SK280522B6 - Deriváty 2,3,4,5-tetrahydro-1,4-benzotiazepínov, s - Google Patents
Deriváty 2,3,4,5-tetrahydro-1,4-benzotiazepínov, s Download PDFInfo
- Publication number
- SK280522B6 SK280522B6 SK588-95A SK58895A SK280522B6 SK 280522 B6 SK280522 B6 SK 280522B6 SK 58895 A SK58895 A SK 58895A SK 280522 B6 SK280522 B6 SK 280522B6
- Authority
- SK
- Slovakia
- Prior art keywords
- tetrahydro
- benzothiazepine
- formula
- chloro
- group
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 171
- 238000002360 preparation method Methods 0.000 title claims abstract description 20
- 238000000034 method Methods 0.000 title claims abstract description 17
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 14
- SUBDEKBXSIKCSA-UHFFFAOYSA-N 2,3,4,5-tetrahydro-1,4-benzothiazepine Chemical class C1NCCSC2=CC=CC=C21 SUBDEKBXSIKCSA-UHFFFAOYSA-N 0.000 title claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 33
- 206010010904 Convulsion Diseases 0.000 claims abstract description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 13
- 238000011282 treatment Methods 0.000 claims abstract description 13
- 208000012902 Nervous system disease Diseases 0.000 claims abstract description 10
- 208000025966 Neurological disease Diseases 0.000 claims abstract description 10
- 206010015037 epilepsy Diseases 0.000 claims abstract description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 8
- 239000004090 neuroprotective agent Substances 0.000 claims abstract description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 56
- 239000001257 hydrogen Substances 0.000 claims description 55
- -1 imino, methylimino, phenylimino Chemical group 0.000 claims description 55
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 44
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 33
- 150000003839 salts Chemical class 0.000 claims description 30
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 29
- 150000002431 hydrogen Chemical class 0.000 claims description 25
- 125000005843 halogen group Chemical group 0.000 claims description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 12
- SGHFCTZTSKLZLQ-UHFFFAOYSA-N 6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine Chemical compound S1CCNCC2=C1C=CC=C2Cl SGHFCTZTSKLZLQ-UHFFFAOYSA-N 0.000 claims description 10
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 230000002829 reductive effect Effects 0.000 claims description 9
- BSCYHWYMSHHZLI-UHFFFAOYSA-N 1-(6-chloro-3,5-dihydro-2h-1,4-benzothiazepin-4-yl)ethanone Chemical compound C1N(C(=O)C)CCSC2=CC=CC(Cl)=C21 BSCYHWYMSHHZLI-UHFFFAOYSA-N 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 8
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 8
- 230000004224 protection Effects 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 6
- GQKWMROFTREIMB-UHFFFAOYSA-N 4-methylsulfonyl-3,5-dihydro-2h-1,4-benzothiazepine Chemical compound C1N(S(=O)(=O)C)CCSC2=CC=CC=C21 GQKWMROFTREIMB-UHFFFAOYSA-N 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 6
