首页> 外国专利> Use of a quinolone derivative containing a Group 7 - (4 - Aminomethyl - 3 oxime) pyrrolidine is able to induce granulocyte colony-stimulating factor for the treatment of neutropenia and the Recovery of hematopoiesis

Use of a quinolone derivative containing a Group 7 - (4 - Aminomethyl - 3 oxime) pyrrolidine is able to induce granulocyte colony-stimulating factor for the treatment of neutropenia and the Recovery of hematopoiesis

机译:包含第7-(4--氨基甲基-3肟)吡咯烷的喹诺酮衍生物能够诱导粒细胞集落刺激因子用于中性粒细胞减少症和造血功能的恢复。

摘要

An antibiotic compound of pentachlorophenol, which can promote the production of G-CSF in vivo and neutron openia therapy, as well as the early recovery of immune inoculation as an active component. Item 1: a drug for the treatment of neutron openia, which contains an effective treatment quantity represented by the formula (1),A pharmaceutically acceptable dissolved salt, including hydrate, ester, isocyanate or isocyanate, wherein R represents hydrogen, methyl or amine, Q represents C-H, C-F, C-Cl, c-oh, c-ch3, c-o-ch3 or N, R1 represents hydrogen, cyclopentane, methyl or ethyl, or phenyl, and is replaced by one or more fluorine atoms, R2 represents one of (a) to (E): (a) hydrocarbon, C1-C4 rectum or resin, cycloacrylonitrile, cyclopropylmethyl, acrylonitrile C3-6, 2- haloethyl ester, methoxy, methoxymethanol, phenyl or propylene; (b) a group of formulations (2), wherein X represents hydrogen, 2-.3-o4-fluorine, cyanogen, nitric acid, thyroid, C1-4 hydrocarbon or 2.4-fluorine, c) one of the following formulas (3);(d) A set of the following formulas (4);(e) A group of the following formulas (5), n for 0 or 1, m for 0, 1 or 2; X for methylene, O or N, R3 for - ch2nr5r6, wherein R5 and R6 independently represent c1-3 or R5 and R6 hydrogen or hydrocarbon, together with the nitrogen atom connected with them, can form a ring, R4 stands for hydrogen, or R3 and R4, plus the carbon atoms connected to them, stands for a formula structure (6) combining a helical pyridine ring, where R7 stands for C1-4 hydrogen or tar. Second requirement: drugs according to the first requirement,Its characteristic is that the formula compound (1) is gem amide. Item 6: drug according to Item 1 or item 2, which is characterized by neutron surgery to induce cancer patients to receive non chemotherapeutic polio treatment. Item 7: the drug meets the requirements of item 6, which is characterized by non chemotherapy myelosuppression therapy selected from gancicvir, acclovir, valaciclovir, valganciclovir, pencelovir, famciclovir, vidabina, citanabina, idosukuridina, trifluridina, edoxana, brivudina. Item 20: drugs provided in accordance with item 11,Hematological reconstruction is characterized by (a) or (b) the addition of a formula compound (1) to a medium containing a mixture of citoquin and growth factor to culture a group of cells, including blood stem cells, Therefore, increasing the innate bone marrow cells in the cell group, and (b) a method of adding a formula compound (1) to an appropriate pharmaceutical environment for the management of mammalian hosts and the reactivation of the innate bone marrow cells.
机译:五氯苯酚的抗生素化合物,可以促进体内G-CSF的产生和中子Openia治疗,以及早期恢复免疫接种作为有效成分。第1项:治疗中子性痴呆的药物,其包含式(1)表示的有效治疗量;药学上可接受的溶解盐,包括水合物,酯,异氰酸酯或异氰酸酯,其中R表示氢,甲基或胺, Q代表CH,CF,C1-Cl,c-oh,c-ch3,co-ch3或N,R1代表氢,环戊烷,甲基或乙基或苯基,并被一个或多个氟原子取代,R2代表一个(a)至(E):(a)烃,C 1 -C 4直肠或树脂,环丙烯腈,环丙基甲基,丙烯腈C 3-6,2-卤代乙基酯,甲氧基,甲氧基甲醇,苯基或丙烯; (b)一组配方(2),其中X代表氢,2-.3-o4-氟,氰,硝酸,甲状腺,C1-4烃或2.4-氟,c)下式(3)之一);(d)一组下式(4);(e)一组下式(5),n表示0或1,m表示0、1或2; X为亚甲基,O或N,R3为-ch2nr5r6,其中R5和R6独立地代表c1-3或R5和R6为氢或烃,以及与其相连的氮原子可以形成环,R4代表氢,或R 3和R 4,加上与它们相连的碳原子,代表结合螺旋吡啶环的式(6),其中R 7代表C 1-4氢或焦油。第二要求:根据第一要求的药物,其特征在于式化合物(1)为酰胺。项目6:根据项目1或项目2的药物,其特征在于中子手术以诱导癌症患者接受非化学治疗脊髓灰质炎治疗。第7项:该药物符合第6项的要求,其特征在于非化疗性骨髓抑制治疗选自gancicvir,acclovir,valaciclovir,valganciclovir,pencelovir,泛昔洛韦,vidabina,citanabina,idosukuridina,trifluridina,edoxana,bruvudina。第20项:根据第11项提供的药物,血液学重建的特征在于(a)或(b)将式化合物(1)添加到含有citoquin和生长因子混合物的培养基中以培养一组细胞,因此,增加了细胞群中的先天骨髓细胞,以及(b)向适当的药物环境中添加式化合物(1)来管理哺乳动物宿主和激活先天骨骼的方法骨髓细胞。

著录项

  • 公开/公告号AR078453A1

    专利类型

  • 公开/公告日2011-11-09

    原文格式PDF

  • 申请/专利权人 LG LIFE SCIENCES LTD.;

    申请/专利号AR2010P103492

  • 发明设计人 PARK JUNG-GYU;PARK HEE-DONG;CHOI JU HYUN;

    申请日2010-09-27

  • 分类号A61K31/4375;A61K31/4725;A61P37/04;A61P35/00;

  • 国家 AR

  • 入库时间 2022-08-21 18:07:23

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