IL266548A - Crystalline forms of magl inhibitor - Google Patents

Crystalline forms of magl inhibitor

Info

Publication number
IL266548A
IL266548A IL266548A IL26654819A IL266548A IL 266548 A IL266548 A IL 266548A IL 266548 A IL266548 A IL 266548A IL 26654819 A IL26654819 A IL 26654819A IL 266548 A IL266548 A IL 266548A
Authority
IL
Israel
Prior art keywords
crystalline forms
magl inhibitor
magl
inhibitor
crystalline
Prior art date
Application number
IL266548A
Other languages
English (en)
Hebrew (he)
Original Assignee
Abide Therapeutics Inc
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 Abide Therapeutics Inc filed Critical Abide Therapeutics Inc
Publication of IL266548A publication Critical patent/IL266548A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/10Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
    • C07D295/205Radicals derived from carbonic acid
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • C07C57/15Fumaric acid
    • 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

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Rheumatology (AREA)
  • Psychiatry (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)
IL266548A 2016-11-16 2019-05-12 Crystalline forms of magl inhibitor IL266548A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662423126P 2016-11-16 2016-11-16
PCT/US2017/061875 WO2018093953A1 (en) 2016-11-16 2017-11-15 Crystalline forms of a magl inhibitor

Publications (1)

Publication Number Publication Date
IL266548A true IL266548A (en) 2019-07-31

Family

ID=62145805

Family Applications (1)

Application Number Title Priority Date Filing Date
IL266548A IL266548A (en) 2016-11-16 2019-05-12 Crystalline forms of magl inhibitor

Country Status (38)