- NABPZJKIWLALLY-UHFFFAOYSA-N n-(6-chloro-2,5-dihydro-1,4-benzothiazepin-3-yl)hydroxylamine Chemical compound C1NC(=NO)CSC2=CC=CC(Cl)=C21 NABPZJKIWLALLY-UHFFFAOYSA-N 0.000 claims description 6
- DPMRVEKZRBXCIW-UHFFFAOYSA-N 6-chloro-4-methylsulfinyl-3,5-dihydro-2h-1,4-benzothiazepine Chemical compound C1N(S(=O)C)CCSC2=CC=CC(Cl)=C21 DPMRVEKZRBXCIW-UHFFFAOYSA-N 0.000 claims description 5
- 125000004423 acyloxy group Chemical group 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 5
- 150000002367 halogens Chemical group 0.000 claims description 5
- IYNOWXHALNJVTD-UHFFFAOYSA-N 6-chloro-2,3,4,5-tetrahydro-1$l^{4},4-benzothiazepine 1-oxide Chemical compound C1NCCS(=O)C2=C1C(Cl)=CC=C2 IYNOWXHALNJVTD-UHFFFAOYSA-N 0.000 claims description 4
- NTHZSPUSDHLYTG-UHFFFAOYSA-N 6-chloro-4-methylsulfonyl-3,5-dihydro-2h-1,4-benzothiazepine Chemical compound C1N(S(=O)(=O)C)CCSC2=CC=CC(Cl)=C21 NTHZSPUSDHLYTG-UHFFFAOYSA-N 0.000 claims description 4
- GAQRNLNAUIIXEZ-UHFFFAOYSA-N 6-chloro-n-phenyl-2,5-dihydro-1,4-benzothiazepin-3-amine Chemical compound N1CC=2C(Cl)=CC=CC=2SCC1=NC1=CC=CC=C1 GAQRNLNAUIIXEZ-UHFFFAOYSA-N 0.000 claims description 4
- YAZUSGHZMAPMQE-UHFFFAOYSA-N 6-fluoro-2,3,4,5-tetrahydro-1,4-benzothiazepine Chemical compound S1CCNCC2=C1C=CC=C2F YAZUSGHZMAPMQE-UHFFFAOYSA-N 0.000 claims description 4
- QKIVZDWLNQMALJ-UHFFFAOYSA-N 6-fluoro-4-methylsulfonyl-3,5-dihydro-2h-1,4-benzothiazepine Chemical compound C1N(S(=O)(=O)C)CCSC2=CC=CC(F)=C21 QKIVZDWLNQMALJ-UHFFFAOYSA-N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 claims description 4
- XSKMMXNLEXKYOY-UHFFFAOYSA-N n-(2,5-dihydro-1,4-benzothiazepin-3-yl)hydroxylamine Chemical compound C1NC(=NO)CSC2=CC=CC=C21 XSKMMXNLEXKYOY-UHFFFAOYSA-N 0.000 claims description 4
- UVLUXVGGWULYRA-UHFFFAOYSA-N (6-chloro-3,5-dihydro-2h-1,4-benzothiazepin-4-yl)-phenylmethanone Chemical compound C1C=2C(Cl)=CC=CC=2SCCN1C(=O)C1=CC=CC=C1 UVLUXVGGWULYRA-UHFFFAOYSA-N 0.000 claims description 3
- RCZYGXYJABXFPK-UHFFFAOYSA-N 1-(1-oxo-3,5-dihydro-2h-1$l^{4},4-benzothiazepin-4-yl)ethanone Chemical compound C1N(C(=O)C)CCS(=O)C2=CC=CC=C21 RCZYGXYJABXFPK-UHFFFAOYSA-N 0.000 claims description 3
- HEFUIQDDJAUWNE-UHFFFAOYSA-N 1-(6-chloro-3,5-dihydro-2h-1,4-benzothiazepin-4-yl)propan-1-one Chemical compound C1N(C(=O)CC)CCSC2=CC=CC(Cl)=C21 HEFUIQDDJAUWNE-UHFFFAOYSA-N 0.000 claims description 3
- AQEDFPDRXSRDPJ-UHFFFAOYSA-N 1-(6-fluoro-3,5-dihydro-2h-1,4-benzothiazepin-4-yl)ethanone Chemical compound C1N(C(=O)C)CCSC2=CC=CC(F)=C21 AQEDFPDRXSRDPJ-UHFFFAOYSA-N 0.000 claims description 3
- SKXSNICLTSJDDZ-UHFFFAOYSA-N 1-(6-methyl-3,5-dihydro-2h-1,4-benzothiazepin-4-yl)ethanone Chemical compound C1N(C(=O)C)CCSC2=CC=CC(C)=C21 SKXSNICLTSJDDZ-UHFFFAOYSA-N 0.000 claims description 3
