JP6193268B2 - Cdk8/cdk19選択的阻害剤、ならびに癌のための抗転移および化学防御の方法におけるそれらの使用 - Google Patents

Cdk8/cdk19選択的阻害剤、ならびに癌のための抗転移および化学防御の方法におけるそれらの使用 Download PDF

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JP6193268B2
JP6193268B2 JP2014555805A JP2014555805A JP6193268B2 JP 6193268 B2 JP6193268 B2 JP 6193268B2 JP 2014555805 A JP2014555805 A JP 2014555805A JP 2014555805 A JP2014555805 A JP 2014555805A JP 6193268 B2 JP6193268 B2 JP 6193268B2
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pharmaceutical formulation
patient
cdk8
cancer
tumor
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JP2015506376A5 (enExample
JP2015506376A (ja
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ロビンソン,イゴール,ビー.
ポーター,ドナルド,シー.
ウェントランド,マーク,ピー.
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Senex Biotechnology Inc
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    • 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
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JP2014555805A 2012-02-02 2013-02-01 Cdk8/cdk19選択的阻害剤、ならびに癌のための抗転移および化学防御の方法におけるそれらの使用 Expired - Fee Related JP6193268B2 (ja)

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US201261594023P 2012-02-02 2012-02-02
US61/594,023 2012-02-02
US201261673419P 2012-07-19 2012-07-19
US61/673,419 2012-07-19
PCT/US2013/024515 WO2013116786A1 (en) 2012-02-02 2013-02-01 Cdk8/cdk19 selective inhibitors and their use in anti-metastatic and chemopreventative methods for cancer

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JP2015506376A JP2015506376A (ja) 2015-03-02
JP2015506376A5 JP2015506376A5 (enExample) 2016-05-19
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KR (1) KR20150023223A (enExample)
CN (1) CN104363913B (enExample)
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Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2671194T3 (es) * 2012-07-27 2018-06-05 Biogen Ma Inc. Compuestos que son agentes moduladores de S1P y/o agentes moduladores de ATX
BR112015003698A2 (pt) * 2012-08-23 2017-07-04 Hoffmann La Roche compostos, processo para a preparação de um composto, composição farmacêutica, uso de um composto e método para o tratamento de câncer
CA2890108C (en) 2012-11-01 2021-03-02 University Of South Carolina Method for treating prostate cancer
EP2961409A1 (en) * 2013-02-26 2016-01-06 Senex Biotechnology, Inc. Inhibitors of cdk8/19 for use in treating estrogen receptor positive breast cancer
CN110183461A (zh) 2013-12-24 2019-08-30 哈佛学院院长等 皮质抑素类似物及其合成和用途
EP3205645B1 (en) * 2014-04-18 2019-10-23 Takeda Pharmaceutical Company Limited Heterocyclic compound
CA2959762A1 (en) * 2014-06-10 2016-02-04 University Of South Carolina Methods and compositions for treatment of her-positive cancers
US20210322651A1 (en) 2014-12-18 2021-10-21 Senex Biotechnology, Inc. Suppression of neointimal formation following vascular surgeru using cdk8 inhibitors
EP3294298A4 (en) 2015-05-08 2018-10-17 President and Fellows of Harvard College Cortistatin analogues, syntheses, and uses thereof
EP3294418A4 (en) * 2015-05-08 2019-01-02 President and Fellows of Harvard College Targeted selection of patients for treatment with cortistatin derivatives
WO2017004411A1 (en) 2015-07-01 2017-01-05 President And Fellows Of Harvard College Cortistatin analogues and syntheses and uses thereof
EP3370720A1 (en) * 2015-11-03 2018-09-12 Lu License AB Compounds for treatment of hypoproliferative disorders
WO2017091836A1 (en) * 2015-11-25 2017-06-01 University Of South Carolina Enhancement of cytarabine activity by inhibiting cdk8/19
WO2017164230A1 (ja) * 2016-03-23 2017-09-28 国立大学法人 岡山大学 リン酸化sarm1、抗体、sarm1リン酸化阻害剤、神経変性疾患の予防又は治療薬、スクリーニング方法、sarm1改変体及び使用
US11285144B2 (en) 2016-08-03 2022-03-29 The Broad Institute, Inc. Use of CDK8 inhibitors to treat diseases of inflammation and autoimmunity
US11578067B2 (en) * 2017-01-30 2023-02-14 Kyoto University Compound, and method for producing regulatory T cells
WO2018151633A1 (ru) * 2017-02-20 2018-08-23 Закрытое Акционерное Общество "Биокад" Способы получения производных 4-(((нафталин-2-ил)алкил)амино)хинозалин-6-карбонитрилов
WO2018156858A1 (en) * 2017-02-23 2018-08-30 University Of South Carolina Use of cdk8/19 inhibitors for treatment of established colon cancer hepatic metastasis
JPWO2018159805A1 (ja) * 2017-03-03 2020-01-09 国立大学法人京都大学 膵前駆細胞の製造方法
US11013728B2 (en) 2017-04-03 2021-05-25 Kyoto Pharmaceutical Industries, Ltd. Cyclin-dependent kinase 8 and/or 19 inhibitor
RU2641001C1 (ru) * 2017-04-03 2018-01-15 Закрытое Акционерное Общество "Биокад" Соли 4-((2-(6-(4-метилпиперазин-1-карбонил)нафталин-2-ил)этил)амино)хиназолин-6-карбонитрила и фармацевтическая композиция
CN111278469A (zh) * 2017-09-18 2020-06-12 陈扎克伯格生物中心公司 用于治疗三阴性乳腺癌的方法
US11261184B2 (en) 2017-10-02 2022-03-01 Boehringer Ingelheim International Gmbh [1,6]naphthyridine compounds and derivatives as CDK8/CDK19 inhibitors
RU2763347C2 (ru) * 2018-03-01 2021-12-28 Закрытое Акционерное Общество "Биокад" Новые ингибиторы cdk8/19
US12281080B2 (en) 2018-08-21 2025-04-22 University Of South Carolina Quinoline-based compounds and methods of inhibiting CDK8/19
US11014906B2 (en) 2018-08-21 2021-05-25 University Of South Carolina Quinoline-based compounds and methods of inhibiting CDK8/19
WO2020160537A1 (en) 2019-02-01 2020-08-06 University Of South Carolina Bicyclic pyridine compositions and methods of using the same for cancer therapy
TW202237818A (zh) 2020-11-20 2022-10-01 日商千紙鶴治療公司 成熟化劑
CA3208794A1 (en) 2021-02-09 2022-08-18 Orizuru Therapeutics, Inc. Maturation agent
WO2022204534A1 (en) * 2021-03-25 2022-09-29 University Of South Carolina Cdk8/19 inhibitors for the treatment of cytokine storm
US20240400993A1 (en) 2021-09-27 2024-12-05 Kyoto University Method for producing t cell
JPWO2023095802A1 (enExample) 2021-11-24 2023-06-01
WO2023095801A1 (ja) 2021-11-24 2023-06-01 レグセル株式会社 ヒト誘導性制御性t細胞およびその作製方法
EP4497822A1 (en) 2022-03-23 2025-01-29 Kyoto University Method for producing regulatory t cells
WO2023210578A1 (ja) 2022-04-25 2023-11-02 オリヅルセラピューティクス株式会社 Alk5阻害活性とcdk8/19阻害活性とを有する成熟化剤
CN119546748A (zh) 2022-07-14 2025-02-28 千纸鹤治疗公司 细胞移植用纤维蛋白凝胶片
TW202421780A (zh) 2022-09-26 2024-06-01 國立大學法人京都大學 T細胞的製造方法
WO2024071039A1 (ja) 2022-09-26 2024-04-04 レグセル株式会社 キメラ抗原受容体(car)を含む誘導性制御性t細胞
CN120676951A (zh) 2023-02-08 2025-09-19 雷格细胞股份有限公司 用于治疗或预防天疱疮的药物组合物

