메뉴 건너뛰기




Volumn 6, Issue 14, 2006, Pages 1529-1543

Fluorinated natural products with clinical significance

Author keywords

Artemisinin; Campothecin; Epothilones; Fluorine; Natural products; Taxanes; Vinca alkaloids

Indexed keywords

7 ETHYL 10 HYDROXYCAMPTOTHECIN; ACETYLSALICYLIC ACID; ANTIMALARIAL AGENT; ANTINEOPLASTIC AGENT; ARTEETHER; ARTEMISIA ANNUA EXTRACT; ARTEMISININ; ARTEMISININ DERIVATIVE; CAMPTOTHECIN; CAMPTOTHECIN DERIVATIVE; CHLOROQUINE; CIPROFLOXACIN; DE 310; DIFLOMOTECAN; EPOTHILONE DERIVATIVE; ESSENTIAL OIL; EXATECAN; FLUDROCORTISONE; FLUORINE; FLUOROACETIC ACID; FLUOROCITRIC ACID; FLUOROPYRIMIDINE DERIVATIVE; FLUOROURACIL; FLUOXETINE; IRINOTECAN; NATURAL PRODUCT; NAVELBINE; PLATINUM; TAXANE DERIVATIVE; UNINDEXED DRUG; VINCA ALKALOID;

EID: 33746611885     PISSN: 15680266     EISSN: None     Source Type: Journal    
DOI: 10.2174/156802606777951109     Document Type: Review
Times cited : (33)

References (133)
  • 1
    • 0000362773 scopus 로고    scopus 로고
    • Fluorine-containing natural products
    • O'Hagan, D. Harper, D. B. Fluorine-containing natural products. J. Fluor. Chem. 1999, 100, 127-133.
    • (1999) J. Fluor. Chem. , vol.100 , pp. 127-133
    • O'Hagan, D.1    Harper, D.B.2
  • 2
    • 0028886897 scopus 로고
    • The composition of the continental crust
    • Wedepohl, K. H. The composition of the continental crust. Geochimica et Cosmochimica Acta. 1995, 59, 1217-1232.
    • (1995) Geochimica Et Cosmochimica Acta , vol.59 , pp. 1217-1232
    • Wedepohl, K.H.1
  • 6
    • 1842633759 scopus 로고    scopus 로고
    • The Importance of Fluorine in the Life Science Industry
    • Maienfisch, P.; Hall, R. G. The Importance of Fluorine in the Life Science Industry. Chimia 2004, 58, 93-99.
    • (2004) Chimia , vol.58 , pp. 93-99
    • Maienfisch, P.1    Hall, R.G.2
  • 8
    • 0001365893 scopus 로고
    • 9α-Fluoro Derivatives of Cortisone and Hydrocortisone
    • Fried, J.; Sabo, E. F. 9α-Fluoro Derivatives of Cortisone and Hydrocortisone. J. Am. Chem. Soc. 1954, 76, 1455-1456.
    • (1954) J. Am. Chem. Soc. , vol.76 , pp. 1455-1456
    • Fried, J.1    Sabo, E.F.2
  • 10
    • 4544278491 scopus 로고    scopus 로고
    • Organic Fluorine: Odd Man Out
    • Dunitz, J. D. Organic Fluorine: Odd Man Out. ChemBioChem 2004, 5, 614-621.
    • (2004) ChemBioChem , vol.5 , pp. 614-621
    • Dunitz, J.D.1
  • 11
    • 4544316921 scopus 로고    scopus 로고
    • The Polar Hydrophobicity of Fluorinated Compounds
    • Biffinger, J. C.; Kim, H. W.; DiMagno, S. G. The Polar Hydrophobicity of Fluorinated Compounds. ChemBioChem 2004, 5, 622-627.
    • (2004) ChemBioChem , vol.5 , pp. 622-627
    • Biffinger, J.C.1    Kim, H.W.2    DiMagno, S.G.3
  • 12
    • 0035960060 scopus 로고    scopus 로고
    • Quantitative Structure-Antitumor Activity Relationships of Camptothecin Analogues: Cluster Analysis and Genetic Algorithm-Based Studies
    • Fan, Y.; Shi, L. M.; Kohn, K. W.; Pommier, Y.; Weinstein, J. N. Quantitative Structure-Antitumor Activity Relationships of Camptothecin Analogues: Cluster Analysis and Genetic Algorithm-Based Studies. J. Med. Chem. 2001, 44, 3254-3263.
    • (2001) J. Med. Chem. , vol.44 , pp. 3254-3263
    • Fan, Y.1    Shi, L.M.2    Kohn, K.W.3    Pommier, Y.4    Weinstein, J.N.5
  • 13
    • 9744232909 scopus 로고    scopus 로고
    • Time-Related Differences in the Physical Property Profiles of Oral Drugs
    • Leeson, P. D.; Davis, A. M. Time-Related Differences in the Physical Property Profiles of Oral Drugs. J. Med. Chem. 2004, 47, 6338-6348.
    • (2004) J. Med. Chem. , vol.47 , pp. 6338-6348
    • Leeson, P.D.1    Davis, A.M.2
  • 15
    • 0002683907 scopus 로고    scopus 로고
    • Uses of Fluorine in Chemotherapy
    • in Eds Banks, R. E.; Smart B. E.; Tatlow J. C. Plenum Press, New York
    • Edwards, P. N. Uses of Fluorine in Chemotherapy. In Organo-fluorine Chemistry: Principles and Commercial Applications, Eds Banks, R. E.; Smart B. E.; Tatlow J. C. Plenum Press, New York, 1994, 501-542.
    • Organo-fluorine Chemistry: Principles and Commercial Applications , vol.1994 , pp. 501-542
    • Edwards, P.N.1
  • 17
    • 0035953321 scopus 로고    scopus 로고
    • Antitumor Benzothiazoles 14. Synthesis and in vitro biological properties of fluorinated 2-(4-aminophenyl)benzothiazoles
    • Hutchinson, I.; Chua, M. S.; Browne, H. L.; Trapani, V.; Bradshaw, T. D.; Westwell, A. D.; Stevens, M. F. G. Antitumor Benzothiazoles 14. Synthesis and in vitro biological properties of fluorinated 2-(4-aminophenyl)benzothiazoles. J. Med. Chem. 2001, 44, 1446-1455.
