SU1450742A3 - Способ получени производных бензоатных эфиров 3-оксиморфинана - Google Patents
Способ получени производных бензоатных эфиров 3-оксиморфинана Download PDFInfo
- Publication number
- SU1450742A3 SU1450742A3 SU853920678A SU3920678A SU1450742A3 SU 1450742 A3 SU1450742 A3 SU 1450742A3 SU 853920678 A SU853920678 A SU 853920678A SU 3920678 A SU3920678 A SU 3920678A SU 1450742 A3 SU1450742 A3 SU 1450742A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dogs
- bioavailability
- base
- oxymorphinan
- cyclobutylmethyl
- Prior art date
Links
- -1 derivatives of benzoate ethers Chemical class 0.000 title claims abstract 4
- 238000000034 method Methods 0.000 title claims description 12
- 241000282472 Canis lupus familiaris Species 0.000 claims description 10
- NETZHAKZCGBWSS-CEDHKZHLSA-N nalbuphine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]1(O)CC[C@@H]3O)CN2CC1CCC1 NETZHAKZCGBWSS-CEDHKZHLSA-N 0.000 claims description 9
- 229960000805 nalbuphine Drugs 0.000 claims description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 6
- 241000124008 Mammalia Species 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 claims description 3
- 241000282693 Cercopithecidae Species 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 229960005181 morphine Drugs 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 claims 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 239000000010 aprotic solvent Substances 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- IYNWSQDZXMGGGI-NUEKZKHPSA-N 3-hydroxymorphinan Chemical class C1CCC[C@H]2[C@H]3CC4=CC=C(O)C=C4[C@]21CCN3 IYNWSQDZXMGGGI-NUEKZKHPSA-N 0.000 abstract description 3
- 229940035676 analgesics Drugs 0.000 abstract description 2
- 239000000730 antalgic agent Substances 0.000 abstract description 2
- 239000003887 narcotic antagonist Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 description 18
- 229940079593 drug Drugs 0.000 description 17
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 241000700159 Rattus Species 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000005557 antagonist Substances 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000282412 Homo Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000556 agonist Substances 0.000 description 2
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 2
- UZHSEJADLWPNLE-GRGSLBFTSA-N naloxone Chemical compound O=C([C@@H]1O2)CC[C@@]3(O)[C@H]4CC5=CC=C(O)C2=C5[C@@]13CCN4CC=C UZHSEJADLWPNLE-GRGSLBFTSA-N 0.000 description 2
- 229960004127 naloxone Drugs 0.000 description 2
- DQCKKXVULJGBQN-XFWGSAIBSA-N naltrexone Chemical compound N1([C@@H]2CC3=CC=C(C=4O[C@@H]5[C@](C3=4)([C@]2(CCC5=O)O)CC1)O)CC1CC1 DQCKKXVULJGBQN-XFWGSAIBSA-N 0.000 description 2
- 229960003086 naltrexone Drugs 0.000 description 2
- 238000009101 premedication Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- RMRJXGBAOAMLHD-IHFGGWKQSA-N buprenorphine Chemical compound C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]11CC[C@]3([C@H](C1)[C@](C)(O)C(C)(C)C)OC)CN2CC1CC1 RMRJXGBAOAMLHD-IHFGGWKQSA-N 0.000 description 1
- 229960001736 buprenorphine Drugs 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D489/00—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
