SG11201807982UA - Substituted inhibitors of menin-mll and methods of use - Google Patents
Substituted inhibitors of menin-mll and methods of useInfo
- Publication number
- SG11201807982UA SG11201807982UA SG11201807982UA SG11201807982UA SG11201807982UA SG 11201807982U A SG11201807982U A SG 11201807982UA SG 11201807982U A SG11201807982U A SG 11201807982UA SG 11201807982U A SG11201807982U A SG 11201807982UA SG 11201807982U A SG11201807982U A SG 11201807982UA
- Authority
- SG
- Singapore
- Prior art keywords
- huron
- floor
- international
- ann arbor
- parkway
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title 1
- 102100022103 Histone-lysine N-methyltransferase 2A Human genes 0.000 abstract 2
- 101001045846 Homo sapiens Histone-lysine N-methyltransferase 2A Proteins 0.000 abstract 2
- 102100022102 Histone-lysine N-methyltransferase 2B Human genes 0.000 abstract 1
- 101001045848 Homo sapiens Histone-lysine N-methyltransferase 2B Proteins 0.000 abstract 1
- 101001008894 Homo sapiens Histone-lysine N-methyltransferase 2D Proteins 0.000 abstract 1
- 102100030550 Menin Human genes 0.000 abstract 1
- 101710169972 Menin Proteins 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 102000037865 fusion proteins Human genes 0.000 abstract 1
- 108020001507 fusion proteins Proteins 0.000 abstract 1
- 208000032839 leukemia Diseases 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000008520 organization Effects 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
- C07D295/205—Radicals derived from carbonic acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Abstract
INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property -, Organization M1111101110101011111 HO 111110111011110110101101011110111110111011 11 International Bureau ... .jd ..... .,,,, (10) International Publication Number (43) International Publication Date WO 2017/161028 Al 21 September 2017 (21.09.2017) WIP0 I PCT (51) International Patent Classification: (US). GREMBECKA, Jolanta; 1600 Huron Parkway, A61K 31/535 (2006.01) 2nd Floor, Ann Arbor, MI 48109 (US). CIERPICKI, To- (21) International Application Number: masz; 1600 Huron Parkway, 2nd Floor, Ann Arbor, MI 48109 (US). KLOSSOWSKI, Szymon; 1600 Huron Park- PCT/US2017/022564 way, 2nd Floor, Ann Arbor, MI 48109 (US). POLLOCK, (22) International Filing Date: Jonathan; 1600 Huron Parkway, 2nd Floor, Ann Arbor, 15 March 2017 (15.03.2017) MI 48109 (US). BORKIN, Dmitry; 1600 Huron Parkway, 2nd Floor, Ann Arbor, MI 48109 (US). (25) Filing Language: English (74) Agents: CHANG, Andrew, L. et al.; Wilson Sonsini (26) Publication Language: English Goodrich & Rosati, 650 Page Mill Road, Palo Alto, CA (30) Priority Data: 94304-1050 (US). 62/309,372 16 March 2016 (16.03.2016) US (81) Designated States (unless otherwise indicated, for every 62/334,369 10 May 2016 (10.05.2016) US kind of national protection available): AE, AG, AL, AM, 62/431,389 7 December 2016 (07.12.2016) US AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, 62/446,640 16 January 2017 (16.01.2017) US BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, — (71) Applicants: KURA ONCOLOGY, INC. [US/US]; 11119 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, North Torrey Pines Road, Suite 125, La Jolla, CA 92037 HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KH, KN, (US). THE REGENTS OF THE UNIVERSITY OF KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MICHIGAN [US/US]; 1600 Huron Parkway, 2nd Floor, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, Ann Arbor, MI 48109 (US). NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, (72) Inventors: WU, Tao; 2355 Terraza Guitara, Carlsbad, CA TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, 92009 (US). LI, Liansheng; 13569 Arroyo Dale Lane, San ZA, ZM, ZW. Diego, CA 92130 (US). WANG, Yi; 7556 Charmant Drive, Apartment 1732, San Diego, CA 92122 (US). REN, (84) Designated States (unless otherwise indicated, for every Pingda; 5534 Havenridge Way, San Diego, CA 92130 kind of regional protection available): ARIPO (BW, GH, [Continued on next page] Title: SUBSTITUTED INHIBITORS OF MENIN-MLL AND METHODS OF USE (54) FIG. 4 MV4;11 s.c. model 2000 -0-vehicle Control 1500 --Compound B, 50 mg/kg/bid, po -9-Compound B, 100 mg/kg/bid, po E ) -IEI-Compound B, 200 mg/kg/qd, po > 1000 8 -0-Compound B, 200 mg/kg/bid, po E +., c w as 500 1-1 ei 2 © 0 2 4 6 8 10 12 14 16 18 1-1 Treatment period (day) 1-1 1-1 (57) : The present disclosure provides methods of inhibiting the interaction of menin with MLL1, MLL2 and MLL-fusion N oncoproteins. The methods are useful for the treatment of leukemia, solid cancers, diabetes and other diseases dependent on activity of MLL1, MLL2, MLL fusion proteins, and/or menin. Compositions for use in these methods are also provided. C WO 2017/161028 Al 1#110HOMOIDEIRMEMOMMIDEMIMMOIMEN GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, Published: TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, DE, LT, — with international search report (Art. 21(3)) — before the expiration of the time limit for amending the LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, SE, GA, claims and to be republished in the event amendments (Rule 48.2(h)) of receipt of GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG).
