NL8420316A - Analgetische en ontstekingsremmende preparaten met daarin xanthinen en een werkwijze voor het toepassen daarvan. - Google Patents
Analgetische en ontstekingsremmende preparaten met daarin xanthinen en een werkwijze voor het toepassen daarvan. Download PDFInfo
- Publication number
- NL8420316A NL8420316A NL8420316A NL8420316A NL8420316A NL 8420316 A NL8420316 A NL 8420316A NL 8420316 A NL8420316 A NL 8420316A NL 8420316 A NL8420316 A NL 8420316A NL 8420316 A NL8420316 A NL 8420316A
- Authority
- NL
- Netherlands
- Prior art keywords
- derivative
- composition
- alkyl
- xanthine
- xanthine derivative
- Prior art date
Links
- 230000000202 analgesic effect Effects 0.000 title claims description 121
- 230000003110 anti-inflammatory effect Effects 0.000 title claims description 69
- 238000002360 preparation method Methods 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 17
- 229940065721 systemic for obstructive airway disease xanthines Drugs 0.000 title description 11
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical class O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 claims description 186
- 239000000203 mixture Substances 0.000 claims description 116
- 239000004084 narcotic analgesic agent Substances 0.000 claims description 67
- 239000003814 drug Substances 0.000 claims description 53
- 229940079593 drug Drugs 0.000 claims description 45
- 125000000217 alkyl group Chemical group 0.000 claims description 34
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical group O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 claims description 34
- -1 methylthio, ethylthio, nitro, methylamino, dimethylamino, phenyl Chemical group 0.000 claims description 29
- 150000003839 salts Chemical class 0.000 claims description 27
- 229940075420 xanthine Drugs 0.000 claims description 26
- 230000036592 analgesia Effects 0.000 claims description 25
- 239000001257 hydrogen Substances 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 24
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 claims description 19
- 150000002431 hydrogen Chemical group 0.000 claims description 19
- HUPFGZXOMWLGNK-UHFFFAOYSA-N diflunisal Chemical compound C1=C(O)C(C(=O)O)=CC(C=2C(=CC(F)=CC=2)F)=C1 HUPFGZXOMWLGNK-UHFFFAOYSA-N 0.000 claims description 18
- 229960000278 theophylline Drugs 0.000 claims description 18
- 238000011282 treatment Methods 0.000 claims description 18
- CMWTZPSULFXXJA-UHFFFAOYSA-N Naproxen Natural products C1=C(C(C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-UHFFFAOYSA-N 0.000 claims description 17
- 229960000616 diflunisal Drugs 0.000 claims description 17
- 229960001680 ibuprofen Drugs 0.000 claims description 17
- 229960002009 naproxen Drugs 0.000 claims description 17
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical compound C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 claims description 17
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 16
- 241000124008 Mammalia Species 0.000 claims description 15
- 238000009472 formulation Methods 0.000 claims description 15
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 12
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 12
