UY38721A - INHIBIDORES DE MOLÉCULAS PEQUEÑAS DE QUINASA INDUCTORA DE NF-kB - Google Patents
INHIBIDORES DE MOLÉCULAS PEQUEÑAS DE QUINASA INDUCTORA DE NF-kBInfo
- Publication number
- UY38721A UY38721A UY0001038721A UY38721A UY38721A UY 38721 A UY38721 A UY 38721A UY 0001038721 A UY0001038721 A UY 0001038721A UY 38721 A UY38721 A UY 38721A UY 38721 A UY38721 A UY 38721A
- Authority
- UY
- Uruguay
- Prior art keywords
- inductive
- small molecule
- molecule inhibitors
- kinase small
- disorders
- Prior art date
Links
Classifications
-
- 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
-
- 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
- A61K31/4365—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 having sulfur as a ring hetero atom, e.g. ticlopidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- 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
- 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
- C07D401/10—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 carbon chain containing aromatic 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
- C07D403/10—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 linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Neurology (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La presente invención se relaciona con agentes farmacéuticos útiles para terapia y/o profilaxis en un mamífero, y en particular a los inhibidores de quinasa inductora de NF-kB (NIK - también conocidos como MAP3K14) útiles para tratar enfermedades tales como el cáncer (en particular malignidades de células B que incluyen leucemias, linfomas y mieloma), trastornos inflamatorios, trastornos autoinmunes y trastornos metabólicos que incluyen obesidad y diabetes.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201962855144P | 2019-05-31 | 2019-05-31 | |
US201962907833P | 2019-09-30 | 2019-09-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY38721A true UY38721A (es) | 2020-11-30 |
Family
ID=71108552
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY0001038721A UY38721A (es) | 2019-05-31 | 2020-05-29 | INHIBIDORES DE MOLÉCULAS PEQUEÑAS DE QUINASA INDUCTORA DE NF-kB |
Country Status (22)
Country | Link |
---|---|
US (3) | US11254673B2 (es) |
EP (1) | EP3976597B1 (es) |
JP (1) | JP7547387B2 (es) |
KR (1) | KR20220027871A (es) |
CN (1) | CN114222737B (es) |
AU (1) | AU2020282005A1 (es) |
BR (1) | BR112021023796A2 (es) |
CA (1) | CA3143350A1 (es) |
CL (1) | CL2021003142A1 (es) |
CO (1) | CO2021017838A2 (es) |
CR (1) | CR20210587A (es) |
DK (1) | DK3976597T3 (es) |
DO (1) | DOP2021000244A (es) |
EC (1) | ECSP21093623A (es) |
IL (1) | IL288387A (es) |
JO (1) | JOP20210318A1 (es) |
MA (1) | MA56038A (es) |
MX (1) | MX2021014679A (es) |
PE (1) | PE20220768A1 (es) |
SG (1) | SG11202112994WA (es) |
UY (1) | UY38721A (es) |
WO (1) | WO2020239999A1 (es) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020239999A1 (en) * | 2019-05-31 | 2020-12-03 | Janssen Pharmaceutica Nv | SMALL MOLECULE INHIBITORS OF NF-kB INDUCING KINASE |
MX2021014441A (es) | 2019-05-31 | 2022-01-06 | Ikena Oncology Inc | Inhibidores del dominio asociado mejorador de la transcripcion (tead) y usos de los mismos. |
