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公开(公告)号:US20090082343A1
公开(公告)日:2009-03-26
申请号:US12099779
申请日:2008-04-08
IPC分类号: A61K31/5415 , C07D401/04 , A61P9/00 , A61P1/00
CPC分类号: C07D417/04 , A61K31/5415 , C07D417/14
摘要: This invention provides a compound represented by the formula (I): wherein R1 is a hydrogen atom, a halogen atom, hydroxy, nitro, optionally halogenated alkyl, alkoxy optionally having substituents, acyl or amino optionally having substituents; R2 is pyridyl, furyl, thienyl, pyrrolyl, quinolyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolyl, tetrahydroquinolyl or thiazolyl, each of which may have substituents; n is 1 or 2; or a salt. And this invention provides a safe pharmaceutical comprising the compound of the formula (I), which has an excellent apoptosis inhibitory effect and MIF binding effect, for preventing and/or treating heart disease, nervous degenerative disease, cerebrovascular disease, central nervous infectious disease, traumatorathy, demyelinating disease, bone and articular disease, kidney disease, liver disease, osteomyelodysplasia, AIDS, cancer, and the like.
摘要翻译: 本发明提供由式(I)表示的化合物:其中R1是氢原子,卤素原子,羟基,硝基,任选卤代烷基,任选具有取代基的烷氧基,任选具有取代基的酰基或氨基; R 2是可以具有取代基的吡啶基,呋喃基,噻吩基,吡咯基,喹啉基,吡嗪基,嘧啶基,哒嗪基,吲哚基,四氢喹啉基或噻唑基。 n为1或2; 或盐。 本发明提供了一种安全药物,其包含具有优异的细胞凋亡抑制作用和MIF结合作用的式(I)化合物,用于预防和/或治疗心脏病,神经退行性疾病,脑血管病,中枢神经感染性疾病, 外伤,脱髓鞘疾病,骨和关节疾病,肾脏疾病,肝病,骨发育不良,艾滋病,癌症等。
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公开(公告)号:US07767665B2
公开(公告)日:2010-08-03
申请号:US12099779
申请日:2008-04-08
IPC分类号: C07D417/04 , A61K31/538
CPC分类号: C07D417/04 , A61K31/5415 , C07D417/14
摘要: This invention provides a compound represented by the formula (I): wherein R1 is a hydrogen atom, a halogen atom, hydroxy, nitro, optionally halogenated alkyl, alkoxy optionally having substituents, acyl or amino optionally having substituents; R2 is pyridyl, furyl, thienyl, pyrrolyl, quinolyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolyl, tetrahydroquinolyl or thiazolyl, each of which may have substituents; n is 1 or 2; or a salt. And this invention provides a safe pharmaceutical comprising the compound of the formula (I), which has an excellent apoptosis inhibitory effect and MIF binding effect, for preventing and/or treating heart disease, nervous degenerative disease, cerebrovascular disease, central nervous infectious disease, traumatorathy, demyelinating disease, bone and articular disease, kidney disease, liver disease, osteomyelodysplasia, AIDS, cancer, and the like.
摘要翻译: 本发明提供由式(I)表示的化合物:其中R1是氢原子,卤素原子,羟基,硝基,任选卤代烷基,任选具有取代基的烷氧基,任选具有取代基的酰基或氨基; R 2是可以具有取代基的吡啶基,呋喃基,噻吩基,吡咯基,喹啉基,吡嗪基,嘧啶基,哒嗪基,吲哚基,四氢喹啉基或噻唑基。 n为1或2; 或盐。 本发明提供一种安全药物,其包含具有优异的细胞凋亡抑制作用和MIF结合作用的式(I)化合物,用于预防和/或治疗心脏病,神经退行性疾病,脑血管病,中枢神经感染性疾病, 外伤,脱髓鞘疾病,骨和关节疾病,肾脏疾病,肝病,骨发育不良,艾滋病,癌症等。
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公开(公告)号:US07399759B2
公开(公告)日:2008-07-15
申请号:US10488384
申请日:2002-09-02
IPC分类号: C07D417/04 , A61K31/538
CPC分类号: C07D417/04 , A61K31/5415 , C07D417/14
摘要: This invention provides a compound represented by the formula (I): wherein R1 is a hydrogen atom, a halogen atom, hydroxy, nitro, optionally halogenated alkyl, alkoxy optionally having substituents, acyl or amino optionally having substituents; R2 is pyridyl, furyl, thienyl, pyrrolyl, quinolyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolyl, tetrahydroquinolyl or thiazolyl, each of which may have substituents; n is 1 or 2; or a salt. And this invention provides a safe pharmaceutical comprising the compound of the formula (I), which has an excellent apoptosis inhibitory effect and MIF binding effect, for preventing and/or treating heart disease, nervous degenerative disease, cerebrovascular disease, central nervous infectious disease, traumatorathy, demyelinating disease, bone and articular disease, kidney disease, liver disease, osteomyelodysplasia, AIDS, cancer, and the like.
