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公开(公告)号:CN1471984A
公开(公告)日:2004-02-04
申请号:CN02124297.6
申请日:2002-07-16
Abstract: 本发明心率同步倍频经络穴位治疗仪能够侦测到患者肌体发出的声、光、电、压力等生命信息,经电路处理后发出与患者心跳同步的倍频信号,转换成适当的电压和电流,通过电极施加到人体的经络或穴位,对某些神经、肌肉疾病进行治疗。本发明有如下优点:1,该装置是由患者的心率控制着治疗的过程。发出的电信号与人的心率同步并呈倍频共振关系。在血供、血氧改善的同时对肌体经络、穴位给以刺激。2,患者能在心理上有所准备地配合治疗。对那些患有中风、神经传导障碍、截瘫、肌肉萎缩疾病的患者,可以提高他们治愈疾病的信心,从而增强疗效。
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公开(公告)号:WO2013013639A1
公开(公告)日:2013-01-31
申请号:PCT/CN2012/079233
申请日:2012-07-27
Applicant: 山东先声麦得津生物制药有限公司 , 江苏先声药物研究有限公司 , 周兵 , 周宇 , 姜静
IPC: C07K19/00 , C07K14/47 , C12N15/62 , C12N15/63 , C12N5/10 , C12N1/21 , A01K67/00 , A61K38/17 , A61P35/00 , A61P37/02
CPC classification number: C07K14/52 , A61K38/00 , A61K38/17 , A61K38/19 , A61K38/191 , C07K14/70575 , C07K2319/73 , C12N5/10 , C12N15/63 , C12P21/02
Abstract: 公开了一种肿瘤坏死因子相关凋亡诱导配体融合蛋白、编码该融合蛋白的DNA序列、含有该DNA序列的载体、含该载体的宿主细胞或者转基因动物、该融合蛋白的制备方法以及该融合蛋白的应用,其中所述融合蛋白包含:(1)人源亮氨酸拉链结构域;(2)人源TRAIL蛋白、人源TRAIL蛋白胞外区或人源TRAIL蛋白胞外区的片段。
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公开(公告)号:WO2008125008A1
公开(公告)日:2008-10-23
申请号:PCT/CN2008/000722
申请日:2008-04-09
IPC: C07D221/04 , A61K31/438 , A61P25/28
CPC classification number: C07D221/04
Abstract: The invention provides a cyclohepta[b]pyridine compound described as formula I and pharmaceutically acceptable salts thereof. The invention also provides the method for preparation of these cyclohepta[b]pyridine compounds as well as the use of these cyclohepta[b]pyridine compounds and compositions thereof in preparing medicines for treatment and prophylaxis of Alzheimer's disease, children mental retardation, amnesia and other cardiovascular and cerebrovascular diseases. The compounds of present invention can be used as agonist or/and inhibitor of a, ß, ?-secretase. The compounds prevent production of amyloid by actuation or inhibition activity of enzymes and can effectually treat and/or prevent Alzheimer's disease, children mental retardation, amnesia and other cardiovascular and cerebrovascular diseases.
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公开(公告)号:WO2007036113A1
公开(公告)日:2007-04-05
申请号:PCT/CN2006/001783
申请日:2006-07-20
IPC: A61K31/7048 , A61P37/06 , A61P37/08
CPC classification number: A61K31/7048
Abstract: The invention discloses Pharmaceutical use of periplocoside A and E. The test shows that periplocoside A and E possesse the action of obvious immunosuppression and advantages of high effect and low toxic by-effect,so periplocoside A and E can be used to prepare the medicines of immunosuppression and which is safe and low-cost.
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公开(公告)号:WO2007095812A1
公开(公告)日:2007-08-30
申请号:PCT/CN2006/003428
申请日:2006-12-15
Applicant: 中国科学院上海药物研究所 , 柳红 , 蒋华良 , 沈旭 , 丁健 , 朱兴族 , 林莉萍 , 郑鸣芳 , 郑明月 , 周宇 , 季新泉 , 罗海彬 , 罗小民 , 沈建华 , 陈凯先
IPC: C07D251/18 , C07D251/52 , C07D251/54 , C07D401/04 , C07D403/04 , C07D417/04 , C07D413/04 , A61K31/395 , A61K31/435 , A61K31/496 , A61K31/497 , A61K31/5377 , A61K31/5395 , A61K31/541 , A61P29/00 , A61P35/00
CPC classification number: C07D403/04 , C07D251/54 , C07D413/04
Abstract: This invention discloses the substituted [1,3,5] triazine compounds of following formula, their pharmaceutically acceptable salts and solvates or hydrates, the pharmaceutical compositions containing the compounds and the uses thereof. The compositions of the present invention may be used for the prevention and/or treatment of inflammation diseases, which have good effect. The substituted [1,3,5] triazine compounds or their pharmaceutically acceptable salts show remarkable EGFR enzyme inhibitory activity and antitumor activity in a serious of selective tests of EGFR enzyme level and tumor cell level (human HT-29 and HCT-116). So The compositions of the present invention may be used for the prevention and/or treatment and/or aid treatment of tumor diseases.