- XRHNTUDLOFKUFB-UHFFFAOYSA-N 4-ethylsulfonyl-3,5-dihydro-2h-1,4-benzothiazepine Chemical compound C1N(S(=O)(=O)CC)CCSC2=CC=CC=C21 XRHNTUDLOFKUFB-UHFFFAOYSA-N 0.000 claims description 3
- MVONUVDATWXOLI-UHFFFAOYSA-N 4-methylsulfonyl-3,5-dihydro-2h-1$l^{4},4-benzothiazepine 1-oxide Chemical compound C1N(S(=O)(=O)C)CCS(=O)C2=CC=CC=C21 MVONUVDATWXOLI-UHFFFAOYSA-N 0.000 claims description 3
- VQGBJTNOBPJBCI-UHFFFAOYSA-N 6-chloro-4-ethylsulfonyl-3,5-dihydro-2h-1,4-benzothiazepine Chemical compound C1N(S(=O)(=O)CC)CCSC2=CC=CC(Cl)=C21 VQGBJTNOBPJBCI-UHFFFAOYSA-N 0.000 claims description 3
- YNEUTBJJWJUGNL-UHFFFAOYSA-N 6-chloro-4-methylsulfonyl-3,5-dihydro-2h-1$l^{4},4-benzothiazepine 1-oxide Chemical compound C1N(S(=O)(=O)C)CCS(=O)C2=CC=CC(Cl)=C21 YNEUTBJJWJUGNL-UHFFFAOYSA-N 0.000 claims description 3
- BJWRKQPKTFGOSR-UHFFFAOYSA-N 6-chloro-n-methoxy-2,5-dihydro-1,4-benzothiazepin-3-amine Chemical compound C1NC(=NOC)CSC2=CC=CC(Cl)=C21 BJWRKQPKTFGOSR-UHFFFAOYSA-N 0.000 claims description 3
- ZSOSRXSUDMSECL-UHFFFAOYSA-N 6-methyl-2,3,4,5-tetrahydro-1,4-benzothiazepine Chemical compound S1CCNCC2=C1C=CC=C2C ZSOSRXSUDMSECL-UHFFFAOYSA-N 0.000 claims description 3
- SAWVIKJOESZFIK-UHFFFAOYSA-N 6-methyl-4-methylsulfonyl-3,5-dihydro-2h-1,4-benzothiazepine Chemical compound S1CCN(S(C)(=O)=O)CC2=C1C=CC=C2C SAWVIKJOESZFIK-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- MRHCFUAGRDCRIP-UHFFFAOYSA-N n-methyl-2,5-dihydro-1,4-benzothiazepin-3-amine Chemical compound C1NC(=NC)CSC2=CC=CC=C21 MRHCFUAGRDCRIP-UHFFFAOYSA-N 0.000 claims description 3
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims description 2
- UREQFTSPNGUYSJ-UHFFFAOYSA-N 1-(3,5-dihydro-2h-1,4-benzothiazepin-4-yl)ethanone Chemical compound C1N(C(=O)C)CCSC2=CC=CC=C21 UREQFTSPNGUYSJ-UHFFFAOYSA-N 0.000 claims description 2
- ZTNADGMRKJZOJT-UHFFFAOYSA-N 1-(3,5-dihydro-2h-1,4-benzothiazepin-4-yl)propan-1-one Chemical compound C1N(C(=O)CC)CCSC2=CC=CC=C21 ZTNADGMRKJZOJT-UHFFFAOYSA-N 0.000 claims description 2
- PBUVSAUCKUNQRD-UHFFFAOYSA-N 1-(6-chloro-1-oxo-3,5-dihydro-2h-1$l^{4},4-benzothiazepin-4-yl)ethanone Chemical compound C1N(C(=O)C)CCS(=O)C2=CC=CC(Cl)=C21 PBUVSAUCKUNQRD-UHFFFAOYSA-N 0.000 claims description 2
- ISNYZTVJXZYPCX-UHFFFAOYSA-N 3,5-dihydro-2h-1,4-benzothiazepine-4-carbaldehyde Chemical compound C1N(C=O)CCSC2=CC=CC=C21 ISNYZTVJXZYPCX-UHFFFAOYSA-N 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 125000001589 carboacyl group Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- JPGSKUHVFVQTAA-UHFFFAOYSA-N n-methoxy-2,5-dihydro-1,4-benzothiazepin-3-amine Chemical compound C1NC(=NOC)CSC2=CC=CC=C21 JPGSKUHVFVQTAA-UHFFFAOYSA-N 0.000 claims description 2
- 230000004112 neuroprotection Effects 0.000 claims description 2
- FHGWEHGZBUBQKL-UHFFFAOYSA-N 1,2-benzothiazepine Chemical compound S1N=CC=CC2=CC=CC=C12 FHGWEHGZBUBQKL-UHFFFAOYSA-N 0.000 claims 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims 1