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662309372P | 2016-03-16 | 2016-03-16 | |
| US201662334369P | 2016-05-10 | 2016-05-10 | |
| US201662431389P | 2016-12-07 | 2016-12-07 | |
| US201762446640P | 2017-01-16 | 2017-01-16 | |
| PCT/US2017/022564 WO2017161028A1 (en) | 2016-03-16 | 2017-03-15 | Substituted inhibitors of menin-mll and methods of use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SG11201807982UA true SG11201807982UA (en) | 2018-10-30 |
Family
ID=59851028
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11201807982UA SG11201807982UA (en) | 2016-03-16 | 2017-03-15 | Substituted inhibitors of menin-mll and methods of use |
Country Status (28)
| Country | Link |
|---|---|
| US (2) | US10781218B2 (en) |
| EP (2) | EP4219449A3 (en) |
| JP (3) | JP6919977B2 (en) |
| KR (1) | KR102419531B1 (en) |
| CN (2) | CN109152784B (en) |
| AU (1) | AU2017232516B2 (en) |
| BR (1) | BR112018068703B1 (en) |
| CA (1) | CA3015847A1 (en) |
| CY (1) | CY1126066T1 (en) |
| DK (1) | DK3429591T3 (en) |
| ES (1) | ES2947636T3 (en) |
| FI (1) | FI3429591T3 (en) |
| HK (1) | HK1259232A1 (en) |
| HR (1) | HRP20230537T1 (en) |
| HU (1) | HUE061989T2 (en) |
| IL (1) | IL261606B (en) |
| LT (1) | LT3429591T (en) |
| MD (1) | MD3429591T2 (en) |
| MX (1) | MX2018011105A (en) |
| MY (1) | MY201450A (en) |
| PH (1) | PH12018501952A1 (en) |
| PL (1) | PL3429591T3 (en) |
| PT (1) | PT3429591T (en) |
| RS (1) | RS64261B1 (en) |
| SG (1) | SG11201807982UA (en) |
| SI (1) | SI3429591T1 (en) |
| TW (1) | TWI747889B (en) |
| WO (1) | WO2017161028A1 (en) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG10201802911RA (en) | 2013-03-15 | 2018-05-30 | Global Blood Therapeutics Inc | Compounds and uses thereof for the modulation of hemoglobin |
| EA201992707A1 (en) | 2013-11-18 | 2020-06-30 | Глобал Блад Терапьютикс, Инк. | COMPOUNDS AND THEIR APPLICATIONS FOR HEMOGLOBIN MODULATION |
| WO2016040330A1 (en) | 2014-09-09 | 2016-03-17 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| AR104020A1 (en) | 2015-06-04 | 2017-06-21 | Kura Oncology Inc | METHODS AND COMPOSITIONS TO INHIBIT THE INTERACTION OF MENINA WITH MILL PROTEINS |
| EP3302057A4 (en) | 2015-06-04 | 2018-11-21 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with mll proteins |
| GB201516504D0 (en) | 2015-09-17 | 2015-11-04 | Astrazeneca Ab | Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer |
| HUE047684T2 (en) | 2016-01-22 | 2020-05-28 | Janssen Pharmaceutica Nv | New substituted cyanoindoline derivatives as nik inhibitors |
| ES2776658T3 (en) | 2016-01-22 | 2020-07-31 | Janssen Pharmaceutica Nv | New 6-membered heteroaromatic substituent cyanoindoline derivatives as NIK inhibitors |
| ES2947636T3 (en) | 2016-03-16 | 2023-08-14 | Kura Oncology Inc | Substituted thieno[2,3-d]pyrimidine derivatives as inhibitors of menin-MLL and methods of use |
| US10752639B2 (en) | 2016-03-16 | 2020-08-25 | Kura Oncology, Inc. | Bridged bicyclic inhibitors of menin-MLL and methods of use |
| SG11201809714TA (en) | 2016-05-02 | 2018-11-29 | Univ Michigan Regents | Piperidines as menin inhibitors |
| US20190119299A1 (en) | 2016-06-30 | 2019-04-25 | Janssen Pharmaceutica Nv | Cyanoindoline derivatives as nik inhibitors |
| WO2018002217A1 (en) | 2016-06-30 | 2018-01-04 | Janssen Pharmaceutica Nv | Heteroaromatic derivatives as nik inhibitors |
| JOP20190024A1 (en) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | Substituted pyrrolizine compounds and uses thereof |
| WO2018047081A1 (en) | 2016-09-09 | 2018-03-15 | Novartis Ag | Compounds and compositions as inhibitors of endosomal toll-like receptors |
