JP2003507421A5 - - Google Patents
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- Publication number
- JP2003507421A5 JP2003507421A5 JP2001518042A JP2001518042A JP2003507421A5 JP 2003507421 A5 JP2003507421 A5 JP 2003507421A5 JP 2001518042 A JP2001518042 A JP 2001518042A JP 2001518042 A JP2001518042 A JP 2001518042A JP 2003507421 A5 JP2003507421 A5 JP 2003507421A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- tramadol
- cyclohexanol
- dimethylamino
- 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.)
- Granted
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- 239000008194 pharmaceutical composition Substances 0.000 description 32
- TVYLLZQTGLZFBW-ZBFHGGJFSA-N (R,R)-tramadol Chemical compound COC1=CC=CC([C@]2(O)[C@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-ZBFHGGJFSA-N 0.000 description 21
- TVYLLZQTGLZFBW-GOEBONIOSA-N tramadol Natural products COC1=CC=CC([C@@]2(O)[C@@H](CCCC2)CN(C)C)=C1 TVYLLZQTGLZFBW-GOEBONIOSA-N 0.000 description 19
- 229960004380 tramadol Drugs 0.000 description 17
- 239000000126 substance Substances 0.000 description 16
- 239000000203 mixture Substances 0.000 description 13
- 230000001773 anti-convulsant effect Effects 0.000 description 10
- 239000001961 anticonvulsive agent Substances 0.000 description 10
- 229960003965 antiepileptics Drugs 0.000 description 10
- UGJMXCAKCUNAIE-UHFFFAOYSA-N Gabapentin Chemical compound OC(=O)CC1(CN)CCCCC1 UGJMXCAKCUNAIE-UHFFFAOYSA-N 0.000 description 8
- -1 N-oxide derivatives of (1R, 2R) -2-[(dimethylamino) methyl] -1- (3-methoxyphenyl) -cyclohexanol Chemical class 0.000 description 6
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical compound N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 5
- KJADKKWYZYXHBB-XBWDGYHZSA-N Topiramic acid Chemical group C1O[C@@]2(COS(N)(=O)=O)OC(C)(C)O[C@H]2[C@@H]2OC(C)(C)O[C@@H]21 KJADKKWYZYXHBB-XBWDGYHZSA-N 0.000 description 5
- OLBWFRRUHYQABZ-MRVPVSSYSA-N carisbamate Chemical compound NC(=O)OC[C@@H](O)C1=CC=CC=C1Cl OLBWFRRUHYQABZ-MRVPVSSYSA-N 0.000 description 5
- 229960004394 topiramate Drugs 0.000 description 5
- 229960002870 gabapentin Drugs 0.000 description 4
- PYZRQGJRPPTADH-UHFFFAOYSA-N lamotrigine Chemical compound NC1=NC(N)=NN=C1C1=CC=CC(Cl)=C1Cl PYZRQGJRPPTADH-UHFFFAOYSA-N 0.000 description 4
- 229960001848 lamotrigine Drugs 0.000 description 4
- 229960002036 phenytoin Drugs 0.000 description 4
- PPKXEPBICJTCRU-XMZRARIVSA-N (R,R)-tramadol hydrochloride Chemical group Cl.COC1=CC=CC([C@]2(O)[C@H](CCCC2)CN(C)C)=C1 PPKXEPBICJTCRU-XMZRARIVSA-N 0.000 description 3
- UWJUQVWARXYRCG-HIFRSBDPSA-N O-Desmethyltramadol Chemical group CN(C)C[C@H]1CCCC[C@]1(O)C1=CC=CC(O)=C1 UWJUQVWARXYRCG-HIFRSBDPSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- DXASQZJWWGZNSF-UHFFFAOYSA-N n,n-dimethylmethanamine;sulfur trioxide Chemical group CN(C)C.O=S(=O)=O DXASQZJWWGZNSF-UHFFFAOYSA-N 0.000 description 3
- 229960003107 tramadol hydrochloride Drugs 0.000 description 3
- NIJJYAXOARWZEE-UHFFFAOYSA-N di-n-propyl-acetic acid Natural products CCCC(C(O)=O)CCC NIJJYAXOARWZEE-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- SSJXIUAHEKJCMH-WDSKDSINSA-N (1s,2s)-cyclohexane-1,2-diamine Chemical compound N[C@H]1CCCC[C@@H]1N SSJXIUAHEKJCMH-WDSKDSINSA-N 0.000 description 1
