CL2017002660A1 - Derivados de pirazol útiles como inhibidores de proteína activadora de 5-lipoxigenasa (flap) - Google Patents

Derivados de pirazol útiles como inhibidores de proteína activadora de 5-lipoxigenasa (flap)

Info

Publication number
CL2017002660A1
CL2017002660A1 CL2017002660A CL2017002660A CL2017002660A1 CL 2017002660 A1 CL2017002660 A1 CL 2017002660A1 CL 2017002660 A CL2017002660 A CL 2017002660A CL 2017002660 A CL2017002660 A CL 2017002660A CL 2017002660 A1 CL2017002660 A1 CL 2017002660A1
Authority
CL
Chile
Prior art keywords
flap
inhibitors
pyrazole derivatives
derivatives useful
activator protein
Prior art date
Application number
CL2017002660A
Other languages
English (en)
Spanish (es)
Inventor
Johan Olof Broddefalk
Hans Fredrik Emtenäs
Kenneth Lars Granberg
Malin Anita Lemurell
Daniel Tor Pettersen
Alleyn Thomas Plowright
Lars Johan Andreas Ulander
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of CL2017002660A1 publication Critical patent/CL2017002660A1/es

Links

Classifications

    • 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
    • C07D403/12—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 chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/38—Nitrogen atoms
    • C07D231/40—Acylated on said nitrogen atom
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A61K31/4155—1,2-Diazoles non 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
    • A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
    • C07D231/46—Oxygen atom in position 3 or 5 and nitrogen atom in position 4
    • C07D231/50—Acylated on said nitrogen atom
    • 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
    • C07D413/12—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 chain containing hetero atoms as chain links
    • 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
    • C07D417/12—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 chain containing hetero atoms as chain links
    • 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
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Vascular Medicine (AREA)
  • Pulmonology (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
CL2017002660A 2015-05-04 2017-10-19 Derivados de pirazol útiles como inhibidores de proteína activadora de 5-lipoxigenasa (flap) CL2017002660A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562156424P 2015-05-04 2015-05-04

Publications (1)

Publication Number Publication Date
CL2017002660A1 true CL2017002660A1 (es) 2018-04-13

Family

ID=55910253

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2017002660A CL2017002660A1 (es) 2015-05-04 2017-10-19 Derivados de pirazol útiles como inhibidores de proteína activadora de 5-lipoxigenasa (flap)

Country Status (38)

Country Link
US (6) US10183947B2 (enExample)
EP (2) EP3670499B1 (enExample)
JP (1) JP6564062B2 (enExample)
KR (1) KR102623474B1 (enExample)
CN (1) CN107646036B (enExample)
AR (1) AR104512A1 (enExample)
AU (1) AU2016258874B2 (enExample)
BR (1) BR112017022757B1 (enExample)
CA (1) CA2983668C (enExample)
CL (1) CL2017002660A1 (enExample)
CO (1) CO2017011506A2 (enExample)
CR (1) CR20170513A (enExample)
CY (2) CY1122689T1 (enExample)
DK (2) DK3670499T3 (enExample)
DO (1) DOP2017000244A (enExample)
EA (1) EA032221B1 (enExample)
ES (2) ES2902139T3 (enExample)
GT (1) GT201700220A (enExample)
HR (2) HRP20211993T1 (enExample)
HU (2) HUE047445T2 (enExample)
IL (1) IL255069B (enExample)
LT (1) LT3670499T (enExample)
ME (1) ME03663B (enExample)
MX (1) MX372755B (enExample)
MY (1) MY186647A (enExample)
PE (1) PE20180247A1 (enExample)
PH (1) PH12017502112B1 (enExample)
PL (2) PL3292105T3 (enExample)
PT (2) PT3670499T (enExample)
RS (2) RS59671B1 (enExample)
SG (1) SG11201708558RA (enExample)
SI (2) SI3670499T1 (enExample)
SM (2) SMT202100722T1 (enExample)
SV (1) SV2017005549A (enExample)
TN (1) TN2017000458A1 (enExample)
TW (1) TWI718146B (enExample)
WO (1) WO2016177703A1 (enExample)
ZA (1) ZA201708189B (enExample)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA032221B1 (ru) 2015-05-04 2019-04-30 Астразенека Аб Производные пиразола, пригодные в качестве ингибиторов белка, активирующего 5-липоксигеназу (flap)
CN109890385B (zh) * 2016-10-28 2022-08-02 阿斯利康(瑞典)有限公司 (1r,2r)-2-[4-(3-甲基-1h-吡唑-5-基)苯甲酰基]-n-(4-氧代-4,5,6,7-四氢吡唑并[1,5-a]吡嗪-3-基)环己烷甲酰胺的结晶形式
GB201905721D0 (en) 2019-04-24 2019-06-05 Univ Dundee Compounds
CN110169969B (zh) * 2019-06-28 2022-05-27 南京医科大学 Mk571在制备预防和治疗心脏病药物中应用
CN111084775A (zh) * 2020-02-17 2020-05-01 牡丹江医学院 一种用于治疗癫痫的药物组合物
CN111419800B (zh) * 2020-04-23 2021-03-19 温州医科大学附属第二医院、温州医科大学附属育英儿童医院 用于治疗红斑狼疮的药物制剂及其制备方法
CN111643498B (zh) * 2020-07-20 2021-05-07 黑龙江中医药大学 一种治疗肾结石的药物组合物及其用途
CN111714499B (zh) * 2020-07-27 2021-05-11 黑龙江中医药大学 一种用于治疗多囊卵巢综合征的药物组合物