- RDJGLLICXDHJDY-NSHDSACASA-N (2s)-2-(3-phenoxyphenyl)propanoic acid Chemical compound OC(=O)[C@@H](C)C1=CC=CC(OC=2C=CC=CC=2)=C1 RDJGLLICXDHJDY-NSHDSACASA-N 0.000 claims description 11
- 229960001419 fenoprofen Drugs 0.000 claims description 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 11
- 230000002708 enhancing effect Effects 0.000 claims description 10
- YZLZPSJXMWGIFH-BCXQGASESA-N nalbuphine hydrochloride Chemical compound [H+].[Cl-].C([C@]12[C@H]3OC=4C(O)=CC=C(C2=4)C[C@@H]2[C@]1(O)CC[C@@H]3O)CN2CC1CCC1 YZLZPSJXMWGIFH-BCXQGASESA-N 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 9
- 230000003111 delayed effect Effects 0.000 claims description 9
- 231100000252 nontoxic Toxicity 0.000 claims description 9
- 230000003000 nontoxic effect Effects 0.000 claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- RJMIEHBSYVWVIN-LLVKDONJSA-N (2r)-2-[4-(3-oxo-1h-isoindol-2-yl)phenyl]propanoic acid Chemical compound C1=CC([C@H](C(O)=O)C)=CC=C1N1C(=O)C2=CC=CC=C2C1 RJMIEHBSYVWVIN-LLVKDONJSA-N 0.000 claims description 7
- BRUQQQPBMZOVGD-XFKAJCMBSA-N Oxycodone Chemical compound O=C([C@@H]1O2)CC[C@@]3(O)[C@H]4CC5=CC=C(OC)C2=C5[C@@]13CCN4C BRUQQQPBMZOVGD-XFKAJCMBSA-N 0.000 claims description 7
- 229960004187 indoprofen Drugs 0.000 claims description 7
- XADCESSVHJOZHK-UHFFFAOYSA-N Meperidine Chemical compound C=1C=CC=CC=1C1(C(=O)OCC)CCN(C)CC1 XADCESSVHJOZHK-UHFFFAOYSA-N 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 6
- 229960002085 oxycodone Drugs 0.000 claims description 6
- YAPQBXQYLJRXSA-UHFFFAOYSA-N theobromine Chemical compound CN1C(=O)NC(=O)C2=C1N=CN2C YAPQBXQYLJRXSA-UHFFFAOYSA-N 0.000 claims description 6
- BCXHDORHMMZBBZ-DORFAMGDSA-N (4r,4ar,7s,7ar,12bs)-9-methoxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC BCXHDORHMMZBBZ-DORFAMGDSA-N 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 125000004414 alkyl thio group Chemical group 0.000 claims description 5
- 229960004415 codeine phosphate Drugs 0.000 claims description 5
- 229960003871 codeine sulfate Drugs 0.000 claims description 5
- 229960000805 nalbuphine Drugs 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- OQGYMIIFOSJQSF-DTOXXUQYSA-N pentazocine hcl Chemical compound Cl.C1C2=CC=C(O)C=C2[C@@]2(C)[C@@H](C)[C@@H]1N(CC=C(C)C)CC2 OQGYMIIFOSJQSF-DTOXXUQYSA-N 0.000 claims description 5
- 229960003809 pentazocine hydrochloride Drugs 0.000 claims description 5
- GIMNFISWKTZFKJ-UHFFFAOYSA-N 1,3-diethyl-7h-purine-2,6-dione Chemical group O=C1N(CC)C(=O)N(CC)C2=C1NC=N2 GIMNFISWKTZFKJ-UHFFFAOYSA-N 0.000 claims description 4
- QUNWUDVFRNGTCO-UHFFFAOYSA-N 1,7-dimethylxanthine Chemical compound N1C(=O)N(C)C(=O)C2=C1N=CN2C QUNWUDVFRNGTCO-UHFFFAOYSA-N 0.000 claims description 4
- MVOYJPOZRLFTCP-UHFFFAOYSA-N 1-methyl-7H-xanthine Chemical compound O=C1N(C)C(=O)NC2=C1NC=N2 MVOYJPOZRLFTCP-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- IFKLAQQSCNILHL-QHAWAJNXSA-N butorphanol Chemical compound N1([C@@H]2CC3=CC=C(C=C3[C@@]3([C@]2(CCCC3)O)CC1)O)CC1CCC1 IFKLAQQSCNILHL-QHAWAJNXSA-N 0.000 claims description 4
- 229960001513 nalbuphine hydrochloride Drugs 0.000 claims description 4
- 230000003389 potentiating effect Effects 0.000 claims description 4
- 230000003637 steroidlike Effects 0.000 claims description 4
- WZBKGWBHAPBSBF-UHFFFAOYSA-N 1,3,8-trimethyl-7h-purine-2,6-dione Chemical group CN1C(=O)N(C)C(=O)C2=C1N=C(C)N2 WZBKGWBHAPBSBF-UHFFFAOYSA-N 0.000 claims description 3
