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METHOD OF MANUFACTURING NOVEL ANTIITUMOR ANTIBIOTICS* VII7501
METHOD OF MANUFACTURING NOVEL ANTIITUMOR ANTIBIOTICS* VII7501
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机译:制造新型抗微生物剂的方法* VII7501
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1513344 Biochemical composition HITACHI CHEMICAL CO Ltd 31 Aug 1976 [3 Sept 1975] 35929/76 Heading C3H A biochemically active composition V1-7051 is made by growing a culture of Streptomyces griseus, bachijoeusis, collinus, griseoruben, lin. coleneusis, cinereornber, imichiganesis, lavendulae, xanthochromogenus, viridifaciens, netropsis, flavogenseus, vendargensis or Actinanices albolayus or coerukscens, in a nutrient medium at 28‹ to 29‹ C. for 24 to 60 hours and then recovering the fraction having a molecular weight range of 1À5 x 104 to 3À5 x 104 from the cultivation liquid, cell walls and cell bodies. The product may be soluble in water and insoluble in methanol, ethanol, acetone, ethyl acetate, benzene and chloroform and it may show a positive reaction with anhydrin o# fluorescamine and negative reaction with anthinone V1-7051 inhibits the activity of succinic dehydrogenase in a tumour cell and its physical and chemical characteristics are detailed. Unlike other antitumour polypeptides it has no antimicrobial activity. Examples are given.
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机译:1513344生化组合物HITACHI CHEMICAL CO Ltd 1976年8月31日[1975年9月3日] 35929/76标题C3H通过生长灰链霉菌,条状芽孢杆菌,collinus,灰麻黄素,林的培养物来制备生物化学活性组合物V1-7051。在营养液中,在28℃至29℃的温度条件下,将结肠炎,灰质,革兰,薰衣草,薰衣草,黄原色,绿头藻,netropsis,黄草,vendargensis或华氏猕猴桃或coerukscens发酵24至60小时,然后回收分子量范围的部分从培养液,细胞壁和细胞体中取出1×5 x 10 4到3×5 x 10 4。该产品可能溶于水,而不溶于甲醇,乙醇,丙酮,乙酸乙酯,苯和氯仿,并且它可能与酸酐o#氟胺发生正反应,而与蒽醌V1-7051发生负反应会抑制琥珀酸脱氢酶的活性。详细介绍了肿瘤细胞及其理化特性。与其他抗肿瘤多肽不同,它没有抗菌活性。举了例子。
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