KR20190077544A - Magl 억제제 - Google Patents
Magl 억제제 Download PDFInfo
- Publication number
- KR20190077544A KR20190077544A KR1020197016924A KR20197016924A KR20190077544A KR 20190077544 A KR20190077544 A KR 20190077544A KR 1020197016924 A KR1020197016924 A KR 1020197016924A KR 20197016924 A KR20197016924 A KR 20197016924A KR 20190077544 A KR20190077544 A KR 20190077544A
- Authority
- KR
- South Korea
- Prior art keywords
- pharmaceutically acceptable
- solvate
- acceptable salt
- compound
- formula
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- 0 C*CC1(CCCC1)C(O)=O Chemical compound C*CC1(CCCC1)C(O)=O 0.000 description 7
- OWHAHLXCBFEAJK-UHFFFAOYSA-N OC(Cc1cc(C(F)(F)F)cc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c1)=O Chemical compound OC(Cc1cc(C(F)(F)F)cc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c1)=O OWHAHLXCBFEAJK-UHFFFAOYSA-N 0.000 description 2
- ATUQTWQLBGTEOL-UHFFFAOYSA-N CC(C)(C(O)=O)C#Cc(c(CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)ccc1)c1F Chemical compound CC(C)(C(O)=O)C#Cc(c(CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)ccc1)c1F ATUQTWQLBGTEOL-UHFFFAOYSA-N 0.000 description 1
- BMFOHZZKYBARQT-UHFFFAOYSA-N CC(C)(C(O)=O)C#Cc(c(CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)ccc1C)c1F Chemical compound CC(C)(C(O)=O)C#Cc(c(CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)ccc1C)c1F BMFOHZZKYBARQT-UHFFFAOYSA-N 0.000 description 1
- VSFMIZAHCAVEKM-UHFFFAOYSA-N CC(C)(C(O)=O)C#Cc1cc(C(F)(F)F)ccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O Chemical compound CC(C)(C(O)=O)C#Cc1cc(C(F)(F)F)ccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O VSFMIZAHCAVEKM-UHFFFAOYSA-N 0.000 description 1
- LIYXNXMFTOEUQK-UHFFFAOYSA-N CC(C)(C)C(OCOC(CCCN(Cc1ccccc1)c1cc(C(F)(F)F)ccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)=O)=O Chemical compound CC(C)(C)C(OCOC(CCCN(Cc1ccccc1)c1cc(C(F)(F)F)ccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)=O)=O LIYXNXMFTOEUQK-UHFFFAOYSA-N 0.000 description 1
- GCSRKLYGGIDREC-UHFFFAOYSA-N CC(C)(C)C(OCOC(CCCNc1cc(C(F)(F)F)ccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)=O)=O Chemical compound CC(C)(C)C(OCOC(CCCNc1cc(C(F)(F)F)ccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)=O)=O GCSRKLYGGIDREC-UHFFFAOYSA-N 0.000 description 1
- UPBJZEVZBJBXDX-UHFFFAOYSA-N CC(C)(C)OC(N1CCN(C[B](F)(F)F)CC1)=O Chemical compound CC(C)(C)OC(N1CCN(C[B](F)(F)F)CC1)=O UPBJZEVZBJBXDX-UHFFFAOYSA-N 0.000 description 1
- LHGSERYYEGVXOP-UHFFFAOYSA-N CC(C)(C)OC(N1CCN(Cc2cc(O)cc(C(F)(F)F)c2)CC1)=O Chemical compound CC(C)(C)OC(N1CCN(Cc2cc(O)cc(C(F)(F)F)c2)CC1)=O LHGSERYYEGVXOP-UHFFFAOYSA-N 0.000 description 1
- OMPKWOGDEJPZKA-UHFFFAOYSA-N COC(C1(CC1)Oc1cc(C(F)(F)F)ccc1C=O)=O Chemical compound COC(C1(CC1)Oc1cc(C(F)(F)F)ccc1C=O)=O OMPKWOGDEJPZKA-UHFFFAOYSA-N 0.000 description 1
- LLQSDPHAQQIKNO-UHFFFAOYSA-N CS(NCCN(C(c1c2cccc1)=O)C2=O)(=O)=O Chemical compound CS(NCCN(C(c1c2cccc1)=O)C2=O)(=O)=O LLQSDPHAQQIKNO-UHFFFAOYSA-N 0.000 description 1
- JUYXSZKVQBFLEX-UHFFFAOYSA-N Cc(c(F)c1O)ccc1Br Chemical compound Cc(c(F)c1O)ccc1Br JUYXSZKVQBFLEX-UHFFFAOYSA-N 0.000 description 1
