KR101911560B1 - 이온 채널 조정제로서의 융합된 헤테로시클릭 화합물 - Google Patents
이온 채널 조정제로서의 융합된 헤테로시클릭 화합물 Download PDFInfo
- Publication number
- KR101911560B1 KR101911560B1 KR1020137001153A KR20137001153A KR101911560B1 KR 101911560 B1 KR101911560 B1 KR 101911560B1 KR 1020137001153 A KR1020137001153 A KR 1020137001153A KR 20137001153 A KR20137001153 A KR 20137001153A KR 101911560 B1 KR101911560 B1 KR 101911560B1
- Authority
- KR
- South Korea
- Prior art keywords
- pyridin
- triazolo
- trifluoromethoxy
- phenyl
- methyl
- 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.)
- Expired - Fee Related
Links
- 0 *c(cc1)ccc1C(C(*)=C(*)C1=NN2*)=C(*)N1C2=O Chemical compound *c(cc1)ccc1C(C(*)=C(*)C1=NN2*)=C(*)N1C2=O 0.000 description 2
- LOZNQJGOYFAIMZ-UHFFFAOYSA-N COc(cc(c(Cl)c1)Cl)c1OCC(CN1N=C(C=CC(c2ccc(C(F)(F)F)cc2)=C2)N2C1=O)O Chemical compound COc(cc(c(Cl)c1)Cl)c1OCC(CN1N=C(C=CC(c2ccc(C(F)(F)F)cc2)=C2)N2C1=O)O LOZNQJGOYFAIMZ-UHFFFAOYSA-N 0.000 description 2
- WVTQLJBWCSRDMW-UHFFFAOYSA-N CC(C)Oc(cccc1)c1OCC(CN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O)O Chemical compound CC(C)Oc(cccc1)c1OCC(CN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O)O WVTQLJBWCSRDMW-UHFFFAOYSA-N 0.000 description 1
- RXDTZKUGJLWLJC-UHFFFAOYSA-N CC(OCc1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1)=O Chemical compound CC(OCc1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1)=O RXDTZKUGJLWLJC-UHFFFAOYSA-N 0.000 description 1
- CSOAIKTXKJYPAL-UHFFFAOYSA-N CC(c1nc(C)n[o]1)N1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O Chemical compound CC(c1nc(C)n[o]1)N1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O CSOAIKTXKJYPAL-UHFFFAOYSA-N 0.000 description 1
- MJKBHISAVSPHNM-UHFFFAOYSA-N CCOc(cccc1)c1OCc1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1 Chemical compound CCOc(cccc1)c1OCc1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1 MJKBHISAVSPHNM-UHFFFAOYSA-N 0.000 description 1
- MHMIMAVFPOBQAN-UHFFFAOYSA-N CN(C(CN1)[Br]=C)NC1=O Chemical compound CN(C(CN1)[Br]=C)NC1=O MHMIMAVFPOBQAN-UHFFFAOYSA-N 0.000 description 1
- FXEVEXAZTVDNCC-UHFFFAOYSA-N COCc1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1 Chemical compound COCc1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1 FXEVEXAZTVDNCC-UHFFFAOYSA-N 0.000 description 1
- HAAFFTHBNFBVKY-UHFFFAOYSA-N COc(cc(c(Cl)c1)Cl)c1O Chemical compound COc(cc(c(Cl)c1)Cl)c1O HAAFFTHBNFBVKY-UHFFFAOYSA-N 0.000 description 1
- GKAJUYNXBRLXRT-UHFFFAOYSA-N COc(cc(c(Cl)c1)Cl)c1OCC1OC1 Chemical compound COc(cc(c(Cl)c1)Cl)c1OCC1OC1 GKAJUYNXBRLXRT-UHFFFAOYSA-N 0.000 description 1
- SXPRBFVBXBOHMC-UHFFFAOYSA-N COc(cc(cc1)F)c1OCCCN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O Chemical compound COc(cc(cc1)F)c1OCCCN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O SXPRBFVBXBOHMC-UHFFFAOYSA-N 0.000 description 1
- QCHBVKBITVXFML-UHFFFAOYSA-N COc(cccc1)c1-c1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1 Chemical compound COc(cccc1)c1-c1nc(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)n[o]1 QCHBVKBITVXFML-UHFFFAOYSA-N 0.000 description 1
- WNCIIWSWCMIMQU-UHFFFAOYSA-N Cc(cc1)ccc1OCCN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O Chemical compound Cc(cc1)ccc1OCCN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O WNCIIWSWCMIMQU-UHFFFAOYSA-N 0.000 description 1
- UTIFATCBAZTAGS-UHFFFAOYSA-N Cc1n[o]c(CN(C2=O)N=C(C=C3)N2C(C)=C3c(cc2)ccc2OC(F)(F)F)n1 Chemical compound Cc1n[o]c(CN(C2=O)N=C(C=C3)N2C(C)=C3c(cc2)ccc2OC(F)(F)F)n1 UTIFATCBAZTAGS-UHFFFAOYSA-N 0.000 description 1
