[go: up one dir, main page]

PE20231303A1 - Forma solida de compuesto - Google Patents

Forma solida de compuesto

Info

Publication number
PE20231303A1
PE20231303A1 PE2023000209A PE2023000209A PE20231303A1 PE 20231303 A1 PE20231303 A1 PE 20231303A1 PE 2023000209 A PE2023000209 A PE 2023000209A PE 2023000209 A PE2023000209 A PE 2023000209A PE 20231303 A1 PE20231303 A1 PE 20231303A1
Authority
PE
Peru
Prior art keywords
compound
formula
theta
degrees
crystalline form
Prior art date
Application number
PE2023000209A
Other languages
English (en)
Inventor
Zaiqi Wang
Jing Gao
Yingxia Sang
Original Assignee
Inxmed Nanjing Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Inxmed Nanjing Co Ltd filed Critical Inxmed Nanjing Co Ltd
Publication of PE20231303A1 publication Critical patent/PE20231303A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C57/00Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
    • C07C57/02Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • C07C57/13Dicarboxylic acids
    • C07C57/145Maleic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/235Saturated compounds containing more than one carboxyl group
    • C07C59/245Saturated compounds containing more than one carboxyl group containing hydroxy or O-metal groups
    • C07C59/255Tartaric acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C63/00Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
    • C07C63/04Monocyclic monocarboxylic acids
    • C07C63/06Benzoic acid
    • C07C63/08Salts thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invencion se refiere a una forma solida de un compuesto de formula (I) o una sal o solvato del mismo, el cual se caracteriza porque es: a) la forma cristalina A de la base libre del compuesto de formula (I), caracterizado por los datos de difraccion de polvo de rayos X (XRPD) que incluye los siguientes picos: 4.781, 7.361, 7.619, 9.58, 10.54, 10.979, 11.459, 12.34, 12.96, 13.278, 14.678, 17.402, 18.54, 19.26, 19.918, 21.581, 22.26, 22.54, 23.521, 24.217, 24.801, 25.181 y 29.219 grados dos-theta, b) la forma cristalina I de la sal tartrato del compuesto de formula (I), caracterizado por los datos de difraccion de polvo de rayos X (XRPD) que incluye los siguientes picos: 4.627, 10.34, 13.019, 15.76, 16.54, 17.159, 17.981, 18.281, 20.538, 21.2, 21.901, 23.121, 24.721, 25.659, 27.299, 27.541, 29.879, 32.277 y 41.821 grados dos-theta, c) la forma cristalina I de la sal fosfato del compuesto de formula (I), caracterizado por los datos de difraccion de polvo de rayos X (XRPD) que incluye los siguientes picos: 9.121, 10.082, 12.6, 13.76, 14.52, 15.941, 18.581, 19.08, 19.781, 20.581, 22.319, 23.381, 23.818, 24.642, 25.66, 26.537, 28.219, 29.419 y 33.98 grados dos-theta, d) la forma cristalina I de la sal maleato del compuesto de formula (I), caracterizado por los datos de difraccion de polvo de rayos X (XRPD) que incluye los siguientes picos: 6.801, 9.575, 10.32, 13.258, 13.662, 15.041, 15.998, 18.459, 19.761, 20.237, 20.781, 21.498, 21.78, 22.185, 24.12, 25.599, 27.062, 28.203 y 35.258 grados dos-theta, o e) la forma cristalina I de la sal benzoato del compuesto de formula (I), caracterizado por los datos de difraccion de polvo de rayos X (XRPD) que incluye los siguientes picos: 3.981, 6.639, 8.461, 9.6, 12.119, 12.602, 14.52, 15.441, 16.882, 18.12, 18.941, 20.16, 20.639, 51.699, 23.378, 23.719, 24.659, 28.418 y 29.259 grados dos-theta. Tambien se refiere a una composicion farmaceutica. Dichos compuestos son inhibidores de a proteina tirosina cinasa 2 (PTK2 o tambien conocida como FAK), siendo utiles en el tratamiento del cancer.
PE2023000209A 2020-08-03 2021-08-02 Forma solida de compuesto PE20231303A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CN202010768730 2020-08-03
CN202010837005 2020-08-19
PCT/CN2021/110069 WO2022028367A1 (zh) 2020-08-03 2021-08-02 化合物的固体形式

Publications (1)

Publication Number Publication Date
PE20231303A1 true PE20231303A1 (es) 2023-08-24

Family

ID=80119956

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2023000209A PE20231303A1 (es) 2020-08-03 2021-08-02 Forma solida de compuesto

Country Status (15)

Country Link
US (2) US20230278985A1 (es)
EP (1) EP4190774B1 (es)
JP (1) JP2023536491A (es)
KR (1) KR20230048089A (es)
CN (1) CN116096713B (es)
AU (1) AU2021323235A1 (es)
BR (1) BR112023001962A2 (es)
CA (1) CA3188244A1 (es)
CL (1) CL2023000313A1 (es)
ES (1) ES3049298T3 (es)
MX (1) MX2023001418A (es)
PE (1) PE20231303A1 (es)
TW (1) TW202206425A (es)
WO (1) WO2022028367A1 (es)
ZA (1) ZA202301378B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2023224815A1 (en) * 2022-02-28 2024-09-26 Wigen Biomedicine Technology (shanghai) Co., Ltd. Compound as fak inhibitor and use thereof
TW202408528A (zh) 2022-06-24 2024-03-01 大陸商應世生物科技(南京)有限公司 治療腫瘤的藥物組合及用途
CN118580221A (zh) * 2023-03-02 2024-09-03 应世生物科技(南京)有限公司 化合物的固体形式

