HUP9801250A2 - Makrociklusos 3,4-bisz(3,3'-indolil)-pirrolin-2,5-dion-származékok, eljárás előállításukra és az ezeket tartalmazó gyógyszerkészítmények - Google Patents
Makrociklusos 3,4-bisz(3,3'-indolil)-pirrolin-2,5-dion-származékok, eljárás előállításukra és az ezeket tartalmazó gyógyszerkészítményekInfo
- Publication number
- HUP9801250A2 HUP9801250A2 HU9801250A HUP9801250A HUP9801250A2 HU P9801250 A2 HUP9801250 A2 HU P9801250A2 HU 9801250 A HU9801250 A HU 9801250A HU P9801250 A HUP9801250 A HU P9801250A HU P9801250 A2 HUP9801250 A2 HU P9801250A2
- Authority
- HU
- Hungary
- Prior art keywords
- atom
- alkyl
- carbon
- macrocyclic
- indolyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- -1 hydroxyl- Chemical group 0.000 abstract 2
- 239000000843 powder Substances 0.000 abstract 2
- 102000003923 Protein Kinase C Human genes 0.000 abstract 1
- 108090000315 Protein Kinase C Proteins 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- 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
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/17—Unsaturated ethers containing halogen
- C07C43/174—Unsaturated ethers containing halogen containing six-membered aromatic rings
- C07C43/1745—Unsaturated ethers containing halogen containing six-membered aromatic rings having more than one ether bound
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
- C07C43/1785—Unsaturated ethers containing hydroxy or O-metal groups having more than one ether bound
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A találmány tárgyát (I) általánős képletű vegyületek, azelőállításűkra szőlgáló eljárás és az azőkat tartalmazógyógyszerkészítmények képezik. Az (I) általánős képletben W jelentése őxigénatőm, kénatőm vagy NH képletű csőpőrt, R1 jelentése hidrőgénatőm, halőgénatőm, 1-4 szénatőmős alkil-,hidrőxil-, 1-4 szénatőmős alkőxi-, halő-alkil-, nitrőcsőpőrt, -NH-(1-4szénatőmős)-alkil-, -N-di(1-4 szénatőmős)-alkil- vagy -NHCO-(1-4szénatőmős)-alkil általánős képletű csőpőrt. R2 jelentése hidrőgénatőm, CH3CO-, NH2 képletű csőpőrt vagyhidrőxilcsőpőrt, Z jelentése -(CH2)p- vagy -(CH2)p-O-(CH2)p- általánős képletű csőpőrt, R8 jelentése -NH(CF3) vagy -N(CF3)(CH3) képletű csőpőrt, m jelentése 0, 1, 2 vagy 3, és p jelentése 0, 1 vagy 2. A találmány szerinti vegyületek prőtein-kináz C gátló hatásúak. ŕ
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/413,735 US5624949A (en) | 1993-12-07 | 1995-03-30 | Protein kinase C inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP9801250A2 true HUP9801250A2 (hu) | 1998-09-28 |
HUP9801250A3 HUP9801250A3 (en) | 1998-12-28 |
Family
ID=23638401
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU9801250A HUP9801250A3 (en) | 1995-03-30 | 1996-03-28 | Macrocyclic 3,4-bis(3,31-indolyl)-pyrrole-2,5-dione derivatives, process for their preparation and pharmaceutical compositions containing them |
Country Status (16)
Country | Link |
---|---|
US (10) | US5624949A (hu) |
EP (1) | EP0735038A1 (hu) |
JP (1) | JPH11507327A (hu) |
KR (1) | KR100319945B1 (hu) |
CN (1) | CN1093767C (hu) |
AU (1) | AU701988B2 (hu) |
CA (1) | CA2216535C (hu) |
CZ (1) | CZ286301B6 (hu) |
EA (1) | EA000598B1 (hu) |
