KR102231637B1 - 염증 질환의 치료를 위한 화합물 및 그의 약학 조성물 - Google Patents
염증 질환의 치료를 위한 화합물 및 그의 약학 조성물 Download PDFInfo
- Publication number
- KR102231637B1 KR102231637B1 KR1020157029122A KR20157029122A KR102231637B1 KR 102231637 B1 KR102231637 B1 KR 102231637B1 KR 1020157029122 A KR1020157029122 A KR 1020157029122A KR 20157029122 A KR20157029122 A KR 20157029122A KR 102231637 B1 KR102231637 B1 KR 102231637B1
- Authority
- KR
- South Korea
- Prior art keywords
- pyridin
- methyl
- ethyl
- imidazo
- fluorophenyl
- 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.)
- Expired - Fee Related
Links
- 0 Cc1c(*)c2nc(*)c(N(C)C)[n]2cc1* Chemical compound Cc1c(*)c2nc(*)c(N(C)C)[n]2cc1* 0.000 description 12
- UTYLRZXQSIMWJU-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)N3CCNCC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)N3CCNCC3)c2n1 UTYLRZXQSIMWJU-UHFFFAOYSA-N 0.000 description 2
- DSJPHLSVLZQIKM-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCNCC2)c(C)c2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCNCC2)c(C)c2)c2n1 DSJPHLSVLZQIKM-UHFFFAOYSA-N 0.000 description 2
- PGZHYJGQWOOUAY-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2C)N3CCN(CC(N(C4)CC4O)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2C)N3CCN(CC(N(C4)CC4O)=O)CC3)c2n1 PGZHYJGQWOOUAY-UHFFFAOYSA-N 0.000 description 2
- YHNZERBUMVGYEI-UHFFFAOYSA-N CCc1c(N(CC)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)C(CC3)=CCN3S(C)(=O)=O)c2n1 Chemical compound CCc1c(N(CC)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)C(CC3)=CCN3S(C)(=O)=O)c2n1 YHNZERBUMVGYEI-UHFFFAOYSA-N 0.000 description 2
- JJNKQZFOEYFMBP-UHFFFAOYSA-N CCc1c(NC)[n](cc(cc2F)Br)c2n1 Chemical compound CCc1c(NC)[n](cc(cc2F)Br)c2n1 JJNKQZFOEYFMBP-UHFFFAOYSA-N 0.000 description 2
- UDNOOZRMVQMNNO-VQHVLOKHSA-N CNc1c(/C=C/c2ccccc2)nc(cc2)[n]1cc2Br Chemical compound CNc1c(/C=C/c2ccccc2)nc(cc2)[n]1cc2Br UDNOOZRMVQMNNO-VQHVLOKHSA-N 0.000 description 2
- VFPXJIDOSVVFDQ-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1c1c[n]2c(N(C)c3nc(-c(cc4)ccc4F)c[s]3)c(CCC#N)nc2cc1)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1c1c[n]2c(N(C)c3nc(-c(cc4)ccc4F)c[s]3)c(CCC#N)nc2cc1)=O VFPXJIDOSVVFDQ-UHFFFAOYSA-N 0.000 description 1
- YKVJZSZZQKQJMO-UHFFFAOYSA-N CCC(N(C)OC)=O Chemical compound CCC(N(C)OC)=O YKVJZSZZQKQJMO-UHFFFAOYSA-N 0.000 description 1
- YKBJCDYADGZXJJ-UHFFFAOYSA-N CCC(N(C1)CC1(C)O)=O Chemical compound CCC(N(C1)CC1(C)O)=O YKBJCDYADGZXJJ-UHFFFAOYSA-N 0.000 description 1
- JAOJQNVJBBEAEZ-UHFFFAOYSA-N CCc1c(N(C)C=O)[n](cc(cc2)C(CC3)=CCN3C(OC(C)(C)C)=O)c2n1 Chemical compound CCc1c(N(C)C=O)[n](cc(cc2)C(CC3)=CCN3C(OC(C)(C)C)=O)c2n1 JAOJQNVJBBEAEZ-UHFFFAOYSA-N 0.000 description 1
- VJNDCQREUFNPPF-UHFFFAOYSA-N CCc1c(N(C)C=O)[n](cc(cc2F)Br)c2n1 Chemical compound CCc1c(N(C)C=O)[n](cc(cc2F)Br)c2n1 VJNDCQREUFNPPF-UHFFFAOYSA-N 0.000 description 1
- VVRCMCTVUXYZQU-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(c(C#N)c3)ccc3F)c(C)[s]2)[n](cc(cc2)N3CCNCC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(c(C#N)c3)ccc3F)c(C)[s]2)[n](cc(cc2)N3CCNCC3)c2n1 VVRCMCTVUXYZQU-UHFFFAOYSA-N 0.000 description 1
- HAPNIGCORXRNGZ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3Cl)c[s]2)[n](cc(cc2)C(CC3)=CCN3S(C)(=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3Cl)c[s]2)[n](cc(cc2)C(CC3)=CCN3S(C)(=O)=O)c2n1 HAPNIGCORXRNGZ-UHFFFAOYSA-N 0.000 description 1
- FAVHBKUDJCJEKF-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3Cl)c[s]2)[n](cc(cc2)N(CC3)CCN3C(OC(C)(C)C)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3Cl)c[s]2)[n](cc(cc2)N(CC3)CCN3C(OC(C)(C)C)=O)c2n1 FAVHBKUDJCJEKF-UHFFFAOYSA-N 0.000 description 1
- DUDFDEKBJHPARI-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3Cl)c[s]2)[n](cc(cc2)N(CC3)CCS3(=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3Cl)c[s]2)[n](cc(cc2)N(CC3)CCS3(=O)=O)c2n1 DUDFDEKBJHPARI-UHFFFAOYSA-N 0.000 description 1
- ZGRHWBVRQHQLMZ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(C(CC2)CCN2C(OC(C)(C)C)=O)cc2C)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(C(CC2)CCN2C(OC(C)(C)C)=O)cc2C)c2n1 ZGRHWBVRQHQLMZ-UHFFFAOYSA-N 0.000 description 1
- CURUUZHLEFADRH-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(C2CCN(CC(N(C3)CC3O)=O)CC2)cc2C)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(C2CCN(CC(N(C3)CC3O)=O)CC2)cc2C)c2n1 CURUUZHLEFADRH-UHFFFAOYSA-N 0.000 description 1
- LUOGCZVRNOALIE-XMMPIXPASA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(C2CCN(CC(N(CC3)C[C@@H]3O)=O)CC2)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(C2CCN(CC(N(CC3)C[C@@H]3O)=O)CC2)cc2)c2n1 LUOGCZVRNOALIE-XMMPIXPASA-N 0.000 description 1
