AR114998A1 - Compuestos de benzamida - Google Patents
Compuestos de benzamidaInfo
- Publication number
- AR114998A1 AR114998A1 ARP190100053A ARP190100053A AR114998A1 AR 114998 A1 AR114998 A1 AR 114998A1 AR P190100053 A ARP190100053 A AR P190100053A AR P190100053 A ARP190100053 A AR P190100053A AR 114998 A1 AR114998 A1 AR 114998A1
- Authority
- AR
- Argentina
- Prior art keywords
- unsubstituted
- substituted
- group
- alkyl
- haloalkyl
- Prior art date
Links
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical class NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 title 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 101100439664 Arabidopsis thaliana CHR8 gene Proteins 0.000 abstract 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 1
- 101100490437 Mus musculus Acvrl1 gene Proteins 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000005265 dialkylamine group Chemical group 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- -1 hydroxy, amino Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
Classifications
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/535—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
- A61K31/5355—Non-condensed oxazines 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
- A61K31/535—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
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D207/12—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/112—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/155—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic 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
- C07D413/12—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
- 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
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Virology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pyrrole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
- Pyridine Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Cephalosporin Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto de la fórmula (1), o una sal farmacéuticamente aceptable de este, que tiene la estructura mostrada a continuación, en donde: R¹ se selecciona del grupo que consiste en hidrógeno, halógeno, un alquilo C₁₋₆ sustituido o no sustituido, un haloalquilo C₁₋₆ sustituido o no sustituido, un cicloalquilo C₃₋₆ sustituido o no sustituido, un alcoxi C₁₋₆ sustituido o no sustituido, una monoalquilamina C₁₋₆ no sustituida y una dialquilamina C₁₋₆ no sustituida, con la condición de que R¹ no sea -CH₂F, -CHF₂ o -CF₃; cada R² se selecciona independientemente del grupo que consiste en halógeno, un alquilo C₁₋₆ sustituido o no sustituido, un haloalquilo C₁₋₆ sustituido o no sustituido y un cicloalquilo C₃₋₆ sustituido o no sustituido; o cuando m es 2 ó 3, cada R² se selecciona independientemente del grupo que consiste en halógeno, un alquilo C₁₋₆ sustituido o no sustituido, un haloalquilo C₁₋₆ sustituido o no sustituido y un cicloalquilo C₃₋₆ sustituido o no sustituido, o dos grupos R² tomados junto con el(los) átomo(s) a los que están unidos forman un cicloalquilo C₃₋₆ sustituido o no sustituido o un heterociclilo de 3 a 6 miembros sustituido o no sustituido; R³ se selecciona del grupo que consiste en, X-R³A, un compuesto