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公开(公告)号:WO2008006276A1
公开(公告)日:2008-01-17
申请号:PCT/CN2007/001518
申请日:2007-05-09
IPC: C07C39/06 , C07C43/23 , C07C69/80 , C07C319/14 , C07C15/16 , C07D295/03 , C07D295/02 , C07D307/28 , A61K31/085 , A61K31/10 , A61K31/135 , A61P25/28
CPC classification number: C07C69/92 , C07C43/23 , C07C2601/14 , C07D209/48 , C07D295/088 , C07D307/68
Abstract: A type of novel compounds having the symmetric structure of formula I, which can inhibit the congregation and fibrosis of ß-amyloid protein, their pharmaceutically accepted salts, and preparation methods thereof. The pharmaceutical compositions containing these compounds or their pharmaceutically accepted salts, and the uses of these compounds or their pharmaceutically accepted salts or their pharmaceutical compositions for the manufacture of a medicament for the prevention or treatment of an Alzheimer's disease. The compounds or their pharmaceutically accepted salts discloses in present invention can inhibit the congregation and fibrosis of ß-amyloid protein by combining with Aß polypeptide. So they can be used to prevent or treat Alzheimer's diseases.
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公开(公告)号:WO2007009388A1
公开(公告)日:2007-01-25
申请号:PCT/CN2006/001782
申请日:2006-07-20
IPC: C07D493/18 , A61K31/357 , C07D323/00 , C07D321/00 , C07D311/00 , A61P37/06
CPC classification number: C07D493/18
Abstract: Water-soluble artemisinin derivatives, their preparation methods, the pharmaceutical compositions containing them and the use thereof are disclosed. The artemisinin derivatives have the structure as following(formula I): These compounds and compositions have immuno-suppressive activities which has been proved by pharmacological test, and may be used to prepare novel immuno-suppressants for treating the diseases caused by hypofunction of human immunity( e. g. auto-immune diseases such as lupus erythematosus, rheumatoid arthritis, multiple sclerosis and the like), and may be useful as anti-rejection agents in organ transplantation.
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公开(公告)号:WO2006081771A1
公开(公告)日:2006-08-10
申请号:PCT/CN2006/000182
申请日:2006-01-27
IPC: C07D493/18 , A61K31/335 , C07D323/00 , C07D321/00 , C07D311/00 , A61P37/00
CPC classification number: C07D493/18
Abstract: The invention provides a artemisine derivative of the following formula I, its preparation method and use, as well as a pharmaceutical composition containing such artemisine derivative and its use. The artemisinin derivatives of the present invetion and the pharmaceutical compositions containing the same have immunosuppressive activities and can be used safely. The compositions which comprise the artemisine derivatives can be made into long-term dosage forms such as tablet, pellet and the like, and have widely productive and use value.
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公开(公告)号:WO2012149699A1
公开(公告)日:2012-11-08
申请号:PCT/CN2011/077462
申请日:2011-07-21
Applicant: 中兴通讯股份有限公司 , 周宇
Inventor: 周宇
IPC: H04W4/02
CPC classification number: H04W4/02
Abstract: 本发明公开了一种定时事务提醒的处理方法及装置,该方法包括:获取移动终端当前的定位信息;根据定位信息,更新移动终端的系统时间;根据更新后的系统时间,调整预先设置的定时事务提醒的时间。本发明可以简化操作并保证调整的准确性,提高用户体验。
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公开(公告)号:WO2012092808A1
公开(公告)日:2012-07-12
申请号:PCT/CN2011/084164
申请日:2011-12-16
Applicant: 深圳市众明半导体照明有限公司 , 周宇 , 赵西刚 , 薛信燊
IPC: F21S2/00 , F21V19/00 , F21V23/00 , F21V9/10 , F21Y101/02
CPC classification number: H01L27/156 , F21K9/90 , F21S2/005 , F21Y2113/13 , F21Y2115/10
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