- DPQQZPUTETUIQM-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(c(F)c2)N3CCN(CC(N(C4)CC4O)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(c(F)c2)N3CCN(CC(N(C4)CC4O)=O)CC3)c2n1 DPQQZPUTETUIQM-UHFFFAOYSA-N 0.000 description 1
- AGSMPFFGNHMXPJ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(c(F)c2)N3CCNCC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(c(F)c2)N3CCNCC3)c2n1 AGSMPFFGNHMXPJ-UHFFFAOYSA-N 0.000 description 1
- NHKQHDXVPCPCFY-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)Br)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)Br)c2n1 NHKQHDXVPCPCFY-UHFFFAOYSA-N 0.000 description 1
- SMXOUWHYLQYXII-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)N(CC3)CCN3C(OC(C)(C)C)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)N(CC3)CCN3C(OC(C)(C)C)=O)c2n1 SMXOUWHYLQYXII-UHFFFAOYSA-N 0.000 description 1
- IVRDWWUBDXJIFB-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)N3CCN(C)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)N3CCN(C)CC3)c2n1 IVRDWWUBDXJIFB-UHFFFAOYSA-N 0.000 description 1
- FVIVERHBPGMJQX-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2F)Br)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2F)Br)c2n1 FVIVERHBPGMJQX-UHFFFAOYSA-N 0.000 description 1
- NYUJXWNROHMKSK-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C(C)=O)[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C(C)=O)[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 NYUJXWNROHMKSK-UHFFFAOYSA-N 0.000 description 1
- SLWLOCBCOHDDDJ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C(N)=O)[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(C(N)=O)[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 SLWLOCBCOHDDDJ-UHFFFAOYSA-N 0.000 description 1
- NLTMATIFSHCSRB-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(CC#N)[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(CC#N)[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 NLTMATIFSHCSRB-UHFFFAOYSA-N 0.000 description 1
- NIRYRKWSLNFJEF-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(CO)[s]2)[n](cc(cc2)N3CCN(CC(N(C)C)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c(CO)[s]2)[n](cc(cc2)N3CCN(CC(N(C)C)=O)CC3)c2n1 NIRYRKWSLNFJEF-UHFFFAOYSA-N 0.000 description 1
- FWHQIRPUSXDPFF-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2C(OC(C)(C)C)=O)c(C)c2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2C(OC(C)(C)C)=O)c(C)c2)c2n1 FWHQIRPUSXDPFF-UHFFFAOYSA-N 0.000 description 1
- URKCAJDOYIRXAA-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(C=C)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(C=C)(=O)=O)cc2)c2n1 URKCAJDOYIRXAA-UHFFFAOYSA-N 0.000 description 1
- HQABZQXPLBOYPA-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(CCCN2CCOCC2)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(CCCN2CCOCC2)(=O)=O)cc2)c2n1 HQABZQXPLBOYPA-UHFFFAOYSA-N 0.000 description 1
- QNJYROLHTDKJEE-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(CCN2CCOCC2)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(CCN2CCOCC2)(=O)=O)cc2)c2n1 QNJYROLHTDKJEE-UHFFFAOYSA-N 0.000 description 1
- VBUZZRDEXJVIEQ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCN(CC(N(C3)CC3O)=O)CC2)c(C)c2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCN(CC(N(C3)CC3O)=O)CC2)c(C)c2)c2n1 VBUZZRDEXJVIEQ-UHFFFAOYSA-N 0.000 description 1
- FBHBZQSDEWXGTJ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCN(CC(N3CC(CO)CC3)=O)CC2)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCN(CC(N3CC(CO)CC3)=O)CC2)cc2)c2n1 FBHBZQSDEWXGTJ-UHFFFAOYSA-N 0.000 description 1
- GSHANZSQZQPMDO-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCN(CC(NC3CC3)=O)CC2)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(C2CCN(CC(NC3CC3)=O)CC2)cc2)c2n1 GSHANZSQZQPMDO-UHFFFAOYSA-N 0.000 description 1
- FOPGCBGTAWHMGC-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)Br)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)Br)c2n1 FOPGCBGTAWHMGC-UHFFFAOYSA-N 0.000 description 1
- YNXIBRAUKJKILJ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(CC3)=CCN3C(Nc3ccc[s]3)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(CC3)=CCN3C(Nc3ccc[s]3)=O)c2n1 YNXIBRAUKJKILJ-UHFFFAOYSA-N 0.000 description 1
- IXRMQXRSZIHASU-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(CC3)=CCN3S(CCCCl)(=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(CC3)=CCN3S(CCCCl)(=O)=O)c2n1 IXRMQXRSZIHASU-UHFFFAOYSA-N 0.000 description 1
- RZEZTSNMQNPOFZ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(CC3)=CCN3S(CCCOC(C)=O)(=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(CC3)=CCN3S(CCCOC(C)=O)(=O)=O)c2n1 RZEZTSNMQNPOFZ-UHFFFAOYSA-N 0.000 description 1
- DFUPHRIWYRIKRO-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(OC)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C(OC)=O)c2n1 DFUPHRIWYRIKRO-UHFFFAOYSA-N 0.000 description 1
