MA45920B1 - Inhibiteurs de pyridopyrimidinone cdk2/4/6 - Google Patents

Inhibiteurs de pyridopyrimidinone cdk2/4/6

Info

Publication number
MA45920B1
MA45920B1 MA45920A MA45920A MA45920B1 MA 45920 B1 MA45920 B1 MA 45920B1 MA 45920 A MA45920 A MA 45920A MA 45920 A MA45920 A MA 45920A MA 45920 B1 MA45920 B1 MA 45920B1
Authority
MA
Morocco
Prior art keywords
pyridopyrimidinone
cdk2
inhibitors
compounds
salts
Prior art date
Application number
MA45920A
Other languages
English (en)
Other versions
MA45920A (fr
Inventor
Sacha Ninkovic
Eugene Yuanjin Rui
Douglas Carl Behenna
Asako Nagata
Sajiv Krishnan Nair
Robert Louis Hoffman
Ping Chen
Kevin Daniel Freeman-Cook
Mehran Jalaie
Martha Alicia Ornelas
Cynthia Louise Palmer
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of MA45920A publication Critical patent/MA45920A/fr
Publication of MA45920B1 publication Critical patent/MA45920B1/fr

Links

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
    • C07D487/02—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 two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

L'invention concerne des composés de formule générale (i), et des sels pharmaceutiquement acceptables de ceux-ci, dans lesquels r1, r2, r2a, r2b, r3, r4, r5a, r5b, r6, r7, r8, r9, p, q et r sont tels que définis dans la description, ainsi que des compositions pharmaceutiques comprenant de tels composés et sels, et sur des procédés d'utilisation de tels composés, sels et compositions pour le traitement d'une croissance cellulaire anormale, y compris le cancer.
MA45920A 2016-08-15 2017-07-31 Inhibiteurs de pyridopyrimidinone cdk2/4/6 MA45920B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662371602P 2016-08-15 2016-08-15
US201762533347P 2017-07-17 2017-07-17
PCT/IB2017/054655 WO2018033815A1 (fr) 2016-08-15 2017-07-31 Inhibiteurs de pyridopyrimidinone cdk2/4/6

Publications (2)

Publication Number Publication Date
MA45920A MA45920A (fr) 2019-06-19
MA45920B1 true MA45920B1 (fr) 2021-08-31

Family

ID=59631834

Family Applications (1)

Application Number Title Priority Date Filing Date
MA45920A MA45920B1 (fr) 2016-08-15 2017-07-31 Inhibiteurs de pyridopyrimidinone cdk2/4/6

Country Status (43)

