BR112022021521A2 - Compostos inovadores úteis como inibidores de poli(adp-ribose)polimerase (parp) - Google Patents
Compostos inovadores úteis como inibidores de poli(adp-ribose)polimerase (parp)Info
- Publication number
- BR112022021521A2 BR112022021521A2 BR112022021521A BR112022021521A BR112022021521A2 BR 112022021521 A2 BR112022021521 A2 BR 112022021521A2 BR 112022021521 A BR112022021521 A BR 112022021521A BR 112022021521 A BR112022021521 A BR 112022021521A BR 112022021521 A2 BR112022021521 A2 BR 112022021521A2
- Authority
- BR
- Brazil
- Prior art keywords
- parp
- cancer
- polymerase
- inhibitors
- poly
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
Abstract
COMPOSTOS INOVADORES ÚTEIS COMO INIBIDORES DE POLI(ADPRIBOSE)POLIMERASE (PARP). A presente invenção fornece novos inibidores de poli(ADP-ribose)polimerase (PARP), métodos de preparação dos mesmos, composições farmacêuticas que contêm os mesmos e métodos para o tratamento, a prevenção e/ou o alívio de doenças ou distúrbios mediados por PARP com o uso dos mesmos. Em particular, os compostos descritos neste documento são úteis para o tratamento de carcinoma da mama, câncer ovariano, carcinoma do fígado, carcinoma do pulmão, câncer de pulmão de células pequenas, câncer esofágico, câncer de vesícula biliar, câncer pancreático e câncer de estômago.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN202041018149 | 2020-04-28 | ||
IN202041047713 | 2020-11-02 | ||
PCT/IB2021/053382 WO2021220120A1 (en) | 2020-04-28 | 2021-04-23 | Novel compounds useful as poly(adp-ribose) polymerase (parp) inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
BR112022021521A2 true BR112022021521A2 (pt) | 2023-01-24 |
Family
ID=75870674
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BR112022021521A BR112022021521A2 (pt) | 2020-04-28 | 2021-04-23 | Compostos inovadores úteis como inibidores de poli(adp-ribose)polimerase (parp) |
Country Status (14)
Country | Link |
---|---|
US (1) | US20230234938A1 (pt) |
EP (1) | EP4143182A1 (pt) |
JP (1) | JP2023524212A (pt) |
KR (1) | KR20230002487A (pt) |
CN (1) | CN115485271A (pt) |
AU (1) | AU2021262569A1 (pt) |
BR (1) | BR112022021521A2 (pt) |
CA (1) | CA3176206A1 (pt) |
CL (1) | CL2022002966A1 (pt) |
CO (1) | CO2022016819A2 (pt) |
IL (1) | IL297537A (pt) |
MX (1) | MX2022013378A (pt) |
TW (1) | TW202140451A (pt) |
WO (1) | WO2021220120A1 (pt) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2022090938A1 (en) * | 2020-10-31 | 2022-05-05 | Rhizen Pharmaceuticals Ag | Phthalazinone derivatives useful as parp inhibitors |
JP2024515338A (ja) | 2021-04-08 | 2024-04-09 | ライゼン ファーマシューティカルズ アーゲー | ポリ(adp-リボース)ポリメラーゼの阻害剤 |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4093448B2 (ja) | 1999-01-11 | 2008-06-04 | アグロン・ファーマシューティカルズ・インコーポレーテッド | ポリ(adp−リボース)ポリメラーゼの三環系阻害剤 |
ECSP003637A (es) | 1999-08-31 | 2002-03-25 | Agouron Pharma | Inhibidores triciclicos de poli (adp-ribosa) polimerasas |
CN100400518C (zh) | 2000-10-30 | 2008-07-09 | 库多斯药物有限公司 | 2,3-二氮杂萘酮衍生物 |
JP2004528376A (ja) | 2001-05-08 | 2004-09-16 | クドス ファーマシューティカルズ リミテッド | Parp阻害薬としてのイソキノリノン誘導体 |
JP4500161B2 (ja) | 2002-04-30 | 2010-07-14 | クドス ファーマシューティカルズ リミテッド | フタラジノン誘導体 |
US20040034078A1 (en) | 2002-06-14 | 2004-02-19 | Agouron Pharmaceuticals, Inc. | Benzimidazole inhibitors of poly(ADP-ribosyl) polymerase |
EP1633724B1 (en) | 2003-03-12 | 2011-05-04 | Kudos Pharmaceuticals Limited | Phthalazinone derivatives |
MXPA05010563A (es) | 2003-03-31 | 2005-11-23 | Pfizer | Sales de los inhibidores triciclicos de las poli(adp-ribosa) polimerasas. |
GB0317466D0 (en) | 2003-07-25 | 2003-08-27 | Univ Sheffield | Use |
NZ544989A (en) | 2003-07-25 | 2009-10-30 | Cancer Rec Tech Ltd | Tricyclic PARP inhibitors |
SG150548A1 (en) | 2003-12-01 | 2009-03-30 | Kudos Pharm Ltd | Dna damage repair inhibitors for treatment of cancer |