- WRZHKEMABNKLMB-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C3=CCNCC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)C3=CCNCC3)c2n1 WRZHKEMABNKLMB-UHFFFAOYSA-N 0.000 description 1
- AIPSXAMYAJLWCX-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCC3=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCC3=O)c2n1 AIPSXAMYAJLWCX-UHFFFAOYSA-N 0.000 description 1
- UETQGPILAFARDJ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCC3O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCC3O)c2n1 UETQGPILAFARDJ-UHFFFAOYSA-N 0.000 description 1
- VQIVHXRWIHNOEM-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3C(C(N)=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3C(C(N)=O)=O)c2n1 VQIVHXRWIHNOEM-UHFFFAOYSA-N 0.000 description 1
- HGFLPGWLQHMLAU-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3C(C(O)=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3C(C(O)=O)=O)c2n1 HGFLPGWLQHMLAU-UHFFFAOYSA-N 0.000 description 1
- IBMBSLBDJTWHKG-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3C(C(OCC)=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3C(C(OCC)=O)=O)c2n1 IBMBSLBDJTWHKG-UHFFFAOYSA-N 0.000 description 1
- NZALMORQKMZTJZ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3S(CC(O)=O)(=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3S(CC(O)=O)(=O)=O)c2n1 NZALMORQKMZTJZ-UHFFFAOYSA-N 0.000 description 1
- ORYRNORNNNECMK-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3S(CCCCl)(=O)=O)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N(CC3)CCN3S(CCCCl)(=O)=O)c2n1 ORYRNORNNNECMK-UHFFFAOYSA-N 0.000 description 1
- BLNDLYMYBGIVIS-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC#N)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC#N)CC3)c2n1 BLNDLYMYBGIVIS-UHFFFAOYSA-N 0.000 description 1
- RPGUQKIZHMPBLL-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N(C)C)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N(C)C)=O)CC3)c2n1 RPGUQKIZHMPBLL-UHFFFAOYSA-N 0.000 description 1
- PDLRHBOQFRLFIO-QHCPKHFHSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N(CC4)C[C@H]4O)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N(CC4)C[C@H]4O)=O)CC3)c2n1 PDLRHBOQFRLFIO-QHCPKHFHSA-N 0.000 description 1
- CNZBGFWSADCVEP-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N4CCC4)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N4CCC4)=O)CC3)c2n1 CNZBGFWSADCVEP-UHFFFAOYSA-N 0.000 description 1
- LGGZTXFXZBKPEW-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N4CCCC4)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCN(CC(N4CCCC4)=O)CC3)c2n1 LGGZTXFXZBKPEW-UHFFFAOYSA-N 0.000 description 1
- QKYUVBKPKKCMJM-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCNCC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)c[s]2)[n](cc(cc2)N3CCNCC3)c2n1 QKYUVBKPKKCMJM-UHFFFAOYSA-N 0.000 description 1
- CDRHPOJZXXBYHL-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3F)n[s]2)[n](cc(cc2)Br)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3F)n[s]2)[n](cc(cc2)Br)c2n1 CDRHPOJZXXBYHL-UHFFFAOYSA-N 0.000 description 1
- PFWBGVPXGZWBJA-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3)ccc3OC(F)(F)F)c[s]2)[n](cc(cc2)C3=CCNCC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3)ccc3OC(F)(F)F)c[s]2)[n](cc(cc2)C3=CCNCC3)c2n1 PFWBGVPXGZWBJA-UHFFFAOYSA-N 0.000 description 1
- YIHHFWPRAIRVHE-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(cc3F)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(cc3F)ccc3F)c[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 YIHHFWPRAIRVHE-UHFFFAOYSA-N 0.000 description 1
- CILREKGZMLVXSQ-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(ccc(F)c3)c3C#N)c[s]2)[n](cc(cc2)N3CCN(CC(N4CCC4)=O)CC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(ccc(F)c3)c3C#N)c[s]2)[n](cc(cc2)N3CCN(CC(N4CCC4)=O)CC3)c2n1 CILREKGZMLVXSQ-UHFFFAOYSA-N 0.000 description 1
- WHDWHJRRBMSVCW-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(ccc(F)c3)c3C#N)c[s]2)[n](cc(cc2)N3CCNCC3)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(ccc(F)c3)c3C#N)c[s]2)[n](cc(cc2)N3CCNCC3)c2n1 WHDWHJRRBMSVCW-UHFFFAOYSA-N 0.000 description 1
- RPOPDLIUTDHBOA-UHFFFAOYSA-N CCc1c(N(C)c2nc(-c(ccc(F)c3)c3NC(C)=O)c[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 Chemical compound CCc1c(N(C)c2nc(-c(ccc(F)c3)c3NC(C)=O)c[s]2)[n](cc(C(CC2)CCN2S(C)(=O)=O)cc2)c2n1 RPOPDLIUTDHBOA-UHFFFAOYSA-N 0.000 description 1
- ZYQCKWKGXBWWEG-UHFFFAOYSA-N CCc1c(N(CC)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)Br)c2n1 Chemical compound CCc1c(N(CC)c2nc(-c(cc3)ccc3F)c(C#N)[s]2)[n](cc(cc2C)Br)c2n1 ZYQCKWKGXBWWEG-UHFFFAOYSA-N 0.000 description 1
- UQZKDCRMFCJUNR-UHFFFAOYSA-N CCc1c(NC)[n](cc(C(CC2)CCN2C(OC(C)(C)C)=O)c(C)c2)c2n1 Chemical compound CCc1c(NC)[n](cc(C(CC2)CCN2C(OC(C)(C)C)=O)c(C)c2)c2n1 UQZKDCRMFCJUNR-UHFFFAOYSA-N 0.000 description 1
