IL301180A - Use of pyrazolopyrimidine derivatives for the treatment of P13K-related disorders - Google Patents

Use of pyrazolopyrimidine derivatives for the treatment of P13K-related disorders

Info

Publication number
IL301180A
IL301180A IL301180A IL30118023A IL301180A IL 301180 A IL301180 A IL 301180A IL 301180 A IL301180 A IL 301180A IL 30118023 A IL30118023 A IL 30118023A IL 301180 A IL301180 A IL 301180A
Authority
IL
Israel
Prior art keywords
methyl
chloro
ethyl
pyrimidin
pyrazolo
Prior art date
Application number
IL301180A
Other languages
English (en)
Hebrew (he)
Original Assignee
Incyte Holdings Corp
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 Incyte Holdings Corp filed Critical Incyte Holdings Corp
Publication of IL301180A publication Critical patent/IL301180A/en

Links

Classifications

    • 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
    • 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
    • A61K31/535Heterocyclic 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
    • 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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
IL301180A 2013-03-01 2014-02-28 Use of pyrazolopyrimidine derivatives for the treatment of P13K-related disorders IL301180A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361771480P 2013-03-01 2013-03-01
PCT/US2014/019372 WO2014134426A1 (en) 2013-03-01 2014-02-28 USE OF PYRAZOLOPYRIMIDINE DERIVATIVES FOR THE TREATMENT OF PI3Kδ RELATED DISORDERS

Publications (1)

Publication Number Publication Date
IL301180A true IL301180A (en) 2023-05-01

Family

ID=50288319

Family Applications (6)

Application Number Title Priority Date Filing Date
IL311666A IL311666A (en) 2013-03-01 2014-02-28 Use of pyrazolopyrimidine derivatives for the treatment of P13K-related disorders
IL301180A IL301180A (en) 2013-03-01 2014-02-28 Use of pyrazolopyrimidine derivatives for the treatment of P13K-related disorders
IL240784A IL240784B (en) 2013-03-01 2015-08-24 Use of pyrazolopyrimidine derivatives for the treatment of p13k-related disorders
IL267853A IL267853B (en) 2013-03-01 2019-07-04 Use of pyrazolopyrimidine derivatives for the treatment of p13k associated disorders
IL274771A IL274771A (en) 2013-03-01 2020-05-19 Use of pyrazolopyrimidine derivatives for the treatment of PI3Kδ associated disorders
IL283943A IL283943B2 (en) 2013-03-01 2021-06-13 Use of pyrazolopyrimidine derivatives for the treatment of p13k associated disorders

Family Applications Before (1)

Application Number Title Priority Date Filing Date
IL311666A IL311666A (en) 2013-03-01 2014-02-28 Use of pyrazolopyrimidine derivatives for the treatment of P13K-related disorders

Family Applications After (4)

Application Number Title Priority Date Filing Date
IL240784A IL240784B (en) 2013-03-01 2015-08-24 Use of pyrazolopyrimidine derivatives for the treatment of p13k-related disorders
IL267853A IL267853B (en) 2013-03-01 2019-07-04 Use of pyrazolopyrimidine derivatives for the treatment of p13k associated disorders
IL274771A IL274771A (en) 2013-03-01 2020-05-19 Use of pyrazolopyrimidine derivatives for the treatment of PI3Kδ associated disorders
IL283943A IL283943B2 (en) 2013-03-01 2021-06-13 Use of pyrazolopyrimidine derivatives for the treatment of p13k associated disorders

Country Status (32)