Country Link
US (4) US10233188B2 (fr)
EP (1) EP3497103B1 (fr)
JP (1) JP6563623B1 (fr)
KR (1) KR102236605B1 (fr)
CN (2) CN109803968A (fr)
AU (1) AU2017311645B2 (fr)
BR (1) BR112019002610A2 (fr)
CA (1) CA2975033C (fr)
CL (1) CL2019000368A1 (fr)
CO (1) CO2019001240A2 (fr)
CR (1) CR20190062A (fr)
CU (1) CU24522B1 (fr)
CY (1) CY1124206T1 (fr)
DK (1) DK3497103T3 (fr)
DO (1) DOP2019000030A (fr)
EC (1) ECSP19011216A (fr)
ES (1) ES2876411T3 (fr)
GE (1) GEP20217234B (fr)
HR (1) HRP20210871T1 (fr)
HU (1) HUE055978T2 (fr)
IL (1) IL264687B (fr)
LT (1) LT3497103T (fr)
MA (1) MA45920B1 (fr)
MD (1) MD3497103T2 (fr)
MX (1) MX389597B (fr)
MY (1) MY198534A (fr)
NI (1) NI201900013A (fr)
NZ (1) NZ750410A (fr)
PE (1) PE20190475A1 (fr)
PH (1) PH12019500329A1 (fr)
PL (1) PL3497103T3 (fr)
PT (1) PT3497103T (fr)
RS (1) RS61934B1 (fr)
RU (1) RU2726115C1 (fr)
SG (1) SG11201900799XA (fr)
SI (1) SI3497103T1 (fr)
SV (1) SV2019005836A (fr)
TN (1) TN2019000039A1 (fr)
TW (1) TWI663169B (fr)
UA (1) UA124804C2 (fr)
UY (1) UY37352A (fr)
WO (1) WO2018033815A1 (fr)
ZA (1) ZA201900716B (fr)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109803968A (zh) * 2016-08-15 2019-05-24 辉瑞公司 吡啶并嘧啶酮cdk2/4/6抑制剂
JP6952747B2 (ja) 2018-09-18 2021-10-20 ファイザー・インク がん処置のためのTGFβ阻害剤およびCDK阻害剤の組合せ
JP2020097562A (ja) 2018-09-25 2020-06-25 ファイザー・インク ピリド[2,3−d]ピリミジン−7(8h)−オンの合成
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
BR112021011894A2 (pt) 2018-12-21 2021-09-08 Daiichi Sankyo Company, Limited Composição farmacêutica
CN113260617A (zh) * 2019-01-17 2021-08-13 辉瑞公司 Cdk抑制剂的结晶形式
WO2020168197A1 (fr) 2019-02-15 2020-08-20 Incyte Corporation Composés de pyrrolo[2,3-d]pyrimidinone en tant qu'inhibiteurs de cdk2
EA202192260A1 (ru) * 2019-02-15 2021-12-17 Инсайт Корпорейшн Биомаркеры циклин-зависимой киназы 2 и их применение
TW202100520A (zh) 2019-03-05 2021-01-01 美商英塞特公司 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物
US11919904B2 (en) 2019-03-29 2024-03-05 Incyte Corporation Sulfonylamide compounds as CDK2 inhibitors
AU2020260018A1 (en) 2019-04-19 2021-11-04 Pfizer Inc. Anti-proliferative agents for treating PAH
WO2020223558A1 (fr) 2019-05-01 2020-11-05 Incyte Corporation Composés aminés tricycliques en tant qu'inhibiteurs de cdk2
WO2020223469A1 (fr) 2019-05-01 2020-11-05 Incyte Corporation Dérivés de n-(1-(méthylsulfonyl)pipéridin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine et composés apparentés utilisés en tant qu'inhibiteurs de kinase 2 dépendante des cyclines (cdk2) pour le traitement du cancer
US20220241412A1 (en) 2019-05-24 2022-08-04 Pfizer Inc. Combination therapies using cdk inhibitors
WO2020240360A1 (fr) 2019-05-24 2020-12-03 Pfizer Inc. Polythérapies à l'aide d'inhibiteurs cdk
WO2021014360A1 (fr) 2019-07-23 2021-01-28 Pfizer Inc. Formes posologiques à libération modifiée par voie orale
WO2021030537A1 (fr) 2019-08-14 2021-02-18 Incyte Corporation Composés imidazolyl-pyrimidinylamines utilisés comme inhibiteurs de la cdk2
CR20220170A (es) * 2019-10-11 2022-10-10 Incyte Corp Aminas bicíclicas como inhibidoras de la cdk2
JP7667147B2 (ja) * 2019-10-17 2025-04-22 シーセン ファーマシューティカル カンパニー リミテッド Cdk2/4/6三重阻害剤としてのアミノピリミジン化合物
JP7369297B2 (ja) 2019-12-17 2023-10-25 ファイザー・インク Cd47、pd-l1に特異的な抗体、およびその使用
JP2023515629A (ja) * 2020-02-28 2023-04-13 フォチョン・バイオサイエンシーズ・リミテッド Cdk2/4/6阻害剤としての化合物
TW202146017A (zh) * 2020-03-05 2021-12-16 美商輝瑞股份有限公司 間變性淋巴瘤激酶抑制劑及周期蛋白依賴型激酶抑制劑之組合
JP2021167301A (ja) 2020-04-08 2021-10-21 ファイザー・インク Cdk2阻害剤に対する腫瘍適応を抑制するためのcdk4/6およびcdk2阻害剤による同時処置