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1h-1,2-benzodiazepine Chemical compound N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FWJKNZONDWOGMI-UHFFFAOYSA-N Metharbital Chemical compound CCC1(CC)C(=O)NC(=O)N(C)C1=O FWJKNZONDWOGMI-UHFFFAOYSA-N 0.000 description 1
- AJXPJJZHWIXJCJ-UHFFFAOYSA-N Methsuximide Chemical compound O=C1N(C)C(=O)CC1(C)C1=CC=CC=C1 AJXPJJZHWIXJCJ-UHFFFAOYSA-N 0.000 description 1
- 150000001204 N-oxides Chemical class 0.000 description 1
- VQASKUSHBVDKGU-UHFFFAOYSA-N Paramethadione Chemical compound CCC1(C)OC(=O)N(C)C1=O VQASKUSHBVDKGU-UHFFFAOYSA-N 0.000 description 1
- BZKPWHYZMXOIDC-UHFFFAOYSA-N acetazolamide Chemical compound CC(=O)NC1=NN=C(S(N)(=O)=O)S1 BZKPWHYZMXOIDC-UHFFFAOYSA-N 0.000 description 1
- 229960000571 acetazolamide Drugs 0.000 description 1
- 229940049706 benzodiazepine Drugs 0.000 description 1
- 229960000623 carbamazepine Drugs 0.000 description 1
- FFGPTBGBLSHEPO-UHFFFAOYSA-N carbamazepine Chemical compound C1=CC2=CC=CC=C2N(C(=O)N)C2=CC=CC=C21 FFGPTBGBLSHEPO-UHFFFAOYSA-N 0.000 description 1
- 229960001403 clobazam Drugs 0.000 description 1
- CXOXHMZGEKVPMT-UHFFFAOYSA-N clobazam Chemical compound O=C1CC(=O)N(C)C2=CC=C(Cl)C=C2N1C1=CC=CC=C1 CXOXHMZGEKVPMT-UHFFFAOYSA-N 0.000 description 1
- 229960003120 clonazepam Drugs 0.000 description 1
- DGBIGWXXNGSACT-UHFFFAOYSA-N clonazepam Chemical compound C12=CC([N+](=O)[O-])=CC=C2NC(=O)CN=C1C1=CC=CC=C1Cl DGBIGWXXNGSACT-UHFFFAOYSA-N 0.000 description 1
- 229940064790 dilantin Drugs 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 229960002767 ethosuximide Drugs 0.000 description 1
- HAPOVYFOVVWLRS-UHFFFAOYSA-N ethosuximide Chemical compound CCC1(C)CC(=O)NC1=O HAPOVYFOVVWLRS-UHFFFAOYSA-N 0.000 description 1
- 229960001596 famotidine Drugs 0.000 description 1
- XUFQPHANEAPEMJ-UHFFFAOYSA-N famotidine Chemical compound NC(N)=NC1=NC(CSCCC(N)=NS(N)(=O)=O)=CS1 XUFQPHANEAPEMJ-UHFFFAOYSA-N 0.000 description 1
- 229940098829 magnesium sulfate injection Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229960000906 mephenytoin Drugs 0.000 description 1
- GMHKMTDVRCWUDX-UHFFFAOYSA-N mephenytoin Chemical compound C=1C=CC=CC=1C1(CC)NC(=O)N(C)C1=O GMHKMTDVRCWUDX-UHFFFAOYSA-N 0.000 description 1
- 229960003729 mesuximide Drugs 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229960002057 metharbital Drugs 0.000 description 1
- 230000000926 neurological effect Effects 0.000 description 1
- 229960003274 paramethadione Drugs 0.000 description 1
- 229960002695 phenobarbital Drugs 0.000 description 1
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229960001233 pregabalin Drugs 0.000 description 1
- AYXYPKUFHZROOJ-ZETCQYMHSA-N pregabalin Chemical compound CC(C)C[C@H](CN)CC(O)=O AYXYPKUFHZROOJ-ZETCQYMHSA-N 0.000 description 1
- DQMZLTXERSFNPB-UHFFFAOYSA-N primidone Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NCNC1=O DQMZLTXERSFNPB-UHFFFAOYSA-N 0.000 description 1
- 229960002393 primidone Drugs 0.000 description 1
- IBALRBWGSVJPAP-HEHNFIMWSA-N progabide Chemical compound C=1C(F)=CC=C(O)C=1C(=N/CCCC(=O)N)/C1=CC=C(Cl)C=C1 IBALRBWGSVJPAP-HEHNFIMWSA-N 0.000 description 1
- 229960002752 progabide Drugs 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- AEQFSUDEHCCHBT-UHFFFAOYSA-M sodium valproate Chemical compound [Na+].CCCC(C([O-])=O)CCC AEQFSUDEHCCHBT-UHFFFAOYSA-M 0.000 description 1