- LVIVCBYJGVUQAJ-UHFFFAOYSA-N Cc1n[o]nc1CN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O Chemical compound Cc1n[o]nc1CN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O LVIVCBYJGVUQAJ-UHFFFAOYSA-N 0.000 description 1
- SQZWPCQKGINHDT-UHFFFAOYSA-N Cc1nc(CN2N=C(C=CC(c(cc3)ccc3Oc(cc3)ccc3Cl)=C3)N3C2=O)n[o]1 Chemical compound Cc1nc(CN2N=C(C=CC(c(cc3)ccc3Oc(cc3)ccc3Cl)=C3)N3C2=O)n[o]1 SQZWPCQKGINHDT-UHFFFAOYSA-N 0.000 description 1
- CPZBZRZORXDGGZ-UHFFFAOYSA-N Cc1nc(CN2N=C(C=CC(c3ccc(C(F)(F)F)cc3)=C3)N3C2=O)n[o]1 Chemical compound Cc1nc(CN2N=C(C=CC(c3ccc(C(F)(F)F)cc3)=C3)N3C2=O)n[o]1 CPZBZRZORXDGGZ-UHFFFAOYSA-N 0.000 description 1
- KWNBHJZWBRZVEO-UHFFFAOYSA-N Cc1nc(ccc(OCC(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)O)c2)c2[s]1 Chemical compound Cc1nc(ccc(OCC(CN2N=C(C=CC(c(cc3)ccc3OC(F)(F)F)=C3)N3C2=O)O)c2)c2[s]1 KWNBHJZWBRZVEO-UHFFFAOYSA-N 0.000 description 1
- KEJHEWPVIDRSDW-UHFFFAOYSA-N Cc1nccnc1CCN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O Chemical compound Cc1nccnc1CCN1N=C(C=CC(c(cc2)ccc2OC(F)(F)F)=C2)N2C1=O KEJHEWPVIDRSDW-UHFFFAOYSA-N 0.000 description 1
- VBSBEBORTDSJNK-UHFFFAOYSA-N N=C(C=C1)N(CN=O)C=C1c1ccc(C(F)(F)F)cc1 Chemical compound N=C(C=C1)N(CN=O)C=C1c1ccc(C(F)(F)F)cc1 VBSBEBORTDSJNK-UHFFFAOYSA-N 0.000 description 1
- QOIYCDICXKRPQE-UHFFFAOYSA-N N=C(C=CC(c(cc1)ccc1OC(F)(F)F)=C1)N1C(NCc1nc(C2CC2)c[o]1)=O Chemical compound N=C(C=CC(c(cc1)ccc1OC(F)(F)F)=C1)N1C(NCc1nc(C2CC2)c[o]1)=O QOIYCDICXKRPQE-UHFFFAOYSA-N 0.000 description 1
- QYQLEYTXFMOLEI-UHFFFAOYSA-N NNc(nc1)ccc1Br Chemical compound NNc(nc1)ccc1Br QYQLEYTXFMOLEI-UHFFFAOYSA-N 0.000 description 1
- GPVLBTKDPJWJQG-UHFFFAOYSA-N O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1CCCOc1c(C(F)(F)F)cccc1 Chemical compound O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1CCCOc1c(C(F)(F)F)cccc1 GPVLBTKDPJWJQG-UHFFFAOYSA-N 0.000 description 1
- OMPOZZVWEMYHAA-UHFFFAOYSA-N O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1CCOc(nc1N(C2)CC2(F)F)ncc1F Chemical compound O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1CCOc(nc1N(C2)CC2(F)F)ncc1F OMPOZZVWEMYHAA-UHFFFAOYSA-N 0.000 description 1
- WTMKJIOBWCFNNX-UHFFFAOYSA-N O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1CCc(cc1)ccc1F Chemical compound O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1CCc(cc1)ccc1F WTMKJIOBWCFNNX-UHFFFAOYSA-N 0.000 description 1
- IISQOFPCGIIYLN-UHFFFAOYSA-N O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1Cc1nc(-c2ccccc2Cl)n[o]1 Chemical compound O=C1N(C=C(C=C2)c(cc3)ccc3OC(F)(F)F)C2=NN1Cc1nc(-c2ccccc2Cl)n[o]1 IISQOFPCGIIYLN-UHFFFAOYSA-N 0.000 description 1
- FHOXTMMDQPXGEB-UHFFFAOYSA-N O=C1N(C=C(C=C2)c3ccc(C(F)(F)F)cc3)C2=NN1 Chemical compound O=C1N(C=C(C=C2)c3ccc(C(F)(F)F)cc3)C2=NN1 FHOXTMMDQPXGEB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
-
- 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
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- 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
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- 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]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36105610P | 2010-07-02 | 2010-07-02 | |
| US61/361,056 | 2010-07-02 | ||
| PCT/US2011/042700 WO2012003392A1 (en) | 2010-07-02 | 2011-06-30 | Fused heterocyclic compounds as ion channel modulators |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20130043158A KR20130043158A (ko) | 2013-04-29 |
| KR101911560B1 true KR101911560B1 (ko) | 2018-10-24 |
Family
ID=44338422
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137001153A Expired - Fee Related KR101911560B1 (ko) | 2010-07-02 | 2011-06-30 | 이온 채널 조정제로서의 융합된 헤테로시클릭 화합물 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US8703759B2 (enExample) |