摘要翻译: 本发明提供由式(I)表示的化合物:其中R 1是氢原子,卤素原子,羟基,硝基,任选卤代烷基,任选具有取代基的烷氧基,任选具有 取代基; R 2是吡啶基,呋喃基,噻吩基,吡咯基,喹啉基,吡嗪基,嘧啶基,哒嗪基,吲哚基,四氢喹啉基或噻唑基,它们各自可以具有取代基; n为1或2; 或盐。 本发明提供了一种安全药物,其包含具有优异的细胞凋亡抑制作用和MIF结合作用的式(I)化合物,用于预防和/或治疗心脏病,神经退行性疾病,脑血管病,中枢神经感染性疾病, 外伤,脱髓鞘疾病,骨和关节疾病,肾脏疾病,肝病,骨发育不良,艾滋病,癌症等。
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公开(公告)号:US20050032786A1
公开(公告)日:2005-02-10
申请号:US10488384
申请日:2002-09-02
IPC分类号: A61K31/5415 , A61P1/00 , A61P9/00 , A61P9/08 , A61P9/10 , A61P13/12 , A61P17/00 , A61P19/00 , A61P19/02 , A61P25/00 , A61P31/00 , A61P43/00 , C07D417/04 , C07D417/14 , C07D279/16
CPC分类号: C07D417/04 , A61K31/5415 , C07D417/14
摘要: This invention provides a compound represented by the formula (I): wherein R1 is a hydrogen atom, a halogen atom, hydroxy, nitro, optionally halogenated alkyl, alkoxy optionally having substituents, acyl or amino optionally having substituents; R2 is pyridyl, furyl, thienyl, pyrrolyl, quinolyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolyl, tetrahydroquinolyl or thiazolyl, each of which may have substituents; n is 1 or 2; or a salt. And this invention provides a safe pharmaceutical comprising the compound of the formula (I), which has an excellent apoptosis inhibitory effect and MIF binding effect, for preventing and/or treating heart disease, nervous degenerative disease, cerebrovascular disease, central nervous infectious disease, traumatorathy, demyelinating disease, bone and articular disease, kidney disease, liver disease, osteomyelodysplasia, AIDS, cancer, and the like.
摘要翻译: 本发明提供由式(I)表示的化合物:其中R 1为氢原子,卤素原子,羟基,硝基,任选卤代烷基,任选具有取代基的烷氧基,任选具有取代基的酰基或氨基; R 2是吡啶基,呋喃基,噻吩基,吡咯基,喹啉基,吡嗪基,嘧啶基,哒嗪基,吲哚基,四氢喹啉基或噻唑基,其各自可以具有取代基; n为1或2; 或盐。 本发明提供一种安全药物,其包含具有优异的细胞凋亡抑制作用和MIF结合作用的式(I)化合物,用于预防和/或治疗心脏病,神经退行性疾病,脑血管病,中枢神经感染性疾病, 外伤,脱髓鞘疾病,骨和关节疾病,肾脏疾病,肝病,骨发育不良,艾滋病,癌症等。
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公开(公告)号:US5883075A
公开(公告)日:1999-03-16
申请号:US680534
申请日:1996-07-09
IPC分类号: A61K38/00 , A61P3/06 , A61P9/00 , A61P9/12 , A61P11/00 , A61P13/02 , A61P15/00 , A61P29/00 , A61P35/00 , C07K7/64 , C07K14/575 , A61K38/12
CPC分类号: C07K14/57536 , C07K7/64 , A61K38/00 , Y02P20/55
摘要: Disclosed are (1) a cyclic hexapeptide represented by formula I or a salt thereof: ##STR1## wherein X and Y each represent .alpha.-amino acid residues, A represents a D-acidic-.alpha.-amino acid residue, B represents a neutral-.alpha.-amino acid residue, C represents an L-.alpha.-amino acid residue and D represents a D-.alpha.-amino acid residue having an aromatic ring group; and (2) a pharmaceutical composition comprising the peptide represented by formula I or a pharmaceutically aceptable salt thereof as an active ingredient.
