Cushman, M.7
-
25
-
-
2942596235
-
Synthesis of nitrated indenoisoquinolines as topoisomerase I inhibitors
-
Morrell, A.; Antony, S.; Kohlhagen, G.; Pommier, Y.; Cushman, M. Synthesis of nitrated indenoisoquinolines as topoisomerase I inhibitors. Bioorg. Med. Chem. Lett. 2004, 14, 3659-3663.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 3659-3663
-
-
Morrell, A.1
Antony, S.2
Kohlhagen, G.3
Pommier, Y.4
Cushman, M.5
-
26
-
-
35948968756
-
Novel indenoisoquinolines NSC 725775 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multidrug resistance
-
Antony, S.; Agama, K. K.; Miao, Z.-H.; Takagi, K.; Wright, M. H.; Robles, A. I.; Varticovski, L.; Nagarajan, M.; Morrell, A.; Cushman, M.; Pommier, Y. Novel indenoisoquinolines NSC 725775 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multidrug resistance. Cancer Res. 2007, 67 (21), 10397-10405.
-
(2007)
Cancer Res
, vol.67
, Issue.21
, pp. 10397-10405
-
-
Antony, S.1
Agama, K.K.2
Miao, Z.-H.3
Takagi, K.4
Wright, M.H.5
Robles, A.I.6
Varticovski, L.7
Nagarajan, M.8
Morrell, A.9
Cushman, M.10
Pommier, Y.11
-
27
-
-
0038155266
-
Design, synthesis, and biological evaluation of cytotoxic 11-alkenylindenoisoquinoline topoisomerase I inhibitors and indenoisoquinoline-camptothecin hybrids
-
Fox, B. M.; Xiao, X.; Antony, S.; Kohlhagen, G.; Pommier, Y.; Staker, B. L.; Stewart, L.; Cushman, M. Design, synthesis, and biological evaluation of cytotoxic 11-alkenylindenoisoquinoline topoisomerase I inhibitors and indenoisoquinoline-camptothecin hybrids. J. Med. Chem. 2003, 46, 3275-3282.
-
(2003)
J. Med. Chem
, vol.46
, pp. 3275-3282
-
-
Fox, B.M.1
Xiao, X.2
Antony, S.3
Kohlhagen, G.4
Pommier, Y.5
Staker, B.L.6
Stewart, L.7
Cushman, M.8
-
28
-
-
33144456499
-
Total synthesis and biological evaluation of 22-hydroxyacuminatine
-
Xiao, X.; Antony, S.; Pommier, Y.; Cushman, M. Total synthesis and biological evaluation of 22-hydroxyacuminatine. J. Med. Chem. 2006, 49, 1408-1412.
-
(2006)
J. Med. Chem
, vol.49
, pp. 1408-1412
-
-
Xiao, X.1
Antony, S.2
Pommier, Y.3
Cushman, M.4
-
29
-
-
41149097270
-
A domino N- amidoacylation/aldol-type condensation approach to the synthesis of the Topo-I inhibitor rosettacin and derivatives
-
Pin, F.; Comesse, S.; Sanselme, M.; Daích, A. A domino N- amidoacylation/aldol-type condensation approach to the synthesis of the Topo-I inhibitor rosettacin and derivatives. J. Org. Chem. 2008, 73 (5), 1975-1978.
-
(2008)
J. Org. Chem
, vol.73
, Issue.5
, pp. 1975-1978
-
-
Pin, F.1
Comesse, S.2
Sanselme, M.3
Daích, A.4
-
30
-
-
12444272662
-
14-Azacamptothecin: A potent water-soluble topoisomerase I poison
-
Cheng, K.; Rahier, N. J.; Eisenhauer, B. M.; Gao, R.; Thomas, S. J.; Hecht, S. M. 14-Azacamptothecin: a potent water-soluble topoisomerase I poison. J. Am. Chem. Soc. 2005, 127 (3), 838-839.
-
(2005)
J. Am. Chem. Soc
, vol.127
, Issue.3
, pp. 838-839
-
-
Cheng, K.1
Rahier, N.J.2
Eisenhauer, B.M.3
Gao, R.4
Thomas, S.J.5
Hecht, S.M.6
-
31
-
-
0242407122
-
A naturally occurring human DNA topoisomerase I poison
-
Cagir, A.; Jones, S. H.; Gao, R.; Eisenhauer, B. M.; Hecht, S. M.; Luotonin, A. A naturally occurring human DNA topoisomerase I poison. J. Am. Chem. Soc. 2003, 125, 13628-13629.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 13628-13629
-
-
Cagir, A.1
Jones, S.H.2
Gao, R.3
Eisenhauer, B.M.4
Hecht, S.M.5
Luotonin, A.6
-
32
-
-
7444265432
-
Synthesis and topoisomerase I inhibitory properties of luotonin A analogues
-
Cagir, A.; Eisenhauer, B. M.; Gao, R.; Jones, S. H.; Hecht, S. M. Synthesis and topoisomerase I inhibitory properties of luotonin A analogues. Bioorg. Med. Chem. 2004, 12, 6287-6299.
