ES2353055T1 - Uso de compuestos antagonistas de crth2. - Google Patents
Uso de compuestos antagonistas de crth2. Download PDFInfo
- Publication number
- ES2353055T1 ES2353055T1 ES08851028T ES08851028T ES2353055T1 ES 2353055 T1 ES2353055 T1 ES 2353055T1 ES 08851028 T ES08851028 T ES 08851028T ES 08851028 T ES08851028 T ES 08851028T ES 2353055 T1 ES2353055 T1 ES 2353055T1
- Authority
- ES
- Spain
- Prior art keywords
- methyl
- acid
- fluoro
- acetic acid
- indole
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 150000001875 compounds Chemical class 0.000 title claims abstract 33
- 229940124003 CRTH2 antagonist Drugs 0.000 title claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 11
- 125000000217 alkyl group Chemical group 0.000 claims abstract 10
- 125000005843 halogen group Chemical group 0.000 claims abstract 8
- 125000001424 substituent group Chemical group 0.000 claims abstract 8
- 125000003118 aryl group Chemical group 0.000 claims abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 6
- 239000001257 hydrogen Substances 0.000 claims abstract 6
- 239000013566 allergen Substances 0.000 claims abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 4
- 206010027654 Allergic conditions Diseases 0.000 claims abstract 3
- 229910052736 halogen Inorganic materials 0.000 claims abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 2
- 150000003839 salts Chemical class 0.000 claims abstract 2
- 239000012453 solvate Substances 0.000 claims abstract 2
- 239000002253 acid Substances 0.000 claims 121
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 27
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims 8
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 claims 7
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 6
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 5
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 5
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 5
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 3
- 229930192474 thiophene Natural products 0.000 claims 3
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 claims 2
- UEMGWPRHOOEKTA-UHFFFAOYSA-N 1,3-difluorobenzene Chemical compound FC1=CC=CC(F)=C1 UEMGWPRHOOEKTA-UHFFFAOYSA-N 0.000 claims 2
- VHZQRDXTXVSINR-UHFFFAOYSA-N 2-[3-[(2-benzylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)CC1=CC=CC=C1 VHZQRDXTXVSINR-UHFFFAOYSA-N 0.000 claims 2
- DJBHJFYUQAZFRB-UHFFFAOYSA-N 2-[3-[(2-cyclobutylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)C1CCC1 DJBHJFYUQAZFRB-UHFFFAOYSA-N 0.000 claims 2
- WIOOBYGJMHMUPJ-UHFFFAOYSA-N 2-[3-[(2-cyclohexylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)C1CCCCC1 WIOOBYGJMHMUPJ-UHFFFAOYSA-N 0.000 claims 2
- DSIZPFACZSRXAM-UHFFFAOYSA-N 2-[3-[(2-cyclopentylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)C1CCCC1 DSIZPFACZSRXAM-UHFFFAOYSA-N 0.000 claims 2
- OJAHKYMVSLLQPG-UHFFFAOYSA-N 2-[3-[(3-benzylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=1)=CC=CC=1S(=O)(=O)CC1=CC=CC=C1 OJAHKYMVSLLQPG-UHFFFAOYSA-N 0.000 claims 2
- BRNIUXLBABJPPA-UHFFFAOYSA-N 2-[3-[(4-benzylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=C1)=CC=C1S(=O)(=O)CC1=CC=CC=C1 BRNIUXLBABJPPA-UHFFFAOYSA-N 0.000 claims 2
- GRCSJFWAKMMIDQ-UHFFFAOYSA-N 2-[3-[(4-cyclohexylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=C1)=CC=C1S(=O)(=O)C1CCCCC1 GRCSJFWAKMMIDQ-UHFFFAOYSA-N 0.000 claims 2
- JZSPIXAOOJTSGW-UHFFFAOYSA-N 2-[3-[(4-cyclopentylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=C1)=CC=C1S(=O)(=O)C1CCCC1 JZSPIXAOOJTSGW-UHFFFAOYSA-N 0.000 claims 2
- GHYFLKZMAHTBNE-UHFFFAOYSA-N 2-[3-[[2-(benzenesulfonyl)phenyl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1 GHYFLKZMAHTBNE-UHFFFAOYSA-N 0.000 claims 2
- HKWZIRZRRMVZLR-UHFFFAOYSA-N 2-[3-[[2-(benzenesulfonyl)pyridin-3-yl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CN=C1S(=O)(=O)C1=CC=CC=C1 HKWZIRZRRMVZLR-UHFFFAOYSA-N 0.000 claims 2
- RCDLAJQERQUBRP-UHFFFAOYSA-N 2-[3-[[4-[(4-chlorophenyl)methylsulfonyl]phenyl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=C1)=CC=C1S(=O)(=O)CC1=CC=C(Cl)C=C1 RCDLAJQERQUBRP-UHFFFAOYSA-N 0.000 claims 2
- FUQCZYPTBHJSQX-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-3-[(2-phenoxyphenyl)methyl]indol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1OC1=CC=CC=C1 FUQCZYPTBHJSQX-UHFFFAOYSA-N 0.000 claims 2
- NRPMXZUNAFYCRH-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-3-[(2-piperidin-1-ylsulfonylphenyl)methyl]indol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)N1CCCCC1 NRPMXZUNAFYCRH-UHFFFAOYSA-N 0.000 claims 2
- PAKMLKICQKNIQV-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-3-[(2-pyrrolidin-1-ylsulfonylphenyl)methyl]indol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)N1CCCC1 PAKMLKICQKNIQV-UHFFFAOYSA-N 0.000 claims 2
- UFWCTHMEWOEIES-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-3-[(3-piperidin-1-ylsulfonylphenyl)methyl]indol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=1)=CC=CC=1S(=O)(=O)N1CCCCC1 UFWCTHMEWOEIES-UHFFFAOYSA-N 0.000 claims 2