- UOOOWRVLSKCKGJ-UHFFFAOYSA-N 1-methyl-8-phenyl-3,7-dihydropurine-2,6-dione Chemical group N1C=2C(=O)N(C)C(=O)NC=2N=C1C1=CC=CC=C1 UOOOWRVLSKCKGJ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- MPJUSISYVXABBH-UHFFFAOYSA-N 3-(3-ethyl-1-methylazepan-3-yl)phenol;hydron;chloride Chemical compound Cl.C=1C=CC(O)=CC=1C1(CC)CCCCN(C)C1 MPJUSISYVXABBH-UHFFFAOYSA-N 0.000 claims description 3
- KTJSVELYMZTQJB-UHFFFAOYSA-N 8-ethyl-1,3-dimethyl-7h-purine-2,6-dione Chemical group CN1C(=O)N(C)C(=O)C2=C1N=C(CC)N2 KTJSVELYMZTQJB-UHFFFAOYSA-N 0.000 claims description 3
- PJFMAVHETLRJHJ-UHFFFAOYSA-N 8-phenyltheophylline Chemical group N1C=2C(=O)N(C)C(=O)N(C)C=2N=C1C1=CC=CC=C1 PJFMAVHETLRJHJ-UHFFFAOYSA-N 0.000 claims description 3
- 229960001736 buprenorphine Drugs 0.000 claims description 3
- 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 claims description 3
- GMTYREVWZXJPLF-AFHUBHILSA-N butorphanol D-tartrate Chemical compound OC(=O)[C@@H](O)[C@H](O)C(O)=O.N1([C@@H]2CC3=CC=C(C=C3[C@@]3([C@]2(CCCC3)O)CC1)O)CC1CCC1 GMTYREVWZXJPLF-AFHUBHILSA-N 0.000 claims description 3
- 229960001590 butorphanol tartrate Drugs 0.000 claims description 3
- 229960004473 meptazinol hydrochloride Drugs 0.000 claims description 3
- 229960000482 pethidine Drugs 0.000 claims description 3
- DKSZLDSPXIWGFO-BLOJGBSASA-N (4r,4ar,7s,7ar,12bs)-9-methoxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol;phosphoric acid;hydrate Chemical compound O.OP(O)(O)=O.OP(O)(O)=O.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC DKSZLDSPXIWGFO-BLOJGBSASA-N 0.000 claims description 2
- MJVIGUCNSRXAFO-UHFFFAOYSA-N 1,3-dipropyl-7h-purine-2,6-dione Chemical compound O=C1N(CCC)C(=O)N(CCC)C2=C1NC=N2 MJVIGUCNSRXAFO-UHFFFAOYSA-N 0.000 claims description 2
- ZCUPBJOZMPROIJ-UHFFFAOYSA-N 1-butyl-3,7-dimethylpurine-2,6-dione Chemical group O=C1N(CCCC)C(=O)N(C)C2=C1N(C)C=N2 ZCUPBJOZMPROIJ-UHFFFAOYSA-N 0.000 claims description 2
- APIXJSLKIYYUKG-UHFFFAOYSA-N 3 Isobutyl 1 methylxanthine Chemical group O=C1N(C)C(=O)N(CC(C)C)C2=C1N=CN2 APIXJSLKIYYUKG-UHFFFAOYSA-N 0.000 claims description 2
- PFWLFWPASULGAN-UHFFFAOYSA-N 7-Methylxanthine Natural products N1C(=O)NC(=O)C2=C1N=CN2C PFWLFWPASULGAN-UHFFFAOYSA-N 0.000 claims description 2
- SCVHFRLUNIOSGI-UHFFFAOYSA-N 8-cyclopentyl-1,3-dimethyl-7H-purine-2,6-dione Chemical group N1C=2C(=O)N(C)C(=O)N(C)C=2N=C1C1CCCC1 SCVHFRLUNIOSGI-UHFFFAOYSA-N 0.000 claims description 2
- SZMWFUBOZRDQPO-UHFFFAOYSA-N 8-cyclopropyl-1,3-dimethyl-7h-purine-2,6-dione Chemical group N1C=2C(=O)N(C)C(=O)N(C)C=2N=C1C1CC1 SZMWFUBOZRDQPO-UHFFFAOYSA-N 0.000 claims description 2
- 229960001113 butorphanol Drugs 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 125000001188 haloalkyl group Chemical group 0.000 claims description 2
- WVLOADHCBXTIJK-YNHQPCIGSA-N hydromorphone Chemical compound O([C@H]1C(CC[C@H]23)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O WVLOADHCBXTIJK-YNHQPCIGSA-N 0.000 claims description 2
- 229960001410 hydromorphone Drugs 0.000 claims description 2
- 229960000365 meptazinol Drugs 0.000 claims description 2
- JLICHNCFTLFZJN-HNNXBMFYSA-N meptazinol Chemical compound C=1C=CC(O)=CC=1[C@@]1(CC)CCCCN(C)C1 JLICHNCFTLFZJN-HNNXBMFYSA-N 0.000 claims description 2