CN113773315A (zh) * 2020-06-10 2021-12-10 无锡佰翱得生物科学有限公司 细胞周期蛋白依赖性激酶2(cdk2)高选择性氘代抑制剂
CN115702155B (zh) * 2020-06-17 2025-01-24 微境生物医药科技(上海)有限公司 新型吡啶并[2,3-d]嘧啶-7(8H)-酮衍生物
WO2022015670A1 (fr) * 2020-07-14 2022-01-20 Nikang Therapeutics, Inc. Dérivés de pyrido[2,3-d]pyrimidin-7(8h)-one utilisés en tant qu'inhibiteurs de kinase 2 dépendant de la cycline
WO2022018667A1 (fr) 2020-07-24 2022-01-27 Pfizer Inc. Polythérapies utilisant des inhibiteurs de cdk2 et de cdc25a
MX2023003054A (es) 2020-09-15 2023-04-05 Pfizer Formas solidas de un inhibidor de cdk4.
EP4217356B1 (fr) 2020-09-25 2025-05-14 JANSSEN Pharmaceutica NV Inhibiteurs non covalents de la kinase cycline-dépendante 7 (cdk7)
WO2022113003A1 (fr) 2020-11-27 2022-06-02 Rhizen Pharmaceuticals Ag Inhibiteurs de cdk
CN116783205A (zh) * 2020-12-22 2023-09-19 尼坎治疗公司 用于通过泛素蛋白酶体途径降解细胞周期蛋白依赖性激酶2的化合物
AU2021409561A1 (en) * 2020-12-22 2023-07-06 Nikang Therapeutics, Inc. Compounds for degrading cyclin-dependent kinase 2 via ubiquitin proteosome pathway
WO2022149057A1 (fr) 2021-01-05 2022-07-14 Rhizen Pharmaceuticals Ag Inhibiteurs de cdk
CN117858879A (zh) * 2021-01-15 2024-04-09 南京再明医药有限公司 Cdk2/4/6抑制剂及其制备方法和应用
CA3217792A1 (fr) 2021-05-07 2022-11-10 Kymera Therapeutics, Inc Agents de degradation de cdk2 et leurs utilisations
JP7822578B2 (ja) * 2021-06-09 2026-03-03 ティーワイケー メディシンズ(ジョンジョウ),インコーポレーテッド Cdkキナーゼ阻害剤として使用される化合物およびその応用
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
WO2023281413A1 (fr) 2021-07-09 2023-01-12 Pfizer Inc. Méthodes et schémas posologiques comprenant pf-06873600 pour le traitement du cancer
WO2023051302A1 (fr) * 2021-09-29 2023-04-06 中国医药研究开发中心有限公司 Composé hétérocyclique ayant une activité inhibitrice de kinase cycline-dépendante, son procédé de préparation et son utilisation médicale
IL312844A (en) * 2021-11-18 2024-07-01 Onconova Therapeutics Inc Methods and compositions for treating cancer
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
US20250049802A1 (en) 2021-12-14 2025-02-13 Pfizer Inc. Combination therapies and uses for treating cancer
WO2023141522A2 (fr) * 2022-01-21 2023-07-27 Slap Pharmaceuticals Llc Composés multicycliques
AU2023212957A1 (en) * 2022-01-25 2024-08-22 Kinnate Biopharma Inc. Inhibitors of cdk4/6 kinase
CN119451967A (zh) * 2022-06-22 2025-02-14 霖康疗法公司 用于经由泛素蛋白酶体途径降解细胞周期蛋白依赖性激酶2的含有吡啶并[2,3-d]嘧啶-7(8H)-酮衍生物的双功能化合物
US20240174665A1 (en) * 2022-08-19 2024-05-30 Kymera Therapeutics, Inc. Cdk2 inhibitors and uses thereof
EP4604961A1 (fr) 2022-10-18 2025-08-27 Pfizer Inc. Composés pour le traitement du cancer
WO2024173766A1 (fr) * 2023-02-17 2024-08-22 Differentiated Therapeutics, Inc. Agents de dégradation de kinase dépendant de la cycline et leurs méthodes d'utilisation
JP2026518313A (ja) 2023-06-01 2026-06-04 ハー・ルンドベック・アクチエゼルスカベット スピロ大環状オレキシン2受容体アゴニスト
AU2025220986A1 (en) * 2024-02-17 2026-08-13 Padarn Therapeutics, Inc. Inhibitors of cdk2
WO2025207957A1 (fr) * 2024-03-28 2025-10-02 Yale University Inhibiteurs de pi5p4k alpha/bêta à petites molécules et procédés les utilisant
CN120842218A (zh) * 2024-04-26 2025-10-28 郑州同源康医药有限公司 一种嘧啶并氮杂环类化合物的晶型及其制备方法及应用
WO2026024674A1 (fr) 2024-07-22 2026-01-29 Genesis Therapeutics, Inc. Méthodes de traitement de cancers associés à skp2
WO2026114911A1 (fr) 2024-11-27 2026-06-04 H. Lundbeck A/S Agonistes du récepteur 2 de l'oréxine
US20260144795A1 (en) 2024-11-27 2026-05-28 H. Lundbeck A/S Spiromacrocyclic orexin 2 receptor agonists

