JPWO2021020585A5 - - Google Patents
Download PDFInfo
- Publication number
- JPWO2021020585A5 JPWO2021020585A5 JP2021535473A JP2021535473A JPWO2021020585A5 JP WO2021020585 A5 JPWO2021020585 A5 JP WO2021020585A5 JP 2021535473 A JP2021535473 A JP 2021535473A JP 2021535473 A JP2021535473 A JP 2021535473A JP WO2021020585 A5 JPWO2021020585 A5 JP WO2021020585A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- thieno
- piperidin
- methyl
- oxy
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2019141699 | 2019-07-31 | ||
PCT/JP2020/029589 WO2021020585A1 (ja) | 2019-07-31 | 2020-07-31 | 複素環化合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPWO2021020585A1 JPWO2021020585A1 (US06656730-20031202-C00002.png) | 2021-02-04 |
JPWO2021020585A5 true JPWO2021020585A5 (US06656730-20031202-C00002.png) | 2023-08-03 |
Family
ID=74228959
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2021535473A Pending JPWO2021020585A1 (US06656730-20031202-C00002.png) | 2019-07-31 | 2020-07-31 |
Country Status (4)
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2024026256A1 (en) * | 2022-07-25 | 2024-02-01 | Celgene Corporation | Substituted imidazopyrazine compounds as ligand directed degraders of irak3 |
WO2024026262A1 (en) * | 2022-07-25 | 2024-02-01 | Celgene Corporation | Substituted pyrazolyl-pyridinyl compounds as ligand directed degraders of irak3 |
Family Cites Families (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005017116A1 (de) | 2005-04-13 | 2006-10-26 | Novartis Ag | Hemmstoffe für Inhibitoren von Apoptose Proteinen (IAP) |
JP2009512719A (ja) | 2005-10-25 | 2009-03-26 | アエゲラ セラピューティクス インコーポレイテッド | Iapbirドメイン結合化合物 |
CN101374829A (zh) | 2005-12-19 | 2009-02-25 | 健泰科生物技术公司 | Iap的抑制剂 |
TWI543988B (zh) | 2006-03-16 | 2016-08-01 | 科學製藥股份有限公司 | 結合於細胞凋亡抑制蛋白(iap)之桿狀病毒iap重複序列(bir)區域之化合物 |
MY159563A (en) | 2006-05-16 | 2017-01-13 | Pharmascience Inc | Iap bir domain binding compounds |
PE20110218A1 (es) | 2006-08-02 | 2011-04-01 | Novartis Ag | DERIVADOS DE 2-OXO-ETIL-AMINO-PROPIONAMIDA-PIRROLIDIN-2-IL-SUSTITUIDOS COMO INHIBIDORES DEL ENLACE DE LA PROTEINA Smac AL INHIBIDOR DE LA PROTEINA DE APOPTOSIS |
RU2009117701A (ru) | 2006-10-12 | 2010-11-20 | Новартис АГ (CH) | Производные пирролидина в качестве ингибиторов iap |
AU2007337104A1 (en) | 2006-12-19 | 2008-07-03 | Genentech, Inc. | Imidazopyridine inhibitors of IAP |
NZ580468A (en) | 2007-04-13 | 2012-02-24 | Univ Michigan | Diazo bicyclic smac mimetics and the uses thereof |
US20100317593A1 (en) | 2009-06-12 | 2010-12-16 | Astrazeneca Ab | 2,3-dihydro-1h-indene compounds |
US8283372B2 (en) | 2009-07-02 | 2012-10-09 | Tetralogic Pharmaceuticals Corp. | 2-(1H-indol-3-ylmethyl)-pyrrolidine dimer as a SMAC mimetic |
BR112012000828A8 (pt) | 2009-07-06 | 2017-10-10 | Ontorii Inc | Novas pró-drogas de ácido nucleico e métodos de uso das mesmas |
US9271980B2 (en) | 2009-08-03 | 2016-03-01 | Daljit Singh Dhanoa | Deuterium-enriched pyrimidine compounds and derivatives |
RU2567544C2 (ru) | 2010-02-12 | 2015-11-10 | Фармасайенс Инк. | Bir домен iap связывающие соединения |
JP2012106958A (ja) | 2010-11-18 | 2012-06-07 | Takeda Chem Ind Ltd | 複素環化合物 |
JP2012176934A (ja) | 2011-02-03 | 2012-09-13 | Takeda Chem Ind Ltd | 複素環化合物 |
GB201106817D0 (en) | 2011-04-21 | 2011-06-01 | Astex Therapeutics Ltd | New compound |
WO2013019966A1 (en) | 2011-08-04 | 2013-02-07 | Allergan, Inc. | Aromatic bycyclic derivatives as cxcr4 receptor modulators |
JP5934986B2 (ja) | 2011-09-07 | 2016-06-15 | 公益財団法人ヒューマンサイエンス振興財団 | アポトーシス阻害タンパク質リガンド−エストロゲン受容体リガンドハイブリッド化合物並びにそれを利用したエストロゲン受容体分解誘導剤及び乳癌、子宮頚癌又は卵巣癌の予防及び治療剤 |
NO2755614T3 (US06656730-20031202-C00002.png) | 2012-01-03 | 2018-03-31 | ||
US9394263B2 (en) | 2012-08-09 | 2016-07-19 | F. Hoffmann-La Roche Ag | Substituted hetero-azepinones |