EP1791827A1 (en) | 2004-08-26 | 2007-06-06 | Kudos Pharmaceuticals Limited | 4-heteroarylmethyl substituted phthalazinone derivatives |
EP1793830A2 (en) | 2004-09-22 | 2007-06-13 | Pfizer, Inc. | Therapeutic combinations comprising poly(adp-ribose) polymerases inhibitor |
DE602005018506D1 (de) | 2004-09-22 | 2010-02-04 | Pfizer | Verfahren zur herstellung von poly(adp-ribose)polymeraseinhibitoren |
ATE551345T1 (de) | 2004-09-22 | 2012-04-15 | Pfizer | Polymorphe formen des phosphatsalzes von 8-fluor- 2-ä4-ä(methylamino)methylüphenylü-1,3,4,5- tetrahydro-6h-azepinoä5,4,3-cdüindol-6-on |
GB0428111D0 (en) | 2004-12-22 | 2005-01-26 | Kudos Pharm Ltd | Pthalazinone derivatives |
US20090281086A1 (en) | 2006-06-15 | 2009-11-12 | Kudos Pharmaceuticals Limited | 2 -oxyheteroarylamide derivatives as parp inhibitors |
US20090209520A1 (en) | 2006-06-15 | 2009-08-20 | Kudos Pharmaceuticals Limited | 2 -oxybenzamide derivatives as parp inhibitors |
WO2007144652A2 (en) | 2006-06-15 | 2007-12-21 | Kudos Pharmaceuticals Limited | Parp inhibitors |
TWI404716B (zh) | 2006-10-17 | 2013-08-11 | Kudos Pharm Ltd | 酞嗪酮(phthalazinone)衍生物 |
WO2008114114A2 (en) | 2007-03-16 | 2008-09-25 | Pfizer Products Inc. | Poly(adp-ribose) polymerases inhibitor for treating ophthalmic condition |
WO2009050469A1 (en) | 2007-10-17 | 2009-04-23 | Kudos Pharmaceuticals Limited | 4- [3- (4-cyclopropanecarbonyl-piperazine-i-carbonyl) -4 -fluoro-benzyl] -2h-phthalaz in-1-one |
LT3150610T (lt) | 2010-02-12 | 2019-11-11 | Pfizer | 8-fluor-2-{4-[(metilamino}metil]fenil}-1,3,4,5-tetrahidro-6h-azepino[5,4,3-cd]indol-6-ono druskos ir polimorfai |
EP3094752A4 (en) | 2014-01-16 | 2017-08-16 | Clovis Oncology, Inc. | Use of parp inhibitors to treat breast or ovarian cancer patients showing a loss of heterozygosity |
KR20210132233A (ko) * | 2014-04-14 | 2021-11-03 | 아비나스 오퍼레이션스, 인코포레이티드 | 단백질분해의 이미드-기초된 조절인자 및 연관된 이용 방법 |
EP3182975A4 (en) | 2014-08-22 | 2018-04-18 | Clovis Oncology, Inc. | High dosage strength tablets of rucaparib |
CN105753789B (zh) | 2015-04-17 | 2018-09-25 | 苏州晶云药物科技有限公司 | 奥拉帕尼与尿素的共晶及其制备方法 |
US20170204067A1 (en) | 2016-01-14 | 2017-07-20 | Scinopharm Taiwan, Ltd. | Crystalline forms of olaparib and manufacturing processes therefor |
CZ201682A3 (cs) | 2016-02-15 | 2017-08-23 | Zentiva, K.S. | Solvatované krystalické formy olaparibu, jejich příprava a použití |
WO2017153958A1 (en) | 2016-03-11 | 2017-09-14 | Lupin Limited | Novel polymorphic forms and amorphous form of olaparib |
WO2017191562A1 (en) | 2016-05-04 | 2017-11-09 | Alembic Pharmaceuticals Limited | Process for the preparation of olaparib and polymorphs thereof |
WO2018038680A1 (en) | 2016-08-24 | 2018-03-01 | Scinopharm Taiwan, Ltd. | Processes for preparing olaparib |
CN108201536A (zh) | 2016-12-16 | 2018-06-26 | 中国科学院上海药物研究所 | 一种奥拉帕尼口服缓控释药物组合物及其用途 |
DK3615034T3 (da) | 2017-04-28 | 2021-08-23 | Akribes Biomedical Gmbh | Rucaparib, talazoparib, veliparib, olaparib og azd 2461 til behandling af forringet hudsårheling |
-
2021
- 2021-04-23 MX MX2022013378A patent/MX2022013378A/es unknown
- 2021-04-23 CA CA3176206A patent/CA3176206A1/en active Pending
- 2021-04-23 WO PCT/IB2021/053382 patent/WO2021220120A1/en active Application Filing
- 2021-04-23 BR BR112022021521A patent/BR112022021521A2/pt unknown
- 2021-04-23 KR KR1020227037119A patent/KR20230002487A/ko unknown
- 2021-04-23 IL IL297537A patent/IL297537A/en unknown
- 2021-04-23 JP JP2022564815A patent/JP2023524212A/ja active Pending
- 2021-04-23 EP EP21724373.2A patent/EP4143182A1/en active Pending
- 2021-04-23 US US17/996,030 patent/US20230234938A1/en active Pending
- 2021-04-23 CN CN202180030479.1A patent/CN115485271A/zh active Pending
- 2021-04-23 AU AU2021262569A patent/AU2021262569A1/en active Pending