- 239000000829 suppository Substances 0.000 claims description 2
- 229960004559 theobromine Drugs 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 2
- LVSWNSHUTPWCNF-UHFFFAOYSA-N 1,3-diethyl-8-phenyl-7h-purine-2,6-dione Chemical group N1C=2C(=O)N(CC)C(=O)N(CC)C=2N=C1C1=CC=CC=C1 LVSWNSHUTPWCNF-UHFFFAOYSA-N 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- 125000004188 dichlorophenyl group Chemical group 0.000 claims 2
- 125000005059 halophenyl group Chemical group 0.000 claims 2
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000006501 nitrophenyl group Chemical group 0.000 claims 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
- RUZDFVZSCVNECE-UHFFFAOYSA-N 1,3,7-triethylpurine-2,6-dione Chemical compound CCN1C(=O)N(CC)C(=O)C2=C1N=CN2CC RUZDFVZSCVNECE-UHFFFAOYSA-N 0.000 claims 1
- NUZFZZOVBJUJQN-UHFFFAOYSA-N 1,3-bis(prop-2-enyl)-7h-purine-2,6-dione Chemical compound O=C1N(CC=C)C(=O)N(CC=C)C2=C1NC=N2 NUZFZZOVBJUJQN-UHFFFAOYSA-N 0.000 claims 1
- KNYQVLUUOXITIT-UHFFFAOYSA-N 1,3-dimethyl-8-(2-nitrophenyl)-7h-purine-2,6-dione Chemical compound N1C=2C(=O)N(C)C(=O)N(C)C=2N=C1C1=CC=CC=C1[N+]([O-])=O KNYQVLUUOXITIT-UHFFFAOYSA-N 0.000 claims 1
- KPSYSSQIKZMIBA-UHFFFAOYSA-N 1,3-dimethyl-8-(methylamino)-7h-purine-2,6-dione Chemical group CN1C(=O)N(C)C(=O)C2=C1N=C(NC)N2 KPSYSSQIKZMIBA-UHFFFAOYSA-N 0.000 claims 1
- RLOPOZUJNIRHCF-UHFFFAOYSA-N 1,3-dimethyl-8-methylsulfanyl-7h-purine-2,6-dione Chemical group CN1C(=O)N(C)C(=O)C2=C1N=C(SC)N2 RLOPOZUJNIRHCF-UHFFFAOYSA-N 0.000 claims 1
- LMQXNURVVYWBSR-UHFFFAOYSA-N 1,3-dimethyl-8-propyl-7h-purine-2,6-dione Chemical group CN1C(=O)N(C)C(=O)C2=C1N=C(CCC)N2 LMQXNURVVYWBSR-UHFFFAOYSA-N 0.000 claims 1
- KRVVZPXPQUPXJE-UHFFFAOYSA-N 1-ethyl-3,7-dimethylpurine-2,6-dione Chemical group O=C1N(CC)C(=O)N(C)C2=C1N(C)C=N2 KRVVZPXPQUPXJE-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- BOZIQSRPJXHQKO-UHFFFAOYSA-N 7-methoxy-1,3-dimethyl-8-phenylpurine-2,6-dione Chemical group N=1C=2N(C)C(=O)N(C)C(=O)C=2N(OC)C=1C1=CC=CC=C1 BOZIQSRPJXHQKO-UHFFFAOYSA-N 0.000 claims 1
- SEMSUTFLQPJDSD-UHFFFAOYSA-N 8-(2-chlorophenyl)-1,3-dimethyl-7h-purine-2,6-dione Chemical compound N1C=2C(=O)N(C)C(=O)N(C)C=2N=C1C1=CC=CC=C1Cl SEMSUTFLQPJDSD-UHFFFAOYSA-N 0.000 claims 1
- VQMYLWUQXXVMKB-UHFFFAOYSA-N 8-(4-bromophenyl)-1,3-dimethyl-7h-purine-2,6-dione Chemical compound N1C=2C(=O)N(C)C(=O)N(C)C=2N=C1C1=CC=C(Br)C=C1 VQMYLWUQXXVMKB-UHFFFAOYSA-N 0.000 claims 1
- QOFFIYLUCIEBBX-UHFFFAOYSA-N 8-(dimethylamino)-1,3-dimethyl-7h-purine-2,6-dione Chemical group CN1C(=O)N(C)C(=O)C2=C1N=C(N(C)C)N2 QOFFIYLUCIEBBX-UHFFFAOYSA-N 0.000 claims 1
- HHDUZSJKCAQOTP-UHFFFAOYSA-N 8-[2-(dimethylamino)phenyl]-1,3-dimethyl-7h-purine-2,6-dione Chemical compound CN(C)C1=CC=CC=C1C(N1)=NC2=C1C(=O)N(C)C(=O)N2C HHDUZSJKCAQOTP-UHFFFAOYSA-N 0.000 claims 1
- DRWCPERSPGFNIK-UHFFFAOYSA-N 8-ethyl-1,3,7-trimethylpurine-2,6-dione Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=C(CC)N2C DRWCPERSPGFNIK-UHFFFAOYSA-N 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- QDVLGXHRLYOKBK-UHFFFAOYSA-N chembl10579 Chemical compound CC1=CC(O)=CC(C)=C1C(N1)=NC2=C1C(=O)N(C)C(=O)N2C QDVLGXHRLYOKBK-UHFFFAOYSA-N 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- MRWQRJMESRRJJB-UHFFFAOYSA-N pentifylline Chemical group O=C1N(CCCCCC)C(=O)N(C)C2=C1N(C)C=N2 MRWQRJMESRRJJB-UHFFFAOYSA-N 0.000 claims 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 80