- XUYPKIUZNJXPOQ-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-3-[(3-pyrrolidin-1-ylsulfonylphenyl)methyl]indol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=1)=CC=CC=1S(=O)(=O)N1CCCC1 XUYPKIUZNJXPOQ-UHFFFAOYSA-N 0.000 claims 2
- ZENZJBGBJVAPCX-UHFFFAOYSA-N 2-[5-fluoro-2-methyl-3-[(4-piperidin-1-ylsulfonylphenyl)methyl]indol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=C1)=CC=C1S(=O)(=O)N1CCCCC1 ZENZJBGBJVAPCX-UHFFFAOYSA-N 0.000 claims 2
- CCZUSMXZUULADP-UHFFFAOYSA-N 2-[5-fluoro-3-[[2-(4-methoxyphenoxy)phenyl]methyl]-2-methylindol-1-yl]acetic acid Chemical compound C1=CC(OC)=CC=C1OC1=CC=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 CCZUSMXZUULADP-UHFFFAOYSA-N 0.000 claims 2
- WYZCOQATIZDSDW-UHFFFAOYSA-N 2-[5-fluoro-3-[[3-[(4-fluorophenyl)methylsulfonyl]phenyl]methyl]-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=1)=CC=CC=1S(=O)(=O)CC1=CC=C(F)C=C1 WYZCOQATIZDSDW-UHFFFAOYSA-N 0.000 claims 2
- NVXAOBKIOMYHKS-UHFFFAOYSA-N 2-[5-fluoro-3-[[4-[(4-fluorophenyl)methylsulfonyl]phenyl]methyl]-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(C=C1)=CC=C1S(=O)(=O)CC1=CC=C(F)C=C1 NVXAOBKIOMYHKS-UHFFFAOYSA-N 0.000 claims 2
- 108060003345 Adrenergic Receptor Proteins 0.000 claims 2
- 102000017910 Adrenergic receptor Human genes 0.000 claims 2
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- 239000000556 agonist Substances 0.000 claims 2
- NDAUXUAQIAJITI-UHFFFAOYSA-N albuterol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C(CO)=C1 NDAUXUAQIAJITI-UHFFFAOYSA-N 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 208000010247 contact dermatitis Diseases 0.000 claims 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims 2
- LMOINURANNBYCM-UHFFFAOYSA-N metaproterenol Chemical compound CC(C)NCC(O)C1=CC(O)=CC(O)=C1 LMOINURANNBYCM-UHFFFAOYSA-N 0.000 claims 2
- 229960002657 orciprenaline Drugs 0.000 claims 2
- -1 pentan-3-ylsulfonyl Chemical group 0.000 claims 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims 2
- 229940044551 receptor antagonist Drugs 0.000 claims 2
- 239000002464 receptor antagonist Substances 0.000 claims 2
- 229960002052 salbutamol Drugs 0.000 claims 2
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 claims 2
- XWTYSIMOBUGWOL-UHFFFAOYSA-N (+-)-Terbutaline Chemical compound CC(C)(C)NCC(O)C1=CC(O)=CC(O)=C1 XWTYSIMOBUGWOL-UHFFFAOYSA-N 0.000 claims 1
- CNIIGCLFLJGOGP-UHFFFAOYSA-N 2-(1-naphthalenylmethyl)-4,5-dihydro-1H-imidazole Chemical compound C=1C=CC2=CC=CC=C2C=1CC1=NCCN1 CNIIGCLFLJGOGP-UHFFFAOYSA-N 0.000 claims 1
- YGWFCQYETHJKNX-UHFFFAOYSA-N 2-[(4-tert-butyl-2,6-dimethylphenyl)methyl]-4,5-dihydro-1h-imidazol-3-ium;chloride Chemical compound [Cl-].CC1=CC(C(C)(C)C)=CC(C)=C1CC1=NCC[NH2+]1 YGWFCQYETHJKNX-UHFFFAOYSA-N 0.000 claims 1
- ZKLPARSLTMPFCP-OAQYLSRUSA-N 2-[2-[4-[(R)-(4-chlorophenyl)-phenylmethyl]-1-piperazinyl]ethoxy]acetic acid Chemical compound C1CN(CCOCC(=O)O)CCN1[C@@H](C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 ZKLPARSLTMPFCP-OAQYLSRUSA-N 0.000 claims 1
- AUHRDYPGCRKIKZ-UHFFFAOYSA-N 2-[2-methyl-3-(quinolin-2-ylmethyl)indol-1-yl]acetic acid Chemical compound C12=CC=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=C(C=CC=C2)C2=N1 AUHRDYPGCRKIKZ-UHFFFAOYSA-N 0.000 claims 1
- RJDBTFKKUDPQCO-UHFFFAOYSA-N 2-[3-[(1-benzylpyrazol-4-yl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(=C1)C=NN1CC1=CC=CC=C1 RJDBTFKKUDPQCO-UHFFFAOYSA-N 0.000 claims 1
- YVLZYLQOFHWRHB-UHFFFAOYSA-N 2-[3-[(2-benzylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1CC1=CC=CC=C1 YVLZYLQOFHWRHB-UHFFFAOYSA-N 0.000 claims 1
- AVMIPJYSHKQHCN-UHFFFAOYSA-N 2-[3-[(2-butan-2-ylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound CCC(C)S(=O)(=O)C1=CC=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 AVMIPJYSHKQHCN-UHFFFAOYSA-N 0.000 claims 1
- KTZAXDGOJAJDPM-UHFFFAOYSA-N 2-[3-[(2-butylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound CCCCS(=O)(=O)C1=CC=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 KTZAXDGOJAJDPM-UHFFFAOYSA-N 0.000 claims 1
- DMLDQWFRMAXMNY-UHFFFAOYSA-N 2-[3-[(2-ethylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound CCS(=O)(=O)C1=CC=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 DMLDQWFRMAXMNY-UHFFFAOYSA-N 0.000 claims 1
- NFXQLCUFDMEXQW-UHFFFAOYSA-N 2-[3-[(2-tert-butylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1S(=O)(=O)C(C)(C)C NFXQLCUFDMEXQW-UHFFFAOYSA-N 0.000 claims 1
- FJGYKUGWEQGURY-UHFFFAOYSA-N 2-[3-[(4,4-dimethyl-2,3-dihydrothiochromen-6-yl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=C(SCCC2(C)C)C2=C1 FJGYKUGWEQGURY-UHFFFAOYSA-N 0.000 claims 1
- MBFPGMJHQDRALK-UHFFFAOYSA-N 2-[3-[(4-butylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C1=CC(S(=O)(=O)CCCC)=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 MBFPGMJHQDRALK-UHFFFAOYSA-N 0.000 claims 1
