JP2012505836A5 - - Google Patents
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- JP2012505836A5 JP2012505836A5 JP2011531305A JP2011531305A JP2012505836A5 JP 2012505836 A5 JP2012505836 A5 JP 2012505836A5 JP 2011531305 A JP2011531305 A JP 2011531305A JP 2011531305 A JP2011531305 A JP 2011531305A JP 2012505836 A5 JP2012505836 A5 JP 2012505836A5
- Authority
- JP
- Japan
- Prior art keywords
- amino
- benzofuran
- oxadiazol
- diol
- propane
- 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 claims 27
- 150000003839 salts Chemical class 0.000 claims 20
- 239000011780 sodium chloride Substances 0.000 claims 20
- 230000000155 isotopic Effects 0.000 claims 19
- 125000000217 alkyl group Chemical group 0.000 claims 17
- 125000000623 heterocyclic group Chemical group 0.000 claims 17
- -1 amino, hydroxy Chemical group 0.000 claims 13
- 239000008194 pharmaceutical composition Substances 0.000 claims 13
- 125000003118 aryl group Chemical group 0.000 claims 10
- 102000011011 Sphingosine 1-phosphate receptors Human genes 0.000 claims 7
- 108050001083 Sphingosine 1-phosphate receptors Proteins 0.000 claims 7
- YZCKVEUIGOORGS-OUBTZVSYSA-N deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 7
- 229910052805 deuterium Inorganic materials 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- 230000000051 modifying Effects 0.000 claims 7
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000003282 alkyl amino group Chemical group 0.000 claims 6
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 239000003814 drug Substances 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 238000009169 immunotherapy Methods 0.000 claims 6
- 238000004519 manufacturing process Methods 0.000 claims 6
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims 5
- 125000004432 carbon atoms Chemical group C* 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 5
- 229910052760 oxygen Inorganic materials 0.000 claims 5
- 230000002265 prevention Effects 0.000 claims 5
- 229910052717 sulfur Inorganic materials 0.000 claims 5
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims 4
- 230000000694 effects Effects 0.000 claims 4
- 239000001301 oxygen Substances 0.000 claims 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 4
- 239000011593 sulfur Substances 0.000 claims 4
- 206010060945 Bacterial infection Diseases 0.000 claims 3
- 206010017533 Fungal infection Diseases 0.000 claims 3
- 208000001756 Virus Disease Diseases 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- 206010021143 Hypoxia Diseases 0.000 claims 2
- 206010022114 Injury Diseases 0.000 claims 2
- 210000004072 Lung Anatomy 0.000 claims 2
- 102000030002 Prion Proteins Human genes 0.000 claims 2
- 108091000054 Prion Proteins Proteins 0.000 claims 2
- FDDDEECHVMSUSB-UHFFFAOYSA-N Sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 claims 2
- 150000001408 amides Chemical class 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 201000009910 diseases by infectious agent Diseases 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 230000001146 hypoxic Effects 0.000 claims 2
- 230000003053 immunization Effects 0.000 claims 2
- 238000002649 immunization Methods 0.000 claims 2
- 230000001404 mediated Effects 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 244000045947 parasites Species 0.000 claims 2
- 230000001717 pathogenic Effects 0.000 claims 2
- 244000052769 pathogens Species 0.000 claims 2
- 210000000130 stem cell Anatomy 0.000 claims 2
- 229960001663 sulfanilamide Drugs 0.000 claims 2
- 238000002255 vaccination Methods 0.000 claims 2
- WEOSPBLWGYWELY-UHFFFAOYSA-N 1-[[5-[5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]methyl]azetidine-3-carboxylic acid Chemical compound C1=C(OCC)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(CN4CC(C4)C(O)=O)OC3=CC=2)=NO1 WEOSPBLWGYWELY-UHFFFAOYSA-N 0.000 claims 1
- CTTGGWIQLLTQGV-UHFFFAOYSA-N 2-amino-2-[5-[5-(2-cyclopropyl-1-benzofuran-5-yl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C=1C=C2OC(C(CO)(CO)N)=CC2=CC=1C(N=1)=NOC=1C(C=C1C=2)=CC=C1OC=2C1CC1 CTTGGWIQLLTQGV-UHFFFAOYSA-N 0.000 claims 1