- C07D489/06—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with a hetero atom directly attached in position 14
- C07D489/08—Oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/22—Bridged ring systems
- C07D221/28—Morphinans
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D489/00—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
- C07D489/02—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with oxygen atoms attached in positions 3 and 6, e.g. morphine, morphinone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62792384A | 1984-07-05 | 1984-07-05 | |
| US06/733,464 US4668685A (en) | 1984-07-05 | 1985-05-14 | Substituted benzoate ester prodrug derivatives of 3-hydroxymorphinans, which are analgesics or narcotic antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1450742A3 true SU1450742A3 (ru) | 1989-01-07 |
Family
ID=27090564
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU853920678A SU1450742A3 (ru) | 1984-07-05 | 1985-07-04 | Способ получени производных бензоатных эфиров 3-оксиморфинана |
| SU874202841A SU1508960A3 (ru) | 1984-07-05 | 1987-07-03 | Способ получени производных бензоатных эфиров 3-оксиморфинанов |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU874202841A SU1508960A3 (ru) | 1984-07-05 | 1987-07-03 | Способ получени производных бензоатных эфиров 3-оксиморфинанов |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4668685A (enExample) |
| EP (1) | EP0170090B1 (enExample) |
| AU (1) | AU578391B2 (enExample) |
| CA (1) | CA1301150C (enExample) |
| DE (1) | DE3573251D1 (enExample) |
| DK (1) | DK160501C (enExample) |
| ES (1) | ES8704443A1 (enExample) |
| FI (1) | FI83215C (enExample) |
| GR (1) | GR851653B (enExample) |
| HK (1) | HK39790A (enExample) |
| HU (1) | HU193995B (enExample) |
| IE (1) | IE58136B1 (enExample) |
| IL (1) | IL75721A (enExample) |
| MX (1) | MX160445A (enExample) |
| NO (1) | NO171209C (enExample) |
| NZ (1) | NZ212641A (enExample) |
| PT (1) | PT80773B (enExample) |
| SU (2) | SU1450742A3 (enExample) |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4673679A (en) * | 1986-05-14 | 1987-06-16 | E. I. Du Pont De Nemours And Company | Use of prodrugs of 3-hydroxymorphinans to prevent bitter taste upon buccal, nasal or sublingual administration |
| DK107688D0 (da) * | 1988-03-01 | 1988-03-01 | Novo Industri As | Carbaminsyreestere af substituerede 7-hydroxy-2,3,4,5-tetrahydro-1h-3-benzazepiner |
| US6702705B1 (en) | 1988-05-04 | 2004-03-09 | Igen International, Inc. | Prodrugs activated by targeted catalytic proteins |
| DK24089D0 (da) * | 1989-01-20 | 1989-01-20 | Hans Bundgaard | Novel prodrug derivatives of biologically active agents containing hydroxyl groups or nh-acidic groups |
| US6258360B1 (en) * | 1989-05-04 | 2001-07-10 | Igen International, Inc. | Prodrugs activated by targeted catalytic proteins |
| AU673335B2 (en) * | 1991-08-05 | 1996-11-07 | Igen, Inc. | Prodrugs activated by targeted catalytic proteins |
| US5968551A (en) * | 1991-12-24 | 1999-10-19 | Purdue Pharma L.P. | Orally administrable opioid formulations having extended duration of effect |
