HUP9903741A2 - Asztmaellenes, allergiaellenes, immunvisszaszorító és/vagy immunmoduláló hatású N-helyettesített indol-3-glioxilamidok - Google Patents
Asztmaellenes, allergiaellenes, immunvisszaszorító és/vagy immunmoduláló hatású N-helyettesített indol-3-glioxilamidokInfo
- Publication number
- HUP9903741A2 HUP9903741A2 HU9903741A HUP9903741A HUP9903741A2 HU P9903741 A2 HUP9903741 A2 HU P9903741A2 HU 9903741 A HU9903741 A HU 9903741A HU P9903741 A HUP9903741 A HU P9903741A HU P9903741 A2 HUP9903741 A2 HU P9903741A2
- Authority
- HU
- Hungary
- Prior art keywords
- antiallergic
- immunosuppressive
- glyoxylamid
- antiasthmatic
- immunomodulating effect
- Prior art date
Links
- 230000003266 anti-allergic effect Effects 0.000 title abstract 2
- 230000002519 immonomodulatory effect Effects 0.000 title abstract 2
- 230000001506 immunosuppresive effect Effects 0.000 title abstract 2
- -1 N-substituted indol-3-glyoxylamid Chemical class 0.000 title 1
- 230000001088 anti-asthma Effects 0.000 title 1
- 239000000924 antiasthmatic agent Substances 0.000 title 1
- DWLVFWDCSFTDOD-UHFFFAOYSA-N 2-(1h-indol-3-yl)-2-oxoacetic acid Chemical class C1=CC=C2C(C(=O)C(=O)O)=CNC2=C1 DWLVFWDCSFTDOD-UHFFFAOYSA-N 0.000 abstract 1
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 abstract 1
- 230000001387 anti-histamine Effects 0.000 abstract 1
- 239000000739 antihistaminic agent Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—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
- C07D209/22—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 with an aralkyl radical attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
A találmány (I) általánős képletű N-helyettesített indől-3-gliőxőlamidőkra, ezek előállítására és gyógyszerészeti alkalmazásűkravőnatkőzik. A vegyületek hisztamingátló, allergiaellenes ésimműngátló/imműnmődűláló hatással rendelkeznek. (I) ŕ
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19636150A DE19636150A1 (de) | 1996-09-06 | 1996-09-06 | N-substituierte Indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender Wirkung |
PCT/EP1997/004474 WO1998009946A1 (de) | 1996-09-06 | 1997-08-16 | N-substituierte indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender wirkung |
Publications (3)
Publication Number | Publication Date |
---|---|
HUP9903741A2 true HUP9903741A2 (hu) | 2000-04-28 |
HUP9903741A3 HUP9903741A3 (en) | 2001-01-29 |
HU227797B1 HU227797B1 (en) | 2012-03-28 |
Family
ID=7804772
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU9903741A HU227797B1 (en) | 1996-09-06 | 1997-08-16 | N-substituted indol-3-glyoxylamid with antiasthmatic, antiallergic and immunosuppressive/immunomodulating effect |
Country Status (26)
Country | Link |
---|---|
US (4) | US6008231A (hu) |
EP (1) | EP0931063B3 (hu) |
JP (1) | JP3296437B2 (hu) |
KR (1) | KR100516321B1 (hu) |
CN (3) | CN100376554C (hu) |
AR (1) | AR008630A1 (hu) |
AT (1) | ATE342889T1 (hu) |
AU (1) | AU726521B2 (hu) |
BR (1) | BR9712808B1 (hu) |
CA (1) | CA2215013C (hu) |
