JP6947651B2 - 4,6−ピリミジニレン誘導体およびこれらの使用 - Google Patents
4,6−ピリミジニレン誘導体およびこれらの使用 Download PDFInfo
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- JP6947651B2 JP6947651B2 JP2017567060A JP2017567060A JP6947651B2 JP 6947651 B2 JP6947651 B2 JP 6947651B2 JP 2017567060 A JP2017567060 A JP 2017567060A JP 2017567060 A JP2017567060 A JP 2017567060A JP 6947651 B2 JP6947651 B2 JP 6947651B2
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- 0 CCCc1c2c(*)c(*)c(*)c(*)c2n[n]1* Chemical compound CCCc1c2c(*)c(*)c(*)c(*)c2n[n]1* 0.000 description 21
- QMFJIJFIHIDENY-UHFFFAOYSA-N CC1=CC=CCC1 Chemical compound CC1=CC=CCC1 QMFJIJFIHIDENY-UHFFFAOYSA-N 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N CCC1CCCCC1 Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- OXAGJGKZKOBWGA-QPJJXVBHSA-N CN(C)C/C=C/C(NC(CC1)CCC1C(Nc1cccc(N)c1)=O)=O Chemical compound CN(C)C/C=C/C(NC(CC1)CCC1C(Nc1cccc(N)c1)=O)=O OXAGJGKZKOBWGA-QPJJXVBHSA-N 0.000 description 2
- FOEYMRPOKBCNCR-UHFFFAOYSA-N C(C1)C11CCCCC1 Chemical compound C(C1)C11CCCCC1 FOEYMRPOKBCNCR-UHFFFAOYSA-N 0.000 description 1
- XMOAFHWYJBRRRN-UHFFFAOYSA-N CC(C)(C)OC(NC(CC1)CCC1C(Nc1cccc(Nc2ncnc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)c2)c1)=O)=O Chemical compound CC(C)(C)OC(NC(CC1)CCC1C(Nc1cccc(Nc2ncnc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)c2)c1)=O)=O XMOAFHWYJBRRRN-UHFFFAOYSA-N 0.000 description 1
- VSLZIENXJCBPAV-UHFFFAOYSA-N CC(C)[O]=S(c1ccccc1)([n](cc1)c(nc2)c1cc2-c1ncnc(NC(CCC2)CN2C(OC(C)(C)C)=O)c1)=O Chemical compound CC(C)[O]=S(c1ccccc1)([n](cc1)c(nc2)c1cc2-c1ncnc(NC(CCC2)CN2C(OC(C)(C)C)=O)c1)=O VSLZIENXJCBPAV-UHFFFAOYSA-N 0.000 description 1
- YZXNQXAMZKETPE-UHFFFAOYSA-N CC/C(/NS(c1ccccc1)(=O)=O)=N\C=C Chemical compound CC/C(/NS(c1ccccc1)(=O)=O)=N\C=C YZXNQXAMZKETPE-UHFFFAOYSA-N 0.000 description 1
- JWZOFFHGENGYHZ-UHFFFAOYSA-N CCC(C)(C)/C(/NC)=N\CC Chemical compound CCC(C)(C)/C(/NC)=N\CC JWZOFFHGENGYHZ-UHFFFAOYSA-N 0.000 description 1
- OGFQGQKVPCBOCQ-UHFFFAOYSA-N CCC(CC)/C(/NS(c1ccccc1)(=O)=O)=N\C=C Chemical compound CCC(CC)/C(/NS(c1ccccc1)(=O)=O)=N\C=C OGFQGQKVPCBOCQ-UHFFFAOYSA-N 0.000 description 1
- PNSADXNZUWCLQX-UHFFFAOYSA-N CCC1CCC2(CC2)CC1 Chemical compound CCC1CCC2(CC2)CC1 PNSADXNZUWCLQX-UHFFFAOYSA-N 0.000 description 1
- YJZTYXAYZOGRLF-QYBLAXJSSA-N CCNC(CC1)CCC1C(Nc1cccc(N/C(/N)=C/C(/c2cc(cc[n]3S(c4ccccc4)(=O)=O)c3nc2)=N\CC)c1)=O Chemical compound CCNC(CC1)CCC1C(Nc1cccc(N/C(/N)=C/C(/c2cc(cc[n]3S(c4ccccc4)(=O)=O)c3nc2)=N\CC)c1)=O YJZTYXAYZOGRLF-QYBLAXJSSA-N 0.000 description 1
- FIOYXRBEYSGKAE-QPJJXVBHSA-N CN(C)C/C=C/C(Nc(cc1)ccc1C(NC(CCC1)CC1Nc1cc(-c2cnc3[nH]ccc3c2)ncn1)=O)=O Chemical compound CN(C)C/C=C/C(Nc(cc1)ccc1C(NC(CCC1)CC1Nc1cc(-c2cnc3[nH]ccc3c2)ncn1)=O)=O FIOYXRBEYSGKAE-QPJJXVBHSA-N 0.000 description 1
