发明授权
- 专利标题: Antibiotic, Spicamycin
- 专利标题(中): 抗生素,Spicamycin
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申请号: US583108申请日: 1984-02-24
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公开(公告)号: US4565781A公开(公告)日: 1986-01-21
- 发明人: Noboru Otake , Yoichi Hayakawa , Hiroyuki Kawai , Masaya Nakagawa , Kozo Tanabe , Junichiro Mochizuki
- 申请人: Noboru Otake , Yoichi Hayakawa , Hiroyuki Kawai , Masaya Nakagawa , Kozo Tanabe , Junichiro Mochizuki
- 申请人地址: JPX Tokyo
- 专利权人: Kirin Beer Kabushiki Kaisha
- 当前专利权人: Kirin Beer Kabushiki Kaisha
- 当前专利权人地址: JPX Tokyo
- 优先权: JPX58-35662 19830304
- 主分类号: A61K31/70
- IPC分类号: A61K31/70 ; A61K31/7042 ; A61K31/7052 ; A61P31/04 ; A61P35/00 ; C07H17/02 ; C12P1/06 ; C12P19/28 ; C12P19/32 ; C12R1/465 ; C12P19/40 ; C07H19/06
摘要:
An antibiotic, Spicamycin, having the physicochemical properties set forth below is produced by aerobically cultivating a Spicamycin-producing Streptomyces strain in a suitable culture medium, and recovering from the culture the antibiotic, Spicamycin.(1) Color and properties: Weakly acidic white powder(2) Melting point: 215.degree. to 220.degree. C. (decomposed)(3) Specific rotatory power: [.alpha.].sub.D.sup.25 =+15.degree. (C: 0.15, in methanol)(4) Elementary analysis (Found): C: 57.4%, H: 8.3%; N: 15.7%, O: 18.6%(5) Ultraviolet absorption spectrum (maximum):______________________________________ CH.sub.3 OH 264 nm (E.sub.1cm.sup.1% 257) 0.01N NaOH + CH.sub.3 OH 272 nm (E.sub.1cm.sup.1% 226) 0.01N HCl + CH.sub.3 OH 273 nm (E.sub.1cm.sup.1% 258) ______________________________________ (6) Infrared absorption spectrum (as measured by the potassium bromide method): As shown in FIG. 2.(7) Solubility in Solvent: Soluble in basic water, dimethyl sulfoxide, methanol, ethanol, n-propanol, and n-butanol. Sparingly soluble in water, acetone, ethyl acetate, and chloroform. Insoluble in benzene, ethyl ether, and hexane.(8) Thin layer chromatography (using "Silica Gel 60F.sub.254 " plate supplied by Merck & Co., Inc.):______________________________________ Developing solvent Rf value ______________________________________ Chloroform:Methanol (1:1) 0.34 ______________________________________ (9) NMR spectrum (400 MHz, in deuteromethanol): As shown in FIG. 3.
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