-
1
-
-
0027383682
-
Recognition of Phar-macophore of ar-Turmerone for its anticancer Activity
-
Baik, K. U., Jung, S. H. and Ahn, B. Z. Recognition of Phar-macophore of ar-Turmerone for its anticancer Activity. Arch.Pharm.Res.16, 254-256 (1993a).
-
(1993)
Arch.Pharm.Res.
, vol.16
, pp. 254-256
-
-
Baik, K.U.1
Jung, S.H.2
Ahn, B.Z.3
-
2
-
-
0027432781
-
Structure-Activity Relationship of ar-Turmerone Analogues
-
Baik, K. U., Jung, S. H. and Ahn, B. Z Structure-Activity Relationship of ar-Turmerone Analogues. Arch. Pharm. Res. 16, 219 (1993b)
-
(1993)
Arch. Pharm. Res.
, vol.16
, pp. 219
-
-
Baik, K.U.1
Jung, S.H.2
Ahn, B.Z.3
-
3
-
-
0025950675
-
Evidence for oxidative activation of mitoxantrone in humane
-
Blanz, J., Mewes, K., Ehninger, G., Gebhardt, R., Zeller, K. P., Evidence for oxidative activation of mitoxantrone in humane. Drug. Metab. Dispos., 19, 871-880 (1991).
-
(1991)
Drug. Metab. Dispos.
, vol.19
, pp. 871-880
-
-
Blanz, J.1
Mewes, K.2
Ehninger, G.3
Gebhardt, R.4
Zeller, K.P.5
-
4
-
-
0025255167
-
Pharmacokinetics and metabolism of mitoxantrone. A review
-
Ehninger, G., Chuler, U., Proksch, B., Zeller, K. P., Blanz, J., Pharmacokinetics and metabolism of mitoxantrone. A review. Clin. Pharmacokinet., 18 365-38- (1990).
-
(1990)
Clin. Pharmacokinet.
, vol.18
, pp. 365-338
-
-
Ehninger, G.1
Chuler, U.2
Proksch, B.3
Zeller, K.P.4
Blanz, J.5
-
5
-
-
0032424310
-
1,4,9,10-Anthraquinone Derivatives: Synthesis and Antitumor Activity
-
Jin, G. Z., Kim, Y., Ho, C. J., Sok, D. E., and Ahn, B. Z., 1,4,9,10-Anthraquinone Derivatives: Synthesis and Antitumor Activity, Arch. Pharm. Pharm. Med. Chem., 331, 380-384 (1998a).
-
(1998)
Arch. Pharm. Pharm. Med. Chem.
, vol.331
, pp. 380-384
-
-
Jin, G.Z.1
Kim, Y.2
Ho, C.J.3
Sok, D.E.4
Ahn, B.Z.5
-
6
-
-
0032035470
-
2- (1-Oxyalkyl)-1,4-dioxy-9,10-anthraquinones: Synthesis and Evaluation of antitumor Activity
-
Jin, G. Z., Song, G. Y., Zheng, S. G., Kim, Y., Sok, D. E., and Ahn, B. Z., 2- (1-Oxyalkyl)-1,4-dioxy-9,10-anthraquinones: Synthesis and Evaluation of antitumor Activity. Arch. Pharm. Res., 21(2), 208-206 (1998b).
-
(1998)
Arch. Pharm. Res.
, vol.21
, Issue.2
, pp. 208-1206
-
-
Jin, G.Z.1
Song, G.Y.2
Zheng, S.G.3
Kim, Y.4
Sok, D.E.5
Ahn, B.Z.6
-
7
-
-
0027420344
-
Cytochrome p-450-induced Cytotoxicity of Mitoxantrone by Formation of Electrophilic Intermediates
-
Mewes, K.., Blanz, J.., Ehninger, G., Gebhardt, R., and Zeller, K. P., Cytochrome p-450-induced Cytotoxicity of Mitoxantrone by Formation of Electrophilic Intermediates. Cancer Res., 2093, 1, 5135-5142 (1993).
-
(1993)
Cancer Res.
, vol.2093
, Issue.1
, pp. 5135-5142
-
-
Mewes, K.1
Blanz, J.2
Ehninger, G.3
Gebhardt, R.4
Zeller, K.P.5
-
8
-
-
21044444317
-
-
National Cancer Institute Protocol, U. S. A (1972)
-
National Cancer Institute Protocol, U. S. A (1972)
-
-
-
-
9
-
-
0033575723
-
Naphthazarin derivatives (II): Formation of glutathione conjugate, inhibition of DNA topoisomerase-I and cytotoxicity
-
Song, G. Y, Zheng, X. G., Kim, Y., You, Y. J., Sok, D. E., and Ahn, B. Z., Naphthazarin derivatives (II): Formation of glutathione conjugate, inhibition of DNA topoisomerase-I and cytotoxicity. Bioorg. Chem. Med. Chem. Letter, 9, 2407-2412 (1999).
-
(1999)
Bioorg. Chem. Med. Chem. Letter
, vol.9
, pp. 2407-2412
-
-
Song, G.Y.1
Zheng, X.G.2
Kim, Y.3
You, Y.J.4
Sok, D.E.5
Ahn, B.Z.6
-
10
-
-
21044459189
-
Naphthazarin Derivatives (IV). Synthesis, Inhibition of DNA topoisomerase-I and Cytotoxicity of 2- or 6-Acyl-5, 8-dimethoxy-1,4-naphthoquinones
-
in press
-
Song, G. Y., Kim, Y., Zheng, X, G., You, Y. J., Cho, H., Chung, J. H., Sok, D. E. and Ahn, B. Z. Naphthazarin Derivatives (IV). Synthesis, Inhibition of DNA topoisomerase-I and Cytotoxicity of 2- or 6-Acyl-5, 8-dimethoxy-1,4-naphthoquinones. European J. Med. Chem. (1999) in press.
-
(1999)
European J. Med. Chem.
-
-
Song, G.Y.1
Kim, Y.2
Zheng, X.G.3
You, Y.J.4
Cho, H.5
Chung, J.H.6
Sok, D.E.7
Ahn, B.Z.8
-
11
-
-
0015046669
-
-
Thayer, P. S., Himnelfarb, L. A., Watt, G. L., Cancer Chemotherapy 2, 1-25 (1971).
-
(1971)
Cancer Chemotherapy
, vol.2
, pp. 1-25
-
-
Thayer, P.S.1
Himnelfarb, L.A.2
Watt, G.L.3
|