de fórmula (2) y un compuesto de fórmula (3); R³A es un heteroarilo de 5 a 10 miembros sustituido o no sustituido; R⁴ se selecciona del grupo que consiste en NO₂, S(O)R⁶, SO₂R⁶, halógeno, ciano y un haloalquilo C₁₋₆ no sustituido; R⁵ se selecciona del grupo que consiste en -X¹-(AIk¹)ₙ-R⁷ y -X²(CHR⁸)-(AIk²)ₚ-X³-R⁹; Alk¹ y Alk² se seleccionan independientemente de un alquileno C₁₋₄ no sustituido y un alquileno C₁₋₄ sustituido con 1, 2 ó 3 sustituyentes seleccionados independientemente de fluoro, cloro, un alquilo C₁₋₃ no sustituido y un haloalquilo C₁₋₆ no sustituido; R⁶ se selecciona del grupo que consiste en un alquilo C₁₋₆ sustituido o no sustituido, un haloalquilo C₁₋₆ sustituido o no sustituido y un cicloalquilo C₃₋₆ sustituido o no sustituido; R⁷ se selecciona de un alcoxi C₁₋₆ sustituido o no sustituido, un cicloalquilo C₃₋₁₀ sustituido o no sustituido, un heterociclilo de 3 a 10 miembros sustituido o no sustituido, hidroxi, amino, un grupo amina monosustituido sustituido o no sustituido, un grupo amina disustituido sustituido o no sustituido, un N-carbamilo sustituido o no sustituido, un C-amido sustituido o no sustituido y un N-amido sustituido o no sustituido; R⁸ se selecciona de un heterociclil(alquilo C₁₋₆) de 3 a 10 miembros sustituido o no sustituido, una di-alquilamina C₁₋₆-(alquilo C₁₋₆) sustituida o no sustituida y una mono-alquilamina C₁₋₆-(alquilo C₁₋₆) sustituida o no sustituida; R⁹ se selecciona de un heteroarilo de 5 a 10 miembros sustituido o no sustituido y un arilo C₆₋₁₀ sustituido o no sustituido; m es 0, 1, 2 ó 3; n y p se seleccionan independientemente de 0 y 1; X¹ y X² son -NH-; y X y X³ se seleccionan independientemente del grupo que consiste en -O-, -S- y -NH-.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862615857P | 2018-01-10 | 2018-01-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR114998A1 true AR114998A1 (es) | 2020-11-18 |
Family
ID=67218673
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP190100050A AR114948A1 (es) | 2018-01-10 | 2019-01-10 | Compuestos de benzamida |
ARP190100051A AR114949A1 (es) | 2018-01-10 | 2019-01-10 | Compuesto de benzamida |
ARP190100052A AR114950A1 (es) | 2018-01-10 | 2019-01-10 | Compuestos de benzamida |
ARP190100053A AR114998A1 (es) | 2018-01-10 | 2019-01-10 | Compuestos de benzamida |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP190100050A AR114948A1 (es) | 2018-01-10 | 2019-01-10 | Compuestos de benzamida |
ARP190100051A AR114949A1 (es) | 2018-01-10 | 2019-01-10 | Compuesto de benzamida |
ARP190100052A AR114950A1 (es) | 2018-01-10 | 2019-01-10 | Compuestos de benzamida |
Country Status (15)
Country | Link |
---|---|
US (6) | US11344546B2 (es) |
EP (3) | EP3737681A4 (es) |
JP (4) | JP2021510165A (es) |
KR (3) | KR20200108302A (es) |
CN (5) | CN111801320A (es) |
AR (4) | AR114948A1 (es) |
AU (4) | AU2019207608B2 (es) |
BR (3) | BR112020014160A2 (es) |
CA (3) | CA3087263A1 (es) |
IL (3) | IL275763A (es) |
MX (4) | MX2020007014A (es) |
RU (2) | RU2020120928A (es) |
SG (3) | SG11202005784YA (es) |
TW (5) | TW201934538A (es) |
WO (4) | WO2019139899A1 (es) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3565815B1 (en) | 2017-01-07 | 2024-03-13 | Fochon Pharmaceuticals, Ltd. | Compounds as bcl-2-selective apoptosis-inducing agents |
