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Volumn 3, Issue 1, 2007, Pages 37-66

Podophyllotoxin: Current perspectives

Author keywords

Biological activity; Chemical modification; Mechanism of actions; Medicinal application; Podophyllotoxin; Reviews; Short chronology; Structure activity relationships

Indexed keywords

2 CHLOROPODOPHYLLOTOXIN; 2 FLUOROPODOPHYLLOTOXIN; 2'' DEOXY 2'' (DIMETHYLAMINO)ETOPOSIDE; ALPHA PELTATIN; APOPICROPODOPHYLLOTOXIN; AZATOXIN; BENZOPODOPHENAZINE; BMY 404811; DEHYDROPODOPHYLLOTOXIN; DIPROPHYLLINE; DNA TOPOISOMERASE; DNA TOPOISOMERASE (ATP HYDROLYSING); EPIPODOPHYLLOTOXIN; ETOPOFOS; ETOPOSIDE; ETOPOSIDE DERIVATIVE; FLUOROURACIL; GL 331; GYRASE INHIBITOR; JUSTICIDIN A; MERCAPTOPURINE; MITOPODOZIDE; PODOPHENAZINE; PODOPHYLLIN; PODOPHYLLOTOXIN; PODOPHYLLOTOXIN DERIVATIVE; TAFLUPOSIDE; TENIPOSIDE; THIOTEPA; TOP 53; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 34248221211     PISSN: 15734072     EISSN: None     Source Type: Journal    
DOI: 10.2174/157340707780126499     Document Type: Review
Times cited : (161)

References (216)
  • 1
    • 34248186644 scopus 로고
    • Lignans, Chemical, Biological and Clinical Properties, Cambridge University Press, Cambridge
    • Ayres, D.C., Loike. J. D. (1990) Lignans, Chemical, Biological and Clinical Properties, Cambridge University Press, Cambridge. Chap 3 and 4.
    • (1990) Chap 3 and 4
    • Ayres, D.C.1    Loike, J.D.2
  • 3
    • 0010683515 scopus 로고
    • Discovery of Podophyllin
    • King, J. (1857) Discovery of Podophyllin. Coll. J. M. Sci., 2, 557-559.
    • (1857) Coll. J. M. Sci , vol.2 , pp. 557-559
    • King, J.1
  • 5
    • 77049217359 scopus 로고
    • The Biological effects and Chemical composition of Podophyllin. A review
    • Kelly, M.G., Hartwell, J. L. (1954) The Biological effects and Chemical composition of Podophyllin. A review. J. Natl. Cancer Inst., 14, 967-1010.
    • (1954) J. Natl. Cancer Inst , vol.14 , pp. 967-1010
    • Kelly, M.G.1    Hartwell, J.L.2
  • 6
    • 0024404351 scopus 로고
    • From Podophyllotoxin gluocoside to Etoposide
    • Stahelin, H., von Wartburg, A. (1989) From Podophyllotoxin gluocoside to Etoposide. Prog. Drug Res., 33, 169-267.
    • (1989) Prog. Drug Res , vol.33 , pp. 169-267
    • Stahelin, H.1    von Wartburg, A.2
  • 7
    • 0001595402 scopus 로고
    • Components of podophyllin. V. The constitution of podophyllotoxin
    • Hartwell, J. L., Schrecker, A. W. (1951) Components of podophyllin. V. The constitution of podophyllotoxin. J. Am. Chem. Soc., 73, 2909-2916.
    • (1951) J. Am. Chem. Soc , vol.73 , pp. 2909-2916
    • Hartwell, J.L.1    Schrecker, A.W.2
  • 9
    • 0032033637 scopus 로고    scopus 로고
    • Discovery of Podophyllotoxins
    • Imbert T. F. (1998) Discovery of Podophyllotoxins. Biochimie, 80, 207-222.
    • (1998) Biochimie , vol.80 , pp. 207-222
    • Imbert, T.F.1
  • 10
    • 0008851694 scopus 로고    scopus 로고
    • Current Research Status of Podophyllotoxin Lignans
    • Liu, C. J., Hou, S. S. (1997) Current Research Status of Podophyllotoxin Lignans. Nat. Prod. Res. Develop., 9, 81-89.
    • (1997) Nat. Prod. Res. Develop , vol.9 , pp. 81-89
    • Liu, C.J.1    Hou, S.S.2
  • 11
    • 0004160423 scopus 로고
    • A Study of the Resources of Chinese Podophyllin Plants
    • Chen, Y. H. (1979) A Study of the Resources of Chinese Podophyllin Plants. Acta Pharm. Sin., 14, 101-107.
    • (1979) Acta Pharm. Sin , vol.14 , pp. 101-107
    • Chen, Y.H.1
  • 16
    • 0001635377 scopus 로고    scopus 로고
    • Podophyllotoxin derivatives: Drug disrovery and development
    • Bohlin, L., Rosen, B. (1996) Podophyllotoxin derivatives: drug disrovery and development. Drug Discov. Today, 1, 343-351.
    • (1996) Drug Discov. Today , vol.1 , pp. 343-351
    • Bohlin, L.1    Rosen, B.2
  • 18
    • 0032168167 scopus 로고    scopus 로고
    • Etoposide: Four decades of development of a topoisomerase II inhibitor
    • Hande, K. R. (1998) Etoposide: four decades of development of a topoisomerase II inhibitor. Eur. J. Cancer, 34, 1514-1521.
    • (1998) Eur. J. Cancer , vol.34 , pp. 1514-1521
    • Hande, K.R.1
  • 19
    • 34248233185 scopus 로고    scopus 로고
    • Species Plantrum, p.505. Stockholm: salvius. 1753.
    • Species Plantrum, p.505. Stockholm: salvius. 1753.
  • 20
    • 34248224292 scopus 로고    scopus 로고
    • Podwyssotzki, V. (1881) The active constituent of podophyllin. Pharm. J. Trans., 12, 217-218.
    • Podwyssotzki, V. (1881) The active constituent of podophyllin. Pharm. J. Trans., 12, 217-218.
  • 21
    • 0010640203 scopus 로고
    • On the active constituents of podophyllin
    • Podwyssotzki, V. (1882) On the active constituents of podophyllin. Am. J. Pharm., 12, 102-115.
    • (1882) Am. J. Pharm , vol.12 , pp. 102-115
    • Podwyssotzki, V.1
  • 22
    • 0002851391 scopus 로고
    • Pharmakologische Studien uber podophyllum peltatum
    • Podwyssotzki, V. (1884) Pharmakologische Studien uber podophyllum peltatum. Naunyn. Schmied Arch Exp. Path. Phar., 13, 29-52.
    • (1884) Naunyn. Schmied Arch Exp. Path. Phar , vol.13 , pp. 29-52
    • Podwyssotzki, V.1
  • 24
    • 0007470441 scopus 로고
    • Sythesis of DL- stereoisomer of Podophyllic acid
    • Gensler, W. J., Samour, C.M., Wang, S.Y., (1954) Sythesis of DL- stereoisomer of Podophyllic acid. J. Am. Chem. Soc., 76, 315.
    • (1954) J. Am. Chem. Soc , vol.76 , pp. 315
    • Gensler, W.J.1    Samour, C.M.2    Wang, S.Y.3
  • 25
    • 0007470442 scopus 로고
    • Sythesis of Picropodophyl-lotoxin
    • Gensler, W. J., Wang, S.Y. (1954) Sythesis of Picropodophyl-lotoxin. J. Am. Chem. Soc., 76, 5890.
    • (1954) J. Am. Chem. Soc , vol.76 , pp. 5890
    • Gensler, W.J.1    Wang, S.Y.2
  • 26
    • 37049139426 scopus 로고
    • Crystal Structure and Absolute Configuration of 2′-Bromopodo-phyllotoxin-0.5 Ehtyl Acetate
    • Petcher, T. J., Weber, H. P., Kuhn, M., von Wartburg, A. J. (1973) Crystal Structure and Absolute Configuration of 2′-Bromopodo-phyllotoxin-0.5 Ehtyl Acetate. J. C. S. Perkin. II, 288-292.
    • (1973) J. C. S. Perkin , vol.2 , pp. 288-292
    • Petcher, T.J.1    Weber, H.P.2    Kuhn, M.3    von Wartburg, A.J.4
  • 27
    • 0001526026 scopus 로고
    • The similarity of the effects of podophyllin and colchicines and their use in the treatment of Codylomata acuminata
    • King, J. L., Sullivan, M. (1946) The similarity of the effects of podophyllin and colchicines and their use in the treatment of Codylomata acuminata. Science, 104, 244-245.
    • (1946) Science , vol.104 , pp. 244-245
    • King, J.L.1    Sullivan, M.2
  • 28
    • 0000258592 scopus 로고
    • The cytological effects of podophyllin
    • Sullivan, B. J., Weshler, H. J. (1947) The cytological effects of podophyllin. Science, 105, 433.
    • (1947) Science , vol.105 , pp. 433
    • Sullivan, B.J.1    Weshler, H.J.2
  • 29
    • 0001117674 scopus 로고
    • The isolation of podophyllotoxin gluooside
    • Stoll, A., Renz, J., Wartburg, A. V. (1954) The isolation of podophyllotoxin gluooside. J. Am. Chem. Soc., 76, 3103-3104.
    • (1954) J. Am. Chem. Soc , vol.76 , pp. 3103-3104
    • Stoll, A.1    Renz, J.2    Wartburg, A.V.3
  • 30
    • 0010679870 scopus 로고
    • The isolation of 4′-Demethylpodophyllotoxin gluooside from rhizomes podophyllum emodi wall
    • Stoll, A., von Wartburg, A., Angliker, E., Renz, J. (1954) The isolation of 4′-Demethylpodophyllotoxin gluooside from rhizomes podophyllum emodi wall. J. Am. Chem. Soc., 76, 5004-5005.
    • (1954) J. Am. Chem. Soc , vol.76 , pp. 5004-5005
    • Stoll, A.1    von Wartburg, A.2    Angliker, E.3    Renz, J.4
  • 32
    • 0014436936 scopus 로고
    • Mitosis-inhibiting substances. XXI. Synthesis of epipodophyllotoxin β-D-glucopyranoside
    • Kuhn, M., von Wartburg, A. (1968) Mitosis-inhibiting substances. XXI. Synthesis of epipodophyllotoxin β-D-glucopyranoside. Helv. Chim. Acta, 51, 1631-1641.
    • (1968) Helv. Chim. Acta , vol.51 , pp. 1631-1641
    • Kuhn, M.1    von Wartburg, A.2
  • 33
    • 0014453173 scopus 로고
    • Mitosis-inhibiting substances. glycosidation process.II. glycosides of 4′-demethylepipodo-phyllotoxin
    • Kuhn, M., von Wartburg, A. (1969) Mitosis-inhibiting substances. glycosidation process.II. glycosides of 4′-demethylepipodo-phyllotoxin. Helv. Chim. Acta, 52, 948-955.
    • (1969) Helv. Chim. Acta , vol.52 , pp. 948-955
    • Kuhn, M.1    von Wartburg, A.2
  • 34
    • 0015138239 scopus 로고
    • Mitosis-inhibiting natural products. 24. Synthesis and antimitotic activity of glycosidic lignan derivatives related to podophyllotoxin
    • Keller-Juslen, C., Kuhn, M., Von Wartburg, A., Staehelin, H. (1971) Mitosis-inhibiting natural products. 24. Synthesis and antimitotic activity of glycosidic lignan derivatives related to podophyllotoxin. J. Med. Chem., 14, 936-940.
    • (1971) J. Med. Chem , vol.14 , pp. 936-940
    • Keller-Juslen, C.1    Kuhn, M.2    Von Wartburg, A.3    Staehelin, H.4
  • 35
    • 0029780802 scopus 로고    scopus 로고
    • The clinical pharmacology of etoposide. An update
    • Joel, S. (1996) The clinical pharmacology of etoposide. An update. Cancer Treat. Rev., 22, 179-221.