-
(2004)
Bioorg. Med. Chem
, vol.12
, pp. 6287-6299
-
-
Cagir, A.1
Eisenhauer, B.M.2
Gao, R.3
Jones, S.H.4
Hecht, S.M.5
-
33
-
-
34547141228
-
Total synthesis of luotonin A and 14-substituted analogues
-
Mason, J. J.; Bergman, J. Total synthesis of luotonin A and 14-substituted analogues. Org. Biomol. Chem. 2007, 5, 2486-2490.
-
(2007)
Org. Biomol. Chem
, vol.5
, pp. 2486-2490
-
-
Mason, J.J.1
Bergman, J.2
-
34
-
-
7044241040
-
Synthesis and cytotoxic activity of substituted luotonin A derivatives
-
Dallavalle, S.; Merlini, L.; Beretta, G. L.; Tinelli, S.; Zunino, F. Synthesis and cytotoxic activity of substituted luotonin A derivatives. Bioorg. Med. Chem. Lett. 2004, 14, 5757-5761.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, pp. 5757-5761
-
-
Dallavalle, S.1
Merlini, L.2
Beretta, G.L.3
Tinelli, S.4
Zunino, F.5
-
35
-
-
0004670744
-
Quinoline alkaloids from Camptotheca acuminata
-
Lin, L. Z.; Cordell, G. A. Quinoline alkaloids from Camptotheca acuminata. Phytochemistry 1989, 28, 1295-1297.
-
(1989)
Phytochemistry
, vol.28
, pp. 1295-1297
-
-
Lin, L.Z.1
Cordell, G.A.2
-
36
-
-
0013617922
-
Synthetic approaches to camptothecin
-
Shamma, M.; Novak, L. Synthetic approaches to camptothecin. Tetrahedron 1969, 25, 2275-2279.
-
(1969)
Tetrahedron
, vol.25
, pp. 2275-2279
-
-
Shamma, M.1
Novak, L.2
-
37
-
-
34247613433
-
Investigation of the lactam side chain length necessary for optimal indenoisoquinoline topoisomerase I inhibition and cytotoxicity in human cancer cell cultures
-
Morrell, A.; Placzek, M. S.; Steffen, J. D.; Antony, S.; Agama, K.; Pommier, Y.; Cushman, M. Investigation of the lactam side chain length necessary for optimal indenoisoquinoline topoisomerase I inhibition and cytotoxicity in human cancer cell cultures. J. Med. Chem. 2007, 50, 2040-2048.
-
(2007)
J. Med. Chem
, vol.50
, pp. 2040-2048
-
-
Morrell, A.1
Placzek, M.S.2
Steffen, J.D.3
Antony, S.4
Agama, K.5
Pommier, Y.6
Cushman, M.7
-
38
-
-
33645232024
-
Concise synthesis of 22-hydroxyacuminatine, cytotoxic camptothecinoid from Camptotheca acuminata, by pyridone benzannulation
-
Babjak, M.; Kanazawa, A.; Anderson, R. J.; Greene, A. E. Concise synthesis of 22-hydroxyacuminatine, cytotoxic camptothecinoid from Camptotheca acuminata, by pyridone benzannulation. Org. Biomol. Chem. 2006, 4, 407-409.
-
(2006)
Org. Biomol. Chem
, vol.4
, pp. 407-409
-
-
Babjak, M.1
Kanazawa, A.2
Anderson, R.J.3
Greene, A.E.4
-
39
-
-
34547619277
-
Short and efficient total synthesis of luotonin A and 22-hydroxyacuminatine using a common cascade strategy
-
Zhou, H.-B.; Liu, G.-S.; Yao, Z.-J. Short and efficient total synthesis of luotonin A and 22-hydroxyacuminatine using a common cascade strategy. J. Org. Chem. 2007, 72, 6270-6272.
-
(2007)
J. Org. Chem
, vol.72
, pp. 6270-6272
-
-
Zhou, H.-B.1
Liu, G.-S.2
Yao, Z.-J.3
-
40
-
-
0028938438
-
Convenient method for the synthesis of N-(ethyloxycarbonyl) ester derivatives from amino acids
-
Bhaskar Kanth, J. V.; Periasamy, M. Convenient method for the synthesis of N-(ethyloxycarbonyl) ester derivatives from amino acids. Synth. Commun. 1995, 25, 1523-1530.