| KR102493644B1 (en) | 2016-09-14 | 2023-01-30 | 얀센 파마슈티카 엔.브이. | Spiro bicyclic inhibitor of the menin-MLL interaction |
| EP3512858B1 (en) | 2016-09-14 | 2023-11-08 | Janssen Pharmaceutica NV | Fused bicyclic inhibitors of menin-mll interaction |
| EP3538101A4 (en) | 2016-11-14 | 2020-08-05 | Virginia Commonwealth University | Inhibitors of cancer invasion, attachment, and/or metastasis |
| KR102513564B1 (en) | 2016-12-15 | 2023-03-22 | 얀센 파마슈티카 엔.브이. | An azepane inhibitor of the menin-MLL interaction |
| WO2018109088A1 (en) | 2016-12-15 | 2018-06-21 | Janssen Pharmaceutica Nv | Azepane inhibitors of menin-mll interaction |
| WO2018175746A1 (en) * | 2017-03-24 | 2018-09-27 | Kura Oncology, Inc. | Methods for treating hematological malignancies and ewing's sarcoma |
| CN110636843A (en) | 2017-03-31 | 2019-12-31 | 密歇根大学董事会 | Piperidines as inhibitors of covalent multiple endocrine adenoma proteins |
| US11542248B2 (en) | 2017-06-08 | 2023-01-03 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
| WO2019014100A1 (en) | 2017-07-10 | 2019-01-17 | Celgene Corporation | Antiproliferative compounds and methods of use thereof |
| PE20201164A1 (en) | 2017-07-11 | 2020-10-28 | Vertex Pharma | CARBOXAMIDES AS MODULATORS OF SODIUM CHANNELS |
| TW201920170A (en) | 2017-09-20 | 2019-06-01 | 美商庫拉腫瘤技術股份有限公司 | Substituted inhibitors of MENIN-MLL and methods of use |
| CN111148743B (en) | 2017-10-06 | 2023-12-15 | 福马治疗有限公司 | Inhibition of ubiquitin-specific peptidase 30 |
| SI3700902T1 (en) | 2017-10-27 | 2023-10-30 | Boehringer Ingelheim International Gmbh | Inhibitors of trpc6 |
| WO2019120212A1 (en) * | 2017-12-19 | 2019-06-27 | 基石药业（苏州）有限公司 | Ido inhibitor |
| US11396517B1 (en) | 2017-12-20 | 2022-07-26 | Janssen Pharmaceutica Nv | Exo-aza spiro inhibitors of menin-MLL interaction |
| CN111788204B (en) | 2018-02-26 | 2023-05-05 | 吉利德科学公司 | Substituted pyrrolizine compounds as inhibitors of HBV replication |
| CN112384515A (en) | 2018-02-27 | 2021-02-19 | 因赛特公司 | Imidazopyrimidines and triazolopyrimidines as A2A/A2B inhibitors |
| CN110204552B (en) * | 2018-02-28 | 2021-08-17 | 中国科学院上海药物研究所 | Thieno [3,2-d ] pyrimidine derivatives, preparation method, pharmaceutical composition and application thereof |
| CN117285532A (en) | 2018-03-09 | 2023-12-26 | 里科瑞尔姆Ip控股有限责任公司 | Substituted 1, 2-dihydro-3H-pyrazolo [3,4-d ] pyrimidin-3-ones |
| EP3765459A1 (en) | 2018-03-13 | 2021-01-20 | Shire Human Genetic Therapies, Inc. | Substituted imidazopyridines as inhibitors of plasma kallikrein and uses thereof |
| JP7239562B2 (en) | 2018-03-30 | 2023-03-14 | 住友ファーマ株式会社 | Optically active crosslinked cyclic secondary amine derivatives |
| EP3773577A4 (en) | 2018-04-12 | 2021-12-01 | Terns, Inc. | Tricyclic ask1 inhibitors |
| HRP20231199T1 (en) | 2018-04-23 | 2024-01-19 | Celgene Corporation | Substituted 4-aminoisoindoline-1,3-dione compounds and their use for treating lymphoma |
| MA52940A (en) | 2018-05-18 | 2021-04-28 | Incyte Corp | FUSION PYRIMIDINE DERIVATIVES USED AS A2A / A2B INHIBITORS |
| EP3818063A1 (en) | 2018-07-05 | 2021-05-12 | Incyte Corporation | Fused pyrazine derivatives as a2a / a2b inhibitors |
| CA3113234A1 (en) | 2018-09-18 | 2020-03-26 | Nikang Therapeutics, Inc. | Tri-substituted heteroaryl derivatives as src homology-2 phosphatase inhibitors |
| WO2020069027A1 (en) * | 2018-09-26 | 2020-04-02 | Kura Oncology, Inc. | Treatment of hematological malignancies with inhibitors of menin |
| EP4218934A1 (en) | 2018-10-05 | 2023-08-02 | Forma Therapeutics, Inc. | Inhibiting ubiquitin-specific protease 30 (usp30) |
