HRP20231467T1 - Spojevi - Google Patents

Spojevi Download PDF

Info

Publication number
HRP20231467T1
HRP20231467T1 HRP20231467TT HRP20231467T HRP20231467T1 HR P20231467 T1 HRP20231467 T1 HR P20231467T1 HR P20231467T T HRP20231467T T HR P20231467TT HR P20231467 T HRP20231467 T HR P20231467T HR P20231467 T1 HRP20231467 T1 HR P20231467T1
Authority
HR
Croatia
Prior art keywords
substituted
compound
salt
hydroxy
phenyl
Prior art date
Application number
HRP20231467TT
Other languages
English (en)
Inventor
Paul Anthony Stupple
Helen Rachel LAGIAKOS
Benjamin Joseph MORROW
Richard Charles FOITZIK
Catherine Fae HEMLEY
Michelle Ang CAMERINO
Ylva Elisabet Bergman BOZIKIS
Scott Raymond WALKER
Original Assignee
Ctxt Pty Ltd
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 Ctxt Pty Ltd filed Critical Ctxt Pty Ltd
Publication of HRP20231467T1 publication Critical patent/HRP20231467T1/hr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/20Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/42Oxazoles
    • A61K31/423Oxazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/4245Oxadiazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/10Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)

Claims (14)

1. Spoj formule (I): [image] , ili njegova farmaceutski prihvatljiva sol, naznačen time što: R1, R2, R3 i R4 se neovisno bira između: (i) H; (ii) C1-3 alkila, koji može biti supstituiran s: hidroksi, C1-2 alkoksi, NH2, fenilom, C5-6 heteroarilom, C1-4 alkil-karbamoilom, ili acilamido; (iii) C1-3 alkoksi, koji može biti supstituiran s C3-6 cikloalkilom, ili s jednom ili više fluornih skupina; (iv) C3-6 cikloalkil; (v) halogena; (vi) CORC, gdje se RC bira između NRN1RN2, gdje se RN1 i RN2 neovisno bira između H i metila; (vii) cijano, NH2, ili NO2; i (viii) fenila ili C5-6 heteroarila, koji može biti supstituiran s metilom, hidroksi ili metoksi; Ar je fenil, koji može biti supstituiran s jednom ili više skupina koje se bira između: (i) C1-4 alkila, koji može biti supstituiran s hidroksi, C1-2 alkoksi, NH2, C1-4 alkil-karbamoilom, ili s jednom ili više fluornih skupina; (ii) C3-6 cikloalkila; (iii) hidroksi; cijano; NRN3RN4, gdje se RN3 i RN4 neovisno bira između H i metila; ili acilamido; (iv) halogena; (v) C1-3 alkoksi, koji može biti supstituiran s hidroksi, C(O)NH2, C3-6 cikloalkilom, fenilom, C5-6 heteroarilom, ili s jednom ili više fluornih skupina; (vi) fenoksi, koji može biti supstituiran s fluorom; (vii) fenila ili C5-6 heteroarila; ili (viii) SF5 ili SO2CH3; i gdje najmanje jedan od R1, R2, R3 i R4 nije H.
2. Spoj, ili sol, u skladu s patentnim zahtjevom 1, naznačen time što je najmanje jedan od R1, R2, R3 i R4 C1-3 alkil, koji može biti supstituiran s: hidroksi, C1-2 alkoksi, NH2, fenilom, C5-6 heteroarilom, C1-4 alkil-karbamoilom, ili acilamido.
3. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 2, naznačen time što je najmanje jedan od R1, R2, R3 i R4 C1-3 alkoksi, koji može biti supstituiran s C3-6 cikloalkilom, ili jednom ili više fluornih skupina.
4. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 3, naznačen time što je najmanje jedan od R1, R2, R3 i R4: (a) C3-6 cikloalkil; (b) CORC, gdje se RC bira između NRN1RN2, gdje se RN1 i RN2 neovisno bira između H i metila; (c) cijano, NH2 ili NO2; ili (d) fenil ili C5-6 heteroaril, koji može biti supstituiran s metilom, hidroksi ili metoksi.
5. Spoj, ili sol, u skladu s patentnim zahtjevom 1, naznačen time što: (a) R4 je metoksi, R2 je CH2OCH3 ili CH2OCH2CH3, a R1 i R3 su H; (b) R4 je metoksi, R2 je fenil, koji može biti supstituiran s metilom ili metoksi, a R1 i R3 su H; (c) R4 je metoksi, R2 je C5-6 heteroaril, koji može biti supstituiran s metilom; (d) R4 je metoksi, a R1, R2 i R3 su H; (e) R4 je klor, R2 je C1-3 alkil ili brom, a R1 i R3 su H; ili (f) R3 je C1-3 alkil, a R1, R2 i R4 su H.
6. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time što je Ar supstituiran s C1-4 alkilom, koji može biti supstituiran s hidroksi, C1-2 alkoksi, NH2, C1-4 alkil-karbamoilom, ili jednom ili više fluornih skupina.
7. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time što je Ar supstituiran s C1-3 alkoksi, koji može biti supstituiran s hidroksi, C(O)NH2, C3-6 cikloalkilom, fenilom, C5-6 heteroarilom, ili jednom ili više fluornih skupina.
8. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time što je Ar supstituiran s: (a) C3-6 cikloalkilom; (b) hidroksi; (c) cijano; (d) NRN3RN4, gdje se RN3 i RN4 neovisno bira između H i metila; ili acilamido; (e) fenoksi, koji može biti supstituiran s fluorom; (f) fenilom ili C5-6 heteroarilom; ili (g) SF5 ili SO2CH3.
9. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 5, naznačen time što je Ar: (a) 5-etil-2-metoksifenil; (b) 5-CF3-2-metoksifenil; ili (c) 2,6-dimetoksifenil.
10. Farmaceutski pripravak, naznačen time što sadrži spoj u skladu s bilo kojim od patentnih zahtjeva 1 do 9, ili njegovu farmaceutski prihvatljivu sol, kao i farmaceutski prihvatljivo pomoćno sredstvo.
11. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 9, naznačen time što je namijenjen upotrebi u postupku terapije.
12. Spoj, ili sol, u skladu s bilo kojim od patentnih zahtjeva 1 do 9, naznačen time što je namijenjen upotrebi u liječenju raka.
13. Spoj, ili sol, namijenjen upotrebi u skladu s patentnim zahtjevom 12, naznačen time što se rak bira između leukemije, akutne limfocitne leukemije, akutne mijeloidne leukemije, kronične limfocitne leukemije, kronične mijeloidne leukemije, nehodgkinovske leukemije, Hodgkinove bolesti, raka prostate, raka pluća, melanoma, raka dojke, raka debelog crijeva i rektuma, raka debelog crijeva, karcinoma pločastih stanica i raka želuca.
14. Spoj, ili sol, namijenjen upotrebi u skladu s patentnim zahtjevom 12, naznačen time što se spoj primijenjuje istodobno ili uzastopno u odnosu na radioterapiju i/ili kemoterapiju.
HRP20231467TT 2018-06-20 2019-06-20 Spojevi HRP20231467T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1810092.5A GB201810092D0 (en) 2018-06-20 2018-06-20 Compounds
EP19734722.2A EP3810602B1 (en) 2018-06-20 2019-06-20 Compounds
PCT/EP2019/066337 WO2019243491A1 (en) 2018-06-20 2019-06-20 Compounds

