JP2021529172A5 - - Google Patents

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Publication number
JP2021529172A5
JP2021529172A5 JP2020570902A JP2020570902A JP2021529172A5 JP 2021529172 A5 JP2021529172 A5 JP 2021529172A5 JP 2020570902 A JP2020570902 A JP 2020570902A JP 2020570902 A JP2020570902 A JP 2020570902A JP 2021529172 A5 JP2021529172 A5 JP 2021529172A5
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JP
Japan
Prior art keywords
pharmaceutically acceptable
acceptable salt
prodrug
alkyl
compound according
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JP2020570902A
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English (en)
Japanese (ja)
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JP2021529172A (ja
JP7538047B2 (ja
JPWO2019246403A5 (https=
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Priority claimed from PCT/US2019/038245 external-priority patent/WO2019246403A1/en
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Publication of JPWO2019246403A5 publication Critical patent/JPWO2019246403A5/ja
Publication of JP2021529172A5 publication Critical patent/JP2021529172A5/ja
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JP2020570902A 2018-06-21 2019-06-20 エクトヌクレオチダーゼ阻害剤及びその使用方法 Active JP7538047B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201862688225P 2018-06-21 2018-06-21
US62/688,225 2018-06-21
US201962827505P 2019-04-01 2019-04-01
US62/827,505 2019-04-01
PCT/US2019/038245 WO2019246403A1 (en) 2018-06-21 2019-06-20 Ectonucleotidase inhibitors and methods of use thereof

Publications (4)

Publication Number Publication Date
JP2021529172A JP2021529172A (ja) 2021-10-28
JPWO2019246403A5 JPWO2019246403A5 (https=) 2022-05-16
JP2021529172A5 true JP2021529172A5 (https=) 2022-05-16
JP7538047B2 JP7538047B2 (ja) 2024-08-21

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JP2020570902A Active JP7538047B2 (ja) 2018-06-21 2019-06-20 エクトヌクレオチダーゼ阻害剤及びその使用方法

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US (3) US11078228B2 (https=)
EP (1) EP3810617A4 (https=)
JP (1) JP7538047B2 (https=)
KR (1) KR102902754B1 (https=)
CN (1) CN112888696B (https=)
AU (1) AU2019288495B2 (https=)
BR (1) BR112020025132B1 (https=)
CA (1) CA3104088A1 (https=)
CL (1) CL2020003339A1 (https=)
CO (1) CO2021000049A2 (https=)
IL (1) IL279475B2 (https=)
MX (1) MX2020013320A (https=)
PH (1) PH12020552214A1 (https=)
SG (1) SG11202012001YA (https=)
TW (1) TWI911140B (https=)
WO (1) WO2019246403A1 (https=)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7138351B2 (ja) * 2016-12-22 2022-09-16 キャリセラ バイオサイエンシーズ, インコーポレイテッド エクトヌクレオチダーゼ阻害剤およびその使用方法
WO2018208980A1 (en) 2017-05-10 2018-11-15 Oric Pharmaceuticals, Inc. Cd73 inhibitors
US11377469B2 (en) 2017-11-03 2022-07-05 Oric Pharmaceuticals, Inc. CD73 inhibitors
CN112423764A (zh) 2018-04-30 2021-02-26 欧瑞克制药公司 Cd73抑制剂
AU2019288495B2 (en) 2018-06-21 2024-02-08 Antengene Therapeutics Limited Ectonucleotidase inhibitors and methods of use thereof
TWI821559B (zh) * 2019-04-28 2023-11-11 大陸商上海和譽生物醫藥科技有限公司 一種cd73抑制劑,其製備方法和應用
KR20220024629A (ko) * 2019-06-20 2022-03-03 칼리테라 바이오사이언시즈, 인코포레이티드 엑토뉴클레오티다제 억제제 및 이의 사용 방법
US12544391B2 (en) 2019-07-16 2026-02-10 Oric Pharmaceuticals, Inc. CD73 inhibitors
HUE072504T2 (hu) 2019-10-30 2025-11-28 Oric Pharmaceuticals Inc CD73-inhibitorok
CN119173276A (zh) 2022-04-13 2024-12-20 吉利德科学公司 用于治疗表达Trop-2的癌症的组合疗法
CN115873049B (zh) * 2023-02-13 2023-05-02 北京先通国际医药科技股份有限公司 腺苷的制备方法及其用途
WO2025137640A1 (en) 2023-12-22 2025-06-26 Gilead Sciences, Inc. Azaspiro wrn inhibitors