| TWI767148B (en) | 2018-10-10 | 2022-06-11 | 美商弗瑪治療公司 | Inhibiting fatty acid synthase (fasn) |
| US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
| PE20211871A1 (en) | 2018-11-22 | 2021-09-21 | Qilu Regor Therapeutics Inc | GLP-1R AGONISTS AND USES OF THEM |
| WO2020116662A1 (en) | 2018-12-06 | 2020-06-11 | 第一三共株式会社 | Cycloalkane-1,3-diamine derivative |
| TW202043205A (en) | 2018-12-31 | 2020-12-01 | 美商拜歐米富士恩有限公司 | Inhibitors of menin-mll interaction |
| AU2020209216A1 (en) | 2019-01-18 | 2021-08-26 | Astrazeneca Ab | PCSK9 inhibitors and methods of use thereof |
| TWI829857B (en) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | Pyrazolopyridines and triazolopyridines as a2a / a2b inhibitors |
| US11384083B2 (en) | 2019-02-15 | 2022-07-12 | Incyte Corporation | Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors |
| TW202100520A (en) | 2019-03-05 | 2021-01-01 | 美商英塞特公司 | Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors |
| WO2020205560A1 (en) | 2019-03-29 | 2020-10-08 | Incyte Corporation | Sulfonylamide compounds as cdk2 inhibitors |
| US10954221B2 (en) | 2019-04-12 | 2021-03-23 | Qilu Regor Therapeutics Inc. | GLP-1R agonists and uses thereof |
| WO2020223469A1 (en) | 2019-05-01 | 2020-11-05 | Incyte Corporation | N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer |
| WO2020223558A1 (en) | 2019-05-01 | 2020-11-05 | Incyte Corporation | Tricyclic amine compounds as cdk2 inhibitors |
| US11529350B2 (en) | 2019-07-03 | 2022-12-20 | Sumitomo Pharma Oncology, Inc. | Tyrosine kinase non-receptor 1 (TNK1) inhibitors and uses thereof |
| CR20220066A (en) | 2019-08-14 | 2022-11-28 | Incyte Corp | Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors |
| WO2021055589A1 (en) | 2019-09-18 | 2021-03-25 | Shire Human Genetic Therapies, Inc. | Heteroaryl plasma kallikrein inhibitors |
| CN114728962A (en) | 2019-09-18 | 2022-07-08 | 武田药品工业有限公司 | Plasma kallikrein inhibitors and uses thereof |
| CN115298177A (en) | 2019-10-11 | 2022-11-04 | 因赛特公司 | Bicyclic amines as CDK2 inhibitors |
| CA3157525A1 (en) | 2019-10-25 | 2021-04-29 | Gilead Sciences, Inc. | Glp-1r modulating compounds |
| US11834441B2 (en) | 2019-12-06 | 2023-12-05 | Vertex Pharmaceuticals Incorporated | Substituted tetrahydrofurans as modulators of sodium channels |
| WO2021133809A1 (en) | 2019-12-23 | 2021-07-01 | Blueprint Medicines Corporation | Inhibitors of mutant forms of egfr |
| AU2020417293A1 (en) | 2020-01-03 | 2022-09-01 | Berg Llc | Polycyclic amides as UBE2K modulators for treating cancer |
| TWI794742B (en) | 2020-02-18 | 2023-03-01 | 美商基利科學股份有限公司 | Antiviral compounds |
| CN111297863B (en) * | 2020-03-30 | 2021-06-25 | 四川大学华西医院 | Application of menin-MLL inhibitor in preparation of medicine for treating endometrial cancer |
| CA3178813A1 (en) | 2020-05-15 | 2021-11-18 | Algen Biotechnologies, Inc. | Certain chemical compositions and methods of use thereof |
| EP4247804A1 (en) | 2020-11-20 | 2023-09-27 | Gilead Sciences, Inc. | Polyheterocyclic glp-1 r modulating compounds |
| KR20230159421A (en) | 2021-02-19 | 2023-11-21 | 수도 바이오사이언시즈 리미티드 | TYK2 inhibitors and uses thereof |
| US11697666B2 (en) | 2021-04-16 | 2023-07-11 | Gilead Sciences, Inc. | Methods of preparing carbanucleosides using amides |
| KR20230173708A (en) | 2021-04-21 | 2023-12-27 | 길리애드 사이언시즈, 인코포레이티드 | Carboxy-benzimidazole GLP-1R modulating compound |
| JP2024518434A (en) | 2021-05-08 | 2024-05-01 | ヤンセン ファーマシューティカ エヌ．ベー． | Substituted Spiro Derivatives |
| CA3214746A1 (en) | 2021-05-08 | 2022-11-17 | Olivier Alexis Georges Querolle | Substituted spiro derivatives |