- LTPLDADXDHQQNG-UHFFFAOYSA-N Cc1ccc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c(OCC(NS(C)(=O)=O)=O)c1F Chemical compound Cc1ccc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c(OCC(NS(C)(=O)=O)=O)c1F LTPLDADXDHQQNG-UHFFFAOYSA-N 0.000 description 1
- KUOMIDXYDQJQBC-UHFFFAOYSA-N Cc1ccc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c(OCC(NS(C2CC2)(=O)=O)=O)c1F Chemical compound Cc1ccc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c(OCC(NS(C2CC2)(=O)=O)=O)c1F KUOMIDXYDQJQBC-UHFFFAOYSA-N 0.000 description 1
- KFZGPLRZCJDUHB-UHFFFAOYSA-N Cc1ccc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c(OCC2(CC2)C(O)=O)c1Cl Chemical compound Cc1ccc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c(OCC2(CC2)C(O)=O)c1Cl KFZGPLRZCJDUHB-UHFFFAOYSA-N 0.000 description 1
- UNJQOFVMMSPQKP-UHFFFAOYSA-N N#Cc(cc(cc1CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)F)c1OCC1(CC1)C(O)=O Chemical compound N#Cc(cc(cc1CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)F)c1OCC1(CC1)C(O)=O UNJQOFVMMSPQKP-UHFFFAOYSA-N 0.000 description 1
- UVGYSEIWAOOIJR-UHFFFAOYSA-N O=Cc(c(F)c1)ccc1Cl Chemical compound O=Cc(c(F)c1)ccc1Cl UVGYSEIWAOOIJR-UHFFFAOYSA-N 0.000 description 1
- KFEHNXLFIGPWNB-UHFFFAOYSA-N O=Cc(ccc(C(F)(F)F)c1)c1F Chemical compound O=Cc(ccc(C(F)(F)F)c1)c1F KFEHNXLFIGPWNB-UHFFFAOYSA-N 0.000 description 1
- GHVCPFRHGFZWMO-UHFFFAOYSA-N OC(C1(CC1)Oc1c(C(F)(F)F)cccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)=O Chemical compound OC(C1(CC1)Oc1c(C(F)(F)F)cccc1CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)=O GHVCPFRHGFZWMO-UHFFFAOYSA-N 0.000 description 1
- FBXXQGXIRNXAGS-UHFFFAOYSA-N OC(C1(CC1)Oc1cc(C(F)(F)F)cc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c1)=O Chemical compound OC(C1(CC1)Oc1cc(C(F)(F)F)cc(CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)c1)=O FBXXQGXIRNXAGS-UHFFFAOYSA-N 0.000 description 1
- QWMVXCRSOICZJV-UHFFFAOYSA-N OC(C1(COc2cc(C(F)(F)F)cc(CN(CC3)CCN3C(OC(C(F)(F)F)C(F)(F)F)=O)c2)CC1)=O Chemical compound OC(C1(COc2cc(C(F)(F)F)cc(CN(CC3)CCN3C(OC(C(F)(F)F)C(F)(F)F)=O)c2)CC1)=O QWMVXCRSOICZJV-UHFFFAOYSA-N 0.000 description 1
- VBIBDPOWQZCXDI-UHFFFAOYSA-N OC(C1(COc2cc(C(F)(F)F)ccc2CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)CC1)=O Chemical compound OC(C1(COc2cc(C(F)(F)F)ccc2CN(CC2)CCN2C(OC(C(F)(F)F)C(F)(F)F)=O)CC1)=O VBIBDPOWQZCXDI-UHFFFAOYSA-N 0.000 description 1
- VTVMGZJBOAKWCY-UHFFFAOYSA-N OC(COCCNc(c(CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)ccc1)c1F)=O Chemical compound OC(COCCNc(c(CN(CC1)CCN1C(OC(C(F)(F)F)C(F)(F)F)=O)ccc1)c1F)=O VTVMGZJBOAKWCY-UHFFFAOYSA-N 0.000 description 1
- BWJBVICFLRSNNM-UHFFFAOYSA-N Oc1cc(C(F)(F)F)cc(Br)c1 Chemical compound Oc1cc(C(F)(F)F)cc(Br)c1 BWJBVICFLRSNNM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic 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
- C07D295/16—Heterocyclic 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
- C07D295/18—Heterocyclic 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 carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/195—Radicals derived from nitrogen analogues of carboxylic acids