Country Link
US (6) US9932341B2 (enExample)
EP (3) EP4233869A3 (enExample)
JP (5) JP6545106B2 (enExample)
KR (5) KR102298150B1 (enExample)
CN (2) CN105120871B (enExample)
AR (1) AR094964A1 (enExample)
AU (5) AU2014223257B2 (enExample)
BR (1) BR112015020941A2 (enExample)
CA (1) CA2901993C (enExample)
CL (1) CL2015002442A1 (enExample)
CR (1) CR20150472A (enExample)
CY (1) CY1122712T1 (enExample)
DK (1) DK2961410T3 (enExample)
EA (2) EA201591612A1 (enExample)
ES (2) ES2945212T3 (enExample)
HR (1) HRP20200263T1 (enExample)
HU (1) HUE047719T2 (enExample)
IL (6) IL311666A (enExample)
LT (1) LT2961410T (enExample)
MX (2) MX367713B (enExample)
MY (1) MY177875A (enExample)
PE (1) PE20151996A1 (enExample)
PH (3) PH12021552233A1 (enExample)
PL (1) PL2961410T3 (enExample)
PT (1) PT2961410T (enExample)
RS (1) RS59958B1 (enExample)
SG (3) SG11201506654UA (enExample)
SI (1) SI2961410T1 (enExample)
SM (1) SMT202000043T1 (enExample)
TW (5) TWI736135B (enExample)
UA (1) UA119641C2 (enExample)
WO (1) WO2014134426A1 (enExample)

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW201602113A (zh) 2009-06-29 2016-01-16 英塞特公司 作為pi3k抑制劑之嘧啶酮
SG10201912484RA (en) 2011-09-02 2020-02-27 Incyte Corp Heterocyclylamines as pi3k inhibitors
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
CA2897200C (en) 2013-01-14 2021-07-06 Incyte Corporation Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors
AR094664A1 (es) 2013-01-15 2015-08-19 Incyte Corp Compuestos de tiazolcarboxamidas y piridinacarboxamida utiles como inhibidores de quinasa pim
TWI736135B (zh) 2013-03-01 2021-08-11 美商英塞特控股公司 吡唑并嘧啶衍生物治療PI3Kδ相關病症之用途
US9556197B2 (en) 2013-08-23 2017-01-31 Incyte Corporation Furo- and thieno-pyridine carboxamide compounds useful as pim kinase inhibitors
JP6537527B2 (ja) 2014-04-08 2019-07-03 インサイト・コーポレイションIncyte Corporation Jak及びpi3k阻害剤併用によるb細胞悪性腫瘍の処置
US10077277B2 (en) 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
US9822124B2 (en) 2014-07-14 2017-11-21 Incyte Corporation Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors
US9580418B2 (en) 2014-07-14 2017-02-28 Incyte Corporation Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors
US9586949B2 (en) 2015-02-09 2017-03-07 Incyte Corporation Aza-heteroaryl compounds as PI3K-gamma inhibitors
EP4183789A1 (en) * 2015-02-27 2023-05-24 Incyte Holdings Corporation Salts of pi3k inhibitor and processes for their preparation