- CMUBATJXNUXZRE-UHFFFAOYSA-N 2-[3-[(4-chlorophenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=C(Cl)C=C1 CMUBATJXNUXZRE-UHFFFAOYSA-N 0.000 claims 1
- CJRMMJVISVGLBQ-UHFFFAOYSA-N 2-[3-[(4-ethylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C1=CC(S(=O)(=O)CC)=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 CJRMMJVISVGLBQ-UHFFFAOYSA-N 0.000 claims 1
- ZCUYLCQVFFSXST-UHFFFAOYSA-N 2-[3-[(4-tert-butylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=C(C(C)(C)C)C=C1 ZCUYLCQVFFSXST-UHFFFAOYSA-N 0.000 claims 1
- GFKLIKDQNJMYMM-UHFFFAOYSA-N 2-[3-[(4-tert-butylsulfonylphenyl)methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=C(S(=O)(=O)C(C)(C)C)C=C1 GFKLIKDQNJMYMM-UHFFFAOYSA-N 0.000 claims 1
- BHEFOTSBJZWUIS-UHFFFAOYSA-N 2-[3-[1-(4-chlorophenyl)ethyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound CC=1N(CC(O)=O)C2=CC=C(F)C=C2C=1C(C)C1=CC=C(Cl)C=C1 BHEFOTSBJZWUIS-UHFFFAOYSA-N 0.000 claims 1
- XYLOSFUTUBOLNB-UHFFFAOYSA-N 2-[3-[1-(4-tert-butylphenyl)ethyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound CC=1N(CC(O)=O)C2=CC=C(F)C=C2C=1C(C)C1=CC=C(C(C)(C)C)C=C1 XYLOSFUTUBOLNB-UHFFFAOYSA-N 0.000 claims 1
- HGJOOXHUFSXPAI-UHFFFAOYSA-N 2-[3-[[1-(2,4-dichlorophenyl)sulfonylpyrrol-2-yl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CN1S(=O)(=O)C1=CC=C(Cl)C=C1Cl HGJOOXHUFSXPAI-UHFFFAOYSA-N 0.000 claims 1
- JNXAGAQABMLZMP-UHFFFAOYSA-N 2-[3-[[1-(benzenesulfonyl)indol-2-yl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC2=CC=CC=C2N1S(=O)(=O)C1=CC=CC=C1 JNXAGAQABMLZMP-UHFFFAOYSA-N 0.000 claims 1
- YSVZRJDOEFUDEM-UHFFFAOYSA-N 2-[3-[[1-(benzenesulfonyl)pyrrol-2-yl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CN1S(=O)(=O)C1=CC=CC=C1 YSVZRJDOEFUDEM-UHFFFAOYSA-N 0.000 claims 1
- YCQINVWJJWUOHH-UHFFFAOYSA-N 2-[3-[[2-(4-chlorophenyl)phenyl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC1=CC=CC=C1C1=CC=C(Cl)C=C1 YCQINVWJJWUOHH-UHFFFAOYSA-N 0.000 claims 1
- XBJNKUJGGZDKGY-UHFFFAOYSA-N 2-[3-[[2-(benzenesulfonyl)-1,3-thiazol-5-yl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C12=CC(F)=CC=C2N(CC(O)=O)C(C)=C1CC(S1)=CN=C1S(=O)(=O)C1=CC=CC=C1 XBJNKUJGGZDKGY-UHFFFAOYSA-N 0.000 claims 1
- RENDLZVWZMAZHA-UHFFFAOYSA-N 2-[3-[[2-(butylsulfamoyl)phenyl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound CCCCNS(=O)(=O)C1=CC=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 RENDLZVWZMAZHA-UHFFFAOYSA-N 0.000 claims 1
- GGFNCDSUSUQDDS-UHFFFAOYSA-N 2-[3-[[3-(butylsulfamoyl)phenyl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound CCCCNS(=O)(=O)C1=CC=CC(CC=2C3=CC(F)=CC=C3N(CC(O)=O)C=2C)=C1 GGFNCDSUSUQDDS-UHFFFAOYSA-N 0.000 claims 1
- VGKDMJLXTGOBSW-UHFFFAOYSA-N 2-[3-[[4-(butylsulfamoyl)phenyl]methyl]-5-fluoro-2-methylindol-1-yl]acetic acid Chemical compound C1=CC(S(=O)(=O)NCCCC)=CC=C1CC1=C(C)N(CC(O)=O)C2=CC=C(F)C=C12 VGKDMJLXTGOBSW-UHFFFAOYSA-N 0.000 claims 1
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- JCCNYMKQOSZNPW-UHFFFAOYSA-N loratadine Chemical compound C1CN(C(=O)OCC)CCC1=C1C2=NC=CC=C2CCC2=CC(Cl)=CC=C21 JCCNYMKQOSZNPW-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- VNXBKJFUJUWOCW-UHFFFAOYSA-N methylcyclopropane Chemical compound CC1CC1 VNXBKJFUJUWOCW-UHFFFAOYSA-N 0.000 claims 1
- JCDWETOKTFWTHA-UHFFFAOYSA-N methylsulfonylbenzene Chemical compound CS(=O)(=O)C1=CC=CC=C1 JCDWETOKTFWTHA-UHFFFAOYSA-N 0.000 claims 1
- 229960002744 mometasone furoate Drugs 0.000 claims 1
- WOFMFGQZHJDGCX-ZULDAHANSA-N mometasone furoate Chemical compound O([C@]1([C@@]2(C)C[C@H](O)[C@]3(Cl)[C@@]4(C)C=CC(=O)C=C4CC[C@H]3[C@@H]2C[C@H]1C)C(=O)CCl)C(=O)C1=CC=CO1 WOFMFGQZHJDGCX-ZULDAHANSA-N 0.000 claims 1
- 230000003551 muscarinic effect Effects 0.000 claims 1
- BEEDODBODQVSIM-UHFFFAOYSA-N oxymetazoline hydrochloride Chemical compound Cl.CC1=CC(C(C)(C)C)=C(O)C(C)=C1CC1=NCCN1 BEEDODBODQVSIM-UHFFFAOYSA-N 0.000 claims 1
- 229960005162 oxymetazoline hydrochloride Drugs 0.000 claims 1
- 208000022719 perennial allergic rhinitis Diseases 0.000 claims 1
- 229960001802 phenylephrine Drugs 0.000 claims 1
- SONNWYBIRXJNDC-VIFPVBQESA-N phenylephrine Chemical compound CNC[C@H](O)C1=CC=CC(O)=C1 SONNWYBIRXJNDC-VIFPVBQESA-N 0.000 claims 1
- DLNKOYKMWOXYQA-APPZFPTMSA-N phenylpropanolamine Chemical compound C[C@@H](N)[C@H](O)C1=CC=CC=C1 DLNKOYKMWOXYQA-APPZFPTMSA-N 0.000 claims 1
- 229960000395 phenylpropanolamine Drugs 0.000 claims 1
- 229960005414 pirbuterol Drugs 0.000 claims 1
- 229960005205 prednisolone Drugs 0.000 claims 1
- OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 claims 1
- 229960004618 prednisone Drugs 0.000 claims 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 claims 1
- JCRIVQIOJSSCQD-UHFFFAOYSA-N propylhexedrine Chemical compound CNC(C)CC1CCCCC1 JCRIVQIOJSSCQD-UHFFFAOYSA-N 0.000 claims 1
- 229960000786 propylhexedrine Drugs 0.000 claims 1
- KWGRBVOPPLSCSI-WCBMZHEXSA-N pseudoephedrine Chemical compound CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WCBMZHEXSA-N 0.000 claims 1
- 229960003908 pseudoephedrine Drugs 0.000 claims 1
