CZ20004896A3 - Pharmaceutical preparation containing inhibitor COX-2 and inhibitor iNOS - Google Patents
Pharmaceutical preparation containing inhibitor COX-2 and inhibitor iNOS Download PDFInfo
- Publication number
- CZ20004896A3 CZ20004896A3 CZ20004896A CZ20004896A CZ20004896A3 CZ 20004896 A3 CZ20004896 A3 CZ 20004896A3 CZ 20004896 A CZ20004896 A CZ 20004896A CZ 20004896 A CZ20004896 A CZ 20004896A CZ 20004896 A3 CZ20004896 A3 CZ 20004896A3
- Authority
- CZ
- Czechia
- Prior art keywords
- quinazoline
- piperidine
- amine
- spiro
- amino
- Prior art date
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- 239000003112 inhibitor Substances 0.000 title abstract description 32
- 102100029438 Nitric oxide synthase, inducible Human genes 0.000 title description 35
- 101710089543 Nitric oxide synthase, inducible Proteins 0.000 title 1
- 102100038280 Prostaglandin G/H synthase 2 Human genes 0.000 title 1
- 108050003267 Prostaglandin G/H synthase 2 Proteins 0.000 title 1
- 239000000825 pharmaceutical preparation Substances 0.000 title 1
- 238000011282 treatment Methods 0.000 claims abstract description 14
- 208000027866 inflammatory disease Diseases 0.000 claims abstract description 11
- -1 nitro, hydroxymethyl Chemical group 0.000 claims description 107
- 239000000203 mixture Substances 0.000 claims description 37
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 29
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 26
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 25
- 239000003255 cyclooxygenase 2 inhibitor Substances 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 229940111134 coxibs Drugs 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- 229910052717 sulfur Chemical group 0.000 claims description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- 229910052736 halogen Inorganic materials 0.000 claims description 17
- 150000002367 halogens Chemical class 0.000 claims description 17
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 16
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 15
- 239000001301 oxygen Substances 0.000 claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 14
- 125000005842 heteroatom Chemical group 0.000 claims description 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 239000011593 sulfur Chemical group 0.000 claims description 11
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 9
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 201000010099 disease Diseases 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 239000003814 drug Substances 0.000 claims description 7
- 238000011321 prophylaxis Methods 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 125000004434 sulfur atom Chemical group 0.000 claims description 7
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 229960000590 celecoxib Drugs 0.000 claims description 6
- RZEKVGVHFLEQIL-UHFFFAOYSA-N celecoxib Chemical compound C1=CC(C)=CC=C1C1=CC(C(F)(F)F)=NN1C1=CC=C(S(N)(=O)=O)C=C1 RZEKVGVHFLEQIL-UHFFFAOYSA-N 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 239000002671 adjuvant Substances 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 4
- 125000002541 furyl group Chemical group 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000001544 thienyl group Chemical group 0.000 claims description 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 125000003386 piperidinyl group Chemical group 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 238000002560 therapeutic procedure Methods 0.000 claims description 3
