IL124417A - Dietary salt of -13 [(dimethyl amino) methyl] - 10, 11, 14, 15 - tetra hydro- 4, 9:16, 21 - our image - H13, H1 - Divenzo {E, K} pyrrole [H-4, 3] [1, 4, 13] Oxadiazacyclohexadecin - 1, 3 (H2) - Discussion, preparation and pharmacological preparations for the inhibition of protein kinase C containing it - Google Patents

Dietary salt of -13 [(dimethyl amino) methyl] - 10, 11, 14, 15 - tetra hydro- 4, 9:16, 21 - our image - H13, H1 - Divenzo {E, K} pyrrole [H-4, 3] [1, 4, 13] Oxadiazacyclohexadecin - 1, 3 (H2) - Discussion, preparation and pharmacological preparations for the inhibition of protein kinase C containing it

Info

Publication number
IL124417A
IL124417A IL12441796A IL12441796A IL124417A IL 124417 A IL124417 A IL 124417A IL 12441796 A IL12441796 A IL 12441796A IL 12441796 A IL12441796 A IL 12441796A IL 124417 A IL124417 A IL 124417A
Authority
IL
Israel
Prior art keywords
salt
compound
reaction
water
methyl
Prior art date
Application number
IL12441796A
Other languages
English (en)
Hebrew (he)
Other versions
IL124417A0 (en
Original Assignee
Lilly Co Eli
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of IL124417A0 publication Critical patent/IL124417A0/xx
Publication of IL124417A publication Critical patent/IL124417A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/22Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/48Drugs for disorders of the endocrine system of the pancreatic hormones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Neurology (AREA)
  • Obesity (AREA)
  • Neurosurgery (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Rheumatology (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Enzymes And Modification Thereof (AREA)
IL12441796A 1995-11-20 1996-11-18 Dietary salt of -13 [(dimethyl amino) methyl] - 10, 11, 14, 15 - tetra hydro- 4, 9:16, 21 - our image - H13, H1 - Divenzo {E, K} pyrrole [H-4, 3] [1, 4, 13] Oxadiazacyclohexadecin - 1, 3 (H2) - Discussion, preparation and pharmacological preparations for the inhibition of protein kinase C containing it IL124417A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US697095P 1995-11-20 1995-11-20
PCT/US1996/018512 WO1997018809A1 (fr) 1995-11-20 1996-11-18 Inhibiteur de la proteine kinase c

Publications (2)

Publication Number Publication Date
IL124417A0 IL124417A0 (en) 1998-12-06
IL124417A true IL124417A (en) 2002-11-10

Family

ID=21723527

Family Applications (1)

Application Number Title Priority Date Filing Date
IL12441796A IL124417A (en) 1995-11-20 1996-11-18 Dietary salt of -13 [(dimethyl amino) methyl] - 10, 11, 14, 15 - tetra hydro- 4, 9:16, 21 - our image - H13, H1 - Divenzo {E, K} pyrrole [H-4, 3] [1, 4, 13] Oxadiazacyclohexadecin - 1, 3 (H2) - Discussion, preparation and pharmacological preparations for the inhibition of protein kinase C containing it

Country Status (34)