- USFKUZLRWZPVGG-UHFFFAOYSA-N CCc1c(NC)[n](cc(cc2)Br)c2n1 Chemical compound CCc1c(NC)[n](cc(cc2)Br)c2n1 USFKUZLRWZPVGG-UHFFFAOYSA-N 0.000 description 1
- UJVUQAQBHSQIIB-UHFFFAOYSA-N CCc1c(NC)[n](cc(cc2C)Br)c2n1 Chemical compound CCc1c(NC)[n](cc(cc2C)Br)c2n1 UJVUQAQBHSQIIB-UHFFFAOYSA-N 0.000 description 1
- JVPSSQQQZKCLNA-UHFFFAOYSA-N CCc1c(NC=O)[n](cc(c(C)c2)Br)c2n1 Chemical compound CCc1c(NC=O)[n](cc(c(C)c2)Br)c2n1 JVPSSQQQZKCLNA-UHFFFAOYSA-N 0.000 description 1
- BQMDLOKNCBCYQB-UHFFFAOYSA-N CCc1c(NC=O)[n](cc(cc2)C(OC)=O)c2n1 Chemical compound CCc1c(NC=O)[n](cc(cc2)C(OC)=O)c2n1 BQMDLOKNCBCYQB-UHFFFAOYSA-N 0.000 description 1
- HIMYRXPWOHYYSO-UHFFFAOYSA-N CN(C)C(CN(CC1)CCC1c1c[n]2c(N(C)c3nc(-c(cc4)ccc4F)c[s]3)c(CCC#N)nc2cc1)=O Chemical compound CN(C)C(CN(CC1)CCC1c1c[n]2c(N(C)c3nc(-c(cc4)ccc4F)c[s]3)c(CCC#N)nc2cc1)=O HIMYRXPWOHYYSO-UHFFFAOYSA-N 0.000 description 1
- LGCHCYHSWGIUCG-NTUHNPAUSA-N CN(c1c(/C=C/c2ccccc2)nc(cc2)[n]1cc2Br)c1nc(-c(cc2)ccc2F)c[s]1 Chemical compound CN(c1c(/C=C/c2ccccc2)nc(cc2)[n]1cc2Br)c1nc(-c(cc2)ccc2F)c[s]1 LGCHCYHSWGIUCG-NTUHNPAUSA-N 0.000 description 1
- ULNIBMFURRNYGK-UHFFFAOYSA-N CN(c1c(C2CC2)nc(cc2)[n]1cc2Br)c1nc(-c(cc2)ccc2F)c[s]1 Chemical compound CN(c1c(C2CC2)nc(cc2)[n]1cc2Br)c1nc(-c(cc2)ccc2F)c[s]1 ULNIBMFURRNYGK-UHFFFAOYSA-N 0.000 description 1
- GGUKQCAXTMDKPC-UHFFFAOYSA-N CN(c1c(CCC#N)nc2[n]1cc(C1CCNCC1)cc2)c1nc(-c(cc2)ccc2F)c[s]1 Chemical compound CN(c1c(CCC#N)nc2[n]1cc(C1CCNCC1)cc2)c1nc(-c(cc2)ccc2F)c[s]1 GGUKQCAXTMDKPC-UHFFFAOYSA-N 0.000 description 1
- MZOODILXYVSPKB-UHFFFAOYSA-N N#Cc(cc(cc1)F)c1C(CBr)=O Chemical compound N#Cc(cc(cc1)F)c1C(CBr)=O MZOODILXYVSPKB-UHFFFAOYSA-N 0.000 description 1
- GGHBRLQYBZMEPV-UHFFFAOYSA-N Nc(nc1)cc(F)c1Br Chemical compound Nc(nc1)cc(F)c1Br GGHBRLQYBZMEPV-UHFFFAOYSA-N 0.000 description 1
- QLXASFJHUCKEHU-UHFFFAOYSA-N Nc(ncc(Br)c1)c1F Chemical compound Nc(ncc(Br)c1)c1F QLXASFJHUCKEHU-UHFFFAOYSA-N 0.000 description 1
- WCCFLOQQACDOAX-UHFFFAOYSA-N Nc1cc(F)ccn1 Chemical compound Nc1cc(F)ccn1 WCCFLOQQACDOAX-UHFFFAOYSA-N 0.000 description 1
- WWEINXQNCAWBPD-UHFFFAOYSA-N Nc1ncccc1F Chemical compound Nc1ncccc1F WWEINXQNCAWBPD-UHFFFAOYSA-N 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
- A61K31/41—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
- A61K31/426—1,3-Thiazoles
-
- 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
- A61K31/435—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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/435—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
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- 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
- A61K31/435—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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Vascular Medicine (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Child & Adolescent Psychology (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361781174P | 2013-03-14 | 2013-03-14 | |
| US61/781,174 | 2013-03-14 | ||
| PCT/EP2014/054440 WO2014139882A1 (en) | 2013-03-14 | 2014-03-07 | Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020217008013A Division KR20210034098A (ko) | 2013-03-14 | 2014-03-07 | 염증 질환의 치료를 위한 화합물 및 그의 약학 조성물 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20150128995A KR20150128995A (ko) | 2015-11-18 |
| KR102231637B1 true KR102231637B1 (ko) | 2021-03-25 |
Family
ID=50236198
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020157029122A Expired - Fee Related KR102231637B1 (ko) | 2013-03-14 | 2014-03-07 | 염증 질환의 치료를 위한 화합물 및 그의 약학 조성물 |
| KR1020217008013A Ceased KR20210034098A (ko) | 2013-03-14 | 2014-03-07 | 염증 질환의 치료를 위한 화합물 및 그의 약학 조성물 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020217008013A Ceased KR20210034098A (ko) | 2013-03-14 | 2014-03-07 | 염증 질환의 치료를 위한 화합물 및 그의 약학 조성물 |
Country Status (29)
| Country | Link |
|---|---|
| US (7) | US8993590B2 (enExample) |
| EP (3) | EP3269716B1 (enExample) |
| JP (2) | JP6339595B2 (enExample) |
| KR (2) | KR102231637B1 (enExample) |
| CN (1) | CN105143221B (enExample) |
| AR (1) | AR095280A1 (enExample) |
| AU (3) | AU2014231009B2 (enExample) |
| BR (1) | BR112015020998B1 (enExample) |
| CA (1) | CA2902103C (enExample) |
| CY (2) | CY1119352T1 (enExample) |
| DK (2) | DK3269716T3 (enExample) |
| ES (2) | ES2824723T3 (enExample) |
| HR (2) | HRP20171219T1 (enExample) |
| HU (2) | HUE051195T2 (enExample) |
| IL (2) | IL240531B (enExample) |
| LT (2) | LT2970255T (enExample) |
| MX (1) | MX358342B (enExample) |
| MY (1) | MY170260A (enExample) |
| NZ (1) | NZ711202A (enExample) |
| PH (1) | PH12015502055B1 (enExample) |