US9988401B2 (en) 2015-05-11 2018-06-05 Incyte Corporation Crystalline forms of a PI3K inhibitor
US9540347B2 (en) 2015-05-29 2017-01-10 Incyte Corporation Pyridineamine compounds useful as Pim kinase inhibitors
AR105967A1 (es) 2015-09-09 2017-11-29 Incyte Corp Sales de un inhibidor de pim quinasa
TW201718546A (zh) 2015-10-02 2017-06-01 英塞特公司 適用作pim激酶抑制劑之雜環化合物
PT3371190T (pt) 2015-11-06 2022-07-08 Incyte Corp Compostos heterocíclicos como inibidores de pi3k-gamma
ES2833955T3 (es) 2016-01-05 2021-06-16 Incyte Corp Piridinas sustituidas con pirazol/imidazol como inhibidores de PI3K-Gamma
WO2017172368A1 (en) 2016-03-31 2017-10-05 Oncternal Therapeutics, Inc. Indoline analogs and uses thereof
WO2017223414A1 (en) 2016-06-24 2017-12-28 Incyte Corporation HETEROCYCLIC COMPOUNDS AS PI3K-γ INHIBITORS
IL272988B (en) * 2017-09-08 2022-08-01 Beigene Ltd Imidazo[1,5-a]pyrazine derivatives as pi3kdelta inhibitors
MD3697789T2 (ro) 2017-10-18 2022-02-28 Incyte Corp Derivați imidazol condensați substituiți cu grupări hidroxi terțiare ca inhibitori PI3K-GAMA
AR113922A1 (es) 2017-12-08 2020-07-01 Incyte Corp Terapia de combinación de dosis baja para el tratamiento de neoplasias mieloproliferativas
MY198902A (en) * 2018-01-10 2023-10-02 Idorsia Pharmaceuticals Ltd 2,4,6,7-tetrahydro-pyrazolo[4,3-d]pyrimidin-5-one derivatives and related compounds as c5a receptor modulators for treating vasculitis and inflammatory diseases
RS63124B1 (sr) 2018-03-08 2022-05-31 Incyte Corp Aminopirazin diol jedinjenja kao pi3k-y inhibitori
CN119258070A (zh) * 2018-06-01 2025-01-07 因赛特公司 治疗pi3k相关病症的给药方案
WO2020010003A1 (en) 2018-07-02 2020-01-09 Incyte Corporation AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS
TWI727392B (zh) * 2018-08-13 2021-05-11 美商基利科學股份有限公司 噻二唑irak4抑制劑
CN110833552A (zh) * 2018-08-15 2020-02-25 广西梧州制药(集团)股份有限公司 吡唑并嘧啶衍生物在治疗狼疮肾炎的用途
CR20250050A (es) * 2018-09-05 2025-03-19 Incyte Corp Formas cristalinas de un inhibidor de fosfoinositida 3–quinasa (pi3k) (divisional 2021-0165)
WO2022115120A1 (en) 2020-11-30 2022-06-02 Incyte Corporation Combination therapy with an anti-cd19 antibody and parsaclisib
TW202241436A (zh) 2020-11-30 2022-11-01 美商英塞特公司 抗cd19抗體及帕薩昔布(parsaclisib)之組合療法
CN112808550B (zh) * 2020-12-28 2021-10-01 青岛理工大学 用于海洋工程的劣化免疫仿生防护界面及制备方法
AR127966A1 (es) 2021-12-16 2024-03-13 Incyte Corp Formulaciones tópicas de inhibidores de pi3k-delta