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 claims description 2
- ZRVUJXDFFKFLMG-UHFFFAOYSA-N Meloxicam Chemical compound OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=NC=C(C)S1 ZRVUJXDFFKFLMG-UHFFFAOYSA-N 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 229950005722 flosulide Drugs 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 2
- 229960001929 meloxicam Drugs 0.000 claims description 2
- CXJONBHNIJFARE-UHFFFAOYSA-N n-[6-(2,4-difluorophenoxy)-1-oxo-2,3-dihydroinden-5-yl]methanesulfonamide Chemical compound CS(=O)(=O)NC1=CC=2CCC(=O)C=2C=C1OC1=CC=C(F)C=C1F CXJONBHNIJFARE-UHFFFAOYSA-N 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000004043 oxo group Chemical group O=* 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000005493 quinolyl group Chemical group 0.000 claims description 2
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- MIMJSJSRRDZIPW-UHFFFAOYSA-N tilmacoxib Chemical compound C=1C=C(S(N)(=O)=O)C(F)=CC=1C=1OC(C)=NC=1C1CCCCC1 MIMJSJSRRDZIPW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003003 spiro group Chemical group 0.000 claims 67
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims 37
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 3
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 claims 3
- 150000001412 amines Chemical class 0.000 claims 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- JLAKCHGEEBPDQI-UHFFFAOYSA-N 4-(4-fluorobenzyl)piperidine Chemical compound C1=CC(F)=CC=C1CC1CCNCC1 JLAKCHGEEBPDQI-UHFFFAOYSA-N 0.000 claims 2
- 125000002672 4-bromobenzoyl group Chemical group BrC1=CC=C(C(=O)*)C=C1 0.000 claims 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 2
- 125000003232 p-nitrobenzoyl group Chemical group [N+](=O)([O-])C1=CC=C(C(=O)*)C=C1 0.000 claims 2
- KOCBGBJUDZNSJE-UHFFFAOYSA-N (4-amino-5,7-difluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-thiophen-2-ylmethanone Chemical compound N1C2=CC(F)=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=CS1 KOCBGBJUDZNSJE-UHFFFAOYSA-N 0.000 claims 1
- NSMOJXCJICOFKS-UHFFFAOYSA-N (4-amino-5,8-difluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(6-chloropyridin-3-yl)methanone Chemical compound N1C2=C(F)C=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=C(Cl)N=C1 NSMOJXCJICOFKS-UHFFFAOYSA-N 0.000 claims 1
- KFHRZNJUQDYBJY-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(1,2-oxazol-3-yl)methanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C=1C=CON=1 KFHRZNJUQDYBJY-UHFFFAOYSA-N 0.000 claims 1
- LPHXOGYMVXBMGV-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(4-bromothiophen-2-yl)methanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC(Br)=CS1 LPHXOGYMVXBMGV-UHFFFAOYSA-N 0.000 claims 1
- ISYQOHGPHWEVDP-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(5-chlorothiophen-2-yl)methanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=C(Cl)S1 ISYQOHGPHWEVDP-UHFFFAOYSA-N 0.000 claims 1
- SJSUYOCGLNUZHL-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(5-methylpyrazin-2-yl)methanone Chemical compound C1=NC(C)=CN=C1C(=O)N1CCC2(N=C(N)C3=C(F)C=CC=C3N2)CC1 SJSUYOCGLNUZHL-UHFFFAOYSA-N 0.000 claims 1
- IZTDKOVHEGYKPL-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(6-chloropyridin-3-yl)methanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=C(Cl)N=C1 IZTDKOVHEGYKPL-UHFFFAOYSA-N 0.000 claims 1
- MPTWCHUKDCSDPV-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(furan-2-yl)methanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=CO1 MPTWCHUKDCSDPV-UHFFFAOYSA-N 0.000 claims 1
