YU37001A - Analgesic drug combination - Google Patents
Analgesic drug combinationInfo
- Publication number
- YU37001A YU37001A YU37001A YU37001A YU37001A YU 37001 A YU37001 A YU 37001A YU 37001 A YU37001 A YU 37001A YU 37001 A YU37001 A YU 37001A YU 37001 A YU37001 A YU 37001A
- Authority
- YU
- Yugoslavia
- Prior art keywords
- compound
- methyl
- xanthine
- analgesic
- analgin
- Prior art date
Links
- 229940035676 analgesics Drugs 0.000 title 1
- 239000000730 antalgic agent Substances 0.000 title 1
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical group O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- YAPQBXQYLJRXSA-UHFFFAOYSA-N theobromine Chemical compound CN1C(=O)NC(=O)C2=C1N=CN2C YAPQBXQYLJRXSA-UHFFFAOYSA-N 0.000 abstract 4
- GMSNIKWWOQHZGF-UHFFFAOYSA-N 3-methyl-9H-xanthine Chemical compound O=C1NC(=O)N(C)C2=C1N=CN2 GMSNIKWWOQHZGF-UHFFFAOYSA-N 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 2
- 230000000202 analgesic effect Effects 0.000 abstract 2
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 abstract 2
- 229960001259 diclofenac Drugs 0.000 abstract 2
- DCOPUUMXTXDBNB-UHFFFAOYSA-N diclofenac Chemical compound OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl DCOPUUMXTXDBNB-UHFFFAOYSA-N 0.000 abstract 2
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 abstract 2
- DJGAAPFSPWAYTJ-UHFFFAOYSA-M metamizole sodium Chemical compound [Na+].O=C1C(N(CS([O-])(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 DJGAAPFSPWAYTJ-UHFFFAOYSA-M 0.000 abstract 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 abstract 2
- 229960004559 theobromine Drugs 0.000 abstract 2
- RYQVRAILJXPCMZ-UHFFFAOYSA-N 3-methyl-7-[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]purine-2,6-dione Chemical compound O1C(C)=NC(CN2C=3C(=O)NC(=O)N(C)C=3N=C2)=N1 RYQVRAILJXPCMZ-UHFFFAOYSA-N 0.000 abstract 1
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 abstract 1
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 abstract 1
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N Aminoantipyrine Natural products CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 abstract 1
- RMMXTBMQSGEXHJ-UHFFFAOYSA-N Aminophenazone Chemical compound O=C1C(N(C)C)=C(C)N(C)N1C1=CC=CC=C1 RMMXTBMQSGEXHJ-UHFFFAOYSA-N 0.000 abstract 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 abstract 1
- 229960000212 aminophenazone Drugs 0.000 abstract 1
- 239000000812 cholinergic antagonist Substances 0.000 abstract 1
- 229960004126 codeine Drugs 0.000 abstract 1
- HEFNNWSXXWATRW-JTQLQIEISA-N dexibuprofen Chemical compound CC(C)CC1=CC=C([C@H](C)C(O)=O)C=C1 HEFNNWSXXWATRW-JTQLQIEISA-N 0.000 abstract 1
- OMFNSKIUKYOYRG-MOSHPQCFSA-N drotaverine Chemical compound C1=C(OCC)C(OCC)=CC=C1\C=C/1C2=CC(OCC)=C(OCC)C=C2CCN\1 OMFNSKIUKYOYRG-MOSHPQCFSA-N 0.000 abstract 1
- 229960002065 drotaverine Drugs 0.000 abstract 1
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 abstract 1
- 229960001680 ibuprofen Drugs 0.000 abstract 1
- 229960000905 indomethacin Drugs 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229960005181 morphine Drugs 0.000 abstract 1
- 210000002460 smooth muscle Anatomy 0.000 abstract 1
- 230000002048 spasmolytic effect Effects 0.000 abstract 1
- 229940075420 xanthine Drugs 0.000 abstract 1
- -1 xanthine compound Chemical class 0.000 abstract 1
Classifications
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61K31/60—Salicylic acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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]
-
- 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]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
Abstract