    • (2001) J. Med. Chem. , vol.44 , pp. 1446-1455
    • Hutchinson, I.1    Chua, M.S.2    Browne, H.L.3    Trapani, V.4    Bradshaw, T.D.5    Westwell, A.D.6    Stevens, M.F.G.7
  • 18
    • 0033246945 scopus 로고    scopus 로고
    • Hundredth Anniversary of Aspirin
    • Kuhnert, N. Hundredth Anniversary of Aspirin. Chemie in Unserer Zeit 1999, 33, 213-220.
    • (1999) Chemie in Unserer Zeit , vol.33 , pp. 213-220
    • Kuhnert, N.1
  • 19
    • 0038413902 scopus 로고    scopus 로고
    • Fluorinated natural products: The biosynthesis of fluoroacetate and 4-fluorothreonine in Streptomyces cattleya
    • Murphy, C. D.; Schaffrath, C.; O'Hagan, D. O. Fluorinated natural products: the biosynthesis of fluoroacetate and 4-fluorothreonine in Streptomyces cattleya. Chemosphere 2003, 52, 455-461.
    • (2003) Chemosphere , vol.52 , pp. 455-461
    • Murphy, C.D.1    Schaffrath, C.2    O'Hagan, D.O.3
  • 21
    • 1542267777 scopus 로고    scopus 로고
    • Fluorinated Aminoglycosides and their Mechanistic Implication for Aminoglycoside 3′-Phosphotransferases from Gram-Negative Bacteria
    • Kim, C.; Haddad, J.; Vakulenko, S. B.; Meroueh, S. O.; Wu, Y.; Yan, H.; Mobashery, S. Fluorinated Aminoglycosides and their Mechanistic Implication for Aminoglycoside 3′-Phosphotransferases from Gram-Negative Bacteria. Biochemistry 2004, 43, 2373-2383.
    • (2004) Biochemistry , vol.43 , pp. 2373-2383
    • Kim, C.1    Haddad, J.2    Vakulenko, S.B.3    Meroueh, S.O.4    Wu, Y.5    Yan, H.6    Mobashery, S.7
  • 22
    • 0032554903 scopus 로고    scopus 로고
    • Synthetic Studies of Huperazine A and its Fluorinated Analogues. 2. Synthesis and Acetylcholinesterase Inhibitory Activity of Novel Fluorinated Huperazine A Analogues
    • Kaneko, S.; Nakajima, N.; Shikano, M.; Katoh, T.; Terashima, S. Synthetic Studies of Huperazine A and its Fluorinated Analogues. 2. Synthesis and Acetylcholinesterase Inhibitory Activity of Novel Fluorinated Huperazine A Analogues. Tetrahedron 1998, 54, 5485-5506.
    • (1998) Tetrahedron , vol.54 , pp. 5485-5506
    • Kaneko, S.1    Nakajima, N.2    Shikano, M.3    Katoh, T.4    Terashima, S.5
  • 24
    • 0037459717 scopus 로고    scopus 로고
    • Synthesis of Two Fluoro Analogues of the Nicontinic Acetylcholine Receptor Agonist UB-165
    • Sutherland, A.; Gallagher, T.; Sharples, C. G. V.; Wonnacott, S. Synthesis of Two Fluoro Analogues of the Nicontinic Acetylcholine Receptor Agonist UB-165. J. Org. Chem. 2003, 68, 2475-2478.
    • (2003) J. Org. Chem. , vol.68 , pp. 2475-2478
    • Sutherland, A.1    Gallagher, T.2    Sharples, C.G.V.3    Wonnacott, S.4
  • 29
    • 23944437163 scopus 로고    scopus 로고
    • A novel fluorinated erythromycin antibiotic
    • Goss, R. J. M.; Hong, H. A novel fluorinated erythromycin antibiotic. Chem. Commun. 2005, 3983-3985.
    • (2005) Chem. Commun. , pp. 3983-3985
    • Goss, R.J.M.1    Hong, H.2
  • 30
    • 11844274689 scopus 로고    scopus 로고
    • Modern Synthetic Methods for Fluorine-Substituted Target Molecules
    • Shimizu, M.; Hiyama, T. Modern Synthetic Methods for Fluorine-Substituted Target Molecules. Angew. Chem. Int. Ed. 2005, 44, 214-231.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 214-231
    • Shimizu, M.1    Hiyama, T.2
  • 31
    • 11144341001 scopus 로고    scopus 로고
    • Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions
    • Ma, J.-A.; Cahard, D. Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions. Chem. Rev. 2004, 104, 6119-6146.
    • (2004) Chem. Rev. , vol.104 , pp. 6119-6146
    • Ma, J.-A.1    Cahard, D.2
  • 32
    • 7144248725 scopus 로고
    • Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminata
    • Wall, M. E.; Wani, M. C.; Cook, C. E.; Palmer, K. H.; McPhail, A. T.; Sim, G. A. Plant antitumor agents. I. The isolation and structure of camptothecin, a novel alkaloidal leukemia and tumor inhibitor from Camptotheca acuminata. J. Am. Chem. Soc. 1966, 88, 3888-3890.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 3888-3890
    • Wall, M.E.1    Wani, M.C.2    Cook, C.E.3    Palmer, K.H.4    McPhail, A.T.5    Sim, G.A.6
  • 33
    • 0022340594 scopus 로고
    • Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I
    • Hsiang, Y.-H.; Hertzberg, R.; Hecht, S.; Liu, L. F. Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I. J. Biol. Chem. 1985, 260, 14873-14878.
    • (1985) J. Biol. Chem. , vol.260 , pp. 14873-14878
    • Hsiang, Y.-H.1    Hertzberg, R.2    Hecht, S.3    Liu, L.F.4
  • 34
    • 0141927373 scopus 로고    scopus 로고
    • Towards new anticancer drugs: A decade of advances in synthesis of camptothecins and related alkaloids
    • Du, W. Towards new anticancer drugs: a decade of advances in synthesis of camptothecins and related alkaloids. Tetrahedron 2003, 59, 8649-8687.