| PL (2) | PL2970255T3 (enExample) |
| PT (2) | PT2970255T (enExample) |
| RU (1) | RU2675818C2 (enExample) |
| SG (1) | SG11201507224RA (enExample) |
| SI (2) | SI2970255T1 (enExample) |
| TW (2) | TWI749290B (enExample) |
| UY (1) | UY35437A (enExample) |
| WO (1) | WO2014139882A1 (enExample) |
| ZA (1) | ZA201505909B (enExample) |
Families Citing this family (77)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2012308570B2 (en) | 2011-09-14 | 2016-11-10 | Samumed, Llc | Indazole-3-carboxamides and their use as Wnt/b-catenin signaling pathway inhibitors |
| PH12017500997A1 (en) | 2012-04-04 | 2018-02-19 | Samumed Llc | Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof |
| CA2902103C (en) | 2013-03-14 | 2021-09-21 | Galapagos Nv | Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
| EP3010922B1 (en) | 2013-06-19 | 2017-03-15 | Galapagos NV | Novel compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
| US9943677B2 (en) | 2013-10-15 | 2018-04-17 | Radux Devices, LLC | Securing a medical device to a valve instrument |
| WO2016033440A1 (en) | 2014-08-29 | 2016-03-03 | Chdi Foundation, Inc. | Probes for imaging huntingtin protein |
| WO2016040181A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof |
| WO2016040193A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridine and therapeutic uses thereof |
| WO2016040184A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(3h-imidazo[4,5-b]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof |
| WO2016040185A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 2-(1h-indazol-3-yl)-3h-imidazo[4,5-b]pyridine and therapeutic uses thereof |
| WO2016040180A1 (en) | 2014-09-08 | 2016-03-17 | Samumed, Llc | 3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[3,4-c]pyridine and therapeutic uses thereof |
| GB201501870D0 (en) | 2015-02-04 | 2015-03-18 | Cancer Rec Tech Ltd | Autotaxin inhibitors |
| GB201502020D0 (en) | 2015-02-06 | 2015-03-25 | Cancer Rec Tech Ltd | Autotaxin inhibitory compounds |
| CA2988306A1 (en) | 2015-06-05 | 2016-12-08 | Vertex Pharmaceuticals Incorporated | Triazoles for the treatment of demyelinating diseases |
| JP6871919B2 (ja) | 2015-06-16 | 2021-05-19 | ナノファギックス エルエルシー | 薬物送達及びイメージング化学コンジュゲート、製剤及びその使用方法 |
| US10226453B2 (en) | 2015-08-03 | 2019-03-12 | Samumed, Llc | 3-(1H-indol-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
| WO2017023996A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-pyrazolo[3,4-b]pyridines and therapeutic uses thereof |
| US10519169B2 (en) | 2015-08-03 | 2019-12-31 | Samumed, Llc | 3-(1H-pyrrolo[2,3-C]pyridin-2-yl)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
| WO2017023989A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-benzo[d]imidazol-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof |
| US10329309B2 (en) | 2015-08-03 | 2019-06-25 | Samumed, Llc | 3-(3H-imidazo[4,5-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
| WO2017023986A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc | 3-(1h-indol-2-yl)-1h-indazoles and therapeutic uses thereof |
| US10206909B2 (en) | 2015-08-03 | 2019-02-19 | Samumed, Llc | 3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
| WO2017024010A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-pyrrolo[3,2-c]pyridin-2-yl)-1h-indazoles and therapeutic uses thereof |
| US10285982B2 (en) | 2015-08-03 | 2019-05-14 | Samumed, Llc | 3-(1H-pyrrolo[2,3-B]pyridin-2-yl)-1H-pyrazolo[3,4-C]pyridines and therapeutic uses thereof |
| WO2017023984A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-pyrrolo[3,2-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridines and therapeutic uses thereof |
| US10350199B2 (en) | 2015-08-03 | 2019-07-16 | Samumed, Llc | 3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-indazoles and therapeutic uses thereof |
| WO2017023972A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-imidazo[4,5-c]pyridin-2-yl)-1h-pyrazolo[4,3-b]pyridines and therapeutic uses thereof |
| US10226448B2 (en) | 2015-08-03 | 2019-03-12 | Samumed, Llc | 3-(1H-pyrrolo[3,2-C]pyridin-2-yl)-1H-pyrazolo[3,4-B]pyridines and therapeutic uses thereof |
| WO2017023975A1 (en) | 2015-08-03 | 2017-02-09 | Samumed, Llc. | 3-(1h-pyrrolo[2,3-c]pyridin-2-yl)-1h-pyrazolo[3,4-c]pyridines and therapeutic uses thereof |
| US10231956B2 (en) | 2015-08-03 | 2019-03-19 | Samumed, Llc | 3-(1H-pyrrolo[3,2-C]pyridin-2-YL)-1 H-pyrazolo[4,3-B]pyridines and therapeutic uses thereof |
| EP3370721A4 (en) | 2015-11-06 | 2019-05-22 | Samumed, LLC | TREATMENT OF OSTEOARTHRITIS |
| US11065251B2 (en) | 2016-05-06 | 2021-07-20 | Albert Einstein College Of Medicine | PAK1 inhibitors and uses thereof |