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AP9400632A0 (en) 1993-04-29 1995-10-07 Zeneca Ltd Ether derivatives.
US5773422A (en) 1996-01-29 1998-06-30 Komer; Gene Avermectin formulation
EP1670804A2 (en) * 2003-09-10 2006-06-21 GPC Biotech AG Heterobicyclic compounds as pharmaceutically active agents
GB2431927B (en) * 2005-11-04 2010-03-17 Amira Pharmaceuticals Inc 5-Lipoxygenase-activating protein (FLAP) inhibitors
TW200815351A (en) * 2006-05-02 2008-04-01 Astrazeneca Ab Novel compounds
WO2008097930A1 (en) * 2007-02-05 2008-08-14 Amira Pharmaceuticals, Inc. Reverse indoles as 5-lipoxygenase-activating protein (flap) inhibitors
GB0702456D0 (en) * 2007-02-08 2007-03-21 Astrazeneca Ab New combination
JP2010524944A (ja) * 2007-04-20 2010-07-22 シェーリング コーポレイション テトラヒドロピリド[4,3−d]ピリミジノン誘導体およびそれらの使用方法
BRPI0811204A8 (pt) * 2007-05-10 2015-09-22 Bristol Myers Squibb Co Tetra-hidroibenzo-1,4-diazepinas substituídas por arila e heteroarila e uso das mesmas para bloquear a recaptação de norepinefrina, dopamina e serotonina
EP2207547A4 (en) * 2007-10-05 2010-11-17 Amira Pharmaceuticals Inc PROTEIN INHIBITORS THAT ACTIVATE 5-LIPOXYGENASE
EA032221B1 (ru) * 2015-05-04 2019-04-30 Астразенека Аб Производные пиразола, пригодные в качестве ингибиторов белка, активирующего 5-липоксигеназу (flap)