- UBMUMMLAFYHPLD-QPJJXVBHSA-N CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Nc3cc(cc[nH]4)c4nc3)c2)ccc1)=O)=O Chemical compound CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Nc3cc(cc[nH]4)c4nc3)c2)ccc1)=O)=O UBMUMMLAFYHPLD-QPJJXVBHSA-N 0.000 description 1
- RSZOKHXOALBCJI-WEVVVXLNSA-N CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Nc3cccnc3)c2)ccc1)=O)=O Chemical compound CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Nc3cccnc3)c2)ccc1)=O)=O RSZOKHXOALBCJI-WEVVVXLNSA-N 0.000 description 1
- QRMUIGFWPNYCHG-WEVVVXLNSA-N CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Oc3cccnc3)c2)ccc1)=O)=O Chemical compound CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Oc3cccnc3)c2)ccc1)=O)=O QRMUIGFWPNYCHG-WEVVVXLNSA-N 0.000 description 1
- AERVPJVOKMQGFB-WEVVVXLNSA-N CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Sc3cccnc3)c2)ccc1)=O)=O Chemical compound CN(C)C/C=C/C(Nc(cc1)ccc1C(Nc1cc(Nc2ncnc(Sc3cccnc3)c2)ccc1)=O)=O AERVPJVOKMQGFB-WEVVVXLNSA-N 0.000 description 1
- WONDADPWHXUCJW-WEVVVXLNSA-N CN(C)C/C=C/C(Nc1cc(NC(N(CCC2)CC2N)=O)ccc1)=O Chemical compound CN(C)C/C=C/C(Nc1cc(NC(N(CCC2)CC2N)=O)ccc1)=O WONDADPWHXUCJW-WEVVVXLNSA-N 0.000 description 1
- AJPKQEAXOXNVJX-RIYZIHGNSA-N CN(C)C/C=C/C(Nc1cc(NC(N(CCC2)CC2Nc2ncnc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)c2)=O)ccc1)=O Chemical compound CN(C)C/C=C/C(Nc1cc(NC(N(CCC2)CC2Nc2ncnc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)c2)=O)ccc1)=O AJPKQEAXOXNVJX-RIYZIHGNSA-N 0.000 description 1
- ITGIYLMMAABTHC-ONEGZZNKSA-N CN(C)C/C=C/C(O)=O Chemical compound CN(C)C/C=C/C(O)=O ITGIYLMMAABTHC-ONEGZZNKSA-N 0.000 description 1
- BPVJSKXIWKALTH-SNAWJCMRSA-N CNC(/C=C/CN(C)C)=O Chemical compound CNC(/C=C/CN(C)C)=O BPVJSKXIWKALTH-SNAWJCMRSA-N 0.000 description 1
- ZMJOLIMVZAAMDI-NSCUHMNNSA-N CNC(/C=C/CN(CC1)CCN1C1CC1)=O Chemical compound CNC(/C=C/CN(CC1)CCN1C1CC1)=O ZMJOLIMVZAAMDI-NSCUHMNNSA-N 0.000 description 1
- SGVUHPSBDNVHKL-OCAPTIKFSA-N C[C@H]1C[C@@H](C)CCC1 Chemical compound C[C@H]1C[C@@H](C)CCC1 SGVUHPSBDNVHKL-OCAPTIKFSA-N 0.000 description 1
- RNTQCUJYWGNHJR-UHFFFAOYSA-N NC(CCC1)CN1C(Nc1cccc(N=O)c1)=O Chemical compound NC(CCC1)CN1C(Nc1cccc(N=O)c1)=O RNTQCUJYWGNHJR-UHFFFAOYSA-N 0.000 description 1
- XUQQHCPJKBYNJQ-UHFFFAOYSA-N Nc1cc(NC(N(CCC2)CC2Nc2cc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)ncn2)=O)ccc1 Chemical compound Nc1cc(NC(N(CCC2)CC2Nc2cc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)ncn2)=O)ccc1 XUQQHCPJKBYNJQ-UHFFFAOYSA-N 0.000 description 1
- SJNNSYZMWLOUIH-UHFFFAOYSA-N Nc1cccc(Nc2cc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)ncn2)c1 Chemical compound Nc1cccc(Nc2cc(-c3cc(cc[n]4S(c5ccccc5)(=O)=O)c4nc3)ncn2)c1 SJNNSYZMWLOUIH-UHFFFAOYSA-N 0.000 description 1