-
(1995)
Synth. Commun
, vol.25
, pp. 1523-1530
-
-
Bhaskar Kanth, J.V.1
Periasamy, M.2
-
41
-
-
0343698975
-
Lycorine: Studies in synthesis
-
Dyke, S. F.; Sainsbury, M.; Evans, J. R. Lycorine: studies in synthesis. Tetrahedron 1973, 29, 213-220.
-
(1973)
Tetrahedron
, vol.29
, pp. 213-220
-
-
Dyke, S.F.1
Sainsbury, M.2
Evans, J.R.3
-
42
-
-
0026510348
-
Preparation of 3-pyrrolidone and 4-perhydroazepinone
-
Roglans, A.; Marquet, J.; Moreno-Manas, M. Preparation of 3-pyrrolidone and 4-perhydroazepinone. Synth. Commun. 1992, 22, 1249-1258.
-
(1992)
Synth. Commun
, vol.22
, pp. 1249-1258
-
-
Roglans, A.1
Marquet, J.2
Moreno-Manas, M.3
-
43
-
-
0010329456
-
N2 reactions of amines with (acyloxy)alkyl α-halides: A product distribution study
-
N2 reactions of amines with (acyloxy)alkyl α-halides: a product distribution study. J. Org. Chem. 1983, 48, 635-640.
-
(1983)
J. Org. Chem
, vol.48
, pp. 635-640
-
-
Sloan, K.B.1
Koch, S.A.M.2
-
44
-
-
37049075631
-
-
Houghton, P. G.; Humphrey, G. R.; Kennedy, D. J.; Roberts, D. C.; Wright, S. H. B. Enantiospecific synthesis of the (4R)-1-azabicyclo[2.2.1] heptane ring system. J. Chem. Soc., Perkin Trans. 1 1993, 1421-1424.
-
Houghton, P. G.; Humphrey, G. R.; Kennedy, D. J.; Roberts, D. C.; Wright, S. H. B. Enantiospecific synthesis of the (4R)-1-azabicyclo[2.2.1] heptane ring system. J. Chem. Soc., Perkin Trans. 1 1993, 1421-1424.
-
-
-
-
45
-
-
33847464972
-
Aminohaloborane in organic synthesis. 1. Specific ortho substitution reaction of anilines
-
Sugasawa, T.; Toyoda, T.; Adachi, M.; Sasakura, K. Aminohaloborane in organic synthesis. 1. Specific ortho substitution reaction of anilines. J. Am. Chem. Soc. 1978, 100, 4842-4852.
-
(1978)
J. Am. Chem. Soc
, vol.100
, pp. 4842-4852
-
-
Sugasawa, T.1
Toyoda, T.2
Adachi, M.3
Sasakura, K.4
-
46
-
-
49449102720
-
-
Cevasco, A. A. Process for the Manufacture of Cycloalkyl and Haloalkyl o-Aminophenyl Ketones. U.S. Patent 5,405,998, 1995
-
Cevasco, A. A. Process for the Manufacture of Cycloalkyl and Haloalkyl o-Aminophenyl Ketones. U.S. Patent 5,405,998, 1995.
-
-
-
-
47
-
-
0025341331
-
New colorimetric cytotoxicity assay for anticancer-drug screening
-
Skehan, P.; Storeng, R.; Scudiero, D.; Monks, A.; McMahon, J. New colorimetric cytotoxicity assay for anticancer-drug screening. J. Natl. Cancer Inst. 1990, 82 (13), 1107-1112.
-
(1990)
J. Natl. Cancer Inst
, vol.82
, Issue.13
, pp. 1107-1112
-
-
Skehan, P.1
Storeng, R.2
Scudiero, D.3
Monks, A.4
McMahon, J.5
-
48
-
-
0028906786
-
Some practical considerations and applications of the national cancer institute in-vitro anticancer drug discovery screen
-
Boyd, M. R.; Paull, K. D. Some practical considerations and applications of the national cancer institute in-vitro anticancer drug discovery screen. Drug Dev. Res. 1995, 34, 91-109.
-
(1995)
Drug Dev. Res
, vol.34
, pp. 91-109
-
-
Boyd, M.R.1
Paull, K.D.2
-
49
-
-
0242610818
-
Differential induction of topoisomerase I - DNA cleavage complexes by the indenoisoquinoline MJ-III-65 (NSC 706744) and camptothecin: Base sequence analysis and activity against camptothecin-resistant topoisomerase I
-
Antony, S.; Jayaraman, M.; Laco, G.; Kohlhagen, G.; Kohn, K. W.; Cushman, M.; Pommier, Y. Differential induction of topoisomerase I - DNA cleavage complexes by the indenoisoquinoline MJ-III-65 (NSC 706744) and camptothecin: base sequence analysis and activity against camptothecin-resistant topoisomerase I. Cancer Res. 2003, 63, 7428-7435.
