PE20140188A1 - Co-cristales y sales de inhibidores de ccr3 - Google Patents

Co-cristales y sales de inhibidores de ccr3

Info

Publication number
PE20140188A1
PE20140188A1 PE2013000781A PE2013000781A PE20140188A1 PE 20140188 A1 PE20140188 A1 PE 20140188A1 PE 2013000781 A PE2013000781 A PE 2013000781A PE 2013000781 A PE2013000781 A PE 2013000781A PE 20140188 A1 PE20140188 A1 PE 20140188A1
Authority
PE
Peru
Prior art keywords
crystals
salts
alkyl
acid
ccr3 inhibitors
Prior art date
Application number
PE2013000781A
Other languages
English (en)
Inventor
Marcus Frank
Hans Haeberle
Manuel Henry
Thorsten Pachur
Marco Santagostino
Uwe Stertz
Thomas Trebing
Ulrike Werthmann
Original Assignee
Boehringer Ingelheim Int
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 Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of PE20140188A1 publication Critical patent/PE20140188A1/es

Links

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
    • C07D401/14—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
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • 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
    • 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
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • 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
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • 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
    • A61P37/08—Antiallergic agents
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • 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
    • C07D401/04—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 directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Immunology (AREA)
  • Communicable Diseases (AREA)
  • Rheumatology (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Pain & Pain Management (AREA)
  • Virology (AREA)
  • Cardiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Ophthalmology & Optometry (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

SE REFIERE A CO-CRISTALES Y SALES DE INHIBIDORES DE CCR3 DE FORMULA (1), DONDE: R1 ES ALQUILO C1-C6, HALOALQUILO C1-C6, HALOGENOS ENTRE OTROS; m ES 1, 2 Y 3; R2a Y R2b SE SELECCIONA INDEPENDIENTEMENTE DE H, ALQUILO C1-C6, HALOGENO ENTRE OTROS; R3 ES H, ALQUILO C1-C6; X ES CLORURO, BROMURO ENTRE OTROS; J ES 0, 0.5, 1, 1.5 Y 2; CON UN AGENTE DE FORMACION DE CO-CRISTALES SELECIONADO DEL GRUPO DE ACIDO PROTICO, ACIDO HIPURICO, ACIDO L-PIROGLUTAMICO ENTRE OTROS. DICHOS COMPUESTOS SON UTILES EN EL TRATAMIENTO DE ASMA, ENFERMEDADES ALERGICAS, ENFERMEDAD PULMONAR OBSTRUCTIVA CRONICA, ENTRE OTROS.
PE2013000781A 2010-10-07 2011-10-06 Co-cristales y sales de inhibidores de ccr3 PE20140188A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP10186901 2010-10-07

Publications (1)

Publication Number Publication Date
PE20140188A1 true PE20140188A1 (es) 2014-02-26

Family

ID=44741339

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2013000781A PE20140188A1 (es) 2010-10-07 2011-10-06 Co-cristales y sales de inhibidores de ccr3

Country Status (36)

