HUP0401644A2 - Aminobenzofenon-származékok, az ezeket tartalmazó gyógyszerkészítmények és alkalmazásuk - Google Patents
Aminobenzofenon-származékok, az ezeket tartalmazó gyógyszerkészítmények és alkalmazásukInfo
- Publication number
- HUP0401644A2 HUP0401644A2 HU0401644A HUP0401644A HUP0401644A2 HU P0401644 A2 HUP0401644 A2 HU P0401644A2 HU 0401644 A HU0401644 A HU 0401644A HU P0401644 A HUP0401644 A HU P0401644A HU P0401644 A2 HUP0401644 A2 HU P0401644A2
- Authority
- HU
- Hungary
- Prior art keywords
- group
- alkyl
- olefinic
- cyclic hydrocarbon
- same
- Prior art date
Links
- MAOBFOXLCJIFLV-UHFFFAOYSA-N (2-aminophenyl)-phenylmethanone Chemical class NC1=CC=CC=C1C(=O)C1=CC=CC=C1 MAOBFOXLCJIFLV-UHFFFAOYSA-N 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- -1 olefinic Chemical group 0.000 abstract 10
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 229940079593 drug Drugs 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical group [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 208000030507 AIDS Diseases 0.000 abstract 1
- 208000002874 Acne Vulgaris Diseases 0.000 abstract 1
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- 208000011231 Crohn disease Diseases 0.000 abstract 1
- 206010012438 Dermatitis atopic Diseases 0.000 abstract 1
- 201000005569 Gout Diseases 0.000 abstract 1
- 206010020751 Hypersensitivity Diseases 0.000 abstract 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 201000004681 Psoriasis Diseases 0.000 abstract 1
- 206010040070 Septic Shock Diseases 0.000 abstract 1
- 206010046851 Uveitis Diseases 0.000 abstract 1
- 206010000496 acne Diseases 0.000 abstract 1
- 208000026935 allergic disease Diseases 0.000 abstract 1
- 230000007815 allergy Effects 0.000 abstract 1
- 206010003246 arthritis Diseases 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 201000008937 atopic dermatitis Diseases 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 230000002757 inflammatory effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000036303 septic shock Effects 0.000 abstract 1
- 208000017520 skin disease Diseases 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
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- C07C225/02—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton
- C07C225/14—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being unsaturated
- C07C225/16—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
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- C07C225/22—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- C07C229/44—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton with carboxyl groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by unsaturated carbon chains
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Abstract
A találmány az aminobenzofenon-származékok új körére vonatkozik,ezeket tartalmazó gyógyászati készítményekre, a készítményekegységdózisaira, és a vegyületek alkalmazására gyógyszerek, különösenasztma, allergia, artritisz, reumatoid artritisz, köszvény,ateroszklerózis, krónikus gyulladásos bélbetegség (Crohn-kór),proliferatív és gyulladásos bőrrendellenességek, pszoriázis, atopiásdermatitisz, uveitisz, szeptikus sokk, AIDS, oszteoporózis és aknekezelésére vagy megelőzésére szolgáló gyógyszer előállítására. Atalálmány szerinti vegyületek az (I) általános képletnek megfelelőek -a képletben X jelentése oxigénatom; R1 jelentése halogénatom,hidroxil-, merkapto-, trifluormetil-, amino-, alkil-, olefines-,alkoxi-, alkiltio-, alkilamino-, alkoxikarbonil-, ciano-, -CONH2,fenil