RS63603B1 (sr) | 2017-04-18 | 2022-10-31 | Shanghai Fochon Pharmaceutical Co Ltd | Sredstva za indukciju apoptoze |
JP2021510165A (ja) | 2018-01-10 | 2021-04-15 | リキュリウム アイピー ホールディングス リミテッド ライアビリティー カンパニー | ベンズアミド化合物 |
AR119379A1 (es) * | 2019-07-10 | 2021-12-15 | Recurium Ip Holdings Llc | Inhibidores de la proteína bcl-2 |
KR20220034038A (ko) * | 2019-07-10 | 2022-03-17 | 리커리엄 아이피 홀딩스, 엘엘씨 | Bcl-2 억제제의 나노입자 제형 |
KR20230127372A (ko) | 2019-12-06 | 2023-08-31 | 록쏘 온콜로지, 인코포레이티드 | 브루톤 티로신 키나제 억제제의 투여 |
US20230065577A1 (en) * | 2019-12-20 | 2023-03-02 | Recurium Ip Holdings, Llc | Combinations |
AU2020407068A1 (en) * | 2019-12-20 | 2022-07-14 | Recurium Ip Holdings, Llc | Combinations |
BR112022012283A2 (pt) * | 2019-12-20 | 2022-08-30 | Recurium Ip Holdings Llc | Combinações |
CN115427042A (zh) * | 2019-12-20 | 2022-12-02 | 里科瑞尔姆Ip控股有限责任公司 | 组合 |
WO2021167987A1 (en) * | 2020-02-21 | 2021-08-26 | Recurium Ip Holdings, Llc | Difluoromethyl iodo compounds and methods |
US20230167105A1 (en) * | 2020-04-28 | 2023-06-01 | Recurium Ip Holdings, Llc | Bcl-2 protein inhibitors |
KR20230007360A (ko) * | 2020-05-07 | 2023-01-12 | 리커리엄 아이피 홀딩스, 엘엘씨 | 복합제 |
EP4138837A4 (en) * | 2020-05-19 | 2024-05-22 | Recurium IP Holdings, LLC | TREATMENT OF AMYLOIDOSIS |
WO2022082180A1 (en) * | 2020-10-16 | 2022-04-21 | Recurium Ip Holdings, Llc | Combinations of bcl-2 inhibitors with chemotherapeutic agents |
WO2022133446A1 (en) * | 2020-12-16 | 2022-06-23 | Recurium Ip Holdings, Llc | Combinations |
CN113143930B (zh) * | 2021-04-08 | 2023-05-30 | 深圳湾实验室 | 化合物在制备SARS-Cov-2 E蛋白抑制剂中的用途 |
CN113816889B (zh) * | 2021-10-11 | 2023-08-22 | 中国药科大学 | 一类4-磺酰亚胺-1H-吡咯类Mcl-1抑制剂及其抗肿瘤医药用途 |
Family Cites Families (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003096461A (ja) | 2001-09-25 | 2003-04-03 | Fuji Photo Film Co Ltd | 液晶組成物およびそれを用いた液晶素子 |
DE10217814A1 (de) | 2002-04-22 | 2003-11-13 | Ibfb Pharma Gmbh | Neue tricyclische Mercaptane, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
US8614318B2 (en) | 2003-11-13 | 2013-12-24 | Abbvie Inc. | Apoptosis promoters |
US7767684B2 (en) | 2003-11-13 | 2010-08-03 | Abbott Laboratories | Apoptosis promoters |
WO2005049593A2 (en) * | 2003-11-13 | 2005-06-02 | Abbott Laboratories | N-acylsulfonamide apoptosis promoters |
US7642260B2 (en) | 2003-11-13 | 2010-01-05 | Abbott Laboratories, Inc. | Apoptosis promoters |
WO2005079803A1 (en) | 2004-02-13 | 2005-09-01 | Pfizer Products, Inc. | Compounds for treatment of cardiovascular diseases |
JP4628140B2 (ja) | 2005-03-03 | 2011-02-09 | 富士フイルム株式会社 | セルロースアシレートフィルム、偏光板および液晶表示装置 |
JP5132550B2 (ja) | 2005-05-12 | 2013-01-30 | アボット・ラボラトリーズ | アポトーシス促進剤 |
US8624027B2 (en) | 2005-05-12 | 2014-01-07 | Abbvie Inc. | Combination therapy for treating cancer and diagnostic assays for use therein |
WO2008008374A2 (en) | 2006-07-14 | 2008-01-17 | Chemocentryx, Inc. | Ccr2 inhibitors and methods of use thereof |
US7842681B2 (en) | 2006-09-05 | 2010-11-30 | Abbott Laboratories | Treatment of myeoproliferative diseases |
WO2008033747A2 (en) | 2006-09-11 | 2008-03-20 | Curis, Inc. | Multi-functional small molecules as anti-proliferative agents |
ES2423029T3 (es) | 2006-11-15 | 2013-09-17 | Genentech, Inc. | Compuestos de arilsulfonamida |