- 2021-04-27 TW TW110115180A patent/TW202140451A/zh unknown
-
2022
- 2022-10-26 CL CL2022002966A patent/CL2022002966A1/es unknown
- 2022-11-23 CO CONC2022/0016819A patent/CO2022016819A2/es unknown
Also Published As
Publication number | Publication date |
---|---|
CL2022002966A1 (es) | 2023-04-21 |
MX2022013378A (es) | 2023-02-15 |
IL297537A (en) | 2022-12-01 |
US20230234938A1 (en) | 2023-07-27 |
CO2022016819A2 (es) | 2023-02-16 |
CN115485271A (zh) | 2022-12-16 |
WO2021220120A1 (en) | 2021-11-04 |
EP4143182A1 (en) | 2023-03-08 |
JP2023524212A (ja) | 2023-06-09 |
TW202140451A (zh) | 2021-11-01 |
AU2021262569A1 (en) | 2022-11-24 |
KR20230002487A (ko) | 2023-01-05 |
CA3176206A1 (en) | 2021-11-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR112022008535A2 (pt) | Composto, composição farmacêutica, métodos para tratar câncer e um distúrbio relativo à proteína ras | |
BR112022008565A2 (pt) | Composto, composição farmacêutica, conjugado, métodos para tratar câncer e um distúrbio relativo à proteína ras | |
BR112022021521A2 (pt) | Compostos inovadores úteis como inibidores de poli(adp-ribose)polimerase (parp) | |
BR112021025034A2 (pt) | Imunoconjugado, composto aminobenzazepina-ligante, composição farmacêutica, métodos para tratar câncer e para preparar um imunoconjugado e uso de um imunoconjugado | |
JOP20200288A1 (ar) | مشتقات تترا هيدرو – إيميدازو[4، 5-c]بيريدين كمعدِّلات مناعية pd-l1 | |
CY1124791T1 (el) | Μορια δεσμευσης ειδικα για cd73 και χρησεις αυτων | |
BR112012015745A2 (pt) | compostos e métodos para a modulação de quinase, e indicações dos mesmos | |
MX2022012780A (es) | Inhibidores de homologo de oncogen viral de sarcoma de rata kirsten (kras) triciclicos fusionados. | |
EA201890730A1 (ru) | Производные пиразолопиримидина в качестве ингибиторов btk для лечения злокачественного новообразования | |
BR112022020769A2 (pt) | Compostos de 2,4-dioxopirimidina de inibição de cd73 | |
BR112022006001A2 (pt) | Imunoconjugado, composto de 8-amido-2-aminobenzazepina-ligante, composto de 5-amino-pirazoloazepina-ligante, composto de aminoquinolina-ligante, uso de um imunoconjugado e métodos para tratar câncer e para preparar um imunoconjugado | |
Suzuki et al. | Aripiprazole, an antipsychotic and partial dopamine agonist, inhibits cancer stem cells and reverses chemoresistance | |
Tessema et al. | SULF2 methylation is prognostic for lung cancer survival and increases sensitivity to topoisomerase-I inhibitors via induction of ISG15 | |
BR112012012694A2 (pt) | "derivados de naftiridina e uso dos mesmos como inibidores de cinase" | |
BRPI0617162B8 (pt) | compostos inibidores de fosfatidilinositol 3-quinase composições farmacêuticas que os contem e métodos de uso dos mesmos | |
BR112021025102A2 (pt) | Derivados de quinazolin-4-ona úteis para o tratamento de doenças e distúrbios associados a braf | |
BR112018074961A2 (pt) | derivados de nucleosídeo de fosforamidato como agentes anticâncer | |
BR112016015983A2 (pt) | Compostos de indazol como inibidores de irak4, seus usos, e composição farmacêutica | |
EA201790502A1 (ru) | Ингибиторы гистоновых диметилаз | |
BR112019024830A2 (pt) | inibidores de bcl6 derivados de benzimidazolona | |
BR112022007719A2 (pt) | Imunoconjugados, composto ligante, composição farmacêutica, método para tratar câncer, uso de um imunoconjugado e método de preparação de um imunoconjugado | |
BR112022011998A2 (pt) | Usos de anticorpos anti-tgfss e inibidores de checkpoint para o tratamento de doenças proliferativas | |
BR112023005160A2 (pt) | Terapia de combinação para o tratamento de câncer | |
BR112023022819A2 (pt) | Compostos, composição farmacêutica, conjugados e métodos para tratar câncer em um sujeito, para tratar um distúrbio e para inibir uma proteína ras em uma célula | |
BR112022019532A2 (pt) | Conjugados de neodegrader |