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Volumn 48, Issue 4, 2009, Pages 725-727

The ammosamides: Structures of cell cycle modulators from a marine-derived Streptomyces species

Author keywords

Actinomycetes; Alkaloids; Natural products; Quinolines; Thiolactams

Indexed keywords

CHEMICAL REACTIONS;

EID: 58249097269     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200804890     Document Type: Article
Times cited : (165)

References (25)
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    • 0037455147 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 355-357;
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 355-357
  • 7
    • 58249102151 scopus 로고    scopus 로고
    • Strain CNR-698 was isolated from a sediment sample collected at Little San Salvador, Bahamas. The strain does not require seawater for growth. Its partial 16S rRNA sequence (Genbank #EU863183) is 100% identical to another bacterium of the family Streptomycetaceae, also isolated from marine sediments (20 m) (#EU099411).
    • Strain CNR-698 was isolated from a sediment sample collected at Little San Salvador, Bahamas. The strain does not require seawater for growth. Its partial 16S rRNA sequence (Genbank #EU863183) is 100% identical to another bacterium of the family Streptomycetaceae, also isolated from marine sediments (20 m) (#EU099411).
  • 8
    • 58249114957 scopus 로고    scopus 로고
    • X-ray measurements were made on a SMART CCD area detector with graphite monochromated MoKa radiation (λ, 1.54178 Å, 1 (C 12H10ClN5OS, crystal dimensions 0.30 x 0.20 x 0.10 mm, monoclinic, space group P21/c, a, 9.3766(8, b, 18.2930(12, c, 7.0462(6) Å, V, 1208.55(17) Å3, Z, 4, ρcalcd, 1.691 mg m -3, μ, 4.456 mm-1, T, 100(2) K, 2θmax, 136.3°, 7060 measured reflections, 1872 independent reflections (Rint, 0.0399, 183 parameters refined, R, 0.0541 (for 4205 reflections with I > 2.00σI, Rw, 0.1523, max/min residual peaks in the final difference map 0.495/-0.817 e Å-3. CCDC 694293 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Ca
    • -3. CCDC 694293 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 11
    • 0141483364 scopus 로고    scopus 로고
    • Amines (and alcohols) react with Lawesson's reagent to afford a variety of N-phosphorus heterocycles: M. Jesberger, T. P. Davis, L. Barner, Synthesis 2003, 1929-1953;
    • Amines (and alcohols) react with Lawesson's reagent to afford a variety of N-phosphorus heterocycles: M. Jesberger, T. P. Davis, L. Barner, Synthesis 2003, 1929-1953;
  • 13
    • 58249119529 scopus 로고    scopus 로고
    • Conversion to the amide occurs via the thioamide S oxide: J. H. Hillhouse, I. A. Blair, L. Field, Phosphorus Sulfur Relat. Elem. 1986, 26, 169-184.
    • Conversion to the amide occurs via the thioamide S oxide: J. H. Hillhouse, I. A. Blair, L. Field, Phosphorus Sulfur Relat. Elem. 1986, 26, 169-184.
  • 22
    • 0001231828 scopus 로고
    • For a review of sulfur-containing metabolites from marine organisms, see
    • For a review of sulfur-containing metabolites from marine organisms, see: C. Christophersen, U. Anthoni, Sulfur Rep. 1986, 4, 365-442.
    • (1986) Sulfur Rep , vol.4 , pp. 365-442
    • Christophersen, C.1    Anthoni, U.2
  • 23
    • 0032581731 scopus 로고    scopus 로고
    • A common strategy in the total synthesis of C-7-N containing natural products, like makaluvamine A (6), is the displacement of a C-7 leaving group with a primary amine. See: M. Iwao, O. Motoi, T. Fukuda, F. Ishibashi, Tetrahedron 1998, 54, 8999-9010.
    • A common strategy in the total synthesis of C-7-N containing natural products, like makaluvamine A (6), is the displacement of a C-7 leaving group with a primary amine. See: M. Iwao, O. Motoi, T. Fukuda, F. Ishibashi, Tetrahedron 1998, 54, 8999-9010.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.