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6046206A (en) * 1995-06-07 2000-04-04 Cell Pathways, Inc. Method of treating a patient having a precancerous lesions with amide quinazoline derivatives
SI20324A (sl) * 1997-10-27 2001-02-28 Agouron Pharmaceuticals, Inc. Substituirane 4-amino-tiazol-2-il spojine kot cdk inhibitorji
US6440959B1 (en) * 1999-04-21 2002-08-27 Hoffman-La Roche Inc. Pyrazolobenzodiazepines
US20040180848A1 (en) 2003-03-10 2004-09-16 Fesik Stephen W. Method of killing cancer cells
US20040180844A1 (en) 2003-03-10 2004-09-16 Fesik Stephen W. Method of killing cancer cells
JP2006522794A (ja) * 2003-04-10 2006-10-05 ファイザー株式会社 Nr2b受容体拮抗物質としての二環系化合物
US20080033000A1 (en) * 2006-05-15 2008-02-07 Senex Biotechnology, Inc. Identification of CDKI pathway inhibitors
US8598344B2 (en) 2009-11-30 2013-12-03 Senex Biotechnology CDKI pathway inhibitors and uses thereof

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EP2809324B1 (en) 2018-08-01
US20170071942A1 (en) 2017-03-16
CN104363913A (zh) 2015-02-18
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CO7151516A2 (es) 2014-12-29
AU2013214783A1 (en) 2014-08-28
KR20150023223A (ko) 2015-03-05
EP2809324A1 (en) 2014-12-10
EA201791284A1 (ru) 2017-10-31
US9321737B2 (en) 2016-04-26
GEP20186818B (en) 2018-02-12
US10993945B2 (en) 2021-05-04
CN104363913B (zh) 2018-08-21
PH12014501862A1 (en) 2014-11-24
UA117342C2 (uk) 2018-07-25
EA201491399A1 (ru) 2015-04-30
JP2015506376A (ja) 2015-03-02
GEP201706688B (en) 2017-06-26
BR112014019052A2 (enExample) 2017-06-20
WO2013116786A1 (en) 2013-08-08
EP3431087A1 (en) 2019-01-23
US20140038958A1 (en) 2014-02-06
EA032429B1 (ru) 2019-05-31
AU2013214783B2 (en) 2017-07-06
EA028595B1 (ru) 2017-12-29
SG11201404596UA (en) 2014-10-30
CL2014002062A1 (es) 2015-03-20

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