HU (1) | HUP9801250A3 (hu) |
MX (1) | MX9707431A (hu) |
NO (1) | NO309271B1 (hu) |
NZ (1) | NZ305276A (hu) |
PL (1) | PL183600B1 (hu) |
TR (1) | TR199701073T1 (hu) |
WO (1) | WO1996030048A1 (hu) |
Families Citing this family (90)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5723456A (en) * | 1993-12-07 | 1998-03-03 | Eli Lilly & Company | Therapeutic treatment for cardiovascular diseases |
US5843935A (en) * | 1993-12-07 | 1998-12-01 | Eli Lilly And Company | Protein kinase C inhibitors |
RU2147304C1 (ru) * | 1993-12-07 | 2000-04-10 | Эли Лилли Энд Компани | Бис-индолмалеимидные макроциклические производные, способ их получения (варианты) и фармацевтическая композиция |
CZ150398A3 (cs) * | 1995-11-20 | 1998-12-16 | Eli Lilly And Company | Nové meziprodukty a jejich použití pro přípravu N,N´- můstkových bisindolylmaleimidů |
CA2237221C (en) * | 1995-11-20 | 2003-03-25 | Eli Lilly And Company | Protein kinase c inhibitor |
UA54427C2 (uk) * | 1996-05-01 | 2003-03-17 | Елі Ліллі Енд Компані | Спосіб лікування очних захворювань, які пов'язані з фактором васкулярного ендотеліального росту |
NZ332645A (en) | 1996-05-01 | 2000-07-28 | Lilly Co Eli | use of a bis-indolylmaleimide derivative for treating VEGF related diseases |
BR9709301A (pt) * | 1996-05-01 | 1999-08-10 | Univ Mississipi | Inibidores da proteína quinase c halo-substituídos |
US6232299B1 (en) * | 1996-05-01 | 2001-05-15 | Eli Lilly And Company | Use of protein kinase C inhibitors to enhance the clinical efficacy of oncolytic agents and radiation therapy |
US6093709A (en) * | 1996-08-22 | 2000-07-25 | Eli Lilly And Company | Therapeutic treatment for sexual dysfunctions |
KR20000068323A (ko) * | 1996-08-23 | 2000-11-25 | 피터 지. 스트링거 | 비스인돌릴말리미드의 합성 |
US6107327A (en) * | 1996-08-30 | 2000-08-22 | Eli Lilly And Company | Therapeutic treatment for HIV infection |
US5962446A (en) * | 1996-08-30 | 1999-10-05 | Eli Lilly And Company | Therapetutic treatment for human T cell lymphotrophic virus type 1 infection |
US6040152A (en) * | 1996-12-31 | 2000-03-21 | National Jewish Medical And Research Center | Method and assay for regulation of T cell proliferation |
US6093740A (en) * | 1997-04-30 | 2000-07-25 | Eli Lilly And Company | Therapeutic treatment for skin disorders |
JPH1180026A (ja) * | 1997-09-02 | 1999-03-23 | Yoshitomi Pharmaceut Ind Ltd | 新規免疫抑制剤、その使用方法およびその同定方法 |
WO1999026609A2 (en) * | 1997-11-26 | 1999-06-03 | Eli Lilly And Company | Therapeutic treatment for chronic myeloid leukemia and acute lymphoid leukemia |
CA2227688C (en) | 1998-01-16 | 2007-07-31 | James W. Critchfield | Methods and compositions for inhibition of viral replication |
US6103713A (en) * | 1998-03-05 | 2000-08-15 | Eli Lilly And Company | Therapeutic treatment for autoimmune diseases |
US6103712A (en) * | 1998-03-05 | 2000-08-15 | Eli Lilly And Company | Therapeutic treatment for asthma |
US6291446B1 (en) * | 1998-03-05 | 2001-09-18 | Eli Lilly And Company | Therapeutic treatment for cytomegalovirus infection |
US6225301B1 (en) | 1998-03-05 | 2001-05-01 | Eli Lilly And Company | Therapeutic treatment for renal dysfunction |
