HUP9800051A2 - 1-Aril-2-acil-amino-etán-vegyületek, alkalmazásuk neurokinin-antagonista gyógyszerkészítmények előállítására és a vegyületeket tartalmazó gyógyszerkészítmények - Google Patents
1-Aril-2-acil-amino-etán-vegyületek, alkalmazásuk neurokinin-antagonista gyógyszerkészítmények előállítására és a vegyületeket tartalmazó gyógyszerkészítményekInfo
- Publication number
- HUP9800051A2 HUP9800051A2 HU9800051A HUP9800051A HUP9800051A2 HU P9800051 A2 HUP9800051 A2 HU P9800051A2 HU 9800051 A HU9800051 A HU 9800051A HU P9800051 A HUP9800051 A HU P9800051A HU P9800051 A2 HUP9800051 A2 HU P9800051A2
- Authority
- HU
- Hungary
- Prior art keywords
- powder
- aryl
- neurokinin
- pipe
- medicaments
- Prior art date
Links
- 239000003814 drug Substances 0.000 title 2
- 239000005557 antagonist Substances 0.000 title 1
- 239000000843 powder Substances 0.000 abstract 15
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 150000001412 amines Chemical class 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 229940127387 Neurokinin 1 Antagonists Drugs 0.000 abstract 1
- HEAUFJZALFKPBA-YRVBCFNBSA-N Neurokinin A Chemical compound C([C@@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(N)=O)C(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CC=1NC=NC=1)C(C)O)C1=CC=CC=C1 HEAUFJZALFKPBA-YRVBCFNBSA-N 0.000 abstract 1
- 102400000097 Neurokinin A Human genes 0.000 abstract 1
- 101800000399 Neurokinin A Proteins 0.000 abstract 1
- 125000004450 alkenylene group Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 208000024891 symptom Diseases 0.000 abstract 1
Classifications
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
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- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
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- C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
- C07C255/29—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton containing cyano groups and acylated amino groups bound to the carbon skeleton
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- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
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Abstract
A találmány tárgya (I) általánős képletű vegyületekre és azők sóiravőnatkőzik - ahől a képletbenR1jelentése arilcsőpőrt vagy heterőarilcsőpőrt,R2jelentése hidrőgénatőm, rövid szénláncú alkilcsőpőrt vagy aril-rövidszénláncú alkilcsőpőrt,R3jelentése hidrőgénatőm, rövid szénláncú alkilcsőpőrt, arilcsőpőrt vagyheterőarilcsőpőrt,R4jelentése arilcsőpőrt vagy heterőarilcsőpőrt,Xjelentése 1-7 szénatőmős alkiléncsőpőrt, 2-7 szénatőmősalkeniléncsőpőrt vagy 4-7 szénatőmős alkándieniléncsőpőrt, ésAmjelentése szűbsztitűálatlan vagy mőnő- vagy diszűbsztitűáltaminőcsőpőrt, ahől a diszűbsztitűált aminőcsőpőrt alatt őlyanaminőcsőpőrtőt is értenek, amelynek az aminő nitrőgénje egy gyűrűbekapcsőlódik -.A találmány szerinti vegyületek neűrőkinin-1 antagőnisták, és ezértalkalmasak őlyan betegségtünetek megegőzésére, amelyeket több között Panyag és a neűrőkinin A idéznek elő.(I)ŕ
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95810117 | 1995-02-22 | ||
PCT/EP1996/000555 WO1996026183A1 (en) | 1995-02-22 | 1996-02-09 | 1-aryl-2-acylamino-ethane compounds and their use as neurokinin especially neurokinin 1 antagonists |
Publications (3)
Publication Number | Publication Date |
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HUP9800051A2 true HUP9800051A2 (hu) | 1998-05-28 |
HUP9800051A3 HUP9800051A3 (en) | 1998-08-28 |
HU226562B1 HU226562B1 (en) | 2009-04-28 |
Family
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Application Number | Title | Priority Date | Filing Date |
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HU9800051A HU226562B1 (en) | 1995-02-22 | 1996-02-09 | 1-aryl-2-acylamino-ethane compounds as neurokinin, especially neurokinin-1 antagonists, and medicaments containing the said compounds. |
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US (1) | US5929067A (hu) |
EP (1) | EP0810991B1 (hu) |
JP (1) | JP3506714B2 (hu) |
KR (1) | KR100389253B1 (hu) |
CN (1) | CN1081625C (hu) |
AT (1) | ATE178886T1 (hu) |
AU (1) | AU701560B2 (hu) |
BR (1) | BR9607335A (hu) |
CA (1) | CA2213080C (hu) |
CY (1) | CY2198B1 (hu) |
CZ (1) | CZ288345B6 (hu) |
DE (1) | DE69602087T2 (hu) |
DK (1) | DK0810991T3 (hu) |
EA (1) | EA002348B1 (hu) |
ES (1) | ES2132882T3 (hu) |
FI (1) | FI120304B (hu) |
GR (1) | GR3030626T3 (hu) |
HU (1) | HU226562B1 (hu) |
IL (1) | IL117209A (hu) |
MX (1) | MX9706394A (hu) |
NO (1) | NO325605B1 (hu) |
NZ (1) | NZ300942A (hu) |
PL (1) | PL184226B1 (hu) |
SK (1) | SK282237B6 (hu) |
TR (1) | TR199700834T1 (hu) |
WO (1) | WO1996026183A1 (hu) |
ZA (1) | ZA961364B (hu) |
Families Citing this family (17)
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JP2000511193A (ja) * | 1996-05-24 | 2000-08-29 | イーライ・リリー・アンド・カンパニー | 高血圧の処置法 |
MY132550A (en) | 1996-08-22 | 2007-10-31 | Novartis Ag | Acylaminoalkenylene-amide derivatives as nk1 and nk2 antogonists |
GB0010958D0 (en) * | 2000-05-05 | 2000-06-28 | Novartis Ag | Organic compounds |
GB0203061D0 (en) * | 2002-02-08 | 2002-03-27 | Novartis Ag | Organic compounds |
GB2394417A (en) * | 2002-10-24 | 2004-04-28 | Novartis Ag | Solid dispersion comprising a piperidine substance P antagonist and a carrier |
GB0224788D0 (en) * | 2002-10-24 | 2002-12-04 | Novartis Ag | Organic compounds |
TWI356821B (en) * | 2003-12-01 | 2012-01-21 | Cambridge Entpr Ltd | Anti-inflammatory agents |
US20090156465A1 (en) | 2005-12-30 | 2009-06-18 | Sattigeri Jitendra A | Derivatives of beta-amino acid as dipeptidyl peptidase-iv inhibitors |
GB0607532D0 (en) * | 2006-04-13 | 2006-05-24 | Novartis Ag | Organic compounds |
JO2630B1 (en) | 2006-04-13 | 2012-06-17 | نوفارتيس ايه جي | Organic compounds |
JP4983616B2 (ja) | 2008-01-16 | 2012-07-25 | ソニー株式会社 | 熱転写記録媒体 |
ES2672099T3 (es) | 2011-07-04 | 2018-06-12 | Irbm - Science Park S.P.A. | Antagonistas del receptor NK-1 para el tratamiento de la neovascularización corneal |
EP3109239A4 (en) * | 2014-02-18 | 2017-07-05 | Daiichi Sankyo Company, Limited | Aminopyrazolone derivative |
US20210015834A1 (en) | 2018-02-26 | 2021-01-21 | Ospedale San Raffaele S.R.L. | Nk-1 antagonists for use in the treatment of ocular pain |
RU2697414C1 (ru) * | 2018-05-11 | 2019-08-14 | Общество с ограниченной ответственностью "АЙ БИ ДИ Терапевтикс" | Новый антагонист тахикининовых рецепторов и его применение |
WO2021150499A1 (en) | 2020-01-20 | 2021-07-29 | Monomer Software LLC | Optical device field of view cleaning apparatus |
US20230134843A1 (en) | 2020-03-11 | 2023-05-04 | Ospedale San Raffaele S.R.L. | Treatment of stem cell deficiency |
Family Cites Families (4)
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AU7880991A (en) * | 1990-05-10 | 1991-11-27 | Novo Nordisk A/S | A pharmaceutical preparation containing n-glycofurols and n-ethylene glycols |
US5472978A (en) * | 1991-07-05 | 1995-12-05 | Merck Sharp & Dohme Ltd. | Aromatic compounds, pharmaceutical compositions containing them and their use in therapy |
MY110227A (en) * | 1991-08-12 | 1998-03-31 | Ciba Geigy Ag | 1-acylpiperindine compounds. |
US5217996A (en) * | 1992-01-22 | 1993-06-08 | Ciba-Geigy Corporation | Biaryl substituted 4-amino-butyric acid amides |
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