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Volumn 65, Issue 4, 2000, Pages 1059-1068

The oxetane ring in Taxol

Author keywords

[No Author keywords available]

Indexed keywords

PACLITAXEL;

EID: 0034712232     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9916075     Document Type: Article
Times cited : (96)

References (77)
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    • Taxol is a registered trademark of Bristol-Myers Squibb Co., Princeton, NJ
    • (b) Taxol is a registered trademark of Bristol-Myers Squibb Co., Princeton, NJ.
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    • (c) McGuire, W. P.; Ozols, R. F. Semin. Oncol. 1998, 25, 340-348; 25, 707.
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  • 24
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    • Submitted for publication
    • A novel T-shaped conformation of Taxol resides in the largely hydrophobic β-tubulin binding pocket: Snyder, J. P.; Nettles, J.; Cornett, B.; Downing, K.; Nogales, E. Submitted for publication.
    • Snyder, J.P.1    Nettles, J.2    Cornett, B.3    Downing, K.4    Nogales, E.5
  • 26
    • 0343737537 scopus 로고    scopus 로고
    • note
    • 14 Insofar as the present study is concerned, the two models differ significantly in the oxetane H-bond donor; Arg for the minireceptor, Thr for the protein-ligand complex. The former was chosen prior to knowledge of the 3-D character of the β-tubulin structure. The next generation anti-tubulin minireceptor will rectify this and other points of difference.
  • 37
    • 0001843250 scopus 로고
    • Taxane Anticancer Agents
    • Georg, G. I., Chen, T. T., Ojima, I., Vyas, D. M., Eds.; American Chemical Society: Washington, DC
    • Kingston, D. G. I. In Taxane Anticancer Agents; Georg, G. I., Chen, T. T., Ojima, I., Vyas, D. M., Eds.; ACS Symposium Series 583; American Chemical Society: Washington, DC, 1995; pp 207-208.
    • (1995) ACS Symposium Series 583 , vol.583 , pp. 207-208
    • Kingston, D.G.I.1
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    • Taxane Anticancer Agents
    • Georg, G. I., Chen, T. T., Ojima, I., Vyas, D. M., Eds.; American Chemical Society: Washington, DC
    • Chen, S.-H.; Farina, V. In Taxane Anticancer Agents; Georg, G. I., Chen, T. T., Ojima, I., Vyas, D. M., Eds.; ACS Symposium Series 583; American Chemical Society: Washington, DC, 1995; pp 257-259.
    • (1995) ACS Symposium Series 583 , vol.583 , pp. 257-259
    • Chen, S.-H.1    Farina, V.2
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    • Virtual Activity, Real Pharmacology
    • Verotta, L., Ed.
    • Bombardelli, E.; Riva, A. In Virtual Activity, Real Pharmacology; Verotta, L., Ed.; Research Signpost: Trivandrum 1997; pp 61-83.
    • (1997) Research Signpost: Trivandrum , pp. 61-83
    • Bombardelli, E.1    Riva, A.2
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    • 0342866909 scopus 로고    scopus 로고
    • note
    • The free energies of aqueous solvation for benzene and 2-methylpropane are -0.87 and 2.3 kcal/mol, respectively; cf. ref 22.
  • 51
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    • (Scripps Institute), private communication
    • Nicolaou, K. C. (Scripps Institute), private communication.
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    • private communication
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    • Klar, U.1
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    • Copenhagen, Denmark, June 8-12, Abstracts
    • (a) Preliminary studies on a common pharmacophore for Taxol, epothilone B, and diseodermolide were presented at the Alfred Benzon Symposium 42, Copenhagen, Denmark, June 8-12, 1997; Snyder, J. P. Abstracts.
    • (1997) Alfred Benzon Symposium , vol.42
    • Snyder, J.P.1
  • 68
    • 0343302004 scopus 로고    scopus 로고
    • note
    • The current version of the software is PrGen 2.0.
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    • MacroModel web site: http://www.schrodinger.com/macromodel.html
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    • Halgren, T. A. J. Comput. Chem. 1996, 17, 490-519; 520-552; 553-586; 616-641. Halgren, T. A.; Nachbar, R. B. Ibid. 1996, 17, 587- 615.
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  • 76
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    • Halgren, T. A. J. Comput. Chem. 1996, 17, 490-519; 520-552; 553-586; 616-641. Halgren, T. A.; Nachbar, R. B. Ibid. 1996, 17, 587-615.
    • (1996) J. Comput. Chem. , vol.17 , pp. 587-615
    • Halgren, T.A.1    Nachbar, R.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.