摘要翻译: 公开了(1)由式I表示的环状六肽或其盐:其中X和Y各自表示α-氨基酸残基,A表示D-酸性-α-氨基酸残基,B表示中性 α-氨基酸残基,C代表L-α-氨基酸残基,D代表具有芳环基团的D-α-氨基酸残基; 和(2)包含由式I表示的肽或其药学上可接受的盐作为活性成分的药物组合物。
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公开(公告)号:US20120277204A1
公开(公告)日:2012-11-01
申请号:US13543207
申请日:2012-07-06
申请人: Takahiko TANIGUCHI , Akira Kawada , Mitsuyo Kondo , John F. Quinn , Jun Kunitomo , Masato Yoshikawa , Makoto Fushimi
发明人: Takahiko TANIGUCHI , Akira Kawada , Mitsuyo Kondo , John F. Quinn , Jun Kunitomo , Masato Yoshikawa , Makoto Fushimi
IPC分类号: A61K31/501 , C07D413/14 , A61K31/5377 , C07D401/14 , A61P25/18 , C07D409/04 , C07D405/14 , C07D409/14 , C07D403/14 , C07D403/04 , C07D413/04
CPC分类号: C07D403/04 , A61K9/2059 , C07D401/14 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/14 , C07D413/04 , C07D413/14
摘要: The present invention provides a compound which has the effect of PDE inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound of formula (I0), wherein R1 represents a substituent; R2 represents a hydrogen atom, or a substituent; R3 represents a hydrogen atom, or a substituent; Ring A represents an aromatic ring which can be substituted, and Ring B represents a 5-membered heteroaromatic ring which can be substituted, or a salt thereof.
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公开(公告)号:US20120028951A1
公开(公告)日:2012-02-02
申请号:US13148172
申请日:2010-02-04
申请人: Takahiko Taniguchi , Akira Kawada , Mitsuyo Kondo , John F. Quinn , Jun Kunitomo , Masato Yoshikawa , Makoto Fushimi
发明人: Takahiko Taniguchi , Akira Kawada , Mitsuyo Kondo , John F. Quinn , Jun Kunitomo , Masato Yoshikawa , Makoto Fushimi
IPC分类号: A61K31/501 , C07D413/14 , C07D401/14 , C07D403/14 , A61P25/18 , C07D405/04 , C07D409/04 , C07D405/14 , C07D409/14 , A61K31/5377 , C07D403/04 , C07D413/04
CPC分类号: C07D403/04 , A61K9/2059 , C07D401/14 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/14 , C07D413/04 , C07D413/14
摘要: The present invention provides a compound which has the effect of PDE inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound of formula (I0), wherein R1 represents a substituent; R2 represents a hydrogen atom, or a substituent; R3 represents a hydrogen atom, or a substituent; Ring A represents an aromatic ring which can be substituted, and Ring B represents a 5-membered heteroaromatic ring which can be substituted, or a salt thereof.
摘要翻译: 本发明提供具有PDE抑制作用的化合物,其可用作预防或治疗精神分裂症等的药物。 式(I0)的化合物,其中R1表示取代基; R2表示氢原子或取代基; R3表示氢原子或取代基; 环A表示可被取代的芳环,环B表示可被取代的5元杂芳环或其盐。
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公开(公告)号:US08778944B2
公开(公告)日:2014-07-15
申请号:US13543207
申请日:2012-07-06
申请人: Takahiko Taniguchi , Akira Kawada , John F. Quinn , Jun Kunitomo , Masato Yoshikawa , Makoto Fushimi
发明人: Takahiko Taniguchi , Akira Kawada , John F. Quinn , Jun Kunitomo , Masato Yoshikawa , Makoto Fushimi
IPC分类号: A61K31/50 , A61K31/501
CPC分类号: C07D403/04 , A61K9/2059 , C07D401/14 , C07D403/14 , C07D405/04 , C07D405/14 , C07D409/04 , C07D409/14 , C07D413/04 , C07D413/14
摘要: The present invention provides a compound which has the effect of PDE inhibition, and which is useful as a medicament for preventing or treating schizophrenia or so on. A compound of formula (I0), wherein R1 represents a substituent; R2 represents a hydrogen atom, or a substituent; R3 represents a hydrogen atom, or a substituent; Ring A represents an aromatic ring which can be substituted, and Ring B represents a 5-membered heteroaromatic ring which can be substituted, or a salt thereof.
