JP2009542658A5

JP2009542658A5 -

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Publication number: JP2009542658A5
Authority: JP; Japan
Prior art keywords: ethyl; phenylsulfamic acid; thiazol; tert; methoxycarbonylamino
Prior art date: 2007-06-27
Legal status : Granted

Application number

JP2009518226A

Other languages

English (en)

Japanese (ja)

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JP2009542658A (ja

JP5232778B2 (ja

Filing date

2007-06-27

Publication date

2010-04-15

2007-06-27 Application filed filed Critical

2007-06-27 Priority claimed from PCT/US2007/014822 external-priority patent/WO2008002569A2/en

2009-12-03 Publication of JP2009542658A publication Critical patent/JP2009542658A/ja

2010-04-15 Publication of JP2009542658A5 publication Critical patent/JP2009542658A5/ja

2013-07-10 Application granted granted Critical

2013-07-10 Publication of JP5232778B2 publication Critical patent/JP5232778B2/ja

Status Expired - Fee Related legal-status Critical Current

2027-06-27 Anticipated expiration legal-status Critical

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-1 2,2- difluoro Cyclopropyl Chemical group 0.000 claims description 271
150000001875 compounds Chemical class 0.000 claims description 172
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 114
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 94
230000033115 angiogenesis Effects 0.000 claims description 84
238000000034 method Methods 0.000 claims description 72
229910052739 hydrogen Inorganic materials 0.000 claims description 61
239000001257 hydrogen Substances 0.000 claims description 61
239000000203 mixture Substances 0.000 claims description 57
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 52
208000035475 disorder Diseases 0.000 claims description 52
210000001519 tissue Anatomy 0.000 claims description 51
125000006626 methoxycarbonylamino group Chemical group 0.000 claims description 44
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 44
201000010099 disease Diseases 0.000 claims description 42
125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 claims description 39
125000000217 alkyl group Chemical group 0.000 claims description 36
125000001072 heteroaryl group Chemical group 0.000 claims description 34
125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims description 32
BEHLMOQXOSLGHN-UHFFFAOYSA-N benzenamine sulfate Chemical compound OS(=O)(=O)NC1=CC=CC=C1 BEHLMOQXOSLGHN-UHFFFAOYSA-N 0.000 claims description 31
238000002360 preparation method Methods 0.000 claims description 28
125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 26
150000003839 salts Chemical class 0.000 claims description 25
206010028980 Neoplasm Diseases 0.000 claims description 24
230000017423 tissue regeneration Effects 0.000 claims description 23
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 20
239000003814 drug Substances 0.000 claims description 19
239000002253 acid Substances 0.000 claims description 18
125000003545 alkoxy group Chemical group 0.000 claims description 17
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
125000004429 atom Chemical group 0.000 claims description 16
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 16
125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 15
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 14
239000011734 sodium Substances 0.000 claims description 14
208000029078 coronary artery disease Diseases 0.000 claims description 13
230000012010 growth Effects 0.000 claims description 13
125000006633 tert-butoxycarbonylamino group Chemical group 0.000 claims description 13
125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 12
230000001737 promoting effect Effects 0.000 claims description 12
229920006395 saturated elastomer Polymers 0.000 claims description 12
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 12
229910052717 sulfur Inorganic materials 0.000 claims description 12
230000001684 chronic effect Effects 0.000 claims description 11
230000000302 ischemic effect Effects 0.000 claims description 11
201000000306 sarcoidosis Diseases 0.000 claims description 11
150000002367 halogens Chemical group 0.000 claims description 10
239000007787 solid Substances 0.000 claims description 10
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
