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Volumn 64, Issue 47, 2008, Pages 10649-10663

Synthesis and evaluation of the bioactivity of simplified analogs of the seco-pseudopterosins; progress toward determining a pharmacophore

Author keywords

Adenosine receptors; Anti inflammatory activity; Marine natural products; Minimal pharmacophore; Phagocytosis; Pseudopterosins; Seco pseudopterosins; Structural analogs; Total synthesis

Indexed keywords

2 [5 (5 METHYLHEX 4 ENYL) 5,6,7,8 TETRAHYDRONAPHTHALEN 1 YLOXY]BETA DEXTRO XYLOPYRANOSIDE; 2 [5 (5 METHYLHEX 4 ENYL) 5,6,7,8 TETRAHYDRONAPHTHALEN 1 YLOXY]BETA LEVO ARABINOPYRANOSIDE; 2 [5 (5 METHYLHEX 4 ENYL) 5,6,7,8 TETRAHYDRONAPHTHALEN 2 HYDROXY 1 YLOXY]BETA DEXTRO XYLOPYRANOSIDE; 2 [5 (5 METHYLHEX 4 ENYL) 5,6,7,8 TETRAHYDRONAPTHALEN 2 HYDROXY 1 YLOXY]BETA LEVO ARABINOPYRANOSIDE; 2 METHYL 6 [5 (5 METHYLHEX 4 ENYL) 5,6,7,8 TETRAHYDRONAPHTHALEN 1 YLOXY]BETA LEVO FUCOPYRANOSIDE; 2 METHYL 6 [5 (5 METHYLHEX 4 ENYL) 5,6,7,8 TETRAHYDRONAPHTHALEN 2 HYDROXY 1 YLOXY]BETA LEVO FUCOPYRANOSIDE; ADENOSINE A2A RECEPTOR; AGLYCONE; AROMATIC COMPOUND; DITERPENE; NATURAL PRODUCT; OXYGEN; PSEUDOPTEROSIN DERIVATIVE; PYRANOSIDE; UNCLASSIFIED DRUG;

EID: 53149154805     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.09.025     Document Type: Article
Times cited : (22)

References (56)
  • 1
    • 53149122131 scopus 로고    scopus 로고
    • Taken in part from the thesis of: V.A. Tanis. Studies toward an SAR understanding of the anti-inflammatory/wound healing activity of simplified seco-pseudopterosins and titanium (III)-mediated formation of C-glycosides: A continuation of the little/Parrish study, M.S. Thesis; University of California: Santa Barbara, CA, September 2007.
    • Taken in part from the thesis of: V.A. Tanis. Studies toward an SAR understanding of the anti-inflammatory/wound healing activity of simplified seco-pseudopterosins and titanium (III)-mediated formation of C-glycosides: A continuation of the little/Parrish study, M.S. Thesis; University of California: Santa Barbara, CA, September 2007.
  • 3
    • 53149126933 scopus 로고    scopus 로고
    • Luedke, E. The identification and characterization of the pseudopterosins:anti-inflammatory agents isolated from the gorgonian coral Pseudopterogorgia elisabethae. Ph.D. Thesis; University of California: Santa Barbara, CA, 1990;
    • Luedke, E. The identification and characterization of the pseudopterosins:anti-inflammatory agents isolated from the gorgonian coral Pseudopterogorgia elisabethae. Ph.D. Thesis; University of California: Santa Barbara, CA, 1990;
  • 36
    • 0002931771 scopus 로고    scopus 로고
    • For use of LiSEt in pseudopterosins, see:
    • For use of LiSEt in pseudopterosins, see:. Majdalani A., and Schmalz H.-G. Synlett (1997) 1303-1305
    • (1997) Synlett , pp. 1303-1305
    • Majdalani, A.1    Schmalz, H.-G.2
  • 39
    • 53149127720 scopus 로고    scopus 로고
    • Carpino, P.A. Enantioselective syntheses of the pseudopterosins and (+)-brefeldin A. Ph.D. Thesis; Harvard University: Cambridge, MA, 1991, p 86.
    • Carpino, P.A. Enantioselective syntheses of the pseudopterosins and (+)-brefeldin A. Ph.D. Thesis; Harvard University: Cambridge, MA, 1991, p 86.
  • 48
    • 0004937424 scopus 로고
    • For an application of Eaton's Reagent to tetralone synthesis see:
    • For an application of Eaton's Reagent to tetralone synthesis see:. Inouye Y., Uchida Y., and Kakisawa H. Bull. Chem. Soc. Jpn. 50 (1977) 961-966
    • (1977) Bull. Chem. Soc. Jpn. , vol.50 , pp. 961-966
    • Inouye, Y.1    Uchida, Y.2    Kakisawa, H.3
  • 54
    • 53149121360 scopus 로고    scopus 로고
    • note
    • These studies were performed by Cerep, Inc., Seattle, Washington and Paris, France.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.