US20080182845A1 (en) | 2006-11-16 | 2008-07-31 | Abbott Laboratories | Method of preventing or treating organ, hematopoietic stem cell or bone marrow transplant rejection |
CA2671399A1 (en) | 2006-12-04 | 2008-06-12 | Abbott Laboratories | Companion diagnostic assays for cancer therapy |
WO2009036051A1 (en) | 2007-09-10 | 2009-03-19 | Curis, Inc. | Bcl-2 inhibitors containing a zinc binding moiety |
US20100160322A1 (en) | 2008-12-04 | 2010-06-24 | Abbott Laboratories | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
US8557983B2 (en) | 2008-12-04 | 2013-10-15 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
UA108193C2 (uk) | 2008-12-04 | 2015-04-10 | Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань | |
KR101692705B1 (ko) * | 2008-12-05 | 2017-01-04 | 애브비 인코포레이티드 | 암 및 면역 질환의 치료를 위한 Bcl2선택적 아폽토시스-유도제로서의 설폰아미드 유도체 |
US8563735B2 (en) * | 2008-12-05 | 2013-10-22 | Abbvie Inc. | Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases |
CN102282128B (zh) | 2009-01-19 | 2015-06-17 | Abbvie公司 | 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂 |
US8546399B2 (en) | 2009-05-26 | 2013-10-01 | Abbvie Inc. | Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases |
US9034875B2 (en) | 2009-05-26 | 2015-05-19 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
KR20190086591A (ko) | 2009-05-26 | 2019-07-22 | 애브비 아일랜드 언리미티드 컴퍼니 | 암,면역 질환 및 자가면역 질환의 치료를 위한 아폽토시스-유도제 |
TWI532484B (zh) | 2009-06-08 | 2016-05-11 | 艾伯維有限公司 | 包含凋亡促進劑之固態分散劑 |
CN102802609A (zh) | 2009-06-18 | 2012-11-28 | 雅培制药有限公司 | 稳定的纳米颗粒药物悬浮液 |
WO2010148422A1 (en) | 2009-06-25 | 2010-12-29 | Walter And Eliza Hall Institute Of Medical Research | Compounds and methods for treating parasitic infestations |
IN2012DN01325A (es) | 2009-08-20 | 2015-06-05 | Karus Therapeutics Ltd | |
CN101798292A (zh) | 2010-03-29 | 2010-08-11 | 无锡好芳德药业有限公司 | ABT-263衍生的新型Bcl-2蛋白抑制剂的制备 |
TWI520960B (zh) | 2010-05-26 | 2016-02-11 | 艾伯維有限公司 | 用於治療癌症及免疫及自體免疫疾病之細胞凋亡誘導劑 |
TWI535712B (zh) | 2010-08-06 | 2016-06-01 | 阿斯特捷利康公司 | 化合物 |
WO2012058392A1 (en) | 2010-10-29 | 2012-05-03 | Abbott Laboratories | Solid dispersions containing an apoptosis-inducing agent |
UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
EP2638007A2 (en) | 2010-11-11 | 2013-09-18 | Redx Pharma Limited | Drug derivatives |
CN105664164B (zh) | 2010-11-23 | 2020-05-05 | 艾伯维巴哈马有限公司 | 使用选择性的bcl-2抑制剂的治疗方法 |
US8691184B2 (en) | 2011-01-25 | 2014-04-08 | The Regents Of The University Of Michigan | Bcl-2/Bcl-xL inhibitors and therapeutic methods using the same |
WO2013185202A1 (en) | 2012-06-14 | 2013-12-19 | Beta Pharma Canada Inc | Apoptosis inducers |
ES2819232T3 (es) | 2013-01-16 | 2021-04-15 | Univ Michigan Regents | Inhibidores de Bcl-2/Bcl-xL y su uso en el tratamiento de cáncer |
RS57569B1 (sr) | 2013-03-13 | 2018-10-31 | Abbvie Inc | Postupci za pripremanje agensa koji uzrokuje apoptozu |
US20140275082A1 (en) | 2013-03-14 | 2014-09-18 | Abbvie Inc. | Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases |
US9168257B2 (en) | 2013-05-22 | 2015-10-27 | Children's Hospital Medical Center | Combination therapy for MDS |
NZ714357A (en) | 2013-05-24 | 2018-12-21 | Mark Barry Hampton | Polycyclic ether compounds and their use in anticancer therapy |