    • (1996) Cancer Treat. Rev , vol.22 , pp. 179-221
    • Joel, S.1
  • 36
    • 0026011121 scopus 로고
    • The Chemical and Biological Route from Podophyllotoxin Glucoside to Etoposide: Ninth Cain Memorial Award Lecture
    • Stahelin, H.F., von Wartburg, A. (1991) The Chemical and Biological Route from Podophyllotoxin Glucoside to Etoposide: Ninth Cain Memorial Award Lecture. Cancer Res., 51, 5-15.
    • (1991) Cancer Res , vol.51 , pp. 5-15
    • Stahelin, H.F.1    von Wartburg, A.2
  • 37
    • 0021688805 scopus 로고
    • Role of topoisomerase II in mediating epipodophyllotoxin-induced DNA cleavage
    • Ross, W., Rowe, T., Glisson, B., Yalowich, J., Liu, L. (1984) Role of topoisomerase II in mediating epipodophyllotoxin-induced DNA cleavage. Cancer Res., 44, 5857-5860.
    • (1984) Cancer Res , vol.44 , pp. 5857-5860
    • Ross, W.1    Rowe, T.2    Glisson, B.3    Yalowich, J.4    Liu, L.5
  • 38
    • 34248147133 scopus 로고    scopus 로고
    • Long, B. H., Brattain, M.G. (1984) The Activity of Etoposide and Teniposide against Human Lung Tumour in vitro: cytotoxicity and DNA breakage. In: Etoposide: Current Status and New Developments. Issell BF. Muggia FM.Carter SA, eds. Academic Press, New York. pp. 223.
    • Long, B. H., Brattain, M.G. (1984) The Activity of Etoposide and Teniposide against Human Lung Tumour in vitro: cytotoxicity and DNA breakage. In: Etoposide: Current Status and New Developments. Issell BF. Muggia FM.Carter SA, eds. Academic Press, New York. pp. 223.
  • 39
    • 0001571565 scopus 로고
    • Inhibition of topoisomerase II by VP-16 (etoposide), VM-26 (teniposide) and structure congeners as explanation for in vivo DNA breakage and cytotoxicitry
    • Long, B. H., Minocha, A. (1983) Inhibition of topoisomerase II by VP-16 (etoposide), VM-26 (teniposide) and structure congeners as explanation for in vivo DNA breakage and cytotoxicitry. Proc. Am. Ass. Cancer Res., 24, 1271.
    • (1983) Proc. Am. Ass. Cancer Res , vol.24 , pp. 1271
    • Long, B.H.1    Minocha, A.2
  • 40
    • 0021329758 scopus 로고
    • Comparison of cytotoxicity and DNA breakage activity of congeners of podophyllotoxin including VP16-213 and VM26: A quantitative structure-activity relationship
    • Long, B. H., Musial, S. T., Brattain, M.G. (1984) Comparison of cytotoxicity and DNA breakage activity of congeners of podophyllotoxin including VP16-213 and VM26: a quantitative structure-activity relationship. Biochemistry, 23, 1183-1188.
    • (1984) Biochemistry , vol.23 , pp. 1183-1188
    • Long, B.H.1    Musial, S.T.2    Brattain, M.G.3
  • 41
    • 0033168569 scopus 로고    scopus 로고
    • Antitumour Agents. 194. Synthesis and Biological Evaluations of 4-β-Mono-, -Di-, and -Trisubstituted Aniline-4′-O-demethyl-podo-phyllotoxin and Related Compounds with Improved Pharma-cological Profiles
    • Zhu, X. K., Guan, J., Tachibana, Y., Bastow, K. F., Cho, S. J., Cheng, H. H., Cheng, Y. C., Gurwith, M., Lee, K. H. (1999) Antitumour Agents. 194. Synthesis and Biological Evaluations of 4-β-Mono-, -Di-, and -Trisubstituted Aniline-4′-O-demethyl-podo-phyllotoxin and Related Compounds with Improved Pharma-cological Profiles. J. Med. Chem., 42, 2441-2446.
    • (1999) J. Med. Chem , vol.42 , pp. 2441-2446
    • Zhu, X.K.1    Guan, J.2    Tachibana, Y.3    Bastow, K.F.4    Cho, S.J.5    Cheng, H.H.6    Cheng, Y.C.7    Gurwith, M.8    Lee, K.H.9
  • 42
    • 4744341416 scopus 로고    scopus 로고
    • Antitumor Agents. 234. Design, Synthesis, and Biological Evaluation of Novel 4β-[4′ ′-Benzamido)-Amino]-4′-O-Demethyl-Epipodophyllotoxin Derivatives
    • Xiao, Z., Bastow, K. F., Vance, J. R., Sidwell, R. S., Wang, H.-K., Chen, M. S., Shi, Q., Lee, K. H. (2004) Antitumor Agents. 234. Design, Synthesis, and Biological Evaluation of Novel 4β-[4′ ′-Benzamido)-Amino]-4′-O-Demethyl-Epipodophyllotoxin Derivatives. J. Med. Chem., 47, 5140-5148.
    • (2004) J. Med. Chem , vol.47 , pp. 5140-5148
    • Xiao, Z.1    Bastow, K.F.2    Vance, J.R.3    Sidwell, R.S.4    Wang, H.-K.5    Chen, M.S.6    Shi, Q.7    Lee, K.H.8
  • 43
    • 0028144884 scopus 로고
    • Clinical and pharmacokinetic over view of parental etoposide phosphate
    • Schacter, L. P., Igwemezie, L. N., Seyedsadr, M. (1994) Clinical and pharmacokinetic over view of parental etoposide phosphate. Cancer Chemother. Pharmacol., 34 (Suppl), s58-s63.
    • (1994) Cancer Chemother. Pharmacol , vol.34 , Issue.SUPPL.
    • Schacter, L.P.1    Igwemezie, L.N.2    Seyedsadr, M.3
  • 44
    • 0030464546 scopus 로고    scopus 로고
    • Early studies of etoposide phosphate, a water prodrug
    • Budman, D.R. (1996) Early studies of etoposide phosphate, a water prodrug. Semin. Oncol., 23(suppl), 8-14.
    • (1996) Semin. Oncol , vol.23 , Issue.SUPPL. , pp. 8-14
    • Budman, D.R.1
  • 45
    • 0030468414 scopus 로고    scopus 로고
    • Clinical Studies of Etoposide phosphate
    • Greco, F. A., Hainsworth, J. D. (1996) Clinical Studies of Etoposide phosphate. Semin. Oncol., 23 (suppl), 45-50.
    • (1996) Semin. Oncol , vol.23 , Issue.SUPPL. , pp. 45-50
    • Greco, F.A.1    Hainsworth, J.D.2
  • 46
    • 0023037509 scopus 로고
    • Studies on Lignan Lactone Antitumour Agents. II. Synthesis of N-Alkylamino- and 2,6-Dideoxy-2-Aminoglycosidic Lignan Variants Related to Podophyllotoxin
    • Saito, H., Yoshikawa, H., Nishimura, Y., Kondo, S., Takeuchi, T., Umezawa, H. (1986) Studies on Lignan Lactone Antitumour Agents. II. Synthesis of N-Alkylamino- and 2,6-Dideoxy-2-Aminoglycosidic Lignan Variants Related to Podophyllotoxin. Chem. Pharm. Bull., 34, 3741-3746.
    • (1986) Chem. Pharm. Bull , vol.34 , pp. 3741-3746
    • Saito, H.1    Yoshikawa, H.2    Nishimura, Y.3    Kondo, S.4    Takeuchi, T.5    Umezawa, H.6
  • 48
    • 0344994511 scopus 로고    scopus 로고
    • Novel Antitumour Agents from Higher Plants
    • Lee, K. H. (1999) Novel Antitumour Agents from Higher Plants. Med. Res. Rev., 19, 569-596.
    • (1999) Med. Res. Rev , vol.19 , pp. 569-596
    • Lee, K.H.1
  • 49
    • 0025350760 scopus 로고
    • Antitumour agents. 111. New 4-hydroxylated and 4-halogenated anilino derivatives of 4′-demethylepipodophyllotoxin as potent inhibitors of human DNA topoisomerase II
    • Lee, K. H., Beers, S. A., Mori, M., Wang, Z. Q., Kuo, Y. H., Li, L., Liu, S. Y., Chang, J. Y., Han, F. S., Cheng, Y. C. (1990) Antitumour agents. 111. New 4-hydroxylated and 4-halogenated anilino derivatives of 4′-demethylepipodophyllotoxin as potent inhibitors of human DNA topoisomerase II. J. Med. Chem., 33, 1364-1368.
    • (1990) J. Med. Chem , vol.33 , pp. 1364-1368
    • Lee, K.H.1    Beers, S.A.2    Mori, M.3    Wang, Z.Q.4    Kuo, Y.H.5    Li, L.6    Liu, S.Y.7    Chang, J.Y.8    Han, F.S.9    Cheng, Y.C.10
  • 50
    • 0024988752 scopus 로고
    • Antitumour agents. 113. New 4.beta.-arylamino derivatives of 4′-O-demethylepipodophyllotoxin and related compounds as potent inhibitors of human DNA topoisomerase II
    • Wang, Z. Q., Kuo, Y. H., Schnur, D., Bowen, J. P., Liu, S. Y., Han, F. S., Chang, J. Y., Cheng, Y. C., Lee, K. H. (1990) Antitumour agents. 113. New 4.beta.-arylamino derivatives of 4′-O-demethylepipodophyllotoxin and related compounds as potent inhibitors of human DNA topoisomerase II. J. Med. Chem., 33, 2660-2666.
    • (1990) J. Med. Chem , vol.33 , pp. 2660-2666
    • Wang, Z.Q.1    Kuo, Y.H.2    Schnur, D.3    Bowen, J.P.4    Liu, S.Y.5    Han, F.S.6    Chang, J.Y.7    Cheng, Y.C.8    Lee, K.H.9
  • 52
    • 0024345610 scopus 로고
    • Synthesis and Antitumour Activity of Podopyllotoxin aza-analogues
    • Tomioka, K., Kubuta, Y., Koga, K. (1989) Synthesis and Antitumour Activity of Podopyllotoxin aza-analogues. Tetradron Lett., 30, 2953-2954.
    • (1989) Tetradron Lett , vol.30 , pp. 2953-2954
    • Tomioka, K.1    Kubuta, Y.2    Koga, K.3
  • 53
    • 0027195713 scopus 로고
    • Dual Inhibition of Topoisomerase II and Tubulin Polymerization by azatoxin, a novel cytotoxic agent
    • Solary, E., Leteurture, F., Paull, K. D., Scudiero, D., Hamel, E., Prommier, Y. (1993) Dual Inhibition of Topoisomerase II and Tubulin Polymerization by azatoxin, a novel cytotoxic agent. Biochem. Pharmacol., 45, 2449-2456.
    • (1993) Biochem. Pharmacol , vol.45 , pp. 2449-2456
    • Solary, E.1    Leteurture, F.2    Paull, K.D.3    Scudiero, D.4    Hamel, E.5    Prommier, Y.6
  • 54
    • 0027208041 scopus 로고
    • Antitumour agents. 3. Synthesis and biological activity of 4.beta.-alkyl derivatives containing hydroxy, amino, and amido groups of 4′-O-demethyl-4-desoxypodophyllotoxin as antitumour agents
    • Terada, T., Fujimoto, K., Nomura, M., Yamashita, J., Wierzba, K., Yamazaki, R., Shibata, J., Sugimoto, Y., Yamada, Y. (1993) Antitumour agents. 3. Synthesis and biological activity of 4.beta.-alkyl derivatives containing hydroxy, amino, and amido groups of 4′-O-demethyl-4-desoxypodophyllotoxin as antitumour agents. J. Med. Chem., 36, 1689-1699.
    • (1993) J. Med. Chem , vol.36 , pp. 1689-1699
    • Terada, T.1    Fujimoto, K.2    Nomura, M.3    Yamashita, J.4    Wierzba, K.5    Yamazaki, R.6    Shibata, J.7    Sugimoto, Y.8    Yamada, Y.9
  • 55
    • 0001766983 scopus 로고
    • in vitro and in vivo Antitumour Activity against lung cancer of TOP53, a novel podophyllotoxin derivative
    • Abst 2154
    • Kobunai, T., Saito, H., Yoshida, M., Toko, T., Takeda, S., Unemi, N. (1994) in vitro and in vivo Antitumour Activity against lung cancer of TOP53, a novel podophyllotoxin derivative. Proc. Am. Assoc. Cancer Res., 35, Abst 2154.
