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Volumn 56, Issue 2, 2003, Pages 181-185

FR235222, a fungal metabolite, is a novel immunosuppressant that inhibits mammalian histone deacetylase. III. Structure determination

Author keywords

[No Author keywords available]

Indexed keywords

CALCINEURIN INHIBITOR; CYCLOSPORIN A; DRUG METABOLITE; FR 235222; HISTONE DEACETYLASE; HISTONE DEACETYLASE INHIBITOR; IMMUNOSUPPRESSIVE AGENT; TACROLIMUS; UNCLASSIFIED DRUG;

EID: 0037300543     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.56.181     Document Type: Article
Times cited : (36)

References (17)
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    • MORI, H.: FR235222, a fungal metabolite, is a novel immunosuppressant that inhibits mammalian histone deacetylase (HDAC). I. Taxonomy, fermentation, isolation and biological activities. J. Antibiotics 56: 72-79, 2003
    • (2003) J. Antibiotics , vol.56 , pp. 72-79
    • Mori, H.1
  • 3
    • 0037300480 scopus 로고    scopus 로고
    • FR235222, a fungal metabolite, is a novel immunosuppressant that inhibits mammalian histone deacetylase (HDAC). II. Biological activities in animal models
    • MORi, H.: FR235222, a fungal metabolite, is a novel immunosuppressant that inhibits mammalian histone deacetylase (HDAC). II. Biological activities in animal models. J. Antibiotics 56: 80-86, 2003
    • (2003) J. Antibiotics , vol.56 , pp. 80-86
    • Mori, H.1
  • 4
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    • Direct-space methods in phase extension and phase determination. I. Low-density elimination
    • SHIONO, M. & M. M. WOOLFSON: Direct-space methods in phase extension and phase determination. I. Low-density elimination. Acta Cryst. A48: 451-456, 1992
    • (1992) Acta Cryst. , vol.48 A , pp. 451-456
    • Shiono, M.1    Woolfson, M.M.2
  • 5
    • 0001479941 scopus 로고    scopus 로고
    • A non-empirical method using LC/MS for determination of the absolute configuration of constituent amino acids in a peptide: Combination of Marfey's method with mass spectrometry and its practical application
    • FUJII, K.; Y. IKAI, H. OKA, M. SUZUKI & K-I. HARADA: A non-empirical method using LC/MS for determination of the absolute configuration of constituent amino acids in a peptide: Combination of Marfey's method with mass spectrometry and its practical application. Anal. Chem. 69: 5146-5151, 1997
    • (1997) Anal. Chem. , vol.69 , pp. 5146-5151
    • Fujii, K.1    Ikai, Y.2    Oka, H.3    Suzuki, M.4    Harada, K.-I.5
  • 6
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
    • OHTANI, I.; T. KUSUMI, Y. KASHMAN & H. KAKISAWA: High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. J. Am. Chem. Soc. 113: 4092-4096, 1991
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092-4096
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  • 7
    • 85038454921 scopus 로고    scopus 로고
    • Hydrogenation of Trapoxin A yielded an α-hydroxyketone derivative and the configuration of the alcohol was established to be S by this method as expected
    • Hydrogenation of Trapoxin A yielded an α-hydroxyketone derivative and the configuration of the alcohol was established to be S by this method as expected.
  • 10
    • 0016031841 scopus 로고
    • Mass spectrometric determination of amino acid sequence in Cy1-2, a novel cyclotetrapeptide from Cylindrocladium scoparium
    • HIROTA, A.; A. SUZUKI, K. AIZAWA & S. MURA: Mass spectrometric determination of amino acid sequence in Cy1-2, a novel cyclotetrapeptide from Cylindrocladium scoparium. Biomed. Mass Spectrom. 1 (1): 15-19, 1974
    • (1974) Biomed. Mass Spectrom. , vol.1 , Issue.1 , pp. 15-19
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    • Isolierung und strukturäufklarung von chlamydocin
    • CLOSSE, A. & R. HUGUENIN: Isolierung und strukturäufklarung von chlamydocin. Helv. Chim. Acta. 57: 533, 1974
    • (1974) Helv. Chim. Acta , vol.57 , pp. 533
    • Closse, A.1    Huguenin, R.2
  • 15
    • 85038451812 scopus 로고
    • This residue has been seen in TAN-1746 in a patent where it was described as an anti-cancer agent. See, Japan Pat. 07-196686
    • This residue has been seen in TAN-1746 in a patent where it was described as an anti-cancer agent. See, YOSHIMURA, K.; S. TSUBOTANI & K. OKAZAKI: Japan Pat. 07-196686, 1995
    • (1995)
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  • 16
    • 0028106671 scopus 로고
    • Characterization of a phytotoxic cyclotetrapeptide, a novel chlamydocin analogue, from Verticillium coccosporum
    • The amino acid residue was also observed in a chlamydocin analogue with phytotoxic activities. We believe that this product is identical with TAN-1746. See
    • The amino acid residue was also observed in a chlamydocin analogue with phytotoxic activities. We believe that this product is identical with TAN-1746. See, Gupta, S.; G. Peiser, T. Nakajima & Y-S. Hwang: Characterization of a phytotoxic cyclotetrapeptide, a novel chlamydocin analogue, from Verticillium coccosporum. Tetrahedron Letters 35 (33): 6009-6012, 1994
    • (1994) Tetrahedron Letters , vol.35 , Issue.33 , pp. 6009-6012
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  • 17
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    • Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase
    • KIJIMA, M.; M. YOSHIDA, K. SUGITA, S. HORINOUCHI & T. BEPPU: Trapoxin, an antitumor cyclic tetrapeptide, is an irreversible inhibitor of mammalian histone deacetylase. J. Biol. Chem. 268 (30): 22429-22435, 1993
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    • Kijima, M.1    Yoshida, M.2    Sugita, K.3    Horinouchi, S.4    Beppu, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.