    • (2003) Tetrahedron , vol.59 , pp. 8649-8687
    • Du, W.1
  • 36
    • 0036304427 scopus 로고    scopus 로고
    • Currrent Perspectives on the Clinical Experience, Pharmacology, and Continued Development of the Campthothecins
    • Garcia-Carbonero, R.; Supko, J. G. Currrent Perspectives on the Clinical Experience, Pharmacology, and Continued Development of the Campthothecins. Clin. Cancer Res. 2002, 8, 641-661.
    • (2002) Clin. Cancer Res. , vol.8 , pp. 641-661
    • Garcia-Carbonero, R.1    Supko, J.G.2
  • 37
    • 12644265333 scopus 로고    scopus 로고
    • Irinotecan (CPT-11) metabolites in human bile and urine
    • Lokiec, F.; Du Sorbier, B. M.; Sanderink, G.-J. Irinotecan (CPT-11) metabolites in human bile and urine. Clin. Cancer Res. 1996, 2, 1943-1949.
    • (1996) Clin. Cancer Res. , vol.2 , pp. 1943-1949
    • Lokiec, F.1    Du Sorbier, B.M.2    Sanderink, G.-J.3
  • 38
    • 0038193608 scopus 로고    scopus 로고
    • Identification of the metabolites of 9-nitro-20(S)-Camptothecin in Rats
    • Li, K.; Chen, X.; Zhong, D.; Li, Y. Identification of the metabolites of 9-nitro-20(S)-Camptothecin in Rats. Drug Metab. Dispos. 2003, 31, 792-797.
    • (2003) Drug Metab. Dispos. , vol.31 , pp. 792-797
    • Li, K.1    Chen, X.2    Zhong, D.3    Li, Y.4
  • 39
    • 0027184132 scopus 로고
    • Ethyl Substitution at the 7 position extends the half-life of 10-hydroxycamptothecin in the presence of Human Serum Albumin
    • Burke, T. G.; Mi, Z. Ethyl Substitution at the 7 position extends the half-life of 10-hydroxycamptothecin in the presence of Human Serum Albumin. J. Med. Chem. 1993, 36, 2580-2582.
    • (1993) J. Med. Chem. , vol.36 , pp. 2580-2582
    • Burke, T.G.1    Mi, Z.2
  • 41
    • 0344074659 scopus 로고    scopus 로고
    • 7-Silylcamptothecins (silatecans): A new family of camptothecin antitumor agents
    • Josien, H.; Bom. D.; Curran, D. P.; Zheng, Y.-H.; Chou, T.-C. 7-Silylcamptothecins (silatecans): A new family of camptothecin antitumor agents. Bioorg. Med. Chem. Lett. 1997, 7, 3189-3194.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 3189-3194
    • Josien, H.1    Bom, D.2    Curran, D.P.3    Zheng, Y.-H.4    Chou, T.-C.5
  • 42
    • 0030931517 scopus 로고    scopus 로고
    • BN 80245: An E-ring modified camptothecin with potent antiproliferative and topoisomerase I inhibitory activities
    • Lavergne, O.; Lesueur-Ginot, L.; Pla Rodas, F.; Bigg, D. C. H. BN 80245: An E-ring modified camptothecin with potent antiproliferative and topoisomerase I inhibitory activities. Bioorg. Med. Chem. Lett. 1997, 7, 2235-2238.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 2235-2238
    • Lavergne, O.1    Lesueur-Ginot, L.2    Pla Rodas, F.3    Bigg, D.C.H.4
  • 45
    • 0001593967 scopus 로고    scopus 로고
    • An E-ring modified camptothecin, BN 80915, shows unusual stability and high activity both in vitro and in vivo
    • Kasprzyk, P. G.; Carlson, M.; Lauer, J.; Demarquay, D.; Lessueur-Ginot, L. An E-ring modified camptothecin, BN 80915, shows unusual stability and high activity both in vitro and in vivo. Proc. Am. Assoc. Cancer Res. 1999, 40, 739.
    • (1999) Proc. Am. Assoc. Cancer Res. , vol.40 , pp. 739
    • Kasprzyk, P.G.1    Carlson, M.2    Lauer, J.3    Demarquay, D.4    Lessueur-Ginot, L.5
  • 50
    • 0030785681 scopus 로고    scopus 로고
    • DX-8951f, a water-soluble camptothecin analog, exhibits potent antitumor activity against a human lung cancer cell line and its SN-38-resistant variant
    • Joto, N.; Ishii, M.; Minami, M.; Kuga, H.; Mitsui, I.; Tohgo, A. DX-8951f, a water-soluble camptothecin analog, exhibits potent antitumor activity against a human lung cancer cell line and its SN-38-resistant variant. Int. J. Cancer 1997, 72, 680-686.
    • (1997) Int. J. Cancer , vol.72 , pp. 680-686
    • Joto, N.1    Ishii, M.2    Minami, M.3    Kuga, H.4    Mitsui, I.5    Tohgo, A.6
  • 51
    • 4644225194 scopus 로고    scopus 로고
    • A phase IIA study of the topoisomerase I inhibitor, exatecan mesylate (DX-8951f), administered at two different dose schedules in patients with platinum- and taxane-resistant/refractory ovarian cancer
    • Clamp, A.; Adams, M.; Atkinson, R.; Boven, E.; Calvert, A. H.; Cervantes, A.; Ganesan, T.; Lotz, J.; Vasey, P.; Cheverton, P.; Jayson, G. C. A phase IIA study of the topoisomerase I inhibitor, exatecan mesylate (DX-8951f), administered at two different dose schedules in patients with platinum- and taxane-resistant/refractory ovarian cancer. Gynecol. Oncol. 2004, 95, 114-119.
    • (2004) Gynecol. Oncol. , vol.95 , pp. 114-119
    • Clamp, A.1    Adams, M.2    Atkinson, R.3    Boven, E.4    Calvert, A.H.5    Cervantes, A.6    Ganesan, T.7    Lotz, J.8    Vasey, P.9    Cheverton, P.10    Jayson, G.C.11
  • 52
    • 23844507339 scopus 로고    scopus 로고
    • A phase II clinical and pharmacokinetic study of intravenous exatecan mesylate (DX-8951f) in patients with untreated metastatic gastric cancer
    • Ajani, J. A.; Takimoto, C.; Becerra, C. R.; Silva, A.; Baez, L.; Cohn, A.; Major, P.; Kamida, M.; Feit, K.; De Jager, R. A phase II clinical and pharmacokinetic study of intravenous exatecan mesylate (DX-8951f) in patients with untreated metastatic gastric cancer. Invest. New Drugs 2005, 23, 479-484.