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 68
- 239000000730 antalgic agent Substances 0.000 description 47
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 39
- 229960001948 caffeine Drugs 0.000 description 39
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 39
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 37
- 230000000694 effects Effects 0.000 description 31
- 208000002193 Pain Diseases 0.000 description 30
- 230000036407 pain Effects 0.000 description 30
- 229940083747 low-ceiling diuretics xanthine derivative Drugs 0.000 description 28
- 230000003533 narcotic effect Effects 0.000 description 28
- 229940035676 analgesics Drugs 0.000 description 26
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 21
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 19
- 241000282412 Homo Species 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 18
- 229960005489 paracetamol Drugs 0.000 description 18
- 239000000556 agonist Substances 0.000 description 16
- CPJSUEIXXCENMM-UHFFFAOYSA-N phenacetin Chemical compound CCOC1=CC=C(NC(C)=O)C=C1 CPJSUEIXXCENMM-UHFFFAOYSA-N 0.000 description 14
- 239000011734 sodium Substances 0.000 description 13
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- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004648 relaxation of smooth muscle Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 210000003625 skull Anatomy 0.000 description 1
- 210000002460 smooth muscle Anatomy 0.000 description 1
- 239000000050 smooth muscle relaxant Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- JWBPVFVNISJVEM-UHFFFAOYSA-M sodium caffeine benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1.CN1C(=O)N(C)C(=O)C2=C1N=CN2C JWBPVFVNISJVEM-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229960004025 sodium salicylate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- ZJXLSCXDGPDZOL-UHFFFAOYSA-M sodium;2-[5-(4-chlorobenzoyl)-1,4-dimethylpyrrol-2-yl]acetate;dihydrate Chemical compound O.O.[Na+].C1=C(CC([O-])=O)N(C)C(C(=O)C=2C=CC(Cl)=CC=2)=C1C ZJXLSCXDGPDZOL-UHFFFAOYSA-M 0.000 description 1
- 238000002693 spinal anesthesia Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229950005175 sudoxicam Drugs 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229960004492 suprofen Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229940095374 tabloid Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000001550 time effect Effects 0.000 description 1
- 229950002345 tiopinac Drugs 0.000 description 1
- 229960002905 tolfenamic acid Drugs 0.000 description 1
- YEZNLOUZAIOMLT-UHFFFAOYSA-N tolfenamic acid Chemical compound CC1=C(Cl)C=CC=C1NC1=CC=CC=C1C(O)=O YEZNLOUZAIOMLT-UHFFFAOYSA-N 0.000 description 1
- 229960001017 tolmetin Drugs 0.000 description 1
- UPSPUYADGBWSHF-UHFFFAOYSA-N tolmetin Chemical compound C1=CC(C)=CC=C1C(=O)C1=CC=C(CC(O)=O)N1C UPSPUYADGBWSHF-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229940116269 uric acid Drugs 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 230000006442 vascular tone Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229950007802 zidometacin Drugs 0.000 description 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56057683 | 1983-12-12 | ||
