AR092347A1 - Derivados de azaindol - Google Patents

Derivados de azaindol

Info

Publication number
AR092347A1
AR092347A1 ARP130102427A ARP130102427A AR092347A1 AR 092347 A1 AR092347 A1 AR 092347A1 AR P130102427 A ARP130102427 A AR P130102427A AR P130102427 A ARP130102427 A AR P130102427A AR 092347 A1 AR092347 A1 AR 092347A1
Authority
AR
Argentina
Prior art keywords
independently selected
alkyl
hydrogen
haloalkyl
halo
Prior art date
Application number
ARP130102427A
Other languages
English (en)
Original Assignee
Takeda Pharmaceuticals Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=48795966&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR092347(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Takeda Pharmaceuticals Co filed Critical Takeda Pharmaceuticals Co
Publication of AR092347A1 publication Critical patent/AR092347A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/02Nasal agents, e.g. decongestants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • 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
    • A61P17/00Drugs for dermatological disorders
    • A61P17/04Antipruritics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • 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
    • 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
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • 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
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • 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
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/16Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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 two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Dermatology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Transplantation (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Vascular Medicine (AREA)
  • Otolaryngology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Reivindicación 1: Un compuesto de la fórmula (1), o una de sus sales farmacéuticamente aceptable, donde: R¹ se selecciona entre cicloalquilo C₃₋₈, heterociclilo C₂₋₆, arilo C₆₋₁₄, y heteroarilo C₁₋₉, cada uno de los cuales está opcionalmente sustituido con entre uno y cinco sustituyentes que se seleccionan, de manera independiente, entre halo, oxo, -CN, R¹¹, y R¹²; cada uno de R², R⁴, y R⁵ se selecciona, de manera independiente, entre hidrógeno, halo, -OH, -CN, alquilo C₁₋₃, y haloalquilo C₁₋₃; R³ se selecciona entre hidrógeno, alquilo C₁₋₃, y haloalquilo C₁₋₃; cada uno de R⁶ y R⁷ se selecciona, de manera independiente, entre hidrógeno, alquilo C₁₋₃, y haloalquilo C₁₋₃; R⁸ se selecciona de hidrógeno, metilo, y -NH₂; R⁹ se selecciona entre hidrógeno, halo, -CN, haloalquilo C₁₋₃, -OR¹⁶, -C(O)R¹⁶, -C(O)OR¹⁶, -C(O)N(R¹⁶)R¹⁷, -C(O)N(R¹⁶)OR¹⁷, -C(O)N(R¹⁶)S(O)₂R¹⁸, -SR¹⁶, -S(O)R¹⁸, -S(O)₂R¹⁸, y -S(O)₂N(R¹⁶)R¹⁷; o R⁸ se selecciona entre -NH- y -CH₂-, y R⁸ y R⁹, junto con los átomos de carbono a los cuales están unidos, forman un heteroarileno C₂₋₄ que tiene 5 átomos en el anillo y entre 1 y 3 heteroátomos, cada uno de los heteroátomos es nitrógeno, y donde el heteroarileno C₂₋₄ está opcionalmente sustituido con R¹²; R¹⁰ se selecciona entre halo, -OH, alquilo C₁₋₃, -NHR¹⁶, y -NHC(O)R¹⁶; cada R¹¹ se selecciona, de manera independiente, entre -OR¹³, -N(R¹³)R¹⁴, -NR¹³C(O)R¹⁴, -NHC(O)NR¹³R¹⁴, -NR¹³C(O)NHR¹⁴, -C(O)R¹³, -C(O)OR¹³, -C(O)N(R¹³)R¹⁴, -C(O)N(R¹³)OR¹⁴, -C(O)N(R¹³)S(O)₂R¹², -N(R¹³)S(O)₂R¹², -SR¹³, -S(O)R¹², -S(O)₂R¹², y -S(O)₂N(R¹³)R¹⁴; cada R¹² se selecciona, de manera independiente, entre alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈-(CH₂)ₘ-, arilo C₆₋₁₄-(CH₂)ₘ-, heterociclilo C₂₋₆-(CH₂)ₘ-, y heteroarilo C₁₋₉-(CH₂)ₘ-, cada uno de los cuales está opcionalmente sustituido con entre uno y cinco sustituyentes que se seleccionan, de manera independiente, entre halo, oxo, -CN, alquilo C₁₋₆, haloalquilo C₁₋₆ y R¹⁵; cada R¹³ y R¹⁴ se selecciona, de manera independiente, entre (a) hidrógeno; y (b) alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₆-(CH₂)ₘ-, arilo C₆₋₁₄-(CH₂)ₘ-, heterociclilo C₂₋₆-(CH₂)ₘ-, y heteroarilo C₁₋₉-(CH₂)ₘ-, cada uno de los cuales está opcionalmente sustituido con entre uno y cinco sustituyentes que se seleccionan, de manera independiente, entre halo, oxo, -CN, alquilo C₁₋₆, haloalquilo C₁₋₆ y R¹⁵; cada R¹⁵ se selecciona, de manera independiente, entre -OR¹⁶, -N(R¹⁶)R¹⁷, -N(R¹⁶)C(O)R¹⁷, -NHC(O)NR¹⁶R¹⁷, -NR¹⁶C(O)NHR¹⁷, -C(O)R¹⁶, -C(O)OR¹⁶, -C(O)N(R¹⁶)R¹⁷, -C(O)N(R¹⁶)OR¹⁷, -C(O)N(R¹⁶)S(O)₂R¹⁸, -NR¹⁶S(O)₂R¹⁸, -SR¹⁶, -S(O)R¹⁸, -S(O)₂R¹⁸, y -S(O)₂N(R¹⁶)R¹⁷; cada R¹⁶ y R¹⁷ se selecciona, de manera independiente, entre hidrógeno, alquilo C₁₋₆, y cicloalquilo C₃₋₆; cada R¹⁸ se selecciona, de manera independiente, entre alquilo C₁₋₆ y cicloalquilo C₃₋₆; cada m se selecciona, de manera independiente, entre 0, 1, 2, 3 y 4; donde cada una de las fracciones de heteroarilo mencionadas tiene, de manera independiente, 1 a 4 heteroátomos que se seleccionan de manera independiente de N, O, y S, y cada una de las fracciones heterociclilo mencionadas tiene independientemente 1 a 4 heteroátomos que se seleccionan de manera independiente de N, O y S.
ARP130102427A 2012-07-10 2013-07-08 Derivados de azaindol AR092347A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201261670116P 2012-07-10 2012-07-10