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5521184A (en) * 1992-04-03 1996-05-28 Ciba-Geigy Corporation Pyrimidine derivatives and processes for the preparation thereof
ES2342240T3 (es) 1998-08-11 2010-07-02 Novartis Ag Derivados de isoquinolina con actividad que inhibe la angiogenia.
US6133031A (en) 1999-08-19 2000-10-17 Isis Pharmaceuticals Inc. Antisense inhibition of focal adhesion kinase expression
GB9905075D0 (en) 1999-03-06 1999-04-28 Zeneca Ltd Chemical compounds
GB0004890D0 (en) 2000-03-01 2000-04-19 Astrazeneca Uk Ltd Chemical compounds
CA2413330A1 (en) 2000-06-28 2002-01-03 Smithkline Beecham P.L.C. Wet milling process
DE60230890D1 (de) 2001-09-19 2009-03-05 Aventis Pharma Sa Indolizine als kinaseproteinhemmer
IL161156A0 (en) 2001-10-30 2004-08-31 Novartis Ag Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity
AR037647A1 (es) 2002-05-29 2004-12-01 Novartis Ag Derivados de diarilurea utiles para el tratamiento de enfermedades dependientes de la cinasa de proteina
GB0215676D0 (en) 2002-07-05 2002-08-14 Novartis Ag Organic compounds
TWI335913B (en) 2002-11-15 2011-01-11 Vertex Pharma Diaminotriazoles useful as inhibitors of protein kinases
UA80767C2 (en) 2002-12-20 2007-10-25 Pfizer Prod Inc Pyrimidine derivatives for the treatment of abnormal cell growth
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
AR045944A1 (es) 2003-09-24 2005-11-16 Novartis Ag Derivados de isoquinolina 1.4-disustituidas
CA2567662C (en) 2004-06-10 2012-11-27 Irm Llc Compounds and compositions as protein kinase inhibitors
CN101106983A (zh) 2004-11-24 2008-01-16 诺瓦提斯公司 JAK抑制剂与至少一种Bcr-Abl、Flt-3、FAK或RAF激酶抑制剂的组合
WO2007084557A2 (en) 2006-01-17 2007-07-26 Vertex Pharmaceuticals Incorporated Azaindoles useful as inhibitors of janus kinases
TW200916447A (en) 2007-08-29 2009-04-16 Methylgene Inc Sirtuin inhibitors
WO2009157880A1 (en) 2008-06-27 2009-12-30 S*Bio Pte Ltd Pyrazine substituted purines
AR073651A1 (es) * 2008-09-24 2010-11-24 Novartis Ag Formulaciones galenicas de compuestos organicos
JP5731978B2 (ja) * 2008-09-26 2015-06-10 インテリカイン, エルエルシー 複素環キナーゼ阻害剤
US20120046333A1 (en) 2009-04-09 2012-02-23 Oncothyreon Incorporated Methods and Compositions of PI-3 Kinase Inhibitors for Treating Fibrosis
TW201602113A (zh) 2009-06-29 2016-01-16 英塞特公司 作為pi3k抑制劑之嘧啶酮
US8293753B2 (en) 2009-07-02 2012-10-23 Novartis Ag Substituted 2-carboxamide cycloamino ureas
EP2470546B1 (en) 2009-08-28 2013-07-24 Takeda Pharmaceutical Company Limited Hexahydrooxazinopteridine compounds for use as mtor inhibitors
WO2011075630A1 (en) 2009-12-18 2011-06-23 Incyte Corporation Substituted fused aryl and heteroaryl derivatives as pi3k inhibitors
US8759359B2 (en) 2009-12-18 2014-06-24 Incyte Corporation Substituted heteroaryl fused derivatives as PI3K inhibitors
WO2011130342A1 (en) 2010-04-14 2011-10-20 Incyte Corporation FUSED DERIVATIVES AS ΡI3Κδ INHIBITORS
US9062055B2 (en) 2010-06-21 2015-06-23 Incyte Corporation Fused pyrrole derivatives as PI3K inhibitors
CA2822070C (en) 2010-12-20 2019-09-17 Incyte Corporation N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors
AU2012212323A1 (en) 2011-02-01 2013-09-12 The Board Of Trustees Of The University Of Illinois HDAC inhibitors and therapeutic methods using the same
US9108984B2 (en) 2011-03-14 2015-08-18 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
US9126948B2 (en) 2011-03-25 2015-09-08 Incyte Holdings Corporation Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
SG10201912484RA (en) 2011-09-02 2020-02-27 Incyte Corp Heterocyclylamines as pi3k inhibitors
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
TWI736135B (zh) * 2013-03-01 2021-08-11 美商英塞特控股公司 吡唑并嘧啶衍生物治療PI3Kδ相關病症之用途
US10077277B2 (en) * 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
EP4183789A1 (en) * 2015-02-27 2023-05-24 Incyte Holdings Corporation Salts of pi3k inhibitor and processes for their preparation
CN119258070A (zh) 2018-06-01 2025-01-07 因赛特公司 治疗pi3k相关病症的给药方案
WO2020102150A1 (en) * 2018-11-13 2020-05-22 Incyte Corporation Heterocyclic derivatives as pi3k inhibitors