239000008194 pharmaceutical composition Substances 0.000 claims description 9
238000006467 substitution reaction Methods 0.000 claims description 9
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 8
201000011510 cancer Diseases 0.000 claims description 8
150000002431 hydrogen Chemical class 0.000 claims description 8
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims description 8
208000018262 Peripheral vascular disease Diseases 0.000 claims description 7
208000006011 Stroke Diseases 0.000 claims description 7
208000014674 injury Diseases 0.000 claims description 7
208000031225 myocardial ischemia Diseases 0.000 claims description 7
125000004287 oxazol-2-yl group Chemical group [H]C1=C([H])N=C(*)O1 0.000 claims description 7
125000003145 oxazol-4-yl group Chemical group O1C=NC(=C1)* 0.000 claims description 7
125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 claims description 7
230000008733 trauma Effects 0.000 claims description 7
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 6
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 6
208000030507 AIDS Diseases 0.000 claims description 6
208000011231 Crohn disease Diseases 0.000 claims description 6
201000004681 Psoriasis Diseases 0.000 claims description 6
SPXYGWSITXECNH-IBGZPJMESA-N [4-[(2s)-2-(2,2-dimethylpropanoylamino)-2-[4-(3-methoxyphenyl)-1,3-thiazol-2-yl]ethyl]phenyl]sulfamic acid Chemical compound COC1=CC=CC(C=2N=C(SC=2)[C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)C(C)(C)C)=C1 SPXYGWSITXECNH-IBGZPJMESA-N 0.000 claims description 6
XKZOMUWCCBPCCW-SFTDATJTSA-N [4-[(2s)-2-(4-ethyl-1,3-thiazol-2-yl)-2-[[(2s)-2-(methoxycarbonylamino)-3-phenylpropanoyl]amino]ethyl]phenyl]sulfamic acid Chemical compound CCC1=CSC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)[C@H](CC=2C=CC=CC=2)NC(=O)OC)=N1 XKZOMUWCCBPCCW-SFTDATJTSA-N 0.000 claims description 6
OGXLOMHMFQEQGZ-SFHVURJKSA-N [4-[(2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-(4-phenyl-1,3-thiazol-2-yl)ethyl]phenyl]sulfamic acid Chemical compound C([C@H](NC(=O)OC(C)(C)C)C=1SC=C(N=1)C=1C=CC=CC=1)C1=CC=C(NS(O)(=O)=O)C=C1 OGXLOMHMFQEQGZ-SFHVURJKSA-N 0.000 claims description 6
201000011066 hemangioma Diseases 0.000 claims description 6
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 6
206010039073 rheumatoid arthritis Diseases 0.000 claims description 6
210000002027 skeletal muscle Anatomy 0.000 claims description 6
208000011580 syndromic disease Diseases 0.000 claims description 6
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
125000001397 3-pyrrolyl group Chemical group [H]N1C([H])=C([*])C([H])=C1[H] 0.000 claims description 5
208000031104 Arterial Occlusive disease Diseases 0.000 claims description 5
208000009137 Behcet syndrome Diseases 0.000 claims description 5
208000037663 Best vitelliform macular dystrophy Diseases 0.000 claims description 5
208000002691 Choroiditis Diseases 0.000 claims description 5
206010009900 Colitis ulcerative Diseases 0.000 claims description 5
206010012689 Diabetic retinopathy Diseases 0.000 claims description 5
208000019878 Eales disease Diseases 0.000 claims description 5
201000002563 Histoplasmosis Diseases 0.000 claims description 5
241000282412 Homo Species 0.000 claims description 5
206010051151 Hyperviscosity syndrome Diseases 0.000 claims description 5
208000016604 Lyme disease Diseases 0.000 claims description 5
206010062207 Mycobacterial infection Diseases 0.000 claims description 5
208000010191 Osteitis Deformans Diseases 0.000 claims description 5
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 5
208000027868 Paget disease Diseases 0.000 claims description 5
208000003971 Posterior uveitis Diseases 0.000 claims description 5
206010038848 Retinal detachment Diseases 0.000 claims description 5
206010038910 Retinitis Diseases 0.000 claims description 5
206010038933 Retinopathy of prematurity Diseases 0.000 claims description 5
208000027073 Stargardt disease Diseases 0.000 claims description 5
201000005485 Toxoplasmosis Diseases 0.000 claims description 5
201000006704 Ulcerative Colitis Diseases 0.000 claims description 5
206010046851 Uveitis Diseases 0.000 claims description 5
206010047663 Vitritis Diseases 0.000 claims description 5