WO2023217906A1 (en) * | 2022-05-11 | 2023-11-16 | Janssen Pharmaceutica Nv | Pyrrolidinone derivatives as inhibitors of nf kappa b inducing kinase |
WO2023217879A1 (en) * | 2022-05-11 | 2023-11-16 | Janssen Pharmaceutica Nv | Pyrrolidione derivatives as inhibitors of nf kappa b inducing kinase |
US20240279230A1 (en) | 2022-12-22 | 2024-08-22 | Boehringer Ingelheim International Gmbh | Crystalline forms of a her2 inhibitor |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9930616D0 (en) | 1999-12-24 | 2000-02-16 | Mathilda & Terence Kennedy Ins | Activation and inhibition of the immune system |
US7132428B2 (en) | 2003-07-03 | 2006-11-07 | Aventis Pharmaceuticals Inc. | Pyrazoloisoquinoline derivative as kinase inhibitors for the treatment of various disorders |
TW200605886A (en) * | 2004-08-03 | 2006-02-16 | Wyeth Corp | Indazoles useful in treating cardiovascular diseases |
KR101227228B1 (ko) | 2004-11-12 | 2013-01-28 | 스태츠 칩팩, 엘티디. | 와이어 본드 배선 |
AU2009263037B2 (en) | 2008-06-26 | 2011-10-06 | Amgen Inc. | Alkynyl alcohols as kinase inhibitors |
US20110183975A1 (en) | 2008-10-07 | 2011-07-28 | Yasuhiro Goto | Novel 6-azaindole aminopyrimidine derivatives having nik inhibitory activity |
AR085908A1 (es) | 2011-03-16 | 2013-11-06 | Hoffmann La Roche | DERIVADOS DE 3-BUTIN-2-OL Y DE CARBONITRILO CON ACTIVIDAD INHIBIDORA DE LA QUINASA INDUCTORA DE NF-kB (NIK) |
MX2014009624A (es) | 2012-02-17 | 2015-03-19 | Hoffmann La Roche | Compuestos triciclicos y metodos para el uso de los mismos. |
US8859553B2 (en) | 2012-07-30 | 2014-10-14 | Astar Biotech Llc | Protein kinase inhibitors |
TWI663166B (zh) | 2013-04-24 | 2019-06-21 | 健生藥品公司 | 新化合物 |
US20160096850A9 (en) * | 2013-08-22 | 2016-04-07 | Genentech, Inc. | Alkynyl alcohols and methods of use |
JP2016531127A (ja) | 2013-08-22 | 2016-10-06 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | アルキニルアルコール及び使用方法 |
TWI704146B (zh) | 2013-09-26 | 2020-09-11 | 比利時商健生藥品公司 | 用作NIK抑制劑之新的1-(4-嘧啶基)-1H-吡唑並[3,2-c]吡啶衍生物 |
TWI627173B (zh) | 2013-09-26 | 2018-06-21 | 比利時商健生藥品公司 | 作為NIK抑制劑的新穎3-(1H-吡唑-4-基)-1H-吡咯并[2,3-c]吡啶衍生物 |
CA2960336C (en) | 2014-10-23 | 2023-03-07 | Janssen Pharmaceutica Nv | Compounds as nik inhibitors |
ES2715104T3 (es) | 2014-10-23 | 2019-05-31 | Janssen Pharmaceutica Nv | Nuevos derivados de pirazolopirimidina como inhibidores de nik |
ES2704738T3 (es) | 2014-10-23 | 2019-03-19 | Janssen Pharmaceutica Nv | Nuevos derivados de tienopirimidina en calidad de inhibidores de nik |
CN107074818B (zh) | 2014-10-23 | 2020-04-17 | 詹森药业有限公司 | 作为nik抑制剂的吡唑衍生物 |
WO2016135163A1 (en) | 2015-02-25 | 2016-09-01 | F. Hoffmann-La Roche Ag | Alkynyl alcohols and methods of use |
LT3405196T (lt) | 2016-01-22 | 2020-02-25 | Janssen Pharmaceutica Nv | Naujieji pakeistieji cianoindolino dariniai kaip nik inhibitoriai |
KR20180098679A (ko) | 2016-01-22 | 2018-09-04 | 잔센파마슈티카엔.브이. | Nik 억제제로서의 신규 6원 헤테로방향족 치환된 시아노인돌린 유도체 |
WO2018002219A1 (en) | 2016-06-30 | 2018-01-04 | Janssen Pharmaceutica Nv | Cyanoindoline derivatives as nik inhibitors |
ES2805976T3 (es) | 2016-06-30 | 2021-02-16 | Janssen Pharmaceutica Nv | Derivados heteroaromáticos en calidad de inhibidores de NIK |