- 150000003233 pyrroles Chemical class 0.000 claims 1
- MIXMJCQRHVAJIO-TZHJZOAOSA-N qk4dys664x Chemical compound O.C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]2(C)C[C@@H]1O.C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]2(C)C[C@@H]1O MIXMJCQRHVAJIO-TZHJZOAOSA-N 0.000 claims 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 1
- 229960004017 salmeterol Drugs 0.000 claims 1
- 208000017022 seasonal allergic rhinitis Diseases 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 229960000195 terbutaline Drugs 0.000 claims 1
- BJORNXNYWNIWEY-UHFFFAOYSA-N tetrahydrozoline hydrochloride Chemical compound Cl.N1CCN=C1C1C2=CC=CC=C2CCC1 BJORNXNYWNIWEY-UHFFFAOYSA-N 0.000 claims 1
- 229940021790 tetrahydrozoline hydrochloride Drugs 0.000 claims 1
- 229960000278 theophylline Drugs 0.000 claims 1
- LERNTVKEWCAPOY-DZZGSBJMSA-N tiotropium Chemical compound O([C@H]1C[C@@H]2[N+]([C@H](C1)[C@@H]1[C@H]2O1)(C)C)C(=O)C(O)(C=1SC=CC=1)C1=CC=CS1 LERNTVKEWCAPOY-DZZGSBJMSA-N 0.000 claims 1
- 229940110309 tiotropium Drugs 0.000 claims 1
- 229960002117 triamcinolone acetonide Drugs 0.000 claims 1
- YNDXUCZADRHECN-JNQJZLCISA-N triamcinolone acetonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O YNDXUCZADRHECN-JNQJZLCISA-N 0.000 claims 1
- 229960001095 xylometazoline hydrochloride Drugs 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 1
- 101100134925 Gallus gallus COR6 gene Proteins 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
Classifications
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- 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
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- A—HUMAN NECESSITIES
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- 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
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- A—HUMAN NECESSITIES
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- 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
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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Abstract
Un compuesto de fórmula general (I): **(Ver fórmula)** en el que R1 es alquilo C1-C6; R2 es halógeno; y R3 es arilo o heteroarilo opcionalmente sustituidos con uno o más sustituyentes seleccionados de halo, OH, CN, R6, COR6, CH2R6, OR6, SR6, SO2R6 o SO2YR6; R6 es alquilo C1-C6, cicloalquilo C3-C8, heterociclilo, arilo o heteroarilo, cualquiera de los cuales puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados de halo, OH, CN, NO2, alquilo C1-C6 u O(alquilo C1-C6); e Y es NH o una cadena de alquileno C1-C4 lineal o ramificada; R4 es H o alquilo C1-C4; R5 es hidrógeno, alquilo C1-C6, arilo, (CH2)mOC(=O)-alquilo(C1-C6), ((CH2)mO)nCH2CH2X, (CH2)mN(R7)2 o CH((CH2)mO(C=O)R8)2; m es 1 ó 2; n es 1-4; X es OR7 o N(R7)2; R7 es hidrógeno o metilo; R8 es alquilo C1-C18; o una sal, un hidrato, un solvato o un complejo farmacéuticamente aceptable del mismo; para el tratamiento de una afección alérgica que está inducida por la presencia de un alérgeno al que es sensible el paciente, en donde el tratamiento comprende al menos un ciclo de tratamiento que comprende: a. un primer período de dos a ocho días durante el cual se administra al paciente el compuesto de fórmula general (I); y b. un segundo período de al menos siete días durante el cual se administra al paciente el compuesto de fórmula general (I) en una cantidad reducida; en donde el alérgeno está presente o se sospecha que está presente a lo largo del tratamiento y en donde el compuesto de fórmula general (I) retiene al menos 50% de sus eficacia durante el segundo período del ciclo de tratamiento.
Claims (15)
1. Un compuesto de fórmula general (I):
en el
que
R^{1} es alquilo
C_{1}-C_{6};
R^{2} es halógeno; y
R^{3} es arilo o heteroarilo opcionalmente
sustituidos con uno o más sustituyentes seleccionados de halo, OH,
CN, R^{6}, COR^{6}, CH_{2}R^{6}, OR^{6}, SR^{6},
SO_{2}R^{6} o SO_{2}YR^{6};
- R^{6} es alquilo C_{1}-C_{6}, cicloalquilo C_{3}-C_{8}, heterociclilo, arilo o heteroarilo, cualquiera de los cuales puede estar opcionalmente sustituido con uno o más sustituyentes seleccionados de halo, OH, CN, NO_{2}, alquilo C_{1}-C_{6} u O(alquilo C_{1}-C_{6}); e
- Y es NH o una cadena de alquileno C_{1}-C_{4} lineal o ramificada;
R^{4} es H o alquilo
C_{1}-C_{4};
R^{5} es hidrógeno, alquilo
C_{1}-C_{6}, arilo,
(CH_{2})_{m}OC(=O)-alquilo(C_{1}-C_{6}),
((CH_{2})_{m}O)_{n}CH_{2}CH_{2}X,
(CH_{2})_{m}N(R^{7})_{2} o
CH((CH_{2})_{m}O(C=O)R^{8})_{2};
- m es 1 ó 2;
- n es 1-4;
- X es OR^{7} o N(R^{7})_{2};
- R^{7} es hidrógeno o metilo;
- R^{8} es alquilo C_{1}-C_{18};
o una sal, un hidrato, un solvato o un complejo
farmacéuticamente aceptable del mismo;
para el tratamiento de una afección alérgica que
está inducida por la presencia de un alérgeno al que es sensible el
paciente, en donde el tratamiento comprende al menos un ciclo de
tratamiento que comprende:
- a.