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic 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
- C07D295/16—Heterocyclic 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
- C07D295/20—Heterocyclic 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
- C07D295/205—Radicals derived from carbonic acid
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)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662423099P | 2016-11-16 | 2016-11-16 | |
| US62/423,099 | 2016-11-16 | ||
| PCT/US2017/061868 WO2018093947A1 (en) | 2016-11-16 | 2017-11-15 | Magl inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20190077544A true KR20190077544A (ko) | 2019-07-03 |
Family
ID=62106678
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020197016924A Abandoned KR20190077544A (ko) | 2016-11-16 | 2017-11-15 | Magl 억제제 |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US10093635B2 (enExample) |
| EP (1) | EP3541821A4 (enExample) |
| JP (1) | JP7042547B2 (enExample) |
| KR (1) | KR20190077544A (enExample) |
| CN (1) | CN110267963B (enExample) |
| AR (1) | AR110089A1 (enExample) |
| AU (1) | AU2017361251B2 (enExample) |
| BR (1) | BR112019009994A2 (enExample) |
| CA (1) | CA3043615A1 (enExample) |
| CL (1) | CL2019001339A1 (enExample) |
| CO (1) | CO2019005059A2 (enExample) |
| CR (1) | CR20190241A (enExample) |
| DO (1) | DOP2019000122A (enExample) |
| EA (1) | EA038090B1 (enExample) |
| EC (1) | ECSP19035077A (enExample) |
| GE (1) | GEP20237470B (enExample) |
| IL (1) | IL266523B (enExample) |
| JO (1) | JOP20190106A1 (enExample) |
| MA (1) | MA46857A (enExample) |
| MX (1) | MX391117B (enExample) |
| NI (1) | NI201900051A (enExample) |
| PE (1) | PE20191144A1 (enExample) |
| PH (1) | PH12019501097A1 (enExample) |
| RU (1) | RU2754536C1 (enExample) |
| TN (1) | TN2019000153A1 (enExample) |
| TW (1) | TWI756299B (enExample) |
| UA (1) | UA124542C2 (enExample) |
| WO (1) | WO2018093947A1 (enExample) |
| ZA (1) | ZA201903100B (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2800565T3 (pl) | 2012-01-06 | 2020-09-21 | Lundbeck La Jolla Research Center, Inc. | Związki karbaminianowe i sposoby ich wytwarzania oraz zastosowanie |
| AU2016262459A1 (en) | 2015-05-11 | 2017-12-21 | H. Lundbeck A/S. | Methods of treating inflammation or neuropathic pain |
| US10899737B2 (en) | 2016-09-19 | 2021-01-26 | Lundbeck La Jolla Research Center, Inc. | Piperazine carbamates and methods of making and using same |
| BR112019009992A2 (pt) | 2016-11-16 | 2019-08-27 | Abide Therapeutics Inc | formulações farmacêuticas |
| JOP20190107A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
| CA3043610A1 (en) | 2016-11-16 | 2018-05-24 | Abide Therapeutics, Inc. | Crystalline forms of a magl inhibitor |
| ES2940111T3 (es) | 2017-05-23 | 2023-05-03 | H Lundbeck As | Inhibidores de MAGL de pirazol |
| MA50041A (fr) | 2017-08-29 | 2020-07-08 | Lundbeck La Jolla Research Center Inc | Composés spirocycliques et procédés de préparation et d'utilisation de ceux-ci |
| SG11202011228TA (en) | 2018-05-15 | 2020-12-30 | Lundbeck La Jolla Research Center Inc | Magl inhibitors |
