CN107249593A - 调节染色质结构的组合物用于移植物抗宿主疾病(gvhd)的用途 - Google Patents
调节染色质结构的组合物用于移植物抗宿主疾病(gvhd)的用途 Download PDFInfo
- Publication number
- CN107249593A CN107249593A CN201580066388.8A CN201580066388A CN107249593A CN 107249593 A CN107249593 A CN 107249593A CN 201580066388 A CN201580066388 A CN 201580066388A CN 107249593 A CN107249593 A CN 107249593A
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- substituted
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- hydrogen
- inhibitor
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- 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
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- 0 CC1OC1N(C)*CC(C)(*)* Chemical compound CC1OC1N(C)*CC(C)(*)* 0.000 description 28
- MQLNQYVZVZHRDH-UHFFFAOYSA-N CC(C)C1COCCC1 Chemical compound CC(C)C1COCCC1 MQLNQYVZVZHRDH-UHFFFAOYSA-N 0.000 description 1
- BIZSJKULZKHUPS-UHFFFAOYSA-N CC1CC(C)(C)NC(C)(C)C1 Chemical compound CC1CC(C)(C)NC(C)(C)C1 BIZSJKULZKHUPS-UHFFFAOYSA-N 0.000 description 1
- SXAHDROJSOYBGU-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C(C)C)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C(C)C)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O SXAHDROJSOYBGU-UHFFFAOYSA-N 0.000 description 1
- HBTSUMQRONNOKJ-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C4CCOCC4)c3cc(-c(cn3)ccc3S)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C4CCOCC4)c3cc(-c(cn3)ccc3S)c2)=O)C1=O HBTSUMQRONNOKJ-UHFFFAOYSA-N 0.000 description 1
- ZNKNGYYEXVVJDY-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C4CCOCC4)c3cc(-c3ccc(C(N)=O)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C4CCOCC4)c3cc(-c3ccc(C(N)=O)nc3)c2)=O)C1=O ZNKNGYYEXVVJDY-UHFFFAOYSA-N 0.000 description 1
- PLWZLLCZKGEVAX-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C4CCOCC4)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3C4CCOCC4)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O PLWZLLCZKGEVAX-UHFFFAOYSA-N 0.000 description 1
- ZJMPHMIRNGOBLZ-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CC(C=C)=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CC(C=C)=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O ZJMPHMIRNGOBLZ-UHFFFAOYSA-N 0.000 description 1
- AQLRQTHYDPTCEH-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CCCCNC(C=C)=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CCCCNC(C=C)=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O AQLRQTHYDPTCEH-UHFFFAOYSA-N 0.000 description 1
- CKUINYQCECMMLS-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CCCN(C(C=C4)=O)C4=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CCCN(C(C=C4)=O)C4=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O CKUINYQCECMMLS-UHFFFAOYSA-N 0.000 description 1
- GHYMBYBJJQIIGB-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CCCNC(C=[IH])=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cc[n]3CCCNC(C=[IH])=O)c3cc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O GHYMBYBJJQIIGB-UHFFFAOYSA-N 0.000 description 1
- LQTWDAYNGMMHLV-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cn[n]3C(C)C)c3nc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cn[n]3C(C)C)c3nc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O LQTWDAYNGMMHLV-UHFFFAOYSA-N 0.000 description 1
