MX2022014168A - Sal y formas de cristal de 4-amino-5-(6-(4-metilpiperazin-1-il)-ih benzo[d]imidazol-2-il)tieno[2,3-b]piridin-6(7h)-ona. - Google Patents
Sal y formas de cristal de 4-amino-5-(6-(4-metilpiperazin-1-il)-ih benzo[d]imidazol-2-il)tieno[2,3-b]piridin-6(7h)-ona.Info
- Publication number
- MX2022014168A MX2022014168A MX2022014168A MX2022014168A MX2022014168A MX 2022014168 A MX2022014168 A MX 2022014168A MX 2022014168 A MX2022014168 A MX 2022014168A MX 2022014168 A MX2022014168 A MX 2022014168A MX 2022014168 A MX2022014168 A MX 2022014168A
- Authority
- MX
- Mexico
- Prior art keywords
- salt
- methylpiperazin
- thieno
- imidazol
- pyridin
- Prior art date
Links
- 150000003839 salts Chemical group 0.000 title abstract 2
- WKFZMTSRRQSGEY-UHFFFAOYSA-N NC=1C2=C(NC(C=1C1=NC3=C(N1)C=C(C=C3)N1CCN(CC1)C)=O)SC=C2 Chemical compound NC=1C2=C(NC(C=1C1=NC3=C(N1)C=C(C=C3)N1CCN(CC1)C)=O)SC=C2 WKFZMTSRRQSGEY-UHFFFAOYSA-N 0.000 title 1
- 239000013078 crystal Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000000053 physical method Methods 0.000 abstract 1
- 150000003892 tartrate salts 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
- C07D495/02—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 two hetero rings
- C07D495/04—Ortho-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
- A61K31/495—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
-
- 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
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/235—Saturated compounds containing more than one carboxyl group
- C07C59/245—Saturated compounds containing more than one carboxyl group containing hydroxy or O-metal groups
- C07C59/255—Tartaric acid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Abstract
Se describe una forma de sal novedosa del Compuesto (I) representado por la siguiente fórmula estructural y sus correspondientes composiciones farmacéuticas, N H S O NH2 N H N N N (I), formas cristalinas individuales particulares de la sal tartrato del Compuesto (I) 1:1 son caracterizadas por una variedad de propiedades y mediciones físicas; también se describen métodos para preparar formas cristalinas específicas; la presente descripción también proporciona métodos para tratar cáncer en un sujeto.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202063022867P | 2020-05-11 | 2020-05-11 | |
PCT/CA2021/050645 WO2021226707A1 (en) | 2020-05-11 | 2021-05-10 | Salt and crystal forms of 4-amino-5-(6-(4-methylpiperazin-1-yl)-1h-benzo[d]imidazol-2-yl)thieno[2,3-b]pyridin-6(7h)-one |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2022014168A true MX2022014168A (es) | 2023-02-22 |
Family
ID=78525916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2022014168A MX2022014168A (es) | 2020-05-11 | 2021-05-10 | Sal y formas de cristal de 4-amino-5-(6-(4-metilpiperazin-1-il)-ih benzo[d]imidazol-2-il)tieno[2,3-b]piridin-6(7h)-ona. |
Country Status (12)
Country | Link |
---|---|
US (1) | US20230174549A1 (es) |
EP (1) | EP4149946A1 (es) |
JP (1) | JP2023526054A (es) |
KR (1) | KR20230019110A (es) |
CN (1) | CN115803330A (es) |
AU (1) | AU2021272064A1 (es) |
BR (1) | BR112022022946A2 (es) |
CA (1) | CA3178415A1 (es) |
IL (1) | IL298132A (es) |
MX (1) | MX2022014168A (es) |
TW (1) | TW202208375A (es) |
WO (1) | WO2021226707A1 (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3873608A1 (en) | 2018-10-31 | 2021-09-08 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds having hpk1 inhibitory activity |
CA3117556A1 (en) | 2018-10-31 | 2020-05-07 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
TWI826690B (zh) | 2019-05-23 | 2023-12-21 | 美商基利科學股份有限公司 | 經取代之烯吲哚酮化物及其用途 |
US20240002394A1 (en) * | 2020-11-24 | 2024-01-04 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Deuterium-modified thienopyridone compound |
TW202333712A (zh) * | 2021-12-22 | 2023-09-01 | 加拿大健康網路大學 | 於急性骨髓性白血病或淋巴瘤之治療 |