    • (1994) Proc. Am. Assoc. Cancer Res , vol.35
    • Kobunai, T.1    Saito, H.2    Yoshida, M.3    Toko, T.4    Takeda, S.5    Unemi, N.6
  • 57
    • 1442310087 scopus 로고    scopus 로고
    • A Tale of Two Tumour Targets: Topoisomerase I and Tubulin. The Wall and Wani Contribution to Cancer Chemotherapy
    • Cragg, G. M., Newman, D. J. (2004) A Tale of Two Tumour Targets: Topoisomerase I and Tubulin. The Wall and Wani Contribution to Cancer Chemotherapy. J. Nat. Prod., 67, 232-244.
    • (2004) J. Nat. Prod , vol.67 , pp. 232-244
    • Cragg, G.M.1    Newman, D.J.2
  • 58
    • 18444404643 scopus 로고    scopus 로고
    • Synthesis and Biological Activity of New Class of Dioxygenated Anticancer Agents
    • Maria, D. P., Manel, R. and Isabel, S. (2005) Synthesis and Biological Activity of New Class of Dioxygenated Anticancer Agents. Anti-Cancer Agents Med. Chem., 5, 215-237.
    • (2005) Anti-Cancer Agents Med. Chem , vol.5 , pp. 215-237
    • Maria, D.P.1    Manel, R.2    Isabel, S.3
  • 60
    • 0020406202 scopus 로고
    • An Investigation of the Antiviral Activity of Podophyllum peltatum
    • Bedows, E., Hatfield, G. M. (1982) An Investigation of the Antiviral Activity of Podophyllum peltatum. J. Nat. Prod., 45, 725-729.
    • (1982) J. Nat. Prod , vol.45 , pp. 725-729
    • Bedows, E.1    Hatfield, G.M.2
  • 62
    • 0029791770 scopus 로고    scopus 로고
    • Studies to show that with podophyllotoxin the early replicative stages of herpes simplex virus type I depend upon functional cytoplasmic microtubules
    • Hammonds, T. R., Denyer, S. P., Jackson, D. E., Irving, W. L. (1996) Studies to show that with podophyllotoxin the early replicative stages of herpes simplex virus type I depend upon functional cytoplasmic microtubules. J. Med. Microbiol., 45, 167-172.
    • (1996) J. Med. Microbiol , vol.45 , pp. 167-172
    • Hammonds, T.R.1    Denyer, S.P.2    Jackson, D.E.3    Irving, W.L.4
  • 63
    • 0000672896 scopus 로고
    • Aryletralin Lignans from Linum Flavum and Linum Capitatum
    • Broomhead, A. J., Dewick, P. M. (1990) Aryletralin Lignans from Linum Flavum and Linum Capitatum. Phytochemistry, 29, 3839-3844.
    • (1990) Phytochemistry , vol.29 , pp. 3839-3844
    • Broomhead, A.J.1    Dewick, P.M.2
  • 65
    • 0031730202 scopus 로고    scopus 로고
    • Antiviral Activity of Lignans
    • Charlton, J. L. (1998) Antiviral Activity of Lignans. J. Nat. Prod., 61, 1447-1451.
    • (1998) J. Nat. Prod , vol.61 , pp. 1447-1451
    • Charlton, J.L.1
  • 67
    • 0035204088 scopus 로고    scopus 로고
    • The Successful Treatment of molluscum contagiosum with Podophyllotoxin(0.5%) self-application
    • Markos, A. R. (2001) The Successful Treatment of molluscum contagiosum with Podophyllotoxin(0.5%) self-application. Int. J. STD. AIDS, 12, 833.
    • (2001) Int. J. STD. AIDS , vol.12 , pp. 833
    • Markos, A.R.1
  • 68
    • 34248171986 scopus 로고
    • Medicinal used for podophyllotoxin
    • US patent, 4,788,216
    • Leander, K., Rosen, B. (1988) Medicinal used for podophyllotoxin. US patent, 4,788,216.
    • (1988)
    • Leander, K.1    Rosen, B.2
  • 69
    • 0036828143 scopus 로고    scopus 로고
    • Useful plants of dermatology.VI. The mayapple (podophyllum)
    • Schwartz, J., Norton, S. A. (2002) Useful plants of dermatology.VI. The mayapple (podophyllum). J. Am. Acad. Dermatol., 47, 774-775.
    • (2002) J. Am. Acad. Dermatol , vol.47 , pp. 774-775
    • Schwartz, J.1    Norton, S.A.2
  • 70
    • 18744373344 scopus 로고    scopus 로고
    • Podophyllotoxin Derivatives: Current Synthetic Approaches for New Anticancer Agents
    • You, Y. J. (2005) Podophyllotoxin Derivatives: Current Synthetic Approaches for New Anticancer Agents. Curr. Pharm. Des., 11, 1695-1717.
    • (2005) Curr. Pharm. Des , vol.11 , pp. 1695-1717
    • You, Y.J.1
  • 71
    • 0034831086 scopus 로고    scopus 로고
    • Advances in Cancer Therapy with Plant Based Natural Products
    • Mukherjee, A. K., Basu, S., Sarkar, N., Ghosh, A. C. (2001) Advances in Cancer Therapy with Plant Based Natural Products. Curr. Med. Chem., 8, 1467-1486.
    • (2001) Curr. Med. Chem , vol.8 , pp. 1467-1486
    • Mukherjee, A.K.1    Basu, S.2    Sarkar, N.3    Ghosh, A.C.4
  • 72
    • 0035073578 scopus 로고    scopus 로고
    • Podophyllotoxin lignans enhance IL-1E but suppress TNF-a mRNA expression in LPS-treated monocytes
    • Pugh, N. I., Khan, I., Moraes, R. M., Pasco, D. (2001) Podophyllotoxin lignans enhance IL-1E but suppress TNF-a mRNA expression in LPS-treated monocytes. Immunopharmacol. Immunotoxicol., 23, 83-95.
    • (2001) Immunopharmacol. Immunotoxicol , vol.23 , pp. 83-95
    • Pugh, N.I.1    Khan, I.2    Moraes, R.M.3    Pasco, D.4
  • 73
    • 0034741843 scopus 로고    scopus 로고
    • Aryltetralin Lignans: Chemistry, Pharmacology and Biotrans-formations
    • Botta, B., Monache, G. D., Misiti, D., Vitali, A., Zappia, G. (2001) Aryltetralin Lignans: Chemistry, Pharmacology and Biotrans-formations. Curr. Med. Chem., 8, 1363-1381.
    • (2001) Curr. Med. Chem , vol.8 , pp. 1363-1381
    • Botta, B.1    Monache, G.D.2    Misiti, D.3    Vitali, A.4    Zappia, G.5
  • 74
    • 0031728637 scopus 로고    scopus 로고
    • Podophyllotoxin-induced acantholysis and cytolysis in a skin equivalent model
    • Hermanns, L.T., Arrese, J. E., Goffin, V., Pierard, G. E. (1998) Podophyllotoxin-induced acantholysis and cytolysis in a skin equivalent model. Eur. J. Morphol., 36, 183-187.
    • (1998) Eur. J. Morphol , vol.36 , pp. 183-187
    • Hermanns, L.T.1    Arrese, J.E.2    Goffin, V.3    Pierard, G.E.4
  • 75
    • 0021267999 scopus 로고
    • Mechanisms of insecticidal action of deoxypodophyl-lotoxin (Anthricin). II. Histopathological studies on tissues of silkworm larvae intoxicated by deoxypodophyllotoxin
    • Inamori, Y., Kato, Y., Kubo, M., Waku, Y., Hayashiya, K., Sakai, M. (1984) Mechanisms of insecticidal action of deoxypodophyl-lotoxin (Anthricin). II. Histopathological studies on tissues of silkworm larvae intoxicated by deoxypodophyllotoxin. Chem. Pharm. Bull., 32, 2015-2019.
    • (1984) Chem. Pharm. Bull , vol.32 , pp. 2015-2019
    • Inamori, Y.1    Kato, Y.2    Kubo, M.3    Waku, Y.4    Hayashiya, K.5    Sakai, M.6
  • 76
    • 85008096966 scopus 로고
    • Components of the root of Anthriscus sylvestris Hoffm II. Insecticidal activity
    • Kozawa, M., Baba, K., Matsuyama, Y., Kido, T. (1982) Components of the root of Anthriscus sylvestris Hoffm II. Insecticidal activity. Chem. Pharm. Bull., 30, 2885-2888.
    • (1982) Chem. Pharm. Bull , vol.30 , pp. 2885-2888
    • Kozawa, M.1    Baba, K.2    Matsuyama, Y.3    Kido, T.4
  • 78
    • 85008113047 scopus 로고
    • Mechanisms of insecticidal action of deoxypodophyllotoxin (Anthricin). III. The mode of delayed insecticidal action of deoxypodophyllotoxin
    • Inamori, Y., Kubo, M., Tsujibo, H., Oki, S., Kodama, Y. (1986) Mechanisms of insecticidal action of deoxypodophyllotoxin (Anthricin). III. The mode of delayed insecticidal action of deoxypodophyllotoxin. Chem. Pharm. Bull., 34, 2247-2250.
    • (1986) Chem. Pharm. Bull , vol.34 , pp. 2247-2250
    • Inamori, Y.1    Kubo, M.2    Tsujibo, H.3    Oki, S.4    Kodama, Y.5
  • 79
    • 7044236118 scopus 로고    scopus 로고
    • A study on the relationship between structure and insecticidal activity of podophyllotoxin analogues I. The synthesis of podophyllotoxin analogues and their insecticidal activities
    • Gao, R., Tian, X., Zhang, X. (2000) A study on the relationship between structure and insecticidal activity of podophyllotoxin analogues I. The synthesis of podophyllotoxin analogues and their insecticidal activities. Acta Universitatis agriculturalis Boreali-occidentalis, 28, 8-13.
    • (2000) Acta Universitatis agriculturalis Boreali-occidentalis , vol.28 , pp. 8-13
    • Gao, R.1    Tian, X.2    Zhang, X.3
  • 81
    • 0036516128 scopus 로고    scopus 로고
    • Synthesis and insecticidal activity of novel 4 β-halogenated benzoylaminopo-dophyllotoxins against Pieris rapae Linnaeus
    • Xu, H., Zhang, X., Tian, X., Lu, M., Wang, Y.G. (2002) Synthesis and insecticidal activity of novel 4 β-halogenated benzoylaminopo-dophyllotoxins against Pieris rapae Linnaeus. Chem. Pharm. Bull., 50, 399-402.
    • (2002) Chem. Pharm. Bull , vol.50 , pp. 399-402
    • Xu, H.1    Zhang, X.2    Tian, X.3    Lu, M.4    Wang, Y.G.5
  • 82
    • 7044269114 scopus 로고    scopus 로고
    • Insecticidal activity of deoxypodophyllotoxin, isolated from Juniperus sabina L, and related lignans against larvae of Pieris rapae L
    • Gao, R., Gan, C. F., Tian, X., Yu, X. Y., Di, X. D., Xiao, H., Zhang, X. (2004) Insecticidal activity of deoxypodophyllotoxin, isolated from Juniperus sabina L, and related lignans against larvae of Pieris rapae L. Pest Manag. Sci., 60, 1131-1136.
    • (2004) Pest Manag. Sci , vol.60 , pp. 1131-1136
    • Gao, R.1    Gan, C.F.2    Tian, X.3    Yu, X.Y.4    Di, X.D.5    Xiao, H.6    Zhang, X.7
  • 83
    • 7044239894 scopus 로고    scopus 로고
    • Study on the relationship between structure and insecticidal activity of podophyllotoxin analogues II. Analysis of structure-activity relationship and prediction of optimal structure
    • Tian, X., Gao, R., Zhang, X. (2000) Study on the relationship between structure and insecticidal activity of podophyllotoxin analogues II. Analysis of structure-activity relationship and prediction of optimal structure. Acta Universitatis Agriculturalis Boreali-occidentalis., 28, 19-24.