| CA3218479A1 (en) | 2021-06-01 | 2022-12-08 | Wei Cai | Substituted phenyl-1h-pyrrolo[2, 3-c]pyridine derivatives |
| BR112023025436A2 (en) | 2021-06-03 | 2024-02-27 | Janssen Pharmaceutica Nv | PYIDAZINES OR 1,2,4-TRIAZINES REPLACED BY SPIROCYCLIC AMINES |
| WO2022253309A1 (en) * | 2021-06-03 | 2022-12-08 | 首药控股(北京)股份有限公司 | Substituted heterocyclic compounds and application thereof |
| EP4347031A1 (en) | 2021-06-04 | 2024-04-10 | Vertex Pharmaceuticals Incorporated | N-(hydroxyalkyl (hetero)aryl) tetrahydrofuran carboxamides as modulators of sodium channels |
| IL309359A (en) | 2021-06-17 | 2024-02-01 | Janssen Pharmaceutica Nv | (r)-n-ethyl-5-fluoro-n-isopropyl-2-((5-(2-(6-((2-methoxyethyl)(methyl)amino)-2-methylhexan-3-yl)-2,6-diazaspiro[3.4]octan-6-yl)-1,2,4-triazin-6-yl)oxy)benzamide besylate salt for the treatment of diseases such as cancer |
| US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
| CN115515958B (en) * | 2021-08-04 | 2023-09-29 | 成都苑东生物制药股份有限公司 | Novel sulfonamide (Menin-MLL) interaction inhibitor, preparation method and medical application thereof |
| WO2023011446A1 (en) * | 2021-08-04 | 2023-02-09 | 成都苑东生物制药股份有限公司 | Novel sulfonamide menin-mll interaction inhibitor, preparation method therefor, and medical use thereof |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| WO2023150635A1 (en) * | 2022-02-04 | 2023-08-10 | Kura Oncology, Inc. | Treatment of hematological malignancies with menin inhibitors and p-glycoprotein inhibitors |
Family Cites Families (102)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5863A (en) | 1848-10-17 | Matthias p | ||
| US5861A (en) | 1848-10-17 | Locking umbrella and parasol | ||
| US510A (en) | 1837-12-07 | soeel | ||
| US949A (en) | 1838-09-27 | Improvement in roller cotton-gins for ginning long-staple and other kinds of cotton | ||
| US5052558A (en) | 1987-12-23 | 1991-10-01 | Entravision, Inc. | Packaged pharmaceutical product |
| US5033252A (en) | 1987-12-23 | 1991-07-23 | Entravision, Inc. | Method of packaging and sterilizing a pharmaceutical product |
| GB8827305D0 (en) | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
| US5323907A (en) | 1992-06-23 | 1994-06-28 | Multi-Comp, Inc. | Child resistant package assembly for dispensing pharmaceutical medications |
| DE4239169A1 (en) | 1992-11-21 | 1994-05-26 | Merck Patent Gmbh | Cyclobutane - benzene derivatives |
| US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| DE69519751T2 (en) | 1995-04-20 | 2001-04-19 | Pfizer | ARYLSULFONAMIDO-SUBSTITUTED HYDROXAMIC ACID DERIVATIVES AS INHIBITORS OF MMP AND TNF |
| ATE225343T1 (en) | 1995-12-20 | 2002-10-15 | Hoffmann La Roche | MATRIX METALLOPROTEASE INHIBITORS |
| JP3195756B2 (en) | 1996-07-04 | 2001-08-06 | 公子 吉水 | Lubrication auxiliary |
| WO1998003516A1 (en) | 1996-07-18 | 1998-01-29 | Pfizer Inc. | Phosphinate based inhibitors of matrix metalloproteases |
| SK21499A3 (en) | 1996-08-23 | 2000-05-16 | Pfizer | Arylsulfonylamino hydroxamic acid derivatives |
| US5866562A (en) | 1996-10-25 | 1999-02-02 | Bayer Aktiengesellschaft | Ring-bridged bis-quinolines |
| PT950059E (en) | 1997-01-06 | 2004-10-29 | Pfizer | CYCLIC SULFONA DERIVATIVES |
| EP0977733B1 (en) | 1997-02-03 | 2003-09-03 | Pfizer Products Inc. | Arylsulfonylamino hydroxamic acid derivatives |
| CA2279863A1 (en) | 1997-02-07 | 1998-08-13 | Pfizer Inc. | N-hydroxy-beta-sulfonyl-propionamide derivatives and their use as inhibitors of matrix metalloproteinases |
| CN1247531A (en) | 1997-02-11 | 2000-03-15 | 辉瑞大药厂 | Arylsulfonyl hydroxamic acid derivatives |
