메뉴 건너뛰기




Volumn 48, Issue 7, 1995, Pages 696-702

Isochromophilones III ~ VI, Inhibitors of Acyl-CoA: Cholesterol Acyltransferase Produced by Penicillium multicolor FO-3216

Author keywords

[No Author keywords available]

Indexed keywords

AZAPHILONE; CHOLESTEROL ACYLTRANSFERASE; ENZYME INHIBITOR; ISOCHROMOPHILONE; UNCLASSIFIED DRUG;

EID: 0028978482     PISSN: 00218820     EISSN: 18811469     Source Type: Journal    
DOI: 10.7164/antibiotics.48.696     Document Type: Article
Times cited : (65)

References (17)
  • 1
    • 0001324937 scopus 로고
    • Arterial cholesterol esterification by acylCoA: cholesterol acyltransferase, its possible significance in atherogenesis and its inhibition by drugs
    • F. R. Rrous Science Publishers
    • Bell, F. P.: Arterial cholesterol esterification by acylCoA: cholesterol acyltransferase, its possible significance in atherogenesis and its inhibition by drugs. In Pharmacology Control of Hyperlipidemia. Ed., F. R. Rrous, pp. 409-422, Science Publishers, 1986
    • (1986) Pharmacology Control of Hyperlipidemia , pp. 409-422
    • Bell, F.P.1
  • 2
    • 0040155335 scopus 로고
    • Agent which inhibit cholesterol esterification in the intestine and their potential value in the treatment of hypercholesterolemia
    • F. R. Rrous Science Publishers
    • Heider, J. G.: Agent which inhibit cholesterol esterification in the intestine and their potential value in the treatment of hypercholesterolemia. In Pharmacology Control, of Hyperlipidemia. Ed., F. R. Rrous, pp. 423 —438 Science Publishers, 1986
    • (1986) Pharmacology Control, of Hyperlipidemia , pp. 423-438
    • Heider, J.G.1
  • 3
    • 0025756150 scopus 로고
    • Therapeutic potential of ACAT inhibitors as lipid lowing and antiatherosclerotic agents
    • Sliskovic, D. R. & A. D. White: Therapeutic potential of ACAT inhibitors as lipid lowing and antiatherosclerotic agents. Trend Pharmcol. Sci. 12: 194 — 199, 1991
    • (1991) Trend Pharmcol. Sci. , vol.12 , pp. 194-199
    • Sliskovic, D.R.1    White, A.D.2
  • 4
    • 0026030197 scopus 로고
    • Purpactins, new inhibitors of acyl-CoA: cholesterol acyltransferase produced by Penicillium purpurogenum. I. Production, isolation and physico-chemical and biological properties
    • Tomoda, H.; H. Nishida, R. Masuma, J. Cao, S. Okuda & S. Omura: Purpactins, new inhibitors of acyl-CoA: cholesterol acyltransferase produced by Penicillium purpurogenum. I. Production, isolation and physico-chemical and biological properties. J. Antibiotics 44: 136–143, 1991
    • (1991) J. Antibiotics , vol.44 , pp. 136-143
    • Tomoda, H.1    Nishida, H.2    Masuma, R.3    Cao, J.4    Okuda, S.5    Omura, S.6
  • 5
    • 0026474969 scopus 로고
    • New cyclodepsipeptides, 'enniatins D, E and F produced by Fusarium sp. FO-1305
    • Tomoda, H.; H. Nishida, X. H. Huang, R. Masuma, Y. K. Kim & S. Omura: New cyclodepsipeptides, 'enniatins D, E and F produced by Fusarium sp. FO-1305. J. Antibiotics 45: 1207–1215, 1992
    • (1992) J. Antibiotics , vol.45 , pp. 1207-1215
    • Tomoda, H.1    Nishida, H.2    Huang, X.H.3    Masuma, R.4    Kim, Y.K.5    Omura, S.6
  • 6
    • 0026479108 scopus 로고
    • Glisoprenins, new inhibitors of acyl-CoA: cholesterol acyltransferase produced by Gliocladium sp. FO-1513 I. Production, isolation and physico-chemical and biological properties
    • Tomoda, H.; X. H. Huang, H. Nishida, R. Masuma, Y. K. Kim& S. ŌMura: Glisoprenins, new inhibitors of acyl-CoA: cholesterol acyltransferase produced by Gliocladium sp. FO-1513 I. Production, isolation and physico-chemical and biological properties. J. Antibiotics 45: 1202–1206, 1992
    • (1992) J. Antibiotics , vol.45 , pp. 1202-1206
    • Tomoda, H.1    Huang, X.H.2    Nishida, H.3    Masuma, R.4    Kim, Y.K.5    ŌMura, S.6
  • 7