    • (2000) Acta Universitatis Agriculturalis Boreali-occidentalis , vol.28 , pp. 19-24
    • Tian, X.1    Gao, R.2    Zhang, X.3
  • 84
    • 32344439156 scopus 로고    scopus 로고
    • A brief review on podophyllotoxin analogues
    • Gao, R., Tian, X., Zhang, X. (2002) A brief review on podophyllotoxin analogues. Chin. J. Pest. Sci., 2, 1-6.
    • (2002) Chin. J. Pest. Sci , vol.2 , pp. 1-6
    • Gao, R.1    Tian, X.2    Zhang, X.3
  • 86
    • 34248195084 scopus 로고    scopus 로고
    • the recent progress in pesticides
    • Wang, M. H., Yang, C. L., Jiang, M. G. (2002) the recent progress in pesticides. World Pest., 24, 13-15.
    • (2002) World Pest , vol.24 , pp. 13-15
    • Wang, M.H.1    Yang, C.L.2    Jiang, M.G.3
  • 87
    • 0036355434 scopus 로고    scopus 로고
    • Aryltetralin Lignans Inhibit Plant Growth by Affecting the Formation of Mitotic Microtubular Organizing Centers
    • Oliva, A., Moraes, R. M., Watson, S. B., Duke, S. O., Dayan, F. E. (2002) Aryltetralin Lignans Inhibit Plant Growth by Affecting the Formation of Mitotic Microtubular Organizing Centers. Pest. Biochem. Phys. 72, 45-54.
    • (2002) Pest. Biochem. Phys , vol.72 , pp. 45-54
    • Oliva, A.1    Moraes, R.M.2    Watson, S.B.3    Duke, S.O.4    Dayan, F.E.5
  • 88
    • 4043124732 scopus 로고    scopus 로고
    • Lignoids in insects: Chemical probes for the study of ecdysis, excretion and Trypanosoma cruzi - triatomine interactions
    • Garcia, E. S., Azambuja, P. (2004) Lignoids in insects: chemical probes for the study of ecdysis, excretion and Trypanosoma cruzi - triatomine interactions. Toxicon, 44, 431-440.
    • (2004) Toxicon , vol.44 , pp. 431-440
    • Garcia, E.S.1    Azambuja, P.2
  • 89
    • 0014144402 scopus 로고
    • the Biochemical Events of Mitosis. II. The in vivo and in vitro Binding of Colchicine in Grasshopper Embryos and Its Possible Relation to Inhibition of Mitosis
    • Wilson, L., Friedkin, M. (1967) the Biochemical Events of Mitosis. II. The in vivo and in vitro Binding of Colchicine in Grasshopper Embryos and Its Possible Relation to Inhibition of Mitosis Biochemistry, 6, 3126-3135.
    • (1967) Biochemistry , vol.6 , pp. 3126-3135
    • Wilson, L.1    Friedkin, M.2
  • 90
    • 0017344821 scopus 로고
    • Podophyllotoxin as a probe for the colchicines binding site of tubulin
    • Cortese, F., Bhattacharyya, B., Wolf, B. (1977) Podophyllotoxin as a probe for the colchicines binding site of tubulin. J. Biol. Chem., 252, 1134-1140.
    • (1977) J. Biol. Chem , vol.252 , pp. 1134-1140
    • Cortese, F.1    Bhattacharyya, B.2    Wolf, B.3
  • 91
    • 0030272619 scopus 로고    scopus 로고
    • Computational and molecular modeling evaluation of the structural basis for tubulin polymerization inhibition by colchicine site agents
    • ter Haar, E., Rosenkranz, H. S., Hamel, E., Day, B. W. (1996) Computational and molecular modeling evaluation of the structural basis for tubulin polymerization inhibition by colchicine site agents. Bioorg. Med Chem., 4, 1659-1671.
    • (1996) Bioorg. Med Chem , vol.4 , pp. 1659-1671
    • ter Haar, E.1    Rosenkranz, H.S.2    Hamel, E.3    Day, B.W.4
  • 92
    • 0036086919 scopus 로고    scopus 로고
    • Drugs that Inhibit Tubulin Polymerization: The Particular Case of Podophyllotoxin and Analogues
    • Desbène, S., Giorgi-Renault, S. (2001) Drugs that Inhibit Tubulin Polymerization: The Particular Case of Podophyllotoxin and Analogues. Curr. Med. Chem. Anti-Cancer Agents, 1, 71-90.
    • (2001) Curr. Med. Chem. Anti-Cancer Agents , vol.1 , pp. 71-90
    • Desbène, S.1    Giorgi-Renault, S.2
  • 93
    • 9144254574 scopus 로고    scopus 로고
    • Microtubulin Binding Sites as Target for Developing Anticancer Agents
    • Islam, M. N., Iskander, M. N. (2004) Microtubulin Binding Sites as Target for Developing Anticancer Agents. Mini-Rev. Med. Chem., 4, 1077-1104.
    • (2004) Mini-Rev. Med. Chem , vol.4 , pp. 1077-1104
    • Islam, M.N.1    Iskander, M.N.2
  • 95
    • 0034923502 scopus 로고    scopus 로고
    • DNA topoisomerases: Structure, function, and mechanism
    • Champoux, J. J. (2001) DNA topoisomerases: structure, function, and mechanism. Annu. Rev. Biochem., 70, 369-413.
    • (2001) Annu. Rev. Biochem , vol.70 , pp. 369-413
    • Champoux, J.J.1
  • 96
    • 0032190561 scopus 로고    scopus 로고
    • Mechanism of action of eukaryotic topoisomerase II and drug targeted to the enzyme
    • Burden, D.A., Osheroff, N. (1998) Mechanism of action of eukaryotic topoisomerase II and drug targeted to the enzyme. Biochim. Biophys. Acta, 1400, 139-154.
    • (1998) Biochim. Biophys. Acta , vol.1400 , pp. 139-154
    • Burden, D.A.1    Osheroff, N.2
  • 97
    • 0030045003 scopus 로고    scopus 로고
    • Structure and Mechanism of DNA Topoisomerase II
    • Berger, J. M., Gambin, S. J., Harrison S. C., Wang, J.C. (1996) Structure and Mechanism of DNA Topoisomerase II. Nature, 379, 225-232.
    • (1996) Nature , vol.379 , pp. 225-232
    • Berger, J.M.1    Gambin, S.J.2    Harrison, S.C.3    Wang, J.C.4
  • 98
    • 0000420523 scopus 로고    scopus 로고
    • DNA topoisomerase II inhibitors
    • Teacher BA, Eds, Human Press, Taotowa, New Jersey. pp
    • Pommier,Y. (1997) DNA topoisomerase II inhibitors. In: Cancer Therapeutic: Experimental and Clinical Agents. Teacher BA, Eds, Human Press, Taotowa, New Jersey. pp. 153-174.
    • (1997) Cancer Therapeutic: Experimental and Clinical Agents , pp. 153-174
    • Pommier, Y.1
  • 99
    • 0022536877 scopus 로고
    • Peroxidative free radical formation and O-demethylation of etoposide and teniposide
    • Haim, N., Nemec, J., Roman, J., Sinha, B. K. (1986) Peroxidative free radical formation and O-demethylation of etoposide and teniposide. Biochem. Biophys. Res. Commun., 135, 215-220.
    • (1986) Biochem. Biophys. Res. Commun , vol.135 , pp. 215-220
    • Haim, N.1    Nemec, J.2    Roman, J.3    Sinha, B.K.4
  • 100
    • 0023552961 scopus 로고
    • peroxidase-catalyzed metabolism of etoposide and covalent binding of reactive intermediates to cellular macromolecules
    • Haim, N., Nemec, J., Roman, J., Sinha, B. K. (1987) peroxidase-catalyzed metabolism of etoposide and covalent binding of reactive intermediates to cellular macromolecules. Cancer Res., 47, 5835-5840.
    • (1987) Cancer Res , vol.47 , pp. 5835-5840
    • Haim, N.1    Nemec, J.2    Roman, J.3    Sinha, B.K.4
  • 101
    • 0024539206 scopus 로고
    • Free radicals in anticancer drug pharmacology
    • Sinha, B. K. (1989) Free radicals in anticancer drug pharmacology. Chem. Biol. Interact., 69, 293-317.
    • (1989) Chem. Biol. Interact , vol.69 , pp. 293-317
    • Sinha, B.K.1
  • 102
    • 0000565780 scopus 로고
    • Partialsynthese der 6, 7-Dimethoxy-Analogen von Podophyllotoxin, Epi-, Neo-, und Desoxy-podophyllotoxin
    • von Schreier, E. (1964) Partialsynthese der 6, 7-Dimethoxy-Analogen von Podophyllotoxin, Epi-, Neo-, und Desoxy-podophyllotoxin. Helv. Chim. Acta, 47, 1529-1554.
    • (1964) Helv. Chim. Acta , vol.47 , pp. 1529-1554
    • von Schreier, E.1
  • 103
    • 0026545101 scopus 로고
    • Antitumour agents. 124. New 4.beta.-substituted aniline derivatives of 6,7-O, O-demethylene-4′-O-demethylpodophyllotoxin and related compounds as potent inhibitors of human DNA topoisomerase II
    • Wang, Z. Q., Hu, H., Chen, H. X., Cheng, Y. C., Lee, K. H. (1992) Antitumour agents. 124. New 4.beta.-substituted aniline derivatives of 6,7-O, O-demethylene-4′-O-demethylpodophyllotoxin and related compounds as potent inhibitors of human DNA topoisomerase II. J. Med. Chem., 35, 871-877.
    • (1992) J. Med. Chem , vol.35 , pp. 871-877
    • Wang, Z.Q.1    Hu, H.2    Chen, H.X.3    Cheng, Y.C.4    Lee, K.H.5
  • 105
    • 0000734820 scopus 로고    scopus 로고
    • Antitumour Agents. 164. Podophenazine, 2″,3″-Dichloropo-dophenazine, Benzopodophenazine, and Their 4β-p-Nitroaniline Derivatives as Novel DNA Topoisomerase II Inhibitors
    • Cho, S. J., Kashiwada, Y., Bastow, K. F., Cheng, Y.C., Lee, K. H. (1996) Antitumour Agents. 164. Podophenazine, 2″,3″-Dichloropo-dophenazine, Benzopodophenazine, and Their 4β-p-Nitroaniline Derivatives as Novel DNA Topoisomerase II Inhibitors. J. Med. Chem., 39, 1396-1402.
    • (1996) J. Med. Chem , vol.39 , pp. 1396-1402
    • Cho, S.J.1    Kashiwada, Y.2    Bastow, K.F.3    Cheng, Y.C.4    Lee, K.H.5
  • 106
    • 16044363432 scopus 로고    scopus 로고
    • Synthesis of podophyllotoxin A-ring pyridazine analogue
    • Bertounesque, E., Imbert, T., Monneret, C. (1996) Synthesis of podophyllotoxin A-ring pyridazine analogue. Tetrahedron, 52, 14235-14246.
    • (1996) Tetrahedron , vol.52 , pp. 14235-14246
    • Bertounesque, E.1    Imbert, T.2    Monneret, C.3
  • 107
    • 0033615756 scopus 로고    scopus 로고
    • Synthetic approaches to condensed aromatic analogues from etoposide. Synthesis of A-ring pyridazine picroetoposide
    • Meresse, P., Bertounesque, E., Imbert, T., Monneret, C. (1999)Synthetic approaches to condensed aromatic analogues from etoposide. Synthesis of A-ring pyridazine picroetoposide. Tetrahedron, 55, 12805-12818.
    • (1999) Tetrahedron , vol.55 , pp. 12805-12818
    • Meresse, P.1    Bertounesque, E.2    Imbert, T.3    Monneret, C.4
  • 110
    • 0042337995 scopus 로고
    • α-Peltatin, a New compound Isolated from podophyllum peltatum
    • Hartwell, J. L. (1947) α-Peltatin, a New compound Isolated from podophyllum peltatum. J. Am. Chem. Soc., 69, 2918-2918.
    • (1947) J. Am. Chem. Soc , vol.69 , pp. 2918-2918
    • Hartwell, J.L.1
  • 111
    • 18444386640 scopus 로고
    • The isolation of α-peltatin glucoside from the rhizomes of Podophyllum peltatum L
    • Stoll, A., von Wartburg, A., Renz, J. (1955) The isolation of α-peltatin glucoside from the rhizomes of Podophyllum peltatum L. J. Am. Chem. Soc., 77, 1710-1711.