    • (2005) Invest. New Drugs , vol.23 , pp. 479-484
    • Ajani, J.A.1    Takimoto, C.2    Becerra, C.R.3    Silva, A.4    Baez, L.5    Cohn, A.6    Major, P.7    Kamida, M.8    Feit, K.9    De Jager, R.10
  • 54
    • 9644302441 scopus 로고    scopus 로고
    • 20-Deoxy-20-fluorocamptothecin: Design and Synthesis of Camptothecin Isostere
    • Shibata, N.; Ishimaru, T.; Nakamura, M.; Toru, T. 20-Deoxy-20-fluorocamptothecin: Design and Synthesis of Camptothecin Isostere. Synlett 2004, 14, 2509-2512.
    • (2004) Synlett , vol.14 , pp. 2509-2512
    • Shibata, N.1    Ishimaru, T.2    Nakamura, M.3    Toru, T.4
  • 56
    • 0000468774 scopus 로고    scopus 로고
    • Electrophilic NF Fluorinating Agents
    • Lal, G. S.; Pez, G. P.; Syvret, R. G. Electrophilic NF Fluorinating Agents. Chem. Rev. 1996, 96, 1737-1755.
    • (1996) Chem. Rev. , vol.96 , pp. 1737-1755
    • Lal, G.S.1    Pez, G.P.2    Syvret, R.G.3
  • 57
    • 0036456479 scopus 로고    scopus 로고
    • Recent Advances in Nucleophilic Fluorination Reactions of Organic Compounds Using Deoxyfluor and DAST
    • Singh, R. P.; Shreeve, J. M. Recent Advances in Nucleophilic Fluorination Reactions of Organic Compounds Using Deoxyfluor and DAST. Synthesis 2002, 17, 2561-2578.
    • (2002) Synthesis , vol.17 , pp. 2561-2578
    • Singh, R.P.1    Shreeve, J.M.2
  • 58
    • 0018612308 scopus 로고
    • Antimalarial studies on qinghaosu
    • Qinghaosu Antimalarial Coordinating Research Group
    • Qinghaosu Antimalarial Coordinating Research Group. Antimalarial studies on qinghaosu. Chin. Med. J. 1979, 92, 811-816.
    • (1979) Chin. Med. J. , vol.92 , pp. 811-816
  • 59
    • 2542640961 scopus 로고    scopus 로고
    • A Medicinal Chemistry Perspective on Artemisinin and Related Endoperoxides
    • O'Neill, P. M.; Posner, G. H. A Medicinal Chemistry Perspective on Artemisinin and Related Endoperoxides. J. Med. Chem. 2004, 47, 2945-2964.
    • (2004) J. Med. Chem. , vol.47 , pp. 2945-2964
    • O'Neill, P.M.1    Posner, G.H.2
  • 61
    • 4344662233 scopus 로고    scopus 로고
    • A Worthy Adversary for Malaria
    • O'Neill, P. M. A Worthy Adversary for Malaria. Nature 2004, 430, 838-839.
    • (2004) Nature , vol.430 , pp. 838-839
    • O'Neill, P.M.1
  • 62
    • 2942654745 scopus 로고    scopus 로고
    • Knowledge of the Proposed Chemical Mechanism of Action and Cytochrome P450 Metabolism of Antimalarial Trioxanes like Artemisinin Allows Rational Design of new Antimalarial Peroxides
    • Posner, G. H.; O'Neill, P. M. Knowledge of the Proposed Chemical Mechanism of Action and Cytochrome P450 Metabolism of Antimalarial Trioxanes like Artemisinin Allows Rational Design of new Antimalarial Peroxides. Acc. Chem. Res. 2004, 37, 397-404.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 397-404
    • Posner, G.H.1    O'Neill, P.M.2
  • 67
    • 0037186497 scopus 로고    scopus 로고
    • Mechanism-Based Desgin of Parasite-Targeted Artemisinin Derivatives: Synthesis and Antimalarial Activity of new Diamine Containing Analogues
    • Hindley, S.; Ward, S. A.; Storr, R. C.; Searle, N. L.; Bray, P. G.; Park, B. K.; Davies, J.; O'Neill, P. M. Mechanism-Based Desgin of Parasite-Targeted Artemisinin Derivatives: Synthesis and Antimalarial Activity of new Diamine Containing Analogues. J. Med. Chem. 2002, 45, 1052-1063.
    • (2002) J. Med. Chem. , vol.45 , pp. 1052-1063
    • Hindley, S.1    Ward, S.A.2    Storr, R.C.3    Searle, N.L.4    Bray, P.G.5    Park, B.K.6    Davies, J.7    O'Neill, P.M.8
  • 68
    • 0032510451 scopus 로고    scopus 로고
    • Orally Active Antimalarial 3-Substituted Trioxanes: New Synthetic Methodology and Biology Evaluation
    • Posner, G. H.; Cumming, J. N.; Woo, S.-H.; Ploypradith, P.; Xie, S.; Shapiro, T. A. Orally Active Antimalarial 3-Substituted Trioxanes: New Synthetic Methodology and Biology Evaluation. J. Med. Chem. 1998, 41, 940-951.
    • (1998) J. Med. Chem. , vol.41 , pp. 940-951
    • Posner, G.H.1    Cumming, J.N.2    Woo, S.-H.3    Ploypradith, P.4    Xie, S.5    Shapiro, T.A.6
  • 69
    • 0035855920 scopus 로고    scopus 로고
    • Antimalarial Simplified 3-Aryltrioxanes: Synthesis and Preclinical Efficacy/Toxicity Testing in Rodents
    • Posner, G. H.; Jeon, H. B.; Parker, M. H.; Krasavin, M.; Paik, I.-H.; Shapiro, T. A. Antimalarial Simplified 3-Aryltrioxanes: Synthesis and Preclinical Efficacy/Toxicity Testing in Rodents. J. Med. Chem. 2001, 44, 3054-3058.