| US06/560,576 US4558051A (en) | 1983-10-11 | 1983-12-12 | Analgesic and anti-inflammatory compositions comprising xanthines and methods of using same |
| US8402035 | 1984-12-12 | ||
| PCT/US1984/002035 WO1985002540A1 (en) | 1983-12-12 | 1984-12-12 | Analgesic and anti-inflammatory compositions comprising xanthines and methods of using same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8420316A true NL8420316A (nl) | 1985-11-01 |
Family
ID=24238396
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8420316A NL8420316A (nl) | 1983-12-12 | 1984-12-12 | Analgetische en ontstekingsremmende preparaten met daarin xanthinen en een werkwijze voor het toepassen daarvan. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4558051A (enExample) |
| EP (1) | EP0165308B1 (enExample) |
| JP (1) | JPS61500665A (enExample) |
| AT (1) | AT389997B (enExample) |
| AU (1) | AU574419B2 (enExample) |
| CA (1) | CA1246453A (enExample) |
| CH (1) | CH669730A5 (enExample) |
| DE (1) | DE3490583T1 (enExample) |
| GB (1) | GB2161076B (enExample) |
| IE (1) | IE58158B1 (enExample) |
| IT (1) | IT1177389B (enExample) |
| NL (1) | NL8420316A (enExample) |
| SE (1) | SE469874B (enExample) |
| WO (1) | WO1985002540A1 (enExample) |
| ZA (1) | ZA849675B (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3508097A1 (de) * | 1984-07-21 | 1986-02-06 | Hoechst Ag, 6230 Frankfurt | Kombinationspraeparat aus xanthinderivaten und o-acetylsalicylsaeure bzw. deren pharmakologisch vertraeglichen salzen und dessen verwendung |
| HU197746B (en) * | 1985-09-05 | 1989-05-29 | Sandoz Ag | Process for producing xantin derivatives and pharmaceutical compositions containing them |
| CH669523A5 (enExample) * | 1986-06-25 | 1989-03-31 | Mepha Ag | |
| DE3779374D1 (en) * | 1986-08-28 | 1992-07-02 | Sandoz Ag | Xanthinderivate. |
| CH670090A5 (enExample) * | 1986-10-27 | 1989-05-12 | Nestle Sa | |
| GB8626098D0 (en) * | 1986-10-31 | 1986-12-03 | Euro Celtique Sa | Controlled release hydromorphone composition |
| GB8629567D0 (en) * | 1986-12-10 | 1987-01-21 | Boots Co Plc | Therapeutic agents |
| US5196430A (en) * | 1986-12-31 | 1993-03-23 | Hoechst-Roussel Pharmaceuticals Inc. | Method of inhibiting the activity of leukocyte derived cytokines |
| US5196429A (en) * | 1986-12-31 | 1993-03-23 | Hoechst-Roussel Pharmaceuticals Inc. | Method of inhibiting the activity of leukocyte derived cytokines |
| US5272153A (en) * | 1986-12-31 | 1993-12-21 | Hoechst-Roussel Pharmaceuticals, Inc. | Method of inhibiting the activity of leukocyte derived cytokines |
| US4861797A (en) * | 1987-10-15 | 1989-08-29 | Oratech Pharmaceutical Development Corporation | Liquid ibuprofen compositions and methods of making them |
| US4859704A (en) * | 1987-10-15 | 1989-08-22 | Oratech Pharmaceutical Development Corporation | Water soluble ibuprofen compositions and methods of making them |
| JPH0228141A (ja) * | 1987-11-13 | 1990-01-30 | Glaxo Group Ltd | フェネタノールアミン誘導体 |
| US4883818A (en) * | 1987-11-17 | 1989-11-28 | Analgesic Associates | Onset-hastened/enhanced analgesia |
| IE882585L (en) * | 1988-08-25 | 1990-02-25 | Prendergast Patrick T | Viral treatment system |
| JP2843634B2 (ja) * | 1989-03-06 | 1999-01-06 | 協和醗酵工業株式会社 | キサンチン誘導体 |