- 229940084026 sodium valproate Drugs 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- MSRILKIQRXUYCT-UHFFFAOYSA-M valproate semisodium Chemical compound [Na+].CCCC(C(O)=O)CCC.CCCC(C([O-])=O)CCC MSRILKIQRXUYCT-UHFFFAOYSA-M 0.000 description 1
- 229960000604 valproic acid Drugs 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15020199P | 1999-08-20 | 1999-08-20 | |
| US60/150,201 | 1999-08-20 | ||
| PCT/US2000/021622 WO2001013904A2 (en) | 1999-08-20 | 2000-08-09 | Composition comprising a tramadol material and an anticonvulsant drug |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003507421A JP2003507421A (ja) | 2003-02-25 |
| JP2003507421A5 true JP2003507421A5 (https=) | 2007-09-27 |
| JP4977297B2 JP4977297B2 (ja) | 2012-07-18 |
Family
ID=22533492
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001518042A Expired - Lifetime JP4977297B2 (ja) | 1999-08-20 | 2000-08-09 | トラマドール物質及び抗痙攣薬を含んで成る組成物 |
Country Status (31)
| Country | Link |
|---|---|
| US (1) | US6562865B1 (https=) |
| EP (1) | EP1210118B1 (https=) |
| JP (1) | JP4977297B2 (https=) |
| KR (1) | KR100758609B1 (https=) |
| CN (1) | CN1198651C (https=) |
| AR (1) | AR032132A1 (https=) |
| AT (1) | ATE284223T1 (https=) |
| AU (1) | AU782759B2 (https=) |
| BG (1) | BG65996B1 (https=) |
| BR (1) | BRPI0013439B8 (https=) |
| CA (1) | CA2381797C (https=) |
| CO (1) | CO5190667A1 (https=) |
| CR (1) | CR6593A (https=) |
| CZ (1) | CZ2002524A3 (https=) |
| DE (1) | DE60016602T2 (https=) |
| EA (1) | EA006598B1 (https=) |
| ES (1) | ES2234651T3 (https=) |
| HU (1) | HUP0203198A3 (https=) |
| IL (2) | IL148019A0 (https=) |
| MX (1) | MXPA02001820A (https=) |
| MY (1) | MY136985A (https=) |
| NO (1) | NO332342B1 (https=) |
| NZ (1) | NZ517106A (https=) |
| PL (1) | PL213323B1 (https=) |
| PT (1) | PT1210118E (https=) |
| SK (1) | SK286621B6 (https=) |
| TR (1) | TR200201067T2 (https=) |
| TW (1) | TWI259769B (https=) |
| UA (1) | UA75868C2 (https=) |
| WO (1) | WO2001013904A2 (https=) |
| ZA (1) | ZA200201403B (https=) |
Families Citing this family (72)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100243956B1 (ko) | 1991-09-06 | 2000-03-02 | 랄프 알. 팔로 | 트라마돌 물질 및 아세트아미노펜을 포함하는 통증 치료용 약제학적 조성물 |
| US7164034B2 (en) | 1999-06-10 | 2007-01-16 | Pfizer Inc. | Alpha2delta ligands for fibromyalgia and other disorders |
| PL213323B1 (pl) | 1999-08-20 | 2013-02-28 | Ortho Mcneil Pharm Inc | Kompozycja farmaceutyczna i jej zastosowanie |
| DE19940740A1 (de) * | 1999-08-31 | 2001-03-01 | Gruenenthal Gmbh | Pharmazeutische Salze |
| DE10049483A1 (de) * | 2000-09-29 | 2002-05-02 | Gruenenthal Gmbh | Substituierte 1-Aminobutan-3-ol-Derivate |
| JP2005512965A (ja) * | 2001-09-24 | 2005-05-12 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 不穏四肢症候群および定期的四肢運動障害の処置に有用な抗痙攣誘導体 |
| US7790905B2 (en) | 2002-02-15 | 2010-09-07 | Mcneil-Ppc, Inc. | Pharmaceutical propylene glycol solvate compositions |
| US7927613B2 (en) | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
| RU2004126093A (ru) * | 2002-02-26 | 2005-04-10 | Орто-Макнейл Фармасьютикал, Инк. (Us) | Комбинированная терапия для лечения мигрени, включающая применение производных противосудорожных средств и средств от мигрени |
