IL123916A - תולדות [(-3 אלקוקסי - פנאוקסי) - אתיל] דיאלקילאמין והשימוש בהן כמאלחשים מקומיים - Google Patents
תולדות [(-3 אלקוקסי - פנאוקסי) - אתיל] דיאלקילאמין והשימוש בהן כמאלחשים מקומייםInfo
- Publication number
- IL123916A IL123916A IL12391696A IL12391696A IL123916A IL 123916 A IL123916 A IL 123916A IL 12391696 A IL12391696 A IL 12391696A IL 12391696 A IL12391696 A IL 12391696A IL 123916 A IL123916 A IL 123916A
- Authority
- IL
- Israel
- Prior art keywords
- compound
- formula
- acceptable salt
- pharmaceutically acceptable
- compounds
- Prior art date
Links
- 229960005015 local anesthetics Drugs 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 58
- 150000003839 salts Chemical class 0.000 claims abstract description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 11
- 230000003444 anaesthetic effect Effects 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 230000000699 topical effect Effects 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 239000002671 adjuvant Substances 0.000 claims 1
- NUZYBIKIXLKGKN-UHFFFAOYSA-N n-methyl-n-[2-(3-propoxyphenoxy)ethyl]propan-2-amine Chemical compound CCCOC1=CC=CC(OCCN(C)C(C)C)=C1 NUZYBIKIXLKGKN-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000000203 mixture Substances 0.000 description 8
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- 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 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229940124326 anaesthetic agent Drugs 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 206010002091 Anaesthesia Diseases 0.000 description 2
- 241000700199 Cavia porcellus Species 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 206010028347 Muscle twitching Diseases 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000037005 anaesthesia Effects 0.000 description 2
- 238000001949 anaesthesia Methods 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000007429 general method Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- -1 methyl ethyl Chemical group 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 241000700198 Cavia Species 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000036592 analgesia Effects 0.000 description 1
- 230000001430 anti-depressive effect Effects 0.000 description 1
- 239000000935 antidepressant agent Substances 0.000 description 1
- 229940005513 antidepressants Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- UTLHDWFDWVOTBY-UHFFFAOYSA-N benzene-1,3-diol;ethanol Chemical compound CCO.OC1=CC=CC(O)=C1 UTLHDWFDWVOTBY-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000002951 depilatory effect Effects 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 208000020016 psychiatric disease Diseases 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
- C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
- C07C217/18—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted
- C07C217/20—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted by halogen atoms, by trihalomethyl, nitro or nitroso groups, or by singly-bound oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
- A61P23/02—Local anaesthetics
-
- 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]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Anesthesiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9503798A SE9503798D0 (sv) | 1995-10-27 | 1995-10-27 | New anaesthetic componds |
| SE9600329A SE9600329D0 (sv) | 1996-01-30 | 1996-01-30 | New anaesthetic compounds |
| PCT/SE1996/001361 WO1997015548A1 (en) | 1995-10-27 | 1996-10-23 | New [(3-alkoxy-phenoxy)-ethyl]-dialkylamine derivatives and their use as local anaesthetics |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL123916A true IL123916A (he) | 2001-10-31 |
Family
ID=26662410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL12391696A IL123916A (he) | 1995-10-27 | 1996-10-23 | תולדות [(-3 אלקוקסי - פנאוקסי) - אתיל] דיאלקילאמין והשימוש בהן כמאלחשים מקומיים |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US6310252B1 (he) |
| EP (1) | EP0858445B1 (he) |
| JP (1) | JP4101877B2 (he) |
| KR (1) | KR100460652B1 (he) |
| CN (1) | CN1113856C (he) |
| AR (1) | AR004691A1 (he) |
| AT (1) | ATE215061T1 (he) |
| AU (1) | AU704635B2 (he) |
| BR (1) | BR9611234A (he) |
| CA (1) | CA2233489C (he) |
| CZ (1) | CZ124198A3 (he) |
| DE (1) | DE69620213T2 (he) |
| DK (1) | DK0858445T3 (he) |
| EE (1) | EE03963B1 (he) |
| ES (1) | ES2174113T3 (he) |
| HU (1) | HUP9901212A3 (he) |
| IL (1) | IL123916A (he) |
| IS (1) | IS1932B (he) |
| MY (1) | MY132329A (he) |
| NO (1) | NO310614B1 (he) |
| NZ (1) | NZ320757A (he) |
| PL (1) | PL186783B1 (he) |