| JPH10330377A (en) | 1997-06-02 | 1998-12-15 | Kyowa Hakko Kogyo Co Ltd | Piperidine derivative |
| GB9725782D0 (en) | 1997-12-05 | 1998-02-04 | Pfizer Ltd | Therapeutic agents |
| GB9801690D0 (en) | 1998-01-27 | 1998-03-25 | Pfizer Ltd | Therapeutic agents |
| US6479487B1 (en) | 1998-02-26 | 2002-11-12 | Aventis Pharmaceuticals Inc. | 6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines |
| PA8469401A1 (en) | 1998-04-10 | 2000-05-24 | Pfizer Prod Inc | BICYCLE DERIVATIVES OF HYDROXAMIC ACID |
| PA8469501A1 (en) | 1998-04-10 | 2000-09-29 | Pfizer Prod Inc | HYDROXAMIDES OF THE ACID (4-ARILSULFONILAMINO) -TETRAHIDROPIRAN-4-CARBOXILICO |
| PA8474101A1 (en) | 1998-06-19 | 2000-09-29 | Pfizer Prod Inc | PYROLEUM [2,3-D] PIRIMIDINE COMPOUNDS |
| US20070208087A1 (en) | 2001-11-02 | 2007-09-06 | Sanders Virginia J | Compounds, compositions and methods for the treatment of inflammatory diseases |
| WO2002088107A1 (en) | 2001-04-26 | 2002-11-07 | Eisai Co., Ltd. | Nitrogenous fused-ring compound having pyrazolyl group as substituent and medicinal composition thereof |
| CN100343258C (en) | 2001-04-30 | 2007-10-17 | 美国拜尔公司 | Novel 4-amino-5,6-substituted thiopheno 2,3-d]pyrimidines |
| WO2003022214A2 (en) | 2001-09-06 | 2003-03-20 | Millennium Pharmaceuticals, Inc. | Piperazine and homopiperazine compounds |
| AU2003255482A1 (en) | 2002-10-02 | 2004-04-23 | Merck Patent Gmbh | Use of 4 amino-quinazolines as anti cancer agents |
| AU2003258662A1 (en) | 2002-10-02 | 2004-04-23 | Merck Patent Gmbh | Use of 4-amino-quinazolines as anti cancer agents |
| US20050222175A1 (en) | 2004-03-31 | 2005-10-06 | Dhanoa Dale S | New piperidinylamino-thieno[2,3-D] pyrimidine compounds |
| US7612078B2 (en) | 2003-03-31 | 2009-11-03 | Epix Delaware, Inc. | Piperidinylamino-thieno[2,3-D] pyrimidine compounds |
| CN1777612A (en) | 2003-03-31 | 2006-05-24 | 普雷迪克医药品控股公司 | New piperidinylamino-thieno[2,3-d] pyrimidine compounds |
| JP5335191B2 (en) | 2003-08-22 | 2013-11-06 | デンドレオン コーポレイション | Compositions and methods for treating diseases associated with Trp-p8 expression |
| US20050123906A1 (en) | 2003-11-06 | 2005-06-09 | Rana Tariq M. | Protein modulation |
| WO2006014420A1 (en) | 2004-07-06 | 2006-02-09 | Angion Biomedica Corporation | Quinazoline modulators of hepatocyte growth factor / c-met activity for the treatment of cancer |
| ATE530519T1 (en) | 2005-06-03 | 2011-11-15 | Abbott Lab | CYCLOBUTYLAMINE DERIVATIVES |
| US20060281769A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators |
| US20060281771A1 (en) | 2005-06-10 | 2006-12-14 | Baumann Christian A | Synergistic modulation of flt3 kinase using aminoquinoline and aminoquinazoline kinase modulators |
| KR20080040032A (en) | 2005-09-02 | 2008-05-07 | 티보텍 파마슈티칼즈 리미티드 | Benzodiazepines as hcv inhibitors |
| EP1926798B1 (en) | 2005-09-19 | 2009-09-30 | Merck Patent GmbH | Cyclobutane and spiro[3.3]heptane compounds |
| FR2891829A1 (en) | 2005-10-12 | 2007-04-13 | Sanofi Aventis Sa | 4-AMINO-QUINAZOLINE DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC USE THEREOF |
| AR057579A1 (en) | 2005-11-23 | 2007-12-05 | Merck & Co Inc | SPIROCICLICAL COMPOUNDS AS INHIBITORS OF ACETYLASE HISTONE (HDAC) |
| ATE541844T1 (en) | 2005-12-21 | 2012-02-15 | Abbott Lab | ANTIVIRAL COMPOUNDS |
| JP5302883B2 (en) | 2006-04-07 | 2013-10-02 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Thienopyrimidine having MNK1 / MNK2 inhibitory activity for pharmaceutical composition |
| EP1903044A1 (en) * | 2006-09-14 | 2008-03-26 | Novartis AG | Adenosine Derivatives as A2A Receptor Agonists |
