-
1
-
-
7144248725
-
Plant antitumor agents. 1. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminata
-
Wall ME, Wani MC, Cook CE, Palmer K, McPhail AT and Sim GA: Plant antitumor agents. 1. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from camptotheca acuminata. J Am Chem Soc 88: 3888-3890, 1966.
-
(1966)
J Am Chem Soc
, vol.88
, pp. 3888-3890
-
-
Wall, M.E.1
Wani, M.C.2
Cook, C.E.3
Palmer, K.4
McPhail, A.T.5
Sim, G.A.6
-
2
-
-
0014895176
-
Preliminary pharmacologic and clinical evaluation of camptothecin sodium (NSC-100880)
-
Gottlieb JA, Guarino AM, Call JB, Oliverio VT and Block JB: Preliminary pharmacologic and clinical evaluation of camptothecin sodium (NSC-100880). Cancer Chemother Rep 54: 461-470, 1970.
-
(1970)
Cancer Chemother Rep
, vol.54
, pp. 461-470
-
-
Gottlieb, J.A.1
Guarino, A.M.2
Call, J.B.3
Oliverio, V.T.4
Block, J.B.5
-
3
-
-
0015292126
-
Treatment of malignant melanoma with camptothecin (NSC-100880)
-
Gottlieb JA and Luce JK: Treatment of malignant melanoma with camptothecin (NSC-100880). Cancer Chemother Rep 56: 103-105, 1972.
-
(1972)
Cancer Chemother Rep
, vol.56
, pp. 103-105
-
-
Gottlieb, J.A.1
Luce, J.K.2
-
4
-
-
0015378084
-
Phase I clinical trial of weekly and daily treatment with camptothecin (NSC-100880): Correlation with preclinical studies
-
Muggia FM, Creaven PJ, Hansen HH, Cohen MH and Selawry OS: Phase I clinical trial of weekly and daily treatment with camptothecin (NSC-100880): Correlation with preclinical studies. Cancer Chemother Rep 56: 515-521, 1972.
-
(1972)
Cancer Chemother Rep
, vol.56
, pp. 515-521
-
-
Muggia, F.M.1
Creaven, P.J.2
Hansen, H.H.3
Cohen, M.H.4
Selawry, O.S.5
-
5
-
-
0015291595
-
Phase II study of camptothecin (NSC-100880) in the treatment of advanced gastrointestinal cancer
-
Moertel CG, Schutt AJ, Reitemeier RJ and Hahn RG: Phase II study of camptothecin (NSC-100880) in the treatment of advanced gastrointestinal cancer. Cancer Chemother Rep 56: 95-101, 1972.
-
(1972)
Cancer Chemother Rep
, vol.56
, pp. 95-101
-
-
Moertel, C.G.1
Schutt, A.J.2
Reitemeier, R.J.3
Hahn, R.G.4
-
7
-
-
0018901322
-
Plant antitumor agents. 18. Synthesis and biological activity of camptothecin analogs
-
Wani MC, Ronman PE, Lindley LT and Wall ME: Plant antitumor agents. 18. Synthesis and biological activity of camptothecin analogs. J Med Chem 23: 554-560, 1980.
-
(1980)
J Med Chem
, vol.23
, pp. 554-560
-
-
Wani, M.C.1
Ronman, P.E.2
Lindley, L.T.3
Wall, M.E.4
-
9
-
-
0025912553
-
Complete growth inhibition of human cancer xenografts in nude mice by treatment with 20-(S)-camptothecin
-
Giovanella BC, Hinz HR, Kozielski AJ, Stehlin JS, Silber R and Potmesil M: Complete growth inhibition of human cancer xenografts in nude mice by treatment with 20-(S)-camptothecin. Cancer Res 51: 3052-3055, 1991.
-
(1991)
Cancer Res
, vol.51
, pp. 3052-3055
-
-
Giovanella, B.C.1
Hinz, H.R.2
Kozielski, A.J.3
Stehlin, J.S.4
Silber, R.5
Potmesil, M.6
-
10
-
-
0030453707
-
Phase I clinical and pharmacological studies of 20-(S)-camptothecin and 20-(S)-9-nitrocamptothecin as anticancer agents
-
Natelson E, Giovanella BC, Verschraegen CF, Fehir KM, De Ipolyi PD, Harris N and Stehlin JS: Phase I clinical and pharmacological studies of 20-(S)-camptothecin and 20-(S)-9-nitrocamptothecin as anticancer agents. Ann NY Acad Sci 803: 224-230, 1996.
-
(1996)
Ann NY Acad Sci
, vol.803
, pp. 224-230
-
-
Natelson, E.1
Giovanella, B.C.2
Verschraegen, C.F.3
Fehir, K.M.4
De Ipolyi, P.D.5
Harris, N.6
Stehlin, J.S.7
-
11
-
-
0030453706
-
Chemistry of the camptothecins in the bloodstream: Drug stabilization and optimization of activity
-
Burke TG: Chemistry of the camptothecins in the bloodstream: Drug stabilization and optimization of activity. Ann NY Acad Sci 803: 29-31, 1996.