| SG11202108008PA (en) * | 2019-01-25 | 2021-08-30 | H Lundbeck As | Methods of treating disease with magl inhibitors |
| MX2022005864A (es) * | 2019-11-15 | 2022-08-16 | H Lundbeck As | Formas cristalinas de un inhibidor de magl. |
| IT202000007150A1 (it) * | 2020-04-03 | 2021-10-03 | Univ Pisa | Inibitori di monoacilglicerolo lipasi (magl) |
| BR112021025516A2 (pt) | 2020-04-21 | 2022-11-01 | H Lundbeck As | Processos para a fabricação de 4-(2-(pirrolidin-1-il)-4-(trifluorometil)benzil)piperazina-1-carboxilato de 1,1,1,3,3,3-hexafluoropropan-2-ila e da forma 2 do sal monocloridrato do mesmo |
| MX2024008337A (es) | 2021-12-29 | 2024-07-30 | Psy Therapeutics Inc | Inhibicion de la monoacilglicerol lipasa (magl). |
| CN119137114A (zh) | 2022-05-04 | 2024-12-13 | H.隆德贝克有限公司 | 作为单酰基甘油脂肪酶抑制剂的(s)-1-(哒嗪-3-基氨基甲酰基)-6-氮杂螺[2.5]辛烷-6-甲酸1,1,1,3,3,3-六氟丙-2-酯的结晶形式 |
Family Cites Families (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1593586A (enExample) | 1967-10-17 | 1970-06-01 | ||
| JPS6183073A (ja) | 1984-10-01 | 1986-04-26 | Oki Electric Ind Co Ltd | 印字装置の用紙送り方法 |
| WO1989011794A1 (fr) | 1988-06-07 | 1989-12-14 | Rikagaku Kenkyusho | Inhibiteur de la croissance de plantes |
| AU3226993A (en) | 1991-11-27 | 1993-06-28 | E.I. Du Pont De Nemours And Company | Herbicidal acylated amino-(phenyl- or pyridinyl- or thienyl-)-phenyl derivatives |
| AU1384795A (en) | 1993-12-22 | 1995-07-10 | Shell Internationale Research Maatschappij B.V. | Process for preparing carbamates |
| EP0863879A1 (en) | 1995-11-15 | 1998-09-16 | Zeneca Limited | Herbicidal substituted pyrazole compounds |
| WO1998000408A1 (en) | 1996-07-02 | 1998-01-08 | Novartis Ag | N-phenylimino heterocyclic derivatives and their use as herbicides |
| RU2167150C2 (ru) | 1998-03-25 | 2001-05-20 | Фокин Александр Васильевич | Полифторалкил-n-арилкарбаматы, обладающие антимикробной активностью |
| EP1218544B1 (en) | 1999-10-04 | 2009-06-03 | The University of Medicine and Dentistry of New Jersey | TAR RNA binding peptides |
| EP1201298A1 (en) | 2000-10-24 | 2002-05-02 | Urea Casale S.A. | Carbamate condensation unit |
| DE10348022A1 (de) | 2003-10-15 | 2005-05-25 | Imtm Gmbh | Neue Dipeptidylpeptidase IV-Inhibitoren zur funktionellen Beeinflussung unterschiedlicher Zellen und zur Behandlung immunologischer, entzündlicher, neuronaler und anderer Erkrankungen |
| FR2864080B1 (fr) | 2003-12-23 | 2006-02-03 | Sanofi Synthelabo | Derives de 1-piperazine-et-1-homopiperazine-carboxylates, leur preparation et leur application en therapeutique |
| AU2003300702A1 (en) | 2003-12-31 | 2005-07-21 | Council Of Scientific And Industrial Research | Process for preparing carbamates |
| KR20070026382A (ko) | 2004-02-18 | 2007-03-08 | 아스트라제네카 아베 | 아세틸린성 피페라진 화합물 및 대사성 글루타메이트수용체 길항제로서 이들의 용도 |
| US7786113B2 (en) | 2004-12-23 | 2010-08-31 | Hoffman-La Roche Inc. | Heterocyclic carbamate derivatives, their manufacture and use as pharmaceutical agents |