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
TW477787B (en) 1996-08-27 2002-03-01 Pfizer Pyrido six-membered nitrogen-containing cyclic ring derivatives having corticotropin releasing factor antagonist activity and pharmaceutical composition containing same
WO2000035298A1 (fr) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Chewing-gum contenant des agents medicamenteux actifs
IL129825A0 (en) 1996-11-27 2000-02-29 Pfizer Fused bicyclic pyrimidine derivatives
ES2301194T3 (es) 1997-02-05 2008-06-16 Warner-Lambert Company Llc Pirido 2,3-d pirimidinas y 4-aminopirimidinas como inhibidores de la proliferacion celular.
US6498163B1 (en) * 1997-02-05 2002-12-24 Warner-Lambert Company Pyrido[2,3-D]pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
SK10772002A3 (sk) * 2000-01-27 2004-01-08 Warner-Lambert Company Pyridopyrimidinónové deriváty na liečbu neurodegeneratívnych ochorení
AP2002002643A0 (en) 2000-03-06 2002-12-31 Warner Lambert Co 5-alkylpyrido[2,3-d]pyrimidines tyrosine kinase inhibitors
SK11322003A3 (en) 2001-02-12 2004-10-05 Hoffmann La Roche 6-Substituted pyrido-pyrimidines
NZ534069A (en) 2002-01-22 2007-03-30 Warner Lambert Co 2-(Pyridin-2-ylamino)-pyrido[2,3-d]pyrimidin-7-ones to be used to treat neurodegenerative disorders, viruses and cancer
US7196090B2 (en) * 2002-07-25 2007-03-27 Warner-Lambert Company Kinase inhibitors
US6951769B2 (en) 2003-06-04 2005-10-04 Texas Instruments Incorporated Method for stripping sacrificial layer in MEMS assembly
DE602004017474D1 (de) 2003-07-11 2008-12-11 Warner Lambert Co Isethionat salz eines selektiven cdk4 inhibitors
CA2555724A1 (fr) 2004-02-18 2005-09-09 Warner-Lambert Company Llc 2-(pyridin-3-ylamino)-pyrido[2,3-d]pyrimidin-7-ones
US20060142312A1 (en) * 2004-12-23 2006-06-29 Pfizer Inc C6-aryl and heteroaryl substituted pyrido[2,3-D] pyrimidin-7-ones
HRP20130902T1 (hr) * 2005-10-07 2013-11-08 Exelixis Inc. PIRIDOPIRIMIDINONSKI INHIBITORI PI3Kalfa
PT1940839E (pt) * 2005-10-07 2013-10-10 Exelixis Inc Inibidores de piridopirimidinona pi3k alfa
KR20090052385A (ko) 2006-09-08 2009-05-25 화이자 프로덕츠 인크. 2-(피리딘-2-일아미노)-피리도[2,3-d]피리미딘-7-온의합성
CA2663401C (fr) * 2006-09-15 2011-07-12 Pfizer Products Inc. Composes de pyrido (2, 3-d) pyrimidin0ne et leur utilisation en tant qu'inhibiteurs de pi3
EP1914234A1 (fr) * 2006-10-16 2008-04-23 GPC Biotech Inc. Pyrido[2,3-d]pyrimidines et leur utilisation comme inhibiteurs de kinases
PT2139484E (pt) * 2007-04-10 2013-10-31 Exelixis Inc Métodos de tratamento de cancro usando inibidores piridopirimidinona de pi3k-alfa
WO2009132980A1 (fr) * 2008-04-29 2009-11-05 F. Hoffmann-La Roche Ag Pyrimidinyle pyridones inhibiteurs de jnk
WO2010022081A1 (fr) 2008-08-19 2010-02-25 Array Biopharma Inc. Composés de triazolopyridine comme inhibiteurs des kinases pim
CN102177161A (zh) 2008-10-22 2011-09-07 霍夫曼-拉罗奇有限公司 Jnk的嘧啶基吡啶酮抑制剂
BR112013025798A2 (pt) * 2011-04-08 2016-12-20 Afraxis Holdings Inc 8-etil-6-(aril)pirido[2,3-d]pirimidin-7(8h)-onas para o tratamento de câncer e distúrbios de sistema nervoso
MX2013012486A (es) * 2011-04-29 2014-05-28 Exelixis Inc Metodo para tratar linfoma usando inhibidores de piridopirimidinona de fosfonio sitol 3-cinasa/diana de rapalamina en celulas de mamifero (pi3k/mtor).
TW201306842A (zh) * 2011-06-15 2013-02-16 Exelixis Inc 使用pi3k/mtor吡啶並嘧啶酮抑制劑及苯達莫司汀及/或利妥昔單抗治療惡性血液疾病之組合療法
AR088082A1 (es) 2011-10-13 2014-05-07 Lilly Co Eli Moduladores selectivos del receptor androgeno
EP2817308B1 (fr) * 2012-02-23 2016-09-07 AbbVie Inc. Dérivés de pyridopyrimidinone et leur utilisation comme inhibiteurs de kinases
DK3431475T3 (da) 2013-02-21 2021-05-25 Pfizer Faste former af en selektiv CDK4/6-hæmmer
TWI647220B (zh) 2013-03-15 2019-01-11 美商西建卡爾有限責任公司 雜芳基化合物及其用途
WO2015084936A1 (fr) * 2013-12-04 2015-06-11 The Scripps Research Institute Nouveaux composés utilisables en tant qu'inhibiteurs des janus kinases
US9734210B2 (en) 2014-07-31 2017-08-15 Linkedin Corporation Personalized search based on searcher interest
CZ201589A3 (cs) * 2015-02-11 2016-08-24 Zentiva, K.S. Pevné formy soli Palbociclibu
CN109803968A (zh) * 2016-08-15 2019-05-24 辉瑞公司 吡啶并嘧啶酮cdk2/4/6抑制剂

