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Volumn 69, Issue 7, 2006, Pages 1101-1104

A meroterpenoid NF-κB inhibitor and drimane sesquiterpenoids from asafetida

Author keywords

[No Author keywords available]

Indexed keywords

8 ACETOXY 5 HYDROXYUMBELLIPRENIN; ANTIINFLAMMATORY AGENT; ASAFETIDA EXTRACT; FETIDONE A; FETIDONE B; HERBACEOUS AGENT; I KAPPA B; MEROTERPENOID; PLANT EXTRACT; RESIN; SESQUITERPENE DERIVATIVE; SESQUITERPENOID; UNCLASSIFIED DRUG; DRIMANE; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; NONSTEROID ANTIINFLAMMATORY AGENT; SESQUITERPENE;

EID: 33747421726     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np0600954     Document Type: Article
Times cited : (50)

References (32)
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    • (a) Kubeczka, K.; Bohn, I. In Hagers Handbuch der Pharmazeutischen Praxis, Folgeband 2; Blaschek, W., Hänsel, R., Keller, K., Reichling, J., Rimpler, H., Schenider, G., Eds.; Springer: Berlin, 1998; pp 696-713.
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  • 2
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    • Borntraeger Verlag: Berlin
    • (b) Tschirch, A.; Stock, E. Die Harze; Borntraeger Verlag: Berlin, 1938; Vol. II, pp 159-183.
    • (1938) Die Harze , vol.2 , pp. 159-183
    • Tschirch, A.1    Stock, E.2
  • 5
    • 33747421227 scopus 로고
    • GB1025372, 1966
    • Interestingly, contraceptive properties have also been attributed to asafetida (Das, P. C. GB1025372, 1966; Chem. Abstr. 1966, 64, 103181).
    • (1966) Chem. Abstr. , vol.64 , pp. 103181
    • Das, P.C.1
  • 7
    • 33747417299 scopus 로고
    • Reprinted
    • Reprinted in Penguin Handbooks, 1980; pp 62-63.
    • (1980) Penguin Handbooks , pp. 62-63
  • 8
    • 33747399621 scopus 로고    scopus 로고
    • (b) For a selection of pharmaceutical preparations based on asafetida, see: British Pharmaceutical Codex 1911. Available on the Web at http://www.ibiblio.org/herbmed/eclectic/bpc1911/main.html.
    • British Pharmaceutical Codex 1911
  • 10
    • 33747448460 scopus 로고
    • This article is available on the Web
    • For a fascinating account on the origin and collection of asafetida, see: Aitchinson, I. E. T. Am. J. Pharm. 1887, 59, 1-7. This article is available on the Web at http://www.swsbm.com/AJP/AJP_1887_No_1.pdf.
    • (1887) Am. J. Pharm. , vol.59 , pp. 1-7
    • Aitchinson, I.E.T.1
  • 20
    • 33747398883 scopus 로고
    • Chem. Abstr. 1959, 53, 73189.
    • (1959) Chem. Abstr. , vol.53 , pp. 73189
  • 26
    • 33747431415 scopus 로고    scopus 로고
    • note
    • Fetidones were unreactive toward cysteamine under conditions where exomethylene-γ-lactones, a known class of electrophilic NF-κB inhibitors, undergo Michael addition (THF, room temperature, 3 days). It is possible that the angular methyl at C-10 and the allylic methyl at C-8 prevent the approach of bulky nucleophiles to the exomethylene.
  • 30
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    • Chem. Abstr. 1959, 53, 73189.
    • (1959) Chem. Abstr. , vol.53 , pp. 73189
  • 31
    • 0031025655 scopus 로고    scopus 로고
    • Euphorbia resinifera Berg. and Thapsia garganica L. are remarkable examples of plants whose medicinal potential was revived by the discovery of a unique mechanism of bioactivity for their constituents (for a discussion, see: Appendino, G.; Szallasi, A. Life Sci. 1997, 60, 681-696).
    • (1997) Life Sci. , vol.60 , pp. 681-696
    • Appendino, G.1    Szallasi, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.