    • (2001) J. Med. Chem. , vol.44 , pp. 3054-3058
    • Posner, G.H.1    Jeon, H.B.2    Parker, M.H.3    Krasavin, M.4    Paik, I.-H.5    Shapiro, T.A.6
  • 70
    • 0028088750 scopus 로고
    • Antimalarial activity of the bicyclic peroxide Ro 42-1611 (arteflene) in experimental models
    • Jaquet, C.; Stohler, H. R.; Chollet, J.; Peters, W. Antimalarial activity of the bicyclic peroxide Ro 42-1611 (arteflene) in experimental models. Trop. Med. Parasitol. 1994, 45, 266-271.
    • (1994) Trop. Med. Parasitol. , vol.45 , pp. 266-271
    • Jaquet, C.1    Stohler, H.R.2    Chollet, J.3    Peters, W.4
  • 71
    • 0032947034 scopus 로고    scopus 로고
    • Metabolism of the Antimalarial Endoperoxide Ro 42-1611 (Arteflene) in the Rat: Evidence for Endoperoxide Bioactivation
    • Bishop, L. P. D.; Maggs, J. L.; O'Neill, P. M.; Park, B. K. Metabolism of the Antimalarial Endoperoxide Ro 42-1611 (Arteflene) in the Rat: Evidence for Endoperoxide Bioactivation. J. Pharmacol. Exp. Ther. 1999, 289, 511-520.
    • (1999) J. Pharmacol. Exp. Ther. , vol.289 , pp. 511-520
    • Bishop, L.P.D.1    Maggs, J.L.2    O'Neill, P.M.3    Park, B.K.4
  • 74
    • 84981860375 scopus 로고
    • Role of Chance Observations in Chemotherapy: Vinca Rosea
    • Noble, R. L.; Beer, C. T.; Cutts, J. H. Role of Chance Observations in Chemotherapy: Vinca Rosea. Ann. N. Y. Acad. Sci. 1958, 76, 882-894.
    • (1958) Ann. N. Y. Acad. Sci. , vol.76 , pp. 882-894
    • Noble, R.L.1    Beer, C.T.2    Cutts, J.H.3
  • 75
    • 0025641040 scopus 로고
    • The discovery of the Vinca alkaloids - Chemotherapeutic agents against cancer
    • Noble, R. L. The discovery of the Vinca alkaloids - chemotherapeutic agents against cancer. Biochem. Cell Biol. 1990, 68, 1344-1351.
    • (1990) Biochem. Cell Biol. , vol.68 , pp. 1344-1351
    • Noble, R.L.1
  • 76
    • 0002837763 scopus 로고
    • Antitumor Bisindole Alkaloids from Catharanthus roseus (L.)
    • Brossi, A.; Suffness, M.; Eds., Academic Press Inc.: San Diego
    • Antitumor Bisindole Alkaloids from Catharanthus roseus (L.). The Alkaloids. Brossi, A.; Suffness, M.; Eds., Academic Press Inc.: San Diego, 1990; Vol. 37.
    • (1990) The Alkaloids , vol.37
  • 77
    • 0002459475 scopus 로고    scopus 로고
    • Plant-derived anticancer agents currently in clinical use or in clinical trials
    • Wang, H.-K. Plant-derived anticancer agents currently in clinical use or in clinical trials. IDrugs 1998, 1, 92-102.
    • (1998) IDrugs , vol.1 , pp. 92-102
    • Wang, H.-K.1
  • 78
    • 0001101470 scopus 로고
    • Effects of vincristine on the fine structure of HeLa cells during mitosis
    • George, P.; Journey, L. J.; Goldstein, M. N. Effects of vincristine on the fine structure of HeLa cells during mitosis. J. Natn. Cancer Inst. 1965, 35, 355-361.
    • (1965) J. Natn. Cancer Inst. , vol.35 , pp. 355-361
    • George, P.1    Journey, L.J.2    Goldstein, M.N.3
  • 79
    • 0026327465 scopus 로고
    • Interactions of the Catharanthus (Vinca) Alkaloids with Tubulin and Microtubules
    • Himes, R. H. Interactions of the Catharanthus (Vinca) Alkaloids with Tubulin and Microtubules. Pharmacol. Ther. 1991, 51, 257-267.
    • (1991) Pharmacol. Ther. , vol.51 , pp. 257-267
    • Himes, R.H.1
  • 80
    • 20044379059 scopus 로고    scopus 로고
    • Review: Tubulin Function, Action of Antitubulin Drugs, and new Drug Development
    • Pellegrini, F.; Budman, D. R. Review: Tubulin Function, Action of Antitubulin Drugs, and new Drug Development. Cancer Invest. 2005, 23, 264-273.
    • (2005) Cancer Invest. , vol.23 , pp. 264-273
    • Pellegrini, F.1    Budman, D.R.2
  • 81
    • 0025824979 scopus 로고
    • Mechanism of inhibition of cell proliferation by Vinca alkaloids
    • Jordan, M. A.; Thrower, D.; Wilson, L. Mechanism of inhibition of cell proliferation by Vinca alkaloids. Cancer Res. 1991, 51, 2212-2222.
    • (1991) Cancer Res. , vol.51 , pp. 2212-2222
    • Jordan, M.A.1    Thrower, D.2    Wilson, L.3
  • 82
    • 0029115509 scopus 로고
    • Vinblastine suppresses dynamics of individual microtubules in living interphase cells
    • Dhamodharan, R.; Jordan, M. A.; Thrower, D.; Wilson, L.; Wadsworth, P. Vinblastine suppresses dynamics of individual microtubules in living interphase cells. Mol. Cell Biol. 1995, 6, 1215-1229.
    • (1995) Mol. Cell Biol. , vol.6 , pp. 1215-1229
    • Dhamodharan, R.1    Jordan, M.A.2    Thrower, D.3    Wilson, L.4    Wadsworth, P.5
  • 83
    • 0034741810 scopus 로고    scopus 로고
    • Modifications in the «upper» or Velbenamine Part of the Vinca Alkaloids have Major Implications for Tubulin Interacting Activities
    • Fahy, J. Modifications in the «upper» or Velbenamine Part of the Vinca Alkaloids have Major Implications for Tubulin Interacting Activities. Curr. Pharm. Design 2001, 7, 1181-1197.