CZ (1) | CZ302301B6 (hu) |
DE (2) | DE19636150A1 (hu) |
DK (1) | DK0931063T5 (hu) |
ES (1) | ES2276433T7 (hu) |
HU (1) | HU227797B1 (hu) |
IL (1) | IL127798A (hu) |
NO (2) | NO314725B3 (hu) |
NZ (1) | NZ334476A (hu) |
PT (1) | PT931063E (hu) |
RU (1) | RU2237661C2 (hu) |
SK (1) | SK285618B6 (hu) |
TR (1) | TR199900469T2 (hu) |
TW (1) | TW550256B (hu) |
UA (1) | UA60312C2 (hu) |
WO (1) | WO1998009946A1 (hu) |
ZA (1) | ZA977475B (hu) |
Families Citing this family (52)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19636150A1 (de) * | 1996-09-06 | 1998-03-12 | Asta Medica Ag | N-substituierte Indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender Wirkung |
AP2000001929A0 (en) * | 1998-03-31 | 2000-09-30 | Inst For Pharm Discovery Inc | Substituted indolealkanoic acids. |
DE19946301A1 (de) | 1998-04-02 | 2001-04-19 | Asta Medica Ag | Indolyl-3-glyoxylsäure-Derivate mit therapeutisch wertvollen Eigenschaften |
CZ302588B6 (cs) * | 1998-04-02 | 2011-07-27 | Ziopharm Oncology, Inc. | Použití N-substituovaného indol-3-glyoxylamidu pro výrobu léciva |
DE19814838C2 (de) * | 1998-04-02 | 2001-01-18 | Asta Medica Ag | Indolyl-3-glyoxylsäure-Derivate mit Antitumorwirkung |
DE19818964A1 (de) * | 1998-04-28 | 1999-11-04 | Dresden Arzneimittel | Neue Hydroxyindole, deren Verwendung als Inhibitoren der Phospodiesterase 4 und Verfahren zu deren Herstellung |
DE19917504A1 (de) * | 1999-04-17 | 2000-10-19 | Dresden Arzneimittel | Verwendung von Hydroxyindolen, die Inhibitoren der Phosphodiesterase 4 sind, zur Therapie chronisch obstruktiver Lungenerkrankungen |
PT1076657E (pt) * | 1998-04-28 | 2004-11-30 | Elbion Ag | Novos hidroxi-indoles, sua utilizacao como inibidores da fosfodiesterase 4 e processo para a sua producao |
ATE320800T1 (de) | 1999-08-21 | 2006-04-15 | Altana Pharma Ag | Synergistische kombination von roflumilast und salmeterol |
TWI269654B (en) * | 1999-09-28 | 2007-01-01 | Baxter Healthcare Sa | N-substituted indole-3-glyoxylamide compounds having anti-tumor action |
DE19962300A1 (de) * | 1999-12-23 | 2001-06-28 | Asta Medica Ag | Substituierte N-Benzyl-Indol-3-yl-glyoxylsäure-Derivate mit Antitumorwirkung |
DE10022925A1 (de) * | 2000-05-11 | 2001-11-15 | Basf Ag | Substituierte Indole als PARP-Inhibitoren |
DE10037310A1 (de) | 2000-07-28 | 2002-02-07 | Asta Medica Ag | Neue Indolderivate und deren Verwendung als Arzneimittel |
AU2002323474B2 (en) * | 2001-09-13 | 2006-10-05 | Synta Pharmaceuticals Corp | 3-glyoxlylamideindoles for treating cancer |
RU2337906C2 (ru) * | 2001-12-03 | 2008-11-10 | Уайт | Ингибиторы цитозольной фосфолипазы а2 |
US6903104B2 (en) * | 2001-12-06 | 2005-06-07 | National Health Research Institutes | Indol-3-YL-2-oxoacetamide compounds and methods of use thereof |
CA2493755A1 (en) * | 2002-07-26 | 2004-02-05 | The Institutes For Pharmaceutical Discovery, Llc | Substituted indolealkanoic acids derivative and formulations containing same for use in treatment of diabetic complications |