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 1710-1711
    • Stoll, A.1    von Wartburg, A.2    Renz, J.3
  • 112
    • 0020406202 scopus 로고
    • An Investigation of the Antiviral Activity of Podophyllum peltatum
    • Bedows, E., Hatfield, G. M. (1982) An Investigation of the Antiviral Activity of Podophyllum peltatum. J. Nat. Prod., 45, 725-729.
    • (1982) J. Nat. Prod , vol.45 , pp. 725-729
    • Bedows, E.1    Hatfield, G.M.2
  • 113
    • 0022504993 scopus 로고
    • Antitumour agents. 78. Inhibition of human DNA topoisomerase II by podophyllotoxin and alpha-peltatin analogs
    • Thurston, L.S., Irie, H., Tani, S., Han, F. S., Liu, Z. C., Cheng, Y. C., Lee, K. H. (1986) Antitumour agents. 78. Inhibition of human DNA topoisomerase II by podophyllotoxin and alpha-peltatin analogs. J. Med. Chem., 29, 1547-1550.
    • (1986) J. Med. Chem , vol.29 , pp. 1547-1550
    • Thurston, L.S.1    Irie, H.2    Tani, S.3    Han, F.S.4    Liu, Z.C.5    Cheng, Y.C.6    Lee, K.H.7
  • 114
    • 0024504542 scopus 로고
    • Antitumour agents. 100. Inhibition of human DNA topoisomerase II by cytotoxic ether and ester derivatives of podophyllotoxin and alpha-peltatin
    • Thurston, L. S., Imakura, Y., Haruna, M., Li, D. H., Liu, Z. C., Liu, S. Y., Cheng, Y. C., Lee, K. H. (1989) Antitumour agents. 100. Inhibition of human DNA topoisomerase II by cytotoxic ether and ester derivatives of podophyllotoxin and alpha-peltatin. J. Med. Chem., 32, 604-608.
    • (1989) J. Med. Chem , vol.32 , pp. 604-608
    • Thurston, L.S.1    Imakura, Y.2    Haruna, M.3    Li, D.H.4    Liu, Z.C.5    Liu, S.Y.6    Cheng, Y.C.7    Lee, K.H.8
  • 115
    • 0023919342 scopus 로고
    • Studies on Lignan Lactone Antitumour Agents.IV. Synthesis of Glycosidic Lignan Variants Related to α- peltatin
    • Saito, H., Nishimura, Y., Kondo, S., Takeuchi, T., Umezawa, H. (1988) Studies on Lignan Lactone Antitumour Agents.IV. Synthesis of Glycosidic Lignan Variants Related to α- peltatin. Bull. Chem. Soc. Jpn., 61, 1259-1263.
    • (1988) Bull. Chem. Soc. Jpn , vol.61 , pp. 1259-1263
    • Saito, H.1    Nishimura, Y.2    Kondo, S.3    Takeuchi, T.4    Umezawa, H.5
  • 116
    • 33947453628 scopus 로고
    • Components of Podophyllin. IX. The Structure of the Apopicropodophyllins
    • Schrecker, A. W., Hartwell, J. L. (1952) Components of Podophyllin. IX. The Structure of the Apopicropodophyllins. J. Am. Chem. Soc., 74, 5676-5683.
    • (1952) J. Am. Chem. Soc , vol.74 , pp. 5676-5683
    • Schrecker, A.W.1    Hartwell, J.L.2
  • 118
    • 33747849809 scopus 로고
    • Compounds Related to Podophyllotoxin. XII. Podophyllotoxone, Picropo-dophyllone and Dehydropodophyllotoxin
    • Gensler, W. J., Johnson, F., Sloan, A. D. B. (1960) Compounds Related to Podophyllotoxin. XII. Podophyllotoxone, Picropo-dophyllone and Dehydropodophyllotoxin. J. Am. Chem. Soc., 82, 6074-6081.
    • (1960) J. Am. Chem. Soc , vol.82 , pp. 6074-6081
    • Gensler, W.J.1    Johnson, F.2    Sloan, A.D.B.3
  • 119
    • 0031576895 scopus 로고    scopus 로고
    • A novel enzymatic dehydrogenation of podophyllotoxin congeners by yeast cells
    • Kamal, A., Damayanthi, Y. (1997) A novel enzymatic dehydrogenation of podophyllotoxin congeners by yeast cells. Bioorg. Med. Chem. Lett., 7, 657-662.
    • (1997) Bioorg. Med. Chem. Lett , vol.7 , pp. 657-662
    • Kamal, A.1    Damayanthi, Y.2
  • 120
    • 0023805939 scopus 로고
    • Antitumour Agents, 99. Synthetic Ring C Aromatized Podophyllotoxin Analogues as Potential Inhibitors of Human DNA Topoisomerase II
    • Beers, S. A., Imakura, Y., Dai, H. J., Li, D. H., Cheng, Y. C., Lee, K. H. (1988) Antitumour Agents, 99. Synthetic Ring C Aromatized Podophyllotoxin Analogues as Potential Inhibitors of Human DNA Topoisomerase II. J. Nat. Prod., 51, 901-905.
    • (1988) J. Nat. Prod , vol.51 , pp. 901-905
    • Beers, S.A.1    Imakura, Y.2    Dai, H.J.3    Li, D.H.4    Cheng, Y.C.5    Lee, K.H.6
  • 121
    • 0005979959 scopus 로고
    • Synthesis of Podophyllotoxin & related analogues: Part II- Synthesis of β-apopicrophyllin analogues with modified Hydroaromatic ring-B
    • Canjanamurthy, K., Lokanatharai, M. (1985) Synthesis of Podophyllotoxin & related analogues: part II- Synthesis of β-apopicrophyllin analogues with modified Hydroaromatic ring-B. Indian J. Chem., 24B, 505-508.
    • (1985) Indian J. Chem , vol.24 B , pp. 505-508
    • Canjanamurthy, K.1    Lokanatharai, M.2
  • 122
    • 0009413517 scopus 로고
    • Synthesis of Podophyllotoxin & related analogues: Part III- Synthesis of β-apopicrophyllin analogues with modified lactone ring
    • Canjanamurthy, K., Lokanatharai, M. (1987) Synthesis of Podophyllotoxin & related analogues: part III- Synthesis of β-apopicrophyllin analogues with modified lactone ring. Indian J. Chem., 26B, 131-135.
    • (1987) Indian J. Chem , vol.26 B , pp. 131-135
    • Canjanamurthy, K.1    Lokanatharai, M.2
  • 123
    • 34248202690 scopus 로고    scopus 로고
    • The effects of unsaturated factors on ring C to chemical Properties of podophyllotoxin analogues
    • He, Y., Ma, W.Y., Zhang, C. N. (2001) The effects of unsaturated factors on ring C to chemical Properties of podophyllotoxin analogues. J. Chin. Pharm. Sci., 10, 81-84.
    • (2001) J. Chin. Pharm. Sci , vol.10 , pp. 81-84
    • He, Y.1    Ma, W.Y.2    Zhang, C.N.3
  • 124
    • 0031810637 scopus 로고    scopus 로고
    • Podophyllotoxins: Current Status and Recent Developments
    • Damayanthi, Y., Lown, J. W. (1998) Podophyllotoxins: Current Status and Recent Developments. Curr. Med. Chem., 5, 205-252.
    • (1998) Curr. Med. Chem , vol.5 , pp. 205-252
    • Damayanthi, Y.1    Lown, J.W.2
  • 125
    • 0000786406 scopus 로고
    • Recent progress in the development of novel antitumour etoposide analogues
    • Zhang, Y. L., Lee, K. H. (1994) Recent progress in the development of novel antitumour etoposide analogues. Chin. Pharm. J., 46, 319-369.
    • (1994) Chin. Pharm. J , vol.46 , pp. 319-369
    • Zhang, Y.L.1    Lee, K.H.2
  • 126
    • 34248180181 scopus 로고    scopus 로고
    • Progress of antitumour drugs of podophyllotoxins
    • Ma, W. Y., Zhang, C. N. (1997) Progress of antitumour drugs of podophyllotoxins. Chin. J. Pharm., 28, 65-69.
    • (1997) Chin. J. Pharm , vol.28 , pp. 65-69
    • Ma, W.Y.1    Zhang, C.N.2
  • 127
    • 1442310071 scopus 로고    scopus 로고
    • Current Developments in the Discovery and Design of New Drug Candidates from Plant Natural Product Leads
    • Lee, K. H. (2004) Current Developments in the Discovery and Design of New Drug Candidates from Plant Natural Product Leads. J. Nat. Prod., 67, 273-283.
    • (2004) J. Nat. Prod , vol.67 , pp. 273-283
    • Lee, K.H.1
  • 128
    • 25844502482 scopus 로고    scopus 로고
    • Plant-based anticancer molecules: A chemical and biological profile of some important leads
    • Srivastava, V., Negi, A. S., Kumar, J.K., Gupta, M.M., Khanuja, S. P.S. (2005) Plant-based anticancer molecules: A chemical and biological profile of some important leads. Bioorg. Med. Chem., 13, 5892-5908.
    • (2005) Bioorg. Med. Chem , vol.13 , pp. 5892-5908
    • Srivastava, V.1    Negi, A.S.2    Kumar, J.K.3    Gupta, M.M.4    Khanuja, S.P.S.5
  • 129
    • 0017656951 scopus 로고
    • Nonenolizable podophyllotoxin derivatives
    • Walter, J., Gensler, C. D., Murthy, M. H. T. (1977) Nonenolizable podophyllotoxin derivatives. J. Med. Chem., 20, 635-644.
    • (1977) J. Med. Chem , vol.20 , pp. 635-644
    • Walter, J.1    Gensler, C.D.2    Murthy, M.H.T.3
  • 130
    • 0000597498 scopus 로고
    • Preparation of 2-substituted podophyllotoxin derivatives
    • Glinski, M.B., Freed, J. C., Durst T. (1987) Preparation of 2-substituted podophyllotoxin derivatives. J. Org. Chem., 52, 2749-2753.
    • (1987) J. Org. Chem , vol.52 , pp. 2749-2753
    • Glinski, M.B.1    Freed, J.C.2    Durst, T.3
  • 131
    • 0033583155 scopus 로고    scopus 로고
    • A high yield preparation of 2-fluoropodophyllotoxin
    • VanVliet, D.S., Lee, K. H. (1999) A high yield preparation of 2-fluoropodophyllotoxin. Tetrahedron Lett., 40, 2259-2262.
    • (1999) Tetrahedron Lett , vol.40 , pp. 2259-2262
    • VanVliet, D.S.1    Lee, K.H.2
  • 132
    • 0035953324 scopus 로고    scopus 로고
    • Antitumour Agents. 207. Design, Synthesis, and Biological Testing of 4β-Anilino-2-fluoro-4′-demethylpodophyllo-toxin Analogues as Cytotoxic and Antiviral Agents
    • VanVliet, D. S., Tachibana, Y., Bastow, K. F., Huang, E. S., Lee, K.-H. (2001) Antitumour Agents. 207. Design, Synthesis, and Biological Testing of 4β-Anilino-2-fluoro-4′-demethylpodophyllo-toxin Analogues as Cytotoxic and Antiviral Agents. J. Med Chem., 44, 1422-1428.
    • (2001) J. Med Chem , vol.44 , pp. 1422-1428
    • VanVliet, D.S.1    Tachibana, Y.2    Bastow, K.F.3    Huang, E.S.4    Lee, K.-H.5
  • 133
    • 33749004000 scopus 로고    scopus 로고
    • Synthesis of Sterically Fixed Podophyllotoxin
    • Laatsch, H., Ernst, B. P., Noltemeyer, M. (1996) Synthesis of Sterically Fixed Podophyllotoxin. Liebigs Ann., 731-737.