Country Link
US (2) US11142517B2 (cg-RX-API-DMAC7.html)
EP (2) EP3541807B1 (cg-RX-API-DMAC7.html)
JP (2) JP7042548B2 (cg-RX-API-DMAC7.html)
KR (1) KR102508739B1 (cg-RX-API-DMAC7.html)
CN (2) CN110291083B (cg-RX-API-DMAC7.html)
AU (1) AU2017361257B2 (cg-RX-API-DMAC7.html)
BR (1) BR112019010003A2 (cg-RX-API-DMAC7.html)
CA (1) CA3043610A1 (cg-RX-API-DMAC7.html)
CL (1) CL2019001340A1 (cg-RX-API-DMAC7.html)
CO (1) CO2019005045A2 (cg-RX-API-DMAC7.html)
CR (1) CR20190242A (cg-RX-API-DMAC7.html)
CY (1) CY1124870T1 (cg-RX-API-DMAC7.html)
DK (1) DK3541807T3 (cg-RX-API-DMAC7.html)
DO (1) DOP2019000120A (cg-RX-API-DMAC7.html)
EA (1) EA201991086A1 (cg-RX-API-DMAC7.html)
EC (1) ECSP19035171A (cg-RX-API-DMAC7.html)
ES (2) ES2966939T3 (cg-RX-API-DMAC7.html)
GE (1) GEP20237559B (cg-RX-API-DMAC7.html)
HR (2) HRP20211863T1 (cg-RX-API-DMAC7.html)
HU (2) HUE056973T2 (cg-RX-API-DMAC7.html)
IL (1) IL266548A (cg-RX-API-DMAC7.html)
JO (1) JOP20190109B1 (cg-RX-API-DMAC7.html)
LT (1) LT3541807T (cg-RX-API-DMAC7.html)
MA (2) MA58133B1 (cg-RX-API-DMAC7.html)
MX (2) MX389459B (cg-RX-API-DMAC7.html)
MY (1) MY199386A (cg-RX-API-DMAC7.html)
NI (1) NI201900053A (cg-RX-API-DMAC7.html)
PE (1) PE20191239A1 (cg-RX-API-DMAC7.html)
PH (1) PH12019501068A1 (cg-RX-API-DMAC7.html)
PL (2) PL3964503T3 (cg-RX-API-DMAC7.html)
PT (1) PT3541807T (cg-RX-API-DMAC7.html)
RS (2) RS65016B1 (cg-RX-API-DMAC7.html)
SI (1) SI3541807T1 (cg-RX-API-DMAC7.html)
SM (2) SMT202100675T1 (cg-RX-API-DMAC7.html)
TN (1) TN2019000151A1 (cg-RX-API-DMAC7.html)
UA (1) UA124585C2 (cg-RX-API-DMAC7.html)
WO (1) WO2018093953A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201903093B (cg-RX-API-DMAC7.html)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2982694T3 (es) 2012-01-06 2024-10-17 H Lundbeck As Compuestos de carbamato para su uso en tratamiento
BR112017024253A2 (pt) 2015-05-11 2018-07-24 Abide Therapeutics Inc métodos de tratamento de inflamação ou dor neuropática.
WO2018053447A1 (en) 2016-09-19 2018-03-22 Abide Therapeutics, Inc. Piperazine carbamates and methods of making and using same
HUE056973T2 (hu) 2016-11-16 2022-04-28 H Lundbeck As MAGL inhibitor kristályos formája
CA3043609A1 (en) 2016-11-16 2018-05-24 Abide Therapeutics, Inc. Pharmaceutical formulations
JOP20190107A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
US10927105B1 (en) 2017-05-23 2021-02-23 Lundbeck La Jolla Research Center, Inc. Pyrazole MAGL inhibitors
JOP20190262B1 (ar) 2017-05-23 2023-09-17 H Lundbeck As مثبطات بيرازول magl
EP3675847B1 (en) 2017-08-29 2023-07-12 H. Lundbeck A/S Spirocycle compounds and methods of making and using same
JOP20200276A1 (ar) * 2018-05-15 2020-11-02 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
US20210309669A1 (en) * 2018-07-19 2021-10-07 Pfizer Inc. Heterocyclic Spiro Compounds As MAGL Inhibitors
WO2020035424A1 (en) 2018-08-13 2020-02-20 F. Hoffmann-La Roche Ag New heterocyclic compounds as monoacylglycerol lipase inhibitors
MX2021008865A (es) * 2019-01-25 2021-10-26 H Lundbeck As Inhibidores de magl para usarse para tratar enfermedades antecedentes.
EP4058431A4 (en) * 2019-11-15 2023-11-15 H. Lundbeck A/S Crystalline forms of a magl inhibitor
MX2022013224A (es) 2020-04-21 2022-11-14 H Lundbeck As Sintesis de un inhibidor de la monoacilglicerol lipasa.
WO2023092079A1 (en) * 2021-11-19 2023-05-25 Bryant Cynthia W Use of cannabinoid compounds to treat gastrointestinal disorders
KR20240128870A (ko) 2021-12-29 2024-08-27 싸이 테라퓨틱스, 인크. 모노아실글리세롤 리파아제(magl) 억제
AU2023264787A1 (en) 2022-05-04 2024-10-31 H. Lundbeck A/S Crystalline form of 1,1,1,3,3,3-hexafluoropropan-2-yl (s)-1-(pyridazin-3-ylcarbamoyl)-6 azaspiro[2.5]octane-6-carboxylate as monoacylglycerol lipase inhibitor.
CN117665187B (zh) * 2023-11-23 2024-08-16 宁波大红鹰药业股份有限公司 一种舒林酸中间体杂质的测定方法