- YPBZKICXUPGWLN-UHFFFAOYSA-N 2-amino-2-[5-[5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(OCC)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 YPBZKICXUPGWLN-UHFFFAOYSA-N 0.000 claims 1
- WQQUFVNZMVJKGC-UHFFFAOYSA-N 2-amino-2-[5-[5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl]-7-methyl-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(OCC)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=C(C)C=2)C(N)(CO)CO)=NO1 WQQUFVNZMVJKGC-UHFFFAOYSA-N 0.000 claims 1
- FVNMEJVPZJKSAP-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-bromo-4-propoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(Br)C(OCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 FVNMEJVPZJKSAP-UHFFFAOYSA-N 0.000 claims 1
- GEVRXICHGPFCQU-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-chloro-4-ethoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(Cl)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 GEVRXICHGPFCQU-UHFFFAOYSA-N 0.000 claims 1
- ZSUWDFCZPVAJHC-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-chloro-4-ethoxyphenyl)-1,2,4-oxadiazol-3-yl]-7-methyl-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(Cl)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=C(C)C=2)C(N)(CO)CO)=NO1 ZSUWDFCZPVAJHC-UHFFFAOYSA-N 0.000 claims 1
- DEXRWGFGZHULRV-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-chloro-4-methoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(Cl)C(OC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 DEXRWGFGZHULRV-UHFFFAOYSA-N 0.000 claims 1
- IDIBDIAUXGPPCT-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-chloro-4-propoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]ethanol Chemical compound C1=C(Cl)C(OCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)CO)=NO1 IDIBDIAUXGPPCT-UHFFFAOYSA-N 0.000 claims 1
- YHNUTRJSCOJJKX-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-chloro-4-propoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(Cl)C(OCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 YHNUTRJSCOJJKX-UHFFFAOYSA-N 0.000 claims 1
- WBPVCLGWJAUETH-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-chloro-4-thiophen-3-ylphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C=1C=C2OC(C(CO)(CO)N)=CC2=CC=1C(N=1)=NOC=1C(C=C1Cl)=CC=C1C=1C=CSC=1 WBPVCLGWJAUETH-UHFFFAOYSA-N 0.000 claims 1
- JXKWEVKZQIEXGR-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-methoxy-4-propoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(OC)C(OCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 JXKWEVKZQIEXGR-UHFFFAOYSA-N 0.000 claims 1
- MVAJLHKPGLWUME-UHFFFAOYSA-N 2-amino-2-[5-[5-(3-nitro-4-propoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C([N+]([O-])=O)C(OCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 MVAJLHKPGLWUME-UHFFFAOYSA-N 0.000 claims 1
- NYXKQRIGTIBHSA-UHFFFAOYSA-N 2-amino-2-[5-[5-(4-bromo-3-chlorophenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C=1C=C2OC(C(CO)(CO)N)=CC2=CC=1C(N=1)=NOC=1C1=CC=C(Br)C(Cl)=C1 NYXKQRIGTIBHSA-UHFFFAOYSA-N 0.000 claims 1
- HQLPQUFUIFCXRU-UHFFFAOYSA-N 2-amino-2-[5-[5-(4-butoxy-3-chlorophenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(Cl)C(OCCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 HQLPQUFUIFCXRU-UHFFFAOYSA-N 0.000 claims 1
- SIJCZRVIAUBDBS-UHFFFAOYSA-N 2-amino-2-[5-[5-(4-ethoxy-3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(OC)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 SIJCZRVIAUBDBS-UHFFFAOYSA-N 0.000 claims 1
- CUPATUDDAXRAIH-UHFFFAOYSA-N 2-amino-2-[5-[5-(4-ethoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=CC(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 CUPATUDDAXRAIH-UHFFFAOYSA-N 0.000 claims 1
- SKAZSVACPVLCRM-UHFFFAOYSA-N 2-amino-2-[5-[5-(4-propylphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=CC(CCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 SKAZSVACPVLCRM-UHFFFAOYSA-N 0.000 claims 1