CA2917767C (en) | 2013-07-12 | 2022-05-03 | Helmholtz-Zentrum Fur Infektionsforschung Gmbh | Cystobactamides |
WO2015085238A1 (en) | 2013-12-05 | 2015-06-11 | The Regents Of The University Of California, A California Corporation | Inhibitors of lpxc |
CN105012318B (zh) | 2014-04-17 | 2020-02-11 | 沈华浩 | 磺酰胺类化合物在气道慢性炎症性疾病中的应用 |
CN104131034B (zh) | 2014-06-19 | 2017-04-05 | 中山大学 | 一种嵌合载体及其制备方法和应用 |
WO2016025652A1 (en) | 2014-08-13 | 2016-02-18 | Celgene Avilomics Research, Inc. | Combinations of an erk inhibitor and a bcl-2 pathway modulator and related methods |
CN106999451B (zh) * | 2014-09-17 | 2021-04-02 | 里科瑞尔姆Ip控股有限责任公司 | 双环化合物 |
UY36391A (es) * | 2014-11-05 | 2016-06-01 | Flexus Biosciences Inc | Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido1), sus métodos de síntesis y composiciones farmacèuticas que las contienen |
US9694084B2 (en) | 2014-12-23 | 2017-07-04 | Dana-Farber Cancer Institute, Inc. | Methods to induce targeted protein degradation through bifunctional molecules |
TW201639573A (zh) | 2015-02-03 | 2016-11-16 | 吉李德科學股份有限公司 | 有關治療癌症之合併治療 |
CN108025006A (zh) | 2015-02-06 | 2018-05-11 | 尤尼蒂生物技术公司 | 化合物及在治疗衰老相关病症中的用途 |
WO2016131100A1 (en) | 2015-02-18 | 2016-08-25 | The Walter And Eliza Hall Institute Of Medical Research | Methods of treating infectious diseases |
BR112017022553A2 (pt) * | 2015-04-20 | 2018-07-17 | Mayo Found Medical Education & Res | métodos e materiais para matar células infectadas por hiv |
MA44645B1 (fr) | 2015-05-26 | 2019-09-30 | Hoffmann La Roche | Traitement combiné d'un anticorps anti-cd20 avec un inhibiteur de bcl-2 et un inhibiteur de mdm2 |
GB201513481D0 (en) | 2015-07-30 | 2015-09-16 | Univ Manchester | Inhibitor compounds |
US10683308B2 (en) | 2015-09-11 | 2020-06-16 | Navitor Pharmaceuticals, Inc. | Rapamycin analogs and uses thereof |
CN106608895A (zh) | 2015-10-21 | 2017-05-03 | 苏州国匡医药科技有限公司 | 一类具有糖环结构的bcl-2选择性抑制剂及其用途 |
WO2017101851A1 (en) | 2015-12-18 | 2017-06-22 | Unity Biotechnology, Inc. | Acylsulfonamide derivatives for treating senescence-associated diseases and disorders |
CN106957315B (zh) | 2016-01-08 | 2019-08-13 | 中国人民解放军第二军医大学 | N-取代苯磺酰基-氮杂吲哚氧基苯甲酰胺类化合物及其制备药物的用途 |
EP3402485A1 (en) | 2016-01-11 | 2018-11-21 | Merrimack Pharmaceuticals, Inc. | Inhibiting b-cell lymphoma 2 (bcl-2) and related proteins |
WO2017132474A1 (en) | 2016-01-30 | 2017-08-03 | Newave Pharmaceutical Inc. | Bcl-2 inhibitors |
CA3018991A1 (en) | 2016-04-21 | 2017-10-26 | Bioventures, Llc | Compounds that induce degradation of anti-apoptotic bcl-2 family proteins and the uses thereof |
AU2017277949B2 (en) | 2016-06-09 | 2023-01-12 | Blinkbio, Inc. | Silanol based therapeutic payloads |
EP3318276A1 (en) | 2016-11-04 | 2018-05-09 | Janssen Biotech, Inc. | Combinations of a telomerase inhibitor and a bcl-2 inhibitor for the treatment of hematological cancers |
CN106565706B (zh) | 2016-10-27 | 2018-05-01 | 广东东阳光药业有限公司 | 一种磺酰胺衍生物及其在药学中的应用 |
CN106749233B (zh) | 2016-11-24 | 2020-04-21 | 中山大学 | 一类磺酰胺衍生物及其应用 |
EP3565815B1 (en) | 2017-01-07 | 2024-03-13 | Fochon Pharmaceuticals, Ltd. | Compounds as bcl-2-selective apoptosis-inducing agents |
WO2018146506A1 (en) | 2017-02-10 | 2018-08-16 | Universitat Politècnica De València | Therapeutic derivatives |
CN107089981A (zh) | 2017-04-24 | 2017-08-25 | 杭州科耀医药科技有限公司 | 一种BCL‑2抑制剂Venetoclax的合成方法 |