GB201218850D0 (en) | 2012-10-19 | 2012-12-05 | Astex Therapeutics Ltd | Bicyclic heterocycle compounds and their uses in therapy |
EP2917218B1 (en) | 2012-11-09 | 2017-01-04 | Ensemble Therapeutics Corporation | Macrocyclic compounds for inhibition of inhibitors of apoptosis |
CN103242341B (zh) | 2013-04-19 | 2015-12-09 | 中国科学院广州生物医药与健康研究院 | 噻吩并2,4取代嘧啶类化合物及其药物组合物与应用 |
WO2016040330A1 (en) | 2014-09-09 | 2016-03-17 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
GB201506871D0 (en) | 2015-04-22 | 2015-06-03 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
GB201506872D0 (en) | 2015-04-22 | 2015-06-03 | Ge Oil & Gas Uk Ltd | Novel compounds |
EP3322986A4 (en) | 2015-07-13 | 2018-09-05 | Arvinas, Inc. | Alanine-based modulators of proteolysis and associated methods of use |
JP2019514878A (ja) | 2016-04-20 | 2019-06-06 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | Ripk2阻害剤を含むコンジュゲート |
JP2019522633A (ja) | 2016-05-20 | 2019-08-15 | ジェネンテック, インコーポレイテッド | Protac抗体コンジュゲート及び使用方法 |
GB201610147D0 (en) * | 2016-06-10 | 2016-07-27 | Glaxosmithkline Ip Dev Ltd | Novel compounds |
JP6899993B2 (ja) | 2016-10-04 | 2021-07-07 | 国立医薬品食品衛生研究所長 | 複素環化合物 |
BR112019012878A2 (pt) | 2016-12-23 | 2019-11-26 | Arvinas Operations Inc | compostos e métodos para a degradação alvo de polipeptídos de fibrossarcoma rapidamente acelerados |
US11191741B2 (en) | 2016-12-24 | 2021-12-07 | Arvinas Operations, Inc. | Compounds and methods for the targeted degradation of enhancer of zeste homolog 2 polypeptide |
WO2019099926A1 (en) | 2017-11-17 | 2019-05-23 | Arvinas, Inc. | Compounds and methods for the targeted degradation of interleukin-1 receptor-associated kinase 4 polypeptides |
JP2021508703A (ja) | 2017-12-26 | 2021-03-11 | カイメラ セラピューティクス, インコーポレイテッド | Irak分解剤およびそれらの使用 |
-
2020
- 2020-07-31 US US17/630,203 patent/US20220402935A1/en active Pending
- 2020-07-31 EP EP20847962.6A patent/EP4006037A4/en active Pending
- 2020-07-31 WO PCT/JP2020/029589 patent/WO2021020585A1/ja unknown
- 2020-07-31 JP JP2021535473A patent/JPWO2021020585A1/ja active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA3089936C (en) | Substituted quinazoline and pyridopyrimidine derivatives useful as anticancer agents | |
US11034685B2 (en) | Aminopyridine derivatives as TAM family kinase inhibitors | |
CN112707893B (zh) | 作为usp30抑制剂的1-氰基吡咯烷化合物 | |
JP2021138734A (ja) | 新規化合物 | |
ES2651843T3 (es) | Derivados de pirazolopirrolidina y su uso en el tratamiento de enfermedades | |
ES2898835T3 (es) | Azol amidas y aminas como inhibidores de la integrina alfav | |
KR20220042204A (ko) | Rip1 억제 화합물 및 그를 제조 및 사용하는 방법 | |
IL258159A (en) | New protein inhibitors | |
WO2018177403A1 (zh) | 1H-咪唑[4,5-h]喹唑啉类化合物作为蛋白激酶抑制剂 | |
KR20190091537A (ko) | C-kit 억제제로서의 아미노티아졸 화합물 | |
AU2015275730A1 (en) | Substituted indazole compounds as IRAK4 inhibitors | |
US20150051185A1 (en) | Chemical Compounds 251 | |
WO2014004863A2 (en) | Compounds, compositions, and therapeutic uses thereof | |
ES2944657T3 (es) | Compuestos de alqueno como moduladores del receptor farnesoide X | |
KR20220079919A (ko) | 헤테로시클릭 rip1 억제 화합물 | |
BR112020008157A2 (pt) | compostos espirocíclicos como moduladores do receptor farnesoide x | |
JPWO2021020585A5 (US06656730-20031202-C00002.png) | ||
EP3600312B1 (en) | Piperidinyl- and piperazinyl-substituted heteroaromatic carboxamides as modulators of gpr6 | |
WO2017073743A1 (ja) | 三環性化合物 | |
TW202320787A (zh) | 一種周期蛋白依賴性激酶抑制劑 | |
IL291418B2 (en) | Substances that function as modulators of cMYC-mRNA translation and their uses for cancer treatment | |
WO2023049199A1 (en) | Azole compounds | |
US20230365551A1 (en) | Inhibitors of human respiratory syncytial virus and metapneumovirus | |
TW202409011A (zh) | 人類呼吸道融合病毒及間質肺病毒抑制劑 | |
TW201247647A (en) | Glycine transport inhibitor |