-
(1996)
Ann NY Acad Sci
, vol.803
, pp. 29-31
-
-
Burke, T.G.1
-
12
-
-
0034725772
-
20-O-acylcamptothecin derivatives: Evidence for lactone stabilization
-
Zhao H, Lee C, Sai P, Choe YH, Boro M, Pendri A, Duan S and Greenwald RB: 20-O-acylcamptothecin derivatives: evidence for lactone stabilization. J Org Chem 65: 4601-4606, 2000.
-
(2000)
J Org Chem
, vol.65
, pp. 4601-4606
-
-
Zhao, H.1
Lee, C.2
Sai, P.3
Choe, Y.H.4
Boro, M.5
Pendri, A.6
Duan, S.7
Greenwald, R.B.8
-
13
-
-
0027201885
-
Preferential binding of the carboxylate form of camptothecin by human serum albumin
-
Burke TG and Mi Z: Preferential binding of the carboxylate form of camptothecin by human serum albumin. Anal Biochem 212: 285-287, 1993.
-
(1993)
Anal Biochem
, vol.212
, pp. 285-287
-
-
Burke, T.G.1
Mi, Z.2
-
14
-
-
0028012774
-
The structural basis of camptothecin interactions with human albumin: Impact on drug stability
-
Burke TG and Mi Z: The structural basis of camptothecin interactions with human albumin: impact on drug stability. J Med Chem 37: 40-46, 1994.
-
(1994)
J Med Chem
, vol.37
, pp. 40-46
-
-
Burke, T.G.1
Mi, Z.2
-
15
-
-
0031952835
-
Alkyl esters of camptothecin and 9-nitrocamptothecin: Synthesis, in vitro pharmacokinetics, toxicity, and antitumor activity
-
Cao Z, Harris N, Kozielski A, Vardeman D and Giovanella B: Alkyl esters of camptothecin and 9-nitrocamptothecin: Synthesis, in vitro pharmacokinetics, toxicity, and antitumor activity. J Med Chem 41: 31-37, 1998.
-
(1998)
J Med Chem
, vol.41
, pp. 31-37
-
-
Cao, Z.1
Harris, N.2
Kozielski, A.3
Vardeman, D.4
Giovanella, B.5
-
16
-
-
0034515727
-
Structure-activity relationship of alkyl camptothecin esters
-
Cao Z, Pantazis P, Mendoza J, Early J, Kozieslki A, Harris N, Vardeman D, Liehr J, Stehlin J and Giovanella B: Structure-activity relationship of alkyl camptothecin esters. Ann NY Acad Sci 992: 122-135, 2000.
-
(2000)
Ann NY Acad Sci
, vol.992
, pp. 122-135
-
-
Cao, Z.1
Pantazis, P.2
Mendoza, J.3
Early, J.4
Kozieslki, A.5
Harris, N.6
Vardeman, D.7
Liehr, J.8
Stehlin, J.9
Giovanella, B.10
-
17
-
-
0037310777
-
Structure-activity relationship of alkyl 9-nitrocamptothecin esters
-
Cao Z, Pantazis P, Mendoza J, Early J, Kozielski A, Harris N and Giovanella B: Structure-activity relationship of alkyl 9-nitrocamptothecin esters. Acta Pharmacol Sin 24: 109-119, 2003.
-
(2003)
Acta Pharmacol Sin
, vol.24
, pp. 109-119
-
-
Cao, Z.1
Pantazis, P.2
Mendoza, J.3
Early, J.4
Kozielski, A.5
Harris, N.6
Giovanella, B.7
-
18
-
-
0026229612
-
Conversion of CPT-11 into SN-38 in human tissues
-
Kono A and Hara Y: Conversion of CPT-11 into SN-38 in human tissues. Jpn J Cancer Chemother 18: 2175-2178, 1991.
-
(1991)
Jpn J Cancer Chemother
, vol.18
, pp. 2175-2178
-
-
Kono, A.1
Hara, Y.2
-
19
-
-
0004093075
-
Production of SN-38, a main metabolite of the camptothecin derivative CPT-11
-
Kawato Y, Aonuma M, Matsumoto K and Sato K: Production of SN-38, a main metabolite of the camptothecin derivative CPT-11. Yakubutsu Dotai 6: 899-907, 1991.
-
(1991)
Yakubutsu Dotai
, vol.6
, pp. 899-907
-
-
Kawato, Y.1
Aonuma, M.2
Matsumoto, K.3
Sato, K.4
-
20
-
-
0028364014
-
Metabolic activation of CPT-11
-
Satoh T, Hosokawa M, Atsumi R, Suzuki W, Hakusui H and Nagai E: Metabolic activation of CPT-11. Biol Pharm Bull 17: 662-664, 1994.
-
(1994)
Biol Pharm Bull
, vol.17
, pp. 662-664
-
-
Satoh, T.1
Hosokawa, M.2
Atsumi, R.3
Suzuki, W.4
Hakusui, H.5
Nagai, E.6
-
21
-
-
0030580064
-
The conversion of irinotecan (CPT-11) to its active metabolite 7-ethyl-10-hydroxycamptothecin (SN38)
-
Rivory LP, Bowles MR, Robert J and Pond SM: The conversion of irinotecan (CPT-11) to its active metabolite 7-ethyl-10-hydroxycamptothecin (SN38). Biochem Pharmacol 52: 1103-1111, 1996.
-
(1996)
Biochem Pharmacol
, vol.52
, pp. 1103-1111
-
-
Rivory, L.P.1
Bowles, M.R.2
Robert, J.3
Pond, S.M.4
-
22
-
-
0019006609
-
Simultaneous purification and comparative characterization of six serine hydrolases from rat liver microsomes
-
Mentlein R, Heiland S, and Heymann E: Simultaneous purification and comparative characterization of six serine hydrolases from rat liver microsomes. Arch Biochem Biophys 200: 547-559, 1980.
-
(1980)
Arch Biochem Biophys
, vol.200
, pp. 547-559
-
-
Mentlein, R.1
Heiland, S.2
Heymann, E.3
-
23
-
-
0021262869
-
Hydrolysis of ester- and amide-type drugs by the purified isoenzymes of nonspecific carboxyl-esterase from rat liver
-
Mentlein R and Heymann E: Hydrolysis of ester- and amide-type drugs by the purified isoenzymes of nonspecific carboxyl-esterase from rat liver. Biochem Pharmacol 33: 1243-1248, 1984.
-
(1984)
Biochem Pharmacol
, vol.33
, pp. 1243-1248
-
-
Mentlein, R.1
Heymann, E.2
-
24
-
-
0000549257
-
Esterification of carboxylic acids with dicyclohexylcarbodiimide/4-dimethylaminopyridine:tert-butyl ethyl fumarate
-
Neises B and Steglich W: Esterification of carboxylic acids with dicyclohexylcarbodiimide/4-dimethylaminopyridine:tert-butyl ethyl fumarate. Org Synth 63: 183-187, 1985.
-
(1985)
Org Synth
, vol.63
, pp. 183-187
-
-
Neises, B.1
Steglich, W.2
-
25
-
-
33748448195
-
Direct room temperature esterification of carboxylic acids
-
Hassner A and Alexanian V: Direct room temperature esterification of carboxylic acids. Tetrahedron Lett 19: 4475-4478, 1978.
-
(1978)
Tetrahedron Lett
, vol.19
, pp. 4475-4478
-
-
Hassner, A.1
Alexanian, V.2
-
26
-
-
84972865137
-
A mild method for the esterification of fatty acids
-
Ziegler FE and Berger GD: A mild method for the esterification of fatty acids. Synth Commun 9: 539-543, 1979.
-
(1979)
Synth Commun
, vol.9
, pp. 539-543
-
-
Ziegler, F.E.1
Berger, G.D.2
-
27
-
-
84981783095
-
N,N-dimethyl-4-pyridinamine, a very effective acylation catalyst
-
Steglich W and Höfle G: N,N-dimethyl-4-pyridinamine, a very effective acylation catalyst. Angew Chem Int Ed Engl 8: 981, 1969.
-
(1969)
Angew Chem Int Ed Engl
, vol.8
, pp. 981
-
-
Steglich, W.1
Höfle, G.2
-
28
-
-
0004442932
-
Water soluble prodrugs of camptothecin
-
US Patent: 4,943,579
-
Rao VB and Garzon-Aburbeh A: Water soluble prodrugs of camptothecin. US Patent: 4,943,579, 1990.
-
(1990)
-
-
Rao, V.B.1
Garzon-Aburbeh, A.2
-
29
-
-
44949142517
-
-
Wall ME and Wani MC: Water-soluble esters of camptothecin compounds: Non-toxic camptothecin prodrugs are prepared by esterifying the 20-position hydroxyl group of camptothecin derivatives. US Patent: 5,646,159, 1997
-
Wall ME and Wani MC: Water-soluble esters of camptothecin compounds: Non-toxic camptothecin prodrugs are prepared by esterifying the 20-position hydroxyl group of camptothecin derivatives. US Patent: 5,646,159, 1997.
-
-
-
-
30
-
-
0032430106
-
Nitration of camptothecin with various inorganic nitrate salts in concentrated sulfuric acid: A new preparation of anticancer drug 9-nitrocamptothecin
-
Cao Z, Armstrong K, Shaw M, Petry E and Harris N: Nitration of camptothecin with various inorganic nitrate salts in concentrated sulfuric acid: a new preparation of anticancer drug 9-nitrocamptothecin. Synthesis pp1724-1730, 1998.
-
(1998)
Synthesis
, pp. 1724-1730
-
-
Cao, Z.1
Armstrong, K.2
Shaw, M.3
Petry, E.4
Harris, N.5
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