- ACFFAMJSFZINGL-OWOJBTEDSA-N O=C(/C=C/CBr)Cl Chemical compound O=C(/C=C/CBr)Cl ACFFAMJSFZINGL-OWOJBTEDSA-N 0.000 description 1
- XOYPFZAJHRTMIF-UHFFFAOYSA-N O=S(c1ccccc1)([n](cc1)c(nc2)c1cc2-c1cc(NC2CNCCC2)ncn1)=O Chemical compound O=S(c1ccccc1)([n](cc1)c(nc2)c1cc2-c1cc(NC2CNCCC2)ncn1)=O XOYPFZAJHRTMIF-UHFFFAOYSA-N 0.000 description 1
- SAHAGUXLUYWVPY-UHFFFAOYSA-N O=S(c1ccccc1)([n](cc1)c(nc2)c1cc2-c1ncnc(Cl)c1)=O Chemical compound O=S(c1ccccc1)([n](cc1)c(nc2)c1cc2-c1ncnc(Cl)c1)=O SAHAGUXLUYWVPY-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim 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
- A61K31/495—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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562185334P | 2015-06-26 | 2015-06-26 | |
| US62/185,334 | 2015-06-26 | ||
| PCT/US2016/039312 WO2016210296A1 (en) | 2015-06-26 | 2016-06-24 | 4,6-pyrimidinylene derivatives and uses thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018522866A JP2018522866A (ja) | 2018-08-16 |
| JP2018522866A5 JP2018522866A5 (enExample) | 2019-07-25 |
| JP6947651B2 true JP6947651B2 (ja) | 2021-10-13 |
Family
ID=57585796
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017567060A Active JP6947651B2 (ja) | 2015-06-26 | 2016-06-24 | 4,6−ピリミジニレン誘導体およびこれらの使用 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US10695346B2 (enExample) |
| EP (1) | EP3313530B1 (enExample) |
| JP (1) | JP6947651B2 (enExample) |
| AU (1) | AU2016283105C1 (enExample) |
| CA (1) | CA2988330A1 (enExample) |
| WO (1) | WO2016210296A1 (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2972239A1 (en) | 2014-12-23 | 2016-06-30 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| CN107427521B (zh) | 2015-03-27 | 2021-08-03 | 达纳-法伯癌症研究所股份有限公司 | 细胞周期蛋白依赖性激酶的抑制剂 |
| WO2017073065A1 (ja) * | 2015-10-28 | 2017-05-04 | 公益財団法人静岡県産業振興財団 | 新規抗がん薬 |
| US11542233B2 (en) * | 2016-12-23 | 2023-01-03 | Aquinnah Pharmaceuticals, Inc. | Compounds, compositions and methods of use |
| JP7569688B2 (ja) * | 2017-12-22 | 2024-10-18 | ハイバーセル,インコーポレイテッド | ホスファチジルイノシトールリン酸キナーゼ阻害剤としてのアミノピリジン誘導体 |
| WO2019126733A1 (en) | 2017-12-22 | 2019-06-27 | Petra Pharma Corporation | Aryl-bipyridine amine derivatives as phosphatidylinositol phosphate kinase inhibitors |
| CN111936484A (zh) * | 2017-12-22 | 2020-11-13 | 拉文纳制药公司 | 作为磷脂酰肌醇磷酸激酶抑制剂的色烯并吡啶衍生物 |
| PT3784664T (pt) | 2018-04-26 | 2025-04-23 | Pfizer | Derivados da 2-amino-piridina ou da 2-amino-pirimidina como inibidores da quinase dependente da ciclina |
| WO2019213403A1 (en) | 2018-05-02 | 2019-11-07 | Kinnate Biopharma Inc. | Inhibitors of cyclin-dependent kinases |
| JP7590185B2 (ja) | 2018-06-25 | 2024-11-26 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | Taireファミリーキナーゼインヒビターおよびそれらの使用 |