- KXQXVFYCBALFOC-UHFFFAOYSA-N CCCC(C=C(C)N1)=C(CNC(c2c(cn[n]3C(C=C)=O)c3nc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O Chemical compound CCCC(C=C(C)N1)=C(CNC(c2c(cn[n]3C(C=C)=O)c3nc(-c3ccc(N4CCN(C)CC4)nc3)c2)=O)C1=O KXQXVFYCBALFOC-UHFFFAOYSA-N 0.000 description 1
- XVGCEWHBWFFBSS-UHFFFAOYSA-N CCCCCCN(C)C(C)=C Chemical compound CCCCCCN(C)C(C)=C XVGCEWHBWFFBSS-UHFFFAOYSA-N 0.000 description 1
- MIVWQSFXCRJPCP-UHFFFAOYSA-N CN(CC1)CCN1c(nc1)ccc1-c1cc(C(NCc(cc(cc2[Br]=C)Br)c2N)=O)c(cc[n]2C3CCOCC3)c2c1 Chemical compound CN(CC1)CCN1c(nc1)ccc1-c1cc(C(NCc(cc(cc2[Br]=C)Br)c2N)=O)c(cc[n]2C3CCOCC3)c2c1 MIVWQSFXCRJPCP-UHFFFAOYSA-N 0.000 description 1
- FXHRAKUEZPSMLJ-UHFFFAOYSA-N CN1CCNCCC1 Chemical compound CN1CCNCCC1 FXHRAKUEZPSMLJ-UHFFFAOYSA-N 0.000 description 1
- ICBYIKRIEVEFCX-UHFFFAOYSA-N NC1OCCCC1 Chemical compound NC1OCCCC1 ICBYIKRIEVEFCX-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462076358P | 2014-11-06 | 2014-11-06 | |
| US62/076,358 | 2014-11-06 | ||
| PCT/US2015/059551 WO2016073903A1 (en) | 2014-11-06 | 2015-11-06 | Use of compositions modulating chromatin structure for graft versus host disease (gvhd) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN107249593A true CN107249593A (zh) | 2017-10-13 |
Family
ID=55909890
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201580066388.8A Pending CN107249593A (zh) | 2014-11-06 | 2015-11-06 | 调节染色质结构的组合物用于移植物抗宿主疾病(gvhd)的用途 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20190000860A1 (enExample) |
| EP (1) | EP3215160A4 (enExample) |
| JP (1) | JP2017533922A (enExample) |
| KR (1) | KR20170098808A (enExample) |
| CN (1) | CN107249593A (enExample) |
| AU (1) | AU2015342895A1 (enExample) |
| BR (1) | BR112017009440A2 (enExample) |
| CA (1) | CA2966336A1 (enExample) |
| WO (1) | WO2016073903A1 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108685880A (zh) * | 2018-04-16 | 2018-10-23 | 广东省人民医院(广东省医学科学院) | Bcl-6小分子抑制剂用于制备预防或治疗cGVHD的药物 |
| CN112341390A (zh) * | 2019-08-07 | 2021-02-09 | 四川大学 | 用于制备靶向组蛋白甲基转移酶ezh2共价抑制剂的化合物及其制备方法和用途 |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL3157527T3 (pl) | 2014-06-17 | 2023-08-07 | Epizyme, Inc. | Inhibitory ezh2 do leczenia chłoniaka |
| WO2016073956A1 (en) | 2014-11-06 | 2016-05-12 | Dana-Farber Cancer Institute, Inc. | Ezh2 inhibitors and uses thereof |
| JP6890097B2 (ja) | 2015-06-10 | 2021-06-18 | エピザイム,インコーポレイティド | リンパ腫を処置するためのezh2阻害剤 |
| CN109069508A (zh) | 2016-04-22 | 2018-12-21 | 达纳-法伯癌症研究所股份有限公司 | Ezh2抑制剂及其用途 |
| CN110191722B (zh) | 2017-01-19 | 2022-03-01 | 第一三共株式会社 | 用于治疗htlv-1相关性脊髓病的药物组合物 |
| US10266542B2 (en) | 2017-03-15 | 2019-04-23 | Mirati Therapeutics, Inc. | EZH2 inhibitors |
| PT4043466T (pt) | 2018-01-31 | 2024-10-14 | Mirati Therapeutics Inc | Inibidores de prc2 |
| WO2020011607A1 (en) | 2018-07-09 | 2020-01-16 | Fondation Asile Des Aveugles | Inhibition of prc2 subunits to treat eye disorders |
| AU2019409868A1 (en) * | 2018-12-21 | 2021-07-08 | The Walter And Eliza Hall Institute Of Medical Research | Methods of treating inflammation |
| EP3959214A1 (en) | 2019-04-22 | 2022-03-02 | Mirati Therapeutics, Inc. | Naphthyridine derivatives as prc2 inhibitors |
| EP3980422A1 (en) | 2019-06-05 | 2022-04-13 | Mirati Therapeutics, Inc. | Imidazo[1,2-c]pyrimidine derivatives as prc2 inhibitors for treating cancer |