| SG11201810683VA (en) | 2016-06-01 | 2018-12-28 | Samumed Llc | Process for preparing n-(5-(3-(7-(3-fluorophenyl)-3h-imidazo[4,5-c]pyridin-2-yl)-1h-indazol-5-yl)pyridin-3-yl)-3-methylbutanamide |
| MX391624B (es) | 2016-10-21 | 2025-03-04 | Samumed Llc | Métodos de uso de indazol-3-carboxamidas y su uso como inhibidores de la ruta de señalización de wnt/b-catenina. |
| WO2018080571A1 (en) | 2016-10-24 | 2018-05-03 | Precison Combustion, Inc. | Solid oxide electrolysis with internal heater |
| KR102558716B1 (ko) | 2016-11-07 | 2023-07-21 | 사뮤메드, 엘엘씨 | 단일-투여량, 즉시-사용가능한 주사용 제제 |
| WO2018106643A1 (en) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Heterocyclic azoles for the treatment of demyelinating diseases |
| WO2018106646A1 (en) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Aminotriazoles for the treatment of demyelinating diseases |
| WO2018106641A1 (en) | 2016-12-06 | 2018-06-14 | Vertex Pharmaceuticals Incorporated | Pyrazoles for the treatment of demyelinating diseases |
| GB201710851D0 (en) | 2017-07-06 | 2017-08-23 | Galápagos Nv | Novel compounds and pharmaceutical compositions thereof for the treatment of fibrosis |
| WO2019030275A1 (en) * | 2017-08-09 | 2019-02-14 | Galapagos Nv | COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREFOR FOR USE IN THE TREATMENT OF FIBROTIC DISEASES |
| WO2019029620A1 (zh) * | 2017-08-09 | 2019-02-14 | 广州市恒诺康医药科技有限公司 | Atx抑制剂及其制备方法和应用 |
| KR20200088844A (ko) | 2017-11-15 | 2020-07-23 | 갈라파고스 엔.브이. | 섬유증성 질병 치료에서의 용도를 위한 화합물 및 그의 약학 조성물 |
| JP2021513551A (ja) * | 2018-02-14 | 2021-05-27 | スーチョウ、シノベント、ファーマスーティカルズ、カンパニー、リミテッドSuzhou Sinovent Pharmaceuticals Co., Ltd. | 複素環式化合物、その応用及びそれを含有する医薬組成物 |
| WO2019223721A1 (zh) * | 2018-05-24 | 2019-11-28 | 广州市恒诺康医药科技有限公司 | 芳杂环化合物、其药物组合物及其应用 |
| US10711000B2 (en) | 2018-05-29 | 2020-07-14 | Fronthera U.S. Pharmaceuticals Llc | Autotaxin inhibitors and uses thereof |
| EP3728257A4 (en) * | 2018-05-29 | 2021-06-23 | Fronthera U.S. Pharmaceuticals LLC | AUTOTAXIN INHIBITORS AND THEIR USES |
| ES2952939T3 (es) | 2018-07-27 | 2023-11-07 | Mitsubishi Tanabe Pharma Corp | Derivados novedosos de piridina 3,5-disustituida y piridazina 3,5-disustituida y uso farmacéutico de los mismos |
| GB201812861D0 (en) | 2018-08-08 | 2018-09-19 | Galapagos Nv | Methods of administering therapy |
| IL282425B2 (en) | 2018-10-29 | 2024-07-01 | Boehringer Ingelheim Int | New pyridazines |
| US11633399B2 (en) | 2018-12-25 | 2023-04-25 | Sol-Gel Technologies Ltd. | Treatment of skin disorders with compositions comprising an EGFR inhibitor |
| GB201904375D0 (en) * | 2019-03-29 | 2019-05-15 | Galapagos Nv | Novel compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
| CN113874354B (zh) * | 2019-06-04 | 2024-02-20 | 江苏恒瑞医药股份有限公司 | 吡啶酮类衍生物、其制备方法及其在医药上的应用 |
| WO2021034414A2 (en) * | 2019-07-03 | 2021-02-25 | Cornell University | Modulation of dendritic cell function by the phospholipid messenger lpa |
| US11485727B2 (en) * | 2019-07-22 | 2022-11-01 | Boehringer Ingelheim International Gmbh | N-methyl, n-(6-(methoxy)pyridazin-3-yl) amine derivatives as autotaxin (ATX) modulators |
| EP4003978B1 (en) * | 2019-07-22 | 2024-05-01 | Boehringer Ingelheim International GmbH | N-methyl, n-(6-(methoxy)pyridazin-3-yl) amine derivatives as autotaxin (atx) modulators for the treatment of inflammatory airway or fibrotic diseases |
| US11465982B2 (en) | 2019-07-22 | 2022-10-11 | Boehringer Ingelheim International Gmbh | Pyridazines |
| EP3782997A1 (en) | 2019-08-19 | 2021-02-24 | Galapagos N.V. | Fused pyrimidine compounds and pharmaceutical compositions thereof for the treatment of fibrotic diseases |
| AU2020342202B2 (en) * | 2019-09-06 | 2023-07-06 | Wuhan Humanwell Innovative Drug Research and Development Center Limited Company | Pyrimidine compound and preparation method therefor |
| WO2021088957A1 (zh) * | 2019-11-07 | 2021-05-14 | 广州市恒诺康医药科技有限公司 | 芳杂环化合物、其药物组合物及其应用 |
| CN111004235A (zh) * | 2019-11-29 | 2020-04-14 | 沈阳药科大学 | 一种ATX抑制剂Ziritaxestat的合成方法 |
| CN113493453B (zh) * | 2020-04-07 | 2023-06-16 | 江苏恒瑞医药股份有限公司 | 稠合芳香环类衍生物、其制备方法及其在医药上的应用 |
| WO2022007882A1 (zh) * | 2020-07-09 | 2022-01-13 | 苏州爱科百发生物医药技术有限公司 | 一种atx抑制剂及其制备方法和应用 |
| CN114315825A (zh) * | 2020-09-30 | 2022-04-12 | 江西济民可信集团有限公司 | 吡啶并咪唑衍生物及其制备方法和应用 |
| KR20230083276A (ko) | 2020-10-06 | 2023-06-09 | 일동제약(주) | 오토탁신 억제제 화합물 |
| EP4242208A4 (en) * | 2020-11-04 | 2025-01-15 | Xizang Haisco Pharmaceutical Co., Ltd. | DEUTERATED DERIVATIVE USED AS ATX INHIBITOR, AND ITS APPLICATION |
| US20240002401A1 (en) * | 2020-11-16 | 2024-01-04 | Guangzhou Henovcom Bioscience Co., Ltd. | Imidazothiazole compounds, pharmaceutical compositions, and uses thereof |
| CN116806150A (zh) | 2021-01-05 | 2023-09-26 | 载度思生命科学有限公司 | 新的自分泌运动因子抑制剂 |
