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Volumn 39, Issue 49, 1998, Pages 8925-8928

Studies related to the absolute configuration of cyclocinamide A: Total synthesis of 4(R),11(R)-cyclocinamide A

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOCINAMIDE A; HEXAPEPTIDE; UNCLASSIFIED DRUG;

EID: 0032481015     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02016-4     Document Type: Article
Times cited : (16)

References (18)
  • 2
    • 85038549439 scopus 로고    scopus 로고
    • 12 This in vitro assay defines solid tumor selective compounds by quantitating differential cytotoxic activity between murine and human solid tumor cells and either murine leukemia or normal cells. Purified 1 was tested against a murine leukemia (L1210) and a murine solid tumor (colon 38). Cyclocinamide A exhibited outstanding solid tumor selecivity against colon 38
    • 12 This in vitro assay defines solid tumor selective compounds by quantitating differential cytotoxic activity between murine and human solid tumor cells and either murine leukemia or normal cells. Purified 1 was tested against a murine leukemia (L1210) and a murine solid tumor (colon 38). Cyclocinamide A exhibited outstanding solid tumor selecivity against colon 38.
  • 5
    • 0000964108 scopus 로고
    • 4. Bednarek, M. A.; Bodansky, M. Int. J. Pept. Protein Res. 1983, 21, 196. Kessler, H.; Siegmeier, R. Tetrahedron Lett. 1983, 24, 281.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 281
    • Kessler, H.1    Siegmeier, R.2
  • 7
    • 85038553583 scopus 로고    scopus 로고
    • Available from Sigma Chemical Company
    • 6. Available from Sigma Chemical Company.
  • 9
    • 0000065810 scopus 로고
    • 8. Paquet, A. Can. J. Chem. 1982, 60, 976. For a review of the use of Fmoc protection in peptide synthesis, see: Atherton, E.; Sheppard, R. C., "The Fluorenylmethoxycarbonyl Amino Protecting Group," in The Peptides., Udenfriend, S.; Meienhofer, J., Eds., Academic Press, Orlando, FL, 1987, Vol. 9, pp. 1-38.
    • (1982) Can. J. Chem. , vol.60 , pp. 976
    • Paquet, A.1
  • 10
    • 0002186442 scopus 로고
    • The fluorenylmethoxycarbonyl amino protecting group
    • Udenfriend, S.; Meienhofer, J., Eds., Academic Press, Orlando, FL
    • 8. Paquet, A. Can. J. Chem. 1982, 60, 976. For a review of the use of Fmoc protection in peptide synthesis, see: Atherton, E.; Sheppard, R. C., "The Fluorenylmethoxycarbonyl Amino Protecting Group," in The Peptides., Udenfriend, S.; Meienhofer, J., Eds., Academic Press, Orlando, FL, 1987, Vol. 9, pp. 1-38.
    • (1987) The Peptides , vol.9 , pp. 1-38
    • Atherton, E.1    Sheppard, R.C.2
  • 13
    • 0025990560 scopus 로고
    • 10. Chen, S.; Xu, J. Tetrahedron Lett. 1991, 32, 6711. Dudash, J.; Jiang, J.; Mayer, S. C.; Joullié, M. M. Syn. Commun. 1993, 23, 349.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 6711
    • Chen, S.1    Xu, J.2
  • 15
  • 18
    • 0029944497 scopus 로고    scopus 로고
    • 12. Valeriote, F.; Corbett, T.; LoRusso, P.; Moore, R. E.; Scheuer, P.J.; Patterson, G.; Paul, V.; Grindey, G.; Bonjouklian, R.; Pearce, H.; Suffness, M. I. J. Pharmacognosy 1995, 33, Suppl. 59. Valeriote, F.; Corbett, T.; Edelstein, M.; Baker, L. Cancer Invest. 1996, 14, 124.
    • (1996) Cancer Invest. , vol.14 , pp. 124
    • Valeriote, F.1    Corbett, T.2    Edelstein, M.3    Baker, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.