SG11201808878UA - Heterocyclic compounds as ret kinase inhibitors - Google Patents
Heterocyclic compounds as ret kinase inhibitorsInfo
- Publication number
- SG11201808878UA SG11201808878UA SG11201808878UA SG11201808878UA SG11201808878UA SG 11201808878U A SG11201808878U A SG 11201808878UA SG 11201808878U A SG11201808878U A SG 11201808878UA SG 11201808878U A SG11201808878U A SG 11201808878UA SG 11201808878U A SG11201808878U A SG 11201808878UA
- Authority
- SG
- Singapore
- Prior art keywords
- manchester
- international
- pct
- cancer research
- compounds
- Prior art date
Links
- 150000002391 heterocyclic compounds Chemical class 0.000 title abstract 2
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 102000020233 phosphotransferase Human genes 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 230000006870 function Effects 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000008520 organization Effects 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- 102220240796 rs553605556 Human genes 0.000 abstract 1
- 238000001890 transfection Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
-
- 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
Abstract
INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property -, Organization 11111111011110111010101111101011111011101011111111111110111011111111101111011111 International Bureau 0.. .... ..Yjd (10) International Publication Number (43) International Publication Date ..... ...,/ WO 2017/178844 Al 19 October 2017(19.10.2017) WIPO I PCT (51) International Patent Classification: (72) Inventors: JORDAN, Allan; Cancer Research UK CO7D 495/04 (2006.01) A61K 31/4985 (2006.01) Manchester Institute, The University of Manchester, A61K 31/519 (2006.01) A61P 35/00 (2006.01) Wilmslow Road, Manchester Greater Manchester M20 A61K 31/437 (2006.01) C07D 487/04 (2006.01) 4BX (GB). NEWTON, Rebecca; Cancer Research UK C07D 471/04 (2006.01) Manchester Institute, The University of Manchester, Wilmslow Road, Manchester Greater Manchester M20 (21) International Application Number: 4BX (GB). PCT/GB2017/051076 (22) (74) International Filing Date: Agent: HGF LIMITED; 4th Floor Merchant Exchange, 17-19 Whitworth Street West, Manchester Greater 18 April 2017 (18.04.2017) Manchester Ml 5WG (GB). (25) Filing Language: English (81) Designated States (unless otherwise indicated, for every (26) Publication Language: English kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (30) Priority Data: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, 1606631.8 15 April 2016 (15.04.2016) GB DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, 1619277.5 14 November 2016 (14.11.2016) GB HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KH, KN, (71) Applicant: CANCER RESEARCH TECHNOLOGY KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, LIMITED [GB/GB]; Angel Building, 407 St John Street, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, — London Greater London EC1V 4AD (GB). 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, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. — _ (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, [Continued on next page] _ = = HETEROCYCLIC COMPOUNDS AS RET KINASE INHIBITORS (54) Title: (57) : The present invention relates to compounds — , X2 R3 of Formula I that function as inhibitors of RET (rearranged \" **.............,./... X 1 - ., a , 1 during transfection) kinase enzyme activity: wherein HET, bonds a, b, c and d, X i , X 2 , , , X 3 X 4 R 2 , and R are each as 3 = _ _ b: defined herein. The present invention also relates to pro - = — 1 cesses for the preparation of these compounds, to pharma- _ X3 ceutical compositions comprising them, and to their use in the treatment of proliferative disorders, such as cancer, as = well as other diseases or conditions in which RET kinase X4 activity is implicated. \ d = % R2 HET ,—, . 4 7r 7r GC GC IN ,—, Formula I IN ,—, © ei O WO 2017/178844 Al MIDEDIMOMOIDEIR01013010MHEIMEMEHOIMIE TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, Declarations under Rule 4.17: TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HR, HU, IE, IS, IT, LT, of inventorship (Rule 4.17w)) LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, Published: SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG). GA, — with international search report (Art. 21(3))