Publications (1)

Publication Number Publication Date
HRP20231467T1 true HRP20231467T1 (hr) 2024-03-01

Family

ID=63042663

Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20231467TT HRP20231467T1 (hr) 2018-06-20 2019-06-20 Spojevi

Country Status (39)

Country Link
US (2) US20200039945A1 (hr)
EP (2) EP4335439A3 (hr)
JP (1) JP2021529738A (hr)
KR (1) KR20210022655A (hr)
CN (1) CN112334466A (hr)
AR (1) AR114972A1 (hr)
AU (1) AU2019289888A1 (hr)
BR (1) BR112020025869A2 (hr)
CA (1) CA3101238A1 (hr)
CL (1) CL2020003219A1 (hr)
CO (1) CO2020014586A2 (hr)
CR (1) CR20210032A (hr)
CU (1) CU20200096A7 (hr)
DK (1) DK3810602T3 (hr)
DO (1) DOP2020000249A (hr)
EA (1) EA202092451A1 (hr)
EC (1) ECSP20075270A (hr)
ES (1) ES2967983T3 (hr)
FI (1) FI3810602T3 (hr)
GB (1) GB201810092D0 (hr)
GE (1) GEP20227403B (hr)
HR (1) HRP20231467T1 (hr)
HU (1) HUE064744T2 (hr)
IL (1) IL279554A (hr)
LT (1) LT3810602T (hr)
MA (1) MA52948B1 (hr)
MD (1) MD3810602T2 (hr)
MX (1) MX2020012723A (hr)
NI (1) NI202000092A (hr)
PE (1) PE20210181A1 (hr)
PH (1) PH12020500673A1 (hr)
PL (1) PL3810602T3 (hr)
PT (1) PT3810602T (hr)
RS (1) RS64932B1 (hr)
SG (1) SG11202010450VA (hr)
SI (1) SI3810602T1 (hr)
TW (1) TWI826471B (hr)
UY (1) UY38270A (hr)
WO (1) WO2019243491A1 (hr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3471271A1 (en) 2017-10-16 2019-04-17 Acoustical Beauty Improved convolutions of digital signals using a bit requirement optimization of a target digital signal
LT3986890T (lt) * 2019-06-18 2023-12-11 Pfizer Inc. Benzizoksazolo sulfonamido dariniai
WO2020254989A1 (en) * 2019-06-19 2020-12-24 Pfizer Inc. Cycloalkyl and heterocycloalkyl benzisoxazole sulfonamide derivatives
EP3999490A4 (en) * 2019-07-12 2023-03-08 Canopy Growth Corporation CANNABINOID DERIVATIVES
JP2022019654A (ja) 2020-07-15 2022-01-27 ファイザー・インク がん処置のためのkat6阻害剤方法および組合せ
CN117881677A (zh) * 2021-05-21 2024-04-12 奥瑞基尼肿瘤有限公司 作为KAT6Aw抑制剂的稠合异噁唑基化合物
EP4368620A1 (en) * 2021-07-05 2024-05-15 Hangzhou Innogate Pharma Co., Ltd. Compound serving as kat6 inhibitor
CA3228411A1 (en) 2021-08-10 2023-02-16 Xiaomin Zhang Sulfonamide derivative, preparation method therefor and medical use thereof
CA3237830A1 (en) * 2021-11-16 2023-05-25 Insilico Medicine Ip Limited Lysine acetyltransferase 6a (kat6a) inhibitors and uses thereof
WO2023114710A1 (en) * 2021-12-13 2023-06-22 Aurigene Oncology Limited Fused benzoisoxazolyl compounds as kat6a inhibitors
TW202400593A (zh) 2022-03-28 2024-01-01 美商艾索司特瑞克斯公司 Myst家族離胺酸乙醯轉移酶之抑制劑
WO2023245150A1 (en) * 2022-06-16 2023-12-21 Prelude Therapeutics Incorporated Kat6 targeting compounds with ubiquitin ligase binding moiety
WO2024023703A1 (en) 2022-07-29 2024-02-01 Pfizer Inc. Dosing regimens comprising a kat6 inhibitor for the treatment of cancer

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
BR9707495A (pt) 1996-02-13 1999-07-27 Zeneca Ltd Derivado de quinazolina processo para a preparação do mesmo composição farmacêutica e processo para a produç o de um efeito antiangiogênico e/ou de redução de permeabilidade vascular em um animal de sangue quente
KR100489174B1 (ko) 1996-03-05 2005-09-30 제네카-파마 소시에떼아노님 4-아닐리노퀴나졸린유도체
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
US20020192228A1 (en) 1997-02-12 2002-12-19 Samir M. Hanash Protein markers for lung cancer and use thereof
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
PL199802B1 (pl) 1999-02-10 2008-10-31 Astrazeneca Ab Pochodne chinazoliny, sposoby ich wytwarzania, ich kompozycje farmaceutyczne i ich zastosowania
EP1676845B1 (en) 1999-11-05 2008-06-11 AstraZeneca AB New quinazoline derivatives
ES2290117T3 (es) 2000-02-15 2008-02-16 Sugen, Inc. Inhibidores de proteina quinasa 2-indolina sustituida con pirrol.
IL152682A0 (en) 2000-05-31 2003-06-24 Astrazeneca Ab Indole derivatives with vascular damaging activity
UA73993C2 (uk) 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
US20050277627A1 (en) 2000-07-07 2005-12-15 Arnould Jean C Colchinol derivatives as vascular damaging agents
KR20030022264A (ko) 2000-07-07 2003-03-15 앤지오젠 파마슈티칼스 리미티드 신생 혈관 형성 억제제인 콜치놀 유도체
GEP20135992B (en) * 2009-01-12 2013-12-25 Icagen Inc Sulfonamide derivatives
WO2014144545A2 (en) * 2013-03-15 2014-09-18 Genentech, Inc. Substituted benzoxazoles and methods of use thereof
KR102458990B1 (ko) * 2014-04-23 2022-10-25 미쓰비시 타나베 파마 코퍼레이션 신규한 바이시클릭 또는 트리시클릭 헤테로시클릭 화합물
GB201510019D0 (en) 2015-06-09 2015-07-22 Cancer Therapeutics Crc Pty Ltd Compounds
EP3548480A1 (en) * 2016-11-29 2019-10-09 Epizyme, Inc. Compounds containing a sulfonic group as kat inhibitors
LT3986890T (lt) * 2019-06-18 2023-12-11 Pfizer Inc. Benzizoksazolo sulfonamido dariniai