QFPXHOSHKYXCBU-VXKWHMMOSA-N [4-[(2s)-2-[[(2s)-2-acetamido-3-phenylpropanoyl]amino]-2-(4-ethyl-1,3-thiazol-2-yl)ethyl]phenyl]sulfamic acid Chemical compound CCC1=CSC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)[C@H](CC=2C=CC=CC=2)NC(C)=O)=N1 QFPXHOSHKYXCBU-VXKWHMMOSA-N 0.000 claims description 5
208000021328 arterial occlusion Diseases 0.000 claims description 5
230000001886 ciliary effect Effects 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
208000013653 hyalitis Diseases 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 claims description 5
125000002140 imidazol-4-yl group Chemical group [H]N1C([H])=NC([*])=C1[H] 0.000 claims description 5
125000001793 isothiazol-3-yl group Chemical group [H]C1=C([H])C(*)=NS1 0.000 claims description 5
125000004500 isothiazol-4-yl group Chemical group S1N=CC(=C1)* 0.000 claims description 5
125000004501 isothiazol-5-yl group Chemical group S1N=CC=C1* 0.000 claims description 5
125000004284 isoxazol-3-yl group Chemical group [H]C1=C([H])C(*)=NO1 0.000 claims description 5
125000004499 isoxazol-5-yl group Chemical group O1N=CC=C1* 0.000 claims description 5
238000013532 laser treatment Methods 0.000 claims description 5
208000002780 macular degeneration Diseases 0.000 claims description 5
208000027202 mammary Paget disease Diseases 0.000 claims description 5
208000027531 mycobacterial infectious disease Diseases 0.000 claims description 5
208000001491 myopia Diseases 0.000 claims description 5
230000004379 myopia Effects 0.000 claims description 5
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
230000006785 proliferative vitreoretinopathy Effects 0.000 claims description 5
230000004264 retinal detachment Effects 0.000 claims description 5
208000007056 sickle cell anemia Diseases 0.000 claims description 5
208000006379 syphilis Diseases 0.000 claims description 5
201000000596 systemic lupus erythematosus Diseases 0.000 claims description 5
125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 claims description 5
125000000335 thiazolyl group Chemical group 0.000 claims description 5
201000007790 vitelliform macular dystrophy Diseases 0.000 claims description 5
208000020938 vitelliform macular dystrophy 2 Diseases 0.000 claims description 5
125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 4
125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 4
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 4
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 4
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
208000031953 Hereditary hemorrhagic telangiectasia Diseases 0.000 claims description 4
208000002158 Proliferative Vitreoretinopathy Diseases 0.000 claims description 4
206010038934 Retinopathy proliferative Diseases 0.000 claims description 4
CXXUQZOTXBDSLC-INIZCTEOSA-N [4-[(2s)-2-(4-ethyl-1,3-thiazol-2-yl)-2-[[3-[(2-methylpropan-2-yl)oxy]-3-oxopropanoyl]amino]ethyl]phenyl]sulfamic acid Chemical compound CCC1=CSC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)CC(=O)OC(C)(C)C)=N1 CXXUQZOTXBDSLC-INIZCTEOSA-N 0.000 claims description 4
229910052797 bismuth Inorganic materials 0.000 claims description 4
JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 4
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 4
208000015181 infectious disease Diseases 0.000 claims description 4
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 4
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 4
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
208000021971 neovascular inflammatory vitreoretinopathy Diseases 0.000 claims description 4
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 4
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 3
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 3
125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 3
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 3
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 3
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 3
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
229910019142 PO4 Inorganic materials 0.000 claims description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
LIOMLBKOFULAIB-MRXNPFEDSA-N [4-[(2S)-2-[4-[2-[(2-methoxy-2-oxoethyl)amino]-2-oxoethyl]-1,3-thiazol-2-yl]-3-[(2-methylpropan-2-yl)oxy]-3-oxopropyl]phenyl]sulfamic acid Chemical compound C(C)(C)(C)OC(=O)[C@H](CC1=CC=C(C=C1)NS(O)(=O)=O)C=1SC=C(N=1)CC(=O)NCC(=O)OC LIOMLBKOFULAIB-MRXNPFEDSA-N 0.000 claims description 3