| ES2639621T3 (es) | 2004-12-30 | 2017-10-27 | Janssen Pharmaceutica N.V. | Derivados de fenilamida del ácido 4-(bencil)-piperazina-1-carboxílico y compuestos relacionados como moduladores de la amida hidrolasa de ácidos grasos (FAAH) para el tratamiento de la ansiedad, el dolor y otras afecciones |
| US20080255150A1 (en) * | 2005-11-05 | 2008-10-16 | Astrazeneca Ab | Novel Compounds |
| JP2009523729A (ja) | 2006-01-13 | 2009-06-25 | ピーティーシー セラピューティクス,インコーポレーテッド | C型肝炎の治療方法 |
| CN101679408B (zh) | 2006-12-22 | 2016-04-27 | Astex治疗学有限公司 | 作为fgfr抑制剂的双环杂环化合物 |
| US7795457B2 (en) | 2007-02-26 | 2010-09-14 | Kosan Biosciences Incorporated | Carbamate compounds |
| US8188098B2 (en) | 2008-05-19 | 2012-05-29 | Hoffmann-La Roche Inc. | GPR119 receptor agonists |
| US20110118286A1 (en) | 2008-07-16 | 2011-05-19 | Santhosh Francis Neelamkavil | Bicyclic heterocycle derivatives and their use as gpcr modulators |
| EP2373315A4 (en) | 2008-11-14 | 2012-06-27 | Scripps Research Inst | METHOD AND COMPOSITIONS RELATED TO TARGETING OF MONOACYLGLYCEROLLIPASE |
| AU2010229134A1 (en) | 2009-03-23 | 2011-11-10 | Msd K.K. | Novel aminopyridine derivatives having Aurora A selective inhibitory action |
| WO2010124114A1 (en) * | 2009-04-22 | 2010-10-28 | Janssen Pharmaceutica Nv | Azetidinyl diamides as monoacylglycerol lipase inhibitors |
| UA107791C2 (en) | 2009-05-05 | 2015-02-25 | Dow Agrosciences Llc | Pesticidal compositions |
| IN2012DN03890A (enExample) | 2009-11-03 | 2015-09-04 | Bayer Materialscience Ag | |
| FR2960875B1 (fr) * | 2010-06-04 | 2012-12-28 | Sanofi Aventis | Derives de carbamates d'hexafluoroisopropyle, leur preparation et leur application en therapeutique |
| SG11201403878QA (en) | 2012-01-06 | 2014-08-28 | Agios Pharmaceuticals Inc | Therapeutically active compounds and their methods of use |
| PL2800565T3 (pl) * | 2012-01-06 | 2020-09-21 | Lundbeck La Jolla Research Center, Inc. | Związki karbaminianowe i sposoby ich wytwarzania oraz zastosowanie |
| WO2013142307A1 (en) | 2012-03-19 | 2013-09-26 | Abide Therapeutics | Carbamate compounds and of making and using same |
| JP2014005245A (ja) * | 2012-06-26 | 2014-01-16 | Dainippon Sumitomo Pharma Co Ltd | 二環性ピリミジン誘導体を含有する医薬組成物 |
| 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 |
| WO2016014975A2 (en) * | 2014-07-25 | 2016-01-28 | Northeastern University | Urea/carbamates faah magl or dual faah/magl inhibitors and uses thereof |
| MX2017011997A (es) | 2015-03-18 | 2018-05-28 | Abide Therapeutics Inc | Carbamatos de piperacina y metodos de preparacion y uso. |
| US10899737B2 (en) * | 2016-09-19 | 2021-01-26 | Lundbeck La Jolla Research Center, Inc. | Piperazine carbamates and methods of making and using same |
| JOP20190105A1 (ar) * | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
-
2017
- 2017-06-16 JO JOP/2019/0106A patent/JOP20190106A1/ar unknown
- 2017-11-15 MA MA046857A patent/MA46857A/fr unknown
- 2017-11-15 CR CR20190241A patent/CR20190241A/es unknown
- 2017-11-15 WO PCT/US2017/061868 patent/WO2018093947A1/en not_active Ceased
- 2017-11-15 IL IL266523A patent/IL266523B/en unknown
- 2017-11-15 PE PE2019001014A patent/PE20191144A1/es unknown
- 2017-11-15 US US15/814,322 patent/US10093635B2/en active Active