| PT (1) | PT858445E (he) |
| SI (1) | SI0858445T1 (he) |
| SK (1) | SK282757B6 (he) |
| TR (1) | TR199800714T2 (he) |
| TW (1) | TW448142B (he) |
| UA (1) | UA59347C2 (he) |
| WO (1) | WO1997015548A1 (he) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7799337B2 (en) | 1997-07-21 | 2010-09-21 | Levin Bruce H | Method for directed intranasal administration of a composition |
| US6432986B2 (en) | 1997-07-21 | 2002-08-13 | Bruce H. Levin | Compositions, kits, and methods for inhibiting cerebral neurovascular disorders and muscular headaches |
| SE9704031D0 (sv) * | 1997-11-05 | 1997-11-05 | Astra Ab | Novel formulation |
| SE9704770D0 (sv) * | 1997-12-19 | 1997-12-19 | Astra Ab | New use |
| SE9704834D0 (sv) * | 1997-12-22 | 1997-12-22 | Astra Ab | New process |
| SE9704835D0 (sv) | 1997-12-22 | 1997-12-22 | Astra Ab | New compound |
| JP2000302737A (ja) * | 1999-04-16 | 2000-10-31 | Shiseido Co Ltd | 二置換ベンゼン誘導体 |
| US8473062B2 (en) | 2008-05-01 | 2013-06-25 | Autonomic Technologies, Inc. | Method and device for the treatment of headache |
| US8412336B2 (en) | 2008-12-29 | 2013-04-02 | Autonomic Technologies, Inc. | Integrated delivery and visualization tool for a neuromodulation system |
| US9012477B2 (en) | 2009-01-06 | 2015-04-21 | Nuvo Research Inc. | Method of treating neuropathic pain |
| US8494641B2 (en) | 2009-04-22 | 2013-07-23 | Autonomic Technologies, Inc. | Implantable neurostimulator with integral hermetic electronic enclosure, circuit substrate, monolithic feed-through, lead assembly and anchoring mechanism |
| US9320908B2 (en) | 2009-01-15 | 2016-04-26 | Autonomic Technologies, Inc. | Approval per use implanted neurostimulator |
| CN102834096A (zh) | 2010-01-14 | 2012-12-19 | 卢福研究公司 | 用于疼痛控制的固态成型局部麻醉制剂 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1173136A (fr) | 1955-11-16 | 1959-02-20 | Rech S Et Tech Appliquees | Dérivés tertio-amino-alcoxylés du benzène et leur procédé de préparation |
| CH380746A (de) | 1958-11-06 | 1964-08-15 | Ciba Geigy | Verfahren zur Herstellung neuer sekundärer Amine |
| GB1027611A (en) * | 1962-01-04 | 1966-04-27 | May & Baker Ltd | Phenoxy- and phenylthio-alkylamines and acid addition salts thereof |
| US3205136A (en) | 1962-12-24 | 1965-09-07 | Smith Kline French Lab | Antidepressant phenyloxyalkylamines |
| DE3233828A1 (de) | 1982-09-11 | 1984-03-15 | Basf Ag, 6700 Ludwigshafen | Aryloxyalkylamine, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
-
1996
- 1996-10-14 AR ARP960104736A patent/AR004691A1/es unknown
- 1996-10-15 TW TW085112594A patent/TW448142B/zh not_active IP Right Cessation
- 1996-10-23 ES ES96935752T patent/ES2174113T3/es not_active Expired - Lifetime
- 1996-10-23 AT AT96935752T patent/ATE215061T1/de active
- 1996-10-23 IL IL12391696A patent/IL123916A/he not_active IP Right Cessation
- 1996-10-23 CA CA002233489A patent/CA2233489C/en not_active Expired - Fee Related
- 1996-10-23 WO PCT/SE1996/001361 patent/WO1997015548A1/en not_active Ceased
- 1996-10-23 CN CN96197845A patent/CN1113856C/zh not_active Expired - Fee Related
- 1996-10-23 AU AU73561/96A patent/AU704635B2/en not_active Ceased
- 1996-10-23 SK SK553-98A patent/SK282757B6/sk unknown
- 1996-10-23 TR TR1998/00714T patent/TR199800714T2/xx unknown
- 1996-10-23 US US08/776,620 patent/US6310252B1/en not_active Expired - Fee Related
- 1996-10-23 JP JP51653997A patent/JP4101877B2/ja not_active Expired - Fee Related
- 1996-10-23 KR KR10-1998-0703023A patent/KR100460652B1/ko not_active Expired - Fee Related
- 1996-10-23 SI SI9630469T patent/SI0858445T1/xx unknown
- 1996-10-23 HU HU9901212A patent/HUP9901212A3/hu unknown
- 1996-10-23 PL PL96326425A patent/PL186783B1/pl not_active IP Right Cessation
- 1996-10-23 PT PT96935752T patent/PT858445E/pt unknown
- 1996-10-23 UA UA98042083A patent/UA59347C2/uk unknown
- 1996-10-23 EE EE9800088A patent/EE03963B1/xx not_active IP Right Cessation
- 1996-10-23 EP EP96935752A patent/EP0858445B1/en not_active Expired - Lifetime
- 1996-10-23 CZ CZ981241A patent/CZ124198A3/cs unknown
- 1996-10-23 NZ NZ320757A patent/NZ320757A/xx not_active IP Right Cessation
- 1996-10-23 DK DK96935752T patent/DK0858445T3/da active
- 1996-10-23 DE DE69620213T patent/DE69620213T2/de not_active Expired - Lifetime
- 1996-10-23 BR BR9611234A patent/BR9611234A/pt not_active IP Right Cessation
- 1996-10-25 MY MYPI96004455A patent/MY132329A/en unknown
-
1998
- 1998-03-25 IS IS4702A patent/IS1932B/is unknown
- 1998-04-23 NO NO19981825A patent/NO310614B1/no not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| KB | Patent renewed | ||
| MM9K | Patent not in force due to non-payment of renewal fees |