Family Cites Families (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4327725A (en) 1980-11-25 1982-05-04 Alza Corporation Osmotic device with hydrogel driving member
US4624848A (en) 1984-05-10 1986-11-25 Ciba-Geigy Corporation Active agent containing hydrogel devices wherein the active agent concentration profile contains a sigmoidal concentration gradient for improved constant release, their manufacture and use
US4968509A (en) 1987-07-27 1990-11-06 Mcneilab, Inc. Oral sustained release acetaminophen formulation and process
IL92966A (en) 1989-01-12 1995-07-31 Pfizer Dispensing devices powered by hydrogel
WO1992018106A1 (fr) 1991-04-16 1992-10-29 Nippon Shinyaku Co., Ltd. Procede de production d'une dispersion solide
WO1993009785A1 (en) 1991-11-22 1993-05-27 Procter & Gamble Pharmaceuticals, Inc. Risedronate delayed-release compositions
US5461140A (en) 1992-04-30 1995-10-24 Pharmaceutical Delivery Systems Bioerodible polymers for solid controlled release pharmaceutical compositions
US5323907A (en) 1992-06-23 1994-06-28 Multi-Comp, Inc. Child resistant package assembly for dispensing pharmaceutical medications
ES2180548T3 (es) 1992-10-16 2003-02-16 Nippon Shinyaku Co Ltd Metodo de obtencion de matrices de cera.
US5686105A (en) 1993-10-19 1997-11-11 The Procter & Gamble Company Pharmaceutical dosage form with multiple enteric polymer coatings for colonic delivery
KR19990014865A (ko) 1995-05-17 1999-02-25 피터 이. 브래이브맨 소장에서의 소화 및 흡수를 증진시키기 위한, 지방산을 함유한조성물들
US6395300B1 (en) 1999-05-27 2002-05-28 Acusphere, Inc. Porous drug matrices and methods of manufacture thereof
AU2001225816B2 (en) 2000-12-18 2005-10-13 Novartis Ag Therapeutic combination of amlodipine and benazepril
US6465014B1 (en) 2001-03-21 2002-10-15 Isp Investments Inc. pH-dependent sustained release, drug-delivery composition
MXPA04008073A (es) 2002-02-20 2004-11-26 Abbott Lab Compuestos azabiciclicos fusionados que inhiben el receptor de subtipo 1 (vr1) del receptor de vainilloide.
US7074805B2 (en) 2002-02-20 2006-07-11 Abbott Laboratories Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor
BRPI0606187A2 (pt) 2005-02-25 2009-06-09 Hoffmann La Roche comprimidos com capacidade de dispersão da substáncia do fármaco melhorada
NZ568700A (en) 2005-11-28 2012-03-30 Marinus Pharmaceuticals Solid stabilized particulate formulations comprising ganaxolone
EP1938804A1 (en) 2006-12-22 2008-07-02 Novartis AG Pharmaceutical formulation comprising neurokinin antagonist
FR2938341A1 (fr) 2008-11-13 2010-05-14 Galderma Res & Dev Modulateurs de la monoglyceride lipase dans le traitement de l'acne, d'une dermatite seborrheique ou de l'hyperseborrhee
WO2010063802A1 (en) 2008-12-05 2010-06-10 Novartis Ag 3, 4-di-substituted cyclobutene- 1, 2 -diones as cxcr2 receptor antagonists
CN101530399B (zh) 2009-04-15 2011-01-26 江苏中兴药业有限公司 一种水飞蓟宾固体自乳化片
ES2982694T3 (es) * 2012-01-06 2024-10-17 H Lundbeck As Compuestos de carbamato para su uso en tratamiento
CN104379578B (zh) 2012-03-19 2017-06-09 阿比德治疗公司 氨基甲酸酯化合物及其制备和使用方法
WO2013159095A1 (en) 2012-04-20 2013-10-24 Anderson Gaweco Ror modulators and their uses
DK2914248T4 (da) 2012-11-02 2024-01-02 Vertex Pharma Farmaceutiske sammensætninger til behandlingen af cftr medierede sygdomme
TW201446286A (zh) 2013-01-31 2014-12-16 Gilead Pharmasset Llc 抗病毒化合物之固態分散調製劑
US9551036B2 (en) 2013-02-25 2017-01-24 Whitehead Institute For Biomedical Research Metabolic gene mesenchymal signatures and uses thereof
WO2015003002A1 (en) 2013-07-03 2015-01-08 Abide Therapeutics, Inc. Pyrrolo-pyrrole carbamate and related organic compounds, pharmaceutical compositions, and medical uses thereof
WO2015030854A1 (en) 2013-08-27 2015-03-05 Gilead Pharmasset Llc Solid dispersion formulation of an antiviral compound
CN103893258B (zh) 2013-12-05 2017-09-29 人福医药集团股份公司 含有广金钱草总黄酮的口服固体制剂及其应用
WO2015164160A1 (en) * 2014-04-21 2015-10-29 Merck Sharp & Dohme Corp. Pharmaceutical salts of an orexin receptor antagonist
WO2015179559A2 (en) 2014-05-21 2015-11-26 Abide Therapeutics, Inc. Pyrazole compounds and methods of making and using same
US9771341B2 (en) 2015-03-18 2017-09-26 Abide Therapeutics, Inc. Piperazine carbamates and methods of making and using same
BR112017024253A2 (pt) 2015-05-11 2018-07-24 Abide Therapeutics Inc métodos de tratamento de inflamação ou dor neuropática.
US10463753B2 (en) * 2016-02-19 2019-11-05 Lundbeck La Jolla Research Center, Inc. Radiolabeled monoacylglycerol lipase occupancy probe
JOP20190107A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
JOP20190106A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
HUE056973T2 (hu) 2016-11-16 2022-04-28 H Lundbeck As MAGL inhibitor kristályos formája
CA3043609A1 (en) 2016-11-16 2018-05-24 Abide Therapeutics, Inc. Pharmaceutical formulations
JOP20190105A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)