    • (1996) Liebigs Ann , pp. 731-737
    • Laatsch, H.1    Ernst, B.P.2    Noltemeyer, M.3
  • 134
    • 0027953563 scopus 로고
    • Antitumour agents. 144. New gamma.- lactone ring-modified arylamino, etoposide analogs as inhibitors of human DNA topoisomerase II
    • Zhou, X. M., Lee, K. J. H., Cheng, J., Wu, S. S., Chen, H. X., Guo, X., Cheng, Y. C., Lee, K. H. (1994) Antitumour agents. 144. New gamma.- lactone ring-modified arylamino, etoposide analogs as inhibitors of human DNA topoisomerase II. J. Med. Chem., 37, 287-292.
    • (1994) J. Med. Chem , vol.37 , pp. 287-292
    • Zhou, X.M.1    Lee, K.J.H.2    Cheng, J.3    Wu, S.S.4    Chen, H.X.5    Guo, X.6    Cheng, Y.C.7    Lee, K.H.8
  • 135
    • 0024345610 scopus 로고
    • Synthesis and antitumour activity of podophyllotoxin aza-analogues
    • Tomioka, K., Kubota, Y., Koga, K. (1989) Synthesis and antitumour activity of podophyllotoxin aza-analogues. Tetrahedron Lett., 30, 2953-2954.
    • (1989) Tetrahedron Lett , vol.30 , pp. 2953-2954
    • Tomioka, K.1    Kubota, Y.2    Koga, K.3
  • 138
    • 0027397585 scopus 로고
    • Design, synthesis, and antitumour activity-absolute configuration relationships of podophyllotoxin aza-analogues
    • Tomioka, K., Kubota, Y., Koga, K. (1993) Design, synthesis, and antitumour activity-absolute configuration relationships of podophyllotoxin aza-analogues. Tetrahedron, 49, 1891-1900.
    • (1993) Tetrahedron , vol.49 , pp. 1891-1900
    • Tomioka, K.1    Kubota, Y.2    Koga, K.3
  • 139
    • 0028033554 scopus 로고
    • Synthesis of 4-Oxa-2-azapodophyllotoxin, a novel analog of the antitumour lignan podophyllotoxin
    • Hitotsuyanagi, Y., Ichihara, Y., Takeya, K., Itokawa, H. (1994) Synthesis of 4-Oxa-2-azapodophyllotoxin, a novel analog of the antitumour lignan podophyllotoxin. Tetrahedron Lett., 35, 9401-9402.
    • (1994) Tetrahedron Lett , vol.35 , pp. 9401-9402
    • Hitotsuyanagi, Y.1    Ichihara, Y.2    Takeya, K.3    Itokawa, H.4
  • 140
    • 0029043214 scopus 로고
    • Syntheses and biological properties of novel aza-podophyllotoxin analogs prossessing pronounced antitumour activity
    • Hitotsuyanagi, Y., Yamagami, K., Fujii, A., Naka, Y., Ito, Y., Tahara, T. (1995) Syntheses and biological properties of novel aza-podophyllotoxin analogs prossessing pronounced antitumour activity. Bioorg. Med. Chem. Lett., 5, 1039-1042.
    • (1995) Bioorg. Med. Chem. Lett , vol.5 , pp. 1039-1042
    • Hitotsuyanagi, Y.1    Yamagami, K.2    Fujii, A.3    Naka, Y.4    Ito, Y.5    Tahara, T.6
  • 141
    • 0030690375 scopus 로고    scopus 로고
    • Targeting DNA topoisomerase II with podophyllotoxin aza-analogue
    • Iida, A., Kano, M., Kubota, Y., Koga, K., Tomioka, K. (1997) Targeting DNA topoisomerase II with podophyllotoxin aza-analogue. Bioorg. Med. Chem. Lett., 7, 2565-2566.
    • (1997) Bioorg. Med. Chem. Lett , vol.7 , pp. 2565-2566
    • Iida, A.1    Kano, M.2    Kubota, Y.3    Koga, K.4    Tomioka, K.5
  • 143
    • 1242317875 scopus 로고    scopus 로고
    • Synthesis of advanced intermediates for the preparation of aza-analogues of podophyllotoxin
    • Marcantoni, E., Petrini, M., Profeta, R. (2004) Synthesis of advanced intermediates for the preparation of aza-analogues of podophyllotoxin. Tetrahedron Lett., 45, 2133-2136.
    • (2004) Tetrahedron Lett , vol.45 , pp. 2133-2136
    • Marcantoni, E.1    Petrini, M.2    Profeta, R.3
  • 144
    • 0000355740 scopus 로고
    • Synthesis of etoposide Lactam via Mitsunobu reaction sequence
    • Kadow, J.F., Vyas, D.M., Doyle, D. M. (1989) Synthesis of etoposide Lactam via Mitsunobu reaction sequence. Tetrahedron Lett., 30, 3299-3302.
    • (1989) Tetrahedron Lett , vol.30 , pp. 3299-3302
    • Kadow, J.F.1    Vyas, D.M.2    Doyle, D.M.3
  • 145
    • 1342281637 scopus 로고    scopus 로고
    • Synthesis of podophyllotoxin analogues: δ-lactone-containing picropodophyllin, podophyllotoxin and 4′-demethyl-epipodophyllotoxin derivatives
    • Meresse, P., Monneret, C., Bertounesque, E. (2004) Synthesis of podophyllotoxin analogues: δ-lactone-containing picropodophyllin, podophyllotoxin and 4′-demethyl-epipodophyllotoxin derivatives. Tetrahedron, 60, 2657-267.
    • (2004) Tetrahedron , vol.60 , pp. 2657-2267
    • Meresse, P.1    Monneret, C.2    Bertounesque, E.3
  • 154
    • 0028866945 scopus 로고    scopus 로고
    • Gordaliza, M., Miguel del Corral, J. M, Castro, M. A., López-Vázquez, M, L., García, P. A., Feliciano, A. S., García-Grávalos M. D. (1995) Selective cytotoxic cyclolignans. Bioorg. Med. Chem. Lett., 5, 2465-2468.
    • Gordaliza, M., Miguel del Corral, J. M,, Castro, M. A., López-Vázquez, M, L., García, P. A., Feliciano, A. S., García-Grávalos M. D. (1995) Selective cytotoxic cyclolignans. Bioorg. Med. Chem. Lett., 5, 2465-2468.
  • 157
    • 1542345035 scopus 로고    scopus 로고
    • Anti-tumour agents. Part 232: Synthesis of cyclosulfite podophyllotoxin analogues as novel prototype antitumour agents
    • Xiao, Z. Y., Han, S. Q., Bastow, K. F., Lee, K. H. (2004) Anti-tumour agents. Part 232: Synthesis of cyclosulfite podophyllotoxin analogues as novel prototype antitumour agents. Bioorg. Med. Chem. Lett., 14, 1581-1584.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 1581-1584
    • Xiao, Z.Y.1    Han, S.Q.2    Bastow, K.F.3    Lee, K.H.4
  • 158
    • 34248227481 scopus 로고    scopus 로고
    • 3 α-Bromo-epipicropo-dophyllin and Its Derivatives: Novel Analogues of Podophyllotoxin with Antitumour Activities
    • He, Y., Ma, W. Y., Zhang, C. N. (2001) 3 α-Bromo-epipicropo-dophyllin and Its Derivatives: Novel Analogues of Podophyllotoxin with Antitumour Activities. J. Chin. Pharm. Sci., 10, 75-80.
    • (2001) J. Chin. Pharm. Sci , vol.10 , pp. 75-80
    • He, Y.1    Ma, W.Y.2    Zhang, C.N.3
  • 159
    • 0024237918 scopus 로고
    • Inhibitors of Topoiso-merase II: Structure-activity relationships and Mechanism of Action of podophyllin Congeners
    • Long, B. H., Stringfellow, D.A. (1988) Inhibitors of Topoiso-merase II: Structure-activity relationships and Mechanism of Action of podophyllin Congeners. Adv. Enz. Regul., 27, 223-256.
    • (1988) Adv. Enz. Regul , vol.27 , pp. 223-256
    • Long, B.H.1    Stringfellow, D.A.2
  • 161
    • 0021023662 scopus 로고
    • Free Radical Metabolism of VP-16 and inhibition of anthracycline-induced lipid peroxidation
    • Sinha, B. K., Trush, M. A. (1983) Free Radical Metabolism of VP-16 and inhibition of anthracycline-induced lipid peroxidation. Biochem. Pharmacol., 32, 3495-3498.
    • (1983) Biochem. Pharmacol , vol.32 , pp. 3495-3498
    • Sinha, B.K.1    Trush, M.A.2
  • 163
    • 0022536877 scopus 로고
    • Peroxidative free radical formation and O-demethylation of etoposide and teniposide
    • Haim, N., Roman, J., Nemec, J., Sinha, B. K. (1986) Peroxidative free radical formation and O-demethylation of etoposide and teniposide. Biochem. Biophys. Res. Comm., 135, 215-220.
    • (1986) Biochem. Biophys. Res. Comm , vol.135 , pp. 215-220
    • Haim, N.1    Roman, J.2    Nemec, J.3    Sinha, B.K.4
  • 164
    • 0024372292 scopus 로고
    • Characterization of free radicals produced during oxidation of etoposide and its catechol and quinone derivatives. An ESR study
    • Kalyanaraman, B., Nemec, J., Sinha, B. K. (1989) Characterization of free radicals produced during oxidation of etoposide and its catechol and quinone derivatives. An ESR study. Biochemistry, 28, 4839-4846.
    • (1989) Biochemistry , vol.28 , pp. 4839-4846
    • Kalyanaraman, B.1    Nemec, J.2    Sinha, B.K.3
  • 166
    • 37049089772 scopus 로고
    • Lignans and related Phenols. Part 18. The synthesis of Quinones fron Podophyllotoxin and its analogues
    • Ayres, D.C., Ritchie, T. J. (1988) Lignans and related Phenols. Part 18. The synthesis of Quinones fron Podophyllotoxin and its analogues. J. Chem. Soc. Perkin. Trans. I., 2573-2578.
    • (1988) J. Chem. Soc. Perkin. Trans , vol.1 , pp. 2573-2578
    • Ayres, D.C.1    Ritchie, T.J.2
  • 167
    • 34248165097 scopus 로고    scopus 로고
    • Vyas, D. M., Saulnier, M. G., Kadow, J. F. (1989) Novel 3′,4′-dinitrogen substituted epipodophyllotoxin glucoside derivatives, their preparation and use as antitumour agents. Eur. Pat. Appl. EP 0,297,594,1989.
    • Vyas, D. M., Saulnier, M. G., Kadow, J. F. (1989) Novel 3′,4′-dinitrogen substituted epipodophyllotoxin glucoside derivatives, their preparation and use as antitumour agents. Eur. Pat. Appl. EP 0,297,594,1989.
  • 168
    • 34248137574 scopus 로고
    • Preparation and Testing of epipodophyllotoxin glucosides as antitumour Agents
    • Vyas, D. M., Saulnier, M. G., Kadow, J. F. (1988) Preparation and Testing of epipodophyllotoxin glucosides as antitumour Agents. Eur.Pat.Appl.EP 291,957,1988.
    • (1988) Eur.Pat.Appl.EP , vol.291 , pp. 957-1988
    • Vyas, D.M.1    Saulnier, M.G.2    Kadow, J.F.3
  • 169
    • 0026667369 scopus 로고
    • Antitumour Agents 130. Novel 4β-Arylamino Derivatives of 3′,4′-Didemethoxy-3′,4′-dioxo-4- deoxypodophyllotoxin as Potent Inhibitors of Human DNA Topoisomerase II
    • Zhang, Y. L., Shen, Y. C., Wang, Z. Q., Chen, H. X., Guo, X., Cheng, Y. C., Lee, K. H. (1992) Antitumour Agents 130. Novel 4β-Arylamino Derivatives of 3′,4′-Didemethoxy-3′,4′-dioxo-4- deoxypodophyllotoxin as Potent Inhibitors of Human DNA Topoisomerase II. J. Nat. Prod., 55, 1100-1111.