    • (2001) Curr. Pharm. Design , vol.7 , pp. 1181-1197
    • Fahy, J.1
  • 85
    • 0017172977 scopus 로고
    • Application of a Modification of the Polonoviski reaction to the Synthesis of Vinblastine-Type Alkaloids
    • Langlois, N.; Guéritte, G.; Langlois, Y.; Potier, P. Application of a Modification of the Polonoviski reaction to the Synthesis of Vinblastine-Type Alkaloids. J. Am. Chem. Soc. 1976, 98, 7017-7024.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 7017-7024
    • Langlois, N.1    Guéritte, G.2    Langlois, Y.3    Potier, P.4
  • 89
    • 0032031453 scopus 로고    scopus 로고
    • Antimitotic and Tubulin-Interacting properties of Vinflunine, a Novel Fluorinated Vinca Alkaloid
    • Kruczynski, A.; Barret, J.-M.; Etiévant, C.; Colpaert, F.; Fahy, J.; Hill, B. T. Antimitotic and Tubulin-Interacting properties of Vinflunine, a Novel Fluorinated Vinca Alkaloid. Biochem. Pharmacol. 1998, 55, 635-648.
    • (1998) Biochem. Pharmacol. , vol.55 , pp. 635-648
    • Kruczynski, A.1    Barret, J.-M.2    Etiévant, C.3    Colpaert, F.4    Fahy, J.5    Hill, B.T.6
  • 90
    • 0034665163 scopus 로고    scopus 로고
    • Novel Actions of the Antitumor Drugs Vinflunine and Vinorelbine on Microtubules
    • Ngan, V. K.; Bellman, K.; Panda, D.; Hill, B. T.; Jordan, M. A.; Wilson, L. Novel Actions of the Antitumor Drugs Vinflunine and Vinorelbine on Microtubules. Cancer Res. 2000, 60, 5045-5051.
    • (2000) Cancer Res. , vol.60 , pp. 5045-5051
    • Ngan, V.K.1    Bellman, K.2    Panda, D.3    Hill, B.T.4    Jordan, M.A.5    Wilson, L.6
  • 91
    • 16644400129 scopus 로고    scopus 로고
    • Vinflunine
    • Shnyder, S. D. Vinflunine. IDrugs 2004, 7, 851-859.
    • (2004) IDrugs , vol.7 , pp. 851-859
    • Shnyder, S.D.1
  • 92
    • 0031820395 scopus 로고    scopus 로고
    • Vinfluinine (20′,20′-difluoro-3′,4′-dihydrovinorelbine), a novel Vinca alkaloid, which participates in P-glycoprotein (PgP)-mediated multidrug resistance in vivo and in vitro
    • Etievant, C.; Barret, J.-M.; Kruczynski, A.; Perrin, D.; Hill, B. T. Vinfluinine (20′,20′-difluoro-3′,4′-dihydrovinorelbine), a novel Vinca alkaloid, which participates in P-glycoprotein (PgP)-mediated multidrug resistance in vivo and in vitro. Invest. New Drugs 1998, 16, 3-17.
    • (1998) Invest. New Drugs , vol.16 , pp. 3-17
    • Etievant, C.1    Barret, J.-M.2    Kruczynski, A.3    Perrin, D.4    Hill, B.T.5
  • 93
    • 0035150786 scopus 로고    scopus 로고
    • Anti-vascular effects of vinflunine in the MAC 15A transplantable adenocarcinoma model
    • Holwell, S. E.; Hill, B. T.; Bibby, M. C. Anti-vascular effects of vinflunine in the MAC 15A transplantable adenocarcinoma model. Br. J. Cancer 2001, 84, 290-295.
    • (2001) Br. J. Cancer , vol.84 , pp. 290-295
    • Holwell, S.E.1    Hill, B.T.2    Bibby, M.C.3
  • 94
    • 0035926851 scopus 로고    scopus 로고
    • Taxol, a molecule for all seasons
    • Kingston, D. G. I. Taxol, a molecule for all seasons. Chem. Commun. 2001, 867-880.
    • (2001) Chem. Commun. , pp. 867-880
    • Kingston, D.G.I.1
  • 95
    • 0015211527 scopus 로고
    • Plant Antitumor Agents. VI. The Isolation and Structure of Taxol, a Novel Antileukemic and Antitumor Agent from Taxus brevifolia
    • Wani, M. C.; Taylor, H. L.; Wall, M. E.; Coggon, P.; McPhail, A. T. Plant Antitumor Agents. VI. The Isolation and Structure of Taxol, a Novel Antileukemic and Antitumor Agent from Taxus brevifolia. J. Am. Chem. Soc. 1971, 93, 2325-2327.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 2325-2327
    • Wani, M.C.1    Taylor, H.L.2    Wall, M.E.3    Coggon, P.4    McPhail, A.T.5
  • 96
    • 0018387446 scopus 로고
    • Promotion of microtubule assembly in vitro by taxol
    • Schiff, P. B.; Fant, J.; Horwitz, S. B. Promotion of microtubule assembly in vitro by taxol. Nature 1979, 277, 665-667.
    • (1979) Nature , vol.277 , pp. 665-667
    • Schiff, P.B.1    Fant, J.2    Horwitz, S.B.3
  • 98
    • 0034789998 scopus 로고    scopus 로고
    • Taxol: Biosynthesis, molecular genetics, and biotechnological applications
    • Jennewein, S.; Croteau, R. Taxol: biosynthesis, molecular genetics, and biotechnological applications. Appl. Microbiol. Biotechnol. 2001, 57, 13-19.
    • (2001) Appl. Microbiol. Biotechnol. , vol.57 , pp. 13-19
    • Jennewein, S.1    Croteau, R.2
  • 99
    • 12344310295 scopus 로고    scopus 로고
    • Recent Progress in Structure Activity Relationship and Mechanistic Studies of Taxol Analogues
    • Fang, W.-S.; Liang, X.-T. Recent Progress in Structure Activity Relationship and Mechanistic Studies of Taxol Analogues. Mini-Rev. Med. Chem. 2005, 5, 1-12.
    • (2005) Mini-Rev. Med. Chem. , vol.5 , pp. 1-12
    • Fang, W.-S.1    Liang, X.-T.2
  • 101
    • 1442285598 scopus 로고    scopus 로고
    • Personal Recollections on the Early Development of Taxol
    • Horwitz, S. B. Personal Recollections on the Early Development of Taxol. J. Nat. Prod. 2004, 67, 136-138.