EP1070068B2 (en) * | 1998-03-13 | 2007-01-17 | The University Of British Columbia | Granulatimide derivatives for use in cancer treatment |
CA2245029A1 (en) | 1998-03-13 | 1999-09-13 | University Of British Columbia | Granulatimide compounds as g2 checkpoint inhibitors |
US6127401A (en) * | 1998-06-05 | 2000-10-03 | Cephalon, Inc. | Bridged indenopyrrolocarbazoles |
US6013646A (en) * | 1998-07-02 | 2000-01-11 | Bayer Corporation | Indolocarbazole derivatives useful for the treatment of neurodegenerative diseases and cancer |
US6841567B1 (en) | 1999-02-12 | 2005-01-11 | Cephalon, Inc. | Cyclic substituted fused pyrrolocarbazoles and isoindolones |
US6284783B1 (en) | 1999-06-09 | 2001-09-04 | The Uab Research Foundation | Use of bisindolylmaleimide compounds to induce Fas-mediated apoptosis |
US6399780B1 (en) | 1999-08-20 | 2002-06-04 | Cephalon, Inc. | Isomeric fused pyrrolocarbazoles and isoindolones |
US6852688B2 (en) | 2000-03-10 | 2005-02-08 | University Of Florida | Compositions for treating diabetic retinopathy and methods of using same |
WO2001081375A2 (en) * | 2000-04-24 | 2001-11-01 | Yale University | Dna & protein binding miniature proteins |
US20020048581A1 (en) * | 2000-07-18 | 2002-04-25 | King George L. | Modulation of nitric oxide synthase by PKC |
US7425537B2 (en) | 2000-08-22 | 2008-09-16 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | SH2 domain binding inhibitors |
MXPA03005139A (es) * | 2000-12-08 | 2004-01-29 | Ortho Mcneil Pharm Inc | Compuestos macroheterociclicos utiles como inhibidores de cinasa. |
ES2263681T3 (es) * | 2000-12-08 | 2006-12-16 | Ortho-Mcneil Pharmaceutical, Inc. | Compuestos de pirrolina indazolil-substituidos como inhibidores de la kinasa. |
DE10109280A1 (de) * | 2001-02-26 | 2002-09-05 | Peter Mayser | Indolderivate mit inhibitorischer Wirkung auf Proteinkinasen |
US6559299B2 (en) * | 2001-03-29 | 2003-05-06 | Merck & Co., Inc. | Preparation and isolation of indolocarbazole glycosides |
GB0125659D0 (en) * | 2001-10-25 | 2001-12-19 | Ssl Int Plc | Spermicides |
GB0125658D0 (en) * | 2001-10-25 | 2001-12-19 | Ssl Int Plc | Medicaments |
ATE352312T1 (de) * | 2001-12-29 | 2007-02-15 | Novo Nordisk As | Kombinierte verwendung einer glp-1-verbindung und eines aldose reduktase inhibitors |
AU2003241398A1 (en) * | 2002-05-06 | 2003-11-17 | Washington University | Methods of treatment of glaucoma and other conditions mediated by nos-2 expression via inhibition of the egfr pathway |
AU2003240517A1 (en) * | 2002-06-05 | 2003-12-22 | Janssen Pharmaceutica N.V. | Substituted pyrrolines as kinase inhibitors |
RU2004135382A (ru) | 2002-06-05 | 2005-06-27 | Янссен Фармацевтика Н.В. (Be) | Замещенные пирролины в качестве ингибиторов киназы |
CA2393720C (en) * | 2002-07-12 | 2010-09-14 | Eli Lilly And Company | Crystalline 2,5-dione-3-(1-methyl-1h-indol-3-yl)-4-[1-(pyridin-2-ylmethyl)piperidin-4-yl]-1h-indol-3-yl]-1h-pyrrole mono-hydrochloride |
US20040175384A1 (en) * | 2003-12-12 | 2004-09-09 | Mohapatra Shyam S. | Protein kinase C as a target for the treatment of respiratory syncytial virus |
AU2004251178A1 (en) * | 2003-06-13 | 2005-01-06 | Janssen Pharmaceutica N.V. | Substituted indazolyl(indolyl)maleimide derivatives as kinase inhibitors |