HRP20050201A2 (en) * | 2002-08-01 | 2005-04-30 | Elbion Ag | Method for producing highly pure hydroxy indolyl glyoxylic acid amideslyoxylic acid amides |
DE10253426B4 (de) * | 2002-11-15 | 2005-09-22 | Elbion Ag | Neue Hydroxyindole, deren Verwendung als Inhibitoren der Phosphodiesterase 4 und Verfahren zu deren Herstellung |
WO2004087211A2 (en) | 2003-04-01 | 2004-10-14 | Applied Research Systems Ars Holding N.V. | Inhibitors of phosphodiesterases in infertility |
DE10318610A1 (de) * | 2003-04-24 | 2004-11-11 | Elbion Ag | 7-Azaindole und deren Verwendung als Therapeutika |
DE10318611A1 (de) * | 2003-04-24 | 2004-11-11 | Elbion Ag | 4-, 6- oder 7-Hydroxyindole mit N-Oxidgruppen und deren Verwendung als Therapeutika |
DE10318609A1 (de) * | 2003-04-24 | 2004-11-11 | Elbion Ag | 5-Hydroxyindole mit N-Oxidgruppen und deren Verwendung als Therapeutika |
US20050075364A1 (en) * | 2003-07-01 | 2005-04-07 | Kap-Sun Yeung | Indole, azaindole and related heterocyclic N-substituted piperazine derivatives |
DE10334040A1 (de) * | 2003-07-25 | 2005-03-10 | Zentaris Gmbh | Neue N-substituierte Indolyl-3-glyoxylsäureamide, deren Verwendung als Arzneimittel und Verfahren zu deren Herstellung |
MXPA06002853A (es) | 2003-09-11 | 2006-06-14 | Kemia Inc | Inhibidores citoquina. |
EP1768662A2 (en) | 2004-06-24 | 2007-04-04 | Novartis Vaccines and Diagnostics, Inc. | Small molecule immunopotentiators and assays for their detection |
DE102004031538A1 (de) * | 2004-06-29 | 2006-02-09 | Baxter International Inc., Deerfield | Pharmazeutische Darreichungsform zur oralen Verabreichung eines schwerlöslichen Wirkstoffs, Verfahren zu deren Herstellung und Kit |
AU2005304952B2 (en) * | 2004-11-08 | 2013-04-04 | Baxter Healthcare S.A. | Nanoparticulate compositions of tubulin inhibitors |
US20060100209A1 (en) * | 2004-11-09 | 2006-05-11 | Chong-Hui Gu | Formulations of 1-(4-benzoyl-piperazin-1-yl)-2-[4-methoxy-7-(3-methyl-[1,2,4]triazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-ethane-1,2-dione |
US20060100432A1 (en) * | 2004-11-09 | 2006-05-11 | Matiskella John D | Crystalline materials of 1-(4-benzoyl-piperazin-1-yl)-2-[4-methoxy-7-(3-methyl-[1,2,4]triazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-ethane-1,2-dione |
US9040558B2 (en) | 2004-12-31 | 2015-05-26 | Dr. Reddy's Laboratories Ltd. | Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors |
US8604055B2 (en) | 2004-12-31 | 2013-12-10 | Dr. Reddy's Laboratories Ltd. | Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors |
JP2006247963A (ja) * | 2005-03-09 | 2006-09-21 | Oji Paper Co Ltd | インクジェット記録用シート |
JP5385605B2 (ja) * | 2005-03-11 | 2014-01-08 | バーテックス ファーマシューティカルズ インコーポレイテッド | Atp結合カセットトランスポーターのモジュレーター |
US7392768B2 (en) | 2005-04-29 | 2008-07-01 | Tendix Development, Llc | Radial impulse engine, pump, and compressor systems, and associated methods of operation |
US20060280787A1 (en) * | 2005-06-14 | 2006-12-14 | Baxter International Inc. | Pharmaceutical formulation of the tubulin inhibitor indibulin for oral administration with improved pharmacokinetic properties, and process for the manufacture thereof |