摘要翻译: 本发明提供具有PDE抑制作用的化合物,其可用作预防或治疗精神分裂症等的药物。 式(I0)的化合物,其中R1表示取代基; R2表示氢原子或取代基; R3表示氢原子或取代基; 环A表示可被取代的芳环,环B表示可被取代的5元杂芳环或其盐。
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公开(公告)号:US4787709A
公开(公告)日:1988-11-29
申请号:US826588
申请日:1986-02-06
申请人: Akira Kawada , Takashi Yasumura , Toshio Koishi
发明人: Akira Kawada , Takashi Yasumura , Toshio Koishi
CPC分类号: C03C25/105 , C03C13/04 , G02B6/02033 , Y10T428/2962
摘要: The invention relates to an optical fiber of the step-index type using quartz glass or an inorganic optical glass as the core material and a fluorine-containing resin as the cladding material. A copolymer of vinylidene fluoride with hexafluoroacetone, preferably at a molar ratio in the range from 96:4 to 88:12, is employed as the cladding material. Using such a copolymer, a highly transparent and very strong and tough cladding layer can easily be formed by a solution coating method.
摘要翻译: 本发明涉及使用石英玻璃或无机光学玻璃作为芯材的分级折射型光纤,含氟树脂作为包层材料。 偏二氟乙烯与六氟丙酮的共聚物优选以96:4至88:12的摩尔比进行包覆材料。 使用这样的共聚物,可以通过溶液涂布法容易地形成高度透明且非常坚固和坚韧的包层。
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公开(公告)号:US4617350A
公开(公告)日:1986-10-14
申请号:US826373
申请日:1986-02-05
申请人: Kazuhiko Maeda , Akira Kawada
发明人: Kazuhiko Maeda , Akira Kawada
IPC分类号: C08L33/00 , C08L1/00 , C08L27/00 , C08L27/12 , C08L27/14 , C08L27/16 , C08L27/20 , C08L33/02 , C08L33/04 , C08L33/08
摘要: A thermoplastic resin composition useful for optical purposes is obtained by blending a polymer of an acrylic ester with a copolymer of vinylidene fluoride (VDF) and hexafluoroacetone (HFA). The blending ratio is not limited, though very good transparency is ensured when the acrylic ester polymer amounts to at least 20 wt %. It is preferable to use a polymer of an acrylic ester with an alkyl alcohol having not more than 4 carbon atoms. When using the resin composition in optical fibers or cylindrical lenses it is suitable to use a VDF/HFA copolymer containing not more than 20 mol % of HFA. The refractive index of a member formed of the resin composition is lower than that of the acrylic ester polymer and falls in the range of about 1.37-1.48. The resin composition is soluble in various organic solvents and accordingly can be used for adhesing and coating purposes too. Besides, this resin composition serves as a thermochromic material.
摘要翻译: 通过将丙烯酸酯的聚合物与偏二氟乙烯(VDF)和六氟丙酮(HFA)的共聚物共混而获得用于光学目的的热塑性树脂组合物。 共混比没有限制,但是当丙烯酸酯聚合物达到至少20重量%时,确保了非常好的透明度。 优选使用具有不超过4个碳原子的烷基醇的丙烯酸酯的聚合物。 当将光学纤维或圆柱形透镜中的树脂组合物使用时,适合使用含有不大于20mol%HFA的VDF / HFA共聚物。 由树脂组合物形成的部件的折射率低于丙烯酸酯聚合物的折射率,并且在约1.37-1.48的范围内。 树脂组合物可溶于各种有机溶剂,因此也可用于粘合和涂布。 此外,该树脂组合物用作热变色材料。
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