- XGEBICJDODHDSM-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(thiadiazol-4-yl)methanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C1=CSN=N1 XGEBICJDODHDSM-UHFFFAOYSA-N 0.000 claims 1
- ABHMXNAQNFTILP-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-imidazol-1-ylmethanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)N1C=CN=C1 ABHMXNAQNFTILP-UHFFFAOYSA-N 0.000 claims 1
- WZEHIPZGALGBOI-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-pyrrolidin-1-ylmethanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)N1CCCC1 WZEHIPZGALGBOI-UHFFFAOYSA-N 0.000 claims 1
- FHRCQQIVIJAXMW-UHFFFAOYSA-N (4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-thiophen-3-ylmethanone Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)C=1C=CSC=1 FHRCQQIVIJAXMW-UHFFFAOYSA-N 0.000 claims 1
- YOGMHFXUEGAVGP-UHFFFAOYSA-N (4-amino-5-hydroxyspiro[1H-quinazoline-2,4'-piperidine]-1'-yl)-(4-bromophenyl)methanone Chemical compound BrC1=CC=C(C(=O)N2CCC3(CC2)NC2=CC=CC(=C2C(=N3)N)O)C=C1 YOGMHFXUEGAVGP-UHFFFAOYSA-N 0.000 claims 1
- HUGDORSEMMDVLL-UHFFFAOYSA-N (4-aminophenyl)-(4-aminospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)methanone Chemical compound N1C2=CC=CC=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=C(N)C=C1 HUGDORSEMMDVLL-UHFFFAOYSA-N 0.000 claims 1
- AGPKOMWNUUEILQ-UHFFFAOYSA-N (4-aminospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(1,3-thiazol-2-yl)methanone Chemical compound N1C2=CC=CC=C2C(N)=NC1(CC1)CCN1C(=O)C1=NC=CS1 AGPKOMWNUUEILQ-UHFFFAOYSA-N 0.000 claims 1
- YTFXUYQLAYFSDK-UHFFFAOYSA-N (4-aminospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(2-nitrophenyl)methanone Chemical compound N1C2=CC=CC=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=CC=C1[N+]([O-])=O YTFXUYQLAYFSDK-UHFFFAOYSA-N 0.000 claims 1
- ZHMUHIIKTOAYBJ-UHFFFAOYSA-N (4-aminospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(4-ethylphenyl)methanone Chemical compound C1=CC(CC)=CC=C1C(=O)N1CCC2(N=C(N)C3=CC=CC=C3N2)CC1 ZHMUHIIKTOAYBJ-UHFFFAOYSA-N 0.000 claims 1
- ZYTYCDYFRYWVRC-UHFFFAOYSA-N (4-aminospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-(4-fluorophenyl)methanone Chemical compound N1C2=CC=CC=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=C(F)C=C1 ZYTYCDYFRYWVRC-UHFFFAOYSA-N 0.000 claims 1
- FOHCTSUZLZRUHD-UHFFFAOYSA-N (4-aminospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-[4-(trifluoromethyl)phenyl]methanone Chemical compound N1C2=CC=CC=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=C(C(F)(F)F)C=C1 FOHCTSUZLZRUHD-UHFFFAOYSA-N 0.000 claims 1
- YCPVARZUSFKJFC-UHFFFAOYSA-N (4-aminospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-thiophen-2-ylmethanone Chemical compound N1C2=CC=CC=C2C(N)=NC1(CC1)CCN1C(=O)C1=CC=CS1 YCPVARZUSFKJFC-UHFFFAOYSA-N 0.000 claims 1
- BANAKXZRCPMACJ-UHFFFAOYSA-N 1'-(1,3-thiazol-2-yl)spiro[1h-quinazoline-2,4'-piperidine]-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1(CC1)CCN1C1=NC=CS1 BANAKXZRCPMACJ-UHFFFAOYSA-N 0.000 claims 1
- LIWDTGMJUGTXEP-UHFFFAOYSA-N 1,2-dihydroquinazolin-4-amine Chemical compound C1=CC=C2C(N)=NCNC2=C1 LIWDTGMJUGTXEP-UHFFFAOYSA-N 0.000 claims 1
- OGXGDEWNXVPOSL-UHFFFAOYSA-N 1-(4-amino-5-fluorospiro[1h-quinazoline-2,4'-piperidine]-1'-yl)-4-phenoxybutan-1-one Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1(CC1)CCN1C(=O)CCCOC1=CC=CC=C1 OGXGDEWNXVPOSL-UHFFFAOYSA-N 0.000 claims 1
- ZCULUGBJSMGCDG-UHFFFAOYSA-N 1-methyl-2-phenyl-2h-quinazolin-4-amine Chemical compound N1=C(N)C2=CC=CC=C2N(C)C1C1=CC=CC=C1 ZCULUGBJSMGCDG-UHFFFAOYSA-N 0.000 claims 1