vagy nitrocsoport; R2 jelentése egy vagy több, azonos vagykülönböző helyettesítő, amelyek jelentése hidrogénatom, halogénatom,hidroxil-, merkapto-, trifluormetil-, amino-, alkil-, olefines-,alkoxi-, alkiltio-, alkilamino-, alkoxikarbonil-, ciano-, -CONH2,fenil- és/vagy nitrocsoport; R3 jelentése egy vagy több, azonos vagykülönböző helyettesítő, amelyek jelentése hidrogénatom, halogénatom,hidroxil-, merkapto-, trifluormetil-, ciano-, karboxil-, karbamoil-,nitro-, alkil-, olefines-, gyűrűs szénhidrogén-, alkoxi-, alkiltio-,alkoxikarbonil- és/vagy fenilcsoport; R4 jelentése hidrogénatom,alkil-, olefines-, gyűrűs szénhidrogén-csoport vagy -C(O)O-C(Rd)(Re)(-O-C(O)-R14)-; ahol az R14 csoport adott esetben egy vagy több, azonosvagy különböző R8 helyettesítővel helyettesített; R5 jelentése egyvagy több, azonos vagy különböző helyettesítő, amelyek hidrogénatomés/vagy az R1 helyettesítőre magadott jelentések; R6 jelentése alkil-heterogyűrűs csoport, alkil(gyűrűs szénhidrogén)-csoport,alkilcsoport, olefines csoport, gyűrűs szénhidrogéncsoport,heterogyűrűs csoport alkinilcsoport, Y1, R21, Y2R22 vagy Y4R24; aholaz alkilcsoport, az olefines csoport és a gyűrűs szénhidrogéncsoportegy vagy több azonos vagy különböző helyettesítővel helyettesítettek,és ahol az (alkil)heterogyűrűs csoport, az (alkil)(gyűrűsszénhidrogén)-csoport, a hetero gyűrűs csoport és a alkinilcsoportadott esetben egy vagy több, azonos vagy különböző helyettesítővelhelyettesítettek; azzal a megkötéssel, hogy a 2-klór-4-(2-[1,1,1-trifluormetil)fenilamino-2'-metil-benzofenon kizárt; valamint a fentivegyületek gyógyászati szempontból elfogadható sói és szolvátjai,például hidrátja. Ó
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31502501P | 2001-08-28 | 2001-08-28 | |
DKPA200200189 | 2002-02-08 | ||
PCT/DK2002/000557 WO2003018535A2 (en) | 2001-08-28 | 2002-08-26 | Novel aminobenzoephenones |
Publications (2)
Publication Number | Publication Date |
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HUP0401644A2 true HUP0401644A2 (hu) | 2004-11-29 |
HUP0401644A3 HUP0401644A3 (en) | 2008-03-28 |
Family
ID=26069134
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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HU0401644A HUP0401644A3 (en) | 2001-08-28 | 2002-08-26 | Aminobenzoephenones, pharmaceutical compositions containing them and use thereof |
Country Status (15)
Country | Link |
---|---|
US (1) | US7034015B2 (hu) |
EP (1) | EP1423356A2 (hu) |
JP (2) | JP4540984B2 (hu) |
KR (1) | KR100896667B1 (hu) |
CN (1) | CN100347151C (hu) |
AU (1) | AU2002331310B2 (hu) |
BR (1) | BR0212249A (hu) |
CA (1) | CA2458611C (hu) |
HK (1) | HK1068606A1 (hu) |
HU (1) | HUP0401644A3 (hu) |
IL (2) | IL160442A0 (hu) |
MX (1) | MXPA04001912A (hu) |
PL (1) | PL207487B1 (hu) |
RU (1) | RU2361855C2 (hu) |
WO (1) | WO2003018535A2 (hu) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7129229B2 (en) * | 2000-08-11 | 2006-10-31 | Nanogen Recognomics Gmbh | Hydrazide building blocks and hydrazide modified biomolecules |
MXPA04001912A (es) * | 2001-08-28 | 2004-07-23 | Leo Pharma As | Aminobenzofenonas novedosas. |
PL377377A1 (pl) * | 2002-12-20 | 2006-02-06 | Leo Pharma A/S | Nowe związki aminobenzofenonu |
CA2530302C (en) * | 2003-07-24 | 2013-12-03 | Leo Pharma A/S | Novel aminobenzophenone compounds |
MX2007006739A (es) | 2004-12-13 | 2007-08-02 | Leo Pharma As | Compuestos de aminobenzofenona sustituidos con triazol. |