    • (2004) J. Nat. Prod. , vol.67 , pp. 136-138
    • Horwitz, S.B.1
  • 102
    • 0033169231 scopus 로고    scopus 로고
    • I-S Cell Cycle Checkpoint Function Sensitizes Cells to Microtubule Inhibitor-induced Apoptosis
    • I-S Cell Cycle Checkpoint Function Sensitizes Cells to Microtubule Inhibitor-induced Apoptosis. Cancer Res. 1999, 59, 3831-3837.
    • (1999) Cancer Res. , vol.59 , pp. 3831-3837
    • Stewart, Z.A.1    Mays, D.2    Pietenpol, J.A.3
  • 105
    • 4544353451 scopus 로고    scopus 로고
    • Use of Fluorine in the Medicinal Chemistry and Chemical Biology of Bioactive Compounds - A case Study of Fluorinated Taxane Anticancer Agents
    • Ojima, I. Use of Fluorine in the Medicinal Chemistry and Chemical Biology of Bioactive Compounds - A case Study of Fluorinated Taxane Anticancer Agents. ChemBioChem 2004, 5, 628-635.
    • (2004) ChemBioChem , vol.5 , pp. 628-635
    • Ojima, I.1
  • 106
    • 0001892688 scopus 로고    scopus 로고
    • Enantiopure fluorine-containing taxoids: Potent anticancer agents and versatile probes for biomedical problems
    • Ojima, I.; Inoue, T.; Chakravarty, S. Enantiopure fluorine-containing taxoids: potent anticancer agents and versatile probes for biomedical problems. J. Fluor. Chem. 1999, 97, 3-10.
    • (1999) J. Fluor. Chem. , vol.97 , pp. 3-10
    • Ojima, I.1    Inoue, T.2    Chakravarty, S.3
  • 109
    • 0029655687 scopus 로고    scopus 로고
    • Syntheses of New Fluorine-Containing Taxoids by Means of β-Lactam Synthon Method
    • Ojima, I.; Kuduk, S. D.; Slater, J. C.; Gimi, R. H.; Sun, C. M. Syntheses of New Fluorine-Containing Taxoids by Means of β-Lactam Synthon Method. Tetrahedron 1996, 52, 209-224.
    • (1996) Tetrahedron , vol.52 , pp. 209-224
    • Ojima, I.1    Kuduk, S.D.2    Slater, J.C.3    Gimi, R.H.4    Sun, C.M.5
  • 110
    • 0345688612 scopus 로고    scopus 로고
    • Mechanisms of Taxol resistance related to microtubules
    • Orr, G. A.; Verdier-Pinard, P.; McDaid, H.; Horwitz, S. B. Mechanisms of Taxol resistance related to microtubules. Oncogene 2003, 22, 7280-7295.
    • (2003) Oncogene , vol.22 , pp. 7280-7295
    • Orr, G.A.1    Verdier-Pinard, P.2    McDaid, H.3    Horwitz, S.B.4
  • 112
    • 0029776766 scopus 로고    scopus 로고
    • Epothilone A and B - Novel 16-Membered Macrolides with Cytotoxic Activity: Isolation, Crystal Structure, and Conformation in Solution
    • Höfle, G.; Bedorf, N.; Steinmetz, H.; Schomburg, D.; Gerth, K.; Reichenbach, H. Epothilone A and B - Novel 16-Membered Macrolides with Cytotoxic Activity: Isolation, Crystal Structure, and Conformation in Solution. Angew. Chem. Int. Ed. Engl. 1996, 35, 1567-1569.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 1567-1569
    • Höfle, G.1    Bedorf, N.2    Steinmetz, H.3    Schomburg, D.4    Gerth, K.5    Reichenbach, H.6
  • 119
    • 0033550167 scopus 로고    scopus 로고
    • Complex Target-Oriented Synthesis in the Drug Discovery Process: A Case History in the dEpoB Series
    • Harris, C. R.; Danishefsky, S. J. Complex Target-Oriented Synthesis in the Drug Discovery Process: A Case History in the dEpoB Series. J. Org. Chem. 1999, 64, 8434-8456.
    • (1999) J. Org. Chem. , vol.64 , pp. 8434-8456
    • Harris, C.R.1    Danishefsky, S.J.2
  • 120
    • 3843053396 scopus 로고    scopus 로고
    • The Binding Mode of Epothilone A on α,β-Tubulin by Electron Crystallography
    • Nettles, J. H.; Li, H.; Cornett, B.; Krahn, J. M.; Snyder, J. P. The Binding Mode of Epothilone A on α,β-Tubulin by Electron Crystallography. Science 2004, 305, 866-869.
    • (2004) Science , vol.305 , pp. 866-869
    • Nettles, J.H.1    Li, H.2    Cornett, B.3    Krahn, J.M.4    Snyder, J.P.5
  • 121
    • 0035942226 scopus 로고    scopus 로고
    • The binding conformation of Taxol in β-tubulin: A model based on electron crystallographic density
    • Snyder, J. P.; Nettles, J. H.; Cornett, B.; Downing, K. H.; Nogales, E. The binding conformation of Taxol in β-tubulin: A model based on electron crystallographic density. Proc. Natl. Acad. Sci. U.S.A. 2001, 98, 5312-5316.
    • (2001) Proc. Natl. Acad. Sci. U.S.A. , vol.98 , pp. 5312-5316
    • Snyder, J.P.1    Nettles, J.H.2    Cornett, B.3    Downing, K.H.4    Nogales, E.5
  • 122
    • 14844338576 scopus 로고    scopus 로고
    • Much Anticipated - The Bioactive Conformation of Epothilone and its Binding to Tubulin
    • Heinz, D. W.; Schubert, W.-D.; Höfle, G. Much Anticipated - The Bioactive Conformation of Epothilone and its Binding to Tubulin. Angew. Chem. Int. Ed. Engl. 2005, 44, 1298-1301.
    • (2005) Angew. Chem. Int. Ed. Engl. , vol.44 , pp. 1298-1301
    • Heinz, D.W.1    Schubert, W.-D.2    Höfle, G.3
  • 123
    • 0031027531 scopus 로고    scopus 로고
    • Activities of the Microtubule-stabilizing Agents Epothilones A and B with Purified Tubulin and in Cells Resistant to Paclitaxel (Taxol)
    • Kowalski, R. J.; Giannakakou, P.; Hamel, E. Activities of the Microtubule-stabilizing Agents Epothilones A and B with Purified Tubulin and in Cells Resistant to Paclitaxel (Taxol). J. Biol. Chem. 1997, 272, 2534-2541.