- WSSKQCCUPWMKSG-UHFFFAOYSA-N 2-amino-2-[5-[5-(6-methoxy-1-benzofuran-2-yl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C2OC(C(N)(CO)CO)=CC2=CC(C=2N=C(ON=2)C2=CC3=CC=C(C=C3O2)OC)=C1 WSSKQCCUPWMKSG-UHFFFAOYSA-N 0.000 claims 1
- TWBVLVVFNQPNAF-UHFFFAOYSA-N 2-amino-2-[5-[5-[3-chloro-4-(2,2,2-trifluoroethoxy)phenyl]-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C=1C=C2OC(C(CO)(CO)N)=CC2=CC=1C(N=1)=NOC=1C1=CC=C(OCC(F)(F)F)C(Cl)=C1 TWBVLVVFNQPNAF-UHFFFAOYSA-N 0.000 claims 1
- CZJMOQSNIBDBTC-UHFFFAOYSA-N 2-amino-2-[5-[5-[4-(2-methylpropoxy)phenyl]-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=CC(OCC(C)C)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 CZJMOQSNIBDBTC-UHFFFAOYSA-N 0.000 claims 1
- NHBQDFXGCMFNDY-UHFFFAOYSA-N 2-amino-2-[6-chloro-5-[5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=C(OCC)C(OCC)=CC=C1C1=NC(C=2C(=CC=3OC(=CC=3C=2)C(N)(CO)CO)Cl)=NO1 NHBQDFXGCMFNDY-UHFFFAOYSA-N 0.000 claims 1
- KTOAAAOGWWGDEA-UHFFFAOYSA-N 2-amino-2-[6-chloro-5-[5-(4-propylphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]propane-1,3-diol Chemical compound C1=CC(CCC)=CC=C1C1=NC(C=2C(=CC=3OC(=CC=3C=2)C(N)(CO)CO)Cl)=NO1 KTOAAAOGWWGDEA-UHFFFAOYSA-N 0.000 claims 1
- WARYWKMETSASTB-UHFFFAOYSA-N 2-amino-2-[[5-[5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]methylamino]propane-1,3-diol Chemical compound C1=C(OCC)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(CNC(N)(CO)CO)OC3=CC=2)=NO1 WARYWKMETSASTB-UHFFFAOYSA-N 0.000 claims 1
- YJVIIBRPTLEUFU-UHFFFAOYSA-N 5-[3-[2-(2-amino-1,3-dihydroxypropan-2-yl)-1-benzofuran-5-yl]-1,2,4-oxadiazol-5-yl]-2-ethoxybenzonitrile Chemical compound C1=C(C#N)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 YJVIIBRPTLEUFU-UHFFFAOYSA-N 0.000 claims 1
- QGJMZSZLXFQNFO-UHFFFAOYSA-N 5-[3-[2-(2-amino-1,3-dihydroxypropan-2-yl)-1-benzofuran-5-yl]-1,2,4-oxadiazol-5-yl]-2-propoxybenzonitrile Chemical compound C1=C(C#N)C(OCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 QGJMZSZLXFQNFO-UHFFFAOYSA-N 0.000 claims 1
- LJCBNYKLIUGIBC-UHFFFAOYSA-N 5-[5-(3,4-diethoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-carboxylic acid Chemical compound C1=C(OCC)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(O)=O)=NO1 LJCBNYKLIUGIBC-UHFFFAOYSA-N 0.000 claims 1
- ANWAZHDMFURBHT-UHFFFAOYSA-N 5-[5-[5-(3-chloro-4-propoxyphenyl)-1,2,4-oxadiazol-3-yl]-1-benzofuran-2-yl]-2-hydroxy-2-oxo-1,3,2$l^{5}-dioxaphosphinan-5-amine Chemical compound C1=C(Cl)C(OCCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C2(N)COP(O)(=O)OC2)=NO1 ANWAZHDMFURBHT-UHFFFAOYSA-N 0.000 claims 1
- 206010003816 Autoimmune disease Diseases 0.000 claims 1
- 208000000350 Central Nervous System Disease Diseases 0.000 claims 1
- 206010015037 Epilepsy Diseases 0.000 claims 1
- 206010021425 Immune system disease Diseases 0.000 claims 1
- 210000004185 Liver Anatomy 0.000 claims 1
- 206010067125 Liver injury Diseases 0.000 claims 1
- MLTVUESQFPDUDP-UHFFFAOYSA-N N-[5-[3-[2-(2-amino-1,3-dihydroxypropan-2-yl)-1-benzofuran-5-yl]-1,2,4-oxadiazol-5-yl]-2-ethoxyphenyl]methanesulfonamide Chemical compound C1=C(NS(C)(=O)=O)C(OCC)=CC=C1C1=NC(C=2C=C3C=C(OC3=CC=2)C(N)(CO)CO)=NO1 MLTVUESQFPDUDP-UHFFFAOYSA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 206010053643 Neurodegenerative disease Diseases 0.000 claims 1
- 210000004258 Portal System Anatomy 0.000 claims 1
- 206010052779 Transplant rejections Diseases 0.000 claims 1
- 206010047461 Viral infection Diseases 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 230000000240 adjuvant Effects 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000004429 atoms Chemical group 0.000 claims 1
- 125000004244 benzofuran-2-yl group Chemical group [H]C1=C(*)OC2=C([H])C([H])=C([H])C([H])=C12 0.000 claims 1
- 201000002393 blood protein disease Diseases 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 230000000271 cardiovascular Effects 0.000 claims 1
- 201000008779 central nervous system disease Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229940079593 drugs Drugs 0.000 claims 1
