CR20200231A - 1H-PIRROLO (2,3-C) PIRIDIN-7 (6H)-ONAS Y PIRAZOLO (3,4-C) PIRIDIN-7 (6H)-ONAS COMO INHIBIDORES DE PROTEINAS BET (Divisional 2016-0542) - Google Patents
1H-PIRROLO (2,3-C) PIRIDIN-7 (6H)-ONAS Y PIRAZOLO (3,4-C) PIRIDIN-7 (6H)-ONAS COMO INHIBIDORES DE PROTEINAS BET (Divisional 2016-0542)Info
- Publication number
- CR20200231A CR20200231A CR20200231A CR20200231A CR20200231A CR 20200231 A CR20200231 A CR 20200231A CR 20200231 A CR20200231 A CR 20200231A CR 20200231 A CR20200231 A CR 20200231A CR 20200231 A CR20200231 A CR 20200231A
- Authority
- CR
- Costa Rica
- Prior art keywords
- pyridin
- ones
- inhibitors
- pyrazolo
- pyrrolo
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 108091005625 BRD4 Proteins 0.000 abstract 1
- 108091052242 Bromo- and Extra-Terminal domain (BET) family Proteins 0.000 abstract 1
- 102100033641 Bromodomain-containing protein 2 Human genes 0.000 abstract 1
- 102100033642 Bromodomain-containing protein 3 Human genes 0.000 abstract 1
- 102100029895 Bromodomain-containing protein 4 Human genes 0.000 abstract 1
- 101000871850 Homo sapiens Bromodomain-containing protein 2 Proteins 0.000 abstract 1
- 101000871851 Homo sapiens Bromodomain-containing protein 3 Proteins 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- TUPZMLLDXCWVKH-UHFFFAOYSA-N pyrazolo[4,3-b]pyridin-3-one Chemical class C1=CN=C2C(=O)N=NC2=C1 TUPZMLLDXCWVKH-UHFFFAOYSA-N 0.000 abstract 1
- ORKUYZDMEWAUEZ-UHFFFAOYSA-N pyrrolo[3,2-b]pyridin-2-one Chemical class N1=CC=CC2=NC(=O)C=C21 ORKUYZDMEWAUEZ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- 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
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- 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
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
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- 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
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- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- A61K31/54—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 sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—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 sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
- A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
- A61K31/546—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine containing further heterocyclic rings, e.g. cephalothin
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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Abstract
La presente invención se relaciona con pirrolopiridinonas sustituidas y pirazolopiridinonas sustituidas que constituyen inhibidores de proteínas BET tales como BRD2, BRD3, BRD4 y BRD-t y son útiles en el tratamiento de las enfermedades como el cáncer.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201461983289P | 2014-04-23 | 2014-04-23 | |
PCT/US2015/027047 WO2015164480A1 (en) | 2014-04-23 | 2015-04-22 | 1H-PYRROLO[2,3-c]PYRIDIN-7(6H)-ONES AND PYRAZOLO[3,4-c]PYRIDIN-7(6H)-ONES AS INHIBITORS OF BET PROTEINS |
Publications (1)
Publication Number | Publication Date |
---|---|
CR20200231A true CR20200231A (es) | 2020-09-11 |
Family
ID=53055117
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CR20200231A CR20200231A (es) | 2014-04-23 | 2015-04-22 | 1H-PIRROLO (2,3-C) PIRIDIN-7 (6H)-ONAS Y PIRAZOLO (3,4-C) PIRIDIN-7 (6H)-ONAS COMO INHIBIDORES DE PROTEINAS BET (Divisional 2016-0542) |
CR20160542A CR20160542A (es) | 2014-04-23 | 2015-04-22 | 1 H-PIRROLO[2,3-c]PIRIDIN-7(6H)-ONAS YPIRAZOLO[3,4-c]PlRIDIN-7(6H)-ONAS COMO INHIBIDORES DE PROTEINAS BET |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CR20160542A CR20160542A (es) | 2014-04-23 | 2015-04-22 | 1 H-PIRROLO[2,3-c]PIRIDIN-7(6H)-ONAS YPIRAZOLO[3,4-c]PlRIDIN-7(6H)-ONAS COMO INHIBIDORES DE PROTEINAS BET |