| US6323212B1 (en) * | 1992-01-23 | 2001-11-27 | Toray Industries, Inc. | Morphinan derivative and its pharmaceutical applications |
| TW372972B (en) * | 1992-10-23 | 1999-11-01 | Novartis Ag | Antiretroviral acyl compounds |
| EP0615756B1 (en) * | 1993-03-15 | 2001-06-27 | National Science Council | Nalbuphine esters and long-acting pharmaceutical compositions containing them |
| JP3843456B2 (ja) * | 1993-07-23 | 2006-11-08 | 東レ株式会社 | モルヒナン誘導体および医薬用途 |
| US5376662A (en) * | 1993-12-08 | 1994-12-27 | Ockert; David M. | Method of attenuating nerve injury induced pain |
| US5869669A (en) * | 1996-07-26 | 1999-02-09 | Penick Corporation | Preparation of 14-hydroxynormorphinones from normorphinone dienol acylates |
| US6225321B1 (en) * | 1997-06-05 | 2001-05-01 | Oliver Yoa-Pu Hu | Long analgesic acting nalbuphine polyester derivative and method of use |
| US6375957B1 (en) | 1997-12-22 | 2002-04-23 | Euro-Celtique, S.A. | Opioid agonist/opioid antagonist/acetaminophen combinations |
| PT1685839E (pt) | 1997-12-22 | 2013-07-08 | Euro Celtique Sa | Forma de dosagem farmacêutica por via oral compreendendo uma combinação de um agonista opióide e de um antagonista opióide |
| ATE233264T1 (de) * | 2000-04-27 | 2003-03-15 | Oliver Yoa-Pu Hu | Polynalbuphinderivat |
| US6569449B1 (en) | 2000-11-13 | 2003-05-27 | University Of Kentucky Research Foundation | Transdermal delivery of opioid antagonist prodrugs |
| DE60238756D1 (de) | 2001-05-11 | 2011-02-10 | Endo Pharmaceuticals Inc | Opioid enthaltende arzneiform gegen missbrauch |
| JP4559730B2 (ja) * | 2001-08-23 | 2010-10-13 | ナームローゼ・フエンノートチヤツプ・オルガノン | １４−ヒドロキシノルモルフィノン誘導体の調製方法。 |
| US20040033253A1 (en) * | 2002-02-19 | 2004-02-19 | Ihor Shevchuk | Acyl opioid antagonists |
| PT2425824T (pt) | 2002-04-05 | 2017-08-23 | Mundipharma Farmacêutica Lda | Preparação farmacêutica contendo oxicodona e naloxona |
| US20040202717A1 (en) | 2003-04-08 | 2004-10-14 | Mehta Atul M. | Abuse-resistant oral dosage forms and method of use thereof |
| US20080020028A1 (en) * | 2003-08-20 | 2008-01-24 | Euro-Celtique S.A. | Transdermal dosage form comprising an active agent and a salt and a free-base form of an adverse agent |
| EP1604666A1 (en) * | 2004-06-08 | 2005-12-14 | Euro-Celtique S.A. | Opioids for the treatment of the Chronic Obstructive Pulmonary Disease (COPD) |
| EP1604667A1 (en) * | 2004-06-08 | 2005-12-14 | Euro-Celtique S.A. | Opioids for the treatment of the restless leg syndrome |
| JP2008514612A (ja) * | 2004-09-23 | 2008-05-08 | ミシャロウ、アレクサンダー | 対抗適応を誘発することにより神経伝達物質系を調節する方法 |
| US20080045610A1 (en) * | 2004-09-23 | 2008-02-21 | Alexander Michalow | Methods for regulating neurotransmitter systems by inducing counteradaptations |
| EP3228308A1 (en) * | 2005-01-28 | 2017-10-11 | Euro-Celtique S.A. | Alcohol resistant dosage forms |
| EP1695700A1 (en) * | 2005-02-28 | 2006-08-30 | Euro-Celtique S.A. | Dosage form containing oxycodone and naloxone |
| EP1702558A1 (en) * | 2005-02-28 | 2006-09-20 | Euro-Celtique S.A. | Method and device for the assessment of bowel function |
| WO2006126529A1 (ja) * | 2005-05-25 | 2006-11-30 | Shionogi & Co., Ltd. | ６，７－不飽和－７－カルバモイル置換モルヒナン誘導体 |
| EP1928881A2 (en) | 2005-08-19 | 2008-06-11 | Pharmacofore, Inc. | Prodrugs of active agents |