JP4928261B2 (ja) | 2003-06-18 | 2012-05-09 | トランザイム・ファーマ・インコーポレイテッド | モチリン受容体の大環状拮抗薬 |
CA2526284C (en) | 2003-06-25 | 2014-11-18 | Crucell Holland B.V. | Binding molecules for the treatment of myeloid cell malignancies |
GB0407315D0 (en) * | 2003-07-15 | 2004-05-05 | Cambridge Antibody Tech | Human antibody molecules |
KR101206206B1 (ko) * | 2003-07-22 | 2012-11-29 | 크루셀 홀란드 비.브이. | 사스-코로나바이러스에 대한 결합분자 및 그것의 용도 |
US7491794B2 (en) | 2003-10-14 | 2009-02-17 | Intermune, Inc. | Macrocyclic compounds as inhibitors of viral replication |
US8592368B2 (en) | 2003-12-19 | 2013-11-26 | University Of South Florida | JAK/STAT inhibitors and MAPK/ERK inhibitors for RSV infection |
JP2007529434A (ja) * | 2004-03-17 | 2007-10-25 | ラース マイケル ラーセン, | 視覚サイクルの阻害による網膜症の予防 |
DK1749029T3 (da) | 2004-05-27 | 2011-06-06 | Crucell Holland Bv | Bindemolekyler, der kan neutralisere rabiesvirus, og anvendelser deraf |
EP1765313A2 (en) | 2004-06-24 | 2007-03-28 | Novartis Vaccines and Diagnostics, Inc. | Compounds for immunopotentiation |
US20080096923A1 (en) * | 2004-07-23 | 2008-04-24 | Aniz Girach | Methods For Diagnosing And Treating Diabetic Microvascular Complications |
JP4852046B2 (ja) | 2004-10-12 | 2012-01-11 | クルセル ホランド ベー ヴェー | 癌の治療及び検出に用いる結合分子 |
US8106170B2 (en) | 2004-11-11 | 2012-01-31 | Crucell Holland B.V. | Compositions against SARS-coronavirus and uses thereof |
WO2006068988A1 (en) * | 2004-12-20 | 2006-06-29 | Eli Lilly And Company | Combination therapy for vascular complications associated with hyperglycemia |
WO2006108270A1 (en) * | 2005-04-11 | 2006-10-19 | Pharmagap Inc. | Inhibitors of protein kinases and uses thereof |
AU2006245734C1 (en) | 2005-05-12 | 2012-05-24 | Crucell Holland B.V. | Host cell specific binding molecules capable of neutralizing viruses and uses thereof |
EP2305697A3 (en) * | 2005-07-25 | 2011-07-27 | Intermune, Inc. | Macrocyclic inhibitors of Hepatitis C virus replication |
WO2007033374A2 (en) | 2005-09-16 | 2007-03-22 | Schering Corporation | Pharmaceutical compositions and methods using temozolomide and a protein kinase inhibitor |
CA2624378A1 (en) * | 2005-09-29 | 2007-04-12 | Janssen Pharmaceutica N.V. | Macroheterocylic compounds as kinase inhibitors |
DE602006019323D1 (de) | 2005-10-11 | 2011-02-10 | Intermune Inc | Verbindungen und verfahren zur inhibierung der replikation des hepatitis-c-virus |
CA2645289A1 (en) * | 2006-03-10 | 2007-09-20 | Janssen Pharmaceutica, N.V. | Pyridine-containing macroheterocylic compounds as kinase inhibitors |
WO2007106884A2 (en) | 2006-03-15 | 2007-09-20 | Theralogics, Inc. | Methods of treating muscular wasting diseases using nf-kb activation inhibitors |
EA031202B1 (ru) | 2006-06-06 | 2018-11-30 | Янссен Вэксинс Энд Превеншн Б.В. | Антитело человека, обладающее фагоцитарной активностью против стафилококков, и его применение |
CA2654502C (en) | 2006-06-06 | 2015-07-14 | Crucell Holland B.V. | Human binding molecules having killing activity against enterococci and uses thereof |
KR20090024834A (ko) * | 2006-07-05 | 2009-03-09 | 인터뮨, 인크. | C형 간염 바이러스 복제의 신규 억제제 |
