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Chromomycin a components of the antibiotic chromomycin

机译:嗜铬菌素是抗生素嗜铬菌素的成分

摘要

The invention relates to (I) chromomycin A group antibiotics, i.e. chromomycin A1, A2, A3, A4 and A5, containing a major proportion but less than 70% by weight of chromomycin A3; (II) chromomycin (A2+A3) containing at least 70% but less than 100% by weight of chromomycin A3; and (III) chromomycin A3, which has a melting point of 185 DEG C., a molecular weight by the Rast method of 467 sB 50 or by the Barger method of 900-1,000, a specific rotation measured at a wavelength of FORM:0898793/IV (b)/1 (c=1.0% ethanol), an antibiotic spectrum according to Table 4 (not shown), a UV-spectrum PICT:0898793/IV (b)/1 PICT:0898793/IV (b)/2 according to Fig. 1 and an IR-spectrum as shown in Fig. 2a. Chromomycin A group is obtained from chromomycin mixture (chromomycin A, B and C groups) by (a) treating chromomycin mixture with a polyhydric alcohol containing water methanol or ethanol in countercurrent with a solvent-immiscible therewith; (b) dissolving chromomycin mixture in an organic solvent of high polarity, adding an organic solvent of low polarity to precipitate first unundesired fractions and then chromomycin A group; (c) dissolving chromomycin mixture in an organic solvent of high polarity, passing the solution through an adsorbent, treating the adsorbed matter with an organic solvent of low polarity and retrieving chromomycin A group as the component which is least adsorbed; (d) partition chromatography using as eluant ether/acetic acid ester, acetic acid ester/acetone and acetone/alcohol solvent systems in succession, the chromomycin being recovered from the ether/acetic acid ester system. Chromomycin (A2 + A3) is obtained by treating chromomycin A group in an organic solvent of high polarity with a non-polar solvent in a step-wise manner, separating each precipitate formed, repeating the treatment on each precipitate and collecting (A2 + A3) from the middle of the final precipitates. Chromomycin A3 is obtained from chromomycin A group by (a) partition chromatography using as eluant ether/acetic acid ester solvent system (90 : 10 ratio); (b) dissolving the chromomycin A group in a polyhydric alcohol containing water, methanol or ethanol with acetic acid ester/ether mobile phase in counter-current distribution apparatus, the chromomycin A3 being recovered from the middle portions of the apparatus. Specification 898,794 is referred to.
机译:本发明涉及(I)含有大量主要成分但少于70%(重量)的嗜铬菌素A类抗生素,即嗜铬菌素A1,A2,A3,A4和A5。 (II)含有至少70%但少于100%重量的霉素A3的霉素(A2 + A3); (III)染色体霉素A3,其熔点为185℃,通过Rast方法的分子量为467 sB 50或通过Barger方法的分子量为900-1,000,在<FORM的波长下测得的比旋光度:0898793 / IV(b)/ 1>(c = 1.0%乙醇),根据表4的抗生素光谱(未显示),紫外光谱 和如图2a所示的IR光谱。嗜铬霉素A基团由嗜铬霉素混合物(嗜铬霉素A,B和C基团)通过以下方法获得:(a)用含有水甲醇或乙醇的多元醇在与其不混溶的溶剂的逆流下处理嗜霉素混合物; (b)将花色霉素混合物溶解在高极性的有机溶剂中,加入低极性的有机溶剂以沉淀出首先不需要的馏分,然后沉淀花色霉素A基团; (c)将花霉素混合物溶解在高极性的有机溶剂中,使溶液通过吸附剂,用低极性的有机溶剂处理被吸附物,并取回作为最不被吸附的组分的花霉素A基团; (d)依次使用醚/乙酸酯,乙酸酯/丙酮和丙酮/醇溶剂体系作为洗脱剂的分配色谱法,从霉素/乙酸酯体系中回收霉素。铬霉素(A2 + A3)是通过在高极性有机溶剂中用非极性溶剂逐步处理铬霉素A基团,分离形成的每个沉淀物,对每个沉淀物重复处理并收集(A2 + A3)而获得的)从最终沉淀物的中间。通过(a)使用醚/乙酸酯溶剂系统(比例为90:10)作为洗脱剂的分配色谱法,从嗜铬菌素A组获得嗜铬菌素A3; (b)在逆流分配装置中,将乙酸霉素A基团溶解在含有水,甲醇或乙醇的带有乙酸酯/醚流动相的多元醇中,从该装置的中间部分回收该霉素霉素A3。参考规格898,794。

著录项

  • 公开/公告号GB898793A

    专利类型

  • 公开/公告日1962-06-14

    原文格式PDF

  • 申请/专利权人 TAKEDA PHARMACEUTICAL INDUSTRIES LTD.;

    申请/专利号GB19580029664

  • 发明设计人

    申请日1958-09-16

  • 分类号C07H15/22;

  • 国家 GB

  • 入库时间 2022-08-23 17:38:04

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