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- 230000002265 prevention Effects 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 5
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-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D281/02—Seven-membered rings
- C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D281/10—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Steroid Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB929223441A GB9223441D0 (en) | 1992-11-09 | 1992-11-09 | Therapeutic agents |
| GB929223443A GB9223443D0 (en) | 1992-11-09 | 1992-11-09 | Therapeutic agents |
| PCT/EP1993/003123 WO1994011360A1 (en) | 1992-11-09 | 1993-11-06 | 1,4-benzothiazepines useful as neurological agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK58895A3 SK58895A3 (en) | 1995-09-13 |
| SK280522B6 true SK280522B6 (sk) | 2000-03-13 |
Family
ID=26301938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK588-95A SK280522B6 (sk) | 1992-11-09 | 1993-11-06 | Deriváty 2,3,4,5-tetrahydro-1,4-benzotiazepínov, s |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US5580866A (cs) |
| EP (1) | EP0667866B1 (cs) |
| JP (1) | JPH08503202A (cs) |
| KR (1) | KR100313649B1 (cs) |
| AT (1) | ATE163927T1 (cs) |
| BG (1) | BG62519B1 (cs) |
| BR (1) | BR9307387A (cs) |
| CA (1) | CA2148584A1 (cs) |
| CZ (1) | CZ288595B6 (cs) |
| DE (1) | DE69317436T2 (cs) |
| DK (1) | DK0667866T3 (cs) |
| ES (1) | ES2113081T3 (cs) |
| FI (1) | FI952204A0 (cs) |
| GR (1) | GR3026386T3 (cs) |
| HU (1) | HUT71819A (cs) |
| NO (1) | NO304467B1 (cs) |
| NZ (1) | NZ257843A (cs) |
| PL (1) | PL179401B1 (cs) |
| RU (1) | RU2115650C1 (cs) |
| SK (1) | SK280522B6 (cs) |
| UA (1) | UA41342C2 (cs) |
| WO (1) | WO1994011360A1 (cs) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5939412A (en) * | 1992-06-26 | 1999-08-17 | Smithkline Beecham Corporation | Bicyclic fibrinogen antagonists |
| AU666318B2 (en) * | 1991-06-28 | 1996-02-08 | Smithkline Beecham Corporation | Bicyclic fibrinogen antagonists |
| MA23420A1 (fr) * | 1994-01-07 | 1995-10-01 | Smithkline Beecham Corp | Antagonistes bicycliques de fibrinogene. |
| US6458784B1 (en) | 1994-06-29 | 2002-10-01 | Smithkline Beecham Corporation | Vitronectin receptor antagonists |
| GB9506382D0 (en) * | 1995-03-29 | 1995-05-17 | Boots Co Plc | Pharmaceutical compositions |
| US5977101A (en) * | 1995-06-29 | 1999-11-02 | Smithkline Beecham Corporation | Benzimidazoles/Imidazoles Linked to a Fibrinogen Receptor Antagonist Template Having Vitronectin Receptor Antagonist Activity |
| ZA9610853B (en) | 1995-12-29 | 1998-04-06 | Smithkline Beecham Corp | Processes and intermediates for preparing pharmaceuticals. |
| GB9616279D0 (en) * | 1996-08-02 | 1996-09-11 | Knoll Ag | Chemical process |
| ATE242258T1 (de) * | 1997-03-14 | 2003-06-15 | Aventis Pharma Gmbh | Hypolipidemische 1,4-benzothiazepin-1,1-dioxide |
| GB9914745D0 (en) * | 1999-06-24 | 1999-08-25 | Knoll Ag | Therapeutic agents |
