发明名称 AMINO ACID DERIVATIVES AND PROCESSES FOR PREPARATION THEREOF
摘要 NEW MATERIAL:The compound of formula I (R<1> is H, amino or protected amino; R<2> is H, carboxy or protected carboxy; R<3> is H, carboxy or protected carboxy; R<4> is lower alkyl, lower aminoalkyl, etc.; R<5> is H or lower alkyl; R<6> is H, lower aralkyl, etc.). EXAMPLE:(2S,3R)-2-[[ (2S)-2-Amino-3-carbamoylpropionyl ]amino]-3-[[(1S)-1-car-boxy-2-(4-imidazolyl)ethyl]amino]butyric acid. USE:An agent effective to recover the colony-forming and antibody-forming activity of a host having immunodeficiency and to inhibit the metastasis of tumor. PREPARATION:The compound of formula I can be produced by reacting the compound of formula II or its reactive derivative at the carboxyl group with the compound of formula III or its reactive derivative at the amino group in a solvent under cooling or at room temperature.
申请公布号 ZA8601281(B) 申请公布日期 1986.10.29
申请号 ZA19860001281 申请日期 1986.02.20
申请人 FUJISAWA PHARMACEUTICAL CO. LTD. 发明人 HIROSHI TERANO;YASUHISA TSURUMI;HIROYUKI SETOI;MASASHI HASHIMOTO;MASANOBU KOHSAKA
分类号 C07D521/00;A61K31/16;A61K31/195;A61K31/215;A61K31/22;A61K31/33;A61K31/403;A61K31/404;A61K31/405;A61K31/415;A61P35/00;A61P37/04;C07C67/00;C07C231/00;C07C231/02;C07C231/08;C07C231/12;C07C233/36;C07C233/47;C07C237/12;C07C237/20;C07C237/22;C07C273/10;C07D209/20;C07D233/64;C07K;C07K5/06;C12P13/04;C12R1/01 主分类号 C07D521/00
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