UCN-01 and UCN-02, new selective inhibitors of protein kinase C. II. Purification, physico-chemical properties, structural determination and biological activities

  • J Antibiot (Tokyo). 1989 Apr;42(4):571-6. doi: 10.7164/antibiotics.42.571.
I Takahashi  1 Y Saitoh M Yoshida H Sano H Nakano M Morimoto T Tamaoki
Affiliations
  • 1. Tokyo Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Tokyo, Japan.
Abstract

A new inhibitor of protein kinase C (PKC), UCN-01, was isolated from the culture broth of Streptomyces sp. N-126. We have found that this strain also produces UCN-02 which is a stereoisomer of UCN-01. The inhibitors have the molecular formula C28H26N4O4 and have an indolo[2,3-alpha]carbazole chromophore. Their structures have been elucidated by mass and NMR spectra. UCN-01 has been shown to inhibit PKC and protein kinase A (PKA) with IC50 values of 0.0041 and 0.042 microM, respectively, and UCN-02 has been shown to inhibit PKC and PKA with IC50 values of 0.062 and 0.25 microM, respectively. UCN-01 and UCN-02 also showed the cytotoxic effect on the growth of HeLa S3 cells.

Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • ≥98.0%, PKC Inhibitor
    target: PKC; PKA
    Research Areas: Cancer