- GOAQIFIXXGXKFF-UHFFFAOYSA-N 2,2-dimethyl-1h-quinazolin-4-amine Chemical compound C1=CC=C2C(N)=NC(C)(C)NC2=C1 GOAQIFIXXGXKFF-UHFFFAOYSA-N 0.000 claims 1
- OESYASHKFVCSTL-UHFFFAOYSA-N 2-(1,3-thiazol-2-yl)-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1=NC=CS1 OESYASHKFVCSTL-UHFFFAOYSA-N 0.000 claims 1
- WPMXZRLXEGVIHU-UHFFFAOYSA-N 2-(1h-imidazol-2-yl)-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1=NC=CN1 WPMXZRLXEGVIHU-UHFFFAOYSA-N 0.000 claims 1
- OSFDRCPUKQFYBL-UHFFFAOYSA-N 2-(2-aminoethyl)-1,2-dihydroquinazolin-4-amine Chemical compound C1=CC=C2C(N)=NC(CCN)NC2=C1 OSFDRCPUKQFYBL-UHFFFAOYSA-N 0.000 claims 1
- SRZVHVKEKUVWKE-UHFFFAOYSA-N 2-(2-nitrophenyl)-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1=CC=CC=C1[N+]([O-])=O SRZVHVKEKUVWKE-UHFFFAOYSA-N 0.000 claims 1
- PZFBPUAOCMMRLZ-UHFFFAOYSA-N 2-(2-trimethylsilylethynyl)-1,2-dihydroquinazolin-4-amine Chemical compound C1=CC=C2C(N)=NC(C#C[Si](C)(C)C)NC2=C1 PZFBPUAOCMMRLZ-UHFFFAOYSA-N 0.000 claims 1
- DRBTXTOYZCLBJI-UHFFFAOYSA-N 2-(3-aminopropyl)-1,2-dihydroquinazolin-4-amine Chemical compound C1=CC=C2C(N)=NC(CCCN)NC2=C1 DRBTXTOYZCLBJI-UHFFFAOYSA-N 0.000 claims 1
- WKAUNVBOSOJUSS-UHFFFAOYSA-N 2-(4-amino-5-fluoro-1,2-dihydroquinazolin-2-yl)phenol Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1C1=CC=CC=C1O WKAUNVBOSOJUSS-UHFFFAOYSA-N 0.000 claims 1
- QFSLLBYFMDJKDY-UHFFFAOYSA-N 2-(4-nitrophenyl)-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1=CC=C([N+]([O-])=O)C=C1 QFSLLBYFMDJKDY-UHFFFAOYSA-N 0.000 claims 1
- HLWCINSTSGDTIB-UHFFFAOYSA-N 2-(5-nitrothiophen-2-yl)-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1=CC=C([N+]([O-])=O)S1 HLWCINSTSGDTIB-UHFFFAOYSA-N 0.000 claims 1
- RIOVUWRMOKFDQS-UHFFFAOYSA-N 2-(furan-2-yl)-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1=CC=CO1 RIOVUWRMOKFDQS-UHFFFAOYSA-N 0.000 claims 1
- KCGIUYAUVHLJJL-UHFFFAOYSA-N 2-[2-(2-aminoethyl)phenyl]-1,2-dihydroquinazolin-4-amine Chemical compound NCCC1=CC=CC=C1C1N=C(N)C2=CC=CC=C2N1 KCGIUYAUVHLJJL-UHFFFAOYSA-N 0.000 claims 1
- PFKHXJPYRVMZLW-UHFFFAOYSA-N 2-[4-(dimethylamino)phenyl]-1,2-dihydroquinazolin-4-amine Chemical compound C1=CC(N(C)C)=CC=C1C1N=C(N)C2=CC=CC=C2N1 PFKHXJPYRVMZLW-UHFFFAOYSA-N 0.000 claims 1
- GTEZSHJBMRWRIG-UHFFFAOYSA-N 2-amino-3-[4-(naphthalene-2-carbonyloxy)phenyl]propanoic acid Chemical group C1=CC(CC(N)C(O)=O)=CC=C1OC(=O)C1=CC=C(C=CC=C2)C2=C1 GTEZSHJBMRWRIG-UHFFFAOYSA-N 0.000 claims 1
- UIIANCNAHLNGKW-UHFFFAOYSA-N 2-anthracen-9-yl-1,2-dihydroquinazolin-4-amine Chemical compound C1=CC=C2C(C3N=C(C4=CC=CC=C4N3)N)=C(C=CC=C3)C3=CC2=C1 UIIANCNAHLNGKW-UHFFFAOYSA-N 0.000 claims 1
- YQSLFNIIJBAELO-UHFFFAOYSA-N 2-cyclobutyl-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1CCC1 YQSLFNIIJBAELO-UHFFFAOYSA-N 0.000 claims 1
- TWDKMKHCHFFGDT-UHFFFAOYSA-N 2-cyclobutyl-5-fluoro-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC(F)=C2C(N)=NC1C1CCC1 TWDKMKHCHFFGDT-UHFFFAOYSA-N 0.000 claims 1
- CODFUQOUEHCCNF-UHFFFAOYSA-N 2-cyclopentyl-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1CCCC1 CODFUQOUEHCCNF-UHFFFAOYSA-N 0.000 claims 1
- MXQUJZRTIGEIOF-UHFFFAOYSA-N 2-cyclopropyl-1,2-dihydroquinazolin-4-amine Chemical compound N1C2=CC=CC=C2C(N)=NC1C1CC1 MXQUJZRTIGEIOF-UHFFFAOYSA-N 0.000 claims 1
- YFDYGSPBBLYHLX-UHFFFAOYSA-N 2-cyclopropyl-1-methyl-2h-quinazolin-4-amine Chemical compound N1=C(N)C2=CC=CC=C2N(C)C1C1CC1 YFDYGSPBBLYHLX-UHFFFAOYSA-N 0.000 claims 1
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- 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
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- A—HUMAN NECESSITIES