| WO2008070303A2 (en) | 2006-10-19 | 2008-06-12 | The University Of Chicago | Therapeutics to inhibit mll-menin interaction for treating leukemia |
| EP1947103A1 (en) | 2007-01-22 | 2008-07-23 | 4Sc Ag | Aryloxypropanolamines, methods of preparation thereof and use of aryloxypropanolamines as medicaments |
| WO2008099019A1 (en) | 2007-02-16 | 2008-08-21 | Tibotec Pharmaceuticals Ltd. | 6-hydroxy-dibenzodiazepinones useful as hepatitis c virus inhibitors |
| FR2913017A1 (en) | 2007-02-23 | 2008-08-29 | Cerep Sa | New N-(substituted alkyl)-piperidine or piperazine derivatives, are cellular proliferation inhibitors useful e.g. for treating cancer or inflammatory or autoimmune diseases |
| ATE496022T1 (en) | 2007-03-19 | 2011-02-15 | Council Scient Ind Res | ANTHRANILIC ACID DERIVATIVE AS AN ANTI-CANCER ACTIVE AND METHOD FOR THE PRODUCTION THEREOF |
| WO2008135232A1 (en) | 2007-05-02 | 2008-11-13 | Riccardo Cortese | Use and compositions of purine derivatives for the treatment of proliferative disorders |
| JP2010530736A (en) | 2007-05-25 | 2010-09-16 | バーンハム インスティトゥート フォー メディカル リサーチ | Inhibitors of cell death induced by thapsigargin. |
| WO2009017838A2 (en) | 2007-08-01 | 2009-02-05 | Exelixis, Inc. | Combinations of jak-2 inhibitors and other agents |
| US20110124649A1 (en) | 2007-11-09 | 2011-05-26 | The Johns Hopkins University | Inhibitors of human methionine aminopeptidase 1 and methods of treating disorders |
| AU2008345225A1 (en) | 2007-12-21 | 2009-07-09 | University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| JP2011523420A (en) | 2008-05-22 | 2011-08-11 | アラーガン インコーポレイテッド | Bicyclic compounds having activity at the CXCR4 receptor |
| DE102008027574A1 (en) * | 2008-06-10 | 2009-12-17 | Merck Patent Gmbh | New pyrrolidine derivatives as MetAP-2 inhibitors |
| US8507491B2 (en) | 2008-08-25 | 2013-08-13 | Irm Llc | Compounds and compositions as hedgehog pathway inhibitors |
| US20100063047A1 (en) | 2008-09-10 | 2010-03-11 | Kalypsys, Inc. | Aminopyrimidine inhibitors of histamine receptors for the treatment of disease |
| GB0904285D0 (en) * | 2009-03-12 | 2009-04-22 | Prosidion Ltd | Compounds for the treatment of metabolic disorders |
| TW201038572A (en) | 2009-03-25 | 2010-11-01 | Gruenenthal Gmbh | Substituted spiro-amide compounds |
| WO2010142402A1 (en) | 2009-06-08 | 2010-12-16 | Grünenthal GmbH | Substituted benzimidazoles, benzothiazoles and benzoxazoles |
| WO2010147234A1 (en) | 2009-06-18 | 2010-12-23 | Banyu Pharmaceutical Co.,Ltd. | Diarylamide-spirodiamine derivative |
| US9346809B2 (en) | 2009-07-08 | 2016-05-24 | Leo Pharma A/S | Heterocyclic compounds as JAK receptor and protein tyrosine kinase inhibitors |
| US8742100B2 (en) | 2009-07-30 | 2014-06-03 | National University Of Singapore | Small molecule inhibitors of isoprenylcysteine carboxyl methyltransferase with potential anticancer activity |
| US8993552B2 (en) | 2009-09-04 | 2015-03-31 | The Regents Of The University Of Michigan | Compositions and methods for treatment of leukemia |
| AU2011217561B2 (en) | 2010-02-22 | 2016-04-21 | Merck Patent Gmbh | Hetarylaminonaphthyridines |
| SG187742A1 (en) | 2010-08-20 | 2013-03-28 | Hutchison Medipharma Ltd | Pyrrolopyrimidine compounds and uses thereof |
| WO2013019966A1 (en) | 2011-08-04 | 2013-02-07 | Allergan, Inc. | Aromatic bycyclic derivatives as cxcr4 receptor modulators |
| GB201114212D0 (en) | 2011-08-18 | 2011-10-05 | Ucb Pharma Sa | Therapeutic agents |
| AR090037A1 (en) * | 2011-11-15 | 2014-10-15 | Xention Ltd | DERIVATIVES OF TIENO AND / OR FURO-PYRIMIDINES AND PYRIDINES INHIBITORS OF THE POTASSIUM CHANNELS |