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB201606631 | 2016-04-15 | ||
GB201619277 | 2016-11-14 | ||
PCT/GB2017/051076 WO2017178844A1 (en) | 2016-04-15 | 2017-04-18 | Heterocyclic compounds as ret kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
SG11201808878UA true SG11201808878UA (en) | 2018-11-29 |
Family
ID=58633035
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201808878UA SG11201808878UA (en) | 2016-04-15 | 2017-04-18 | Heterocyclic compounds as ret kinase inhibitors |
SG10201911665UA SG10201911665UA (en) | 2016-04-15 | 2017-04-18 | Heterocyclic compounds as ret kinase inhibitors |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10201911665UA SG10201911665UA (en) | 2016-04-15 | 2017-04-18 | Heterocyclic compounds as ret kinase inhibitors |
Country Status (23)
Country | Link |
---|---|
US (3) | US10954241B2 (en) |
EP (2) | EP3442980B1 (en) |
JP (3) | JP6943876B2 (en) |
KR (2) | KR102390578B1 (en) |
CN (2) | CN115650985A (en) |
AU (3) | AU2017250448C1 (en) |
BR (2) | BR112018071097B1 (en) |
CA (1) | CA3020778A1 (en) |
CY (1) | CY1124478T1 (en) |
DK (1) | DK3442980T3 (en) |
ES (1) | ES2886587T3 (en) |
HR (1) | HRP20211362T1 (en) |
HU (1) | HUE056135T2 (en) |
IL (3) | IL297192A (en) |
LT (1) | LT3442980T (en) |
MX (2) | MX2018012609A (en) |
PL (1) | PL3442980T3 (en) |
PT (1) | PT3442980T (en) |
RS (1) | RS62322B1 (en) |
RU (1) | RU2742115C2 (en) |
SG (2) | SG11201808878UA (en) |
SI (1) | SI3442980T1 (en) |
WO (1) | WO2017178844A1 (en) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HUE035337T2 (en) | 2010-05-20 | 2018-05-02 | Array Biopharma Inc | Macrocyclic compounds as TRK kinase inhibitors |
TN2018000027A1 (en) | 2015-07-16 | 2019-07-08 | Array Biopharma Inc | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
TWI757256B (en) | 2015-11-02 | 2022-03-11 | 美商纜圖藥品公司 | Inhibitors of ret |
JP6943876B2 (en) | 2016-04-15 | 2021-10-06 | キャンサー・リサーチ・テクノロジー・リミテッドCancer Research Technology Limited | Heterocyclic compounds as RET kinase inhibitors |
RS63609B1 (en) | 2016-04-15 | 2022-10-31 | Cancer Research Tech Ltd | Heterocyclic compounds as ret kinase inhibitors |
JOP20190077A1 (en) | 2016-10-10 | 2019-04-09 | Array Biopharma Inc | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
TWI704148B (en) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
EP3571203B1 (en) | 2017-01-18 | 2023-06-07 | Array BioPharma Inc. | Substituted pyrazolo[1,5-a]pyrazine compounds as ret kinase inhibitors |
WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
JOP20190213A1 (en) | 2017-03-16 | 2019-09-16 | Array Biopharma Inc | Macrocyclic compounds as ros1 kinase inhibitors |
GB201705971D0 (en) | 2017-04-13 | 2017-05-31 | Cancer Res Tech Ltd | Inhibitor compounds |
TWI791053B (en) | 2017-10-10 | 2023-02-01 | 美商亞雷生物製藥股份有限公司 | Crystalline forms of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile and pharmaceutical composition thereof |
TWI812649B (en) | 2017-10-10 | 2023-08-21 | 美商絡速藥業公司 | Formulations of 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile |
JOP20180094A1 (en) | 2017-10-18 | 2019-04-18 | Hk Inno N Corp | Heterocyclic compound as a protein kinase inhibito |
WO2019143977A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
US11524963B2 (en) | 2018-01-18 | 2022-12-13 | Array Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidines as RET kinase inhibitors |
WO2019143994A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors |
SI3773589T1 (en) | 2018-04-03 | 2024-03-29 | Blueprint Medicines Corporation | Ret inhibitor for use in treating cancer having a ret alteration |