| AU2003213719A1 (en) | 2002-03-01 | 2003-09-16 | Regents Of The University Of Michigan | Multiple-component solid phases containing at least one active pharmaceutical ingredient |
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| DE102013009114A1 (de) * | 2013-05-29 | 2014-12-04 | Franz Gerstheimer | Pharmazeutische Zusammensetzung zur Überwindung von Metabolisierungsproblemen |
| WO2017118726A1 (en) | 2016-01-06 | 2017-07-13 | Lonza Ltd | Inhibition of protein degradation for improved production |
| US11464756B1 (en) | 2017-05-19 | 2022-10-11 | Jerry Darm | Mecuna pruriens, L-DOPA and 5-HTP based dietary supplements, pharmaceutical formulations and uses thereof |
| IL277402B1 (en) | 2018-03-20 | 2026-04-01 | Abraxis Bioscience Llc | Methods for treating central nervous system disorders using administration of MTOR inhibitor nanoparticles and albumin |
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| CN114096314A (zh) * | 2019-06-27 | 2022-02-25 | 沼泽敏彦 | 痴呆症的治疗和预防药 |
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| US3652589A (en) | 1967-07-27 | 1972-03-28 | Gruenenthal Chemie | 1-(m-substituted phenyl)-2-aminomethyl cyclohexanols |
| US3562589A (en) * | 1968-09-09 | 1971-02-09 | Ite Imperial Corp | Electrically resetting undervoltage trip for circuit breakers |
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| US4569937A (en) * | 1985-02-11 | 1986-02-11 | E. I. Du Pont De Nemours And Company | Analgesic mixture of oxycodone and ibuprofen |
| CA2077637C (en) | 1991-09-06 | 2007-01-09 | Robert B. Raffa | Compositions comprising a tramadol material and any of codeine, oxycodone or hydrocodone and their use |
| KR100243956B1 (ko) * | 1991-09-06 | 2000-03-02 | 랄프 알. 팔로 | 트라마돌 물질 및 아세트아미노펜을 포함하는 통증 치료용 약제학적 조성물 |
| US5516803A (en) | 1991-10-30 | 1996-05-14 | Mcneilab, Inc. | Composition comprising a tramadol material and a non-steroidal anti-inflammatory drug |
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| WO1998007447A1 (en) * | 1996-08-23 | 1998-02-26 | Algos Pharmaceutical Corporation | Anticonvulsant containing composition for treating neuropathic pain |
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| PL213323B1 (pl) | 1999-08-20 | 2013-02-28 | Ortho Mcneil Pharm Inc | Kompozycja farmaceutyczna i jej zastosowanie |
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- 2000-08-09 WO PCT/US2000/021622 patent/WO2001013904A2/en not_active Ceased
- 2000-08-09 DE DE60016602T patent/DE60016602T2/de not_active Expired - Lifetime
- 2000-08-09 CZ CZ2002524A patent/CZ2002524A3/cs unknown
- 2000-08-09 AT AT00957321T patent/ATE284223T1/de active
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- 2000-08-09 EA EA200200183A patent/EA006598B1/ru not_active IP Right Cessation
- 2000-08-09 AU AU68958/00A patent/AU782759B2/en not_active Expired
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- 2000-08-09 CA CA002381797A patent/CA2381797C/en not_active Expired - Fee Related
- 2000-08-09 SK SK226-2002A patent/SK286621B6/sk not_active IP Right Cessation
- 2000-08-09 CN CNB008144990A patent/CN1198651C/zh not_active Expired - Lifetime
- 2000-08-09 KR KR1020027002005A patent/KR100758609B1/ko not_active Expired - Lifetime
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