Also Published As

Publication number Publication date
EP3964503A1 (en) 2022-03-09
NZ753241A (en) 2021-06-25
CL2019001340A1 (es) 2019-10-04
EP3541807A1 (en) 2019-09-25
CN110291083B (zh) 2022-06-17
KR20190077561A (ko) 2019-07-03
BR112019010003A2 (pt) 2019-08-20
GEP20237559B (en) 2023-10-25
CN110291083A (zh) 2019-09-27
ES2900016T3 (es) 2022-03-15
RU2019116689A3 (cg-RX-API-DMAC7.html) 2021-02-26
SI3541807T1 (sl) 2022-01-31
US11993588B2 (en) 2024-05-28
WO2018093953A1 (en) 2018-05-24
ZA201903093B (en) 2020-11-25
JP7042548B2 (ja) 2022-03-28
HUE064559T2 (hu) 2024-03-28
US20200190063A1 (en) 2020-06-18
JP7350117B2 (ja) 2023-09-25
NI201900053A (es) 2019-10-30
UA124585C2 (uk) 2021-10-13
ES2966939T3 (es) 2024-04-25
MX389459B (es) 2025-03-20
EP3964503C0 (en) 2023-11-08
RU2019116689A (ru) 2020-12-17
EP3541807A4 (en) 2020-04-22
SMT202300494T1 (it) 2024-01-10
PL3541807T3 (pl) 2022-01-17
US11142517B2 (en) 2021-10-12
MY199386A (en) 2023-10-25
MX2022000249A (es) 2022-02-03
MA58133B1 (fr) 2024-02-29
SMT202100675T1 (it) 2022-01-10
US20220235037A1 (en) 2022-07-28
DK3541807T3 (da) 2021-12-06
HRP20231697T1 (hr) 2024-03-15
DOP2019000120A (es) 2019-09-30
CR20190242A (es) 2019-07-09
PH12019501068A1 (en) 2019-08-19
PL3964503T3 (pl) 2024-04-02
RS62665B1 (sr) 2021-12-31
KR102508739B1 (ko) 2023-03-09
CA3043610A1 (en) 2018-05-24
MX2019005767A (es) 2019-12-05
PE20191239A1 (es) 2019-09-16
AU2017361257B2 (en) 2022-02-10
RS65016B1 (sr) 2024-01-31
CY1124870T1 (el) 2022-11-25
LT3541807T (lt) 2021-12-27
EP3964503B1 (en) 2023-11-08
PT3541807T (pt) 2021-12-09
CN115093382A (zh) 2022-09-23
ECSP19035171A (es) 2019-05-31
JOP20190109B1 (ar) 2022-09-15
HRP20211863T1 (hr) 2022-03-04
JOP20190109A1 (ar) 2019-05-09
EP3541807B1 (en) 2021-09-29
MA46866A (fr) 2021-06-02
AU2017361257A1 (en) 2019-05-30
EA201991086A1 (ru) 2019-11-29
JP2022084717A (ja) 2022-06-07
CO2019005045A2 (es) 2019-05-31
MA46866B1 (fr) 2021-11-30
TN2019000151A1 (en) 2020-10-05
HUE056973T2 (hu) 2022-04-28
JP2019537596A (ja) 2019-12-26

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