JP2021510165A (ja) | 2018-01-10 | 2021-04-15 | リキュリウム アイピー ホールディングス リミテッド ライアビリティー カンパニー | ベンズアミド化合物 |
US11420968B2 (en) | 2018-04-29 | 2022-08-23 | Beigene, Ltd. | Bcl-2 inhibitors |
AU2019343044A1 (en) | 2018-09-18 | 2021-03-18 | Signalchem Lifesciences Corporation | Combination therapy for treating blood cancer |
-
2019
- 2019-01-08 JP JP2020538692A patent/JP2021510165A/ja active Pending
- 2019-01-08 RU RU2020120928A patent/RU2020120928A/ru unknown
- 2019-01-08 CN CN201980015896.1A patent/CN111801320A/zh active Pending
- 2019-01-08 JP JP2020538644A patent/JP2021510163A/ja active Pending
- 2019-01-08 BR BR112020014160-7A patent/BR112020014160A2/pt not_active Application Discontinuation
- 2019-01-08 WO PCT/US2019/012695 patent/WO2019139899A1/en unknown
- 2019-01-08 WO PCT/US2019/012719 patent/WO2019139907A1/en unknown
- 2019-01-08 EP EP19738858.0A patent/EP3737681A4/en not_active Withdrawn
- 2019-01-08 AU AU2019207608A patent/AU2019207608B2/en active Active
- 2019-01-08 AU AU2019207616A patent/AU2019207616A1/en not_active Abandoned
- 2019-01-08 CA CA3087263A patent/CA3087263A1/en active Pending
- 2019-01-08 CN CN201980015882.XA patent/CN111801327B/zh active Active
- 2019-01-08 US US16/957,862 patent/US11344546B2/en active Active
- 2019-01-08 BR BR112020014151-8A patent/BR112020014151A2/pt not_active Application Discontinuation
- 2019-01-08 CA CA3087262A patent/CA3087262A1/en active Pending
- 2019-01-08 MX MX2020007014A patent/MX2020007014A/es unknown
- 2019-01-08 EP EP19738922.4A patent/EP3737672A4/en not_active Withdrawn
- 2019-01-08 EP EP19738996.8A patent/EP3740487A4/en active Pending
- 2019-01-08 CA CA3087261A patent/CA3087261A1/en active Pending
- 2019-01-08 CN CN202410225032.5A patent/CN118084905A/zh active Pending
- 2019-01-08 BR BR112020014169-0A patent/BR112020014169A2/pt unknown
- 2019-01-08 RU RU2020120929A patent/RU2020120929A/ru unknown
- 2019-01-08 MX MX2020007392A patent/MX2020007392A/es unknown
- 2019-01-08 SG SG11202005784YA patent/SG11202005784YA/en unknown
- 2019-01-08 SG SG11202005785XA patent/SG11202005785XA/en unknown
- 2019-01-08 SG SG11202005985PA patent/SG11202005985PA/en unknown
- 2019-01-08 US US16/957,865 patent/US11590126B2/en active Active
- 2019-01-08 KR KR1020207022538A patent/KR20200108302A/ko not_active Application Discontinuation
- 2019-01-08 JP JP2020538691A patent/JP7355741B2/ja active Active
- 2019-01-08 WO PCT/US2019/012704 patent/WO2019139902A1/en unknown
- 2019-01-08 KR KR1020207022537A patent/KR20200108301A/ko unknown
- 2019-01-08 US US16/957,861 patent/US11318134B2/en active Active
- 2019-01-08 KR KR1020207022443A patent/KR20200108298A/ko unknown
- 2019-01-08 MX MX2020007388A patent/MX2020007388A/es unknown
- 2019-01-08 CN CN202410225030.6A patent/CN118084904A/zh active Pending
- 2019-01-08 AU AU2019207611A patent/AU2019207611A1/en not_active Abandoned
- 2019-01-08 CN CN201980015923.5A patent/CN111788203A/zh active Pending
- 2019-01-08 WO PCT/US2019/012699 patent/WO2019139900A1/en active Application Filing
- 2019-01-10 AR ARP190100050A patent/AR114948A1/es unknown
- 2019-01-10 TW TW108101046A patent/TW201934538A/zh unknown
- 2019-01-10 TW TW108101045A patent/TW201934550A/zh unknown
- 2019-01-10 AR ARP190100051A patent/AR114949A1/es unknown