-
(2003)
Cancer Res
, vol.63
, pp. 7428-7435
-
-
Antony, S.1
Jayaraman, M.2
Laco, G.3
Kohlhagen, G.4
Kohn, K.W.5
Cushman, M.6
Pommier, Y.7
-
50
-
-
0346996356
-
Design, synthesis, and biological evaluation of indenoisoquinoline topoisomerase I Inhibitors featuring polyamine side chains on the lactam nitrogen
-
Nagarajan, M.; Xiao, X.; Antony, S.; Kohlhagen, G.; Pommier, Y.; Cushman, M. Design, synthesis, and biological evaluation of indenoisoquinoline topoisomerase I Inhibitors featuring polyamine side chains on the lactam nitrogen. J. Med. Chem. 2003, 46, 5712-5724.
-
(2003)
J. Med. Chem
, vol.46
, pp. 5712-5724
-
-
Nagarajan, M.1
Xiao, X.2
Antony, S.3
Kohlhagen, G.4
Pommier, Y.5
Cushman, M.6
-
51
-
-
0024312538
-
Display and analysis of patterns of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm
-
Paull, K. D.; Shoemaker, R. H.; Hodes, L.; Monks, A.; Scudiero, D. A.; Rubinstein, L.; Plowman, J.; Boyd, M. R. Display and analysis of patterns of differential activity of drugs against human tumor cell lines: development of mean graph and COMPARE algorithm. J. Natl. Cancer. Inst. 1989, 81, 1088-1092.
-
(1989)
J. Natl. Cancer. Inst
, vol.81
, pp. 1088-1092
-
-
Paull, K.D.1
Shoemaker, R.H.2
Hodes, L.3
Monks, A.4
Scudiero, D.A.5
Rubinstein, L.6
Plowman, J.7
Boyd, M.R.8
-
52
-
-
0003154873
-
Prediction of Biochemical Mechanism of Action from the in Vitro Antitumor Screen of the National Cancer Institute
-
Foye, W. O, Ed, American Chemical Society: Washington, DC
-
Paull, K. D.; Hamel, E.; Malspeis, L. Prediction of Biochemical Mechanism of Action from the in Vitro Antitumor Screen of the National Cancer Institute. In Cancer Chemotherapeutic Agents; Foye, W. O., Ed.; American Chemical Society: Washington, DC, 1995; pp 9-45.
-
(1995)
Cancer Chemotherapeutic Agents
, pp. 9-45
-
-
Paull, K.D.1
Hamel, E.2
Malspeis, L.3
-
53
-
-
0037038323
-
Effect of spermine conjugation on the cytotoxicity and cellular transport of acridine
-
Delcros, J.-G.; Tomasi, S.; Carrington, S.; Martin, B.; Renault, J.; Blagbrough, I. S.; Uriac, P. Effect of spermine conjugation on the cytotoxicity and cellular transport of acridine. J. Med. Chem. 2002, 45, 5098-5111.
-
(2002)
J. Med. Chem
, vol.45
, pp. 5098-5111
-
-
Delcros, J.-G.1
Tomasi, S.2
Carrington, S.3
Martin, B.4
Renault, J.5
Blagbrough, I.S.6
Uriac, P.7
-
54
-
-
0033946967
-
Synthesis and characterisation of polyamine-poly(ethylene glycol) constructs for DNA binding and gene delivery
-
Garrett, S. W.; Davies, O. R.; Milroy, D. A.; Wood, P. J.; Pouton, C. W.; Threadgill, M. D. Synthesis and characterisation of polyamine-poly(ethylene glycol) constructs for DNA binding and gene delivery. Biooorg. Med. Chem. 2008, 8, 1779-1797.
-
(2008)
Biooorg. Med. Chem
, vol.8
, pp. 1779-1797
-
-
Garrett, S.W.1
Davies, O.R.2
Milroy, D.A.3
Wood, P.J.4
Pouton, C.W.5
Threadgill, M.D.6
-
55
-
-
0033605675
-
Induction of reversible complexes between eukaryotic DNA topoisomerase I and DNA-containing oxidative base damages. 7,8-Dihydro-8-oxoguanine and 5-hydroxycytosine
-
Pourquier, P.; Ueng, L.-M.; Fertala, J.; Wang, D.; Park, H.-K.; Essigmann, J. M.; Bjornsti, M.-A.; Pommier, Y. Induction of reversible complexes between eukaryotic DNA topoisomerase I and DNA-containing oxidative base damages. 7,8-Dihydro-8-oxoguanine and 5-hydroxycytosine. J. Biol. Chem. 1999, 274, 8516-8523.
-
(1999)
J. Biol. Chem
, vol.274
, pp. 8516-8523
-
-
Pourquier, P.1
Ueng, L.-M.2
Fertala, J.3
Wang, D.4
Park, H.-K.5
Essigmann, J.M.6
Bjornsti, M.-A.7
Pommier, Y.8
|