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- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- 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]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
Landscapes
- Health & Medical Sciences (AREA)
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- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
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- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
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| SE9802333A SE9802333D0 (sv) | 1998-06-29 | 1998-06-29 | Novel combination |
Publications (1)
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| CZ20004896A3 true CZ20004896A3 (en) | 2001-06-13 |
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| PL203262B1 (pl) * | 1999-12-08 | 2009-09-30 | Pharmacia Corp | Substancja lecznicza celekoksyb, jej zastosowanie i sposób jej wytwarzania, kompozyt celekoksyb-inhibitor krystalizacji i sposób jego wytwarzania, kompozycja farmaceutyczna i sposób jej wytwarzania |
| JP2003523958A (ja) | 1999-12-23 | 2003-08-12 | ニトロメド インコーポレーテッド | ニトロソ化およびニトロシル化されたシクロオキシゲナーゼ−２の阻害剤、組成物ならびに使用法 |
| WO2002060378A2 (en) * | 2000-12-21 | 2002-08-08 | Nitromed, Inc. | Substituted aryl compounds as cyclooxygenase-2 selective inhibitors, compositions and methods of use |
| US7012098B2 (en) * | 2001-03-23 | 2006-03-14 | Pharmacia Corporation | Inhibitors of inducible nitric oxide synthase for chemoprevention and treatment of cancers |
| CN1638760A (zh) * | 2002-01-07 | 2005-07-13 | 法马西亚公司 | 用环加氧酶－2选择性抑制剂和阿司匹林的组合治疗疼痛、炎症和炎症相关疾病 |
| US7220749B2 (en) | 2002-06-11 | 2007-05-22 | Nitromed, Inc. | Nitrosated and/or nitrosylated cyclooxygenase-2 selective inhibitors, compositions and methods of use |
| US20040077691A1 (en) * | 2002-06-21 | 2004-04-22 | Medinox, Inc. | Hydroxamate derivatives of non-steroidal anti-inflammatory drugs |
| AU2003247792B2 (en) | 2002-07-03 | 2009-09-24 | Nicox S.A. | Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use |
| US7244753B2 (en) | 2002-07-29 | 2007-07-17 | Nitromed, Inc. | Cyclooxygenase-2 selective inhibitors, compositions and methods of use |
| WO2004019986A1 (en) * | 2002-08-29 | 2004-03-11 | Schering Aktiengesellschaft | Methods of treating acute respiratory distress syndrome |
| ES2275218T3 (es) | 2003-05-07 | 2007-06-01 | Osteologix A/S | Sales de estroncio hidrosolubles para el tratamiento de afecciones de cartilagos y/o huesos. |
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| EP2518059A4 (en) * | 2009-12-24 | 2013-05-29 | Shionogi & Co | 4-AMINO-1,3-THIAZINE OR OXAZINE DERIVATIVE |
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| WO2015075040A1 (de) | 2013-11-19 | 2015-05-28 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zum verbinden von silikongummi mit einem substrat |
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| DE202014004532U1 (de) | 2014-05-28 | 2014-08-05 | Hans-Dieter Cornelius | Hygienevorlage |
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| DE102014017938A1 (de) | 2014-12-05 | 2016-06-09 | Florian M. König | Trichter-turbinenartige Vorrichtung mit elektromagnetischer Rotationssteuerung von Flüssigkeits-Mischvorgängen |
| DE102015000003A1 (de) | 2015-01-02 | 2016-07-07 | Solukon Ingenieure GbR (vertretungsberechtigte Gesellschafter: Andreas Hartmann, 86391 Stadtbergen und Dominik Schmid, 86165 Augsburg) | Baubehälter für Produktionsanlagen zur Herstellung von Bauteilen in Schichtbauverfahren |
