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Volumn 11, Issue 20, 2003, Pages 4431-4447

New highly active taxoids from 9β-dihydrobaccatin-9,10-acetals. Part 4

Author keywords

[No Author keywords available]

Indexed keywords

4 ACETOXY 2 BENZOYLOXY 5,20 EPOXY 1 HYDROXY 9,10 [2 (MORPHOLINO)ETHYLIDENEDIOXY]TAX 11 EN 13 YL 3 (TERT BUTOXYCARBONYLAMINO) 2 HYDROXY 3 (5 HYDROXY 2 PYRIDYL)PROPIONATE; ACETAL DERIVATIVE; PROPIONIC ACID DERIVATIVE; PYRIDINE; TAXANE DERIVATIVE; TOXOID; UNCLASSIFIED DRUG;

EID: 0041833673     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(03)00454-1     Document Type: Article
Times cited : (15)

References (16)
  • 4
    • 85127635914 scopus 로고
    • CRC: New York
    • For general reviews on taxoid chemistry, see: (a) Suffness, M., Ed., Taxol® Science and Applications; CRC: New York, 1995. (b) Georg, I. G., Chen, T. T., Ojima, I., Vyas, D. M., Eds., Taxane Anticancer Agents: Basic Science and Current Status; ACS Symposium Series No. 583; American Chemical Society: Washington, DC, 1995. (c) Farina, V., Ed., The Chemistry and Pharmacology of Taxol® and its Derivatives; Elsevier: New York, 1995.
    • (1995) Taxol® Science and Applications
    • Suffness, M.1
  • 5
    • 0003671040 scopus 로고
    • ACS Symposium Series No. 583; American Chemical Society: Washington, DC
    • For general reviews on taxoid chemistry, see: (a) Suffness, M., Ed., Taxol® Science and Applications; CRC: New York, 1995. (b) Georg, I. G., Chen, T. T., Ojima, I., Vyas, D. M., Eds., Taxane Anticancer Agents: Basic Science and Current Status; ACS Symposium Series No. 583; American Chemical Society: Washington, DC, 1995. (c) Farina, V., Ed., The Chemistry and Pharmacology of Taxol® and its Derivatives; Elsevier: New York, 1995.
    • (1995) Taxane Anticancer Agents: Basic Science and Current Status
    • Georg, I.G.1    Chen, T.T.2    Ojima, I.3    Vyas, D.M.4
  • 6
    • 0003897919 scopus 로고
    • Elsevier: New York
    • For general reviews on taxoid chemistry, see: (a) Suffness, M., Ed., Taxol® Science and Applications; CRC: New York, 1995. (b) Georg, I. G., Chen, T. T., Ojima, I., Vyas, D. M., Eds., Taxane Anticancer Agents: Basic Science and Current Status; ACS Symposium Series No. 583; American Chemical Society: Washington, DC, 1995. (c) Farina, V., Ed., The Chemistry and Pharmacology of Taxol® and its Derivatives; Elsevier: New York, 1995.
    • (1995) The Chemistry and Pharmacology of Taxol® and its Derivatives
    • Farina, V.1
  • 7
    • 77956791953 scopus 로고
    • (a) . For review, see: Suffness M. Annu. Rep. Med. Chem. 28:1993;305 (b) Guénard D., Guéritte-Voegelein F., Potier P. Acc. Chem. Res. 26:1993;160.
    • (1993) Annu. Rep. Med. Chem. , vol.28 , pp. 305
    • Suffness, M.1
  • 13
    • 85031072869 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess of 13a, 13b and 22f could not be determined by HPLC analysis with a Chiralcel OD column; however, from the consideration of good yields at the coupling reaction with 16, the enantiomeric excess of each compound was assumed to be high and/or a kinetic resolution might occur.
  • 15
    • 85031072559 scopus 로고    scopus 로고
    • note
    • PC-6/VCR29-9: PC-6 cell line, which is resistant to Vincristine®. PC-6/VP1-1: PC-6 cell line, which is resistant to VP-16 (Etoposide®).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.