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR074210A1 (es) * 2008-11-24 2010-12-29 Boehringer Ingelheim Int Derivados de pirimidina como inhibidores de ptk2-quinasa
CA2991044C (en) * 2015-06-29 2024-11-19 Verastem, Inc. THERAPEUTIC COMPOSITIONS, COMBINATIONS AND METHODS OF USE
KR102861189B1 (ko) * 2019-03-28 2025-09-16 앰플리아 테라퓨틱스 리미티드 Fak 억제제의 염 및 결정 형태
WO2020202005A1 (en) * 2019-04-02 2020-10-08 Inxmed (Shanghai) Co., Ltd. Combination of a fak kinase inhibitor and an agent targeting t-cell co-stimulatory receptors
WO2021098679A1 (zh) * 2019-11-18 2021-05-27 应世生物科技(南京)有限公司 Fak抑制剂在制备用于治疗nras突变的肿瘤的药物中的用途
PE20230180A1 (es) * 2019-11-28 2023-02-01 Inxmed Nanjing Co Ltd Uso de bi853520 en tratamiento contra el cancer
CA3168648A1 (en) * 2020-01-31 2021-08-05 Verastem, Inc. Combination therapy for treating abnormal cell growth
AU2021215747A1 (en) * 2020-02-05 2022-08-18 Inxmed (Nanjing) Co., Ltd. Combination of BI853520 with chemotherapeutic drugs
TW202313044A (zh) * 2021-08-16 2023-04-01 大陸商應世生物科技(南京)有限公司 In10018與pld的聯用
TW202408528A (zh) * 2022-06-24 2024-03-01 大陸商應世生物科技(南京)有限公司 治療腫瘤的藥物組合及用途

Also Published As

Publication number Publication date
BR112023001962A2 (pt) 2023-04-11
US20230278985A1 (en) 2023-09-07
US20240051942A1 (en) 2024-02-15
MX2023001418A (es) 2023-04-10
EP4190774B1 (en) 2025-10-01
CL2023000313A1 (es) 2023-07-28
CN116096713B (zh) 2025-04-29
EP4190774A4 (en) 2024-01-17
ZA202301378B (en) 2025-05-28
EP4190774A1 (en) 2023-06-07
TW202206425A (zh) 2022-02-16
AU2021323235A1 (en) 2023-03-02
WO2022028367A1 (zh) 2022-02-10
ES3049298T3 (en) 2025-12-16
KR20230048089A (ko) 2023-04-10
JP2023536491A (ja) 2023-08-25
CN116096713A (zh) 2023-05-09
CA3188244A1 (en) 2022-02-10
US11999719B2 (en) 2024-06-04

Similar Documents

Publication Publication Date Title
PE20231303A1 (es) Forma solida de compuesto
PE20210392A1 (es) Compuestos utiles para inhibir a cdk7
CY1123353T1 (el) Καινοφανης ενωση συμπυκνωμενης πυριμιδινης ή αλας εξ αυτης
ZA202102999B (en) Inhibitors of cyclin-dependent kinase 7 (cdk7)
MX374513B (es) Compuestos de morfolinona de ácido heteroarilo como inhibidores mdm2 para el tratamiento de cáncer.
CU20200070A7 (es) Derivados de 2-amino-piridina o 2-amino-pirimidina como inhibidores de quinasa dependientes de ciclina
CY1120179T1 (el) Ετεροκυκλικη ενωση που περιεχει αζωτο ή αλας αυτης
UY31072A1 (es) Imidazopiridazinas sustituidas como inhibidores de cinasa de lipido
JOP20190151B1 (ar) مركبات أمينو - ترايازولو بيريدين واستخدامها في علاج سرطان
PE20141855A1 (es) Benzotienilo-pirrolotriazinas disustituidas y sus usos
NZ711376A (en) Heteroaryl compounds and uses thereof
EA201000886A1 (ru) Органические соединения
EA202090413A1 (ru) Пиразоло- и триазолобициклические соединения в качестве ингибиторов jak киназы
MX2018011792A (es) Compuestos de pirrolotriazina como inhibidores de tyro3, axl y mer (tam).
PH12016501048A1 (en) Piperidine derivatives as mdm2 inhibitors for the treatment of cancer
EA201690153A1 (ru) Замещенные бензофуранильные и бензоксазолильные соединения и их применения
EA201790492A1 (ru) СОЕДИНЕНИЯ, КОТОРЫЕ ИНГИБИРУЮТ БЕЛОК Mcl-1
EA201992320A1 (ru) Пиперидины в качестве ковалентных ингибиторов менина
EA201001687A1 (ru) Производные имидазопиридина в качестве ингибиторов активиноподобной рецепторной киназы ( alk-4 или alk-5 )
EA201892436A1 (ru) Пиримидиновые соединения в качестве ингибиторов jak киназы
EA201001772A1 (ru) Производные 3,5-диамино-6-хлорпиразин-2-карбоновой кислоты и их применение в качестве блокаторов эпителиальных натриевых каналов для лечения заболеваний дыхательных путей
PE20181017A1 (es) Compuestos heteroarilo y su uso como farmacos terapeuticos
EA201990902A1 (ru) Ингибиторы тирозинкиназы брутона
EA201792425A1 (ru) Трициклические соединения и их применение в качестве ингибиторов фосфодиэстераз
PE20210002A1 (es) Sales de derivados de pirrolotriazina utiles como inhibidores tam