Country Link
US (3) US8742115B2 (es)
EP (1) EP2625174B1 (es)
JP (1) JP5794713B2 (es)
KR (3) KR102239690B1 (es)
CN (1) CN103140486B (es)
AP (1) AP3268A (es)
AR (1) AR083353A1 (es)
AU (1) AU2011311530B2 (es)
BR (2) BR112013008211B1 (es)
CA (1) CA2807255C (es)
CL (1) CL2013000488A1 (es)
CO (1) CO6710910A2 (es)
CY (1) CY1116168T1 (es)
DK (1) DK2625174T3 (es)
EA (1) EA029097B1 (es)
EC (1) ECSP13012600A (es)
ES (1) ES2535264T3 (es)
GE (1) GEP20166488B (es)
HR (1) HRP20150419T1 (es)
HU (1) HUE024540T2 (es)
IL (1) IL224269A (es)
MA (1) MA34545B1 (es)
ME (1) ME02040B (es)
MX (1) MX2013003785A (es)
MY (1) MY167898A (es)
NZ (1) NZ605827A (es)
PE (1) PE20140188A1 (es)
PL (1) PL2625174T3 (es)
PT (1) PT2625174E (es)
RS (1) RS53858B1 (es)
SG (1) SG188949A1 (es)
SI (1) SI2625174T1 (es)
TW (1) TWI546294B (es)
UA (1) UA109290C2 (es)
UY (1) UY33655A (es)
WO (1) WO2012045803A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8278302B2 (en) 2009-04-08 2012-10-02 Boehringer Ingelheim International Gmbh Substituted piperidines as CCR3 antagonists
UA109290C2 (uk) * 2010-10-07 2015-08-10 Спільні кристали і солі інгібіторів ccr3
AR090566A1 (es) 2012-04-02 2014-11-19 Boehringer Ingelheim Int Proceso para la produccion de inhibidores de crr
US20130261153A1 (en) * 2012-04-03 2013-10-03 Boehringer Ingelheim International Gmbh Use of ccr3-inhibitors
US10213421B2 (en) * 2012-04-04 2019-02-26 Alkahest, Inc. Pharmaceutical formulations comprising CCR3 antagonists
JP7179755B2 (ja) 2017-04-05 2022-11-29 アルカヘスト インコーポレイテッド Ｃｃｒ３阻害剤を使用した網膜関連疾患を治療するための方法および組成物
US20200054622A1 (en) * 2017-04-05 2020-02-20 Alkahest, Inc. Methods and Compositions for Treating Aging-Associated Impairments Using CCR3-Inhibitors
KR20190131078A (ko) * 2017-04-05 2019-11-25 알카헤스트 인코포레이티드 Ccr3-억제제를 사용한 노화 관련 장애 치료를 위한 방법 및 조성물
JP2020536929A (ja) * 2017-10-13 2020-12-17 アルカヘスト，インコーポレイテッド Ｃｃｒ３阻害剤を用いた、そう痒症、乾皮症、及び関連疾患を治療するための方法及び組成物
MX2020011114A (es) 2018-05-15 2021-01-29 Alkahest Inc Tratamiento de enfermedades asociadas con el envejecimiento con moduladores de la leucotrieno a4 hidrolasa.
JP2022502441A (ja) * 2018-09-26 2022-01-11 アルカヘスト，インコーポレイテッド Ｃｃｒ３阻害剤を用いて、加齢性機能障害を治療するための方法および組成物
CA3221177A1 (en) 2021-11-01 2023-05-04 Meghan Kerrisk Campbell Benzodioxane modulators of leukotriene a4 hydrolase (lta4h) for prevention and treatment of aging-associated diseases