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2085994A1 (en) 1991-04-24 1992-10-25 Shinji Sakata 1-beta-d-arabinofuranosyl-(e)-5- (2-halogenovinyl) uracil derivatives
AU5449094A (en) 1992-11-02 1994-05-24 Affymax Technologies N.V. Novel photoreactive protecting groups
US5635608A (en) 1994-11-08 1997-06-03 Molecular Probes, Inc. α-carboxy caged compounds
TW528755B (en) 1996-12-24 2003-04-21 Glaxo Group Ltd 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
NL1005244C2 (nl) 1997-02-10 1998-08-18 Inst Voor Agrotech Onderzoek Oppervlakte-actieve aminen en glycosiden.
WO2004096233A2 (en) 2003-04-25 2004-11-11 Gilead Sciences, Inc. Nucleoside phosphonate conjugates
EP1860113A1 (en) 2006-05-24 2007-11-28 Rheinische Friedrich-Wilhelms-Universität Bonn Ectonucleotidase inhibitors
WO2008011406A2 (en) * 2006-07-18 2008-01-24 Anadys Pharmaceuticals, Inc. Carbonate and carbamate prodrugs of thiazolo [4,5-d] pyrimidines
JP2011503084A (ja) 2007-11-07 2011-01-27 シェーリング コーポレイション 新規の細胞周期チェックポイント調節剤およびこれらの調節剤とチェックポイント阻害剤との併用
EP2070938A1 (en) * 2007-12-13 2009-06-17 Heidelberg Pharma AG Clofarabine dietherphospholipid derivatives
CA2684017A1 (en) 2009-10-22 2011-04-22 Universite Laval Ectonucleotidase pyrophosphate/phosphodiesterase-1 (enpp-1) as a target for the treatment of aortic valve stenosis and cardiovascular calcification
WO2011133871A2 (en) 2010-04-22 2011-10-27 Alnylam Pharmaceuticals, Inc. 5'-end derivatives
EP2590958B1 (en) 2010-07-08 2015-08-26 Life Technologies Corporation In situ chemiluminescent substrates and assays
CN102311472B (zh) 2010-07-09 2014-09-03 神隆(昆山)生化科技有限公司 2-氯-9-(2’-脱氧-2’-氟-β-D-阿拉伯呋喃糖基)-腺嘌呤的制备
US20140154675A1 (en) 2011-05-03 2014-06-05 Life Technologies Corporation Flash and Glow 1,2-Dioxetanes
DK2731947T3 (en) * 2011-07-15 2019-04-23 Boehringer Ingelheim Int SUBSTITUTED DIMERIC QUINAZOLINE DERIVATIVE, PREPARATION AND USE thereof IN PHARMACEUTICAL COMPOSITIONS FOR TREATMENT OF TYPE I AND TYPE II DIABETES
GB201220843D0 (en) 2012-11-20 2013-01-02 Univ College Cork Nat Univ Ie Compound
US10068577B2 (en) * 2014-04-25 2018-09-04 Dolby Laboratories Licensing Corporation Audio segmentation based on spatial metadata
WO2015164573A1 (en) * 2014-04-25 2015-10-29 Vitae Pharmaceuticals, Inc. Purine derivatives as cd73 inhibitors for the treatment of cancer
WO2017066782A1 (en) 2015-10-16 2017-04-20 Modernatx, Inc. Hydrophobic mrna cap analogs
WO2017066781A1 (en) 2015-10-16 2017-04-20 Modernatx, Inc. Mrna cap analogs with modified phosphate linkage
WO2017066791A1 (en) 2015-10-16 2017-04-20 Modernatx, Inc. Sugar substituted mrna cap analogs
US10611790B2 (en) 2015-11-02 2020-04-07 Mitobridge, Inc. Nicotinamide riboside and nicotinamide mononucleotide derivatives for use in the treatments of mitochondrial-related diseases
TWI704154B (zh) * 2015-12-03 2020-09-11 英商葛蘭素史克智慧財產發展有限公司 新穎化合物
TWI767937B (zh) * 2016-09-09 2022-06-21 美商卡利泰拉生物科技公司 外核苷酸酶抑制劑及其使用方法
US10794113B2 (en) * 2016-12-22 2020-10-06 Marketing Displays, Inc. Compact privacy screen
JP7138351B2 (ja) 2016-12-22 2022-09-16 キャリセラ バイオサイエンシーズ, インコーポレイテッド エクトヌクレオチダーゼ阻害剤およびその使用方法
WO2018208727A1 (en) * 2017-05-08 2018-11-15 Eternity Bioscience Inc. Nucleoside and nucleotide analogues as cd73 inhibitors and therapeutic uses thereof
WO2018208980A1 (en) * 2017-05-10 2018-11-15 Oric Pharmaceuticals, Inc. Cd73 inhibitors
CN109503587B (zh) * 2017-09-14 2022-01-11 辽宁利锋科技开发有限公司 双杂环三氮唑核苷类似物的抗肿瘤作用与应用
US11377469B2 (en) * 2017-11-03 2022-07-05 Oric Pharmaceuticals, Inc. CD73 inhibitors
CN112423764A (zh) * 2018-04-30 2021-02-26 欧瑞克制药公司 Cd73抑制剂
EP3810109B1 (en) * 2018-05-31 2024-08-07 Peloton Therapeutics, Inc. Compounds and compositions for inhibiting cd73
AU2019288495B2 (en) 2018-06-21 2024-02-08 Antengene Therapeutics Limited Ectonucleotidase inhibitors and methods of use thereof
KR20220024629A (ko) 2019-06-20 2022-03-03 칼리테라 바이오사이언시즈, 인코포레이티드 엑토뉴클레오티다제 억제제 및 이의 사용 방법

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