메뉴 건너뛰기




Volumn 34, Issue 3, 1999, Pages 307-311

Synthetic routes to lipidic diamines and amino alcohols: A class of potential antiinflammatory agents

Author keywords

[No Author keywords available]

Indexed keywords

1,2 HEXADECANEDIAMINE; 1,3 HEPTADECANEDIAMINE; 2 AMINOHEXADECANOL; DIAMINE; UNCLASSIFIED DRUG;

EID: 0032923791     PISSN: 00244201     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11745-999-0368-6     Document Type: Article
Times cited : (15)

References (10)
  • 1
    • 0025856636 scopus 로고
    • Nonsteroidal anti-inflammatory drugs. Differences and similarities
    • Brooks, P.M., and Day, R.O. (1991) Nonsteroidal Anti-inflammatory Drugs. Differences and Similarities, N. Engl. J. Med. 324, 1716-1725.
    • (1991) N. Engl. J. Med. , vol.324 , pp. 1716-1725
    • Brooks, P.M.1    Day, R.O.2
  • 2
    • 0026443983 scopus 로고
    • NSAIDS, ulcers and prostaglandins
    • Kimmey, M.B. (1992) NSAIDS, Ulcers and Prostaglandins, J. Rheumatol. 19 (Suppl. 36), 68-73.
    • (1992) J. Rheumatol. , vol.19 , Issue.SUPPL. 36 , pp. 68-73
    • Kimmey, M.B.1
  • 4
    • 0029865173 scopus 로고    scopus 로고
    • General approach to the enantiomeric synthesis of lipidic α-amino acids, peptides and vicinal amino alcohols
    • Kokotos, G., Padron, J.M., Noula, C, Gibbons, W.A., and Martin, V.A. (1996) General Approach to the Enantiomeric Synthesis of Lipidic α-Amino Acids, Peptides and Vicinal Amino Alcohols, Tetrahedron: Asymmetry 7, 857-866.
    • (1996) Tetrahedron: Asymmetry , vol.7 , pp. 857-866
    • Kokotos, G.1    Padron, J.M.2    Noula, C.3    Gibbons, W.A.4    Martin, V.A.5
  • 5
    • 0001340433 scopus 로고    scopus 로고
    • A general approach to the asymmetric synthesis of unsaturated lipidic α-amino acids. The first synthesis of α-aminoarachidonic acid
    • Kokotos, G., Padron, J.M., Martin, T., Gibbons, W.A., and Martin, V.A. (1998) A General Approach to the Asymmetric Synthesis of Unsaturated Lipidic α-Amino Acids. The First Synthesis of α-Aminoarachidonic Acid, J. Org. Chem. 63, 3741-3744.
    • (1998) J. Org. Chem. , vol.63 , pp. 3741-3744
    • Kokotos, G.1    Padron, J.M.2    Martin, T.3    Gibbons, W.A.4    Martin, V.A.5
  • 8
    • 0001162640 scopus 로고
    • The identification of N-(2-hydroxy-ethyl)-palmitamide as a naturally occurring anti-inflammatory agent
    • Kuehl, F.A., Jr., Jacob, T.A., Ganley, O.H., Osmond, R.E., and Meisinger, M.A.P. (1957) The Identification of N-(2-hydroxy-ethyl)-Palmitamide as a Naturally Occurring Anti-inflammatory Agent, J. Am. Chem. Soc. 79, 5577-5578.
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 5577-5578
    • Kuehl F.A., Jr.1    Jacob, T.A.2    Ganley, O.H.3    Osmond, R.E.4    Meisinger, M.A.P.5
  • 9
    • 0028906566 scopus 로고
    • Mast cells express a peripheral cannabinoid receptor with differential sensitivity to anandamide and palmitoylethanolamide
    • Facci, L., Dal Toso, R., Romanello, S., Buriani, A., Skaper, S.D., and Leon, A. (1995) Mast Cells Express a Peripheral Cannabinoid Receptor with Differential Sensitivity to Anandamide and Palmitoylethanolamide, Proc. Natl. Acad. Sci. USA 92, 3376-3380.
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 3376-3380
    • Facci, L.1    Dal Toso, R.2    Romanello, S.3    Buriani, A.4    Skaper, S.D.5    Leon, A.6
  • 10
    • 84986665157 scopus 로고
    • Conversion of racemic lipidic amino acids into sphingosine and ceramide analogues and 1,2-diamines
    • Kokotos, G., Constantinou-Kokotou, V., del Olmo, E., Toth, I., and Gibbons, W.A. (1992) Conversion of Racemic Lipidic Amino Acids into Sphingosine and Ceramide Analogues and 1,2-Diamines, Liebigs Ann. Chem., 961-964.
    • (1992) Liebigs Ann. Chem. , pp. 961-964
    • Kokotos, G.1    Constantinou-Kokotou, V.2    Del Olmo, E.3    Toth, I.4    Gibbons, W.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.