EA201692435A1 - Соли присоединения (s)-2-(1-(6-амино-5-цианопиримидин-4-иламино)этил)-4-оксо-3-фенил-3,4-дигидропирроло[1,2-f][1,2,4]триазин-5-карбонитрила - Google Patents
Соли присоединения (s)-2-(1-(6-амино-5-цианопиримидин-4-иламино)этил)-4-оксо-3-фенил-3,4-дигидропирроло[1,2-f][1,2,4]триазин-5-карбонитрилаInfo
- Publication number
- EA201692435A1 EA201692435A1 EA201692435A EA201692435A EA201692435A1 EA 201692435 A1 EA201692435 A1 EA 201692435A1 EA 201692435 A EA201692435 A EA 201692435A EA 201692435 A EA201692435 A EA 201692435A EA 201692435 A1 EA201692435 A1 EA 201692435A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- cyanopyrimidin
- carbonitrile
- oxo
- phenyl
- amino
- Prior art date
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- 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
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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Abstract
Настоящее изобретение относится к новым фармацевтически приемлемым солям присоединения (S)-2-(1-(6-амино-5-цианопиримидин-4-иламино)этил)-4-оксо-3-фенил-3,4-дигидропирроло[1,2-f][1,2,4]триазин-5-карбонитрила с производными сульфоновой кислоты, в частности с метансульфоновой кислотой, нафталин-2-сульфоновой кислотой и паратолуолсульфоновой кислотой, и к их фармацевтически приемлемым сольватам, и к их применению в качестве ингибиторов фосфоинозитид-3-киназы (PI3K).
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP14382192 | 2014-05-27 | ||
EP14382401 | 2014-10-17 | ||
EP14382400 | 2014-10-17 | ||
PCT/EP2015/061307 WO2015181052A1 (en) | 2014-05-27 | 2015-05-21 | Addition salts of (s)-2-(1-(6-amino-5-cyanopyrimidin-4-ylamino)ethyl)-4-oxo-3-phenyl-3,4-dihydropyrrolo[1,2-f][1,2,4]triazine-5-carbonitrile |
Publications (1)
Publication Number | Publication Date |
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EA201692435A1 true EA201692435A1 (ru) | 2017-04-28 |
Family
ID=53269467
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201692436A EA201692436A1 (ru) | 2014-05-27 | 2015-05-21 | Медицинское применение |
EA201692437A EA201692437A1 (ru) | 2014-05-27 | 2015-05-21 | Комбинация |
EA201692435A EA201692435A1 (ru) | 2014-05-27 | 2015-05-21 | Соли присоединения (s)-2-(1-(6-амино-5-цианопиримидин-4-иламино)этил)-4-оксо-3-фенил-3,4-дигидропирроло[1,2-f][1,2,4]триазин-5-карбонитрила |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201692436A EA201692436A1 (ru) | 2014-05-27 | 2015-05-21 | Медицинское применение |
EA201692437A EA201692437A1 (ru) | 2014-05-27 | 2015-05-21 | Комбинация |
Country Status (21)
Country | Link |
---|---|
US (3) | US20170151264A1 (ru) |
EP (3) | EP3148999A1 (ru) |
JP (3) | JP2017516799A (ru) |
KR (3) | KR20170007760A (ru) |
CN (3) | CN106414449A (ru) |
AU (3) | AU2015266191A1 (ru) |
BR (1) | BR112016024538A2 (ru) |
CA (3) | CA2941429A1 (ru) |
CL (2) | CL2016002970A1 (ru) |
CR (3) | CR20160538A (ru) |
EA (3) | EA201692436A1 (ru) |
IL (3) | IL247072A0 (ru) |
MA (3) | MA39828A (ru) |
MD (3) | MD20160138A2 (ru) |
MX (3) | MX2016014864A (ru) |
PE (2) | PE20170145A1 (ru) |
PH (3) | PH12016502256A1 (ru) |
SG (3) | SG11201606763VA (ru) |
TW (3) | TW201625259A (ru) |
