Hydroxynybomycin: isolation, structure and bioactivity.

@article{Nadzan1977HydroxynybomycinIS,
  title={Hydroxynybomycin: isolation, structure and bioactivity.},
  author={Alex M. Nadzan and Kenneth L. Jun. Rinehart and Walter T. Sokolski},
  journal={The Journal of antibiotics},
  year={1977},
  volume={30 6},
  pages={
          523-4
        }
}
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12 Citations

12 Citations

Synthesis of Novel 1,3‐Cyclohexadiene Derivatives Bearing 2‐Oxo‐Quinoline Moiety via a 4‐CR Strategy**

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Structure Determination, Functional Characterization, and Biosynthetic Implications of Nybomycin Metabolites from a Mining Reclamation Site-Associated Streptomyces.

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A facile synthesis of various functionalized 3-substituted quinolin-2(1H)-ones through Ag(i) nitrate-catalyzed cyclization of o-alkynylisocyanobenzenes is described. The reaction allows rapid and…

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La presente invention concerne un compose ou un sel correspondant represente par la formule generale (I) dote d'une forte activite antibacterienne contre des bacteries ayant developpe une resistance…

Facile and efficient synthesis of quinolin-2(1H)-ones via cyclization of penta-2,4-dienamides mediated by H2SO4.

A facile and efficient synthesis of substituted quinolin-2(1H)-ones is developed via intramolecular cyclization of penta-2,4-dienamides mediated by concentrated H(2)SO(4) (98%), and a mechanism…

Pseudonocardians A–C, New Diazaanthraquinone Derivatives from a Deap-Sea Actinomycete Pseudonocardia sp. SCSIO 01299

Three new diazaanthraquinone derivatives, along with a previously synthesized compound deoxynyboquinone, were produced by the strain SCSIO 01299, a marine actinomycete member of the genus Pseudonocardia, isolated from deep-sea sediment of the South China Sea, and exhibited potent cytotoxic activities against three tumor cell lines.

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