| DE102015008129A1 (de) | 2015-01-22 | 2016-07-28 | Liebherr-Hausgeräte Lienz Gmbh | Verfahren zur Bestimmung der Dämmeigenschaft einer Wandung eines wärmeisolierten Behältnisses |
| DE102015000887A1 (de) | 2015-01-23 | 2016-07-28 | Arnulf Deinzer | Zahnreinigungsgerät mit ausfahrbaren Borsten |
| DE102015015877A1 (de) | 2015-12-09 | 2017-06-14 | Bayerisches Zentrum für angewandte Energieforschung, e.V. (ZAE Bayern) | Optisch schaltendes Element |
| DE102016006696A1 (de) | 2016-05-27 | 2017-11-30 | Christoph Jaeger | Flugautosystem |
| DE202016004226U1 (de) | 2016-07-06 | 2016-11-11 | Helmut Senkel | Schienensystem mit verfahrbaren Verbrauchern |
| CN106279585A (zh) * | 2016-08-26 | 2017-01-04 | 宁波圣达精工智能科技有限公司 | 一种阻燃智能密集书架的制备方法 |
| CN108832306B (zh) * | 2018-06-13 | 2023-11-03 | 中国科学院国家天文台 | 一种fast反射面中心孔柔性封堵结构 |
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|---|---|---|---|---|
| EE9800116A (et) * | 1995-10-17 | 1998-10-15 | Astra Pharmaceuticals Limited | Farmatseutiliselt aktiivsed kinasoliini ühendid |
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1998
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1999
- 1999-06-23 BR BR9911666-9A patent/BR9911666A/pt not_active Application Discontinuation
- 1999-06-23 CN CN99810007A patent/CN1313769A/zh active Pending
- 1999-06-23 AU AU49447/99A patent/AU4944799A/en not_active Abandoned
- 1999-06-23 ID IDW20002691A patent/ID27394A/id unknown
- 1999-06-23 JP JP2000556785A patent/JP2002519324A/ja active Pending
- 1999-06-23 US US09/380,379 patent/US6248745B1/en not_active Expired - Fee Related
- 1999-06-23 CA CA002334515A patent/CA2334515A1/en not_active Abandoned
- 1999-06-23 PL PL99345028A patent/PL345028A1/xx not_active Application Discontinuation
- 1999-06-23 CZ CZ20004896A patent/CZ20004896A3/cs unknown
- 1999-06-23 EP EP99933384A patent/EP1100505A1/en not_active Withdrawn
- 1999-06-23 KR KR1020007014933A patent/KR20010053252A/ko not_active Withdrawn
- 1999-06-23 MX MXPA00012162 patent/MXPA00012162A/es unknown
- 1999-06-23 WO PCT/SE1999/001144 patent/WO2000000200A1/en not_active Application Discontinuation
- 1999-06-23 EE EEP200000766A patent/EE200000766A/xx unknown
- 1999-06-23 SK SK1848-2000A patent/SK18482000A3/sk unknown
- 1999-06-23 TR TR2000/03808T patent/TR200003808T2/xx unknown
- 1999-06-23 IL IL14002299A patent/IL140022A0/xx unknown
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2000
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- 2000-11-30 ZA ZA200007076A patent/ZA200007076B/en unknown
- 2000-12-21 NO NO20006559A patent/NO20006559L/no not_active Application Discontinuation
- 2000-12-27 IS IS5794A patent/IS5794A/is unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL140022A0 (en) | 2002-02-10 |
| EP1100505A1 (en) | 2001-05-23 |
| IS5794A (is) | 2000-12-27 |
| AU4944799A (en) | 2000-01-17 |
| ZA200007076B (en) | 2002-02-28 |
| CA2334515A1 (en) | 2000-01-06 |
| EE200000766A (et) | 2002-06-17 |
| SE9802333D0 (sv) | 1998-06-29 |
| NO20006559L (no) | 2001-02-28 |
| US6248745B1 (en) | 2001-06-19 |
| JP2002519324A (ja) | 2002-07-02 |
| MXPA00012162A (es) | 2001-05-01 |
| BR9911666A (pt) | 2001-03-20 |
| IN2000MU00721A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2005-03-18 |
| WO2000000200A1 (en) | 2000-01-06 |
| KR20010053252A (ko) | 2001-06-25 |
| NO20006559D0 (no) | 2000-12-21 |
| CN1313769A (zh) | 2001-09-19 |
| PL345028A1 (en) | 2001-11-19 |
| ID27394A (id) | 2001-04-05 |
| TR200003808T2 (tr) | 2001-06-21 |
| SK18482000A3 (sk) | 2001-07-10 |
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