Country Link
US (3) US5710145A (fr)
EP (1) EP0776895B1 (fr)
JP (1) JP3348859B2 (fr)
KR (1) KR100304210B1 (fr)
CN (1) CN1093759C (fr)
AR (2) AR004717A1 (fr)
AT (1) ATE172199T1 (fr)
AU (1) AU711125B2 (fr)
BR (1) BR9611724A (fr)
CA (1) CA2237221C (fr)
CO (1) CO4750823A1 (fr)
CY (1) CY2103B1 (fr)
CZ (1) CZ297524B6 (fr)
DE (1) DE69600784T2 (fr)
DK (1) DK0776895T3 (fr)
EA (1) EA000967B1 (fr)
EG (1) EG23871A (fr)
ES (1) ES2122764T3 (fr)
HU (1) HU226821B1 (fr)
IL (1) IL124417A (fr)
MX (1) MX9803792A (fr)
MY (1) MY118068A (fr)
NO (1) NO310196B1 (fr)
NZ (1) NZ323571A (fr)
PE (1) PE22798A1 (fr)
PL (1) PL184715B1 (fr)
RO (1) RO120074B1 (fr)
SI (1) SI0776895T1 (fr)
TR (1) TR199800759T2 (fr)
TW (1) TW403754B (fr)
UA (1) UA61897C2 (fr)
WO (1) WO1997018809A1 (fr)
YU (1) YU49315B (fr)
ZA (1) ZA969646B (fr)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5624949A (en) * 1993-12-07 1997-04-29 Eli Lilly And Company Protein kinase C inhibitors
US6093740A (en) * 1997-04-30 2000-07-25 Eli Lilly And Company Therapeutic treatment for skin disorders
AR017200A1 (es) 1997-12-23 2001-08-22 Astrazeneca Ab Compuestos inhibidores de la proteina cinasa c, sales farmaceuticamente aceptables de los mismos, formulaciones farmaceuitcas que los comprenden, usode las mismas y proceso para la sintesis de dichos compuestos
US6620977B1 (en) 1998-01-30 2003-09-16 Daiso Co., Ltd. Process for producing butanetriol derivative
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
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
AU758241B2 (en) * 1998-03-13 2003-03-20 University Of British Columbia, The Granulatimide derivatives for use in cancer treatment
SE9800835D0 (sv) 1998-03-13 1998-03-13 Astra Ab New Compounds
CA2245029A1 (fr) 1998-03-13 1999-09-13 University Of British Columbia Composes granulatimide en tant qu'inhibiteurs de controle g2
US6706721B1 (en) 1998-04-29 2004-03-16 Osi Pharmaceuticals, Inc. N-(3-ethynylphenylamino)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine mesylate anhydrate and monohydrate
US6127401A (en) 1998-06-05 2000-10-03 Cephalon, Inc. Bridged indenopyrrolocarbazoles
TWI223598B (en) * 1998-06-22 2004-11-11 Pfizer Ireland Pharmaceuticals An intranasal pharmaceutical composition for the treatment of male erectile dysfunction or female sexual disorders, an intranasal delivery system or device and sildenafil mesylate
GB9828640D0 (en) * 1998-12-23 1999-02-17 Smithkline Beecham Plc Novel method and compounds
US6841567B1 (en) * 1999-02-12 2005-01-11 Cephalon, Inc. Cyclic substituted fused pyrrolocarbazoles and isoindolones
US6492406B1 (en) 1999-05-21 2002-12-10 Astrazeneca Ab Pharmaceutically active compounds
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
UA74803C2 (uk) 1999-11-11 2006-02-15 Осі Фармасьютікалз, Інк. Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування
US7087613B2 (en) * 1999-11-11 2006-08-08 Osi Pharmaceuticals, Inc. Treating abnormal cell growth with a stable polymorph of N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine hydrochloride
US6852688B2 (en) 2000-03-10 2005-02-08 University Of Florida Compositions for treating diabetic retinopathy and methods of using same
CA2413156C (fr) * 2000-07-03 2009-08-18 Gala Design, Inc. Vecteurs d'expression
US20030224415A1 (en) * 2001-06-29 2003-12-04 Gala Design, Inc. Selection free growth of host cells containing multiple integrating vectors
AU2001271614B2 (en) 2000-07-03 2007-05-31 Catalent Pharma Solutions, Llc Host cells containing multiple integrating vectors
US6300106B1 (en) * 2000-11-22 2001-10-09 Ppg Industries Ohio, Inc. Method of preparing 3-[2-{(Methylsulfonyl)oxy}-ethoxy ]-4-(triphenylmethoxy)-1-butanol, methane sulfonate
