PE20231106A1 - Inhibidores de apol1 y metodos para usar los mismos - Google Patents
Inhibidores de apol1 y metodos para usar los mismosInfo
- Publication number
- PE20231106A1 PE20231106A1 PE2023000722A PE2023000722A PE20231106A1 PE 20231106 A1 PE20231106 A1 PE 20231106A1 PE 2023000722 A PE2023000722 A PE 2023000722A PE 2023000722 A PE2023000722 A PE 2023000722A PE 20231106 A1 PE20231106 A1 PE 20231106A1
- Authority
- PE
- Peru
- Prior art keywords
- apol1
- inhibitors
- methyltriazol
- piran
- spiro
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102100030762 Apolipoprotein L1 Human genes 0.000 title 1
- 101100323521 Homo sapiens APOL1 gene Proteins 0.000 title 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 102000018757 Apolipoprotein L1 Human genes 0.000 abstract 2
- 108010052469 Apolipoprotein L1 Proteins 0.000 abstract 2
- 201000005206 focal segmental glomerulosclerosis Diseases 0.000 abstract 2
- 231100000854 focal segmental glomerulosclerosis Toxicity 0.000 abstract 2
- 208000038001 non-diabetic kidney disease Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
Classifications
-
- 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
- C07D495/12—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 three hetero rings
- C07D495/20—Spiro-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
- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/538—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with carbocyclic ring systems
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
SE REFIERE A COMPUESTOS ESPIROHETEROCICLOS DE FORMULA (I) DONDE LOS RADICALES X1, X2, R1, R3a, R3b, R4, R5, k Y m SON TAL COMO SE DESCRIBEN EN EL PRESENTE DOCUMENTO. SON COMPUESTOS PREFERIDOS: (2'S,6'S,7S)-2-CLORO-2'-METIL-6'-(1-METILTRIAZOL-4-IL)ESPIRO[4,5-DIHIDROTIENO[2,3-C]PIRAN-7,4'-PIPERIDINA]; (2'S,6'S,7S)-2'-METIL-6'-(1-METILTRIAZOL-4-IL)-2-(TRIFLUOROMETIL)ESPIRO[4,5-DIHIDROTIENO[2,3-C]PIRAN-7,4'-PIPERIDINA]; [(2'S,6'S,7S)-2'-METIL-6'-(1-METILTRIAZOL-4-IL)-2-(TRIFLUOROMETIL)ESPIRO[4,5-DIHIDROTIENO[2,3-C]PIRAN-7,4'-PIPERIDIN]-3-IL]METANOL; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA APOLIPOPROTEINA L1 (APOL1) SIENDO UTILES EN EL TRATAMIENTO DE GLOMERULOESCLEROSIS SEGMENTARIA FOCAL (FSGS) Y ENFERMEDAD RENAL NO DIABETICA.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202063070705P | 2020-08-26 | 2020-08-26 | |
PCT/US2021/047754 WO2022047031A1 (en) | 2020-08-26 | 2021-08-26 | Inhibitors of apol1 and methods of using same |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20231106A1 true PE20231106A1 (es) | 2023-07-19 |
Family
ID=77822053
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2023000722A PE20231106A1 (es) | 2020-08-26 | 2021-08-26 | Inhibidores de apol1 y metodos para usar los mismos |
Country Status (20)
Country | Link |
---|---|
US (1) | US11866446B2 (es) |
EP (1) | EP4204423A1 (es) |
JP (1) | JP2023539194A (es) |
KR (1) | KR20230057386A (es) |
CN (1) | CN116547287A (es) |
AR (1) | AR123355A1 (es) |
AU (1) | AU2021333776A1 (es) |
BR (1) | BR112023003423A2 (es) |
CA (1) | CA3190609A1 (es) |
CL (1) | CL2023000536A1 (es) |
CO (1) | CO2023003026A2 (es) |
CR (1) | CR20230132A (es) |
DO (1) | DOP2023000042A (es) |
EC (1) | ECSP23020167A (es) |
IL (1) | IL300298A (es) |
MX (1) | MX2023002269A (es) |
PE (1) | PE20231106A1 (es) |
TW (1) | TW202227456A (es) |
UY (1) | UY39395A (es) |
WO (1) | WO2022047031A1 (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11618746B2 (en) | 2018-12-17 | 2023-04-04 | Vertex Pharmaceuticals Incorporated | Inhibitors of APOL1 and methods of using same |
KR20220151634A (ko) | 2020-03-06 | 2022-11-15 | 버텍스 파마슈티칼스 인코포레이티드 | Apol-1 의존성 국소 분절성 사구체경화증을 치료하는 방법 |