| GB0606124D0 (en) * | 2006-03-28 | 2006-05-03 | Reckitt Benckiser Healthcare | Buprenorphine derivatives and uses thereof |
| US8178551B2 (en) * | 2007-03-09 | 2012-05-15 | Green Cross Corporation | Orally bioavailable prodrugs of (+)-3-hydroxymorphinan for Parkinson'S disease prevention or treatment |
| MX2011000155A (es) * | 2008-07-07 | 2011-03-01 | Euro Celtique Sa | Uso de antagonistas opioides para el tratamiento de retencion urinaria. |
| ME03298B (me) | 2009-03-10 | 2019-07-20 | Euro Celtique Sa | Farmaceutske kombinacije sa trenutnim oslobađanjem које obuhvataju oksikodon i nalokson |
| US10849981B2 (en) | 2009-07-02 | 2020-12-01 | KemPham, Inc. | Benzoic acid, benzoic acid derivatives and heteroaryl carboxylic acid conjugates of hydrocodone, prodrugs, methods of making and use thereof |
| UA102916C2 (uk) | 2009-07-02 | 2013-08-27 | Кемфарм, Інк. | Композиція на основі кон'югату гідрокодону з бензойною кислотою, похідними бензойної кислоти або гетероарилкарбоновою кислотою, проліки, спосіб лікування від зловживань |
| WO2011008636A1 (en) * | 2009-07-15 | 2011-01-20 | Mallinckrodt Inc. | 3-oxy-hydromorphone derivatives |
| RU2643807C1 (ru) | 2010-11-12 | 2018-02-06 | Сионоги Энд Ко., Лтд. | Кристаллы производных 6,7-ненасыщенного-7-карбамоилморфинана и способ их получения |
| PH12014500791A1 (en) | 2011-10-26 | 2022-12-02 | Kempharm Inc | Benzoic acid, benzoic acid derivatives and heteroaryl carboxylic acid conjugates of hydromorphone, prodrugs, methods of making and use thereof |
| CN105517551A (zh) | 2013-07-23 | 2016-04-20 | 欧洲凯尔特公司 | 用于在患有疼痛和导致肠生态失调和/或提高肠细菌移位风险之疾病的患者中治疗疼痛的羟考酮与纳洛酮的组合 |
| SG11201704178UA (en) | 2014-11-25 | 2017-06-29 | Kempharm Inc | Benzoic acid, benzoic acid derivatives and heteroaryl carboxylic acid conjugates of oxycodone |
| MX2017006935A (es) | 2014-12-02 | 2017-08-10 | Kempharm Inc * | Acido benzoico, derivados de acido benzoico y conjugados de acido heteroaril carboxilico de oximorfona, profarmacos, metodos de elaboracion y uso de los mismos. |
| US10155771B2 (en) * | 2015-11-04 | 2018-12-18 | Noramco, Inc. | Selective reduction of morphinan alkaloids |
| US10799496B2 (en) | 2018-07-13 | 2020-10-13 | Alkermes Pharma Ireland Limited | Naphthylenyl compounds for long-acting injectable compositions and related methods |
| WO2020012245A1 (en) | 2018-07-13 | 2020-01-16 | Alkermes Pharma Ireland Limited | Thienothiophene-naltrexone prodrugs for long-acting injectable compositions |
| US11186585B2 (en) | 2018-08-17 | 2021-11-30 | Kappa-Pharma LLC | Compositions and methods of enhancing opioid receptor engagement by opioid hexadienoates and optionally substituted hexadienoates |
| US10975099B2 (en) | 2018-11-05 | 2021-04-13 | Alkermes Pharma Ireland Limited | Thiophene compounds for long-acting injectable compositions and related methods |
| CA3149152A1 (en) | 2019-08-11 | 2021-02-18 | Kappa-Pharma LLC | Compositions and methods of enhancing opioid receptor engagement by opioid hexadienoates and optionally substituted hexadienoates |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE224197C (enExample) * | ||||
| US3254088A (en) * | 1961-03-14 | 1966-05-31 | Lewenstein | Morphine derivative |