US8445437B2 (en) * | 2006-07-27 | 2013-05-21 | The Brigham And Women's Hospital, Inc. | Treatment and prevention of cardiovascular disease using mast cell stabilizers |
MY170607A (en) | 2006-09-07 | 2019-08-20 | Crucell Holland Bv | Human binding molecules capable of neutralizing influenza virus h5n1 and uses thereof |
ES2402217T3 (es) | 2006-09-07 | 2013-04-29 | Crucell Holland B.V. | Moléculas de unión humanas que pueden neutralizar el virus influenza H5N1 y usos de las mismas |
US20090155209A1 (en) * | 2007-05-03 | 2009-06-18 | Blatt Lawrence M | Novel macrocyclic inhibitors of hepatitis c virus replication |
AU2008251425A1 (en) * | 2007-05-10 | 2008-11-20 | Array Biopharma, Inc. | Novel peptide inhibitors of hepatitis C virus replication |
US8445435B2 (en) * | 2007-09-28 | 2013-05-21 | The Brigham And Women's Hospital, Inc. | Mast cell stabilizers in the treatment of obesity |
US20090130195A1 (en) | 2007-10-17 | 2009-05-21 | Mildred Acevedo-Duncan | Prostate carcinogenesis predictor |
US8419332B2 (en) * | 2007-10-19 | 2013-04-16 | Atlas Bolt & Screw Company Llc | Non-dimpling fastener |
JP2011519364A (ja) * | 2008-04-15 | 2011-07-07 | インターミューン・インコーポレーテッド | C型肝炎ウイルス複製の新規大環状阻害剤 |
EP2181999A1 (en) | 2008-11-03 | 2010-05-05 | Zentiva, A.S. | Method of manufacturing ruboxistarin |
AR075584A1 (es) * | 2009-02-27 | 2011-04-20 | Intermune Inc | COMPOSICIONES TERAPEUTICAS QUE COMPRENDEN beta-D-2'-DESOXI-2'-FLUORO-2'-C-METILCITIDINA Y UN DERIVADO DE ACIDO ISOINDOL CARBOXILICO Y SUS USOS. COMPUESTO. |
BRPI1012749B1 (pt) | 2009-05-11 | 2022-01-11 | Janssen Vaccines & Prevention B.V. | Anticorpo monoclonal humano, seu uso e seu método de produção, imunoconjugado, e composição farmacêutica |
CN102741270B (zh) * | 2009-09-28 | 2015-07-22 | 英特穆恩公司 | C型肝炎病毒复制的环肽抑制剂 |
ES2385157B1 (es) * | 2010-02-25 | 2013-07-08 | Universidad Del País Vasco | Compuestos para el tratamiento de alzheimer. |
US8785648B1 (en) | 2010-08-10 | 2014-07-22 | The Regents Of The University Of California | PKC-epsilon inhibitors |
EP3180003B1 (en) | 2014-07-01 | 2022-01-12 | The Regents of the University of California | Pkc-epsilon inhibitors |
BR112019012383A2 (pt) | 2016-12-19 | 2020-02-27 | Chromaderm, Inc. | Métodos de tratamento de distúrbios de hiperpigmentação |
WO2019000224A1 (zh) * | 2017-06-27 | 2019-01-03 | 中国海洋大学 | 双吲哚马来酰亚胺衍生物及其制备方法和用途 |
US11590131B2 (en) | 2017-07-28 | 2023-02-28 | Applied Therapeutics, Inc. | Compositions and methods for treating galactosemia |
CN115996725A (zh) | 2020-05-01 | 2023-04-21 | 应用治疗公司 | 用于治疗山梨糖醇脱氢酶缺乏症的醛糖还原酶抑制剂 |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4785085A (en) * | 1986-11-21 | 1988-11-15 | Bristol-Myers Company | Rebeccamycin analogs |
US4808613A (en) * | 1986-11-21 | 1989-02-28 | Bristol-Myers Company | Rebeccamycin derivative containing pharmaceutical composition |
EP0303697B1 (en) * | 1987-03-09 | 1997-10-01 | Kyowa Hakko Kogyo Co., Ltd. | Derivatives of physiologically active substance k-252 |
JPH07113027B2 (ja) * | 1987-12-24 | 1995-12-06 | 協和醗酵工業株式会社 | K−252誘導体 |
DE3803620A1 (de) * | 1988-02-06 | 1989-08-17 | Goedecke Ag | Indolocarbazol-derivate, verfahren zu deren herstellung und diese enthaltende arzneimittel |