- 2017-11-15 MX MX2019005776A patent/MX391117B/es unknown
- 2017-11-15 AU AU2017361251A patent/AU2017361251B2/en not_active Ceased
- 2017-11-15 TN TNP/2019/000153A patent/TN2019000153A1/en unknown
- 2017-11-15 AR ARP170103184A patent/AR110089A1/es not_active Application Discontinuation
- 2017-11-15 CA CA3043615A patent/CA3043615A1/en active Pending
- 2017-11-15 UA UAA201905620A patent/UA124542C2/uk unknown
- 2017-11-15 KR KR1020197016924A patent/KR20190077544A/ko not_active Abandoned
- 2017-11-15 EA EA201991073A patent/EA038090B1/ru unknown
- 2017-11-15 JP JP2019523587A patent/JP7042547B2/ja active Active
- 2017-11-15 GE GEAP201715088A patent/GEP20237470B/en unknown
- 2017-11-15 EP EP17871753.4A patent/EP3541821A4/en not_active Withdrawn
- 2017-11-15 BR BR112019009994A patent/BR112019009994A2/pt not_active IP Right Cessation
- 2017-11-15 CN CN201780083663.6A patent/CN110267963B/zh not_active Expired - Fee Related
- 2017-11-15 RU RU2019116512A patent/RU2754536C1/ru active
- 2017-11-16 TW TW106139775A patent/TWI756299B/zh not_active IP Right Cessation
-
2019
- 2019-05-16 DO DO2019000122A patent/DOP2019000122A/es unknown
- 2019-05-16 EC ECSENADI201935077A patent/ECSP19035077A/es unknown
- 2019-05-16 NI NI201900051A patent/NI201900051A/es unknown
- 2019-05-16 PH PH12019501097A patent/PH12019501097A1/en unknown
- 2019-05-16 CL CL2019001339A patent/CL2019001339A1/es unknown
- 2019-05-16 CO CONC2019/0005059A patent/CO2019005059A2/es unknown
- 2019-05-17 ZA ZA201903100A patent/ZA201903100B/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR20190077544A (ko) | Magl 억제제 | |
| JP7042468B2 (ja) | Magl阻害剤 | |
| JP6987859B2 (ja) | Magl阻害剤 | |
| JP2021523200A (ja) | Magl阻害剤 | |
| JP7042804B2 (ja) | ピペラジンカルバメート、及びその製造と使用の方法 | |
| JP2020532547A (ja) | スピロ環化合物並びにその作製及び使用方法 | |
| KR20200010366A (ko) | 피라졸 magl 저해제 | |
| KR102756049B1 (ko) | 이중 magl 및 faah 저해제 | |
| EP3793552A1 (en) | Abhd12 inhibitors and methods of making and using same | |
| NZ753264B2 (en) | Magl inhibitors | |
| HK40009161A (en) | Magl inhibitors | |
| HK40009161B (en) | Magl inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| PG1501 | Laying open of application |
St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
|
| PN2301 | Change of applicant |
St.27 status event code: A-3-3-R10-R13-asn-PN2301 St.27 status event code: A-3-3-R10-R11-asn-PN2301 |
|
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| PA0201 | Request for examination |
St.27 status event code: A-1-2-D10-D11-exm-PA0201 |
|
| N231 | Notification of change of applicant | ||
| PN2301 | Change of applicant |
St.27 status event code: A-3-3-R10-R13-asn-PN2301 St.27 status event code: A-3-3-R10-R11-asn-PN2301 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| E13-X000 | Pre-grant limitation requested |
St.27 status event code: A-2-3-E10-E13-lim-X000 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
St.27 status event code: A-1-2-D10-D22-exm-PE0701 |
|
| PC1904 | Unpaid initial registration fee |
St.27 status event code: A-2-2-U10-U14-oth-PC1904 St.27 status event code: N-2-6-B10-B12-nap-PC1904 |