| GB8906792D0 (en) * | 1989-03-23 | 1989-05-10 | Beecham Wuelfing Gmbh & Co Kg | Treatment and compounds |
| AU662297B2 (en) * | 1990-09-11 | 1995-08-31 | Richardson-Vicks Inc. | Method for providing improved analgesic effect |
| AU5132893A (en) * | 1992-09-29 | 1994-04-26 | Mcneil-Ppc, Inc. | Ibuprofen-caffeine combinations |
| US5817662A (en) * | 1992-11-09 | 1998-10-06 | Cell Therapeutics, Inc. | Substituted amino alkyl compounds |
| US5340813A (en) * | 1992-11-09 | 1994-08-23 | Cell Therapeutics, Inc. | Substituted aminoalkyl xanthine compounds |
| WO1994025462A1 (en) * | 1993-05-03 | 1994-11-10 | The United States Of America, Represented By The | 8-substituted 1,3,7-trialkyl-xanthine derivatives as a2-selective adenosine receptor antagonists |
| US5451409A (en) * | 1993-11-22 | 1995-09-19 | Rencher; William F. | Sustained release matrix system using hydroxyethyl cellulose and hydroxypropyl cellulose polymer blends |
| US6103730A (en) * | 1994-03-24 | 2000-08-15 | Cell Therapeutics, Inc. | Amine substituted compounds |
| US5801182A (en) * | 1994-03-24 | 1998-09-01 | Cell Therapeutics, Inc. | Amine substituted compounds |
| US5807861A (en) * | 1994-03-24 | 1998-09-15 | Cell Therapeutics, Inc. | Amine substituted xanthinyl compounds |
| US6348216B1 (en) * | 1996-06-10 | 2002-02-19 | Knoll Pharmaceutical Company | Ibuprofen and narcotic analgesic compositions |
| US6361794B1 (en) | 1996-06-12 | 2002-03-26 | Basf Corporation | Method of making ibuprofen and narcotic analgesic composition |
| US20090149479A1 (en) * | 1998-11-02 | 2009-06-11 | Elan Pharma International Limited | Dosing regimen |
| US6211246B1 (en) | 1999-06-10 | 2001-04-03 | Mcneil-Ppc, Inc. | Rapidly absorbed liquid compositions |
| US6586429B2 (en) * | 2000-11-29 | 2003-07-01 | Cell Therapeutics, Inc. | Tricyclic fused xanthine compounds and their uses |
| DE60223254T2 (de) | 2001-07-06 | 2008-08-14 | Penwest Pharmaceuticals Co. | Verzögert freisetzende formulierungen von oxymorphon |
| US8329216B2 (en) | 2001-07-06 | 2012-12-11 | Endo Pharmaceuticals Inc. | Oxymorphone controlled release formulations |
| JP2005515966A (ja) | 2001-07-06 | 2005-06-02 | エンドー ファーマシューティカルズ， インコーポレイティド | 鎮痛薬としての使用のための６−ヒドロキシ−オキシモルホンの経口投与 |
| US7317017B2 (en) | 2002-11-08 | 2008-01-08 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
| US6977300B2 (en) * | 2001-11-09 | 2005-12-20 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
| US20080318983A1 (en) * | 2001-11-09 | 2008-12-25 | Rao Kalla | A2b adenosine receptor antagonists |
| NZ532816A (en) | 2001-11-09 | 2005-11-25 | Cv Therapeutics Inc | A2B adenosine receptor antagonists |
| US7125993B2 (en) * | 2001-11-09 | 2006-10-24 | Cv Therapeutics, Inc. | A2B adenosine receptor antagonists |
| US20050137262A1 (en) * | 2003-12-22 | 2005-06-23 | Hu Patrick C. | Highly concentrated pourable aqueous solutions of potassium ibuprofen, their preparation and their uses |
| ES2387653T3 (es) * | 2004-09-01 | 2012-09-27 | Gilead Sciences, Inc. | Procedimiento de cicatrización de heridas utilizando antagonistas del receptor de adenosina A2B |
| CL2007002425A1 (es) * | 2006-08-22 | 2008-06-27 | Albermarle Corp | Procedimiento de preparacion controlado de sal sodica de ibuprofeno de tamano de particula mediano; y dichas particulas de sal sodica. |