CA3190609A1 (en) | 2020-08-26 | 2022-03-03 | Vertex Pharmaceuticals Incorporated | Inhibitors of apol1 and methods of using same |
US20230119114A1 (en) * | 2021-08-26 | 2023-04-20 | Vertex Pharmaceuticals Incorporated | Solid forms of apol1 inhibitors and methods of using same |
US11976067B2 (en) | 2022-01-18 | 2024-05-07 | Maze Therapeutics, Inc. | APOL1 inhibitors and methods of use |
WO2023154344A1 (en) * | 2022-02-08 | 2023-08-17 | Vertex Pharmaceuticals Incorporated | 2-methyl-4',5'-dihydrospiro[piperidine-4,7'-thieno[2,3-c]pyran] derivatives as inhibitors of apol1 and methods of using same |
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US4039676A (en) | 1975-06-23 | 1977-08-02 | Ciba-Geigy Corporation | 2-piperidinoalkyl-1,4-benzodioxans |
US6518423B1 (en) | 1996-08-09 | 2003-02-11 | Eisai Co., Ltd. | Benzopiperidine derivatives |
WO2001017965A2 (en) | 1999-09-07 | 2001-03-15 | Syngenta Participations Ag | Cyanopiperidines as pesticides |
FR2801585B1 (fr) | 1999-11-25 | 2002-02-15 | Fournier Ind & Sante | Nouveaux antagonistes des recepteurs de l'ii-8 |
AU2002211828A1 (en) | 2000-10-02 | 2002-04-15 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
FR2824827B1 (fr) | 2001-05-17 | 2004-02-13 | Fournier Lab Sa | Nouveaux derives de 5-phenyl-1h-indole antagoniste des recepteurs de l'interleukine-8 |
FR2824826B1 (fr) | 2001-05-17 | 2003-11-07 | Fournier Lab Sa | Nouveaux derives de 5-cyano-1h-indole antagonistes des recepteurs de l'interleukine-8 |
WO2003104180A1 (en) | 2002-06-05 | 2003-12-18 | Natco Pharma Limited | Process for the preparation of 4-(4-fluorobenzoyl) butyric acid |
EP1723105B1 (en) | 2004-03-03 | 2013-05-15 | Eli Lilly And Company | Bicyclic substituted indole-derivative steroid hormone nuclear receptor modulators |
AR048523A1 (es) | 2004-04-07 | 2006-05-03 | Kalypsys Inc | Compuestos con estructura de aril sulfonamida y sulfonilo como moduladores de ppar y metodos para tratar trastornos metabolicos |
US8222288B2 (en) | 2006-08-30 | 2012-07-17 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
EP2086935A1 (de) | 2006-10-16 | 2009-08-12 | Grünenthal GmbH | Substituierte sulfonamid-derivate als bradykinin 1 rezeptor modulatoren |
RU2009123133A (ru) | 2006-12-22 | 2011-01-27 | Ф.Хоффманн-Ля Рош Аг (Ch) | Производные спиро-пиперидина |
US8053440B2 (en) | 2007-02-01 | 2011-11-08 | Resverlogix Corporation | Compounds for the prevention and treatment of cardiovascular diseases |
EP2020414A1 (en) | 2007-06-20 | 2009-02-04 | Laboratorios del Dr. Esteve S.A. | spiro[piperidine-4,4'-thieno[3,2-c]pyran] derivatives and related compounds as inhibitors of the sigma receptor for the treatment of psychosis |
CN101801965B (zh) | 2007-08-17 | 2014-07-30 | 株式会社Lg生命科学 | 作为细胞坏死抑制剂的吲哚化合物 |
US9101616B2 (en) | 2009-05-29 | 2015-08-11 | Raqualia Pharma Inc. | Aryl substituted carboxamide derivatives as calcium or sodium channel blockers |
SI2501704T1 (sl) | 2009-11-16 | 2013-11-29 | Eli Lilly Company | Spojine spiropiperidina kot antagonisti oral-1 receptorja |
UA107943C2 (en) | 2009-11-16 | 2015-03-10 | Lilly Co Eli | Compounds of spiropiperidines as antagonists of the orl-1 receptors |
WO2012025155A1 (en) | 2010-08-26 | 2012-03-01 | Novartis Ag | Hydroxamate-based inhibitors of deacetylases |
BR102012024778A2 (pt) | 2012-09-28 | 2014-08-19 | Cristalia Prod Quimicos Farm | Compostos heteroaromáticos; processo para preparar os compostos, composições farmacêuticas, usos e método de tratamento para as dores aguda e crônica |