US7598380B2 (en) * | 2005-08-03 | 2009-10-06 | Bristol-Myers Squibb Company | Method of preparation of azaindole derivatives |
ITMI20051999A1 (it) * | 2005-10-21 | 2007-04-22 | Eratech S R L | Formulazioni inalatorie di farmaci in fora di polvere secca per somministrazione come tale o con nebulizzatore e dotate di elevata erogabilita' respirabilita' e stabilita' |
US7851476B2 (en) * | 2005-12-14 | 2010-12-14 | Bristol-Myers Squibb Company | Crystalline forms of 1-benzoyl-4-[2-[4-methoxy-7-(3-methyl-1H-1,2,4-triazol-1-YL)-1-[(phosphonooxy)methyl]-1H-pyrrolo[2,3-C]pyridin-3-YL]-1,2-dioxoethyl]-piperazine |
US7807671B2 (en) | 2006-04-25 | 2010-10-05 | Bristol-Myers Squibb Company | Diketo-piperazine and piperidine derivatives as antiviral agents |
PL2359826T3 (pl) | 2006-07-05 | 2014-04-30 | Astrazeneca Ab | Połączenie inhibitora reduktazy HMG-CoA rosuwastatyny z inhibitorem fosfodiesterazy 4, takim jak roflumilast, N-tlenek roflumilastu, do leczenia chorób zapalnych płuc |
EP2610244A1 (en) | 2006-08-07 | 2013-07-03 | Ironwood Pharmaceuticals, Inc. | Indole compounds |
JP2010509237A (ja) * | 2006-11-02 | 2010-03-25 | アレテ セラピューティクス, インコーポレイテッド | 可溶性エポキシドヒドロラーゼ阻害剤 |
JP2010511041A (ja) * | 2006-11-28 | 2010-04-08 | ジオファーム オンコロジー, インコーポレイテッド | インジブリンを含むインドリル−3−グリオキシル酸誘導体の癌を処置するための単独またはさらなる薬剤との組み合わせでの使用 |
EP3563842A1 (en) | 2009-04-29 | 2019-11-06 | Amarin Pharmaceuticals Ireland Limited | Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same |
AR084433A1 (es) | 2010-12-22 | 2013-05-15 | Ironwood Pharmaceuticals Inc | Inhibidores de la faah y composiciones farmaceuticas que los contienen |
EP2744803A2 (en) | 2011-08-18 | 2014-06-25 | Dr. Reddy's Laboratories Ltd. | Substituted heterocyclic amine compounds as cholestryl ester-transfer protein (cetp) inhibitors |
US9000007B2 (en) | 2011-09-27 | 2015-04-07 | Dr. Reddy's Laboratories Ltd. | 5-benzylaminomethyl-6-aminopyrazolo [3, 4 -B] pyridine derivatives as cholesteryl ester-transfer protein (CETP) inhibitors useful for the treatment of atherosclerosis |
EP3165224A1 (en) | 2015-11-09 | 2017-05-10 | Albert-Ludwigs-Universität Freiburg | Use of pde4 inhibitors for the prophylaxis and/or therapy of dyslipoproteinaemia and related disorders |
WO2017089347A1 (en) | 2015-11-25 | 2017-06-01 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Methods and pharmaceutical compositions for the treatment of braf inhibitor resistant melanomas |
CN109000634B (zh) * | 2018-06-04 | 2022-06-03 | 上海智蕙林医疗科技有限公司 | 一种导航对象行进路线的提醒方法和系统 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB797258A (en) * | 1955-04-11 | 1958-06-25 | Upjohn Co | 3-substituted indoles |
GB944443A (hu) * | 1959-09-25 | 1900-01-01 | ||
GB1028812A (en) * | 1962-08-28 | 1966-05-11 | Ici Ltd | Indole derivatives |
GB1089071A (en) * | 1964-02-28 | 1967-11-01 | Merck & Co Inc | Indole derivatives |