- un primer período de dos a ocho días durante el cual se administra al paciente el compuesto de fórmula general (I); y
- b.
- un segundo período de al menos siete días durante el cual se administra al paciente el compuesto de fórmula general (I) en una cantidad reducida;
en donde el alérgeno está presente o se sospecha
que está presente a lo largo del tratamiento y en donde el compuesto
de fórmula general (I) retiene al menos 50% de sus eficacia durante
el segundo período del ciclo de tratamiento.
2. Un compuesto de acuerdo con la reivindicación
1, en el que, durante el segundo período del ciclo de tratamiento,
el compuesto retiene al menos 80% de su eficacia.
3. Un compuesto de acuerdo con la reivindicación
1 o la reivindicación 2, en el que, durante el segundo período del
ciclo de tratamiento, se interrumpe la administración del compuesto
antagonista de CRTH2.
4. Un compuesto de acuerdo con una cualquiera de
las reivindicaciones 1 a 3, en el que el segundo período del ciclo
de tratamiento dura al menos 28 días.
5. Un compuesto de acuerdo con una cualquiera de
las reivindicaciones 1 a 4, en el que, en el primer período del
ciclo de tratamiento, el compuesto se administra una vez al día.
6. Un compuesto de acuerdo con una cualquiera de
las reivindicaciones 1 a 5, que incluye además uno o más ciclos de
tratamiento adicionales.
7. Un compuesto de acuerdo con una cualquiera de
las reivindicaciones 1 a 6, en el que la afección alérgica es asma
(incluyendo asma alérgica), alergias alimentarias, urticaria aguda y
crónica, rinitis alérgica perenne, rinitis alérgica estacional,
dermatitis atópica, hipersensibilidad por contacto (incluyendo
dermatitis por contacto) o conjuntivitis, especialmente
conjuntivitis alérgica.
8. Un compuesto de acuerdo con una cualquiera de
las reivindicaciones 1 a 7, en el que, en el compuesto de fórmula
general (I), independientemente o en cualquier combinación:
R^{1} es fluoro;
R^{2} es alquilo
C_{1}-C_{4}, particularmente metilo o etilo,
pero más especialmente metilo;
R^{4} es H o metilo;
R^{3} es quinolina, quinoxalina, isoquinolina,
tiazol, fenilo, naftaleno, tiofeno, pirrol o piridina, cualquiera de
los cuales puede estar sustituido según se indica en la
reivindicación 1; y
R_{5} es hidrógeno.
9. Un compuesto de acuerdo con una cualquiera de
las reivindicaciones 1 a 8, en el que, en el compuesto de fórmula
general (I), R^{3} es quinolina, fenilo, naftaleno, tiofeno,
pirrol o piridina opcionalmente sustituido.
10. Un compuesto de acuerdo con la
reivindicación 10, en el que, en el compuesto de fórmula general
(I):
- a.
- R^{3} es quinolina, que no está sustituida o está sustituida con uno o más sustituyentes halo; o
- b.
- R^{3} es fenilo, naftaleno, tiofeno, pirrol o piridina, opcionalmente sustituidos con uno o más sustituyentes seleccionados de OR^{6}, SO_{2}R^{6} o SO_{2}YR^{6};
donde R^{6} y Y son como se definen en la
reivindicación 1.
11. Un compuesto de acuerdo con la
reivindicación 10, en el que, en el compuesto de fórmula general
(I), R^{6} es alquilo C_{1}-C_{6}, un grupo
cicloalquilo de 4 a 6 miembros, un grupo heterociclilo de 5 ó 6
miembros o fenilo, y
cuando R^{3} está sustituido con
SO_{2}R^{6} o SO_{2}YR^{6}, Y es CH_{2} y el grupo R^{6}
no está sustituido o está sustituido con uno o más sustituyentes
elegidos de metilo y halo; o
cuando R^{3} está sustituido con OR^{6}, el
grupo R^{6} no está sustituido o está sustituido con uno o más
sustituyentes elegidos de halo, ciano, alquilo
C_{1}-C_{4} y O(alquilo
C_{1}-C_{4}).
12. Un compuesto de acuerdo con la
reivindicación 10 o la reivindicación 11, en el que R^{3} es un
resto 3-piridilo opcionalmente sustituido con uno o
más sustituyentes seleccionados de OR^{6}, SO_{2}R^{6} o
SO_{2}YR^{6}; donde R^{6} e Y son como se definen en la
reivindicación 1.
13. Un compuesto de acuerdo con una cualquiera
de las reivindicaciones 1 a 8, en el que el compuesto de fórmula
general (I) es:
Ácido
{3-[1-(4-cloro-fenil)-etil]-5-fluoro-2-metil-indol-1-il}-acético;
Ácido
{5-fluoro-2-metil-3-[1-(4-trifluorometil-fenil)-etil]-indol-1-il}-acético;
Ácido
{3-[1-(4-terc-butil-fenil)-etil]-5-fluoro-2-metil-indol-1-il}-acético;
Ácido
{5-fluoro-3-
[1-(4-metanosulfonil-fenil)-etil]-2-metil-indol-1-il}-acético;
Ácido
[5-fluoro-2-metil-3-(1-naftalen-2-il-etil)-indol-1-il]-acético;
Ácido
(5-fluoro-2-metil-3-quinolin-2-ilmetil-indol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-naftalen-2-ilmetil-indol-1-il)-acético;
Ácido
[5-fluoro-3-(8-hidroxiquinolin-2-ilmetil)-2-metil-indol-1-il]-acético;
Ácido
[5-fluoro-2-metil-3-(quinoxalin-2-ilmetil)indol-1-il]-acético;
Ácido
[5-fluoro-3-(4-metoxi-bencil)-2-metil-indol-1-il]-acético;
Ácido
[5-fluoro-2-metil-3-(1,3-tiazol-2-ilmetil)indol-1-il]-acético;
Ácido
[3-(4-cloro-bencil)-5-fluoro-2-metil-indol-1-il]-acético;
Ácido
[5-fluoro-2-metil-3-(4-trifluorometil-bencil)-indol-1-il]-acético;
Ácido
[5-fluoro-2-metil-3-(4-terc-butil-bencil)-indol-1-il]-acético;
Ácido
{5-fluoro-2-metil-3-[(4-fenilfenil)metil]indol-1-il}-acético;
Ácido
[5-fluoro-3-(4-metanosulfonil-bencil)-2-metil-indol-1-il]-acético;
Ácido
{5-fluoro-3-[(6-fluoroquinolin-2-il)metil]-2-metilindol-1-il}-acético;
Ácido
(2-metil-3-quinolin-2-ilmetil-indol-1-il)-acético;
Ácido
(5-cloro-2-metil-3-quinolin-2-ilmetil-indol-1-il)-acético;
Ácido
(3-{[1-(bencenosulfonil)pirrol-2-il]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
