메뉴 건너뛰기




Volumn 54, Issue 7, 2006, Pages 1010-1016

Chemistry of ecteinascidins. Part 2. Preparation of 6′-O-acyl derivatives of stable ecteinascidin and evaluation of cytotoxicity

Author keywords

Acyl derivative; Cytotoxicity; Ecteinascidia thurstoni; Ecteinascidin 770

Indexed keywords

ACETIC ACID DERIVATIVE; ANTINEOPLASTIC ALKALOID; BENZOIC ACID DERIVATIVE; BUFFER; CARBOXYLIC ACID DERIVATIVE; DIACETYLECTEINASCIDIN 743; DIACETYLECTEINASCIDIN 770; DIACETYLECTEINASCIDIN 786; ECTEINASCIDIN 770; ECTEINASCIDIN 770 6' O 1'' ISOQUINOLINECARBOXYLIC ACID; ECTEINASCIDIN 770 6' O 1'' NAPHTHOATE; ECTEINASCIDIN 770 6' O 2'' BROMOBENZOIC ACID; ECTEINASCIDIN 770 6' O 2'' METHOXYBENZOIC ACID; ECTEINASCIDIN 770 6' O 2'' NAPHTHOATE; ECTEINASCIDIN 770 6' O 2'' QUINOLINECARBOXYLIC ACID; ECTEINASCIDIN 770 6' O 3'' ISOQUINOLINECARBOXYLIC ACID; ECTEINASCIDIN 770 6' O 4'' METHOXYBENZOIC ACID; ECTEINASCIDIN 770 6' O 4'' QUINOLINECARBOXYLIC ACID; ECTEINASCIDIN 770 6' O ISONICOTINIC ACID; ECTEINASCIDIN 770 6' O NICOTINIC ACID; ECTEINASCIDIN 770 6'O 2'' NITROBENZOIC ACID; ECTEINASCIDIN 770 6'O 3'' BROMOBENZOIC ACID; ECTEINASCIDIN 770 6'O 3'' NITROBENZOIC ACID; ECTEINASCIDIN 770 6'O 4'' BROMOBENZOIC ACID; ECTEINASCIDIN 770 6'O 4'' NITROBENZOIC ACID; ECTEINASCIDIN 770 6'O BENZOIC ACID; ECTEINASCIDIN 786; ESTER DERIVATIVE; NICOTINIC ACID DERIVATIVE; POTASSIUM CYANIDE; UNCLASSIFIED DRUG;

EID: 33745699988     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.54.1010     Document Type: Article
Times cited : (17)

References (18)
  • 2
    • 33745694025 scopus 로고    scopus 로고
    • note
    • Ecteinascidin 743 (1a) has the international nonproprietary name of trabectedin, and is being developed under the trade name "Yondelis."
  • 8
    • 70449705199 scopus 로고    scopus 로고
    • ed. by Nicolaou K. C., Snyder S. A., Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
    • Corey E. J., "Classics in Total Synthesis II," ed. by Nicolaou K. C., Snyder S. A., Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2003, pp. 109-136.
    • (2003) Classics in Total Synthesis II , pp. 109-136
    • Corey, E.J.1
  • 13
    • 0033616691 scopus 로고    scopus 로고
    • Phthalascidin, one of the saframycin A analogs, is very similar to 1a with regard to in vitro cytotoxicity and mode of action in a variety of cell types. See: Martinez E. J., Owa T., Schreiber S. L., Corey E. J., Proc. Natl. Acad. Sci. U.S.A., 96, 3496-3501 (1999).
    • (1999) Proc. Natl. Acad. Sci. U.S.A. , vol.96 , pp. 3496-3501
    • Martinez, E.J.1    Owa, T.2    Schreiber, S.L.3    Corey, E.J.4
  • 14
    • 0036015848 scopus 로고    scopus 로고
    • Saframycin A analog, which has the most potent quinaldic acid derivative (QAD), was reported by Myers et al. in Plowright A. T., Schaus S. E., Myers A. G., Chemistry & Biology, 9, 607-618 (2002).
    • (2002) Chemistry & Biology , vol.9 , pp. 607-618
    • Plowright, A.T.1    Schaus, S.E.2    Myers, A.G.3
  • 15
  • 18
    • 33745679832 scopus 로고    scopus 로고
    • note
    • Dedicated to the late Professor Kenneth L. Rinehart (University of Illinois, Urbana) for his pioneering work in the field of ecteinascidin natural marine products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.