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US11618746B2 (en) | 2018-12-17 | 2023-04-04 | Vertex Pharmaceuticals Incorporated | Inhibitors of APOL1 and methods of using same |
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CA3168909A1 (en) | 2020-01-29 | 2021-08-05 | Vertex Pharmaceuticals Incorporated | Inhibitors of apol1 and methods of using same |
WO2021158666A1 (en) | 2020-02-04 | 2021-08-12 | Vertex Pharmaceuticals Incorporated | Solid forms of apol1 inhibitor and methods of using same |
KR20220151634A (ko) | 2020-03-06 | 2022-11-15 | 버텍스 파마슈티칼스 인코포레이티드 | Apol-1 의존성 국소 분절성 사구체경화증을 치료하는 방법 |
WO2021216665A1 (en) | 2020-04-22 | 2021-10-28 | Anima Biotech Inc. | Collagen 1 translation inhibitors and methods of use thereof |
WO2021220178A1 (en) | 2020-04-29 | 2021-11-04 | Cominnex Zrt. | Iap antagonists and their therapeutic applications |
CA3182373A1 (en) | 2020-05-07 | 2021-11-11 | Rambam Med-Tech Ltd. | Composition for use in the treatment of apol1-associated disease |
TW202214601A (zh) | 2020-06-12 | 2022-04-16 | 美商維泰克斯製藥公司 | Apol1抑制劑之固體形式及其使用方法 |
AU2021286666A1 (en) | 2020-06-12 | 2023-01-19 | Vertex Pharmaceuticals Incorporated | Inhibitors of APOL1 and use of the same |
CA3185604A1 (en) | 2020-06-12 | 2021-12-16 | Vertex Pharmaceuticals Incorporated | Inhibitors of apol1 and use of the same |
CA3190609A1 (en) | 2020-08-26 | 2022-03-03 | Vertex Pharmaceuticals Incorporated | Inhibitors of apol1 and methods of using same |
US20230119114A1 (en) | 2021-08-26 | 2023-04-20 | Vertex Pharmaceuticals Incorporated | Solid forms of apol1 inhibitors and methods of using same |
-
2021
- 2021-08-26 CA CA3190609A patent/CA3190609A1/en active Pending
- 2021-08-26 EP EP21773242.9A patent/EP4204423A1/en active Pending
- 2021-08-26 CN CN202180072946.7A patent/CN116547287A/zh active Pending
- 2021-08-26 JP JP2023513110A patent/JP2023539194A/ja active Pending
- 2021-08-26 MX MX2023002269A patent/MX2023002269A/es unknown
- 2021-08-26 CR CR20230132A patent/CR20230132A/es unknown
- 2021-08-26 AU AU2021333776A patent/AU2021333776A1/en active Pending
- 2021-08-26 IL IL300298A patent/IL300298A/en unknown
- 2021-08-26 WO PCT/US2021/047754 patent/WO2022047031A1/en active Application Filing
- 2021-08-26 TW TW110131630A patent/TW202227456A/zh unknown
- 2021-08-26 UY UY0001039395A patent/UY39395A/es unknown
- 2021-08-26 AR ARP210102407A patent/AR123355A1/es unknown
- 2021-08-26 KR KR1020237008538A patent/KR20230057386A/ko unknown
- 2021-08-26 US US17/446,135 patent/US11866446B2/en active Active
- 2021-08-26 BR BR112023003423A patent/BR112023003423A2/pt unknown
- 2021-08-26 PE PE2023000722A patent/PE20231106A1/es unknown
-
2023
- 2023-02-23 CL CL2023000536A patent/CL2023000536A1/es unknown
- 2023-02-28 DO DO2023000042A patent/DOP2023000042A/es unknown
- 2023-03-13 CO CONC2023/0003026A patent/CO2023003026A2/es unknown
- 2023-03-20 EC ECSENADI202320167A patent/ECSP23020167A/es unknown
Also Published As
Publication number | Publication date |
---|---|
EP4204423A1 (en) | 2023-07-05 |
MX2023002269A (es) | 2023-05-16 |
TW202227456A (zh) | 2022-07-16 |
CL2023000536A1 (es) | 2023-09-08 |
UY39395A (es) | 2022-03-31 |
DOP2023000042A (es) | 2023-07-09 |
ECSP23020167A (es) | 2023-12-29 |
AU2021333776A1 (en) | 2023-03-16 |
CA3190609A1 (en) | 2022-03-03 |
CO2023003026A2 (es) | 2023-03-17 |
IL300298A (en) | 2023-04-01 |
AR123355A1 (es) | 2022-11-23 |
KR20230057386A (ko) | 2023-04-28 |
US11866446B2 (en) | 2024-01-09 |
CN116547287A (zh) | 2023-08-04 |
WO2022047031A1 (en) | 2022-03-03 |
BR112023003423A2 (pt) | 2023-03-21 |
US20220106327A1 (en) | 2022-04-07 |
JP2023539194A (ja) | 2023-09-13 |
CR20230132A (es) | 2023-06-27 |
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