US3686213A (en) * | 1970-08-28 | 1972-08-22 | American Cyanamid Co | Substituted aminoethyl indoles |
SU457698A1 (ru) * | 1972-10-20 | 1975-01-25 | Всесоюзный научно-исследовательский химико-фармацевтический институт им. Серго Орджоникидзе | Способ получени производных индолил-2-уксусной кислоты |
FR2689888B1 (fr) * | 1992-04-10 | 1994-06-10 | Rhone Poulenc Rorer Sa | Nouveaux derives de perhydroisoindole, leur preparation et les compositions pharmaceutiques qui les contiennent. |
IL113210A (en) * | 1994-04-01 | 2001-01-28 | Lilly Co Eli | 1H-indole-3- glyoxylamide spla2 inhibitors and pharmaceutical compositions containing them |
DE19636150A1 (de) * | 1996-09-06 | 1998-03-12 | Asta Medica Ag | N-substituierte Indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender Wirkung |
DE19946301A1 (de) * | 1998-04-02 | 2001-04-19 | Asta Medica Ag | Indolyl-3-glyoxylsäure-Derivate mit therapeutisch wertvollen Eigenschaften |
US7205299B2 (en) * | 2003-06-05 | 2007-04-17 | Zentaris Gmbh | Indole derivatives having an apoptosis-inducing effect |
-
1996
- 1996-09-06 DE DE19636150A patent/DE19636150A1/de not_active Ceased
-
1997
- 1997-08-16 SK SK271-99A patent/SK285618B6/sk not_active IP Right Cessation
- 1997-08-16 WO PCT/EP1997/004474 patent/WO1998009946A1/de active IP Right Grant
- 1997-08-16 DK DK97937586T patent/DK0931063T5/da active
- 1997-08-16 JP JP51216798A patent/JP3296437B2/ja not_active Expired - Fee Related
- 1997-08-16 TR TR1999/00469T patent/TR199900469T2/xx unknown
- 1997-08-16 RU RU99106782A patent/RU2237661C2/ru not_active IP Right Cessation
- 1997-08-16 UA UA99041907A patent/UA60312C2/uk unknown
- 1997-08-16 AU AU40158/97A patent/AU726521B2/en not_active Ceased
- 1997-08-16 NZ NZ334476A patent/NZ334476A/xx not_active IP Right Cessation
- 1997-08-16 EP EP97937586A patent/EP0931063B3/de not_active Expired - Lifetime
- 1997-08-16 AT AT97937586T patent/ATE342889T1/de active
- 1997-08-16 BR BRPI9712808-2A patent/BR9712808B1/pt not_active IP Right Cessation
- 1997-08-16 CN CNB971971285A patent/CN100376554C/zh not_active Expired - Fee Related
- 1997-08-16 CN CN2008100087226A patent/CN101219985B/zh not_active Expired - Fee Related
- 1997-08-16 CZ CZ0061699A patent/CZ302301B6/cs not_active IP Right Cessation
- 1997-08-16 KR KR10-1999-7001909A patent/KR100516321B1/ko not_active Expired - Fee Related
- 1997-08-16 PT PT97937586T patent/PT931063E/pt unknown
- 1997-08-16 CN CNB021320616A patent/CN100488948C/zh not_active Expired - Fee Related
- 1997-08-16 ES ES97937586T patent/ES2276433T7/es active Active
- 1997-08-16 DE DE59712752T patent/DE59712752D1/de not_active Expired - Lifetime
- 1997-08-16 IL IL12779897A patent/IL127798A/xx not_active IP Right Cessation
- 1997-08-16 HU HU9903741A patent/HU227797B1/hu not_active IP Right Cessation
- 1997-08-20 ZA ZA9707475A patent/ZA977475B/xx unknown
- 1997-09-04 CA CA002215013A patent/CA2215013C/en not_active Expired - Fee Related
- 1997-09-05 AR ARP970104064A patent/AR008630A1/es active IP Right Grant
