ES2574277T3 - Derivados de dibenzotiazepina y su uso en el tratamiento de trastornos del SNC - Google Patents
Derivados de dibenzotiazepina y su uso en el tratamiento de trastornos del SNC Download PDFInfo
- Publication number
- ES2574277T3 ES2574277T3 ES12720266.1T ES12720266T ES2574277T3 ES 2574277 T3 ES2574277 T3 ES 2574277T3 ES 12720266 T ES12720266 T ES 12720266T ES 2574277 T3 ES2574277 T3 ES 2574277T3
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- alkyl
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- 150000003839 salts Chemical class 0.000 claims abstract description 37
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- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 210000000225 synapse Anatomy 0.000 description 1
- 230000000946 synaptic effect Effects 0.000 description 1
- 230000009782 synaptic response Effects 0.000 description 1
- 229960001967 tacrolimus Drugs 0.000 description 1
- QJJXYPPXXYFBGM-SHYZHZOCSA-N tacrolimus Natural products CO[C@H]1C[C@H](CC[C@@H]1O)C=C(C)[C@H]2OC(=O)[C@H]3CCCCN3C(=O)C(=O)[C@@]4(O)O[C@@H]([C@H](C[C@H]4C)OC)[C@@H](C[C@H](C)CC(=C[C@@H](CC=C)C(=O)C[C@H](O)[C@H]2C)C)OC QJJXYPPXXYFBGM-SHYZHZOCSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- MHXBHWLGRWOABW-UHFFFAOYSA-N tetradecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC MHXBHWLGRWOABW-UHFFFAOYSA-N 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- LERNTVKEWCAPOY-DZZGSBJMSA-N tiotropium Chemical compound O([C@H]1C[C@@H]2[N+]([C@H](C1)[C@@H]1[C@H]2O1)(C)C)C(=O)C(O)(C=1SC=CC=1)C1=CC=CS1 LERNTVKEWCAPOY-DZZGSBJMSA-N 0.000 description 1
- 229940110309 tiotropium Drugs 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 125000004665 trialkylsilyl group Chemical group 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
-
- 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
-
- 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
- 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
- A61P17/00—Drugs for dermatological disorders
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D281/12—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D281/14—[b, e]-condensed
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1106520.8A GB201106520D0 (en) | 2011-04-18 | 2011-04-18 | Pharmaceutical compounds |
| GB201106520 | 2011-04-18 | ||
| GB201113163 | 2011-08-01 | ||
| GBGB1113163.8A GB201113163D0 (en) | 2011-04-18 | 2011-08-01 | Pharmaceutical compounds |
| PCT/GB2012/050831 WO2012143703A1 (en) | 2011-04-18 | 2012-04-16 | Dibenzothiazepine derivatives and their use in the treatment of cns disorders |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2574277T3 true ES2574277T3 (es) | 2016-06-16 |
Family
ID=44147160
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12720266.1T Active ES2574277T3 (es) | 2011-04-18 | 2012-04-16 | Derivados de dibenzotiazepina y su uso en el tratamiento de trastornos del SNC |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US9487492B2 (enExample) |
| EP (1) | EP2699559B1 (enExample) |
| JP (1) | JP6030120B2 (enExample) |
| CN (1) | CN103717583B (enExample) |
| CA (1) | CA2833320C (enExample) |
| DK (1) | DK2699559T3 (enExample) |
| ES (1) | ES2574277T3 (enExample) |
| GB (2) | GB201106520D0 (enExample) |
| WO (1) | WO2012143703A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6557674B2 (ja) * | 2014-03-12 | 2019-08-07 | ザ・トラスティーズ・オブ・コランビア・ユニバーシティー・イン・ザ・シティー・オブ・ニューヨーク | 新規クラスのミュー−オピオイド受容体アゴニスト |
