CY1254A - Etomidate-containing compositions - Google Patents
Etomidate-containing compositions Download PDFInfo
- Publication number
- CY1254A CY1254A CY1254A CY125479A CY1254A CY 1254 A CY1254 A CY 1254A CY 1254 A CY1254 A CY 1254A CY 125479 A CY125479 A CY 125479A CY 1254 A CY1254 A CY 1254A
- Authority
- CY
- Cyprus
- Prior art keywords
- etomidate
- solution
- infusion liquid
- hydrochloride
- hydrobromide
- Prior art date
Links
- NPUKDXXFDDZOKR-LLVKDONJSA-N etomidate Chemical compound CCOC(=O)C1=CN=CN1[C@H](C)C1=CC=CC=C1 NPUKDXXFDDZOKR-LLVKDONJSA-N 0.000 title claims description 30
- 229960001690 etomidate Drugs 0.000 title claims description 30
- 239000000203 mixture Substances 0.000 title description 24
- 239000000243 solution Substances 0.000 claims description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- 239000003978 infusion fluid Substances 0.000 claims description 15
- 238000001990 intravenous administration Methods 0.000 claims description 12
- NCDXBSVHIGDPOE-RFVHGSKJSA-N ethyl 3-[(1r)-1-phenylethyl]imidazole-4-carboxylate;hydrochloride Chemical compound Cl.CCOC(=O)C1=CN=CN1[C@H](C)C1=CC=CC=C1 NCDXBSVHIGDPOE-RFVHGSKJSA-N 0.000 claims description 10
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- 239000003708 ampul Substances 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- 238000010790 dilution Methods 0.000 claims 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000002609 medium Substances 0.000 description 8
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 239000003814 drug Substances 0.000 description 6
- 239000008103 glucose Substances 0.000 description 6
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 5
- 238000001802 infusion Methods 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- YCUUCSZGTWIJDW-RFVHGSKJSA-N ethyl 3-[(1r)-1-phenylethyl]imidazole-4-carboxylate;sulfuric acid Chemical compound OS(O)(=O)=O.CCOC(=O)C1=CN=CN1[C@H](C)C1=CC=CC=C1 YCUUCSZGTWIJDW-RFVHGSKJSA-N 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 230000003444 anaesthetic effect Effects 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical compound FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 description 1
- 229960003132 halothane Drugs 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003326 hypnotic agent Substances 0.000 description 1
- 230000000147 hypnotic effect Effects 0.000 description 1
- 229940124327 inhalation anaesthetic agent Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Anesthesiology (AREA)
- Dermatology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94223678A | 1978-09-14 | 1978-09-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY1254A true CY1254A (en) | 1984-08-31 |
Family
ID=25477775
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY1254A CY1254A (en) | 1978-09-14 | 1979-07-27 | Etomidate-containing compositions |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US4289783A (cs) |
| JP (1) | JPS5547858A (cs) |
| BE (1) | BE878709A (cs) |
| CA (1) | CA1140048A (cs) |
| CH (1) | CH651752A5 (cs) |
| CY (1) | CY1254A (cs) |
| DE (1) | DE2937290A1 (cs) |
| DK (1) | DK154926C (cs) |
| ES (1) | ES484160A1 (cs) |
| FR (1) | FR2435945A1 (cs) |
| GB (1) | GB2029700B (cs) |
| GR (1) | GR64915B (cs) |
| HK (1) | HK80984A (cs) |
| HU (1) | HU179989B (cs) |
| IE (1) | IE48689B1 (cs) |
| IT (1) | IT1120537B (cs) |
| KE (1) | KE3426A (cs) |
| NL (1) | NL7906835A (cs) |
| SE (1) | SE447961B (cs) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ225045A (en) * | 1987-07-01 | 1990-06-26 | Janssen Pharmaceutica Nv | Antiviral pharmaceutical compositions containing cyclodextrin and an antiviral agent |