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 1
- 230000001900 immune effect Effects 0.000 claims 1
- 230000036039 immunity Effects 0.000 claims 1
- 230000002458 infectious Effects 0.000 claims 1
- 125000005647 linker group Chemical group 0.000 claims 1
- 201000009673 liver disease Diseases 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000033667 organ regeneration Effects 0.000 claims 1
- 210000000056 organs Anatomy 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 230000001575 pathological Effects 0.000 claims 1
- 239000000546 pharmaceutic aid Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 230000002062 proliferating Effects 0.000 claims 1
- 230000001737 promoting Effects 0.000 claims 1
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 230000001225 therapeutic Effects 0.000 claims 1
- 230000017423 tissue regeneration Effects 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2008905369A AU2008905369A0 (en) | 2008-10-17 | S1P Receptors Modulators and Their use Thereof | |
| AU2008905369 | 2008-10-17 | ||
| AU2009903644A AU2009903644A0 (en) | 2009-08-05 | S1P Receptors Modulators and their use Thereof | |
| AU2009903644 | 2009-08-05 | ||
| PCT/AU2009/001371 WO2010043000A1 (en) | 2008-10-17 | 2009-10-19 | S1p receptors modulators and their use thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014192502A Division JP5963823B2 (ja) | 2008-10-17 | 2014-09-22 | Ｓ１ｐ受容体モジュレーターおよびそれらの使用 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012505836A JP2012505836A (ja) | 2012-03-08 |
| JP2012505836A5 true JP2012505836A5 (US07846941-20101207-C00217.png) | 2013-02-07 |
Family
ID=42106136
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011531305A Pending JP2012505836A (ja) | 2008-10-17 | 2009-10-19 | Ｓ１ｐ受容体モジュレーターおよびそれらの使用 |
| JP2014192502A Active JP5963823B2 (ja) | 2008-10-17 | 2014-09-22 | Ｓ１ｐ受容体モジュレーターおよびそれらの使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014192502A Active JP5963823B2 (ja) | 2008-10-17 | 2014-09-22 | Ｓ１ｐ受容体モジュレーターおよびそれらの使用 |
Country Status (9)
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ592748A (en) | 2008-10-17 | 2013-01-25 | Akaal Pharma Pty Ltd | 2-Amino-(oxadiazol-3-yl)-benzofuran derivatives and their use as S1P receptor modulators |
| US9181182B2 (en) | 2008-10-17 | 2015-11-10 | Akaal Pharma Pty Ltd | S1P receptors modulators |
| RU2011137454A (ru) * | 2009-02-10 | 2013-03-20 | Эбботт Лэборетриз | Агонисты и антагонисты s1p5-рецепторов и способы их применения |
| JP6107660B2 (ja) * | 2010-11-30 | 2017-04-05 | 艾達索高新材料蕪湖有限公司 | 再加工可能なエポキシ樹脂のための新規薬剤 |
| WO2012142268A1 (en) | 2011-04-14 | 2012-10-18 | Allergan, Inc. | Phenyl bicyclic methyl azetidine derivatives as sphingosine-1 phosphate receptors modulators |
| CN102993027B (zh) * | 2011-09-08 | 2014-08-13 | 中化蓝天集团有限公司 | 4-氟-n-异丙基苯胺的定向单烷基化制备方法 |
| AU2012354695B2 (en) | 2011-12-23 | 2016-11-03 | Meiji Seika Pharma Co., Ltd. | Novel S1P receptor modulator |
| WO2013169531A1 (en) * | 2012-05-09 | 2013-11-14 | Boehringer Ingelheim International Gmbh | Methods for making oxetan-3-ylmethanamines |
| AU2013295594B2 (en) | 2012-07-27 | 2018-03-29 | Biogen Ma Inc. | Compounds that are S1P modulating agents and/or ATX modulating agents |
| US8859598B2 (en) | 2012-10-04 | 2014-10-14 | Allergan, Inc. | 1, 2, 4-oxadiazoles azetidine derivatives as sphingosine-1 phosphate receptors modulators |
| WO2014063199A1 (en) * | 2012-10-26 | 2014-05-01 | Akaal Pharma Pty Ltd | Organic compounds |
| WO2014072220A1 (en) | 2012-11-07 | 2014-05-15 | Nerviano Medical Sciences S.R.L. | Substituted pyrimidinyl and pyridinyl-pyrrolopyridinones, process for their preparation and their use as kinase inhibitors |
| US8735433B1 (en) * | 2012-11-14 | 2014-05-27 | Allergan, Inc. | Aryl oxadiazole derivatives as sphingosine 1-phosphate (S1P) receptor modulators |
| CN103304503B (zh) * | 2013-06-02 | 2015-03-04 | 张远强 | 抗糖尿病化合物、其制备方法和用途 |
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