    • (1997) J. Biol. Chem. , vol.272 , pp. 2534-2541
    • Kowalski, R.J.1    Giannakakou, P.2    Hamel, E.3
  • 124
    • 0032483019 scopus 로고    scopus 로고
    • Desoxyepothilone B: An efficacious microtubule-targeted antitumor agent with a promising in vivo profile relative to epothilone B
    • Chou, T.-C.; Zhang, X.-G.; Balog, A.; Su, D.-S.; Meng, D.; Savin, K.; Bertino, J. R.; Danishefsky, S. J. Desoxyepothilone B: An efficacious microtubule-targeted antitumor agent with a promising in vivo profile relative to epothilone B. Proc. Natl. Acad. Sci. U.S.A. 1998, 95, 9642-9647.
    • (1998) Proc. Natl. Acad. Sci. U.S.A. , vol.95 , pp. 9642-9647
    • Chou, T.-C.1    Zhang, X.-G.2    Balog, A.3    Su, D.-S.4    Meng, D.5    Savin, K.6    Bertino, J.R.7    Danishefsky, S.J.8
  • 125
    • 3042701597 scopus 로고    scopus 로고
    • Epothilones: Mechanism of Action and Biologic Activity
    • Goodin, S.; Kane, M. P.; Rubin, E. H. Epothilones: Mechanism of Action and Biologic Activity. J. Clin. Oncol. 2004, 22, 2015-2025.
    • (2004) J. Clin. Oncol. , vol.22 , pp. 2015-2025
    • Goodin, S.1    Kane, M.P.2    Rubin, E.H.3
  • 127
    • 0032543528 scopus 로고    scopus 로고
    • Total Synthesis of 26-Hydroxy-Epothilone B and Related Analogs via a Macrolactonization Based Strategy
    • Nicolaou, K. C.; Finlay, M. R. V.; Ninkovic, S.; Sarabia, F. Total Synthesis of 26-Hydroxy-Epothilone B and Related Analogs via a Macrolactonization Based Strategy. Tetrahedron 1998, 54, 7127-7166.
    • (1998) Tetrahedron , vol.54 , pp. 7127-7166
    • Nicolaou, K.C.1    Finlay, M.R.V.2    Ninkovic, S.3    Sarabia, F.4
  • 128
    • 1642272050 scopus 로고    scopus 로고
    • Total Synthesis of 26-Fluoro-epothilone B
    • Koch, G.; Loiseleur, O.; Altmann, K.-H. Total Synthesis of 26-Fluoro-epothilone B. Synlett 2004, 693-697.
    • (2004) Synlett , pp. 693-697
    • Koch, G.1    Loiseleur, O.2    Altmann, K.-H.3
  • 130
    • 0037433593 scopus 로고    scopus 로고
    • Complex Target-Oriented Total Synthesis in the Drug Discovery Process: The Discovery of a Highly Promising Family of Second Generation Epothilones
    • Rivkin, A.; Yoshimura, F.; Gabarda, A. E.; Chou, T.-C.; Doug, H.; Tong, W. P.; Danishefsky, S. J. Complex Target-Oriented Total Synthesis in the Drug Discovery Process: The Discovery of a Highly Promising Family of Second Generation Epothilones. J. Am. Chem. Soc. 2003, 125, 2899-2901.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2899-2901
    • Rivkin, A.1    Yoshimura, F.2    Gabarda, A.E.3    Chou, T.-C.4    Doug, H.5    Tong, W.P.6    Danishefsky, S.J.7
  • 131
    • 1542541269 scopus 로고    scopus 로고
    • Design and Total Synthesis of a Superior Family of Epothilone Analogues, which Eliminate Xenograft Tumors to a Nonrelapsable State
    • Chao, T.-C.; Dong, H.; Rivkin, A.; Yoshimura, F.; Gabarda, A. E.; Cho, Y. S.; Tong, W. P.; Danishefsky, S. J. Design and Total Synthesis of a Superior Family of Epothilone Analogues, which Eliminate Xenograft Tumors to a Nonrelapsable State. Angew. Chem. Int. Ed. Engl. 2003, 42, 4762-4767.
    • (2003) Angew. Chem. Int. Ed. Engl. , vol.42 , pp. 4762-4767
    • Chao, T.-C.1    Dong, H.2    Rivkin, A.3    Yoshimura, F.4    Gabarda, A.E.5    Cho, Y.S.6    Tong, W.P.7    Danishefsky, S.J.8
  • 132
    • 4444339511 scopus 로고    scopus 로고
    • Discovery of (E)-9,10-Dehydroepothilones through Chemical Synthesis: On the Emergence of 26-Trifluoro-(E)-9,10-dehydro-12,13-desoxyepothilone B as a Promising Anticancer Drug Candidate
    • Rivkin, A.; Yoshimura, F.; Gabarda, A. E.; Cho, Y. S.; Chou, T.-C.; Dong, H.; Danishefsky, S. J. Discovery of (E)-9,10-Dehydroepothilones through Chemical Synthesis: On the Emergence of 26-Trifluoro-(E)-9,10-dehydro-12,13-desoxyepothilone B as a Promising Anticancer Drug Candidate. J. Am. Chem. Soc. 2004, 126, 10913-10922.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 10913-10922
    • Rivkin, A.1    Yoshimura, F.2    Gabarda, A.E.3    Cho, Y.S.4    Chou, T.-C.5    Dong, H.6    Danishefsky, S.J.7
  • 133
    • 27144456478 scopus 로고    scopus 로고
    • Therapeutic Cure against Human Tumor Xenografts in Nude Mice by a Microtubule Stabilization Agent, Fludelone, via Parenteral or Oral Route
    • Chou, T.-C.; Dong, H.; Zhang, X.; Tong, W. P. Danishefsky, S. J. Therapeutic Cure against Human Tumor Xenografts in Nude Mice by a Microtubule Stabilization Agent, Fludelone, via Parenteral or Oral Route. Cancer Res. 2005, 65, 9445-9454.
    • (2005) Cancer Res. , vol.65 , pp. 9445-9454
    • Chou, T.-C.1    Dong, H.2    Zhang, X.3    Tong, W.P.4    Danishefsky, S.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.