| WO2021175432A1 (en) | 2020-03-04 | 2021-09-10 | Boehringer Ingelheim International Gmbh | Method for administration of an anti cancer agent |
| TW202400140A (zh) | 2022-04-27 | 2024-01-01 | 日商第一三共股份有限公司 | 抗體-藥物結合物與ezh1及/或ezh2抑制劑之組合 |
| EP4568946A1 (en) * | 2022-08-09 | 2025-06-18 | Dana-Farber Cancer Institute, Inc. | Macrocyclic bcl6 degraders |
| WO2024211684A1 (en) * | 2023-04-06 | 2024-10-10 | Halda Therapeutics Opco, Inc. | Heterobifunctional compounds and methods of treating disease |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE305777T1 (de) * | 1999-07-16 | 2005-10-15 | Kissei Pharmaceutical | Mittel zur verhinderung der chronischen abstossreaktion infolge einer organtransplantation |
| WO2008066887A2 (en) * | 2006-11-30 | 2008-06-05 | Albert Einstein College Of Medicine Of Yeshiva University | Small molecule inhibitors of bcl6 |
| KR20080107050A (ko) * | 2007-06-05 | 2008-12-10 | 울산대학교 산학협력단 | 항-cd137 단일클론 항체를 포함하는 만성이식편대숙주 질환의 예방 또는 치료용 약학적 조성물 |
| US8637509B2 (en) * | 2010-05-07 | 2014-01-28 | Glaxosmithkline Llc | Azaindazoles |
| US20120014979A1 (en) * | 2010-07-16 | 2012-01-19 | Alexander Dent | Use of bcl6 inhibitors for treating autoimmune diseases |
| JP2014511389A (ja) * | 2011-02-28 | 2014-05-15 | エピザイム インコーポレイテッド | 置換6,5−縮合二環式ヘテロアリール化合物 |
| EP2755962B1 (en) * | 2011-09-13 | 2017-03-01 | Glaxosmithkline LLC | Azaindazoles |
| WO2013067302A1 (en) * | 2011-11-04 | 2013-05-10 | Glaxosmithkline Intellectual Property (No. 2) Limited | Method of treatment |
| KR20140095073A (ko) * | 2011-11-04 | 2014-07-31 | 글락소스미스클라인 인털렉츄얼 프로퍼티 (넘버 2) 리미티드 | 치료 방법 |
| JP2015508780A (ja) * | 2012-02-17 | 2015-03-23 | アンサン バイオファーマ,インコーポレイテッド | 免疫不全患者のインフルエンザ及びパラインフルエンザウイルスを処置するための方法、化合物、及び組成物 |
| WO2014155301A1 (en) * | 2013-03-26 | 2014-10-02 | Piramal Enterprises Limited | Substituted bicyclic compounds as inhibitors of ezh2 |
-
2015
- 2015-11-06 WO PCT/US2015/059551 patent/WO2016073903A1/en not_active Ceased
- 2015-11-06 BR BR112017009440A patent/BR112017009440A2/pt not_active Application Discontinuation
- 2015-11-06 JP JP2017525115A patent/JP2017533922A/ja active Pending
- 2015-11-06 AU AU2015342895A patent/AU2015342895A1/en not_active Abandoned
- 2015-11-06 KR KR1020177014969A patent/KR20170098808A/ko not_active Withdrawn
- 2015-11-06 CA CA2966336A patent/CA2966336A1/en not_active Abandoned
- 2015-11-06 CN CN201580066388.8A patent/CN107249593A/zh active Pending
- 2015-11-06 US US15/524,707 patent/US20190000860A1/en not_active Abandoned
- 2015-11-06 EP EP15856340.3A patent/EP3215160A4/en not_active Withdrawn
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108685880A (zh) * | 2018-04-16 | 2018-10-23 | 广东省人民医院(广东省医学科学院) | Bcl-6小分子抑制剂用于制备预防或治疗cGVHD的药物 |
| CN112341390A (zh) * | 2019-08-07 | 2021-02-09 | 四川大学 | 用于制备靶向组蛋白甲基转移酶ezh2共价抑制剂的化合物及其制备方法和用途 |
| CN112341390B (zh) * | 2019-08-07 | 2022-08-23 | 四川大学 | 用于制备靶向组蛋白甲基转移酶ezh2共价抑制剂的化合物及其制备方法和用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2015342895A1 (en) | 2017-05-18 |
| BR112017009440A2 (pt) | 2017-12-19 |
| CA2966336A1 (en) | 2016-05-12 |
| WO2016073903A1 (en) | 2016-05-12 |
| JP2017533922A (ja) | 2017-11-16 |
| KR20170098808A (ko) | 2017-08-30 |
| EP3215160A1 (en) | 2017-09-13 |
| US20190000860A1 (en) | 2019-01-03 |
| EP3215160A4 (en) | 2018-08-08 |
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Application publication date: 20171013 |