JP7138093B2 (ja) * | 2016-08-24 | 2022-09-15 | エフ.ホフマン-ラ ロシュ アーゲー | 2-アザビシクロ[3.1.0]ヘキサン-3-オン誘導体及び使用方法 |
WO2018037059A1 (en) | 2016-08-24 | 2018-03-01 | F. Hoffmann-La Roche Ag | 2-azabicyclo[3.1.0]hexan-3-one derivatives and methods of use |
EP3649127B1 (en) | 2017-07-06 | 2021-09-08 | Janssen Pharmaceutica NV | Substituted azaindoline derivatives as nik inhibitors |
CN109810110B (zh) | 2017-11-22 | 2023-01-24 | 中国科学院上海药物研究所 | 一种具有2-氨基嘧啶结构的化合物,其制备方法和用途 |
PE20230244A1 (es) | 2019-05-31 | 2023-02-07 | Sage Therapeutics Inc | Esteroides neuroactivos y composiciones de estos |
MX2021014441A (es) | 2019-05-31 | 2022-01-06 | Ikena Oncology Inc | Inhibidores del dominio asociado mejorador de la transcripcion (tead) y usos de los mismos. |
CA3142351A1 (en) | 2019-05-31 | 2020-12-03 | Ikena Oncology, Inc. | Tead inhibitors and uses thereof |
WO2020239999A1 (en) * | 2019-05-31 | 2020-12-03 | Janssen Pharmaceutica Nv | SMALL MOLECULE INHIBITORS OF NF-kB INDUCING KINASE |
MX2021014115A (es) | 2019-05-31 | 2021-12-10 | Chiesi Farm Spa | Derivados de aminoquinazolina como inhibidores del purinoreceptor 3 de p2x (p2x3). |
KR20220075382A (ko) | 2019-09-30 | 2022-06-08 | 인사이트 코포레이션 | 면역조절제로서의 피리도[3,2-d]피리미딘 화합물 |
-
2020
- 2020-05-29 WO PCT/EP2020/065024 patent/WO2020239999A1/en active Application Filing
- 2020-05-29 JO JOP/2021/0318A patent/JOP20210318A1/ar unknown
- 2020-05-29 AU AU2020282005A patent/AU2020282005A1/en active Pending
- 2020-05-29 BR BR112021023796A patent/BR112021023796A2/pt unknown
- 2020-05-29 EP EP20733688.4A patent/EP3976597B1/en active Active
- 2020-05-29 DK DK20733688.4T patent/DK3976597T3/da active
- 2020-05-29 US US16/887,889 patent/US11254673B2/en active Active
- 2020-05-29 KR KR1020217042635A patent/KR20220027871A/ko unknown
- 2020-05-29 SG SG11202112994WA patent/SG11202112994WA/en unknown
- 2020-05-29 JP JP2021570919A patent/JP7547387B2/ja active Active
- 2020-05-29 CR CR20210587A patent/CR20210587A/es unknown
- 2020-05-29 PE PE2021001987A patent/PE20220768A1/es unknown
- 2020-05-29 CN CN202080057418.XA patent/CN114222737B/zh active Active
- 2020-05-29 CA CA3143350A patent/CA3143350A1/en active Pending
- 2020-05-29 MA MA056038A patent/MA56038A/fr unknown
- 2020-05-29 UY UY0001038721A patent/UY38721A/es unknown
- 2020-05-29 MX MX2021014679A patent/MX2021014679A/es unknown
-
2021
- 2021-11-25 IL IL288387A patent/IL288387A/en unknown
- 2021-11-25 CL CL2021003142A patent/CL2021003142A1/es unknown
- 2021-11-26 DO DO2021000244A patent/DOP2021000244A/es unknown
- 2021-12-13 US US17/549,057 patent/US11827634B2/en active Active
- 2021-12-27 CO CONC2021/0017838A patent/CO2021017838A2/es unknown
- 2021-12-28 EC ECSENADI202193623A patent/ECSP21093623A/es unknown
-
2023
- 2023-09-27 US US18/475,499 patent/US20240199605A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
BR112021023796A2 (pt) | 2022-02-08 |
PE20220768A1 (es) | 2022-05-16 |
JOP20210318A1 (ar) | 2023-01-30 |
MA56038A (fr) | 2022-04-06 |
EP3976597A1 (en) | 2022-04-06 |
EP3976597B1 (en) | 2024-08-28 |
DK3976597T3 (da) | 2024-09-09 |
MX2021014679A (es) | 2022-04-06 |
US20230080834A1 (en) | 2023-03-16 |
US20240199605A1 (en) | 2024-06-20 |
SG11202112994WA (en) | 2021-12-30 |