US5438050A (en) * | 1988-02-06 | 1995-08-01 | Godecke Aktiengesellschaft | Indolocarbazole derivatives, processes for their preparation and compositions containing them |
NZ227850A (en) * | 1988-02-10 | 1991-11-26 | Hoffmann La Roche | Indole substituted pyrrole derivatives; preparatory process and medicaments for use against inflammatory immunological, bronchopulmonary or vascular disorders |
MC2096A1 (fr) * | 1989-02-23 | 1991-02-15 | Hoffmann La Roche | Pyrroles substitues |
CA2015996C (en) * | 1989-05-05 | 2001-08-28 | Hartmut Osswald | Bis-(1h-indol-3-yl)-maleinimide derivatives and their use as pharmaceuticals |
DE3914764A1 (de) * | 1989-05-05 | 1990-11-08 | Goedecke Ag | Maleinimid-derivate und deren verwendung als arzneimittel |
US5380746A (en) * | 1989-05-05 | 1995-01-10 | Goedecke Aktiengesellschaft | Bis-(1H-indol-3-YL)-maleinimide derivatives, processes for the preparation thereof and pharmaceutical compositions containing them |
DE3924538A1 (de) * | 1989-07-25 | 1991-01-31 | Goedecke Ag | Indolocarbazol und dessen verwendung |
DE3942296A1 (de) * | 1989-12-21 | 1991-06-27 | Goedecke Ag | Indolocarbazol-derivate, verfahren zu deren herstellung und deren verwendung |
DE4005970A1 (de) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | Neue trisubstituierte maleinimide, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten |
DE4005969A1 (de) * | 1990-02-26 | 1991-08-29 | Boehringer Mannheim Gmbh | Neue trisubstituierte pyrrole, verfahren zu ihrer herstellung sowie arzneimittel, die diese verbindungen enthalten |
CA2046801C (en) * | 1990-08-07 | 2002-02-26 | Peter D. Davis | Substituted pyrroles |
US5292747A (en) * | 1990-08-07 | 1994-03-08 | Hoffman-La Roche Inc. | Substituted pyrroles |
WO1992018507A1 (en) * | 1991-04-11 | 1992-10-29 | Schering Corporation | Anti-tumor and anti-psoriatic agents |
GB9123396D0 (en) * | 1991-11-04 | 1991-12-18 | Hoffmann La Roche | A process for the manufacture of substituted maleimides |
EP0575955B1 (en) * | 1992-06-22 | 1999-09-15 | Kyowa Hakko Kogyo Co., Ltd. | Process for producing staurosporine derivatives |
US5461146A (en) * | 1992-07-24 | 1995-10-24 | Cephalon, Inc. | Selected protein kinase inhibitors for the treatment of neurological disorders |
US5589472A (en) * | 1992-09-25 | 1996-12-31 | Vice; Susan F. | Diindolo compounds and pharmaceutical compositions containing them |
DE4243321A1 (de) * | 1992-12-21 | 1994-06-23 | Goedecke Ag | Aminosäurederivate von Heterocyclen als PKC-Inhibitoren |
PH30300A (en) * | 1993-05-07 | 1997-01-20 | Ciba Geigy Ag | Polycyclic compounds and processes for the preparation thereof |
AU678435B2 (en) * | 1993-05-10 | 1997-05-29 | F. Hoffmann-La Roche Ag | Substituted pyrroles |
RU2147304C1 (ru) * | 1993-12-07 | 2000-04-10 | Эли Лилли Энд Компани | Бис-индолмалеимидные макроциклические производные, способ их получения (варианты) и фармацевтическая композиция |
HUT69164A (en) * | 1993-12-07 | 1995-08-28 | Lilly Co Eli | Improved process for producing bis-indolyl-maleimide derivatives |
US5481003A (en) * | 1994-06-22 | 1996-01-02 | Eli Lilly And Company | Protein kinase C inhibitors |
CA2237221C (en) * | 1995-11-20 | 2003-03-25 | Eli Lilly And Company | Protein kinase c inhibitor |
-
1995