    • (1992) J. Nat. Prod , vol.55 , pp. 1100-1111
    • Zhang, Y.L.1    Shen, Y.C.2    Wang, Z.Q.3    Chen, H.X.4    Guo, X.5    Cheng, Y.C.6    Lee, K.H.7
  • 170
    • 0027417854 scopus 로고
    • Antitumour Agents 126. Novel 4β-Substituted Anilino Derivatives of 3′,4′-O,O-Didemethyl-podophyl-lotoxin as Potent Inhibitors of Human DNA Topoisomerase II
    • Wang, Z. Q., Shen, Y. C., Chen, H. X., Chang, J.Y., Guo, X., Cheng, Y. C., Lee, K. H. (1993) Antitumour Agents 126. Novel 4β-Substituted Anilino Derivatives of 3′,4′-O,O-Didemethyl-podophyl-lotoxin as Potent Inhibitors of Human DNA Topoisomerase II. Pharm. Res., 10, 343-349.
    • (1993) Pharm. Res , vol.10 , pp. 343-349
    • Wang, Z.Q.1    Shen, Y.C.2    Chen, H.X.3    Chang, J.Y.4    Guo, X.5    Cheng, Y.C.6    Lee, K.H.7
  • 172
    • 0029904857 scopus 로고    scopus 로고
    • Chemoenzymatic and Ring E-Modular Approach to the (-)-Podophyllotoxin Skeleton. Synthesis of 3′,4′,5′-Tridemethoxy-(-)-podophyllotoxin
    • Berkowitz, D. B., Maeng, J.H., Dantzig, A. H., Shepard, R. L., Norman, B. H. (1996) Chemoenzymatic and Ring E-Modular Approach to the (-)-Podophyllotoxin Skeleton. Synthesis of 3′,4′,5′-Tridemethoxy-(-)-podophyllotoxin. J. Am. Chem. Soc., 118, 9426-9427.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 9426-9427
    • Berkowitz, D.B.1    Maeng, J.H.2    Dantzig, A.H.3    Shepard, R.L.4    Norman, B.H.5
  • 174
    • 37049124946 scopus 로고
    • Lignans and related Phenols. Part XIII. Halogenated Derivatives of podophyllotoxin
    • Ayres, D. C., Lim C. K. (1972) Lignans and related Phenols. Part XIII. Halogenated Derivatives of podophyllotoxin. J. Chem. Soc. Perkin. Trans. I, 1350-1355.
    • (1972) J. Chem. Soc. Perkin. Trans , vol.1 , pp. 1350-1355
    • Ayres, D.C.1    Lim, C.K.2
  • 175
    • 0020081874 scopus 로고
    • Modification of the Pendant Ring of Podophyllotoxin
    • Ayres, D. C., Lim, C. K. (1982) Modification of the Pendant Ring of Podophyllotoxin. Cancer Chemother. Pharmacol., 7, 99-101.
    • (1982) Cancer Chemother. Pharmacol , vol.7 , pp. 99-101
    • Ayres, D.C.1    Lim, C.K.2
  • 176
    • 0026549112 scopus 로고
    • Antitumour agents. 123. Synthesis and human DNA topoisomerase II inhibitory activity of 2′-chloro derivatives of etoposide and 4.beta.-(arylamino)4′-O-deme thylpodophyllotoxins
    • Hu, H., Liu, S.Y., Cheng, Y. C., Lee, K.H., Wang, Z. Q. (1992) Antitumour agents. 123. Synthesis and human DNA topoisomerase II inhibitory activity of 2′-chloro derivatives of etoposide and 4.beta.-(arylamino)4′-O-deme thylpodophyllotoxins. J. Med. Chem., 35, 866-871.
    • (1992) J. Med. Chem , vol.35 , pp. 866-871
    • Hu, H.1    Liu, S.Y.2    Cheng, Y.C.3    Lee, K.H.4    Wang, Z.Q.5
  • 177
    • 34248152043 scopus 로고
    • US Pat. 4916217
    • Saulnier, M. G. (1990) Preparation of Phosphorus containing etoposide derivatives as antitumour agents. US Pat. 4916217, 1990.
    • (1990)
    • Saulnier, M.G.1
  • 178
    • 34248179632 scopus 로고    scopus 로고
    • Saulnier, M. G, Vyas, M. D, Langley, D. R, 1989 preparation and testing of epipodophyllotoxin glucoside 4′-O-acyl derivatives as antitumour agents. Eur. Pat. Appl. EP 0,320,988,1989
    • Saulnier, M. G., Vyas, M. D., Langley, D. R. (1989) preparation and testing of epipodophyllotoxin glucoside 4′-O-acyl derivatives as antitumour agents. Eur. Pat. Appl. EP 0,320,988,1989.
  • 179
    • 0035912801 scopus 로고    scopus 로고
    • In vivo activity in a catalytic antibody-prodrug system: Antibody catalyzed etoposide prodrug activation for selective chemotherapy
    • Shabat, D., Lode, H. N., Pertl, U., Reisfeld, R. A., Rader, C., Lerner, R. A., Barbas, C. F. (2001) In vivo activity in a catalytic antibody-prodrug system: antibody catalyzed etoposide prodrug activation for selective chemotherapy. Proc. Nat. Acad. Sci. USA, 98, 7528-7533.
    • (2001) Proc. Nat. Acad. Sci. USA , vol.98 , pp. 7528-7533
    • Shabat, D.1    Lode, H.N.2    Pertl, U.3    Reisfeld, R.A.4    Rader, C.5    Lerner, R.A.6    Barbas, C.F.7
  • 180
    • 0036318521 scopus 로고    scopus 로고
    • Synthesis and characterization of a catalytic Antibody-HPMA copolymer-Conjugate as a tool for tumour selective prodrug activation
    • Satchi-Fainaro, R., Wrasidlo, W., Lode, H. N., Shabat, D. (2002) Synthesis and characterization of a catalytic Antibody-HPMA copolymer-Conjugate as a tool for tumour selective prodrug activation. Bioorg. Med. Chem., 10, 3023-3029.
    • (2002) Bioorg. Med. Chem , vol.10 , pp. 3023-3029
    • Satchi-Fainaro, R.1    Wrasidlo, W.2    Lode, H.N.3    Shabat, D.4
  • 182
    • 0037447943 scopus 로고    scopus 로고
    • Prodrug Mono therapy: Synthesis and biological evaluation of an etoposide glucuronide-prodrug
    • Schmidt, F., Monneret, C. (2003) Prodrug Mono therapy: synthesis and biological evaluation of an etoposide glucuronide-prodrug. Bioorg. Med. Chem., 11, 2277-2283.
    • (2003) Bioorg. Med. Chem , vol.11 , pp. 2277-2283
    • Schmidt, F.1    Monneret, C.2
  • 184
  • 185
    • 0037155531 scopus 로고    scopus 로고
    • Protease-Mediated Fragmentation of p-Amidobenzyl Ethers: A New Strategy for the Activation of Anticancer Prodrugs
    • Toki, B. E., Cerveny, C. G., Wahl, A. F., Senter, P. D. (2002) Protease-Mediated Fragmentation of p-Amidobenzyl Ethers: A New Strategy for the Activation of Anticancer Prodrugs. J. Org. Chem., 67, 1866-1872.
    • (2002) J. Org. Chem , vol.67 , pp. 1866-1872
    • Toki, B.E.1    Cerveny, C.G.2    Wahl, A.F.3    Senter, P.D.4
  • 187
    • 2542474272 scopus 로고    scopus 로고
    • Antitumour agents. Part 235: Novel 4′-ester etoposide analogues as potent DNA topoisomerase II inhibitors with improved therapeutic potential
    • Xiao, Z.Y., Vance, J. R., Bastow, K. F., Brossi, A., Wang, H. K., Lee, K. H. (2004) Antitumour agents. Part 235: Novel 4′-ester etoposide analogues as potent DNA topoisomerase II inhibitors with improved therapeutic potential. Bioorg. Med. Chem., 12, 3363-3369.
    • (2004) Bioorg. Med. Chem , vol.12 , pp. 3363-3369
    • Xiao, Z.Y.1    Vance, J.R.2    Bastow, K.F.3    Brossi, A.4    Wang, H.K.5    Lee, K.H.6
  • 188
    • 0036888356 scopus 로고    scopus 로고
    • Prodrugs of 4′-demethyl-4′-deoxypodophyllotoxin: Synthesis and evaluation of the antitumour activity
    • Kim, Y., You, Y. J., Nam, N. H., and Ahn, B. Z. (2002) Prodrugs of 4′-demethyl-4′-deoxypodophyllotoxin: synthesis and evaluation of the antitumour activity. Bioorg. Med. Chem. Lett., 12, 3435-3438.
    • (2002) Bioorg. Med. Chem. Lett , vol.12 , pp. 3435-3438
    • Kim, Y.1    You, Y.J.2    Nam, N.H.3    Ahn, B.Z.4
  • 189
    • 1342281649 scopus 로고    scopus 로고
    • Alkyl and carboxylalkyl esters of 4′-demethyl-4′-deoxypodophyl-lotoxin: Synthesis, cytotoxic, and antitumour activity
    • You, Y. J., Kim, Y., Nam, N. H., Bang, S. C., Ahn, B. Z. (2004) Alkyl and carboxylalkyl esters of 4′-demethyl-4′-deoxypodophyl-lotoxin: synthesis, cytotoxic, and antitumour activity. Eur. J. Med. Chem., 39, 189-193.
    • (2004) Eur. J. Med. Chem , vol.39 , pp. 189-193
    • You, Y.J.1    Kim, Y.2    Nam, N.H.3    Bang, S.C.4    Ahn, B.Z.5
  • 190
    • 0037811439 scopus 로고    scopus 로고
    • Antitumour activity of unsaturated fatty acid esters of 4′-demethyldeoxypodo-phyllotoxin
    • You, Y. J., Kim, Y., Nam, N. H., Ahn, B. Z. (2003) Antitumour activity of unsaturated fatty acid esters of 4′-demethyldeoxypodo-phyllotoxin. Bioorg. Med. Chem. Lett., 13, 2629-2632.
    • (2003) Bioorg. Med. Chem. Lett , vol.13 , pp. 2629-2632
    • You, Y.J.1    Kim, Y.2    Nam, N.H.3    Ahn, B.Z.4
  • 191
    • 0024155186 scopus 로고
    • Progress in spin-labeled antitumour drugs
    • Wang, Y. G., Tian, X., Chen, Y. Z. (1988) Progress in spin-labeled antitumour drugs. Acta Pharmaceut. Sin., 23, 792-798.
    • (1988) Acta Pharmaceut. Sin , vol.23 , pp. 792-798
    • Wang, Y.G.1    Tian, X.2    Chen, Y.Z.3
  • 192
    • 0023431467 scopus 로고
    • Spin-labeled antitumour derivative of podophyllotoxin
    • Chen, Y. Z., Zhang, C.J., Tian, X. (1987) Spin-labeled antitumour derivative of podophyllotoxin. Scientia Sin (series B)., 30, 1070-1079.
    • (1987) Scientia Sin (series B) , vol.30 , pp. 1070-1079
    • Chen, Y.Z.1    Zhang, C.J.2    Tian, X.3
  • 193
    • 34248200520 scopus 로고
    • Spin-labeled antitumour derivative of podophyllotoxin
    • Chen, Y. Z., Tian, X., Wang, Y. G. (1989) Spin-labeled antitumour derivative of podophyllotoxin. Life Sci., 45, 2569-2571.
    • (1989) Life Sci , vol.45 , pp. 2569-2571
    • Chen, Y.Z.1    Tian, X.2    Wang, Y.G.3
  • 194
    • 0027288674 scopus 로고
    • Antitumour activity of a new low immunosuppressive derivative of podophyllotoxin (GP-11) and its mechanisms
    • Wang, J. Z., Tian, X, Tsumura, H. (1993) Antitumour activity of a new low immunosuppressive derivative of podophyllotoxin (GP-11) and its mechanisms. Anti-Cancer Drug Des., 8, 193-202
    • (1993) Anti-Cancer Drug Des , vol.8 , pp. 193-202
    • Wang, J.Z.1    Tian, X.2    Tsumura, H.3
  • 195
    • 7144219663 scopus 로고
    • Anticancer Drugs (V)-Synthesis of etoposide Derivatives
    • Tian, X., Yan, Z.Q., Li, J. X., Chen, Y. Z. (1995)Anticancer Drugs (V)-Synthesis of etoposide Derivatives. Chem. Res. Chin. Univ., 11, 79-83.