YDMOYGLNUKECPA-HNNXBMFYSA-N [4-[(2s)-2-(2,2-dimethylpropanoylamino)-2-(4-ethyl-1,3-thiazol-2-yl)ethyl]phenyl]sulfamic acid Chemical compound CCC1=CSC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)C(C)(C)C)=N1 YDMOYGLNUKECPA-HNNXBMFYSA-N 0.000 claims description 3
QDLLTACANIARFO-AWEZNQCLSA-N [4-[(2s)-2-(2,2-dimethylpropanoylamino)-2-(4-methyl-1,3-thiazol-2-yl)ethyl]phenyl]sulfamic acid Chemical compound CC1=CSC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)C(C)(C)C)=N1 QDLLTACANIARFO-AWEZNQCLSA-N 0.000 claims description 3
IHLNYOYOOXRVFX-SFHVURJKSA-N [4-[(2s)-2-(2,2-dimethylpropanoylamino)-2-(4-phenyl-1,3-thiazol-2-yl)ethyl]phenyl]sulfamic acid Chemical compound C([C@H](NC(=O)C(C)(C)C)C=1SC=C(N=1)C=1C=CC=CC=1)C1=CC=C(NS(O)(=O)=O)C=C1 IHLNYOYOOXRVFX-SFHVURJKSA-N 0.000 claims description 3
ZOLAHFBNGNECSE-IBGZPJMESA-N [4-[(2s)-2-(2,2-dimethylpropanoylamino)-2-(5-methyl-4-phenyl-1,3-thiazol-2-yl)ethyl]phenyl]sulfamic acid Chemical compound CC=1SC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)C(C)(C)C)=NC=1C1=CC=CC=C1 ZOLAHFBNGNECSE-IBGZPJMESA-N 0.000 claims description 3
ZORFECOAEGMFEQ-SFHVURJKSA-N [4-[(2s)-2-(2,2-dimethylpropanoylamino)-2-[4-(thiophen-2-ylmethyl)-1,3-thiazol-2-yl]ethyl]phenyl]sulfamic acid Chemical compound C([C@H](NC(=O)C(C)(C)C)C=1SC=C(CC=2SC=CC=2)N=1)C1=CC=C(NS(O)(=O)=O)C=C1 ZORFECOAEGMFEQ-SFHVURJKSA-N 0.000 claims description 3
XNQLVRONDTXSHT-NRFANRHFSA-N [4-[(2s)-2-(2,2-dimethylpropanoylamino)-2-[4-[(3-methoxyphenyl)methyl]-1,3-thiazol-2-yl]ethyl]phenyl]sulfamic acid Chemical compound COC1=CC=CC(CC=2N=C(SC=2)[C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)C(C)(C)C)=C1 XNQLVRONDTXSHT-NRFANRHFSA-N 0.000 claims description 3
ZKDWAOAVSQQEJN-FQEVSTJZSA-N [4-[(2s)-2-(4-benzyl-1,3-thiazol-2-yl)-2-(2,2-dimethylpropanoylamino)ethyl]phenyl]sulfamic acid Chemical compound C([C@H](NC(=O)C(C)(C)C)C=1SC=C(CC=2C=CC=CC=2)N=1)C1=CC=C(NS(O)(=O)=O)C=C1 ZKDWAOAVSQQEJN-FQEVSTJZSA-N 0.000 claims description 3
DFMNJBSBPRRYMI-GOTSBHOMSA-N [4-[(2s)-2-(4-ethyl-1,3-thiazol-2-yl)-2-[[(2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]amino]ethyl]phenyl]sulfamic acid Chemical compound CCC1=CSC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)[C@H](CC=2C=CC=CC=2)NC(=O)OC(C)(C)C)=N1 DFMNJBSBPRRYMI-GOTSBHOMSA-N 0.000 claims description 3
GRGXZTOMWQBGBV-SFTDATJTSA-N [4-[(2s)-2-(4-tert-butyl-1,3-thiazol-2-yl)-2-[[(2s)-2-(methoxycarbonylamino)-3-phenylpropanoyl]amino]ethyl]phenyl]sulfamic acid Chemical compound C([C@H](NC(=O)OC)C(=O)N[C@@H](CC=1C=CC(NS(O)(=O)=O)=CC=1)C=1SC=C(N=1)C(C)(C)C)C1=CC=CC=C1 GRGXZTOMWQBGBV-SFTDATJTSA-N 0.000 claims description 3
RMUOIGZNNCUUTD-SFHVURJKSA-N [4-[(2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-(5-phenyl-1,3-thiazol-2-yl)ethyl]phenyl]sulfamic acid Chemical compound C([C@H](NC(=O)OC(C)(C)C)C=1SC(=CN=1)C=1C=CC=CC=1)C1=CC=C(NS(O)(=O)=O)C=C1 RMUOIGZNNCUUTD-SFHVURJKSA-N 0.000 claims description 3
SJXHSNZPIWYRNY-SFHVURJKSA-N [4-[(2s)-2-[4-(2,3-dihydro-1,4-benzodioxin-6-yl)-1,3-thiazol-2-yl]-2-(2,2-dimethylpropanoylamino)ethyl]phenyl]sulfamic acid Chemical compound C([C@H](NC(=O)C(C)(C)C)C=1SC=C(N=1)C=1C=C2OCCOC2=CC=1)C1=CC=C(NS(O)(=O)=O)C=C1 SJXHSNZPIWYRNY-SFHVURJKSA-N 0.000 claims description 3
RQOCHQZZERGEFT-IBGZPJMESA-N [4-[(2s)-2-[4-(2,4-dimethoxyphenyl)-1,3-thiazol-2-yl]-2-(2,2-dimethylpropanoylamino)ethyl]phenyl]sulfamic acid Chemical compound COC1=CC(OC)=CC=C1C1=CSC([C@H](CC=2C=CC(NS(O)(=O)=O)=CC=2)NC(=O)C(C)(C)C)=N1 RQOCHQZZERGEFT-IBGZPJMESA-N 0.000 claims description 3
150000001450 anions Chemical class 0.000 claims description 3
239000011575 calcium Substances 0.000 claims description 3
229910052791 calcium Inorganic materials 0.000 claims description 3
150000001768 cations Chemical class 0.000 claims description 3
210000004177 elastic tissue Anatomy 0.000 claims description 3
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 3
QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 3
125000004498 isoxazol-4-yl group Chemical group O1N=CC(=C1)* 0.000 claims description 3
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JP2009518226A 2006-06-27 2007-06-27 ヒトプロテインチロシンホスファターゼβ阻害剤および使用法 Expired - Fee Related JP5232778B2 (ja)