| EP (1) | EP2588197B1 (enExample) |
| JP (2) | JP5858586B2 (enExample) |
| KR (1) | KR101911560B1 (enExample) |
| CN (1) | CN103096977B (enExample) |
| AU (1) | AU2011272787B2 (enExample) |
| BR (1) | BR112012033402A2 (enExample) |
| CA (1) | CA2802288C (enExample) |
| EA (1) | EA026385B9 (enExample) |
| ES (1) | ES2529119T3 (enExample) |
| IL (1) | IL223724A (enExample) |
| MX (1) | MX2012015096A (enExample) |
| NZ (1) | NZ604478A (enExample) |
| PT (1) | PT2588197E (enExample) |
| TW (1) | TWI537266B (enExample) |
| WO (1) | WO2012003392A1 (enExample) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SMT201700456T1 (it) | 2009-07-27 | 2017-11-15 | Gilead Sciences Inc | Composti eterociclici fusi come modulatori dei canali ionici |
| JP5858586B2 (ja) | 2010-07-02 | 2016-02-10 | ギリアード サイエンシーズ, インコーポレイテッド | イオンチャネルモジュレーターとしての縮合複素環式化合物 |
| TWI577670B (zh) | 2011-05-10 | 2017-04-11 | 基利科學股份有限公司 | 充當離子通道調節劑之稠合雜環化合物 |
| TWI478908B (zh) | 2011-07-01 | 2015-04-01 | Gilead Sciences Inc | 作為離子通道調節劑之稠合雜環化合物 |
| NO3175985T3 (enExample) | 2011-07-01 | 2018-04-28 | ||
| US9266881B2 (en) * | 2011-11-14 | 2016-02-23 | Merck Sharp & Dohme Corp. | Triazolopyridinone PDE10 inhibitors |
| US20150045305A1 (en) | 2012-01-27 | 2015-02-12 | Gilead Sciences, Inc. | Combination therapies using late sodium ion channel blockers and potassium ion channel blockers |
| HK1213476A1 (zh) * | 2013-03-14 | 2016-07-08 | 基因泰克公司 | 取代的三唑並吡啶及其使用方法 |
| ME03654B (me) | 2014-02-13 | 2020-07-20 | Incyte Corp | Ciklopropilamini kao lsd1 inhibitori |
| TW201613860A (en) | 2014-02-13 | 2016-04-16 | Incyte Corp | Cyclopropylamines as LSD1 inhibitors |
| PT3105226T (pt) | 2014-02-13 | 2019-11-06 | Incyte Corp | Ciclopropilaminas como inibidores de lsd1 |
| WO2015123437A1 (en) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| EP3159341B8 (en) * | 2014-06-17 | 2020-01-08 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Pyridino[1,2-a]pyrimidone analogue used as pi3k inhibitor |
| WO2016007727A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
| TW201613925A (en) | 2014-07-10 | 2016-04-16 | Incyte Corp | Imidazopyrazines as LSD1 inhibitors |
| WO2016007731A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Imidazopyridines and imidazopyrazines as lsd1 inhibitors |
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Also Published As
| Publication number | Publication date |
|---|---|
| US20150080370A1 (en) | 2015-03-19 |
| AU2011272787B2 (en) | 2015-06-18 |
| TWI537266B (zh) | 2016-06-11 |
| CA2802288A1 (en) | 2012-01-05 |
| HK1184092A1 (en) | 2014-01-17 |
| US8703759B2 (en) | 2014-04-22 |
| MX2012015096A (es) | 2013-05-28 |
| EA201291272A1 (ru) | 2013-12-30 |
| AU2011272787A1 (en) | 2013-01-10 |
| BR112012033402A2 (pt) | 2017-01-24 |
| WO2012003392A1 (en) | 2012-01-05 |
| ES2529119T3 (es) | 2015-02-17 |
| IL223724A (en) | 2016-06-30 |
| US20120010192A1 (en) | 2012-01-12 |
| US9079901B2 (en) | 2015-07-14 |
| JP2013535423A (ja) | 2013-09-12 |
| EP2588197B1 (en) | 2014-11-05 |
| CA2802288C (en) | 2018-08-21 |
| TW201215608A (en) | 2012-04-16 |
| JP5858586B2 (ja) | 2016-02-10 |
| JP2016029107A (ja) | 2016-03-03 |
| EP2588197A1 (en) | 2013-05-08 |
| KR20130043158A (ko) | 2013-04-29 |
| EA026385B9 (ru) | 2017-08-31 |
| NZ604478A (en) | 2014-12-24 |
| CN103096977B (zh) | 2017-02-15 |
| CN103096977A (zh) | 2013-05-08 |
| EA026385B1 (ru) | 2017-04-28 |
| PT2588197E (pt) | 2015-02-09 |
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