| FR1602610A (en) * | 1962-10-10 | 1971-01-04 | 10.10.62.-17.4.63. 38445-15209 thebaine derivs | |
| US3332950A (en) * | 1963-03-23 | 1967-07-25 | Endo Lab | 14-hydroxydihydronormorphinone derivatives |
| IL26896A (en) * | 1966-01-19 | 1970-11-30 | Endo Lab | 14 - Hydroxynormorphinins and 14 - Hydroxynormorphinones |
| GB1097167A (en) * | 1966-05-31 | 1967-12-29 | Shionogi & Co | 3-hydroxy-6-oxo-n-phenethylmorphinan compounds and their production |
| CH543514A (de) * | 1967-08-25 | 1973-10-31 | Hoffmann La Roche | Verfahren zur Herstellung von Morphinanderivaten |
| US3654280A (en) * | 1968-03-21 | 1972-04-04 | Shionogi & Co | L-n allylic-3-hydroxy-6-oxomorphinans |
| DE2323192A1 (de) * | 1972-05-10 | 1973-12-13 | Endo Lab | Injizierbare, langwirkende antagonistpraeparate gegen narkotika und rauschgifte |
| US4161597A (en) * | 1976-12-20 | 1979-07-17 | Research Corporation | N-alkyl-14-hydroxymorphinans and derivatives |
| JPS59184182A (ja) * | 1983-04-02 | 1984-10-19 | Res Inst For Prod Dev | ３−ベンゾイルチオ−４、５α−エポキシ−７α−〔１（Ｒ）−ヒドロキシ−１−メチルベンチル〕−６−メトキシ−１７−メチル−６、１４−エンド−エタノモルヒナン |
| JPS59184163A (ja) * | 1983-04-02 | 1984-10-19 | Res Inst For Prod Dev | ３−ベンゾイルチオ−１７−メチルモルヒナン |
| JPS59184183A (ja) * | 1983-04-02 | 1984-10-19 | Res Inst For Prod Dev | ３−ベンゾイルチオ−４、５α−エポキシ−７α−〔１（Ｒ）−ヒドロキシ−１−メチルブチル〕−６−メトキシ−１７−メチル−６、１４−エンド−エテノモルヒナン |
| JPS59186987A (ja) * | 1983-04-06 | 1984-10-23 | Res Inst For Prod Dev | ３−ベンゾイルチオ−４、５α−エポキシ−７α−〔１（Ｒ）−ヒドロキシ−１−メチルブチル〕−６−メトキシ−１７−メチル−６、１４−エンド−エテノモルヒナン |
-
1985
- 1985-05-14 US US06/733,464 patent/US4668685A/en not_active Expired - Lifetime
- 1985-06-27 CA CA000485661A patent/CA1301150C/en not_active Expired - Lifetime
- 1985-07-03 EP EP85108258A patent/EP0170090B1/en not_active Expired
- 1985-07-03 DE DE8585108258T patent/DE3573251D1/de not_active Expired
- 1985-07-03 AU AU44516/85A patent/AU578391B2/en not_active Ceased
- 1985-07-04 IE IE168385A patent/IE58136B1/en not_active IP Right Cessation
- 1985-07-04 DK DK306885A patent/DK160501C/da not_active IP Right Cessation
- 1985-07-04 HU HU852607A patent/HU193995B/hu not_active IP Right Cessation
- 1985-07-04 SU SU853920678A patent/SU1450742A3/ru active
- 1985-07-04 NZ NZ212641A patent/NZ212641A/xx unknown
- 1985-07-04 IL IL75721A patent/IL75721A/xx not_active IP Right Cessation
- 1985-07-04 ES ES544852A patent/ES8704443A1/es not_active Expired
- 1985-07-04 NO NO852699A patent/NO171209C/no unknown
- 1985-07-04 PT PT80773A patent/PT80773B/pt not_active IP Right Cessation
- 1985-07-04 FI FI852659A patent/FI83215C/fi not_active IP Right Cessation
- 1985-07-04 GR GR851653A patent/GR851653B/el unknown
- 1985-07-05 MX MX6144A patent/MX160445A/es unknown
-
1987
- 1987-07-03 SU SU874202841A patent/SU1508960A3/ru active
-
1990
- 1990-05-24 HK HK397/90A patent/HK39790A/xx unknown
Non-Patent Citations (1)
| Title |
|---|
| Патент US № 3254088, - . .кл. 260-285, 1966. Патент DE № 2323192, кл. С 07 D 489/02, 1973. * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1301150C (en) | 1992-05-19 |
| FI83215C (fi) | 1991-06-10 |
| HUT40132A (en) | 1986-11-28 |
| PT80773B (pt) | 1987-10-20 |
| US4668685A (en) | 1987-05-26 |
| FI852659L (fi) | 1986-01-06 |