| MX2023009060A (es) | 2021-02-02 | 2023-09-29 | Liminal Biosciences Ltd | Antagonistas de gpr84 y usos de estos. |
| CA3206499A1 (en) | 2021-02-02 | 2022-08-11 | Liminal Biosciences Limited | Gpr84 antagonists and uses thereof |
| CN118317958A (zh) * | 2021-11-25 | 2024-07-09 | 上海济煜医药科技有限公司 | 三并环衍生物及其制备方法和应用 |
| WO2023235871A2 (en) * | 2022-06-03 | 2023-12-07 | Seer, Inc. | Systems, compositions, and methods relating to neurodegenerative diseases |
| KR102587919B1 (ko) * | 2022-07-22 | 2023-10-11 | 주식회사 넥스트젠바이오사이언스 | 신규한 헤테로사이클릭 화합물 및 이를 포함하는 오토탁신 저해용 약학 조성물 |
| CN119894873A (zh) | 2022-08-02 | 2025-04-25 | 里米诺生物科学有限公司 | 芳基三唑基和相关gpr84拮抗剂及其用途 |
| AU2023317742A1 (en) | 2022-08-02 | 2025-03-20 | Liminal Biosciences Limited | Substituted pyridone gpr84 antagonists and uses thereof |
| CN120019047A (zh) | 2022-08-02 | 2025-05-16 | 里米诺生物科学有限公司 | 杂芳基甲酰胺和相关gpr84拮抗剂及其用途 |
| GR1010570B (el) | 2022-12-22 | 2023-11-17 | Uni-Pharma Κλεων Τσετης Φαρμακευτικα Εργαστηρια Α.Β.Ε.Ε., | 4-(2-(4-((2,4-διοξοθειαζολιδιν-5-υλ)μεθυλ)φαινοξυ) παραγωγα με δραση αναστολης της αυτοταξινης |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007149395A2 (en) | 2006-06-20 | 2007-12-27 | Amphora Discovery Corporation | 2,5-substituted oxazole derivatives as protein kinase inhibitors for the treatment of cancer |
| WO2012166415A1 (en) | 2011-05-27 | 2012-12-06 | Amira Pharmaceuticals, Inc. | Heterocyclic autotaxin inhibitors and uses thereof |
| US20130052190A1 (en) | 2011-02-22 | 2013-02-28 | Oxagen Limited | CRTH2 Antagonists for Treatment of Eosinophilic Diseases and Conditions |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2382919C (en) * | 1999-10-08 | 2008-12-09 | Gruenenthal Gmbh | Bicyclic imidazo-3-yl-amine derivatives |
| PT1622912E (pt) * | 2003-04-23 | 2009-08-17 | Schering Corp | Antagonistas 2-alcinil- e 2-alcenilpirazolo-[4,3-b]-1,2,4- triazolo-[1,5-c]-pirimidina do receptor a2a da adenosina |
| US8227603B2 (en) * | 2006-08-01 | 2012-07-24 | Cytokinetics, Inc. | Modulating skeletal muscle |
| US8148369B2 (en) * | 2007-05-10 | 2012-04-03 | Janssen Pharmaceutica Nv | Fused pyrazine compounds useful for the treatment of degenerative and inflammatory diseases |
| DE102008059578A1 (de) | 2008-11-28 | 2010-06-10 | Merck Patent Gmbh | Benzo-Naphtyridin Verbindungen |
| JP5697601B2 (ja) * | 2008-12-01 | 2015-04-08 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | 癌に対するオータキシン阻害剤としての2,5−ジアミノ−置換ピリド[4,3−d]ピリミジン |
| CA2757415C (en) | 2009-04-02 | 2018-02-06 | Merck Patent Gmbh | Autotaxin inhibitors |
| TW201120043A (en) * | 2009-11-05 | 2011-06-16 | Galapagos Nv | Fused pyrazine compounds as their salts, useful for the treatment of degenerative and inflammatory diseases |
| EP2338888A1 (en) * | 2009-12-24 | 2011-06-29 | Almirall, S.A. | Imidazopyridine derivatives as JAK inhibitors |
| CN103201262B (zh) * | 2010-08-20 | 2016-06-01 | 艾米拉医药股份有限公司 | 自分泌运动因子抑制剂及其用途 |
| CA2902103C (en) | 2013-03-14 | 2021-09-21 | Galapagos Nv | Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
-
2014
- 2014-03-07 CA CA2902103A patent/CA2902103C/en active Active
- 2014-03-07 MX MX2015011077A patent/MX358342B/es active IP Right Grant
- 2014-03-07 MY MYPI2015703027A patent/MY170260A/en unknown
- 2014-03-07 SI SI201430403T patent/SI2970255T1/sl unknown
- 2014-03-07 WO PCT/EP2014/054440 patent/WO2014139882A1/en not_active Ceased
- 2014-03-07 ES ES17177371T patent/ES2824723T3/es active Active
- 2014-03-07 ES ES14708291.1T patent/ES2638980T3/es active Active
- 2014-03-07 EP EP17177371.6A patent/EP3269716B1/en active Active
- 2014-03-07 HU HUE17177371A patent/HUE051195T2/hu unknown
- 2014-03-07 HU HUE14708291A patent/HUE035966T2/en unknown
- 2014-03-07 KR KR1020157029122A patent/KR102231637B1/ko not_active Expired - Fee Related
- 2014-03-07 PT PT147082911T patent/PT2970255T/pt unknown
- 2014-03-07 EP EP14708291.1A patent/EP2970255B9/en active Active
- 2014-03-07 DK DK17177371.6T patent/DK3269716T3/da active
- 2014-03-07 EP EP20189787.3A patent/EP3760630A1/en not_active Withdrawn
- 2014-03-07 SG SG11201507224RA patent/SG11201507224RA/en unknown
- 2014-03-07 PL PL14708291T patent/PL2970255T3/pl unknown
- 2014-03-07 PL PL17177371T patent/PL3269716T3/pl unknown
- 2014-03-07 KR KR1020217008013A patent/KR20210034098A/ko not_active Ceased
- 2014-03-07 AU AU2014231009A patent/AU2014231009B2/en not_active Ceased
- 2014-03-07 NZ NZ711202A patent/NZ711202A/en not_active IP Right Cessation
- 2014-03-07 LT LTEP14708291.1T patent/LT2970255T/lt unknown
- 2014-03-07 JP JP2015562040A patent/JP6339595B2/ja active Active
- 2014-03-07 BR BR112015020998-0A patent/BR112015020998B1/pt not_active IP Right Cessation
- 2014-03-07 CN CN201480014005.8A patent/CN105143221B/zh active Active