[5-fluoro-2-metil-3-({1-[(4-metilbenceno)sulfonil]pirrol-2-il}metil)indol-1-il]-acético;
Ácido
[3-({1-[(2,4-difluorobenceno)sulfonil]pirrol-2-il}metil)-5-fluoro-2-etilindol-1-il]-acético;
Ácido
(3-{[2-(bencenosulfonil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
[3-({2-[(4-clorobenceno)sulfonil]fenil}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
[5-fluoro-3-({2-[(4-fluorobenceno)sulfonil]fenil}metil)-2-metilindol-1-il]-acético;
Ácido
(3-{[2-(bencenosulfonil)piridin-3-il]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
[5-fluoro-3-({2-[(4-fluorobenceno)sulfonil]piridin-3-il}metil)-2-metilindol-1-il]-acético;
Ácido
[3-({2-[(4-clorobenceno)sulfonil]piridin-3-il}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
2-(3-(4-(bencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(4-(4-clorobencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(3-(bencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-3-(3-(4-fluorobencilsulfonil)bencil)-2-metil-indol-1-il)-acético;
Ácido
2-(3-(2-(bencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(4-(4-fluorobencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(2-(ciclohexilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(2-(piperidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(3-(2-(ciclopentilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(3-(piperidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(2-(pirrolidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(3-(4-(ciclohexilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(4-(ciclopentilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(2-(ciclobutilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(3-(pirrolidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(4-(piperidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
[5-fluoro-2-metil-3-(2-fenoxibencil)-indol-1-il]-acético;
Ácido
[5-fluoro-2-metil-3-(2-(4-metoxifenoxi)bencil)-indol-1-il]-acético;
Ácido
[3-({1-[(2,4-difluorobenceno)sulfonil]pirrol-2-il}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
(3-{[2-(bencenosulfonil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
[3-({2-[(4-clorobenceno)sulfonil]fenil}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
[5-fluoro-3-({2-[(4-fluorobenceno)sulfonil]fenil}metil)-2-metilindol-1-il]-acético;
Ácido
(3-{[2-(bencenosulfonil)piridin-3-il]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
[5-fluoro-3-({2-[(4-fluorobenceno)sulfonil]piridin-3-il}metil)-2-metilindol-1-il]-acético;
Ácido
[3-({2-[(4-clorobenceno)sulfonil]piridin-3-il}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
2-(3-(4-(bencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(4-(4-clorobencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(3-(bencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-3-(3-(4-fluorobencilsulfonil)bencil)-2-metil-indol-1-il)-acético;
Ácido
2-(3-(2-(bencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(4-(4-fluorobencilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(2-(ciclohexilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(2-(piperidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(3-(2-(ciclopentilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(3-(piperidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(2-(pirrolidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(3-(4-(ciclohexilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(4-(ciclopentilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(3-(2-(ciclobutilsulfonil)bencil)-5-fluoro-2-metil-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(3-(pirrolidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
2-(5-fluoro-2-metil-3-(4-(piperidin-1-ilsulfonil)bencil)-indol-1-il)-acético;
Ácido
[5-fluoro-2-metil-3-(2-fenoxibencil)-indol-1-il]-acético;
Ácido
[5-fluoro-2-metil-3-(2-(4-metoxifenoxi)bencil)-indol-1-il]-acético;
Ácido
[3-({4-[(ciclopropilmetil)sulfanil]fenil}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
{3-[(4,4-dimetil-2,3-dihidro-1-benzotiopiran-6-il)metil]-5-fluoro-2-metilindol-l-il}-acético;
Ácido
(3-{[2-(etanosulfonil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[2-(propano-1-sulfonil)fenil]metil}indol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-
{[2-(propano-2-sulfonil)fenil]metil}indol-1-il)-acético;
Ácido
(3-{[2-(butano-1-sulfonil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(3-{[2-(butano-2-sulfonil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[2-(2-metilpropano-2-sulfonil)fenil]metil}indol-1-il)acético;
Ácido
(5-fluoro-2-metil-3-{[2-(pentano-1-sulfonil)fenil]metil}indol-1-il)-acético;
Ácido
(3-{[2-(ciclopropilmetano)sulfonilfenil]metil}-5-fluoro-2-metilindol-1-il)acético;
Ácido
(5-fluoro-2-metil-3-{[2-(propilsulfamoil)fenil]metil}indol-1-il)-acético;
Ácido
(3-{[2-(butilsulfamoil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[3-(propilsulfamoil)fenil]metil}indol-1-il)-acético;
Ácido
(3-{[3-(butilsulfamoil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[4-(trifluorometano)sulfonilfenil]metil}indol-1-il)acético;
Ácido
(3-{[4-(etanosulfonil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[4-(propano-1-sulfonil)fenil]metil}indol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[4-(propano-2-sulfonil)fenil]metil}indol-1-il)-acético;
Ácido
