BE-23372M, a novel protein tyrosine kinase inhibitor. III. Synthesis.

  • TANAKA SEIICHI
    Tsukuba Research Institute in collaboration with Merck Research Laboratories, Banyu Pharmaceutical Co., Ltd.
  • OKABE TAKAYOSHI
    Tsukuba Research Institute in collaboration with Merck Research Laboratories, Banyu Pharmaceutical Co., Ltd.
  • NAKAJIMA SHIGERU
    Tsukuba Research Institute in collaboration with Merck Research Laboratories, Banyu Pharmaceutical Co., Ltd.
  • YOSHIDA EISAKU
    Tsukuba Research Institute in collaboration with Merck Research Laboratories, Banyu Pharmaceutical Co., Ltd.
  • MORISHIMA HAJIME
    Tsukuba Research Institute in collaboration with Merck Research Laboratories, Banyu Pharmaceutical Co., Ltd.

書誌事項

タイトル別名
  • III. SYNTHESIS

この論文をさがす

説明

In a preceding paper, the physico-chemical properties and structural elucidation of BE-23372M, a potent novel protein tyrosine kinase inhibitor, were described. In this paper, we report the synthesis of BE-23372M from 3-(3, 4-dimethoxybenzoyl)propionic acid and veratraldehyde or 3, 4-diacetoxy-benzaldehyde. The structure of BE-23372M was confirmed to be (E)-3-(3, 4-dihydroxybenzylidene)-5-(3, 4-dihydroxyphenyl)-2(3H)-furanone.

収録刊行物

キーワード

詳細情報 詳細情報について

  • CRID
    1390282679127676928
  • NII論文ID
    130003502722
  • DOI
    10.7164/antibiotics.47.297
  • COI
    1:CAS:528:DyaK2cXktlGisrw%3D
  • ISSN
    18811469
    00218820
  • PubMed
    8175482
  • 本文言語コード
    en
  • 資料種別
    journal article
  • データソース種別
    • JaLC
    • Crossref
    • PubMed
    • CiNii Articles
  • 抄録ライセンスフラグ
    使用不可

問題の指摘

ページトップへ