Publications (1)

Publication Number Publication Date
AR092347A1 true AR092347A1 (es) 2015-04-15

Family

ID=48795966

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP130102427A AR092347A1 (es) 2012-07-10 2013-07-08 Derivados de azaindol

Country Status (26)

Country Link
US (2) US8835420B2 (es)
EP (1) EP2872507A1 (es)
JP (1) JP2015522074A (es)
KR (1) KR20150031334A (es)
CN (1) CN104619708A (es)
AP (1) AP2015008236A0 (es)
AR (1) AR092347A1 (es)
AU (1) AU2013288895A1 (es)
BR (1) BR112015000386A2 (es)
CA (1) CA2878502A1 (es)
CO (1) CO7280475A2 (es)
CR (1) CR20150056A (es)
DO (1) DOP2015000002A (es)
EA (1) EA201590183A1 (es)
HK (1) HK1210771A1 (es)
IL (1) IL236535A0 (es)
MA (1) MA37831B1 (es)
MX (1) MX2015000107A (es)
NZ (1) NZ704160A (es)
PE (1) PE20150754A1 (es)
PH (1) PH12015500063B1 (es)
SG (1) SG11201500063UA (es)
TN (1) TN2015000005A1 (es)
TW (1) TW201414734A (es)
UY (1) UY34893A (es)
WO (1) WO2014011568A1 (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA031153B1 (ru) * 2011-06-10 2018-11-30 Мерк Патент Гмбх Применение пиримидиновых соединений с btk ингибирующей активностью
UY35945A (es) * 2014-01-09 2015-08-31 Takeda Pharmaceutical Derivados de azaindol
WO2015106014A1 (en) * 2014-01-09 2015-07-16 Takeda Pharmaceutical Company Limited Azaindole derivatives
WO2016064957A1 (en) 2014-10-22 2016-04-28 Bristol-Myers Squibb Company Bicyclic heteroaryl amine compounds as pi3k inhibitors
WO2016064958A1 (en) 2014-10-22 2016-04-28 Bristol-Myers Squibb Company Heteroaryl substituted pyrrolotriazine amine compounds as pi3k inhibitors
US9997391B2 (en) * 2015-10-19 2018-06-12 QROMIS, Inc. Lift off process for chip scale package solid state devices on engineered substrate
WO2017079542A1 (en) * 2015-11-04 2017-05-11 Merck Patent Gmbh Methods for treating cancer using pyrimidine and pyridine compounds with btk inhibitory activity
FI3377484T3 (fi) * 2015-11-17 2023-11-30 Merck Patent Gmbh Menetelmiä multippeliskleroosin hoitoon käyttämällä pyrimidiini- ja pyridiiniyhdisteitä, joilla on BTK inhiboiva vaikutus
US10792283B2 (en) * 2016-03-05 2020-10-06 Hangzhou Zhengxiang Pharmaceuticals Co., Ltd. Quinoline analogs as phosphatidylinositol 3-kinase inhibitors
US10755986B2 (en) * 2016-03-29 2020-08-25 QROMIS, Inc. Aluminum nitride based Silicon-on-Insulator substrate structure
CN107964018A (zh) * 2016-10-19 2018-04-27 中国人民解放军军事医学科学院毒物药物研究所 取代嘌呤酮类衍生物及其医药用途
CA3142088C (en) * 2019-05-08 2023-02-28 Tyk Medicines, Inc. Compound used as kinase inhibitor and application thereof
CN112794851B (zh) * 2021-01-26 2022-08-23 复旦大学 3-(吡啶-3基)-7-氮杂吲哚衍生物PI3Kδ抑制剂及其制备方法与应用