(3-{[4-(butano-1-sulfonil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[4-(2-metilpropano-2-sulfonil)fenil]metil}indol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[4-(pentano-1-sulfonil)fenil]metil}indol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-1[4-(pentan-3-ilsulfonil)fenil]metil}indol-1-il)-acético;
Ácido
[3-({4-[(ciclopropilmetil)sulfonil]fenil}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
(5-fluoro-2-metil-3-{[4-(propilsulfamoil)fenil]metil}indol-1-il)-acético;
Ácido
(3-{[4-(butilsulfamoil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[4-(trifluorometoxi)fenil]metil}indol-1-il)-acético;
Ácido
(5-fluoro-3-{[4-metanosulfonil-3-(trifluorometil)fenil]metil}-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-3-{[4-metanosulfonil-3-(trifluorometoxi)fenil]metil}-2
metilindol-1-il)-acético;
Ácido
{5-fluoro-3-[(5-metanosulfoniltiofen-2-il)metil]-2-metilindol-1-il}-acético;
Ácido
{3-[(4,4-dimetil-1,1-dioxo-2,3-dihidro-1\lambda^{6}-benzotiopiran-6-il)metil]-5-fluoro-2-metilindol-1-il}-acético;
Ácido
[3-({1-[(4-clorobenceno)sulfonil]pirrol-2-il}metil)-5-fluoro-2-metilindol-1-il]acético;
Ácido
[5-fluoro-3-({1-[(4-fluorobenceno)sulfonil]pirrol-2-il}metil)-2-metilindol-1-il]-acético;
Ácido
[5-fluoro-3-({1-[(4-metoxibenceno)sulfonil]pirrol-2-il}metil)-2-metilindol-1-il]-acético;
Ácido
{3-[1-(2,4-dicloro-bencenosulfonil)pirrol-2-ilmetil]-5-fluoro-2-metil-indol-1-il}-acético;
Ácido
[5-fluoro-3-({1-[(4-metanosulfonilbenceno)sulfonil]pirrol-2-il}metil)-2-metilindol-1-il]-acético;
Ácido
{5-fluoro-2-metil-3-[(2-fenilfenil)metil]indol-1-il}-acético;
Ácido
(3-{[1-(bencenosulfonil)indol-2-il]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(3-{[2-(4-clorofenil)fenil]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
(5-fluoro-2-metil-3-{[2-(4-metilfenil)fenil]metil}indol-1-il)-acético;
Ácido
{5-fluoro-2-metil-3-[(3-fenoxifenil)metil]indol-1-il}-acético;
Ácido
[5-fluoro-3-({4-[(4-fluorofenil)carbonil]-1-metilpirrol-2-il}metil)-2-metilindol-1-il]-acético;
Ácido
{5-fluoro-2-metil-3-[(6-{[3-(trifluorometil)fenil]metil}piridin-3-il)metil]indol-1-il}-acético;
Ácido
{5-fluoro-2-metil-3-[(3-fenoxitiofen-2-il)metil]indol-1-il}-acético;
Ácido
(3-{[2-(bencenosulfonil)-1,3-tiazol-5-il]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
{3-[(1-bencilpirazol-4-il)metil]-5-fluoro-2-metilindol-1-il}-acético;
Ácido
(3-{[5-(4-clorofenoxi)-1-metil-3-(trifluorometil)pirazol-4-il]metil}-5-fluoro-2-metilindol-1-il)-acético;
Ácido
[3-({5-[(4-clorobenceno)sulfonil]furan-2-il}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
[3-({5-[(4-clorobenceno)sulfonil]tiofen-2-il}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
[3-({3-[(4-clorobenceno)sulfonil]tiofen-2-il}metil)-5-fluoro-2-metilindol-1-il]-acético;
Ácido
{3-[(2-bencilfenil)metil]-5-fluoro-2-metilindol-1-il}-acético;
o los ésteres alquílicos
C_{1}-C_{6}, arílicos,
(CH_{2})_{m}OC(=O)-alquílicos(C_{1}-C_{6}),
((CH_{2})_{m}O)_{n}CH_{2}CH_{2}X,
(CH_{2})_{m}N(R^{7})_{2} o
CH((CH_{2})_{m}O(C=O)R^{8})_{2}
de cualquiera de los anteriores; en los que
m es 1 ó 2;
n es 1-4;
X es OR^{7} o
N(R^{7})_{2};
R^{7} es hidrógeno o metilo;
R^{8} es alquilo
C_{1}-C_{18}.
14. Un compuesto de acuerdo con una cualquiera
de las reivindicaciones 1 a 13, en donde el compuesto de fórmula
general (I) se administra en combinación con uno o más agentes
adicionales que se usan en el tratamiento de estas afecciones
alérgicas.
15. Un compuesto de acuerdo con la
reivindicación 14, en el que el agente adicional se selecciona
de:
tosilato de Suplatast y compuestos
similares;
agonistas de adrenorreceptores B_{2} tales
como metaproterenol, isoproterenol, isoprenalina, albuterol,
salbutamol, formoterol, salmeterol, terbutalina, orciprenalina,
mesilato de bitolterol, pirbuterol e indacaterol o metilxantaninas
tales como teofilina y aminofilina, estabilizadores de células
cebadas tales como cromoglicato sódico o antagonistas de receptores
muscarínicos tales como ipratropio y tiotropio;
antihistaminas, por ejemplo antagonistas del
receptor de histamina H_{1} tales como loratadina, cetirizina,
desloratadina, levocetirizina, fexofenadina, astemizol, azelastina y
clorfeniramina o antagonistas del receptor H_{4};
agonistas de adrenorreceptores \alpha_{1} y
\alpha_{2} tales como propilhexedrina, fenilefrina,
fenilpropanolamina, pseudoefedrina, hidrocloruro de nafazolina,
hidrocloruro de oximetazolina, hidrocloruro de tetrahidrozolina,
hidrocloruro de xilometazolina e hidrocloruro de
etilnorepinefrina;
corticosteroides tales como prednisona,
prednisolona, flunisolida, acetónido de triamcinolona, dipropionato
de beclometasona, budesonida, propionato de fluticasona, furoato de
fluticasona, furoato de mometasona y ciclesonida;
inmunoterapia con alérgenos tal como Grazax.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0722203.7A GB0722203D0 (en) | 2007-11-13 | 2007-11-13 | Use of CRTH2 antagonist compounds |
| GB0722203 | 2007-11-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2353055T1 true ES2353055T1 (es) | 2011-02-25 |
Family
ID=38858584
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES08851028T Pending ES2353055T1 (es) | 2007-11-13 | 2008-11-13 | Uso de compuestos antagonistas de crth2. |
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| Country | Link |
|---|---|
| EP (1) | EP2219645A2 (es) |
| JP (1) | JP2011503045A (es) |