SG11202008162WA (en) | 2018-04-05 | 2020-09-29 | Merck Patent Gmbh | Heteroaryl compounds as type ii irak inhibitors and uses hereof |
WO2020055672A1 (en) | 2018-09-10 | 2020-03-19 | Array Biopharma Inc. | Fused heterocyclic compounds as ret kinase inhibitors |
FI3860998T3 (en) | 2018-10-05 | 2024-03-27 | Annapurna Bio Inc | Compounds and compositions for treating conditions associated with apj receptor activity |
EP3950685A4 (en) * | 2019-04-03 | 2022-12-14 | Guangzhou Baiyunshan Pharmaceutical Holdings Co., Ltd. Baiyunshan Pharmaceutical General Factory | Pyrazolopyridine compound as ret inhibitor and application thereof |
CN115210226B (en) * | 2020-02-20 | 2024-01-09 | 广州白云山医药集团股份有限公司白云山制药总厂 | Quinoline compounds |
CN113214294A (en) * | 2020-06-10 | 2021-08-06 | 深圳铂立健医药有限公司 | Tricyclic compound, pharmaceutical composition and application thereof |
MX2023003995A (en) | 2020-10-05 | 2023-06-12 | Enliven Inc | 5- and 6-azaindole compounds for inhibition of bcr-abl tyrosine kinases. |
TW202241419A (en) * | 2020-12-22 | 2022-11-01 | 美商基利科學股份有限公司 | 6-substituted indole compounds |
EP4267559A1 (en) * | 2020-12-22 | 2023-11-01 | Gilead Sciences, Inc. | Substituted indole compounds |
IL307203A (en) | 2021-04-16 | 2023-11-01 | Gilead Sciences Inc | Thienopyrrole compounds |
CN113248518B (en) * | 2021-06-21 | 2022-03-25 | 山东大学 | Pyrimidine piperazine derivative and preparation method and application thereof |
WO2023064843A1 (en) | 2021-10-15 | 2023-04-20 | Stemline Therapeutics, Inc. | Inhibitors of mutant ret kinases for use in treating cancer |
Family Cites Families (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0322779A3 (en) | 1987-12-29 | 1991-05-08 | Yoshitomi Pharmaceutical Industries, Ltd. | Benzolactam compounds and pharmaceutical uses thereof |
US5480883A (en) | 1991-05-10 | 1996-01-02 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
EP1140938B1 (en) * | 1999-01-11 | 2003-08-27 | Princeton University | High affinity inhibitors for target validation and uses thereof |
US7119200B2 (en) | 2002-09-04 | 2006-10-10 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
US7429596B2 (en) | 2003-06-20 | 2008-09-30 | The Regents Of The University Of California | 1H-pyrrolo [2,3-D] pyrimidine derivatives and methods of use thereof |
JP2008520744A (en) | 2004-11-19 | 2008-06-19 | ザ・レジェンツ・オブ・ザ・ユニバーシティ・オブ・カリフォルニア | Anti-inflammatory pyrazolopyrimidine |
WO2006092430A1 (en) | 2005-03-03 | 2006-09-08 | Universität des Saarlandes | Selective inhibitors of human corticosteroid synthases |
DK1951724T3 (en) * | 2005-11-17 | 2011-08-15 | Osi Pharmaceuticals Llc | Merged bicyclic mTOR inhibitors |
AR057960A1 (en) | 2005-12-02 | 2007-12-26 | Osi Pharm Inc | BICYCLE PROTEIN QUINASE INHIBITORS |
US7772231B2 (en) | 2005-12-29 | 2010-08-10 | Abbott Laboratories | Substituted pyrazolo[3,4-d]pyrimidines as protein kinase inhibitors |
GB0610242D0 (en) | 2006-05-23 | 2006-07-05 | Novartis Ag | Organic compounds |
JP2008063278A (en) | 2006-09-07 | 2008-03-21 | Fujifilm Finechemicals Co Ltd | Method for producing 1-pyridin-4-yl-indole |
NZ601278A (en) | 2006-09-22 | 2013-09-27 | Pharmacyclics Inc | Inhibitors of Bruton's tyrosine kinase |
US20090274698A1 (en) * | 2007-07-06 | 2009-11-05 | Shripad Bhagwat | Combination anti-cancer therapy |
KR101653842B1 (en) | 2008-01-04 | 2016-09-02 | 인텔리카인, 엘엘씨 | Certain chemical entities, compositions and methods |
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
CA2730106A1 (en) * | 2008-07-08 | 2010-01-14 | Intellikine, Inc. | Kinase inhibitors and methods of use |
US20110224223A1 (en) * | 2008-07-08 | 2011-09-15 | The Regents Of The University Of California, A California Corporation | MTOR Modulators and Uses Thereof |
US8703778B2 (en) | 2008-09-26 | 2014-04-22 | Intellikine Llc | Heterocyclic kinase inhibitors |
US20110269779A1 (en) | 2008-11-18 | 2011-11-03 | Intellikine, Inc. | Methods and compositions for treatment of ophthalmic conditions |