- 1995-03-30 US US08/413,735 patent/US5624949A/en not_active Expired - Fee Related
- 1995-06-01 US US08/457,060 patent/US5674862A/en not_active Expired - Lifetime
- 1995-06-01 US US08/457,000 patent/US5552396A/en not_active Expired - Lifetime
- 1995-06-01 US US08/457,657 patent/US5621098A/en not_active Expired - Fee Related
-
1996
- 1996-03-28 NZ NZ305276A patent/NZ305276A/xx unknown
- 1996-03-28 CZ CZ19973051A patent/CZ286301B6/cs not_active IP Right Cessation
- 1996-03-28 CN CN96194257A patent/CN1093767C/zh not_active Expired - Fee Related
- 1996-03-28 EP EP96302142A patent/EP0735038A1/en not_active Withdrawn
- 1996-03-28 KR KR1019970706785A patent/KR100319945B1/ko not_active IP Right Cessation
- 1996-03-28 CA CA002216535A patent/CA2216535C/en not_active Expired - Fee Related
- 1996-03-28 PL PL96322584A patent/PL183600B1/pl unknown
- 1996-03-28 JP JP8529640A patent/JPH11507327A/ja not_active Withdrawn
- 1996-03-28 WO PCT/US1996/004245 patent/WO1996030048A1/en active IP Right Grant
- 1996-03-28 AU AU53249/96A patent/AU701988B2/en not_active Ceased
- 1996-03-28 HU HU9801250A patent/HUP9801250A3/hu unknown
- 1996-03-28 TR TR97/01073T patent/TR199701073T1/xx unknown
- 1996-03-28 MX MX9707431A patent/MX9707431A/es unknown
- 1996-03-28 EA EA199700280A patent/EA000598B1/ru not_active IP Right Cessation
- 1996-05-06 US US08/646,703 patent/US5696108A/en not_active Expired - Fee Related
- 1996-05-06 US US08/646,708 patent/US5719175A/en not_active Expired - Fee Related
- 1996-05-06 US US08/643,710 patent/US5780461A/en not_active Expired - Fee Related
-
1997
- 1997-03-20 US US08/822,255 patent/US5739322A/en not_active Expired - Fee Related
- 1997-09-26 NO NO974453A patent/NO309271B1/no not_active IP Right Cessation
- 1997-11-14 US US08/970,891 patent/US6057440A/en not_active Expired - Fee Related
- 1997-11-14 US US08/971,115 patent/US5821365A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
HUP9801250A3 (en) | 1998-12-28 |
US5624949A (en) | 1997-04-29 |
US5696108A (en) | 1997-12-09 |
TR199701073T1 (xx) | 1998-02-21 |
CZ305197A3 (cs) | 1998-05-13 |
AU5324996A (en) | 1996-10-16 |
WO1996030048A1 (en) | 1996-10-03 |
NZ305276A (en) | 1999-02-25 |
CA2216535C (en) | 2002-05-07 |
NO309271B1 (no) | 2001-01-08 |
NO974453D0 (no) | 1997-09-26 |
MX9707431A (es) | 1997-12-31 |
US5739322A (en) | 1998-04-14 |
US5674862A (en) | 1997-10-07 |
NO974453L (no) | 1997-11-19 |
US5780461A (en) | 1998-07-14 |
KR100319945B1 (ko) | 2002-03-08 |
PL322584A1 (en) | 1998-02-02 |
KR19980703380A (ko) | 1998-10-15 |
AU701988B2 (en) | 1999-02-11 |
US6057440A (en) | 2000-05-02 |
CN1185742A (zh) | 1998-06-24 |
CN1093767C (zh) | 2002-11-06 |
JPH11507327A (ja) | 1999-06-29 |
US5821365A (en) | 1998-10-13 |
CZ286301B6 (cs) | 2000-03-15 |
EA199700280A1 (ru) | 1998-02-26 |
EA000598B1 (ru) | 1999-12-29 |
CA2216535A1 (en) | 1996-10-03 |
EP0735038A1 (en) | 1996-10-02 |
US5719175A (en) | 1998-02-17 |
US5552396A (en) | 1996-09-03 |
PL183600B1 (pl) | 2002-06-28 |
US5621098A (en) | 1997-04-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HUP9801250A2 (hu) | Makrociklusos 3,4-bisz(3,3'-indolil)-pirrolin-2,5-dion-származékok, eljárás előállításukra és az ezeket tartalmazó gyógyszerkészítmények | |