CA3143350A1 (en) | 2020-12-03 |
CN114222737A (zh) | 2022-03-22 |
IL288387A (en) | 2022-01-01 |
DOP2021000244A (es) | 2022-04-18 |
CO2021017838A2 (es) | 2022-01-17 |
ECSP21093623A (es) | 2022-01-31 |
KR20220027871A (ko) | 2022-03-08 |
US11254673B2 (en) | 2022-02-22 |
CN114222737B (zh) | 2024-07-26 |
CL2021003142A1 (es) | 2022-08-19 |
US11827634B2 (en) | 2023-11-28 |
JP2022534302A (ja) | 2022-07-28 |
JP7547387B2 (ja) | 2024-09-09 |
US20210300918A1 (en) | 2021-09-30 |
WO2020239999A1 (en) | 2020-12-03 |
CR20210587A (es) | 2022-02-11 |
AU2020282005A1 (en) | 2021-12-23 |
TW202110842A (zh) | 2021-03-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UY38721A (es) | INHIBIDORES DE MOLÉCULAS PEQUEÑAS DE QUINASA INDUCTORA DE NF-kB | |
CO2020002588A2 (es) | Composiciones que comprenden un inhibidor de shp2 y metodos para tratar el cáncer | |
CO2020011908A2 (es) | Imidazopirimidinas y triazolopirimidinas como inhibidores de a2a/a2b | |
NI201900019A (es) | Inhibidores de procesos metabólicos celulares | |
GT201400089A (es) | Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a | |
DOP2019000005A (es) | 3-metil pirazinas 2,5-disustituidas y 3-metil pirazinas 2,5,6-trisustituidas como inhibidores alostéricos de shp2 | |
CO2018013293A2 (es) | Derivados de pirazolopirimidina como inhibidor de quinasa | |
BR112018077136A2 (pt) | composto, e, métodos para tratar um distúrbio associado com proliferação celular anormal e para reduzir o efeito de quimioterapia em células saudáveis. | |
CL2018000803A1 (es) | Composiciones y métodos para inhibir la expresión génica de lpa. | |
CO2017004525A2 (es) | Dihidropirrolopiridinas inhibidoras de ror-gamma | |
CL2020002840A1 (es) | Compuestos inhibidores de rip1 y métodos para preparar y usar los mismos | |
CR20190394A (es) | Compuestos de inhibidores de autotaxina | |
CL2016003301A1 (es) | Compuestos derivados del ácido amino-(piridin-4-carboxílico) sustituidos, inhibidores de la histona desmetilasa; composición farmacéutica, que los comprende, útiles en el tratamiento del cáncer, tales como el cáncer de próstata, mama, vejiga, pulmón y/o melanoma. | |
GT201300215A (es) | Inhibidores de glucosilceramida sintasa | |
BR112015021371A2 (pt) | uso de agonistas de receptor de formil peptídeo 2 para tratar doenças inflamatórias oculares | |
BR112017008045A2 (pt) | compostos como inibidores de nik | |
CL2016001409A1 (es) | Inhibidores de quinasa relacionada con la tropomiosina (trk). | |
ECSP20024210A (es) | Uso de inhibidores de p38 para reducir la expresión de dux4 | |
MX2015016100A (es) | Inhibidores de criopirina para prevenir y tratar la inflamacion. | |
ECSP20061378A (es) | COMPUESTOS DIÓLICOS DE AMINOPIRAZINA COMO INHIBIDORES DE PI3K-gamma | |
BR112017007704A2 (pt) | derivados de pirazolopirimidina como inibidores de nik | |
CO2019000753A2 (es) | Métodos para tratar el cáncer de próstata | |
CR20150496A (es) | Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a | |
UY36416A (es) | 1-[2-(aminometil)bencil]-2-tioxo-1,2,3,5-tetrahidro-4h-pirrolo[3,2-d]pirimidin-4-onas como inhibidores de la mieloperoxidasa | |
BR112022007376A2 (pt) | Terapias de combinação com venetoclax e inibidores de tim-3 |