WO2023143384A1 (zh) * | 2022-01-27 | 2023-08-03 | 四川海思科制药有限公司 | 一种抑制或降解hpk1激酶的化合物及其在医药中的用途 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3322711B1 (en) * | 2015-06-25 | 2021-03-10 | University Health Network | Hpk1 inhibitors and methods of using same |
CN109721620B (zh) * | 2017-10-27 | 2022-05-13 | 药捷安康(南京)科技股份有限公司 | Hpk1抑制剂及其用途 |
-
2021
- 2021-05-10 KR KR1020227043409A patent/KR20230019110A/ko unknown
- 2021-05-10 CN CN202180047337.6A patent/CN115803330A/zh active Pending
- 2021-05-10 US US17/924,220 patent/US20230174549A1/en active Pending
- 2021-05-10 EP EP21803607.7A patent/EP4149946A1/en active Pending
- 2021-05-10 AU AU2021272064A patent/AU2021272064A1/en active Pending
- 2021-05-10 CA CA3178415A patent/CA3178415A1/en active Pending
- 2021-05-10 IL IL298132A patent/IL298132A/en unknown
- 2021-05-10 WO PCT/CA2021/050645 patent/WO2021226707A1/en unknown
- 2021-05-10 TW TW110116763A patent/TW202208375A/zh unknown
- 2021-05-10 MX MX2022014168A patent/MX2022014168A/es unknown
- 2021-05-10 JP JP2022568819A patent/JP2023526054A/ja active Pending
- 2021-05-10 BR BR112022022946A patent/BR112022022946A2/pt unknown
Also Published As
Publication number | Publication date |
---|---|
IL298132A (en) | 2023-01-01 |
BR112022022946A2 (pt) | 2023-01-10 |
EP4149946A1 (en) | 2023-03-22 |
WO2021226707A1 (en) | 2021-11-18 |
US20230174549A1 (en) | 2023-06-08 |
JP2023526054A (ja) | 2023-06-20 |
KR20230019110A (ko) | 2023-02-07 |
AU2021272064A1 (en) | 2023-01-19 |
CA3178415A1 (en) | 2021-11-18 |
TW202208375A (zh) | 2022-03-01 |
CN115803330A (zh) | 2023-03-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX2022014168A (es) | Sal y formas de cristal de 4-amino-5-(6-(4-metilpiperazin-1-il)-ih benzo[d]imidazol-2-il)tieno[2,3-b]piridin-6(7h)-ona. | |
AU2007243457B2 (en) | Pharmaceutical compounds | |
TWI499420B (zh) | 肌醇磷脂3-激酶抑制劑化合物及使用方法 | |
AU2013225533B2 (en) | Amido spirocyclic amide and sulfonamide derivatives | |
CA3215823A1 (en) | Heterocyclic derivative inhibitor and preparation method therefor and application thereof | |
US6770641B2 (en) | Fused heteroaryl derivatives | |
CA2932175C (en) | 3,5-(un)substituted-1h-pyrrolo[2,3-b]pyridine, 1h-pyrazolo[3,4-b]pyridine and 5h-pyrrolo[2,3-b]pyrazine dual itk and jak3 kinase inhibitors | |
AU2014205577A1 (en) | IRAK inhibitors and uses thereof | |
CZ294027B6 (cs) | Derivát thienopyrimidinu, jeho použití a farmaceutický prostředek, který ho obsahuje | |
JP2015508785A (ja) | ピリジニル及びピリミジニルスルホキシド及びスルホン誘導体 | |
TW200924781A (en) | Thieno- and furo-pyrimidine modulators of the histamine H4 receptor | |
TW200821315A (en) | Benzofuro-and benzothienopyrimidine modulators of the histamine H4 receptor | |
AU2013225530A1 (en) | Amido-benzyl sulfone and sulfoxide derivatives | |
NZ599553A (en) | Ethynyl derivatives | |
CN111484494A (zh) | 抑制mnk1和mnk2的多环化合物 | |
Hassan et al. | Utility of thieno [2, 3-b] pyridine derivatives in the synthesis of some condensed heterocyclic compounds with expected biological activity | |
MX2023007641A (es) | Derivados de 4-amino-3-(4-fenoxifenilo)-1,3-dihidro-2h-imidazo[4,5 -c]piridin-2-ona y sales de los mismos. | |
CN107382974B (zh) | 一种嘧啶胺类化合物作为周期蛋白依赖性激酶4/6抑制剂的应用 | |
EA202190322A1 (ru) | ИМИДАЗО[1,2-b]ПИРИДАЗИНОВЫЕ ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ TRK | |
CA3026592C (en) | Fused pyrimidine piperidine cyclic derivative, preparation process and use thereof | |
MX2022000474A (es) | Derivados de camptotecina con un resto disulfuro y un resto piperazina. | |
WO2020006031A8 (en) | Ask1 inhibiting agents | |
Morel et al. | On the problem of the cyclisation of benzothiazolyl-anthranilic acids into thiazolo-acridinones. The case of thiazolo [4, 5-a] acridines | |
NZ755300A (en) | Novel heterocyclic compound, its preparation method, and pharmaceutical composition comprising the same | |
EA201290535A1 (ru) | Способ получения фармацевтических соединений и промежуточных соединений |