US7384738B2 (en) * 2002-03-28 2008-06-10 Bremel Robert D Retrovirus-based genomic screening
US20040038304A1 (en) * 2002-03-28 2004-02-26 Gala Design, Inc. Antibody libraries
US20030232741A1 (en) * 2002-05-06 2003-12-18 Washington University Methods of treatment of glaucoma and other conditions mediated by NOS-2 expression via inhibition of the EGFR pathway
DE10244453A1 (de) * 2002-09-24 2004-04-01 Phenomiques Gmbh Hemmung der Proteinkinase C-alpha zur Behandlung von Krankheiten
US7232842B2 (en) * 2003-01-10 2007-06-19 Board Of Trustees Of The Leland Stanford Junior University Kinase inhibitors and associated pharmaceutical compositions and methods of use
US7521420B2 (en) 2003-06-18 2009-04-21 Tranzyme Pharma, Inc. Macrocyclic antagonists of the motilin receptor
US20050152942A1 (en) * 2003-12-23 2005-07-14 Medtronic Vascular, Inc. Medical devices to treat or inhibit restenosis
US20050221429A1 (en) * 2004-01-16 2005-10-06 Cardinal Health Pts, Llc Host cells containing multiple integrating vectors comprising an amplifiable marker
NZ550340A (en) * 2004-03-17 2010-08-27 Lars Michael Larsen Prevention of retinopathy by inhibition of the visual cycle using a retinoid
DE102004019413A1 (de) * 2004-04-19 2005-11-24 Phenos Gmbh Hemmung der Proteinkinase C epsilon zur Behandlung von Krankheiten
WO2006071451A2 (fr) * 2004-12-03 2006-07-06 The Regents Of The University Of California Composes destines a la prevention de l'apoptose de macrophages et procedes de leur utilisation
US20070281988A1 (en) * 2004-12-20 2007-12-06 Cameron Norman E Combination Therapy for Vascular Complications Associated with Hyperglycemia
US8034823B2 (en) * 2005-02-22 2011-10-11 Savvipharm Inc Method of increasing drug oral bioavailability and compositions of less toxic orotate salts
GB0504203D0 (en) * 2005-03-01 2005-04-06 Novartis Ag Organic compounds
US8158586B2 (en) * 2005-04-11 2012-04-17 Pharmagap Inc. Inhibitors of protein kinases and uses thereof
WO2008027619A2 (fr) 2006-09-01 2008-03-06 Intermec Ip Corp. Système d'étiquette rfid avec encodage de bloc, tel qu'un encodage de bloc espace-temps
PE20091522A1 (es) * 2007-12-21 2009-10-29 Novartis Ag Composicion farmaceutica solida que contiene 3-(1.h-indol-3-il)-4-[2-(4-metil-piperazin-1-il)-quinazolin-4-il]-quinazolin-4-il]-pirrol-2,5-diona
EP2181999A1 (fr) 2008-11-03 2010-05-05 Zentiva, A.S. Procédé de fabrication d'un ruboxistaurine
US9265764B2 (en) * 2009-02-27 2016-02-23 Massachusetts Institute Of Technology Uses of chemicals to modulate GSK-3 signaling for treatment of bipolar disorder and other brain disorders
MX2012011341A (es) 2010-03-30 2012-11-12 Novartis Ag Inhibidores de pkc para el tratamiento de linfoma de celulas-b que tenga señalizacion activa cronica de receptores de celulas-b.
UA115250C2 (uk) 2012-11-29 2017-10-10 Новартіс Аг Фармацевтичні комбінації
WO2014174478A1 (fr) 2013-04-26 2014-10-30 Novartis Ag Combinaisons pharmaceutiques d'un inhibiteur de la pkc et d'un inhibiteur du récepteur tyrosine-kinase c-met
JO3589B1 (ar) 2014-08-06 2020-07-05 Novartis Ag مثبطات كيناز البروتين c وطرق استخداماتها
US20180185259A1 (en) 2016-12-19 2018-07-05 Chromaderm, Inc. Methods of treating hyperpigmentation disorders
EP3600440A1 (fr) 2017-03-20 2020-02-05 Sienna Biopharmaceuticals, Inc. Conjugués d'exposition réduite modulant des cibles thérapeutiques
WO2018175302A1 (fr) 2017-03-20 2018-09-27 Sienna Biopharmaceuticals, Inc. Conjugués polymères ciblant c-src à exposition réduite
EP3658142B1 (fr) 2017-07-28 2024-04-17 Applied Therapeutics, Inc. Compositions et méthodes de traitement de la galactosémie
KR20230005944A (ko) 2020-05-01 2023-01-10 어플라이드 테라퓨틱스 인크. 소르비톨 데히드로게나제 결핍 치료를 위한 알도스 리덕타제 억제제
KR20230128175A (ko) * 2022-02-25 2023-09-04 주식회사 온코크로스 루복시스타우린을 포함하는 항암용 조성물