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
US6187777B1 (en) 1998-02-06 2001-02-13 Amgen Inc. Compounds and methods which modulate feeding behavior and related diseases
MXPA02010618A (es) 2000-04-25 2004-05-05 Icos Corp Inhibidores de fosfatidilinositol 3-quinasa delta.
US6667300B2 (en) 2000-04-25 2003-12-23 Icos Corporation Inhibitors of human phosphatidylinositol 3-kinase delta
US20020183292A1 (en) 2000-10-31 2002-12-05 Michel Pairet Pharmaceutical compositions based on anticholinergics and corticosteroids
US6806272B2 (en) 2001-09-04 2004-10-19 Boehringer Ingelheim Pharma Kg Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions
US7348337B2 (en) 2002-05-28 2008-03-25 Bristol-Myers Squibb Company Indole, azaindole and related heterocyclic 4-alkenyl piperidine amides
US6900206B2 (en) 2002-06-20 2005-05-31 Bristol-Myers Squibb Company Indole, azaindole and related heterocyclic sulfonylureido piperazine derivatives
US6861422B2 (en) 2003-02-26 2005-03-01 Boehringer Ingelheim Pharma Gmbh & Co. Kg Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions
CN100398545C (zh) 2003-09-08 2008-07-02 安万特药物公司 噻吩并吡唑类化合物
DE602004010299T2 (de) 2003-12-22 2008-09-18 Memory Pharmaceuticals Corp. Indole, 1h-indazole, 1,2-benzisoxazole und 1,2-benzisothiazole und deren herstellung und anwendungen
EP1742944B1 (en) 2004-04-22 2010-11-10 Memory Pharmaceuticals Corporation Indoles, 1h-indazoles, 1,2-benzisoxazoles, 1,2-benzoisothiazoles, and preparation and uses thereof
GB0415364D0 (en) 2004-07-09 2004-08-11 Astrazeneca Ab Pyrimidine derivatives
DE102004034623A1 (de) 2004-07-16 2006-02-02 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue 6-Formyl-tetrahydropteridine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
US20060035903A1 (en) 2004-08-14 2006-02-16 Boehringer Ingelheim International Gmbh Storage stable perfusion solution for dihydropteridinones
US7759485B2 (en) 2004-08-14 2010-07-20 Boehringer Ingelheim International Gmbh Process for the manufacture of dihydropteridinones
WO2006021548A1 (de) 2004-08-27 2006-03-02 Boehringer Ingelheim International Gmbh Dihydropteridinone, verfahren zu deren herstellung und deren verwendung als arzneimittel
DE102004058337A1 (de) 2004-12-02 2006-06-14 Boehringer Ingelheim Pharma Gmbh & Co. Kg Verfahren zur Herstellung von annelierten Piperazin-2-on Derivaten
FR2878849B1 (fr) 2004-12-06 2008-09-12 Aventis Pharma Sa Indoles substitues, compositions les contenant, procede de fabrication et utilisation
EP2057129A1 (en) 2006-08-24 2009-05-13 AstraZeneca AB Morpholino pyrimidine derivatives useful in the treatment of proliferative disorders
CL2007003444A1 (es) 2006-11-30 2008-06-27 Genentech Inc Compuestos derivados de pirrolo[3,2-c]piridina; composicion farmaceutica; y uso en el tratamiento de un trastorno hiperproliferativo o una enfermedad inflamatoria.
EP2164850B1 (en) 2007-06-12 2016-01-13 Genentech, Inc. N-substituted azaindoles and methods of use
CN106279283A (zh) 2007-08-13 2017-01-04 症变治疗公司 新颖的葡糖激酶活化剂
WO2010036380A1 (en) 2008-09-26 2010-04-01 Intellikine, Inc. Heterocyclic kinase inhibitors
SG175877A1 (en) 2009-05-04 2011-12-29 Plexxikon Inc Compounds and methods for inhibition of renin, and indications therefor
AR077267A1 (es) * 2009-06-25 2011-08-17 Amgen Inc Derivados nitrogenados heterociclicos inhibidores selectivos de pi3k, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de enfermedades inflamatorias y/o autoinmunes.
JP2012531435A (ja) 2009-06-25 2012-12-10 アムジエン・インコーポレーテツド PI3K阻害剤としての4H−ピリド[1,2−a]ピリミジン−4−オン誘導体
KR101763656B1 (ko) 2009-06-29 2017-08-01 인사이트 홀딩스 코포레이션 Pi3k 저해물질로서의 피리미디논
AR085406A1 (es) 2011-02-25 2013-09-25 Takeda Pharmaceutical Oxazinopteridinas y oxazinopteridinonas n-sustituidas
UY35945A (es) * 2014-01-09 2015-08-31 Takeda Pharmaceutical Derivados de azaindol