Country Status (36)
Country | Link |
---|---|
US (7) | US9540368B2 (es) |
EP (3) | EP3134403B1 (es) |
JP (2) | JP6572237B2 (es) |
KR (3) | KR20240134245A (es) |
CN (1) | CN106414442B (es) |
AR (1) | AR100160A1 (es) |
AU (3) | AU2015249810B2 (es) |
BR (1) | BR112016024626B1 (es) |
CA (1) | CA2946731C (es) |
CL (1) | CL2016002681A1 (es) |
CR (2) | CR20200231A (es) |
CY (2) | CY1122948T1 (es) |
DK (2) | DK3134403T3 (es) |
EA (2) | EA039678B1 (es) |
EC (1) | ECSP16088983A (es) |
ES (2) | ES2784846T3 (es) |
FI (1) | FI3674302T3 (es) |
HR (2) | HRP20230340T1 (es) |
HU (2) | HUE061770T2 (es) |
IL (3) | IL248415B (es) |
LT (2) | LT3674302T (es) |
MA (1) | MA39985B1 (es) |
ME (1) | ME03763B (es) |
MX (2) | MX2016013851A (es) |
MY (1) | MY180775A (es) |
NZ (3) | NZ763737A (es) |
PE (1) | PE20170144A1 (es) |
PH (1) | PH12016502115A1 (es) |
PL (2) | PL3134403T3 (es) |
PT (2) | PT3674302T (es) |
RS (2) | RS64231B1 (es) |
SG (2) | SG10201809353TA (es) |
SI (2) | SI3674302T1 (es) |
TW (2) | TWI672301B (es) |
UA (1) | UA119870C2 (es) |
WO (1) | WO2015164480A1 (es) |
Families Citing this family (47)
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EP3581576B1 (en) | 2013-03-15 | 2022-01-26 | Incyte Holdings Corporation | Tricyclic heterocycles as bet protein inhibitors for use in the treatment of a proliferative disease in combination with a janus kinase inhibitor |
WO2015006193A1 (en) | 2013-07-08 | 2015-01-15 | Incyte Corporation | Tricyclic heterocycles as bet protein inhibitors |
WO2015081203A1 (en) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Bicyclic heterocycles as bet protein inhibitors |
US9315501B2 (en) | 2013-11-26 | 2016-04-19 | Incyte Corporation | Bicyclic heterocycles as BET protein inhibitors |
WO2015095492A1 (en) | 2013-12-19 | 2015-06-25 | Incyte Corporation | Tricyclic heterocycles as bet protein inhibitors |
CA2946731C (en) | 2014-04-23 | 2022-06-07 | Incyte Corporation | 1h-pyrrolo[2,3-c]pyridin-7(6h)-ones and pyrazolo[3,4-c]pyridin-7(6h)-ones as inhibitors of bet proteins |
EP3194406B8 (en) | 2014-09-15 | 2021-03-31 | Incyte Corporation | Tricyclic heterocycles for use as bet protein inhibitors |
WO2016077375A1 (en) | 2014-11-10 | 2016-05-19 | Genentech, Inc. | Bromodomain inhibitors and uses thereof |
MA40943A (fr) | 2014-11-10 | 2017-09-19 | Constellation Pharmaceuticals Inc | Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines |
MA40940A (fr) | 2014-11-10 | 2017-09-19 | Constellation Pharmaceuticals Inc | Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines |
CN107531692B (zh) | 2015-01-29 | 2020-12-25 | 基因泰克公司 | 治疗化合物及其用途 |
AR104259A1 (es) | 2015-04-15 | 2017-07-05 | Celgene Quanticel Res Inc | Inhibidores de bromodominio |
MX2018001751A (es) * | 2015-08-11 | 2018-08-01 | Neomed Inst | Dihidroquinolinonas aril-sustituidas, su preparacion y su uso como farmaceuticos. |
US10836742B2 (en) | 2015-08-11 | 2020-11-17 | Neomed Institute | N-substituted bicyclic lactams, their preparation and their use as pharmaceuticals |
MX2018001756A (es) | 2015-08-12 | 2018-09-06 | Neomed Inst | Benzimidazoles sustituidos, su preparacion y su uso como productos farmaceuticos. |
US10501459B2 (en) | 2015-10-21 | 2019-12-10 | Neomed Institute | Substituted imidazo[1,2-a]pyridines as bromodomain inhibitors |
WO2017075377A1 (en) | 2015-10-29 | 2017-05-04 | Incyte Corporation | Amorphous solid form of a bet protein inhibitor |
WO2017127930A1 (en) | 2016-01-28 | 2017-08-03 | Neomed Institute | Substituted [1,2,4]triazolo[4,3-a]pyridines, their preparation and their use as pharmaceuticals |
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