HUP0002112A2 (hu) | Helyettesített 3-ciano-kinolinok, előállításuk és alkalmazásuk, valamint e vegyületeket tartalmazó gyógyászati készítmények | |
HUP9902471A2 (hu) | Piperazin- és piperidinvegyületek, eljárás előállításukra és az ezeket tartalmazó gyógyszerkészítmények | |
HUP9802694A1 (hu) | Benzamidszármazékok, eljárás előállításukra és ezeket tartalmazó gyógyszerkészítmények | |
GB9024730D0 (en) | Diazine derivatives | |
HUP0001232A2 (hu) | Béta-amiloid peptid kibocsátást és/vagy szintézist gátló cikloalkil-, laktám-, laktonszármazékok, és ezek tio-analógjai, valamint e vegyületeket tartalmazó gyógyászati készítmények | |
HUP9900949A2 (hu) | Triazolilcsoportot tartalmazó foszfátok, eljárás előállításukra és ezeket tartalmazó gyógyszerkészítmények | |
HUP9700992A2 (hu) | 3-(Piperid-4-il)-1,2-benzizoxazol- és 3-(piperazin-4-il)-1,2-benzizoxazol-származékok, eljárás előállításukra, valamint ezeket tartalmazó gyógyászati készítmények | |
HUP9802937A2 (hu) | Benzo[g]kinolin-származékok, e vegyületeket tartalmazó gyógyászati készítmények, eljárás előállításukra és alkalmazásuk | |
HUP0402225A2 (hu) | Makrolid-vegyületek, eljárás az előállításukra és ezeket tartalmazó gyógyszerkészítmények | |
DE69712084D1 (de) | Aminothiazole derivate, ihre herstellung und sie enthaltenden pharmazeutischen zusammensetzungen | |
HUP9904514A2 (hu) | 5H-Pirrolo[2,1-c][1,4]-benzodiazepin-3-karboxamid-származékok, eljárás előállításukra, alkalmazásuk és az azokat tartalmazó gyógyszerkészítmények | |
HUP9802393A2 (hu) | Benzotiazolonszármazékok, alkalmazásuk, az ezeket tartalmazó gyógyszerkészítmények, eljárás a vegyületek előállítására és intermedierjeik | |
ES8605810A1 (es) | Un procedimiento para la preparacion de compuestos de beta-lactama | |
HUP9901376A2 (hu) | 1-Metil-karbapenem-származékok, alkalmazásuk, előállításuk, ezeket tartalmazó gyógyszerkészítmények | |
RU95106653A (ru) | Производные 2-имидазолин-5-онов и 2-имидазолин-5-тионов и фунгицидные композиции на их основе | |
ES8600261A1 (es) | Un compuesto fenoxi | |
HUP9701660A2 (hu) | 10,13,15-trioxa-triciklo[9.2.1.1. 9.6]pentadekanon-származékok, eljárás ezek előállítására, és az e vegyületeket tartalmazó gyógyászati készítmények | |
TR200001222T2 (tr) | Yeni tetrasiklikler, bunların üretimi için işlem ve bu birleşikleri içeren farmasötik preparasyonlar. | |
MY137475A (en) | Chemical compounds. | |
HUP9802042A2 (hu) | Taxoidok, előállításuk és ezeket tartalmazó gyógyszerkészítmények | |
HUP9903514A2 (hu) | Cikloalkilén-lánccal rendelkező új ciklusos vegyületek, eljárás azok előállítására és az azokat tartalmazó gyógyszerkészítmények | |
HUP0402585A2 (hu) | Új benzotiazin- benzotiadiazin-származékok, előállításuk, alkalmazásuk és az ezeket tartalmazó gyógyászati készítmények | |
HUP9802518A2 (hu) | Szulfonamidcsoporttal szubsztituált benzopiránszármazékok, eljárás előállításukra, gyógyszerként történő alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények | |
HUP9701005A2 (hu) | Benzil-oxi-csoporttal szubsztituált fenilszármazékok, e vegyületeket tartalmazó gomba- és rovarirtó készítmények, valamint eljárás a vegyületek előállítására |