| GB9922271D0 (en) * | 1999-09-21 | 1999-11-17 | Zeneca Ltd | Formulation |
| US8022058B2 (en) | 2000-05-10 | 2011-09-20 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
| US7718644B2 (en) * | 2004-01-22 | 2010-05-18 | The Trustees Of Columbia University In The City Of New York | Anti-arrhythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) and uses thereof |
| US20040229781A1 (en) * | 2000-05-10 | 2004-11-18 | Marks Andrew Robert | Compounds and methods for treating and preventing exercise-induced cardiac arrhythmias |
| US7879840B2 (en) | 2005-08-25 | 2011-02-01 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
| US7393652B2 (en) | 2000-05-10 | 2008-07-01 | The Trustees Of Columbia University In The City Of New York | Methods for identifying a chemical compound that directly enhances binding of FKBP12.6 to PKA-phosphorylated type 2 ryanodine receptor (RyR2) |
| US7544678B2 (en) * | 2002-11-05 | 2009-06-09 | The Trustees Of Columbia University In The City Of New York | Anti-arrythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) |
| JP2007525165A (ja) | 2003-03-07 | 2007-09-06 | トラスティーズ・オブ・コロンビア・ユニバーシティ・イン・ザ・シティ・オブ・ニューヨーク | タイプ１ライアノジン受容体に基づく方法 |
| US8710045B2 (en) | 2004-01-22 | 2014-04-29 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the ryanodine receptors |
| US7704990B2 (en) | 2005-08-25 | 2010-04-27 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
| ATE536348T1 (de) | 2008-03-03 | 2011-12-15 | Armgo Pharma Inc | Verfahren zur herstellung von benzothiazepinen aus gamma-aminoalkylbenzolen |
| WO2013064231A1 (en) | 2011-10-31 | 2013-05-10 | Phenex Pharmaceuticals Ag | SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3) |
| EP2708535A1 (en) * | 2012-05-11 | 2014-03-19 | Les Laboratoires Servier | Agents for treating disorders involving modulation of ryanodine receptors |
| KR102157141B1 (ko) | 2018-11-27 | 2020-09-17 | 주식회사 파미니티 | 으아리 추출물을 유효 성분으로 포함하는 인지 기능 개선용 조성물 |
| KR102172916B1 (ko) | 2018-12-07 | 2020-11-02 | 주식회사 파미니티 | 실크 펩타이드 및 천연 추출물을 포함하는 인지 기능 개선용 조성물 |
| BR112023009303A2 (pt) * | 2020-11-17 | 2024-02-06 | Armgo Pharma Inc | Agentes para tratar distúrbios envolvendo receptores de rianodina |
| CN116887839A (zh) | 2021-01-08 | 2023-10-13 | 阿姆果制药有限公司 | 兰诺定受体调节剂的结晶形式及其用途 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3362962A (en) * | 1964-01-24 | 1968-01-09 | Hoffmann La Roche | Certain benzothiazepine derivatives |
| US3682962A (en) * | 1970-03-17 | 1972-08-08 | Sterling Drug Inc | 1-substituted-1,2,3,5-tetrahydro-4,1-benzothiozepines |
| EP0368063B1 (de) * | 1988-11-05 | 1992-06-10 | Bayer Ag | Verfahren zur Kernchlorierung von aromatischen Kohlenwasserstoffen |
| JP2703408B2 (ja) * | 1990-12-28 | 1998-01-26 | 麒麟麦酒株式会社 | １，４‐ベンゾチアゼピン誘導体 |
| GB9111376D0 (en) * | 1991-05-25 | 1991-07-17 | Boots Co Plc | Therapeutic agents |