Also Published As

Publication number Publication date
EP3632442B1 (en) 2023-04-05
JP2025003975A (ja) 2025-01-14
PE20151996A1 (es) 2016-01-13
JP6545106B2 (ja) 2019-07-17
TWI657090B (zh) 2019-04-21
JP7556010B2 (ja) 2024-09-25
SI2961410T1 (sl) 2020-03-31
TW201444846A (zh) 2014-12-01
US20220119393A1 (en) 2022-04-21
US20220106318A1 (en) 2022-04-07
AR094964A1 (es) 2015-09-09
KR102717616B1 (ko) 2024-10-16
CY1122712T1 (el) 2021-03-12
KR102298150B1 (ko) 2021-09-07
TW201929860A (zh) 2019-08-01
JP2016510035A (ja) 2016-04-04
JP6776399B2 (ja) 2020-10-28
KR20210110409A (ko) 2021-09-07
EP4233869A2 (en) 2023-08-30
PH12021552233A1 (en) 2022-07-18
PH12019501321A1 (en) 2020-10-12
AU2022218495B2 (en) 2024-10-03
KR20230145517A (ko) 2023-10-17
CA2901993C (en) 2023-03-07
LT2961410T (lt) 2020-02-10
US9932341B2 (en) 2018-04-03
AU2020210278A1 (en) 2020-08-20
KR102586858B1 (ko) 2023-10-11
IL240784B (en) 2020-06-30
TWI736135B (zh) 2021-08-11
IL240784A0 (en) 2015-10-29
JP2023036609A (ja) 2023-03-14
AU2020210278B2 (en) 2022-05-26
PH12015501920A1 (en) 2016-01-18
IL311666A (en) 2024-05-01
US12152033B2 (en) 2024-11-26
HK1221398A1 (en) 2017-06-02
EP2961410B1 (en) 2019-12-11
HUE047719T2 (hu) 2020-05-28
CL2015002442A1 (es) 2016-02-05
PH12019501321B1 (en) 2020-10-12
CR20150472A (es) 2016-01-04
IL283943B2 (en) 2023-08-01
US20210332059A1 (en) 2021-10-28
HRP20200263T1 (hr) 2020-05-29
US20190040067A1 (en) 2019-02-07
JP2021020914A (ja) 2021-02-18
KR20150135327A (ko) 2015-12-02
IL283943B1 (en) 2023-04-01
AU2014223257A1 (en) 2015-09-24
ES2945212T3 (es) 2023-06-29
US20250289823A1 (en) 2025-09-18
TW202214254A (zh) 2022-04-16
PT2961410T (pt) 2020-03-02
DK2961410T3 (da) 2020-02-17
TWI841376B (zh) 2024-05-01
AU2018264053B2 (en) 2020-08-20
SG10201707130UA (en) 2017-10-30
ES2774436T3 (es) 2020-07-21
KR102454308B1 (ko) 2022-10-14
MX367713B (es) 2019-09-03
EA202192151A1 (ru) 2021-12-31
AU2014223257B2 (en) 2018-11-29
UA119641C2 (uk) 2019-07-25
WO2014134426A1 (en) 2014-09-04
CA2901993A1 (en) 2014-09-04
SMT202000043T1 (it) 2020-03-13
TW202333734A (zh) 2023-09-01
JP2019142941A (ja) 2019-08-29
US20140249132A1 (en) 2014-09-04
EP2961410A1 (en) 2016-01-06
KR20220143146A (ko) 2022-10-24
SG10201912275YA (en) 2020-04-29
PL2961410T3 (pl) 2020-05-18
IL267853B (en) 2020-03-31
PH12015501920B1 (en) 2016-01-18
CN109010343A (zh) 2018-12-18
AU2024287194A1 (en) 2025-01-23
BR112015020941A2 (pt) 2017-07-18
EA201591612A1 (ru) 2016-05-31
EP4233869A3 (en) 2023-11-01
AU2022218495A1 (en) 2022-09-08
KR20240152422A (ko) 2024-10-21
SG11201506654UA (en) 2015-09-29
CN105120871A (zh) 2015-12-02
MX2015011273A (es) 2015-12-03
MX2019010422A (es) 2019-10-15
CN105120871B (zh) 2018-08-10
JP7189185B2 (ja) 2022-12-13
IL274771A (en) 2020-07-30
RS59958B1 (sr) 2020-03-31
EP3632442A1 (en) 2020-04-08
MY177875A (en) 2020-09-24
IL283943A (en) 2021-07-29
AU2018264053A1 (en) 2018-12-06
TWI687220B (zh) 2020-03-11
IL267853A (en) 2019-09-26
TW202019428A (zh) 2020-06-01

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