    • (1995) Chem. Res. Chin. Univ , vol.11 , pp. 79-83
    • Tian, X.1    Yan, Z.Q.2    Li, J.X.3    Chen, Y.Z.4
  • 196
    • 0006880321 scopus 로고    scopus 로고
    • Anticancer Drugs (VI)-Synthesis and activity of Spin Labeled Derivatives of 4-Amino-4-deoxy-4′-demethylepipodophyllotoxin
    • Tian, X., Yang, M.G., Chen, Y. Z. (1996) Anticancer Drugs (VI)-Synthesis and activity of Spin Labeled Derivatives of 4-Amino-4-deoxy-4′-demethylepipodophyllotoxin. Chem. Res. Chin. Univ., 12, 304-308.
    • (1996) Chem. Res. Chin. Univ , vol.12 , pp. 304-308
    • Tian, X.1    Yang, M.G.2    Chen, Y.Z.3
  • 197
    • 0030968703 scopus 로고    scopus 로고
    • Sythesis of Novel Spin Labeled Analogues of podophyllotoxin glycoside
    • Lu, K. K., Wang, Y. G., Chen, Y. Z. (1997) Sythesis of Novel Spin Labeled Analogues of podophyllotoxin glycoside. Synthetic Commun., 27, 1963-1968.
    • (1997) Synthetic Commun , vol.27 , pp. 1963-1968
    • Lu, K.K.1    Wang, Y.G.2    Chen, Y.Z.3
  • 198
    • 0031575394 scopus 로고    scopus 로고
    • Synthesis and antitumour activity of Spin Labeled Derivatives of podophyllotoxin
    • Tian, X., Wang, Y. G., Yang, M. G., Chen, Y. Z. (1997) Synthesis and antitumour activity of Spin Labeled Derivatives of podophyllotoxin. Life Sci., 60, 511-517.
    • (1997) Life Sci , vol.60 , pp. 511-517
    • Tian, X.1    Wang, Y.G.2    Yang, M.G.3    Chen, Y.Z.4
  • 199
    • 0030841950 scopus 로고    scopus 로고
    • New Spin Labeled Analogues of podophyllotoxin as potential antitumour agents
    • Wang, Y. G., Pan, J. L., Shi, J. F., Chen, Y. Z. (1997) New Spin Labeled Analogues of podophyllotoxin as potential antitumour agents. Life Sci., 61, 537-542.
    • (1997) Life Sci , vol.61 , pp. 537-542
    • Wang, Y.G.1    Pan, J.L.2    Shi, J.F.3    Chen, Y.Z.4
  • 200
    • 0031497418 scopus 로고    scopus 로고
    • Synthesis of New Spin Labeled Derivatives of podophyllotoxin as potential anticancer agents
    • Pan, J. L., Wang, Y. G., Shi, J. F., Chen, Y. Z. (1997) Synthesis of New Spin Labeled Derivatives of podophyllotoxin as potential anticancer agents. Chin. Chem. Lett., 8, 207-208.
    • (1997) Chin. Chem. Lett , vol.8 , pp. 207-208
    • Pan, J.L.1    Wang, Y.G.2    Shi, J.F.3    Chen, Y.Z.4
  • 201
    • 0037023256 scopus 로고    scopus 로고
    • Antitumour and antioxidant activity of spin labeled derivatives of podophyllotoxin (GP-1) and congeners
    • Tian, X., Zhang, F. M., Li W. G. (2002) Antitumour and antioxidant activity of spin labeled derivatives of podophyllotoxin (GP-1) and congeners. Life Sci., 70, 2433-2443.
    • (2002) Life Sci , vol.70 , pp. 2433-2443
    • Tian, X.1    Zhang, F.M.2    Li, W.G.3
  • 202
    • 34248196083 scopus 로고    scopus 로고
    • Synthesis of Novel Spin Labeled podophyllotoxin derivatives
    • Liu, Y. Q., Tian, X. (2005) Synthesis of Novel Spin Labeled podophyllotoxin derivatives. Chin. J. Org. Chem (S)., 25, 17.
    • (2005) Chin. J. Org. Chem (S) , vol.25 , pp. 17
    • Liu, Y.Q.1    Tian, X.2
  • 203
    • 34248152763 scopus 로고    scopus 로고
    • Synthesis of Novel Spin Labeled podophyllotoxin derivatives
    • Liu, Y. Q., Tian, X.(2005) Synthesis of Novel Spin Labeled podophyllotoxin derivatives. Synthetic Commun., 27, 1963-1968.
    • (2005) Synthetic Commun , vol.27 , pp. 1963-1968
    • Liu, Y.Q.1    Tian, X.2
  • 204
    • 33644983091 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of new spin-labeled derivatives of podophyllotoxin
    • Jin, Y., Chen, S. W., Tian, X. (2006) Synthesis and biological evaluation of new spin-labeled derivatives of podophyllotoxin. Bioorg. Med. Chem., 14, 3062-3068.
    • (2006) Bioorg. Med. Chem , vol.14 , pp. 3062-3068
    • Jin, Y.1    Chen, S.W.2    Tian, X.3
  • 205
    • 0027269874 scopus 로고
    • Synthesis and biological activity of novel thymidine derivatives of podophyllotoxin and 4′-demethylepipodophyllotoxin
    • Derry, W. B., Pamidi, C. C., Gupta, R. S. (1993) Synthesis and biological activity of novel thymidine derivatives of podophyllotoxin and 4′-demethylepipodophyllotoxin. Anti-Cancer Drug Des., 8, 203-221.
    • (1993) Anti-Cancer Drug Des , vol.8 , pp. 203-221
    • Derry, W.B.1    Pamidi, C.C.2    Gupta, R.S.3
  • 206
    • 0031552141 scopus 로고    scopus 로고
    • Antitumour Agents 177. Design, Synthesis and Biological Evaluation of Novel Etoposide analogues bearing pyrrolecarboxyamidino group as DNA topoisomerase II inhibitors
    • Ji, Z., Wang, H. K., Bastow, K. F., Zhu, X. K., Cho, S. J., Cheng Y. C., Lee, K. H. (1997) Antitumour Agents 177. Design, Synthesis and Biological Evaluation of Novel Etoposide analogues bearing pyrrolecarboxyamidino group as DNA topoisomerase II inhibitors. Bioorg. Med. Chem. lett., 7, 607-612.
    • (1997) Bioorg. Med. Chem. lett , vol.7 , pp. 607-612
    • Ji, Z.1    Wang, H.K.2    Bastow, K.F.3    Zhu, X.K.4    Cho, S.J.5    Cheng, Y.C.6    Lee, K.H.7
  • 207
    • 4544283303 scopus 로고    scopus 로고
    • Synthesis and cytotoxic activity of novel derivatives of 4′-demethylepipodophyllotoxin
    • Chen, S. W., Tian, X., Tu, Y. Q. (2004) Synthesis and cytotoxic activity of novel derivatives of 4′-demethylepipodophyllotoxin. Bioorg. Med. Chem. Lett., 14, 5063-5066.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 5063-5066
    • Chen, S.W.1    Tian, X.2    Tu, Y.Q.3
  • 208
    • 33746047461 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of novel etoposide analogue as cytotoxic agents
    • Liu, Y. Q., Yang, H., Tian, X (2006) Design, synthesis and biological evaluation of novel etoposide analogue as cytotoxic agents. Chin. J. Chem., 24, 785-790.
    • (2006) Chin. J. Chem , vol.24 , pp. 785-790
    • Liu, Y.Q.1    Yang, H.2    Tian, X.3
  • 209
    • 4043052701 scopus 로고    scopus 로고
    • Synthesis and anticancer activity of novel derivatives of 4′-demethylepipodophyllotoxn
    • Zhang, F. M., Tian, X. (2002) Synthesis and anticancer activity of novel derivatives of 4′-demethylepipodophyllotoxn. Acta Chim. Sin., 60, 720-724.
    • (2002) Acta Chim. Sin , vol.60 , pp. 720-724
    • Zhang, F.M.1    Tian, X.2
  • 210
    • 0030747053 scopus 로고    scopus 로고
    • Antitumour Agents-CLXXIII. Synthesis and Evaluation of Camptothecin-4β-amino4′-O-demethyl epipodophyllotoxin conju-gates as Inhibitors of Manumalian DNA Topoisomerases and as Cytotoxic Agents
    • Bastow, K. F., Wang, H. K., Cheng, Y. C., Lee, K. H. (1997) Antitumour Agents-CLXXIII. Synthesis and Evaluation of Camptothecin-4β-amino4′-O-demethyl epipodophyllotoxin conju-gates as Inhibitors of Manumalian DNA Topoisomerases and as Cytotoxic Agents. Bioorg. Med. Chem., 5, 1481-1488.
    • (1997) Bioorg. Med. Chem , vol.5 , pp. 1481-1488
    • Bastow, K.F.1    Wang, H.K.2    Cheng, Y.C.3    Lee, K.H.4
  • 211
    • 0035813468 scopus 로고    scopus 로고
    • Antitumour Agents 210. Synthesis and Evaluation of Taxoid-Epipodophyllotoxin conjugates as novel Cytotoxic Agents
    • Shi, Q., Wang, H. K., Bastow, K.F., Tachibana, Y., Chen, K., Lee, F. K., Lee, K. H. (2001) Antitumour Agents 210. Synthesis and Evaluation of Taxoid-Epipodophyllotoxin conjugates as novel Cytotoxic Agents. Bioorg. Med. Chem., 9, 2999-3004.
    • (2001) Bioorg. Med. Chem , vol.9 , pp. 2999-3004
    • Shi, Q.1    Wang, H.K.2    Bastow, K.F.3    Tachibana, Y.4    Chen, K.5    Lee, F.K.6    Lee, K.H.7
  • 212
    • 0035759195 scopus 로고    scopus 로고
    • Linker length in podophyllotoxin-acridine conjugates determines potency in vivo and in vitro as well as specificity against MDR cell lines
    • Jensen, L.R., Hansen, H. F., Wessel, I., Nitiss, J. L., Schmidt, G., Jensen, P. B., Sehested, M., Jensen, L. H. (2001) Linker length in podophyllotoxin-acridine conjugates determines potency in vivo and in vitro as well as specificity against MDR cell lines. Anti-Cancer Drug Des., 16, 305-315.
    • (2001) Anti-Cancer Drug Des , vol.16 , pp. 305-315
    • Jensen, L.R.1    Hansen, H.F.2    Wessel, I.3    Nitiss, J.L.4    Schmidt, G.5    Jensen, P.B.6    Sehested, M.7    Jensen, L.H.8
  • 215
    • 0032878627 scopus 로고    scopus 로고
    • Drug delivery of anticancer agents: Water soluble 4-poly (ethylene glycol) derivatives of the lignan, podophyllotoxin
    • Greenwald, R. B., Conover, C. D., Pendri A., Choe, Y. H., Martinez, A., Wu, D., Guan, S.Y., Yao, Z. L., Shum, K. L. (1999) Drug delivery of anticancer agents: water soluble 4-poly (ethylene glycol) derivatives of the lignan, podophyllotoxin. J. Control Rel., 61, 281-294.
    • (1999) J. Control Rel , vol.61 , pp. 281-294
    • Greenwald, R.B.1    Conover, C.D.2    Pendri, A.3    Choe, Y.H.4    Martinez, A.5    Wu, D.6    Guan, S.Y.7    Yao, Z.L.8    Shum, K.L.9
  • 216
    • 0037161603 scopus 로고    scopus 로고
    • Antitumour Agents. 213. Modeling of Epipodophyllo-toxin Derivatives Using Variable Selection k Nearest Neighbor QSAR Method
    • Xiao, Z., Xiao, Y. D., Feng, J., Golbraikh, A., Tropsha, A., Lee, K. H. (2002) Antitumour Agents. 213. Modeling of Epipodophyllo-toxin Derivatives Using Variable Selection k Nearest Neighbor QSAR Method. J. Med. Chem., 45, 2294-2309.
    • (2002) J. Med. Chem , vol.45 , pp. 2294-2309
    • Xiao, Z.1    Xiao, Y.D.2    Feng, J.3    Golbraikh, A.4    Tropsha, A.5    Lee, K.H.6


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