| DK3280417T3 (da) | 2015-04-08 | 2020-11-02 | Lewis And Clark Pharmaceuticals Inc | Xanthin-substitueret alkynyl karbamater/omvendte karbamater som a2b antagonister |
| CN109912598B (zh) * | 2019-03-27 | 2022-09-13 | 四川大学华西医院 | 防治炎症反应的核苷类衍生物及其应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3439094A (en) * | 1967-07-20 | 1969-04-15 | Warner Lambert Pharmaceutical | Analgesic compositions containing namol xenyrate,caffeine and acetyl-rho-aminophenol |
| US3936528A (en) * | 1974-02-13 | 1976-02-03 | Syntex Corporation | Analgesic formulations having enhanced therapeutic activity |
| AU532600B2 (en) * | 1977-04-02 | 1983-10-06 | Hoechst A.G. | Alkenyl xanthines and pharmaceutical compositions |
| JPS56154416A (en) * | 1980-04-30 | 1981-11-30 | Kaken Pharmaceut Co Ltd | Antipyretic analgesic composition |
| AU558485B2 (en) * | 1982-07-22 | 1987-01-29 | Richardson-Vicks Inc. | Improved analgesic and anti-inflammatory compositions comprising caffeine and methods of using same |
| US4420483A (en) * | 1982-07-22 | 1983-12-13 | Richardson-Vicks, Inc. | Analgesic and anti-inflammatory compositions comprising ibuprofen and methods of using same |
| US4479956A (en) * | 1983-04-26 | 1984-10-30 | Analgeic Associates | Analgesic compositions comprising propiram and methods of using same |
-
1983
- 1983-12-12 US US06/560,576 patent/US4558051A/en not_active Expired - Lifetime
-
1984
- 1984-12-10 IE IE316684A patent/IE58158B1/en not_active IP Right Cessation
- 1984-12-11 CA CA000469837A patent/CA1246453A/en not_active Expired
- 1984-12-12 AT AT0905384A patent/AT389997B/de not_active IP Right Cessation
- 1984-12-12 AU AU37474/85A patent/AU574419B2/en not_active Expired
- 1984-12-12 IT IT24009/84A patent/IT1177389B/it active
- 1984-12-12 DE DE19843490583 patent/DE3490583T1/de not_active Withdrawn
- 1984-12-12 WO PCT/US1984/002035 patent/WO1985002540A1/en not_active Ceased
- 1984-12-12 EP EP85900409A patent/EP0165308B1/en not_active Expired
- 1984-12-12 ZA ZA849675A patent/ZA849675B/xx unknown
- 1984-12-12 NL NL8420316A patent/NL8420316A/nl unknown
- 1984-12-12 GB GB08519256A patent/GB2161076B/en not_active Expired
- 1984-12-12 JP JP60500078A patent/JPS61500665A/ja active Pending
-
1985
- 1985-08-09 SE SE8503762A patent/SE469874B/sv not_active IP Right Cessation
- 1985-12-12 CH CH3505/85A patent/CH669730A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CH669730A5 (enExample) | 1989-04-14 |
| SE8503762L (sv) | 1985-08-09 |
| SE8503762D0 (sv) | 1985-08-09 |
| GB2161076A (en) | 1986-01-08 |
| GB8519256D0 (en) | 1985-09-04 |
| IT8424009A1 (it) | 1986-06-12 |
| AU3747485A (en) | 1985-06-26 |
| WO1985002540A1 (en) | 1985-06-20 |
| AU574419B2 (en) | 1988-07-07 |
| JPS61500665A (ja) | 1986-04-10 |
| ZA849675B (en) | 1985-07-31 |
| EP0165308B1 (en) | 1989-03-22 |
| EP0165308A1 (en) | 1985-12-27 |
| AT389997B (de) | 1990-02-26 |
| US4558051A (en) | 1985-12-10 |
| GB2161076B (en) | 1988-03-30 |
| IT1177389B (it) | 1987-08-26 |
| IT8424009A0 (it) | 1984-12-12 |
| EP0165308A4 (en) | 1986-05-16 |
| IE843166L (en) | 1985-06-12 |
| SE469874B (sv) | 1993-10-04 |
| IE58158B1 (en) | 1993-07-28 |
| DE3490583T1 (de) | 1986-04-03 |
| ATA905384A (de) | 1989-08-15 |
| CA1246453A (en) | 1988-12-13 |
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