Also Published As

Publication number Publication date
SMT202100722T1 (it) 2022-01-10
EP3292105A1 (en) 2018-03-14
CN107646036B (zh) 2020-05-19
CR20170513A (es) 2018-02-13
US20240317767A1 (en) 2024-09-26
CY1125179T1 (el) 2023-03-24
PT3292105T (pt) 2019-12-13
MY186647A (en) 2021-08-03
PH12017502112B1 (en) 2021-07-02
EA201792341A1 (ru) 2018-05-31
SI3292105T1 (sl) 2020-01-31
LT3670499T (lt) 2021-12-27
PL3670499T3 (pl) 2022-02-14
CN107646036A (zh) 2018-01-30
IL255069B (en) 2019-12-31
JP6564062B2 (ja) 2019-08-21
EP3292105B1 (en) 2019-10-02
US20230219967A1 (en) 2023-07-13
PT3670499T (pt) 2021-12-24
AU2016258874A1 (en) 2017-12-14
DK3670499T3 (da) 2022-01-03
HUE056875T2 (hu) 2022-03-28
EP3670499B1 (en) 2021-09-29
US12024523B2 (en) 2024-07-02
CA2983668A1 (en) 2016-11-10
JP2018514535A (ja) 2018-06-07
KR20180002784A (ko) 2018-01-08
TW201713625A (zh) 2017-04-16
NZ737672A (en) 2020-11-27
CO2017011506A2 (es) 2018-01-31
DOP2017000244A (es) 2017-11-15
HK1245255A1 (en) 2018-08-24
HRP20192172T1 (hr) 2020-02-21
PL3292105T3 (pl) 2020-04-30
EP3670499A1 (en) 2020-06-24
TN2017000458A1 (en) 2019-04-12
HRP20211993T1 (hr) 2022-04-01
KR102623474B1 (ko) 2024-01-09
MX372755B (es) 2020-06-29
MX2017013571A (es) 2018-02-26
ES2760466T3 (es) 2020-05-14
US20210355127A1 (en) 2021-11-18
BR112017022757A2 (pt) 2018-07-17
US10508119B2 (en) 2019-12-17
RS59671B1 (sr) 2020-01-31
ME03663B (me) 2020-07-20
US11001589B2 (en) 2021-05-11
US20180237439A1 (en) 2018-08-23
SG11201708558RA (en) 2017-11-29
BR112017022757B1 (pt) 2023-02-23
PH12017502112A1 (en) 2018-05-07
SI3670499T1 (sl) 2022-02-28
US11691978B2 (en) 2023-07-04
GT201700220A (es) 2018-12-19
SV2017005549A (es) 2018-03-12
ZA201708189B (en) 2018-11-28
SMT201900691T1 (it) 2020-01-14
IL255069A0 (en) 2017-12-31
RS62729B1 (sr) 2022-01-31
HUE047445T2 (hu) 2020-04-28
AU2016258874B2 (en) 2020-04-30
DK3292105T3 (da) 2019-12-09
CA2983668C (en) 2023-06-27
US10183947B2 (en) 2019-01-22
US20200157113A1 (en) 2020-05-21
TWI718146B (zh) 2021-02-11
US20190084991A1 (en) 2019-03-21
PE20180247A1 (es) 2018-02-02
ES2902139T3 (es) 2022-03-25
EA032221B1 (ru) 2019-04-30
CY1122689T1 (el) 2021-03-12
WO2016177703A1 (en) 2016-11-10
AR104512A1 (es) 2017-07-26

Similar Documents

Publication Publication Date Title
CO2017011506A2 (es) Derivados de pirazol útiles como inhibidores de proteína activadora de 5-lipoxigenasa (flap)
CL2017002650A1 (es) Compuestos novedosos
CL2018003681A1 (es) Derivados de ácido borónico y usos terapéuticos de los mismos
DOP2019000005A (es) 3-metil pirazinas 2,5-disustituidas y 3-metil pirazinas 2,5,6-trisustituidas como inhibidores alostéricos de shp2
DOP2017000151A (es) Derivados de quinazolina utilizados para tratar el vih
BR112016018555A8 (pt) Ciclopropilaminas como inibidores de lsd1, seu uso, composição farmacêutica que os compreende e método de inibição de lsd1
CO2018004857A2 (es) Derivados de dihidroimidazopirazinona usados en el tratamiento del cáncer
UA117958C2 (uk) Похідні хіноксаліну, корисні як модулятори кінази fgfr
BR112017003312A2 (pt) compostos de indazol como inibidores de fgfr quinase, preparação e uso dos mesmos
MX2016008131A (es) Compuestos heterociclos biciclicos y sus usos en terapia.
CO6670585A2 (es) Promotores de apotosis n-acilsufonamidas
MX2019012847A (es) Compuestos de c5-anilinoquinazolina y su uso en el tratamiento del cancer.
DOP2014000036A (es) Compuestos de piridazinona y su uso como inhibidores daao
BR112014009006B8 (pt) Compostos heterocíclicos e métodos de uso dos mesmos
BR112016001645A8 (pt) derivados de oxoquinazolinil-butanamida, seu uso, medicamentos e kit
CR20180374A (es) Compuestos heterocíclicos como inmunomoduladores
CL2013003056A1 (es) Compuestos derivados de (fenil o piridin)-etinil-(piridin o pirimidin) sustituido; composición farmacéutica que los comprende; proceso de preparación de esto; y su uso en el tratamiento de la esquizofrenia o enfermedades cognitivas.
BR112017009012A2 (pt) derivados de anel benzo de seis membros como inibidor de dpp-4 e seu uso
BR112016008799A8 (pt) derivados de pirazolopirimidona ou pirrolotriazona, seus usos, seus processos para sua preparação e seus intermediários, e composição farmacêutica
DOP2019000221A (es) Derivados de pirazol como inhibidores de bromodominio
MX2016005437A (es) Derivados de n-(1-hidroxi-3-(pirrolidinil)propan-2-il)pirrolidin-3 -carboxamida como inhibidores de glucosilceramida sintasa.
ECSP18056196A (es) Derivados de indano
BR112017021114A8 (pt) Compostos heterocíclicos como inibidores de lsd1
CU20100172A7 (es) Derivados heterocíclicos de urea y métodos de uso de los mismos-211