DE102005022020A1 (de) * | 2005-05-12 | 2006-11-23 | Merckle Gmbh | Dibenzocycloheptanverbindungen und pharmazeutische Mittel, welche diese Verbindungen enthalten |
EP2206534A1 (de) | 2008-10-09 | 2010-07-14 | c-a-i-r biosciences GmbH | Dibenzocycloheptanonderivate und pharmazeutische Mittel, welche diese Verbindungen enthalten |
PL2484661T3 (pl) * | 2009-09-30 | 2017-10-31 | Toray Industries | Pochodna 2,3-dihydro-1h-inden-2-ylomocznika i jej zastosowanie farmaceutyczne |
BR112015009777A2 (pt) * | 2012-10-31 | 2017-07-11 | Fujifilm Corp | derivado de amina ou sal do mesmo |
WO2015126462A1 (en) * | 2014-02-19 | 2015-08-27 | Materia, Inc. | Preparation of surfactants via cross-metathesis |
US9758445B2 (en) * | 2013-04-09 | 2017-09-12 | Materia, Inc. | Preparation of surfactants via cross-metathesis |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS57177058A (en) | 1981-04-24 | 1982-10-30 | Hodogaya Chem Co Ltd | Novel fluoran compound |
AU702887B2 (en) * | 1995-10-31 | 1999-03-11 | Merck & Co., Inc. | Substituted pyridyl pyrroles, compositions containing such compounds and methods of use |
GB9701453D0 (en) * | 1997-01-24 | 1997-03-12 | Leo Pharm Prod Ltd | Aminobenzophenones |
JPH11349568A (ja) * | 1998-06-08 | 1999-12-21 | Maruho Co Ltd | ラクタム誘導体及びその医薬用途 |
CN1231459C (zh) | 1999-07-16 | 2005-12-14 | 里奥药物制品有限公司 | 新型氨基二苯酮 |
RU2247719C2 (ru) * | 1999-07-16 | 2005-03-10 | Лео Фармасьютикал Продактс Лтд.А/С (Левенс Кемиске Фабрик Продукционсактиесельскаб) | Аминобензофеноны как ингибиторы il-1 бета и tnf-альфа, фармацевтическая композиция и способ лечения и/или профилактики воспалительных заболеваний |
ATE277891T1 (de) * | 1999-07-16 | 2004-10-15 | Leo Pharma As | Aminobenzophenone als inhibitoren von il-1beta und tnf-alpha |
EP1202959B1 (en) * | 1999-07-16 | 2004-09-29 | Leo Pharma A/S | Aminobenzophenones as inhibitors of il-1-beta and tnf-alpha |
CA2379319A1 (en) | 1999-07-16 | 2001-01-25 | Leo Pharmaceutical Products Ltd. A/S (Lovens Kemiske Fabrik Produktionsa Ktieselskab) | Aminobenzophenones as inhibitors of il-1.beta. and tnf-.alpha. |
KR20020071876A (ko) * | 1999-12-06 | 2002-09-13 | 레오 파마 에이/에스 | IL-1β 및 TNF-α의 억제제로서의 아미노벤조페논 |
BR0111034A (pt) * | 2000-05-22 | 2003-06-17 | Leo Pharma S A | Composto, composição farmacêutica, uso de um composto, e, métodos para o tratamento ou profilaxia de condições ou doenças inflamatórias, para o tratamento e/ou profilaxia de osteoporose e para o tratamento de doenças relacionadas à aids |
US20020165286A1 (en) * | 2000-12-08 | 2002-11-07 | Hanne Hedeman | Dermal anti-inflammatory composition |
MXPA04001912A (es) * | 2001-08-28 | 2004-07-23 | Leo Pharma As | Aminobenzofenonas novedosas. |
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EP1423356A2 (en) | 2004-06-02 |
CA2458611A1 (en) | 2003-03-06 |
KR100896667B1 (ko) | 2009-05-14 |
HUP0401644A3 (en) | 2008-03-28 |
MXPA04001912A (es) | 2004-07-23 |
IL160442A (en) | 2011-11-30 |
WO2003018535A3 (en) | 2004-03-18 |
RU2361855C2 (ru) | 2009-07-20 |
RU2004109142A (ru) | 2005-08-20 |
CN1561327A (zh) | 2005-01-05 |
HK1068606A1 (en) | 2005-04-29 |
PL368686A1 (en) | 2005-04-04 |
US20030119902A1 (en) | 2003-06-26 |
BR0212249A (pt) | 2004-10-05 |
JP2010189410A (ja) | 2010-09-02 |
JP4540984B2 (ja) | 2010-09-08 |
PL207487B1 (pl) | 2010-12-31 |
JP2005500400A (ja) | 2005-01-06 |
US7034015B2 (en) | 2006-04-25 |
IL160442A0 (en) | 2004-07-25 |
AU2002331310B2 (en) | 2008-07-17 |
CA2458611C (en) | 2012-05-29 |
KR20040029455A (ko) | 2004-04-06 |
WO2003018535A2 (en) | 2003-03-06 |
CN100347151C (zh) | 2007-11-07 |
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