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)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (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 (https=) |
| EP (1) | EP3541821A4 (https=) |
| JP (1) | JP7042547B2 (https=) |
| KR (1) | KR20190077544A (https=) |
| CN (1) | CN110267963B (https=) |
| AR (1) | AR110089A1 (https=) |
| AU (1) | AU2017361251B2 (https=) |
| BR (1) | BR112019009994A2 (https=) |
| CA (1) | CA3043615A1 (https=) |
| CL (1) | CL2019001339A1 (https=) |
| CO (1) | CO2019005059A2 (https=) |
| CR (1) | CR20190241A (https=) |
| DO (1) | DOP2019000122A (https=) |
| EA (1) | EA038090B1 (https=) |
| EC (1) | ECSP19035077A (https=) |
| GE (2) | GEP20237470B (https=) |
| IL (1) | IL266523B (https=) |
| JO (1) | JOP20190106A1 (https=) |
| MA (1) | MA46857A (https=) |
| MX (1) | MX391117B (https=) |
| NI (1) | NI201900051A (https=) |
| PE (1) | PE20191144A1 (https=) |
| PH (1) | PH12019501097A1 (https=) |
| RU (1) | RU2754536C1 (https=) |
| TN (1) | TN2019000153A1 (https=) |
| TW (1) | TWI756299B (https=) |
| UA (1) | UA124542C2 (https=) |
| WO (1) | WO2018093947A1 (https=) |
| ZA (1) | ZA201903100B (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20141702A1 (es) | 2012-01-06 | 2014-11-19 | Abide Therapeutics Inc | Compuestos de carbamato y preparacion y uso de los mismos |
| CN113413387A (zh) | 2015-05-11 | 2021-09-21 | H.隆德贝克有限公司 | 治疗炎症或神经性疼痛的方法 |
| US10899737B2 (en) | 2016-09-19 | 2021-01-26 | Lundbeck La Jolla Research Center, Inc. | Piperazine carbamates and methods of making and using same |
| UA124884C2 (uk) | 2016-11-16 | 2021-12-08 | Лундбек Ла Джолла Ресеарч Центер, Інк. | Фармацевтичні склади |
| JOP20190107A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
| MA46866B1 (fr) | 2016-11-16 | 2021-11-30 | H Lundbeck As | Une forme cristalline d'un inhibiteur de magl |
| DK3630744T3 (da) | 2017-05-23 | 2023-03-06 | H Lundbeck As | Pyrazol-magl-inhibitorer |
| JP7257387B2 (ja) | 2017-08-29 | 2023-04-13 | ハー・ルンドベック・アクチエゼルスカベット | スピロ環化合物並びにその作製及び使用方法 |
| GEP20227443B (en) * | 2018-05-15 | 2022-11-25 | H Lundbeck As | Magl inhibitors |
| CA3125636A1 (en) * | 2019-01-25 | 2020-07-30 | H. Lundbeck A/S | Methods of treating disease with magl inhibitors |
| KR20220101095A (ko) * | 2019-11-15 | 2022-07-19 | 하. 룬드벡 아크티에셀스카브 | Magl 억제제의 결정형 |
| IT202000007150A1 (it) * | 2020-04-03 | 2021-10-03 | Univ Pisa | Inibitori di monoacilglicerolo lipasi (magl) |
| WO2021214550A1 (en) | 2020-04-21 | 2021-10-28 | H. Lundbeck A/S | Synthesis of a monoacylglycerol lipase inhibitor |
| CA3242372A1 (en) | 2021-12-29 | 2023-07-06 | Psy Therapeutics, Inc. | Inhibiting monoacylglycerol lipase (magl) |
| KR20250005229A (ko) | 2022-05-04 | 2025-01-09 | 하. 룬드벡 아크티에셀스카브 | 모노아실글리세롤 리파제 억제제로서 1,1,1,3,3,3-헥사플루오로프로판-2-일 (s)-1-(피리다진-3-일카르바모일)-6 아자스피로[2.5]옥탄-6-카르복실레이트의 결정질 형태 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1593586A (https=) | 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 |
| EP0619804B1 (en) | 1991-11-27 | 1996-05-22 | E.I. Du Pont De Nemours And Company | Herbicidal acylated amino-(phenyl- or pyridinyl- or thienyl-)-phenyl derivatives |
| DE69408873T2 (de) | 1993-12-22 | 1998-07-09 | Shell Int Research | Verfahren zur herstellung von carbamaten |
| WO1997018196A1 (en) | 1995-11-15 | 1997-05-22 | Zeneca Limited | Herbicidal substituted pyrazole compounds |
| AU3440597A (en) | 1996-07-02 | 1998-01-21 | 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 |
| AU7855900A (en) | 1999-10-04 | 2001-05-10 | University Of Medicine And Dentistry Of New Jersey | Methods for identifying rna binding compounds |
| 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 |
| WO2005063698A1 (en) | 2003-12-31 | 2005-07-14 | Council Of Scientific & Industrial Research | Process for preparing carbamates |
| BRPI0507499A (pt) | 2004-02-18 | 2007-07-24 | Astrazeneca Ab | composto ou um sal farmaceuticamente aceitável ou hidrato dos mesmos, composição farmacêutica, uso do composto, e, métodos para tratar distúrbios mediados por mglur 5 e para inibir a ativação de receptores de mglur 5 |
| US7786113B2 (en) | 2004-12-23 | 2010-08-31 | Hoffman-La Roche Inc. | Heterocyclic carbamate derivatives, their manufacture and use as pharmaceutical agents |
| AR055831A1 (es) | 2004-12-30 | 2007-09-12 | Janssen Pharmaceutica Nv | Pepirazinilureas y piperidinilureas como moduladores de hidrolasa de amida de acidos grasos |
| WO2007052023A2 (en) | 2005-11-05 | 2007-05-10 | Astrazeneca Ab | Novel compounds |
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