专利信息

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专利标题：Aqueous compositions comprising arbekacin

The invention provides aqueous liquid pharmaceutical compositions comprising arbekacin and chloride ions. The compositions are well tolerable for use in a method for treatment or prevention of a disease of the upper or lower respiratory tract, wherein the composition is aerosolized and inhaled by the patient. Furthermore, the invention provides arbekacin hydrochloride.

专利标题：Method for synthesizing dibekacin and arbekacin

专利权人：UNIV BEIJING CHEMICAL;

专利标题：AQUEOUS COMPOSITIONS COMPRISING ARBEKACIN

专利标题：Aqueous compositions comprising arbekacin

专利标题：The synthetic method of arbekacin and intermediate dibekacin thereof

专利标题：Composition for prevention or treatment of inner ear damage comprising an extract of piper longum l

PURPOSE: A composition containing a Piper longum L. extract for preventing and treating inner ear damage is provided to suppress the reduction of sensory hair cells. CONSTITUTION: A pharmaceutical composition for preventing and treating inner ear damage contains a Piper longum L. extract as an active ingredient. The inner ear damage is caused by apoptosis of sensory hair cells and is due to aminoglycoside antibiotics. The aminoglycoside antibiotics include amikacin arbekacin gentamycin kanamycin...

专利标题：New synthetic method of arbekacin and intermediate of dibekacin thereof

专利标题：Convenient high-yield Arbekacin synthesis method

专利标题：A kind of slow releasing injection that contains arbekacin

专利标题：Dibekacin derivative or arbekacin derivative effective for resistant bacteria and their production

专利权人：MICROBIAL CHEM RES FOUND;

PURPOSE: To obtain a new compound useful for treating microbial infectious diseases as a chemotherapeutic agent having a broad antibacterial activity against not only methicillin resistant staphylococci but also against Gram positive and Gram negative bacteria while having low toxicity.CONSTITUTION: The objective compound is expressed by formula I (R is hydroxyl or H) or its salt e.g. 2''-amino-2''-deoxyarbekacin. This compound can be obtained as follows: Amino groups at sites 1 and 3'' of 2'6'-...

当前查询条件: [药品] 包含 'Arbekacin'

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!	专利类型	发明实用新型外观设计
!	公开号			CN1234
!	申请号			CN1234
!	专利标题		扩展	PHARMA
!	专利权人		扩展	pfizer
	发明人
!	申请日			yyyymmdd
!	公开日			yyyymmdd
	优先权号
!	摘要		扩展	PHARMA
	IPC			A01B

1. AU2012307661A1	2014/2/20	AU20120307661	2012/8/3
专利标题：Aqueous compositions comprising arbekacin 专利权人：PARI PHARMA GMBH;MEIJI SEIKA PHARMA CO LTD; The invention provides aqueous liquid pharmaceutical compositions comprising arbekacin and chloride ions. The compositions are well tolerable for use in a method for treatment or prevention of a disease of the upper or lower respiratory tract, wherein the composition is aerosolized and inhaled by the patient. Furthermore, the invention provides arbekacin hydrochloride.

2. CN103204887A	2013/7/17	CN20131125488	2013/4/11
专利标题：Method for synthesizing dibekacin and arbekacin 专利权人：UNIV BEIJING CHEMICAL;

3. WO2013037566A1	2013/3/21	WO2012EP65265	2012/8/3
专利标题：AQUEOUS COMPOSITIONS COMPRISING ARBEKACIN 专利权人：MEIJI SEIKA PHARMA CO LTD [JP];PARI PHARMA GMBH [DE];YAGI YUKIHIRO [JP];TANAKA MASASHI [JP];SUGANO TOSHIE [JP];SHOJI KUNIKO [JP];SANO NAO [JP];KELLER MANFRED [DE];HAHN MICHAEL [DE];EGLE ROMAN [DE]; The invention provides aqueous liquid pharmaceutical compositions comprising arbekacin and chloride ions. The compositions are well tolerable for use in a method for treatment or prevention of a disease of the upper or lower respiratory tract, wherein the composition is aerosolized and inhaled by the patient. Furthermore, the invention provides arbekacin hydrochloride.

4. EP2567691A1	2013/3/13	EP20110180927	2011/9/12
专利标题：Aqueous compositions comprising arbekacin 专利权人：MEIJI SEIKA PHARMA CO LTD [JP];PARI PHARMA GMBH [DE]; The invention provides aqueous liquid pharmaceutical compositions comprising arbekacin and chloride ions. The compositions are well tolerable for use in a method for treatment or prevention of a disease of the upper or lower respiratory tract, wherein the composition is aerosolized and inhaled by the patient. Furthermore, the invention provides arbekacin hydrochloride.

5. CN101575354B	2013/3/13
专利标题：The synthetic method of arbekacin and intermediate dibekacin thereof 专利权人：BEIJING UNIVERSITY OF CHEMICAL TECHNOLOGY;

6. KR20130004949A	2013/1/15	KR20110065870	2011/7/4
专利标题：Composition for prevention or treatment of inner ear damage comprising an extract of piper longum l 专利权人：Dongguk University Industry-academic Cooperation Foundation; PURPOSE: A composition containing a Piper longum L. extract for preventing and treating inner ear damage is provided to suppress the reduction of sensory hair cells. CONSTITUTION: A pharmaceutical composition for preventing and treating inner ear damage contains a Piper longum L. extract as an active ingredient. The inner ear damage is caused by apoptosis of sensory hair cells and is due to aminoglycoside antibiotics. The aminoglycoside antibiotics include amikacin arbekacin gentamycin kanamycin...

7. CN102786564A	2012/11/21	CN20111131544	2011/5/19
专利标题：New synthetic method of arbekacin and intermediate of dibekacin thereof 专利权人：UNIV BEIJING CHEMICAL;QILU TIANHE PHARMACEUTICAL CO LTD;

8. CN102190690A	2011/9/21	CN2011182052	2011/4/1
专利标题：Convenient high-yield Arbekacin synthesis method 专利权人：FUZHOU BORNI PHARMACEUTICAL SCI & TECH CO LTD;

9. CN101278901A	2008/10/8
专利标题：A kind of slow releasing injection that contains arbekacin 专利权人：Jinan Shuaihua Pharmaceutical Technology Co., Ltd.;

10. JP3215732B2	2001/10/9
专利标题：Dibekacin derivative or arbekacin derivative effective for resistant bacteria and their production 专利权人：MICROBIAL CHEM RES FOUND; PURPOSE: To obtain a new compound useful for treating microbial infectious diseases as a chemotherapeutic agent having a broad antibacterial activity against not only methicillin resistant staphylococci but also against Gram positive and Gram negative bacteria while having low toxicity.CONSTITUTION: The objective compound is expressed by formula I (R is hydroxyl or H) or its salt e.g. 2''-amino-2''-deoxyarbekacin. This compound can be obtained as follows: Amino groups at sites 1 and 3'' of 2'6'-...

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