UY (3) | UY36153A (ru) |
WO (3) | WO2015181052A1 (ru) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2647163T3 (es) | 2008-01-04 | 2017-12-19 | Intellikine, Inc. | Derivados de isoquinolinona sustituidos con una purina útiles como inhibidores de la PI3K |
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
CA2824197C (en) | 2011-01-10 | 2020-02-25 | Michael Martin | Processes for preparing isoquinolinones and solid forms of isoquinolinones |
US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
ES2797376T3 (es) | 2013-01-24 | 2020-12-02 | Palvella Therapeutics Inc | Composiciones para la administración transdérmica de inhibidores de mTOR |
WO2015160975A2 (en) | 2014-04-16 | 2015-10-22 | Infinity Pharmaceuticals, Inc. | Combination therapies |
WO2015191677A1 (en) | 2014-06-11 | 2015-12-17 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors |
MD3831833T2 (ro) | 2015-02-27 | 2023-04-30 | Incyte Holdings Corp | Procedee pentru prepararea unui inhibitor PI3K |
KR20240052871A (ko) | 2016-04-27 | 2024-04-23 | 애브비 인코포레이티드 | 항-il-13 항체를 이용한 il-13 활성이 유해한 질환의 치료 방법 |
JP7118509B2 (ja) | 2016-05-18 | 2022-08-16 | トルク アーゲー | 皮膚病変の治療 |
GB201608797D0 (en) * | 2016-05-19 | 2016-07-06 | Ucb Biopharma Sprl | Therapeutic use |
CN107456454A (zh) * | 2016-06-06 | 2017-12-12 | 先声药业有限公司 | 一种预防或治疗炎性疾病的药物组合物 |
MX2018016227A (es) | 2016-06-24 | 2019-07-08 | Infinity Pharmaceuticals Inc | Terapias de combinacion. |
US10722499B2 (en) | 2017-01-06 | 2020-07-28 | Palvella Therapeutics, Inc. | Anyhydrous compositions of mTOR inhibitors and methods of use |
GB201708856D0 (en) * | 2017-06-02 | 2017-07-19 | Ucb Biopharma Sprl | Seletalisib crystalline forms |
IL274132B2 (en) * | 2017-11-23 | 2024-02-01 | Piqur Therapeutics Ag | Treatment of skin problems |
EP3817743A4 (en) | 2018-07-02 | 2022-07-06 | Palvella Therapeutics, Inc. | ANHYDROUS COMPOSITIONS OF MTOR INHIBITORS AND METHODS OF USE |
US11633399B2 (en) | 2018-12-25 | 2023-04-25 | Sol-Gel Technologies Ltd. | Treatment of skin disorders with compositions comprising an EGFR inhibitor |
CN113440614A (zh) * | 2020-03-26 | 2021-09-28 | 长沙晶易医药科技有限公司 | 一种用于治疗类风湿性关节炎的组合物及其应用 |
KR20230065591A (ko) * | 2021-11-05 | 2023-05-12 | 연세대학교 산학협력단 | 피부-특이적 T 세포(skin-specific T cell)의 억제제를 유효성분으로 포함하는 아토피피부염의 예방 또는 치료용 조성물 |
TW202329976A (zh) * | 2021-12-16 | 2023-08-01 | 美商英塞特公司 | P13K—δ抑制劑之局部調配物 |
TWI823476B (zh) * | 2022-07-15 | 2023-11-21 | 中化合成生技股份有限公司 | 托法替尼檸檬酸鹽的製備方法 |
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Publication number | Priority date | Publication date | Assignee | Title |
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JP2008501707A (ja) * | 2004-06-04 | 2008-01-24 | アイコス、コーポレーション | マスト細胞障害を処置するための方法 |
CN101296909B (zh) * | 2005-08-26 | 2011-10-12 | 默克雪兰诺有限公司 | 吡嗪衍生物及其作为pi3k抑制剂的应用 |
CN102439012A (zh) * | 2009-03-24 | 2012-05-02 | 吉里德卡利斯托加公司 | 2-嘌呤基-3-甲苯基-喹唑啉酮衍生物的阻转异构体和使用方法 |
EP2518070A1 (en) * | 2011-04-29 | 2012-10-31 | Almirall, S.A. | Pyrrolotriazinone derivatives as PI3K inhibitors |
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2015
- 2015-05-21 AU AU2015266191A patent/AU2015266191A1/en not_active Abandoned
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