| CN103833759A (en) | 2012-11-23 | 2014-06-04 | 华东理工大学 | Pteridinone derivatives as BLK and FLT3 inhibitors and applications thereof |
| GB201217704D0 (en) | 2012-10-03 | 2012-11-14 | Ucb Pharma Sa | Therapeutic agents |
| US9505781B2 (en) * | 2013-03-13 | 2016-11-29 | The Regents Of The University Of Michigan | Compositions comprising thienopyrimidine and thienopyridine compounds and methods of use thereof |
| US9771327B2 (en) | 2013-03-13 | 2017-09-26 | Flatley Discovery Lab, Llc | Compounds and methods for the treatment of cystic fibrosis |
| US9212180B2 (en) | 2013-06-12 | 2015-12-15 | The Regents Of The University Of Michigan | Menin-MLL inhibitors and methods of use thereof |
| WO2015087151A1 (en) | 2013-12-12 | 2015-06-18 | Chong Kun Dang Pharmaceutical Corp. | Novel azaindole derivatives as selective histone deacetylase (hdac) inhibitors and pharmaceutical compositions comprising the same |
| PT3126352T (en) | 2014-04-04 | 2018-12-27 | Syros Pharmaceuticals Inc | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| WO2015191701A1 (en) | 2014-06-10 | 2015-12-17 | The Trustees Of The University Of Pennsylvania | Scaffolds for inhibitors of menin-mll interactions |
| WO2016040330A1 (en) * | 2014-09-09 | 2016-03-17 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| CN105732636B (en) | 2014-12-30 | 2020-04-21 | 广东东阳光药业有限公司 | Heteroaromatic compounds and their use in medicine |
| AR104020A1 (en) | 2015-06-04 | 2017-06-21 | Kura Oncology Inc | METHODS AND COMPOSITIONS TO INHIBIT THE INTERACTION OF MENINA WITH MILL PROTEINS |
| EP3302057A4 (en) | 2015-06-04 | 2018-11-21 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with mll proteins |
| KR20180022826A (en) | 2015-07-02 | 2018-03-06 | 얀센 사이언시즈 아일랜드 유씨 | Antimicrobial compound |
| EP3394064A1 (en) | 2015-12-22 | 2018-10-31 | Vitae Pharmaceuticals, Inc. | Inhibitors of the menin-mll interaction |
| AR107354A1 (en) | 2016-01-13 | 2018-04-18 | Bristol Myers Squibb Co | SPIROHEPTAN SALICILAMIDS AND RELATED COMPOUNDS AS ROCK INHIBITORS |
| CA3012649A1 (en) | 2016-01-26 | 2017-08-03 | Memorial Sloan-Kettering Cancer Center | Targeting chromatin regulators inhibits leukemogenic gene expression in npm1 mutant leukemia |
| US10752639B2 (en) | 2016-03-16 | 2020-08-25 | Kura Oncology, Inc. | Bridged bicyclic inhibitors of menin-MLL and methods of use |
| ES2947636T3 (en) | 2016-03-16 | 2023-08-14 | Kura Oncology Inc | Substituted thieno[2,3-d]pyrimidine derivatives as inhibitors of menin-MLL and methods of use |
| SG11201809714TA (en) | 2016-05-02 | 2018-11-29 | Univ Michigan Regents | Piperidines as menin inhibitors |
| WO2017207387A1 (en) | 2016-05-31 | 2017-12-07 | Bayer Pharma Aktiengesellschaft | Spiro condensed azetidine derivatives as inhibitors of the menin-mml1 interaction |
| ES2831084T3 (en) | 2016-06-10 | 2021-06-07 | Vitae Pharmaceuticals Inc | Inhibitors of the menin-MLL interaction |
| WO2018024602A1 (en) | 2016-08-04 | 2018-02-08 | Bayer Aktiengesellschaft | 2,7-diazaspiro[4.4]nonanes |
| EP3512858B1 (en) | 2016-09-14 | 2023-11-08 | Janssen Pharmaceutica NV | Fused bicyclic inhibitors of menin-mll interaction |
| MX2019003091A (en) | 2016-09-16 | 2019-07-08 | Vitae Pharmaceuticals Inc | Inhibitors of the menin-mll interaction. |
| EA201990699A1 (en) | 2016-10-05 | 2019-09-30 | Янссен Фармацевтика Нв | SPIROBICYCLIC INhibitors of the MENIN – MLL INTERACTION |
| TW201920170A (en) | 2017-09-20 | 2019-06-01 | 美商庫拉腫瘤技術股份有限公司 | Substituted inhibitors of MENIN-MLL and methods of use |
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