- 2014-03-07 HR HRP20171219TT patent/HRP20171219T1/hr unknown
- 2014-03-07 LT LTEP17177371.6T patent/LT3269716T/lt unknown
- 2014-03-07 PT PT171773716T patent/PT3269716T/pt unknown
- 2014-03-07 DK DK14708291.1T patent/DK2970255T3/en active
- 2014-03-07 RU RU2015143430A patent/RU2675818C2/ru active
- 2014-03-07 SI SI201431673T patent/SI3269716T1/sl unknown
- 2014-03-11 TW TW108104845A patent/TWI749290B/zh not_active IP Right Cessation
- 2014-03-11 TW TW103108497A patent/TWI695002B/zh not_active IP Right Cessation
- 2014-03-12 US US14/205,885 patent/US8993590B2/en active Active
- 2014-03-12 AR ARP140100893A patent/AR095280A1/es active IP Right Grant
- 2014-03-14 UY UY35437A patent/UY35437A/es not_active Application Discontinuation
- 2014-12-17 US US14/572,870 patent/US9249141B2/en active Active
-
2015
- 2015-08-12 IL IL240531A patent/IL240531B/en active IP Right Grant
- 2015-08-17 ZA ZA2015/05909A patent/ZA201505909B/en unknown
- 2015-09-11 PH PH12015502055A patent/PH12015502055B1/en unknown
- 2015-12-22 US US14/977,918 patent/US9670204B2/en not_active Expired - Fee Related
-
2017
- 2017-05-01 US US15/583,161 patent/US10125132B2/en active Active
- 2017-09-06 CY CY20171100940T patent/CY1119352T1/el unknown
- 2017-12-20 AU AU2017286828A patent/AU2017286828B2/en not_active Ceased
- 2017-12-27 IL IL256624A patent/IL256624B/en active IP Right Grant
-
2018
- 2018-04-05 JP JP2018072964A patent/JP6517976B2/ja active Active
- 2018-09-28 US US16/146,450 patent/US10526329B2/en active Active
-
2019
- 2019-06-27 AU AU2019204539A patent/AU2019204539B2/en not_active Ceased
- 2019-11-13 US US16/682,553 patent/US11072611B2/en active Active
-
2020
- 2020-10-09 CY CY20201100953T patent/CY1123521T1/el unknown
- 2020-10-13 HR HRP20201641TT patent/HRP20201641T1/hr unknown
-
2021
- 2021-06-18 US US17/351,765 patent/US20230022534A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007149395A2 (en) | 2006-06-20 | 2007-12-27 | Amphora Discovery Corporation | 2,5-substituted oxazole derivatives as protein kinase inhibitors for the treatment of cancer |
| US20130052190A1 (en) | 2011-02-22 | 2013-02-28 | Oxagen Limited | CRTH2 Antagonists for Treatment of Eosinophilic Diseases and Conditions |
| WO2012166415A1 (en) | 2011-05-27 | 2012-12-06 | Amira Pharmaceuticals, Inc. | Heterocyclic autotaxin inhibitors and uses thereof |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11072611B2 (en) | Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders | |
| US20180127425A1 (en) | Novel compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders | |
| HK1219730B (en) | Compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders | |
| HK1249507B (en) | Novel compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
St.27 status event code: A-0-1-A10-A15-nap-PA0105 |
|
| PG1501 | Laying open of application |
St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
|
| R17-X000 | Change to representative recorded |
St.27 status event code: A-3-3-R10-R17-oth-X000 |
|
| P22-X000 | Classification modified |
St.27 status event code: A-2-2-P10-P22-nap-X000 |
|
| PA0201 | Request for examination |
St.27 status event code: A-1-2-D10-D11-exm-PA0201 |
|
| D13-X000 | Search requested |
St.27 status event code: A-1-2-D10-D13-srh-X000 |
|
| D14-X000 | Search report completed |
St.27 status event code: A-1-2-D10-D14-srh-X000 |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
St.27 status event code: A-1-2-D10-D21-exm-PE0902 |
|
| P11-X000 | Amendment of application requested |
St.27 status event code: A-2-2-P10-P11-nap-X000 |
|
| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
|
| E701 | Decision to grant or registration of patent right | ||
| PE0701 | Decision of registration |
St.27 status event code: A-1-2-D10-D22-exm-PE0701 |
|
| PA0104 | Divisional application for international application |
St.27 status event code: A-0-1-A10-A18-div-PA0104 St.27 status event code: A-0-1-A10-A16-div-PA0104 |
|
| GRNT | Written decision to grant | ||
| PR0701 | Registration of establishment |
St.27 status event code: A-2-4-F10-F11-exm-PR0701 |
|
| PR1002 | Payment of registration fee |
St.27 status event code: A-2-2-U10-U12-oth-PR1002 Fee payment year number: 1 |
|
| PG1601 | Publication of registration |
St.27 status event code: A-4-4-Q10-Q13-nap-PG1601 |
|
| PC1903 | Unpaid annual fee |
St.27 status event code: A-4-4-U10-U13-oth-PC1903 Not in force date: 20240319 Payment event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE |
|
| PC1903 | Unpaid annual fee |
St.27 status event code: N-4-6-H10-H13-oth-PC1903 Ip right cessation event data comment text: Termination Category : DEFAULT_OF_REGISTRATION_FEE Not in force date: 20240319 |