Cytotoxic ergosterols from Paecilomyces sp. J300.

@article{Kwon2002CytotoxicEF,
  title={Cytotoxic ergosterols from Paecilomyces sp. J300.},
  author={Hak Cheol Kwon and Sang Deuk Zee and Sae Yun Cho and Sang Un Choi and Kang Ro Lee},
  journal={Archives of pharmacal research},
  year={2002},
  volume={25 6},
  pages={851-5}
}
Seven ergosterol derivatives (1-7) were isolated from silkworm larvae infected with Paecilomyces sp. J300. On the basis of spectroscopic means, their structures have been elucidated as 3beta,5alpha-dihydroxy-ergosta-7,22-diene (1), 5alpha,6alpha-epoxy-(22E,24R)-ergosta-8(14), 22-diene-3beta, 7alpha-diol (2), 5alpha,6alpha-epoxy-(22E,24R)-ergosta-8,22-diene-3beta,7alpha-diol (3), ergosta-4,6,8(14),22-tetraene-3-one (4), ergosterol (5), ergosterol endoperoxide (6), 3beta,5alpha-dihydroxy-6beta… CONTINUE READING

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