- 1997-09-08 US US08/925,326 patent/US6008231A/en not_active Expired - Lifetime
- 1997-09-30 TW TW086112985A patent/TW550256B/zh not_active IP Right Cessation
-
1999
- 1999-03-04 NO NO19991071A patent/NO314725B3/no not_active IP Right Cessation
- 1999-09-30 US US09/409,263 patent/US6344467B1/en not_active Expired - Lifetime
-
2002
- 2002-01-30 US US10/058,836 patent/US20020161025A1/en not_active Abandoned
-
2003
- 2003-01-30 NO NO20030481A patent/NO20030481D0/no not_active Application Discontinuation
- 2003-04-01 US US10/402,931 patent/US6919344B2/en not_active Expired - Fee Related
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HUP9903741A2 (hu) | Asztmaellenes, allergiaellenes, immunvisszaszorító és/vagy immunmoduláló hatású N-helyettesített indol-3-glioxilamidok | |
WO2001072728A3 (en) | Novel piperazine derivatives | |
PT1193270E (pt) | Pirrolobenzodiazepinas | |
CY2488B1 (en) | New 4-(oxyalkoxyphenyl)-3-oxy-piperidines for trea. | |
MY134129A (en) | Polymorphs of an epothilone analog | |
ES2191208T3 (es) | Oxiimino-pregnano-carbolactonas. | |
CA2216796A1 (en) | Quinazoline derivatives | |
AP9801169A0 (en) | N-hydroxy-B-sulfonyl propionamide derivatives. | |
EP0680328A1 (en) | KETOCONAZOLE COMPOSITIONS FOR LOCAL USE. | |
FR2735127B1 (fr) | Nouvelles piperazines heteroaromatiques utiles comme medicaments. | |
MX9605206A (es) | 1alfa,26-dihidroxi-d-homo-vitamina d3. | |
FI980862A0 (fi) | Kiraalisia metyylifenyylioksatsolidinoneja | |
HUP9901616A3 (en) | Novel benzofuranone derivatives, process for their production and pharmaceutical compositions of the same | |
MY133112A (en) | 3-amino-3-arylpropan-1-ol derivatives, and their preparation and use | |
WO2002032901A3 (en) | Bridged piperazine derivatives | |
BR0114380A (pt) | Derivados-1-aminobutan-3-ol-substituìdos | |
MY133169A (en) | Substituted heterocyclic benzocycloalkenes and the use thereof as substances having an analgesic effect | |
GEP20032924B (en) | Novel Furan Diarylmethylidene Derivatives, Method for Their Preparation and Pharmaceutical Composition | |
EP0816366A4 (en) | IMIDAZOTHIAZOLE COMPOUNDS | |
NO961168L (no) | Nye uretanholdige aminosteroid forbindelser | |
TR199701298T1 (xx) | Tetralinler. | |
AP2002002595A0 (en) | Heterocyclic amide derivatives. | |
PT1246790E (pt) | Bases de mannich de 1- e 2-naftol substituido | |
AU6832498A (en) | Substituted benzyl oximino compounds | |
HUT77174A (hu) | Heterociklusos csoporttal szubsztituált 3-(indol-3-il)-akrilsav-származékok, mint NMDA antagonisták, és a vegyületeket tartalmazó gyógyszerkészítmények |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
GB9A | Succession in title |
Owner name: ZIOPHARM ONCOLOGY, INC., US Free format text: FORMER OWNER(S): ASTA MEDICA AKTIENGESELLSCHAFT, DE |
|
HC9A | Change of name, address |
Owner name: ZIOPHARM ONCOLOGY, INC., US Free format text: FORMER OWNER(S): ASTA MEDICA AKTIENGESELLSCHAFT, DE; ZIOPHARM ONCOLOGY, INC., US |
|
MM4A | Lapse of definitive patent protection due to non-payment of fees |