| GB9203347D0 (en) * | 1992-02-17 | 1992-04-01 | Wellcome Found | Hypolipidaemic compounds |
-
1993
- 1993-11-06 AT AT94900113T patent/ATE163927T1/de not_active IP Right Cessation
- 1993-11-06 NZ NZ257843A patent/NZ257843A/en unknown
- 1993-11-06 CZ CZ19951176A patent/CZ288595B6/cs not_active IP Right Cessation
- 1993-11-06 US US08/424,464 patent/US5580866A/en not_active Expired - Fee Related
- 1993-11-06 UA UA95062705A patent/UA41342C2/uk unknown
- 1993-11-06 WO PCT/EP1993/003123 patent/WO1994011360A1/en active IP Right Grant
- 1993-11-06 KR KR1019950701831A patent/KR100313649B1/ko not_active Expired - Fee Related
- 1993-11-06 SK SK588-95A patent/SK280522B6/sk unknown
- 1993-11-06 JP JP6511695A patent/JPH08503202A/ja not_active Withdrawn
- 1993-11-06 BR BR9307387-9A patent/BR9307387A/pt not_active Application Discontinuation
- 1993-11-06 HU HU9501352A patent/HUT71819A/hu unknown
- 1993-11-06 PL PL93308757A patent/PL179401B1/pl unknown
- 1993-11-06 EP EP94900113A patent/EP0667866B1/en not_active Expired - Lifetime
- 1993-11-06 CA CA002148584A patent/CA2148584A1/en not_active Abandoned
- 1993-11-06 DE DE69317436T patent/DE69317436T2/de not_active Expired - Fee Related
- 1993-11-06 DK DK94900113.5T patent/DK0667866T3/da active
- 1993-11-06 ES ES94900113T patent/ES2113081T3/es not_active Expired - Lifetime
- 1993-11-06 RU RU95112484/04A patent/RU2115650C1/ru not_active IP Right Cessation
-
1995
- 1995-05-08 NO NO951797A patent/NO304467B1/no not_active IP Right Cessation
- 1995-05-08 FI FI952204A patent/FI952204A0/fi unknown
- 1995-05-30 BG BG99679A patent/BG62519B1/bg unknown
-
1998
- 1998-03-17 GR GR980400582T patent/GR3026386T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RU2115650C1 (ru) | 1998-07-20 |
| FI952204A7 (fi) | 1995-05-08 |
| KR100313649B1 (ko) | 2002-02-28 |
| RU95112484A (ru) | 1997-04-20 |
| BG99679A (bg) | 1996-04-30 |
| AU5464494A (en) | 1994-06-08 |
| NZ257843A (en) | 1996-10-28 |
| GR3026386T3 (en) | 1998-06-30 |
| CZ288595B6 (cs) | 2001-07-11 |
| NO951797D0 (no) | 1995-05-08 |
| NO304467B1 (no) | 1998-12-21 |
| ES2113081T3 (es) | 1998-04-16 |
| PL308757A1 (en) | 1995-08-21 |
| CZ117695A3 (en) | 1996-06-12 |
| HUT71819A (en) | 1996-02-28 |
| ATE163927T1 (de) | 1998-03-15 |
| NO951797L (no) | 1995-05-24 |
| BR9307387A (pt) | 1999-08-31 |
| HU9501352D0 (en) | 1995-06-28 |
| DK0667866T3 (da) | 1998-05-25 |
| EP0667866A1 (en) | 1995-08-23 |
| BG62519B1 (bg) | 2000-01-31 |
| US5580866A (en) | 1996-12-03 |
| FI952204A0 (fi) | 1995-05-08 |
| AU680639B2 (en) | 1997-08-07 |
| PL179401B1 (pl) | 2000-08-31 |
| DE69317436T2 (de) | 1998-07-02 |
| UA41342C2 (uk) | 2001-09-17 |
| CA2148584A1 (en) | 1994-05-26 |
| JPH08503202A (ja) | 1996-04-09 |
| SK58895A3 (en) | 1995-09-13 |
| EP0667866B1 (en) | 1998-03-11 |
| WO1994011360A1 (en) | 1994-05-26 |
| KR950704283A (ko) | 1995-11-17 |
| DE69317436D1 (de) | 1998-04-16 |
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