Also Published As

Publication number Publication date
JP2021529738A (ja) 2021-11-04
DOP2020000249A (es) 2021-02-28
CA3101238A1 (en) 2019-12-26
EP4335439A2 (en) 2024-03-13
WO2019243491A1 (en) 2019-12-26
SG11202010450VA (en) 2021-01-28
MX2020012723A (es) 2021-05-14
TWI826471B (zh) 2023-12-21
CR20210032A (es) 2021-02-11
CU20200096A7 (es) 2021-08-06
ECSP20075270A (es) 2021-02-26
GEP20227403B (en) 2022-08-10
NI202000092A (es) 2021-03-23
AR114972A1 (es) 2020-11-11
CO2020014586A2 (es) 2021-03-08
US20220153710A1 (en) 2022-05-19
HUE064744T2 (hu) 2024-04-28
CN112334466A (zh) 2021-02-05
EP3810602A1 (en) 2021-04-28
BR112020025869A2 (pt) 2021-03-23
EP3810602B1 (en) 2023-11-01
US20200039945A1 (en) 2020-02-06
UY38270A (es) 2020-01-31
PE20210181A1 (es) 2021-01-29
IL279554A (en) 2021-01-31
KR20210022655A (ko) 2021-03-03
MD3810602T2 (ro) 2024-03-31
FI3810602T3 (fi) 2023-12-21
MA52948B1 (fr) 2024-02-29
GB201810092D0 (en) 2018-08-08
RS64932B1 (sr) 2023-12-29
EP4335439A3 (en) 2024-05-15
TW202016103A (zh) 2020-05-01
EA202092451A1 (ru) 2021-03-16
DK3810602T3 (da) 2023-12-11
ES2967983T3 (es) 2024-05-06
PL3810602T3 (pl) 2024-03-04
CL2020003219A1 (es) 2021-06-11
LT3810602T (lt) 2024-01-25
PH12020500673A1 (en) 2021-05-31
PT3810602T (pt) 2024-01-03
AU2019289888A1 (en) 2020-11-12
SI3810602T1 (sl) 2024-02-29
MA52948A (fr) 2021-04-28

Similar Documents

Publication Publication Date Title
HRP20231467T1 (hr) Spojevi
WO2008041053A3 (en) Inhibitors of vegf receptor and hgf receptor signaling
CO6190620A2 (es) Triazoles biciclicos como moduladores de la proteina cinasa
HRP20191482T1 (hr) 18f-označeni psma ciljani pet reagensi
RS52862B (en) IMIDASO [1,2-A] Pyridine Compounds as Tyrosine Kinase Receptor Inhibitors
AR121600A1 (es) Compuestos de oxoisoindolina sustituidos
AR115885A1 (es) Compuestos derivados de 1h-pirazolo[4,3-d]pirimidina como agonistas del receptor 7 tipo toll (tlr7) y su uso en combinación con un agente de inmunoterapia anticancerígeno
AR109958A1 (es) Lactamas bicíclicas de piridona y sus métodos de uso
AR048377A1 (es) Benzoimidazol-, benzotriazol- y benzoimidazolona - o- glucosidos sustituidos
RU2019116512A (ru) Ингибиторы magl
TW200612954A (en) Anti-angiogenesis methods
AR117544A1 (es) Heterocíclicos inhibidores de mat2a y métodos de uso para el tratamiento del cáncer
RS54183B1 (en) PIRAZOLE DERIVATIVES
JP2020500178A5 (hr)
AR074409A1 (es) Derivados de arilciclohexileteres de 5,6-dihidro-4h-2,3,5,10-b-tetraaza-benzo[e]azuleno, composiciones farmaceuticas que los contienen, proceso de preparacion y uso de los mismos en disfunciones sexuales y trastornos del snc, entre otras patologias.
RU2019115059A (ru) Модуляторы ror-гамма
RS54337B1 (en) RECEPTORA TRPM8 ANTAGONISTS
RS54248B1 (en) NEW UNITS AS LISTS OF HISTAMINE H3 RECEPTORS
SE9904673D0 (sv) Novel compounds
AR046311A1 (es) Derivados de 1,2,4 tiadiazoles. composiciones farmaceuticas.
AR073008A1 (es) Compuestos de 2- aminopirimidina como potentes inhibidores de hsp-90
JP2019522048A5 (hr)
NO20064882L (no) Kjemisk prosess
SE0101769D0 (sv) Novel compounds
AR118244A1 (es) Compuestos de pirazolil pirimidinilamina como inhibidores de cdk2