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE7907121L (sv) 1979-08-27 1981-02-28 Astra Laekemedel Ab Ftalimidinderivat
JP2807577B2 (ja) 1990-06-15 1998-10-08 エーザイ株式会社 環状アミド誘導体
US6433165B1 (en) 1998-01-21 2002-08-13 Millennium Pharmaceuticals, Inc. Chemokine receptor antagonists and methods of use therefor
US6140349A (en) 1998-02-02 2000-10-31 Merck & Co., Inc. Cyclic amine modulators of chemokine receptor activity
JP2002501898A (ja) 1998-02-02 2002-01-22 メルク エンド カムパニー インコーポレーテッド ケモカイン受容体活性の環状アミン調節剤
EP1448528A2 (en) 2001-11-29 2004-08-25 Schering Corporation Preparation of pharmaceutical salts of 4((z)-(4-bromophenyl)(ethoxyimino)methyl)-1'-((2,4-dimethyl-1-oxido-3-pyridinyl)carbonyl)-4'-methyl-1,4'bipiperidine as ccr5-antagonists for the treatment of aids and related hiv infections
EP1596869B1 (en) 2003-01-21 2014-06-04 New Form Pharmaceuticals Inc. Novel cocrystallization
SG131946A1 (en) 2003-10-24 2007-05-28 Hoffmann La Roche Ccr3 receptor antagonists
CA2554465A1 (en) 2004-02-05 2005-08-25 Schering Corporation Piperidine derivatives useful as ccr3 antagonists
WO2006007448A2 (en) 2004-06-17 2006-01-19 Transform Pharmaceuticals, Inc. Pharmaceutical co-crystal compositions and related methods of use
JP2006137718A (ja) 2004-11-12 2006-06-01 Astellas Pharma Inc インドール若しくはインダゾール誘導体
US8030003B2 (en) 2004-12-07 2011-10-04 Children's Hospital Medical Center Diagnosis of eosinophilic esophagitis based on presence of an elevated level of eotaxin-3
DOP2006000051A (es) 2005-02-24 2006-08-31 Lilly Co Eli Inhibidores de vegf-r2 y métodos
JP3701964B1 (ja) * 2005-03-08 2005-10-05 アステラス製薬株式会社 キヌクリジン誘導体の新規な塩
JP2009533416A (ja) * 2006-04-12 2009-09-17 ファイザー・リミテッド ケモカインｃｃｒ５受容体の調節剤としてのピロリジン誘導体
KR101176697B1 (ko) * 2006-04-20 2012-08-23 에프. 호프만-라 로슈 아게 케모카인 수용체의 다이아제판 유도체 조절자
GB0701992D0 (en) 2007-02-02 2007-03-14 7Tm Pharma As Grehlin Receptor Modulators
US8008092B2 (en) 2007-10-09 2011-08-30 University Of Kentucky Research Foundation CCR3 inhibition for ocular angiogenesis and macular degeneration
TW201000446A (en) 2008-05-30 2010-01-01 Astrazeneca Ab New compounds useful in pain therapy
US8278302B2 (en) * 2009-04-08 2012-10-02 Boehringer Ingelheim International Gmbh Substituted piperidines as CCR3 antagonists
UA109290C2 (uk) * 2010-10-07 2015-08-10 Спільні кристали і солі інгібіторів ccr3
AR090566A1 (es) 2012-04-02 2014-11-19 Boehringer Ingelheim Int Proceso para la produccion de inhibidores de crr
US20130261153A1 (en) 2012-04-03 2013-10-03 Boehringer Ingelheim International Gmbh Use of ccr3-inhibitors
US10213421B2 (en) 2012-04-04 2019-02-26 Alkahest, Inc. Pharmaceutical formulations comprising CCR3 antagonists

Also Published As

Publication number Publication date
UY33655A (es) 2012-04-30
IL224269A (en) 2017-08-31
US20120264729A1 (en) 2012-10-18
MA34545B1 (fr) 2013-09-02
GEP20166488B (en) 2016-06-10
TW201305134A (zh) 2013-02-01
HRP20150419T1 (hr) 2015-05-22
SG188949A1 (en) 2013-05-31
HUE024540T2 (hu) 2016-01-28
MY167898A (en) 2018-09-26
TWI546294B (zh) 2016-08-21
ME02040B (me) 2015-05-20
AU2011311530B2 (en) 2015-04-09
CN103140486A (zh) 2013-06-05
KR20190104645A (ko) 2019-09-10
KR102163874B1 (ko) 2020-10-12
KR20180005717A (ko) 2018-01-16
BR112013008211A8 (pt) 2017-10-10
CA2807255A1 (en) 2012-04-12
SI2625174T1 (sl) 2015-03-31
BR122021010665B1 (pt) 2022-03-15
WO2012045803A1 (en) 2012-04-12
DK2625174T3 (da) 2015-02-02
US20140135307A1 (en) 2014-05-15
JP2013542207A (ja) 2013-11-21
US8742115B2 (en) 2014-06-03
EA201300436A8 (ru) 2018-01-31
AP2013006679A0 (en) 2013-01-31
EP2625174A1 (en) 2013-08-14
EP2625174B1 (en) 2015-01-21
EA201300436A1 (ru) 2013-08-30
BR112013008211A2 (pt) 2016-06-21
ECSP13012600A (es) 2013-07-31
KR20130118313A (ko) 2013-10-29
AP3268A (en) 2015-05-31
CL2013000488A1 (es) 2013-07-05
PL2625174T3 (pl) 2015-06-30
CA2807255C (en) 2018-11-13
BR112013008211B1 (pt) 2021-08-24
US20150105371A1 (en) 2015-04-16
US9233950B2 (en) 2016-01-12
PT2625174E (pt) 2015-03-09
AU2011311530A1 (en) 2013-01-31
KR101844215B1 (ko) 2018-04-03
EA029097B1 (ru) 2018-02-28
UA109290C2 (uk) 2015-08-10
CO6710910A2 (es) 2013-07-15
NZ605827A (en) 2015-09-25
CY1116168T1 (el) 2017-02-08
ES2535264T3 (es) 2015-05-07
MX2013003785A (es) 2013-06-05
RS53858B1 (en) 2015-08-31
JP5794713B2 (ja) 2015-10-14
AR083353A1 (es) 2013-02-21
CN103140486B (zh) 2016-08-03
KR102239690B1 (ko) 2021-04-13