Also Published As

Publication number Publication date
MA37831B1 (fr) 2018-09-28
BR112015000386A2 (pt) 2017-06-27
WO2014011568A1 (en) 2014-01-16
US20140343033A1 (en) 2014-11-20
CR20150056A (es) 2015-05-25
AU2013288895A1 (en) 2015-02-12
CO7280475A2 (es) 2015-05-29
MA37831A1 (fr) 2018-02-28
DOP2015000002A (es) 2015-04-15
CN104619708A (zh) 2015-05-13
US8835420B2 (en) 2014-09-16
PH12015500063A1 (en) 2015-03-02
KR20150031334A (ko) 2015-03-23
CA2878502A1 (en) 2014-01-16
EA201590183A1 (ru) 2015-06-30
JP2015522074A (ja) 2015-08-03
AP2015008236A0 (en) 2015-01-31
MX2015000107A (es) 2015-04-14
TW201414734A (zh) 2014-04-16
EP2872507A1 (en) 2015-05-20
PE20150754A1 (es) 2015-05-15
NZ704160A (en) 2017-01-27
TN2015000005A1 (en) 2016-06-29
PH12015500063B1 (en) 2015-03-02
HK1210771A1 (en) 2016-05-06
UY34893A (es) 2014-02-28
SG11201500063UA (en) 2015-03-30
US20140018344A1 (en) 2014-01-16
IL236535A0 (en) 2015-02-26

Similar Documents

Publication Publication Date Title
AR092347A1 (es) Derivados de azaindol
AR095198A1 (es) Derivados de triazolona de piridinilo y piridinilo fusionado
AR092742A1 (es) Piridinonas antifibroticas
AR103297A1 (es) Pirrolo y pirazolopirimidinas como inhibidores de la proteasa 7 específica de ubiquitina
AR102492A1 (es) Cromanos sustituidos y métodos para su uso
AR103252A1 (es) Compuestos de quinazolina
AR094299A1 (es) Derivados de ftalazin-1(2h)-ona sustituidos
AR091424A1 (es) Compuestos triciclicos sustituidos como inhibidores de receptores del factor de crecimiento del fibroplasto (fgfr)
AR102177A1 (es) Compuestos de heteroarilo como inhibidores de btk y usos de los mismos
AR111407A1 (es) Compuestos inhibidores de ask1 y usos de los mismos
AR103969A1 (es) Inmunomoduladores
AR098872A1 (es) Moduladores de tetrahidropiridopirazinas de gpr6
AR100809A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR097571A1 (es) Compuestos espirocíclicos como inhibidores de la triptofano hidroxilasa
AR100808A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR096979A1 (es) Derivados de pirrol, su procedimiento de preparación y las composiciones farmacéuticas que los contienen
AR106301A1 (es) Composiciones de pirrolpirimidina como inhibidores de quinasas
AR095359A1 (es) Compuestos heteroaromáticos y su uso como ligandos d1 de dopamina
AR104878A1 (es) MODULADORES DE ROR GAMMA (RORg)
AR099890A1 (es) Inhibidores de histona demetilasas
AR112907A1 (es) Pirazoles inhibidores de monoacilglicerol lipasa (magl)
AR104879A1 (es) MODULADORES DE ROR GAMMA (RORg)
AR095136A1 (es) Derivados de pirazol microbiocidas
AR107321A1 (es) Compuestos antiproliferativos, y sus composiciones farmacéuticas y usos
AR101077A1 (es) Triterpenoides con actividad inhibidora de la maduración de hiv

Legal Events

Date Code Title Description
FB Suspension of granting procedure