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HUE055978T2 (hu) 2022-01-28
RU2726115C1 (ru) 2020-07-09
MX389597B (es) 2025-03-20
US11396512B2 (en) 2022-07-26
PL3497103T3 (pl) 2021-10-25
NI201900013A (es) 2019-04-08
JP2019527722A (ja) 2019-10-03
LT3497103T (lt) 2021-07-26
ECSP19011216A (es) 2019-03-29
PT3497103T (pt) 2021-06-17
AU2017311645B2 (en) 2021-05-27
HRP20210871T1 (hr) 2021-07-09
TN2019000039A1 (en) 2020-07-15
CY1124206T1 (el) 2022-05-27
AU2017311645A1 (en) 2019-02-28
PH12019500329A1 (en) 2019-10-28
EP3497103A1 (fr) 2019-06-19
US20180044344A1 (en) 2018-02-15
CA2975033A1 (fr) 2018-02-15
MY198534A (en) 2023-09-04
CN114394966B (zh) 2024-10-11
SV2019005836A (es) 2019-03-19
DK3497103T3 (da) 2021-06-14
JP6563623B1 (ja) 2019-08-21
SG11201900799XA (en) 2019-02-27
KR102236605B1 (ko) 2021-04-05
CL2019000368A1 (es) 2019-05-10
CU20190010A7 (es) 2019-10-04
CA2975033C (fr) 2023-01-24
SI3497103T1 (sl) 2021-07-30
RS61934B1 (sr) 2021-07-30
MX2019001849A (es) 2019-05-09
CN114394966A (zh) 2022-04-26
TW201819383A (zh) 2018-06-01
US10233188B2 (en) 2019-03-19
WO2018033815A1 (fr) 2018-02-22
TWI663169B (zh) 2019-06-21
BR112019002610A2 (pt) 2019-07-02
PE20190475A1 (es) 2019-04-04
US10800783B2 (en) 2020-10-13
US20190135817A1 (en) 2019-05-09
ZA201900716B (en) 2022-03-30
ES2876411T3 (es) 2021-11-12
CO2019001240A2 (es) 2019-02-19
KR20190038915A (ko) 2019-04-09
CN109803968A (zh) 2019-05-24
NZ750410A (en) 2025-06-27
CU24522B1 (es) 2021-06-08
UA124804C2 (uk) 2021-11-24
DOP2019000030A (es) 2019-06-30
GEP20217234B (en) 2021-03-25
CR20190062A (es) 2019-05-22
US20220324872A1 (en) 2022-10-13
MD3497103T2 (ro) 2021-08-31
IL264687B (en) 2021-04-29
US20200392142A1 (en) 2020-12-17
EP3497103B1 (fr) 2021-05-05
UY37352A (es) 2018-03-23
MA45920A (fr) 2019-06-19

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