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Volumn 62, Issue 10, 1999, Pages 1399-1404

Diterpenoids from Euphorbia pithyusa subsp. cupanii

Author keywords

[No Author keywords available]

Indexed keywords

DITERPENOID; LATHYRANE; PLANT EXTRACT; PREMYRSINANE; TIGLIANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0032720648     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np990209u     Document Type: Article
Times cited : (71)

References (23)
  • 1
    • 0344246300 scopus 로고    scopus 로고
    • note
    • Pliny's opening of the paragraph on pityusa in his Naturalis Historia has often been quoted: Cum honore et pityusa simile de causa dicetur, quamdam in tithymali genere numerant (Honorable mention will now be made of pityusa, which some include in the same class as tithymalus) (XXIV, XXXI).
  • 2
    • 0345540075 scopus 로고    scopus 로고
    • Batsford: London
    • Turner, R. Euphorbias; Batsford: London, 1995; pp 148-149.
    • Euphorbias , vol.1995 , pp. 148-149
    • Turner, R.1
  • 8
    • 85027475123 scopus 로고
    • This compound was isolated as early as 1890 but was originally considered a steroid and named "euphorbiasteroid" (Tahara, Y. Chem. Ber. 1890, 23, 3347-3351).
    • (1890) Chem. Ber. , vol.23 , pp. 3347-3351
    • Tahara, Y.1
  • 10
    • 0345540074 scopus 로고    scopus 로고
    • note
    • The use of monomeric triphenylphosphine gave a product which could not be satisfactorily separated from triphenylphosphine oxide by crystallization or chromatography.
  • 14
    • 0345108658 scopus 로고
    • Farina, V., Ed.; Elsevier: Amsterdam
    • ® and its Derivatives; Farina, V., Ed.; Elsevier: Amsterdam, 1995; pp 56-58) and rather different from the ones calculated from Woodward's rules. Ring strain and the presence of a vinyl group adjacent to the endocyclic double bond probably underlay this remarkable bathochromic shift. For these reasons, the differences between the UV spectra of 1c and 3b are difficult to rationalize.
    • (1995) ® and Its Derivatives , pp. 56-58
    • Appendino, G.1
  • 16
    • 0345108657 scopus 로고    scopus 로고
    • Blaschek, W., Hänsel, R., Keller, K., Reichling, J., Rimpler, H., Schneider, G., Eds.; Springer: Berlin, Folgeband 2
    • Hecker, E. in Hagers Handbuch der Pharmazeutischen Praxis; Blaschek, W., Hänsel, R., Keller, K., Reichling, J., Rimpler, H., Schneider, G., Eds.; Springer: Berlin, 1998; Folgeband 2, pp 644-649.
    • (1998) Hagers Handbuch der Pharmazeutischen Praxis , vol.2 , pp. 644-649
    • Hecker, E.1
  • 18
    • 0028979464 scopus 로고
    • This hydrogen bond is typical of all phorboid 13-esters, and was even detected in the X-ray analysis of phorbol 13-acetate bound to a fragment of PKC δ (Zhang, G.; Kazanietz, M. G.; Blumberg, P. M.; Hurley, J. H. Cell 1995, 81, 917-924).
    • (1995) Cell , vol.81 , pp. 917-924
    • Zhang, G.1    Kazanietz, M.G.2    Blumberg, P.M.3    Hurley, J.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.