| DE19709704C2 (de) | 1997-03-10 | 1999-11-04 | Michael Georgieff | Verwendung einer flüssigen Präparation von Xenon zur intravenösen Verabreichung bei Einleitung und/oder Aufrechterhaltung der Anaesthesie |
| WO2008112641A2 (en) * | 2007-03-09 | 2008-09-18 | New York University | Methods and compositions for treating thalamocortical dysrhythmia |
| AU2008340865B2 (en) | 2007-12-20 | 2014-01-23 | Acarix A/S | An adhesive patch for monitoring acoustic signals |
| EP3210976A1 (en) | 2008-03-31 | 2017-08-30 | The General Hospital Corporation | Etomidate analogues with improved pharmacokinetic and pharmacodynamic properties |
| BR112012000606A2 (pt) | 2009-07-10 | 2016-11-22 | Brigham & Womens Hospital | análogos de etomidato que não inibem a síntese de esteróides adrenocorticais |
| EA027976B1 (ru) | 2012-01-13 | 2017-09-29 | Дзе Дженерал Хоспитал Корпорейшн | Анестезирующие соединения и способы их применения |
| US20180022698A1 (en) | 2014-10-16 | 2018-01-25 | The Board Of Trustees Of The Leland Stanford Junior University | Novel methods, compounds, and compositions for anesthesia |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3354173A (en) * | 1964-04-16 | 1967-11-21 | Janssen Pharmaceutica Nv | Imidazole carboxylates |
-
1979
- 1979-07-23 GR GR59677A patent/GR64915B/el unknown
- 1979-07-27 CY CY1254A patent/CY1254A/en unknown
- 1979-07-27 GB GB7926364A patent/GB2029700B/en not_active Expired
- 1979-08-23 IT IT50093/79A patent/IT1120537B/it active
- 1979-09-05 CA CA000335043A patent/CA1140048A/en not_active Expired
- 1979-09-05 FR FR7922235A patent/FR2435945A1/fr active Granted
- 1979-09-11 BE BE0/197088A patent/BE878709A/nl not_active IP Right Cessation
- 1979-09-11 JP JP11579179A patent/JPS5547858A/ja active Granted
- 1979-09-13 DK DK384379A patent/DK154926C/da not_active IP Right Cessation
- 1979-09-13 ES ES484160A patent/ES484160A1/es not_active Expired
- 1979-09-13 SE SE7907621A patent/SE447961B/sv not_active IP Right Cessation
- 1979-09-13 HU HU79JA855A patent/HU179989B/hu not_active IP Right Cessation
- 1979-09-13 NL NL7906835A patent/NL7906835A/nl not_active Application Discontinuation
- 1979-09-13 IE IE1741/79A patent/IE48689B1/en not_active IP Right Cessation
- 1979-09-14 CH CH8358/79A patent/CH651752A5/de not_active IP Right Cessation
- 1979-09-14 DE DE19792937290 patent/DE2937290A1/de not_active Ceased
-
1980
- 1980-01-16 US US06/112,671 patent/US4289783A/en not_active Expired - Lifetime
-
1984
- 1984-07-20 KE KE3426A patent/KE3426A/xx unknown
- 1984-11-25 HK HK809/84A patent/HK80984A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DK154926C (da) | 1989-05-29 |
| GB2029700B (en) | 1983-03-30 |
| US4289783A (en) | 1981-09-15 |
| JPH0214058B2 (cs) | 1990-04-06 |
| GR64915B (en) | 1980-06-09 |
| KE3426A (en) | 1984-08-10 |
| DK384379A (da) | 1980-03-15 |
| DK154926B (da) | 1989-01-09 |
| IE48689B1 (en) | 1985-04-17 |
| DE2937290A1 (de) | 1980-04-03 |
| IT7950093A0 (it) | 1979-08-23 |
| FR2435945A1 (fr) | 1980-04-11 |
| HU179989B (en) | 1983-01-28 |
| FR2435945B1 (cs) | 1983-02-25 |
| HK80984A (en) | 1984-11-25 |
| NL7906835A (nl) | 1980-03-18 |
| ES484160A1 (es) | 1980-10-01 |
| BE878709A (nl) | 1980-03-11 |
| IE791741L (en) | 1980-03-14 |
| CH651752A5 (de) | 1985-10-15 |
| SE447961B (sv) | 1987-01-12 |
| SE7907621L (sv) | 1980-03-15 |
| CA1140048A (en) | 1983-01-25 |
| IT1120537B (it) | 1986-03-26 |
| JPS5547858A (en) | 1980-04-05 |
| GB2029700A (en) | 1980-03-26 |
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| PHILADELPHIA | I am indebted to Dr. Paul S. Pittenger for conducting the careful physiologic tests mentioned in these notes. | |
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