Predmet pronalaska je farmaceutsko jedinjenje koje sadrži kao aktivni analgetički sastojak morfin, aminofenazon, analgin, acetil-salicilnu kiselinu, indometacin, ibuprofen, diklofenak ili kodein i kao jedinjenje ksantinske strukture 3-metilksantin, teobromin ili CH-13584 (1H-purin-2,6-dion-3,7-dihidro-3-metil-7/5-metil-1,2,4-oksadiazol-2-il/metil), gde je proporcija aktivnog sastojka i derivata ksantina (1-20):1, preporučljivo 10:1. Kao analgetičko jedinjenje preferentno se koristi analgin, S(+)ibuprofen, ili diklofenak, a kao jedinjenje ksantinske strukture preferiran je teobromin. Jedinjenja pronalaska mogu sadržati kao drugi aktivni sastojak spazmolitik glatke muskulature, preferentno drotaverin.The subject of the invention is a pharmaceutical compound which contains as active analgesic ingredient morphine, aminophenazone, analgin, acetyl-salicylic acid, indomethacin, ibuprofen, diclofenac or codeine and as a compound of xanthine structure 3-methylxanthine, theobromine or CH-13584 (1H-purine 6-dione-3,7-dihydro-3-methyl-7H-5-methyl-1,2,4-oxadiazol-2-yl / methyl), where the proportion of active ingredient and xanthine derivative (1-20): 1 , 10: 1 recommended. Analgin, S (+) ibuprofen, or diclofenac is preferably used as the analgesic compound, and theobromine is preferred as the xanthine compound. The compounds of the invention may contain as another active ingredient a spasmolytic smooth muscle, preferably drotaverine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU9802716A HUP9802716A3 (en) | 1998-11-25 | 1998-11-25 | Pharmaceutical composition of analgesic activity |
Publications (1)
Publication Number | Publication Date |
---|---|
YU37001A true YU37001A (en) | 2004-05-12 |
Family
ID=89997413
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
YU37001A YU37001A (en) | 1998-11-25 | 1999-11-23 | Analgesic drug combination |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP1131135A1 (en) |
AU (1) | AU1510200A (en) |
BG (1) | BG105616A (en) |
CZ (1) | CZ20011847A3 (en) |
EA (1) | EA004375B1 (en) |
EE (1) | EE200100281A (en) |
HR (1) | HRP20010403A2 (en) |
HU (1) | HUP9802716A3 (en) |
PL (1) | PL348631A1 (en) |
SK (1) | SK6872001A3 (en) |
WO (1) | WO2000030715A1 (en) |
YU (1) | YU37001A (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BG65576B1 (en) * | 2002-04-17 | 2009-01-30 | ПИРИМОВА Румяна | Composition of an analgesic, suitable in particular for headache and migraine |
GB0910375D0 (en) | 2009-06-16 | 2009-07-29 | Biocopea Ltd | Drug composition and its use in therapy |
US9314465B2 (en) | 2009-06-16 | 2016-04-19 | Infirst Healthcare Limited | Drug combinations and uses in treating a coughing condition |
GB0919893D0 (en) * | 2009-11-13 | 2009-12-30 | Biocopea Ltd | Drug composition and its use in therapy |
US10016437B2 (en) | 2009-06-16 | 2018-07-10 | Infirst Healthcare Limited | Drug combinations and uses in treating a coughing condition |
US9308211B2 (en) | 2009-06-16 | 2016-04-12 | Infirst Healthcare Limited | Drug combinations and uses in treating a coughing condition |
AU2015201845B2 (en) * | 2009-11-13 | 2015-11-05 | Infirst Healthcare Limited | Drug combination with theobromine and its use in therapy |
WO2013005226A1 (en) * | 2011-07-04 | 2013-01-10 | Zota Health Care Ltd | A novel combined pharmaceutical composition containing diclofenac and methods of making and using the same |
US8853189B2 (en) | 2012-05-31 | 2014-10-07 | Prima Innovations, Llc | Antispasmodic 1,2-Diols and 1,2,3-triols |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0205492A1 (en) * | 1984-12-26 | 1986-12-30 | SUNSHINE, Abraham | Analgesic, anti-inflammatory and skeletal muscle relaxant compositions |
CA2170488A1 (en) * | 1993-09-07 | 1995-03-16 | Sekhar Mitra | Compositions containing an amino acid salt of propionic acid non-steroidal anti-inflammatory agent and at least one of a decongestant, an expectorant, an antihistamine and an antitussive |
GB9613457D0 (en) * | 1996-06-27 | 1996-08-28 | Procter & Gamble | Pharmaceutical compositions |
-
1998