    • 0027279354 scopus 로고
    • Pyripyropenes, highly potent inhibitors of acyl-CoA: cholesterol acyltransferase produced by Aspergillus fumigatus
    • ŌMura. S.; H. Tomoda, Y. K. Kim & H. Nishida: Pyripyropenes, highly potent inhibitors of acyl-CoA: cholesterol acyltransferase produced by Aspergillus fumigatus. J. Antibiotics 46: 1168 — 1169, 1993
    • (1993) J. Antibiotics , vol.46 , pp. 1168-1169
    • ŌMura, S.1    Tomoda, H.2    Kim, Y.K.3    Nishida, H.4
  • 8
    • 0027759339 scopus 로고    scopus 로고
    • Isochromophilones I and II, novel inhibitors against gp120-CD4 binding from Penicillium sp
    • ŌMura, S.; H. Tanaka, K. Matsuzaki, H. Ikeda & R. Masuma: Isochromophilones I and II, novel inhibitors against gp120-CD4 binding from Penicillium sp. J. Antibiotics 46: 1908 — 1911, 1993
    • J. Antibiotics , vol.46 , pp. 1908-1911
    • ŌMura, S.1    Tanaka, H.2    Matsuzaki, K.3    Ikeda, H.4    Masuma, R.5
  • 9
    • 0000410013 scopus 로고
    • Sclerotiorin, C20H20O5Cl, a chlorine-containing metabolic product of Penicillium sclerotiorum van Beyma: Biochem
    • Curtin, T. P. & J. Reilly: Sclerotiorin, C20H20O5Cl, a chlorine-containing metabolic product of Penicillium sclerotiorum van Beyma: Biochem. J. 34: 1419—1421, 1940
    • (1940) , vol.34 , pp. 1419-1421
    • Curtin, T.P.1    Reilly, J.2
  • 10
    • 0008143712 scopus 로고
    • The chemistry of fungi. part XL. Further evidence for the structure of sclerotiorin
    • Holker, J. S. E.; W. J. Ross, J. Staunton & W. B. Whalley: The chemistry of fungi. part XL. Further evidence for the structure of sclerotiorin. J. Chem. Soc. 4150–4154, 1962
    • (1962) J. Chem. Soc. , pp. 4150-4154
    • Holker, J.S.E.1    Ross, W.J.2    Staunton, J.3    Whalley, W.B.4
  • 11
    • 85007820593 scopus 로고
    • (—)-Sclerotiorin, a major metabolite of Penicillium hirayamae Udagawa
    • Udagawa, S.: (—)-Sclerotiorin, a major metabolite of Penicillium hirayamae Udagawa., Chem. Pharm. Bull. 11: 336–367, 1963
    • (1963) Chem. Pharm. Bull. , vol.11 , pp. 336-367
    • Udagawa, S.1
  • 13
    • 0000373754 scopus 로고
    • Two new fungal azaphilones from Talaromyces luteus, with monoamine oxidase inhibitory effect
    • Fujimoto, H.; T. Matsudo, A. Yamaguchi & M. Yamazaki: Two new fungal azaphilones from Talaromyces luteus, with monoamine oxidase inhibitory effect. Heterocycles 30: 607 — 616, 1990
    • (1990) Heterocycles , vol.30 , pp. 607-616
    • Fujimoto, H.1    Matsudo, T.2    Yamaguchi, A.3    Yamazaki, M.4
  • 14
    • 0000185494 scopus 로고
    • Pyranose benzoates. An additivity relation in the amplitudes of exciton-split CD curves
    • Hung-Wen, L. & K. Nakanishi: Pyranose benzoates. An additivity relation in the amplitudes of exciton-split CD curves. J. Am. Chem. Soc. 104: 1178—1185, 1982
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 1178-1185
    • Hung-Wen, L.1    Nakanishi, K.2
  • 16
    • 85007877911 scopus 로고
    • (Fujisawa Pharmaceutical Co., Ltd.): Inhibitor of phospholipase A2. Jpn. Kokai 255615 ('90) Oct. 16
    • Nakamura, M.; T. Kino, K. Koji, S. Kiyonaga & M. Okuhara (Fujisawa Pharmaceutical Co., Ltd.): Inhibitor of phospholipase A2. Jpn. Kokai 255615 ('90) Oct. 16, 1990
    • (1990)
    • Nakamura, M.1    Kino, T.2    Koji, K.3    Kiyonaga, S.4    Okuhara, M.5
  • 17
    • 0028013360 scopus 로고
    • Azaphilones inhibit tumor promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mice
    • Yasukawa, K.; M. Takahashi, K. Kawai, M. Yamazaki, M. Takeuchi & M. Takido: Azaphilones inhibit tumor promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mice. Oncology 51: 108 —112, 1994
    • (1994) Oncology , vol.51 , pp. 108-112
    • Yasukawa, K.1    Takahashi, M.2    Kawai, K.3    Yamazaki, M.4    Takeuchi, M.5    Takido, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.