| JP2021529740A (ja) | 2018-06-29 | 2021-11-04 | キネート バイオファーマ インク. | サイクリン依存性キナーゼの阻害剤 |
| EP3833353A4 (en) * | 2018-08-10 | 2022-08-24 | Yale University | Small-molecule pi5p4k alpha/beta inhibitors and methods of treatment using same |
| EP3902542A4 (en) | 2018-12-28 | 2022-09-07 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 and uses thereof |
| TW202112767A (zh) * | 2019-06-17 | 2021-04-01 | 美商佩特拉製藥公司 | 作為磷脂酸肌醇磷酸激酶抑制劑之胺基吡啶衍生物 |
| TW202112784A (zh) | 2019-06-17 | 2021-04-01 | 美商佩特拉製藥公司 | 作為磷脂酸肌醇磷酸激酶抑制劑之𠳭唏并嘧啶衍生物 |
| CN113698391B (zh) * | 2020-05-21 | 2023-06-06 | 上海拓界生物医药科技有限公司 | 4-氨基嘧啶或2-氨基三嗪类化合物及其制备方法 |
| JP2023554673A (ja) * | 2020-12-21 | 2023-12-28 | ヤンセン ファーマシューティカ エヌ.ベー. | サイクリン依存性キナーゼ7(cdk7)阻害剤としての三環式ピリミジン |
| CA3173819A1 (en) * | 2020-12-23 | 2022-06-30 | Dana-Farber Cancer Institute, Inc. | Small molecule degraders of phosphatidylinositol-5-phosphate 4-kinase type 2 and uses thereof |
| WO2022246025A1 (en) * | 2021-05-20 | 2022-11-24 | Dana-Farber Cancer Institute, Inc. | Inhibitors and degraders of pip4k protein |
| MX2024002139A (es) | 2021-08-18 | 2024-03-06 | Chemocentryx Inc | Arilsulfonil(hidroxi)piperidinas como inhibidores de ccr6. |
| WO2023023534A2 (en) | 2021-08-18 | 2023-02-23 | Chemocentryx, Inc. | Aryl sulfonyl compounds as ccr6 inhibitors |
| CN113698357A (zh) * | 2021-09-29 | 2021-11-26 | 守恒(厦门)医疗科技有限公司 | 磺胺嘧啶类衍生物及其在抗肿瘤药物的应用 |
| CN113861130A (zh) * | 2021-09-29 | 2021-12-31 | 守恒(厦门)医疗科技有限公司 | 联苯磺胺噻二唑类衍生物及其在抗肿瘤药物的应用 |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
| WO2023227125A1 (zh) * | 2022-05-26 | 2023-11-30 | 杭州德睿智药科技有限公司 | 作为CDKs抑制剂的新型并杂环类新化合物及其应用 |
| CN116903587B (zh) * | 2023-06-01 | 2024-03-22 | 三峡大学 | 一种角鲨烯环氧酶抑制剂及其用途 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1205276A (en) * | 1915-03-29 | 1916-11-21 | Robert C Sharpe | Machine or instrument for cracking nuts. |
| KR100848067B1 (ko) * | 2003-12-25 | 2008-07-23 | 니뽄 신야쿠 가부시키가이샤 | 아미드 유도체 및 의약 |
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2016
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- 2016-06-24 US US15/737,535 patent/US10695346B2/en active Active
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| US20180344733A9 (en) | 2018-12-06 |
| CA2988330A1 (en) | 2016-12-29 |
| EP3313530A4 (en) | 2019-02-20 |
| EP3313530B1 (en) | 2022-10-05 |
| AU2016283105B2 (en) | 2020-09-24 |
| AU2016283105A1 (en) | 2017-12-21 |
| AU2016283105C1 (en) | 2023-02-02 |
| US20180110778A1 (en) | 2018-04-26 |
| WO2016210296A1 (en) | 2016-12-29 |
| JP2018522866A (ja) | 2018-08-16 |
| US20200338075A1 (en) | 2020-10-29 |
| US10695346B2 (en) | 2020-06-30 |
| HK1254654A1 (en) | 2019-07-26 |
| EP3313530A1 (en) | 2018-05-02 |
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