- 1998-11-25 HU HU9802716A patent/HUP9802716A3/en unknown
-
1999
- 1999-11-23 EA EA200100581A patent/EA004375B1/en not_active IP Right Cessation
- 1999-11-23 WO PCT/HU1999/000079 patent/WO2000030715A1/en not_active Application Discontinuation
- 1999-11-23 AU AU15102/00A patent/AU1510200A/en not_active Abandoned
- 1999-11-23 SK SK687-2001A patent/SK6872001A3/en unknown
- 1999-11-23 PL PL99348631A patent/PL348631A1/en unknown
- 1999-11-23 CZ CZ20011847A patent/CZ20011847A3/en unknown
- 1999-11-23 EE EEP200100281A patent/EE200100281A/en unknown
- 1999-11-23 EP EP99957378A patent/EP1131135A1/en not_active Withdrawn
- 1999-11-23 YU YU37001A patent/YU37001A/en unknown
-
2001
- 2001-05-25 HR HR20010403A patent/HRP20010403A2/en not_active Application Discontinuation
- 2001-06-18 BG BG105616A patent/BG105616A/en unknown
Also Published As
Publication number | Publication date |
---|---|
HUP9802716A3 (en) | 2000-08-28 |
EA200100581A1 (en) | 2001-12-24 |
HRP20010403A2 (en) | 2002-06-30 |
SK6872001A3 (en) | 2002-05-09 |
EA004375B1 (en) | 2004-04-29 |
EP1131135A1 (en) | 2001-09-12 |
EE200100281A (en) | 2002-08-15 |
AU1510200A (en) | 2000-06-13 |
BG105616A (en) | 2002-01-31 |
PL348631A1 (en) | 2002-06-03 |
HU9802716D0 (en) | 1999-01-28 |
HUP9802716A2 (en) | 2000-06-28 |
WO2000030715A1 (en) | 2000-06-02 |
CZ20011847A3 (en) | 2002-07-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA200301165A1 (en) | Drug on the basis of oxycodone | |
DE69516540T2 (en) | AMINO-IMIDAZO [4,5-c] CHINOLINE | |
NO20022014L (en) | A solid oral controlled release dosage form containing hydrocodone | |
DE3779500D1 (en) | LEVODOPA METHYL ESTER CONTAINING PHARMACEUTICAL COMPOSITIONS, THEIR PRODUCTION AND THERAPEUTIC USE. | |
ATE359077T1 (en) | ORAL ADMINISTRATION OF 6-HYDROXY-OXYMORPHONE AS ANALGESIC | |
HUP0004383A2 (en) | Pharmaceutical preparation comprising clodronate as active ingredient and silicified microcrystalline cellulose as excipient | |
CA2326517A1 (en) | New galenic preparations of meloxicam for oral administration | |
SE8804629D0 (en) | NEW THERAPEUTICALLY ACTIVE COMPOUNDS | |
DE69629591D1 (en) | FORMULATION FOR INTRANASAL ADMINISTRATION | |
AR015157A1 (en) | DERIVATIVES OF THE ACID 5-RENT-2-ARYLAMINOPHENYLACCETIC, PHARMACEUTICAL COMPOSITION THAT INCLUDES IT, ITS USE IN THE MANUFACTURE OF A MEDICINAL PRODUCT AND METHOD OF PREPARATION OF THE SAME | |
DK1383752T3 (en) | Deuterated 3-piperidinopropiophenones as well as drugs containing these compounds | |
YU37001A (en) | Analgesic drug combination | |
NO991613D0 (en) | Pharmaceutical microspheres of valproic acid for oral administration | |
ES2051834T3 (en) | THE USE OF TETRAHYDROBENZENE (C, D) INDOL-6 CARBOXAMIDES FOR THE PREPARATION OF A MEDICATION FOR THE TREATMENT OF ANXIETY. | |
AR010984A1 (en) | NEW ESTERS OF PLEUROMUTILINE, AND THE ACID 1-AZABICICLO-4- CARBANILCARBANICO; PROCEDURE FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM. | |
DE69824313D1 (en) | PHARMACEUTICAL COMPOSITIONS CONTAINING SIBUTRAMINE AND ORLISTAT | |
LV10267A (en) | A compound for the purpose of obtaining a compound compound | |
AR035006A1 (en) | DERIVATIVE OF NAFTIRIDIN-DIBENZO [A, D] CICLOHEPTENO-10-ACETICO, PHARMACEUTICAL COMPOSITION, AND THE USE OF THAT DERIVATIVE FOR THE MANUFACTURE OF A MEDICINAL PRODUCT. | |
AU2001246999A1 (en) | New neurokinin antagonists for use as medicaments | |
BR9910201A (en) | Transdermal therapeutic system for the use of candesartan | |
CO5170494A1 (en) | PHARMACEUTICAL COMPLEX | |
NO20001894L (en) | Use of TNF antagonists as drugs for the treatment of septic diseases | |
IT8848398A0 (en) | PHARMACEUTICAL USER OF 3-INDOLPYRUVIC ACID AS AN INHIBITING AGENT FOR DEGENERATIVE DISEASES | |
NO882724D0 (en) | PAIN PREPARATION. | |
PT1117420E (en) | ALPHA-CYCLODEXTRIN-BASED PHARMACEUTICAL COMPOSICS FOR ORAL ADMINISTRATION OF LH-RH ANALOGS |