- 2019-01-10 AR ARP190100052A patent/AR114950A1/es unknown
- 2019-01-10 TW TW113101066A patent/TW202417442A/zh unknown
- 2019-01-10 AR ARP190100053A patent/AR114998A1/es unknown
- 2019-01-10 TW TW108101047A patent/TW201930317A/zh unknown
- 2019-01-10 TW TW108101048A patent/TWI829664B/zh active
-
2020
- 2020-06-30 IL IL275763A patent/IL275763A/en unknown
- 2020-06-30 IL IL275762A patent/IL275762A/en unknown
- 2020-06-30 IL IL275761A patent/IL275761A/en unknown
- 2020-07-13 MX MX2023009185A patent/MX2023009185A/es unknown
-
2022
- 2022-03-28 US US17/656,726 patent/US11813259B2/en active Active
-
2023
- 2023-05-26 US US18/202,622 patent/US11813260B1/en active Active
- 2023-09-20 US US18/471,017 patent/US20240180899A1/en active Pending
- 2023-09-21 JP JP2023156385A patent/JP2024001052A/ja active Pending
-
2024
- 2024-06-06 AU AU2024203833A patent/AU2024203833A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR114998A1 (es) | Compuestos de benzamida | |
AR114254A1 (es) | Moduladores del regulador de conductancia transmembrana de fibrosis quística, composiciones farmacéuticas, métodos de tratamiento y proceso de preparación de los moduladores | |
AR112797A1 (es) | Inhibidores de kras g12c y métodos para utilizarlos | |
AR113964A1 (es) | Carbamoíl ciclohexil ácidos ligados a n de triazol como antagonistas de lpa | |
AR100033A1 (es) | Compuestos y composiciones para inhibir la actividad de shp2 | |
AR103990A1 (es) | Ureas cíclicas como inhibidoras de rock | |
AR109709A1 (es) | Inhibidores de la fosfatidilinositol 3-quinasa | |
AR098414A1 (es) | PIPERAZINAS DE PIRAZOLO SUSTITUIDO COMO INHIBIDORES DE CASEÍNA QUINASA 1 d/e | |
AR100808A1 (es) | Inhibidores de fosfatidilinositol 3-quinasa | |
AR107840A1 (es) | INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASA g | |
AR092349A1 (es) | Imidazotriazincarbonitrilos utiles como inhibidores de quinasa | |
AR095430A1 (es) | Compuestos de pirimidina y piridina y su uso como inhibidores de la actividad de fgfr | |
AR091981A1 (es) | Dihidropiridona p1 como inhibidores del factor xia | |
AR099228A1 (es) | Inhibidores macrocíclicos de fxia que tienen grupos heterocíclicos | |
AR091498A1 (es) | DERIVADOS DE 2,3-DIHIDRO-1H-IMIDAZO{1,2-a}PIRIMIDIN-5-ONA Y 1,2,3,4-TETRAHIDRO-PIRIMIDO{1,2-a}PIRIMIDIN-6-ONA QUE CONTIENEN UNA MORFOLINA SUSTITUIDA, SU PREPARACION Y SU UTILIZACION FARMACEUTICA | |
AR117398A1 (es) | Inhibidores de la señalización mediada por tirosina cinasa 2 | |
AR093579A1 (es) | Inhibidores de bmi-1 de pirimidina inversa sustituida | |
AR108387A1 (es) | Compuestos de tipo tetrahidropirimidodiazepina y dihidropiridodiazepina para tratar el dolor y afecciones relacionadas con el dolor | |
AR108185A1 (es) | Amidas terciarias y método para su uso | |
AR093758A1 (es) | Inhibidores de aril lactama quinasa | |
AR114369A1 (es) | Dinucleótidos cíclicos como agentes antineoplásicos | |
AR119379A1 (es) | Inhibidores de la proteína bcl-2 | |
AR123121A1 (es) | Compuestos de dihidropirimidinona o dihidrotriazinona fusionados con anillo saturado y su uso farmacéutico | |
AR120246A1 (es) | Aminas heteroaril-bifenilas para el tratamiento de las enfermedades por pd-l1 | |
AR119378A1 (es) | Formulación de nanopartículas del inhibidor de bcl-2 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |