-
1
-
-
0001398676
-
Polyamine inhibitors and analogues as potential anticancer agents
-
Dowling RH, Fölsch UR, Löser R (eds.), Dordrecht, the Netherlands: Kluwer
-
Porter CW, Regenass U, Bergeron RJ: Polyamine inhibitors and analogues as potential anticancer agents, in: Dowling RH, Fölsch UR, Löser R (eds.), Polyamines in the gastrointestinal tract: Falk Symposium, 62 ed. Dordrecht, the Netherlands: Kluwer, 1992;301-322.
-
(1992)
Polyamines in the Gastrointestinal Tract: Falk Symposium, 62 Ed.
, pp. 301-322
-
-
Porter, C.W.1
Regenass, U.2
Bergeron, R.J.3
-
2
-
-
0026671825
-
Ornithine decarboxylase as an enzyme target for therapy
-
McCann PP, Pegg AE: Ornithine decarboxylase as an enzyme target for therapy. Pharmacol Ther 1992;54:195-215.
-
(1992)
Pharmacol Ther
, vol.54
, pp. 195-215
-
-
McCann, P.P.1
Pegg, A.E.2
-
3
-
-
0027097783
-
S-adenosylmethionine decarboxylase as an enzyme target for therapy
-
Pegg AE, McCann PP: S-adenosylmethionine decarboxylase as an enzyme target for therapy. Pharmacol Ther 1992;56:359-377.
-
(1992)
Pharmacol Ther
, vol.56
, pp. 359-377
-
-
Pegg, A.E.1
McCann, P.P.2
-
4
-
-
0026775528
-
New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity
-
Regenass U, Caravatti G, Mett H, Stanek J, Schneider P, Muller M, Matter A, Vertino P, Porter CW: New S-adenosylmethionine decarboxylase inhibitors with potent antitumor activity. Cancer Res 1992; 52(17):4712-4718.
-
(1992)
Cancer Res
, vol.52
, Issue.17
, pp. 4712-4718
-
-
Regenass, U.1
Caravatti, G.2
Mett, H.3
Stanek, J.4
Schneider, P.5
Muller, M.6
Matter, A.7
Vertino, P.8
Porter, C.W.9
-
5
-
-
0020623560
-
Methylgloxal-bis(guanylhydrazone) (Methyl-GAG): Current status and future prospects
-
Warrell RP, Burchenal JH: Methylgloxal-bis(guanylhydrazone) (Methyl-GAG): current status and future prospects. J Clin Oncol 1983;1:52-65.
-
(1983)
J Clin Oncol
, vol.1
, pp. 52-65
-
-
Warrell, R.P.1
Burchenal, J.H.2
-
6
-
-
0029127116
-
In vivo effects of 4-amidinoindan-1-one 2′-amidinohydrazone (CGP 48664A) and alpha-difluromethylornithine (DFMO) on L1210 growth, cell-cycle phase distribution and polyamine contents
-
Dorhout B, Te Velde RJ, Ferwerda H, Kingma AW, de Hoog E, Muskiet FA: In vivo effects of 4-amidinoindan-1-one 2′-amidinohydrazone (CGP 48664A) and alpha-difluromethylornithine (DFMO) on L1210 growth, cell-cycle phase distribution and polyamine contents. Int J Cancer 1995;62:738-742.
-
(1995)
Int J Cancer
, vol.62
, pp. 738-742
-
-
Dorhout, B.1
Te Velde, R.J.2
Ferwerda, H.3
Kingma, A.W.4
De Hoog, E.5
Muskiet, F.A.6
-
7
-
-
0028361273
-
CGP 48664, an S-adenosylmethionine decarboxylase inhibitor with broad antiproliferative and anti-tumor activity
-
Regenass U, Mett H, Stanek J, Muller M, Kramer D, Porter CW: CGP 48664, an S-adenosylmethionine decarboxylase inhibitor with broad antiproliferative and anti-tumor activity. Cancer Res 1994;54: 3210-3217.
-
(1994)
Cancer Res
, vol.54
, pp. 3210-3217
-
-
Regenass, U.1
Mett, H.2
Stanek, J.3
Muller, M.4
Kramer, D.5
Porter, C.W.6
-
8
-
-
0029004134
-
Treatment of nude mice with 4-amidinoindanon-1-(2′-amidino)hydrazone, a new S-adenosylmethionine decarboxylase inhibitor, delays growth and inhibits metastasis of human melanoma cells
-
Gutman M, Beltran PJ, Fan D, Delworth M, Singh RK, Wilson M, Fidler IJ: Treatment of nude mice with 4-amidinoindanon-1-(2′-amidino)hydrazone, a new S-adenosylmethionine decarboxylase inhibitor, delays growth and inhibits metastasis of human melanoma cells. Melanoma Res 1995;5:147-155.
-
(1995)
Melanoma Res
, vol.5
, pp. 147-155
-
-
Gutman, M.1
Beltran, P.J.2
Fan, D.3
Delworth, M.4
Singh, R.K.5
Wilson, M.6
Fidler, I.J.7
-
9
-
-
0028878823
-
Systemic administration of 4-amidinoindanon-1-(2′-amidino)-hydrazone, a new inhibitor of S-adenosylmethionine decarboxylase, produces cytostasis of human prostate cancer in athymic nude mice
-
Delworth MG, Nishioka K, Pettaway C, Gutman M, Killion JJ, Von Eschenbach AC, Fidler IJ: Systemic administration of 4-amidinoindanon-1-(2′-amidino)-hydrazone, a new inhibitor of S-adenosylmethionine decarboxylase, produces cytostasis of human prostate cancer in athymic nude mice. Int J Oncol 1997;6:293-299.
-
(1997)
Int J Oncol
, vol.6
, pp. 293-299
-
-
Delworth, M.G.1
Nishioka, K.2
Pettaway, C.3
Gutman, M.4
Killion, J.J.5
Von Eschenbach, A.C.6
Fidler, I.J.7
-
10
-
-
0028925525
-
In vivo growth inhibition of L1210 leukemia by 4-amidinoindan-1-one 2′amidinohydrazone (CGP 48664), a new inhibitor of S-adenosylmethionine decarboxylase
-
Dorhout B, Te Velde RJ, Ferwerda H, Kingma AW, De Hoog E, Muskiet FAJ: In vivo growth inhibition of L1210 leukemia by 4-amidinoindan-1-one 2′amidinohydrazone (CGP 48664), a new inhibitor of S-adenosylmethionine decarboxylase. Int J Carcer 1995; 61:214-217.
-
(1995)
Int J Carcer
, vol.61
, pp. 214-217
-
-
Dorhout, B.1
Te Velde, R.J.2
Ferwerda, H.3
Kingma, A.W.4
De Hoog, E.5
Muskiet, F.A.J.6
-
11
-
-
0008445913
-
Phase I and pharmacologic study of CGP 48664, a SAMDC inhibitor, given once weekly × 4 in patients with solid tumors
-
Greim G, Bruntsch U, Eskens F, Hoppener F, Barbet NC, Choi L, Hanauske AR, Verweij J: Phase I and pharmacologic study of CGP 48664, a SAMDC inhibitor, given once weekly × 4 in patients with solid tumors. American Society of Clinical Oncology 34th Annual Meeting Proceedings 1998;17:232a.
-
(1998)
American Society of Clinical Oncology 34th Annual Meeting Proceedings
, vol.17
-
-
Greim, G.1
Bruntsch, U.2
Eskens, F.3
Hoppener, F.4
Barbet, N.C.5
Choi, L.6
Hanauske, A.R.7
Verweij, J.8
-
12
-
-
0008503842
-
A phase I and pharmacokinetic (PK) study of the polyamine biosynthesis inhibitor CGP 48664 in patients with advanced cancer
-
Siu LL, Rowinski EK, Weiss GR, Hammond L, Kraynak M, Moczygemba J, Choi L, Barbet NC, DeMoor C, Von Hoff DD, Eckhardt SG: A phase I and pharmacokinetic (PK) study of the polyamine biosynthesis inhibitor CGP 48664 in patients with advanced cancer. American Society of Clinical Oncology 34th Annual Meeting Proceedings 1998;17:191a.
-
(1998)
American Society of Clinical Oncology 34th Annual Meeting Proceedings
, vol.17
-
-
Siu, L.L.1
Rowinski, E.K.2
Weiss, G.R.3
Hammond, L.4
Kraynak, M.5
Moczygemba, J.6
Choi, L.7
Barbet, N.C.8
DeMoor, C.9
Von Hoff, D.D.10
Eckhardt, S.G.11
-
13
-
-
0008418185
-
Phase I dose escalation and pharmacokinetic study of CGP 48664, a new S-adenosylmethionine decarboxylase (SAMDC) inhibitor, administered in continuous infusion over 5 days in cancer patients with solid tumors
-
Paridaens R, Uges DRA, Barbet N, Seeghers M, Van der Graaf WTA, Lassus M, Groen HJM, Dumez H, Muskiet F, Man A, Van Oosterom AT, De Vries EGE: Phase I dose escalation and pharmacokinetic study of CGP 48664, a new S-adenosylmethionine decarboxylase (SAMDC) inhibitor, administered in continuous infusion over 5 days in cancer patients with solid tumors. American Society of Clinical Oncology 34th Annual Meeting Proceedings 1998;17:190a.
-
(1998)
American Society of Clinical Oncology 34th Annual Meeting Proceedings
, vol.17
-
-
Paridaens, R.1
Uges, D.R.A.2
Barbet, N.3
Seeghers, M.4
Van Der Graaf, W.T.A.5
Lassus, M.6
Groen, H.J.M.7
Dumez, H.8
Muskiet, F.9
Man, A.10
Van Oosterom, A.T.11
De Vries, E.G.E.12
-
14
-
-
0029974939
-
Automated quantitative determination of a new polyamine biosynthesis inhibitor (CGP 48664) and a potential metabolite in human and in animal plasma by high-performance liquid chromatography
-
Degen PH, Zbinden P: Automated quantitative determination of a new polyamine biosynthesis inhibitor (CGP 48664) and a potential metabolite in human and in animal plasma by high-performance liquid chromatography. J Chromatogr 1996;681:339-345.
-
(1996)
J Chromatogr
, vol.681
, pp. 339-345
-
-
Degen, P.H.1
Zbinden, P.2
-
15
-
-
0018091195
-
Application of Akaike's Information Criterion (AIC) in the evaluation of linear pharmacokinetic equations
-
Yamaoka K, Nakagawa T, Uno T: Application of Akaike's Information Criterion (AIC) in the evaluation of linear pharmacokinetic equations. J Pharmacokinet Biopharm 1978;6:165-175.
-
(1978)
J Pharmacokinet Biopharm
, vol.6
, pp. 165-175
-
-
Yamaoka, K.1
Nakagawa, T.2
Uno, T.3
-
16
-
-
0029041029
-
Paclitaxel effect on a leukemia cell line: Importance of paclitaxel concentration
-
Nusbaum NJ, Abraham T: Paclitaxel effect on a leukemia cell line: importance of paclitaxel concentration. Anticancer Drugs 1995; 6(3):427-431.
-
(1995)
Anticancer Drugs
, vol.6
, Issue.3
, pp. 427-431
-
-
Nusbaum, N.J.1
Abraham, T.2
-
17
-
-
0028894301
-
Nonlinear pharmacokinetics and metabolism of paclitaxel and its pharmacokinetic/pharmacodynamic relationships in humans
-
Gianni L, Kearns CM, Giani A, Capri G, Vigano L, Lacatelli A, Bonadonna G, Egorin MJ: Nonlinear pharmacokinetics and metabolism of paclitaxel and its pharmacokinetic/pharmacodynamic relationships in humans. J Clin Oncol 1995;13(1):180-190.
-
(1995)
J Clin Oncol
, vol.13
, Issue.1
, pp. 180-190
-
-
Gianni, L.1
Kearns, C.M.2
Giani, A.3
Capri, G.4
Vigano, L.5
Lacatelli, A.6
Bonadonna, G.7
Egorin, M.J.8
-
18
-
-
0030753473
-
Clinical pharmacokinetics and dose optimisation of carboplatin
-
Duffull SB, Robinson BA: Clinical pharmacokinetics and dose optimisation of carboplatin. Clin Pharmacokinet 1997;33(3):161-183.
-
(1997)
Clin Pharmacokinet
, vol.33
, Issue.3
, pp. 161-183
-
-
Duffull, S.B.1
Robinson, B.A.2
-
19
-
-
0028027813
-
Bioanalysis, pharmacokinetics, and pharmacodynamics of novel anticancer drug paclitxel (Taxol)
-
Beijnen JH, Huizing MT, ten Bokkel Huinink WW, Veenhof CH, Vermorken JB, Giaccone G, Pinedo HM: Bioanalysis, pharmacokinetics, and pharmacodynamics of novel anticancer drug paclitxel (Taxol). Semin Oncol 1994;21(5, Suppl. B):53-62.
-
(1994)
Semin Oncol
, vol.21
, Issue.5 SUPPL. B
, pp. 53-62
-
-
Beijnen, J.H.1
Huizing, M.T.2
Ten Bokkel Huinink, W.W.3
Veenhof, C.H.4
Vermorken, J.B.5
Giaccone, G.6
Pinedo, H.M.7
-
20
-
-
0028227087
-
Saturable pharmacokinetics and paclitaxel pharmacodynamics in children with solid tumors
-
Sonnichsen DS, Hurwitz CA, Pratt CB, Shuster JJ, Relling MV: Saturable pharmacokinetics and paclitaxel pharmacodynamics in children with solid tumors. J Clin Oncol 1994;12(3):532-538.
-
(1994)
J Clin Oncol
, vol.12
, Issue.3
, pp. 532-538
-
-
Sonnichsen, D.S.1
Hurwitz, C.A.2
Pratt, C.B.3
Shuster, J.J.4
Relling, M.V.5
-
21
-
-
0023125107
-
Relationship between the neurotoxicity of the hypoxic cell radiosensitizer SR 2508 and the pharmacokinetic profile
-
Coleman CN, Halsey J, Cox RS, Hirst VK, Blaschke T, Howes AE, Wasserman TH, Urtasun RC, Pajak T, Hancock S, et al: Relationship between the neurotoxicity of the hypoxic cell radiosensitizer SR 2508 and the pharmacokinetic profile. Cancer Res 1987;47(1):319-322.
-
(1987)
Cancer Res
, vol.47
, Issue.1
, pp. 319-322
-
-
Coleman, C.N.1
Halsey, J.2
Cox, R.S.3
Hirst, V.K.4
Blaschke, T.5
Howes, A.E.6
Wasserman, T.H.7
Urtasun, R.C.8
Pajak, T.9
Hancock, S.10
-
22
-
-
0028798952
-
Pharmacokinetics and pharmacodynamics of prolonged oral etoposide in women with metastatic breast cancer
-
Millward MJ, Newell DR, Yuen K, Matthews JP, Balmanno K, Charlton CJ, Gumbrell L, Lind MJ, Chapman F, Proctor M, et al: Pharmacokinetics and pharmacodynamics of prolonged oral etoposide in women with metastatic breast cancer. Cancer Chemother Pharmacol 1995;37(1-2):161-167.
-
(1995)
Cancer Chemother Pharmacol
, vol.37
, Issue.1-2
, pp. 161-167
-
-
Millward, M.J.1
Newell, D.R.2
Yuen, K.3
Matthews, J.P.4
Balmanno, K.5
Charlton, C.J.6
Gumbrell, L.7
Lind, M.J.8
Chapman, F.9
Proctor, M.10
-
23
-
-
0029780751
-
Improved designs for dose escalation studies using pharmacokinetic measurements
-
Piantadosi S, Liu G: Improved designs for dose escalation studies using pharmacokinetic measurements. Stat Med 1996;15(15):1605-1618.
-
(1996)
Stat Med
, vol.15
, Issue.15
, pp. 1605-1618
-
-
Piantadosi, S.1
Liu, G.2
-
24
-
-
0031940674
-
A general model for time-dissociated pharmacokinetic-pharmacodynamic relationship exemplified by paclitaxel myelosuppression
-
Karlsson MO, Molnar V, Bergh J, Freijs A, Larsson R: A general model for time-dissociated pharmacokinetic-pharmacodynamic relationship exemplified by paclitaxel myelosuppression. Clin Pharmacol Ther 1998;63(1):11-25.
-
(1998)
Clin Pharmacol Ther
, vol.63
, Issue.1
, pp. 11-25
-
-
Karlsson, M.O.1
Molnar, V.2
Bergh, J.3
Freijs, A.4
Larsson, R.5
|