KR101061599B1 (en) * | 2008-12-05 | 2011-09-02 | 한국과학기술연구원 | Novel indazole derivatives that are protein kinase inhibitors for the treatment of abnormal cell growth diseases, pharmaceutically acceptable salts thereof, and pharmaceutical compositions containing the same as active ingredients |
LT2496567T (en) | 2009-11-05 | 2017-11-27 | Rhizen Pharmaceuticals S.A. | Novel benzopyran kinase modulators |
WO2011094628A1 (en) | 2010-01-28 | 2011-08-04 | University Of Washington | Compositions and methods for treating toxoplasmosis. cryptosporidiosis and other apicomplexan protozoan related diseases |
US9765037B2 (en) | 2010-01-28 | 2017-09-19 | University Of Washington Through Its Center For Commercialization | Compositions and methods for treating toxoplasmosis, cryptosporidiosis, and other apicomplexan protozoan related diseases |
WO2011153553A2 (en) | 2010-06-04 | 2011-12-08 | The Regents Of The University Of California | Methods and compositions for kinase inhibition |
WO2012006619A2 (en) | 2010-07-09 | 2012-01-12 | Northeastern University | ANTIPARASITIC AGENTS BASED ON mTOR INHIBITORS |
EP2678018A4 (en) | 2011-02-23 | 2015-09-30 | Intellikine Llc | Combination of kanase inhibitors and uses thereof |
US20140357651A1 (en) | 2011-05-04 | 2014-12-04 | Yi Liu | Combination pharmaceutical compositions and uses thereof |
WO2013023119A1 (en) | 2011-08-10 | 2013-02-14 | Novartis Pharma Ag | JAK P13K/mTOR COMBINATION THERAPY |
AU2012341028C1 (en) * | 2011-09-02 | 2017-10-19 | Mount Sinai School Of Medicine | Substituted pyrazolo[3,4-D]pyrimidines and uses thereof |
CN106994126A (en) | 2011-11-08 | 2017-08-01 | 因特利凯有限责任公司 | Use the therapeutic scheme of various medicaments |
CN104363914A (en) | 2011-11-23 | 2015-02-18 | 因特利凯有限责任公司 | Enhanced treatment regimens using mtor inhibitors |
US8501724B1 (en) | 2012-01-31 | 2013-08-06 | Pharmacyclics, Inc. | Purinone compounds as kinase inhibitors |
US8889730B2 (en) | 2012-04-10 | 2014-11-18 | Pfizer Inc. | Indole and indazole compounds that activate AMPK |
US9738610B2 (en) | 2012-09-24 | 2017-08-22 | Whitehead Institute For Biomedical Research | Indazole derivatives and uses thereof |
GB201217285D0 (en) | 2012-09-27 | 2012-11-14 | Univ Central Lancashire | Indole derivatives |
EP2968340A4 (en) | 2013-03-15 | 2016-08-10 | Intellikine Llc | Combination of kinase inhibitors and uses thereof |
WO2014153509A1 (en) | 2013-03-22 | 2014-09-25 | Millennium Pharmaceuticals, Inc. | Combination of catalytic mtorc 1/2 inhibitors and selective inhibitors of aurora a kinase |
CA2922058A1 (en) | 2013-10-18 | 2015-04-23 | Medivation Technologies, Inc. | Heterocyclic compounds and methods of use |
US20160272645A1 (en) | 2013-10-18 | 2016-09-22 | Medivation Technologies, Inc. | Heterocyclic Compounds and Methods of Use |
GB201321146D0 (en) * | 2013-11-29 | 2014-01-15 | Cancer Rec Tech Ltd | Quinazoline compounds |
CA2967125C (en) | 2014-11-14 | 2022-10-25 | Nerviano Medical Sciences S.R.L. | 6-amino-7-bicyclo-7-deaza-purine derivatives as protein kinase inhibitors |
CA2974702C (en) | 2015-01-26 | 2023-10-10 | University Of Washington | Compositions and methods for treating toxoplasmosis, cryptosporidiosis and other apicomplexan protozoan related diseases |
WO2017027883A1 (en) | 2015-08-13 | 2017-02-16 | San Diego State University Research Foundation | Atropisomerism for increased kinase inhibitor selectivity |
WO2017160717A2 (en) | 2016-03-15 | 2017-09-21 | Memorial Sloan Kettering Cancer Center | Method of treating diseases using kinase modulators |
RS63609B1 (en) * | 2016-04-15 | 2022-10-31 | Cancer Research Tech Ltd | Heterocyclic compounds as ret kinase inhibitors |
JP6943876B2 (en) | 2016-04-15 | 2021-10-06 | キャンサー・リサーチ・テクノロジー・リミテッドCancer Research Technology Limited | Heterocyclic compounds as RET kinase inhibitors |
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2017
- 2017-04-18 JP JP2018554114A patent/JP6943876B2/en active Active
- 2017-04-18 WO PCT/GB2017/051076 patent/WO2017178844A1/en active Application Filing
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