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US5292747A (en) * 1990-08-07 1994-03-08 Hoffman-La Roche Inc. Substituted pyrroles
AU5100393A (en) * 1992-09-25 1994-04-26 Schering Corporation Diindolo compounds and pharmaceutical compositions containing them
US5624949A (en) * 1993-12-07 1997-04-29 Eli Lilly And Company Protein kinase C inhibitors
CA2137203C (fr) * 1993-12-07 2006-11-28 William Francis Heath Jr. Inhibiteurs de la proteine kinase c

Also Published As

Publication number Publication date
PL326754A1 (en) 1998-10-26
HU226821B1 (en) 2009-11-30
CA2237221C (fr) 2003-03-25
CA2237221A1 (fr) 1997-05-29
YU60996A (sh) 1999-03-04
TR199800759T2 (xx) 2001-01-22
EG23871A (en) 2007-11-27
EA199800374A1 (ru) 1998-10-29
MX9803792A (es) 1998-09-30
DE69600784T2 (de) 1999-04-08
JPH11500149A (ja) 1999-01-06
NO982182L (no) 1998-05-13
AU711125B2 (en) 1999-10-07
SI0776895T1 (en) 1999-04-30
CN1202825A (zh) 1998-12-23
US5710145A (en) 1998-01-20
RO120074B1 (ro) 2005-08-30
CZ297524B6 (cs) 2007-01-03
CO4750823A1 (es) 1999-03-31
CZ150298A3 (cs) 1998-12-16
KR19990067596A (ko) 1999-08-25
AU1054897A (en) 1997-06-11
IL124417A0 (en) 1998-12-06
US6117861A (en) 2000-09-12
CY2103B1 (en) 2002-04-05
DK0776895T3 (da) 1999-06-23
DE69600784D1 (de) 1998-11-19
JP3348859B2 (ja) 2002-11-20
KR100304210B1 (ko) 2001-11-05
YU49315B (sh) 2005-06-10
HUP9903377A3 (en) 2000-04-28
TW403754B (en) 2000-09-01
PL184715B1 (pl) 2002-12-31
HUP9903377A2 (hu) 2000-02-28
AR004717A1 (es) 1999-03-10
ATE172199T1 (de) 1998-10-15
NO310196B1 (no) 2001-06-05
WO1997018809A1 (fr) 1997-05-29
MY118068A (en) 2004-08-30
AR004336A1 (es) 1998-11-04
EP0776895B1 (fr) 1998-10-14
ZA969646B (en) 1998-05-18
ES2122764T3 (es) 1998-12-16
NO982182D0 (no) 1998-05-13
PE22798A1 (es) 1998-05-11
CN1093759C (zh) 2002-11-06
NZ323571A (en) 1998-12-23
EA000967B1 (ru) 2000-08-28
EP0776895A1 (fr) 1997-06-04
US6015807A (en) 2000-01-18
UA61897C2 (en) 2003-12-15
BR9611724A (pt) 1999-06-01

Similar Documents

Publication Publication Date Title
US6117861A (en) Protein kinase C inhibitor
RU2089550C1 (ru) Производное 1,4-бензотиазепина
PL166209B1 (pl) Sposób wytwarzania nowych pochodnych benzimidazolu PL
BR112021001309A2 (pt) método para a preparação da 2-[(3r)-3-metilmorfolin-4-il]-4-(1-metil-1h-pirazol-5-il)-8-(1h-pirazol-5-il)-1,7-naftiridina
JP2008138006A (ja) N,n’−架橋ビスインドリルマレイミドの製造における新規中間体およびその用途
JPH0249788A (ja) ピラノベンゾオキサジアゾール誘導体
JP2024506387A (ja) 腎線維症を治療するためのオキサジアゾリルジヒドロピラノ[2,3‐b]ピリジン系HIPK2阻害剤
CA2896209A1 (fr) 3,5-diaryl-azaindoles comme inhibiteurs de la proteine dyrk1a pour le traitement des deficiences cognitives liees au syndrome de down et a la maladie d'alzheimer
US5721272A (en) Intermediates and their use to prepare N,N'-bridged bisindolylmaleimides
RU2128043C1 (ru) Лекарственные средства для сердечной недостаточности
RU2051916C1 (ru) Оптически активные производные индолбензохинолина или их фармацевтически приемлемые соли

Legal Events

Date Code Title Description
FF Patent granted
KB Patent renewed
KB Patent renewed
KB Patent renewed
MM9K Patent not in force due to non-payment of renewal fees