Similar Documents

Publication Publication Date Title
PE20140188A1 (es) Co-cristales y sales de inhibidores de ccr3
PE20161064A1 (es) Derivado de sulfonamida o sales de adicion de acido farmaceuticamente aceptables del mismo
PE20141726A1 (es) Heterociclilaminas como inhibidores de pi 3k
PE20141322A1 (es) Ciclopropilaminas como inhibidores de desmetilasa 1 especifica de lisina
PE20161475A1 (es) Pirazolopiridinas y pirazolopirimidinas
PE20070362A1 (es) COMPUESTOS DERIVADOS DE INDAZOL-4-IL-2,4-PIRIMIDINDIAMINA COMO INHIBIDORES DE TIROSINA QUINASA (QUINASA Syk)
MX2020000404A (es) Inhibidores de tirosina quinasa de bazo (syk).
JP2016526024A5 (es)
UY33226A (es) Compuestos de pirrolopirimidina deuterada como inhibidores de la cdk4/6
MX361488B (es) Cocristales de (s)-n-metil-8-(1-((2'-metil-[4,5'-bipirimidin]-6-il ) amino)propan-2-il)quinolina-4-carboxamida y sus derivados deuterados como inhibidores de proteínas cinasa dependientes de adn (adn-pk).
CO7131357A2 (es) Compuestos de n-ariltriazol como antagonistas de lpar
CY1117122T1 (el) Παραγωγα πυραζολοσπειροκετονης για χρηση ως αναστολεις ακετyλ-coa καρβοξυλασης
PE20120690A1 (es) Derivados de 5-fluoropirimidinona
EA201490696A1 (ru) 3-пиримидин-4-ил-оксазолидин-2-оны в качестве ингибиторов мутантной idh
PE20120171A1 (es) Sales de adicion de aminas que contienen grupos hidroxilo y/o carboxilicos con derivados de acidos aminonicotinico como inhibidores de dhodh
EA201390917A1 (ru) Дигетероарильные соединения в качестве ингибиторов vps34
PE20180233A1 (es) Nuevos compuestos biciclicos como inhibidores duales de atx / ca
NZ598208A (en) Inhibitors of flaviviridae viruses
PE20141380A1 (es) Imidazopiridazinas como inhibidores de quinasa akt
PE20140966A1 (es) Quinazolincarboxamida azetidinas
ECSP13012494A (es) Inhibidores de oxadiazol de la producción de leucotrieno.
MX369956B (es) Metodos para preparar compuestos de benzoquinolina.
CY1124179T1 (el) Βελτιωμενη μεθοδος παρασκευης ριβαροξαμπανης με χρηση νεων ενδιαμεσων ενωσεων
EA201591957A1 (ru) Производные глутаримидов, их применение, фармацевтическая композиция на их основе, способы их получения
MX350862B (es) Acidos de piperidinil naftilacetico.

Legal Events

Date Code Title Description
FC Refusal