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Volumn 122, Issue 8, 2000, Pages 1842-1843

Alutacenoic acids A and B, rare naturally occurring cyclopropenone derivatives isolated from fungi: Potent non-peptide factor XIIIa inhibitors [21]

Author keywords

[No Author keywords available]

Indexed keywords

ALUTACENOIC ACID A; ALUTACENOIC ACID B; ANTICOAGULANT AGENT; BLOOD CLOTTING FACTOR 13A; CYCLOPROPENONE; UNCLASSIFIED DRUG;

EID: 0034095071     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja992355s     Document Type: Letter
Times cited : (47)

References (53)
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    • Synthetic peptides: Achyuthan, K. E.; Slaughter, T. F.; Santiago, M. A.; Enghild, J. J.; Greenberg, C. S. J. Biol. Chem. 1993, 268, 21284-21292. Natural peptide: Finney, S.; Seale, L.; Sawyer, R. T.; Wallis, R. B. Biochem. J. 1997, 324, 797-805.
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  • 22
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    • note
    • 3OD) δ (ppm) 26.5, 27.1, 28.1, 30.2, 30.4, 30.5, 35.5, 150.2, 161.8, 171.4, 178.2. 1b was stored in a freezer (-20 °C) without decomposition for at least 2 years.
  • 23
    • 0027254197 scopus 로고
    • For the factor XIIIa assay utilized for this study, see: Usui, T.; Takagi, J.; Saito, Y. J. Biol. Chem. 1993, 268, 12311-12316.
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    • Usui, T.1    Takagi, J.2    Saito, Y.3
  • 24
    • 0342673339 scopus 로고    scopus 로고
    • note
    • Alutacenoic acid B (1b) is also isolated from Aspergillus fumigatus Fresenius.
  • 25
    • 0343979460 scopus 로고    scopus 로고
    • note
    • For a detailed study on structure determination by NMR, see the Supporting Information.
  • 30
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    • Review: (a) Krebs, A. W. Angew. Chem., Int. Ed. Engl. 1965, 4, 10-22. (b) Potts, K. T.; Baum, J. S. Chem. Rev. 1974, 74, 189-213. (c) Eicher, T.; Weber, J. L. Top. Curr. Chem. 1975, 57, 1-109.
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    • Krebs, A.W.1
  • 31
    • 0000995098 scopus 로고
    • Review: (a) Krebs, A. W. Angew. Chem., Int. Ed. Engl. 1965, 4, 10- 22. (b) Potts, K. T.; Baum, J. S. Chem. Rev. 1974, 74, 189-213. (c) Eicher, T.; Weber, J. L. Top. Curr. Chem. 1975, 57, 1-109.
    • (1974) Chem. Rev. , vol.74 , pp. 189-213
    • Potts, K.T.1    Baum, J.S.2
  • 32
    • 0016600810 scopus 로고
    • Review: (a) Krebs, A. W. Angew. Chem., Int. Ed. Engl. 1965, 4, 10- 22. (b) Potts, K. T.; Baum, J. S. Chem. Rev. 1974, 74, 189-213. (c) Eicher, T.; Weber, J. L. Top. Curr. Chem. 1975, 57, 1-109.
    • (1975) Top. Curr. Chem. , vol.57 , pp. 1-109
    • Eicher, T.1    Weber, J.L.2
  • 40
    • 0343979455 scopus 로고    scopus 로고
    • note
    • Formula Presented
  • 42
    • 0343107595 scopus 로고    scopus 로고
    • note
    • Formula Presented
  • 43
    • 0343979454 scopus 로고    scopus 로고
    • note
    • Compound 1d was derived from 4d, which was prepared by methylation of 4b. Further details, see the Supporting Information.
  • 44
    • 0342673338 scopus 로고    scopus 로고
    • note
    • We also prepared various esters, amides, ethers, and acylamines. Further detailed study will be reported elsewhere.
  • 47
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    • obs varied hyperbolically with inhibitor concentration. A detailed study will be reported elsewhere.
    • (1995) Methods Enzymol. , vol.248 , pp. 59-84
    • Bieth, J.G.1
  • 51
    • 0343979451 scopus 로고    scopus 로고
    • note
    • Compound 1d does not fit the active site well because of the steric repulsion of the methyl group.
  • 52
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    • Molecular Simulations Inc., USA
    • Molecular Simulations Inc., USA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.