| ES544852A0 (es) | 1987-04-01 |
| SU1508960A3 (ru) | 1989-09-15 |
| IE58136B1 (en) | 1993-07-14 |
| HK39790A (en) | 1990-06-01 |
| ES8704443A1 (es) | 1987-04-01 |
| IL75721A (en) | 1990-04-29 |
| IL75721A0 (en) | 1985-11-29 |
| GR851653B (enExample) | 1985-11-26 |
| NZ212641A (en) | 1988-10-28 |
| DK306885A (da) | 1986-01-06 |
| FI83215B (fi) | 1991-02-28 |
| PT80773A (en) | 1985-08-01 |
| EP0170090A1 (en) | 1986-02-05 |
| AU578391B2 (en) | 1988-10-20 |
| DK306885D0 (da) | 1985-07-04 |
| NO852699L (no) | 1986-01-06 |
| HU193995B (en) | 1987-12-28 |
| EP0170090B1 (en) | 1989-09-27 |
| FI852659A0 (fi) | 1985-07-04 |
| AU4451685A (en) | 1986-01-09 |
| DK160501B (da) | 1991-03-18 |
| NO171209C (no) | 1993-02-10 |
| DE3573251D1 (en) | 1989-11-02 |
| IE851683L (en) | 1986-01-05 |
| DK160501C (da) | 1991-08-26 |
| MX160445A (es) | 1990-03-02 |
| NO171209B (no) | 1992-11-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU1450742A3 (ru) | Способ получени производных бензоатных эфиров 3-оксиморфинана | |
| Zimmerman et al. | Discovery of a potent, peripherally selective trans-3, 4-dimethyl-4-(3-hydroxyphenyl) piperidine opioid antagonist for the treatment of gastrointestinal motility disorders | |
| JP6947713B2 (ja) | 末梢オピオイド受容体アンタゴニストおよびその使用 | |
| TWI275591B (en) | Opiod and opioid-like coumpounds and uses thereof | |
| CN102325778B (zh) | 盐酸纳美芬二水合物 | |
| Carroll et al. | Optical isomers of aryl-2-piperidylmethanol antimalarial agents. Preparation, optical purity, and absolute stereochemistry | |
| BR112012000569B1 (pt) | composição compreendendo um conjugado de benzoatohidrocodona (bz-hc) e composições para administração oral e intravenosa compreendendo o mesmo | |
| BRPI0612922A2 (pt) | princìpio farmacêutico ativo canabinóide para formas farmacêuticas aperfeiçoadas | |
| TWI501969B (zh) | 丁基原啡因衍生物及其用途 | |
| CN112105602A (zh) | 基于喹啉和异喹啉的hdac抑制剂及其使用方法 | |
| US5750534A (en) | Nalbuphine esters having long acting analgesic action and method of use | |
| EP0615756B1 (en) | Nalbuphine esters and long-acting pharmaceutical compositions containing them | |
| CZ265798A3 (cs) | Morfinové a diamorfinové soli anionických nenarkotických analgetik typu substituovaných karboxylových kyselin, způsob jejich výroby, jejich použití a farmaceutické preparáty tyto soli obsahující | |
| US5298622A (en) | Spiroindane opiate analogs | |
| BR112013009505B1 (pt) | Composto, composição farmacêutica, métodos para ensaio quanto a um receptor, e, usos de um composto | |
| JP2938188B2 (ja) | 医薬としてのベンゾイルエクゴニン誘導体、エクゴニン誘導体、およびエクゴニジン誘導体 | |
| KR20150109456A (ko) | 프로토파녹사다이올 유도체 및 그의 제조방법과 용도 | |
| ES2357250T3 (es) | Composiciones que comprenden trans-(+/-)-delta-9-tetrahidrocannabinol cristalino. | |
| ES2311034T3 (es) | Derivados de indol y uso de los mismos en medicamentos. | |
| US5525613A (en) | Covalently coupled benzoylecgonine ecgonine and ecgonidine | |
| US6271239B1 (en) | Delta opioid receptor-selective benzylidene-substituted morphinans | |
| Frincke et al. | The major metabolite of fentanyl in the horse. | |
| JPWO2007072749A1 (ja) | 鎮咳剤 | |
| JP2000511916A (ja) | ポリオールスクシネートおよびその医薬製剤 | |
| EP3998256A1 (en) | Crystalline form of cxcr2 antagonist and application thereof |