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公开(公告)号:US3992376A
公开(公告)日:1976-11-16
申请号:US496618
申请日:1974-08-12
申请人: Peter Stoss , Gerhard Satzinger , Manfred Herrmann
发明人: Peter Stoss , Gerhard Satzinger , Manfred Herrmann
IPC分类号: A61K31/38 , A61K31/381 , A61K31/382 , A61K31/385 , A61K31/39 , A61K31/445 , A61K31/54 , A61K31/5415 , A61P7/10 , A61P11/14 , A61P25/20 , A61P43/00 , C07D279/34 , C07D285/38 , C07D327/08 , C07D333/76 , C07D335/12 , C07D337/12 , C07D339/08 , C07D279/10
CPC分类号: C07D279/34 , C07D327/08 , C07D333/76 , C07D335/12 , C07D339/08
摘要: The present invention is concerned with novel tricyclic sulphoximides and with the preparation thereof. This family of compounds has been found to possess antihistaminic, antitussive, antiinflammatory, sedative, and diuretic properties.
摘要翻译: 本发明涉及新型三环磺酰亚胺及其制备方法。 已发现这一化合物族具有抗组胺,镇咳,抗炎,镇静,利尿等特性。
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公开(公告)号:US3978109A
公开(公告)日:1976-08-31
申请号:US387860
申请日:1973-08-09
IPC分类号: C07C101/04
摘要: The present invention relates to a process for 3r-N-Monomethylamino-4 cis-phenyl-4 trans-ethoxycarbonyl-cyclohexene and its N-substitution products which are generally useful as analgesics.
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公开(公告)号:US3978052A
公开(公告)日:1976-08-31
申请号:US496600
申请日:1974-08-12
申请人: Peter Stoss , Gerhard Satzinger
发明人: Peter Stoss , Gerhard Satzinger
IPC分类号: C07B61/00 , C07D279/34 , C07D281/14 , C07D327/08 , C07D333/76 , C07D335/12 , C07D335/16 , C07D337/14 , C07D339/00 , C07D339/08 , C07D279/20 , C07D279/22 , C07D279/30
CPC分类号: C07D327/08 , C07D333/76 , C07D339/08 , Y10S514/869
摘要: The present invention is concerned with tricyclic sulphoximides and with the preparation thereof. This family of compounds has been found to possess antihistominic, antitussive, antiinflammatory, sedative, and diuretic properties.
摘要翻译: 本发明涉及三环磺酰亚胺及其制备。 已经发现这种化合物家族具有抗真菌,止咳,抗炎,镇静和利尿的特性。
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64.
公开(公告)号:US3957851A
公开(公告)日:1976-05-18
申请号:US226509
申请日:1972-02-15
IPC分类号: C07D211/14 , C07D211/34 , C07D211/46 , C07D295/155 , C07C101/38
CPC分类号: C07D295/155 , C07D211/14 , C07D211/34 , C07D211/46
摘要: The invention relates to 1-phenyl-4-amino-cyclohex-2-ene-1-carboxylic-acid-esters of the general formula I ##SPC1##wherein R.sub.1 and R.sub.2 may be the same or different and may be H, alkyl, hydroxyalkyl, alkenyl, preferably with 1 to 4 C-atoms, aralkyl which may be bonded to each other, in which connection the heterocyclic system formed may be substituted further by the OH-- group and where attachment takes place by an oxygen or a nitrogen atom, if desired, which in its turn carries an H, alkyl with 1 to 4 C-atoms, aryl which may be substituted by chlorine, preferably in 3 or 4-position, and by methoxy, preferably in 2 or 4-position, acyl, preferably alkanoyl with 1 to 4 C-atoms, and aroyl, or aralkyl, and R.sub.3 represents an alkyl radical with 1 to 4 C-atoms, the salts thereof and quarternary ammonium compounds, and a process for their preparation. These compounds have analgesic and neuroleptic properties.
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公开(公告)号:US4861770A
公开(公告)日:1989-08-29
申请号:US150578
申请日:1988-02-01
IPC分类号: C07D281/10 , A61K31/55 , A61K31/554 , A61P31/12 , A61P31/18 , A61P37/00
CPC分类号: A61K31/55
摘要: The use of benzothiazepine derivatives for the protection of lymphocytes in humans and higher mammals, especially in the treatment of acquired immune deficiency syndrome.