| CN108135866A (zh) | 2015-09-16 | 2018-06-08 | 哥伦比亚大学董事会 | 羧基二芳基硫氮杂胺作为μ-阿片受体激动剂 |
| GB201517133D0 (en) * | 2015-09-28 | 2015-11-11 | Numedicus Ltd | New pharmaceutical use |
| EP4143189A1 (en) | 2020-04-30 | 2023-03-08 | Gilead Sciences, Inc. | Macrocyclic inhibitors of peptidylarginine deiminases |
| US20240092802A1 (en) * | 2020-10-06 | 2024-03-21 | Kures, Inc. | Mu-opioid receptor agonists and uses therefor |
| US20230365519A1 (en) * | 2020-10-06 | 2023-11-16 | Kures, Inc. | Carboxylic diarylthiazepineamines and uses thereof |
| CN118598743A (zh) * | 2024-05-29 | 2024-09-06 | 康龙化成手性医药技术(宁波)有限公司 | 一种2,2-二甲基环丁烷甲酸的合成方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1269551A (en) | 1969-03-27 | 1972-04-06 | Science Union & Cie | New tricyclic derivatives and process for their manufacture |
| US3872102A (en) * | 1971-11-04 | 1975-03-18 | En Nom Collectif Science Union | Tricyclic compounds of aliphatic w-amino alcohols |
| WO2001004106A1 (en) * | 1999-07-09 | 2001-01-18 | Ube Industries, Ltd. | Process for producing dibenzothiazepine derivatives |
| CN1913900B (zh) * | 2003-12-22 | 2010-11-24 | 阿卡蒂亚药品公司 | 作为毒蕈碱激动剂的氨基取代的二芳基[a，d]环庚烯类似物及神经精神疾病的治疗方法 |
| US20050227961A1 (en) * | 2004-04-08 | 2005-10-13 | Vela Pharmaceuticals, Inc. | Compositions and methods for treatment of neuropathic pain, fibromyalgia and chronic fatigue syndrome |
| CN101351210A (zh) * | 2005-01-07 | 2009-01-21 | 阿斯利康公司 | 11－哌嗪－1－基二苯并[b,f][l,4]硫氮杂卓或其药学上可接受的盐的新用途及其用于口服药物组合物的新用途 |
| EP1752143A1 (en) * | 2005-08-08 | 2007-02-14 | NewThera | Novel uses for drugs targeting glutamine synthetase |
| JP5219465B2 (ja) * | 2006-11-10 | 2013-06-26 | 大塚製薬株式会社 | 医薬 |
| US9314469B2 (en) | 2008-05-05 | 2016-04-19 | Tonix Pharma Holdings Limited | Method for treating neurocognitive dysfunction |
| WO2010070667A2 (en) | 2008-11-19 | 2010-06-24 | Biophore India Pharmaceuticals Pvt. Ltd. | Novel process for the preparation of 7-((3-chloro-6-methyl-5,5-dioxo-6,11-dihydrodibenzo(c,f)(1,2) thiazepin-11-yl)amino)heptanoate |
-
2011
- 2011-04-18 GB GBGB1106520.8A patent/GB201106520D0/en not_active Ceased
- 2011-08-01 GB GBGB1113163.8A patent/GB201113163D0/en not_active Ceased
-
2012
- 2012-04-16 ES ES12720266.1T patent/ES2574277T3/es active Active
- 2012-04-16 WO PCT/GB2012/050831 patent/WO2012143703A1/en not_active Ceased
- 2012-04-16 DK DK12720266.1T patent/DK2699559T3/en active
- 2012-04-16 EP EP12720266.1A patent/EP2699559B1/en active Active
- 2012-04-16 JP JP2014505712A patent/JP6030120B2/ja active Active
- 2012-04-16 CA CA2833320A patent/CA2833320C/en active Active
- 2012-04-16 CN CN201280023906.4A patent/CN103717583B/zh active Active
- 2012-04-16 US US14/112,499 patent/US9487492B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US20140243317A1 (en) | 2014-08-28 |
| CN103717583B (zh) | 2016-02-10 |
| CA2833320C (en) | 2019-05-21 |
| WO2012143703A1 (en) | 2012-10-26 |
| GB201106520D0 (en) | 2011-06-01 |
| CN103717583A (zh) | 2014-04-09 |
| DK2699559T3 (en) | 2016-07-04 |
| EP2699559A1 (en) | 2014-02-26 |
| US9487492B2 (en) | 2016-11-08 |
| EP2699559B1 (en) | 2016-04-06 |
| JP6030120B2 (ja) | 2016-11-24 |
| GB201113163D0 (en) | 2011-09-14 |
| CA2833320A1 (en) | 2012-10-26 |
| JP2014511897A (ja) | 2014-05-19 |
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