| DE (1) | DE08851028T1 (es) |
| ES (1) | ES2353055T1 (es) |
| GB (1) | GB0722203D0 (es) |
| WO (1) | WO2009063202A2 (es) |
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| DK2229358T3 (da) * | 2007-12-14 | 2011-07-04 | Pulmagen Therapeutics Asthma Ltd | Indoler og deres terapeutiske anvendelse |
| US7750027B2 (en) | 2008-01-18 | 2010-07-06 | Oxagen Limited | Compounds having CRTH2 antagonist activity |
| CA2712017C (en) * | 2008-01-18 | 2016-08-09 | Oxagen Limited | Compounds having crth2 antagonist activity |
| JP2011509991A (ja) * | 2008-01-22 | 2011-03-31 | オキサジェン リミテッド | Crth2アンタゴニスト活性を有する化合物 |
| EP2265581A1 (en) * | 2008-01-22 | 2010-12-29 | Oxagen Limited | Compounds having crth2 antagonist activity |
| BRPI0907364A2 (pt) | 2008-02-01 | 2015-07-14 | Amira Pharmaceuticals Inc | Antagonistas aminoalquilbifenil n,n-disubstituídos de receptores d2 de prostaglandina |
| WO2009102893A2 (en) | 2008-02-14 | 2009-08-20 | Amira Pharmaceuticals, Inc. | CYCLIC DIARYL ETHER COMPOUNDS AS ANTAGONISTS OF PROSTAGLANDIN D2 receptors |
| US8426449B2 (en) | 2008-04-02 | 2013-04-23 | Panmira Pharmaceuticals, Llc | Aminoalkylphenyl antagonists of prostaglandin D2 receptors |
| WO2010008864A2 (en) | 2008-06-24 | 2010-01-21 | Amira Pharmaceuticals, Inc. | Cycloalkane[b]indole angtagonists of prostaglandin d2 receptors |
| US8071807B2 (en) | 2008-07-03 | 2011-12-06 | Panmira Pharmaceuticals, Llc | Antagonists of prostaglandin D2 receptors |
| GB2463788B (en) | 2008-09-29 | 2010-12-15 | Amira Pharmaceuticals Inc | Heteroaryl antagonists of prostaglandin D2 receptors |
| GB2465062B (en) | 2008-11-06 | 2011-04-13 | Amira Pharmaceuticals Inc | Cycloalkane(B)azaindole antagonists of prostaglandin D2 receptors |
| US8383654B2 (en) | 2008-11-17 | 2013-02-26 | Panmira Pharmaceuticals, Llc | Heterocyclic antagonists of prostaglandin D2 receptors |
| EP2461809A4 (en) | 2009-07-31 | 2013-06-19 | Panmira Pharmaceuticals Llc | OPHTHALMIC PHARMACEUTICAL COMPOSITIONS OF DP2 RECEPTOR ANTAGONSITES |
| US8815917B2 (en) | 2009-08-05 | 2014-08-26 | Panmira Pharmaceuticals, Llc | DP2 antagonist and uses thereof |
| EP2521713A4 (en) | 2010-01-06 | 2013-10-02 | Panmira Pharmaceuticals Llc | ANTAGONIST OF DP2 AND ITS USES |
| AR080703A1 (es) | 2010-03-22 | 2012-05-02 | Actelion Pharmaceuticals Ltd | Derivados de 3-(heteroaril-amino)-1,2,3,4-tetrahidro-9h-carbazol, moduladores de receptores de prostaglandina d2, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de trastornos alergicos o inmunitarios tales como asma. |
| US9469615B2 (en) * | 2010-12-23 | 2016-10-18 | Merck Sharp & Dohme Corp. | Quinoxalines and AZA-quinoxalines as CRTH2 receptor modulators |
| GB201103837D0 (en) | 2011-03-07 | 2011-04-20 | Oxagen Ltd | Amorphous (5-Fluoro-2-Methyl-3-Quinolin-2-Ylmethyl-Indol-1-Yl)-acetic acid |
| DK2697223T3 (en) | 2011-04-14 | 2016-09-05 | Actelion Pharmaceuticals Ltd | 7- (heteroaryl-amino) -6,7,8,9-tetrahydro-pyrido [1,2-a] indole-acetic acid derivatives and their use as prostaglandin D2 receptor |
| CN103086943B (zh) * | 2011-11-04 | 2015-04-15 | 山东亨利医药科技有限责任公司 | 作为crth2受体拮抗剂的吲哚类衍生物 |
| PE20161177A1 (es) | 2014-03-17 | 2016-11-18 | Actelion Pharmaceuticals Ltd | Derivados del acido acetico azaindol y su uso como moduladores del receptor de prostaglandina d2 |
| WO2015140701A1 (en) | 2014-03-18 | 2015-09-24 | Actelion Pharmaceuticals Ltd | Azaindole acetic acid derivatives and their use as prostaglandin d2 receptor modulators |
| GB201407820D0 (en) | 2014-05-02 | 2014-06-18 | Atopix Therapeutics Ltd | Polymorphic form |
| GB201407807D0 (en) | 2014-05-02 | 2014-06-18 | Atopix Therapeutics Ltd | Polymorphic form |
| KR20180053345A (ko) | 2015-09-15 | 2018-05-21 | 이도르시아 파마슈티컬스 리미티드 | 결정질 형태 |
| WO2017104728A1 (ja) * | 2015-12-16 | 2017-06-22 | 国立大学法人東京大学 | 食物アレルギー治療薬 |
| RU2756270C2 (ru) * | 2016-07-21 | 2021-09-29 | Чиа Тай Тянцин Фармасьютикал Груп Ко., Лтд. | Производное индола, используемое в качестве ингибитора CRTH2 |
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| GB0324763D0 (en) * | 2003-10-23 | 2003-11-26 | Oxagen Ltd | Use of compounds in therapy |
| GB0504150D0 (en) * | 2005-03-01 | 2005-04-06 | Oxagen Ltd | Microcrystalline material |
| GB0505048D0 (en) * | 2005-03-11 | 2005-04-20 | Oxagen Ltd | Compounds with PGD antagonist activity |
| GB0605743D0 (en) * | 2006-03-22 | 2006-05-03 | Oxagen Ltd | Salts with CRTH2 antagonist activity |
| CA2658496A1 (en) * | 2006-07-22 | 2008-01-31 | Oxagen Limited | 2-{5-fluoro-2-methyl-3-[2-(phenylsulfonyl)benzyl]-1h-indol-yl} acetic acid derivatives and esters thereof having crth2 antagonist activity |
-
2007
- 2007-11-13 GB GBGB0722203.7A patent/GB0722203D0/en not_active Ceased
-
2008
- 2008-11-13 JP JP2010532660A patent/JP2011503045A/ja active Pending
- 2008-11-13 WO PCT/GB2008/003824 patent/WO2009063202A2/en not_active Ceased
- 2008-11-13 ES ES08851028T patent/ES2353055T1/es active Pending
- 2008-11-13 DE DE08851028T patent/DE08851028T1/de active Pending
- 2008-11-13 EP EP08851028A patent/EP2219645A2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP2011503045A (ja) | 2011-01-27 |
| DE08851028T1 (de) | 2011-02-24 |
| GB0722203D0 (en) | 2007-12-19 |
| WO2009063202A3 (en) | 2009-08-27 |
| WO2009063202A2 (en) | 2009-05-22 |
| EP2219645A2 (en) | 2010-08-25 |
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