摘要翻译: 使用苯并硫氮杂衍生物保护人类和更高级哺乳动物中的淋巴细胞,特别是治疗获得性免疫缺陷综合征。
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公开(公告)号:US4110448A
公开(公告)日:1978-08-29
申请号:US719317
申请日:1976-08-31
申请人: Peter Stoss , Gerhard Satzinger , Manfred Herrmann
发明人: Peter Stoss , Gerhard Satzinger , Manfred Herrmann
IPC分类号: C07D279/34 , C07D327/08 , C07D333/76 , C07D335/12 , C07D339/08 , A61K31/54 , A61K31/38 , A61K31/385 , A61K31/39
CPC分类号: C07D333/76 , C07D279/34 , C07D327/08 , C07D335/12 , C07D339/08 , Y10S514/849 , Y10S514/869
摘要: The present invention is concerned with novel tricyclic sulphoximides and with the preparation thereof. This family of compounds has been found to possess antihistaminic, antitussive, antiinflammatory, sedative, and diuretic properties.
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公开(公告)号:US4082770A
公开(公告)日:1978-04-04
申请号:US785809
申请日:1977-04-08
IPC分类号: C07D333/70 , C07D333/64
CPC分类号: C07D333/70
摘要: The present invention relates to novel benzo(b)thiophene derivatives of the general formula: ##STR1## wherein Y represents a hydrogen or halogen atom; A represents a hydrogen atom or a phenyl group which may be substituted with a halogen atom or a lower alkoxy group; B represents a radical of the formula OR' or NR.sup.2 R.sup.3, wherein R' is an alkyl radical of 1 to 5 carbon atoms which may be substituted with hydroxy, lower alkoxy, phenyl or phenoxy groups or a cycloalkyl or phenyl group which may be substituted by lower alkoxy or halogen atoms; R.sup.2 and R.sup.3, which may be identical or different, represent, if identical, hydrogen, alkyl radicals of 1 to 5 carbon atoms which may be substituted by hydroxy, lower alkoxy, phenoxy, di-lower alkylamino, or phenyl groups; or, if R.sup.2 is hydrogen, R.sup.3 represents either a hydroxyl or an amino group which may be substituted by lower alkyl, dialkyl, alkylidene, phenyl or acyl groups or a lower alkyl group which may be substituted by hydroxy, lower alkoxy, phenoxy, dialkylamino, pyrrolidino, piperidino or morpholino groups; R.sup.3 further is a cycloalkyl or phenyl group, which may be substituted by a halogen or a lower alkoxy radical; R.sup.2 and R.sup.3 together with the nitrogen atom to which they are attached, may form an aziridine, pyrrolidine, piperidine, morpholine or piperazine ring which may be substituted by lower alkyl, hydroxyalkyl, phenylalkyl, phenyl or acetyl groups; or A and B together with the C--N group may form a 5, 6, or 7-membered heterocyclic ring.The present invention further relates to the processes for the preparation of these derivatives and to the salts of these compounds with physiologically acceptable inorganic and organic acids such as hydrochloric acid, sulfuric acid, phosphoric acid, fumaric acid, oxalic acid, citric acid, etc., and the quaternary ammonium compounds.
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公开(公告)号:US4076937A
公开(公告)日:1978-02-28
申请号:US696665
申请日:1976-06-16
IPC分类号: C07D211/14 , C07D221/20 , C07D295/088 , C07D295/10
CPC分类号: C07D221/20 , C07D211/14 , C07D295/088
摘要: The present invention is concerned with new dibenzylglycolic acid derivatives and with the preparation thereof. These derivatives show an extraordinary anti-hypertensive and antisecretory profile.
摘要翻译: 本发明涉及新的二苄基乙醇酸衍生物及其制备方法。 这些衍生物显示出非凡的抗高血压和抗分泌性。
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公开(公告)号:US4076723A
公开(公告)日:1978-02-28
申请号:US769641
申请日:1977-02-17
申请人: Peter Stoss , Gerhard Satzinger
发明人: Peter Stoss , Gerhard Satzinger
IPC分类号: C07D333/76 , C07D337/14 , C07D335/12 , C07D335/16
CPC分类号: C07D333/76
摘要: The present invention is concerned with novel tricyclic sulphoximides and with the preparation thereof. This family of compounds has been found to possess antihistominic, antitussive, antiinflammatory, sedative, and diuretic properties.
摘要翻译: 本发明涉及新型三环磺酰亚胺及其制备方法。 已经发现这种化合物家族具有抗真菌,止咳,抗炎,镇静和利尿的特性。
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公开(公告)号:US4033981A
公开(公告)日:1977-07-05
申请号:US663312
申请日:1976-03-03
申请人: Peter Stoss , Gerhard Satzinger
发明人: Peter Stoss , Gerhard Satzinger
IPC分类号: C07D333/76 , C07D339/08 , C07D327/08
CPC分类号: C07D333/76
摘要: The present invention is concerned with novel tricyclic sulphoximides and with the preparation thereof. This family of compounds has been found to possess antihistominic, antitussive, antiinflammatory, sedative, and diuretic properties.
摘要翻译: 本发明涉及新型三环磺酰亚胺及其制备方法。 已经发现这种化合物家族具有抗真菌,止咳,抗炎,镇静和利尿的特性。
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