JP2017507915A5 - - Google Patents
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- Publication number
- JP2017507915A5 JP2017507915A5 JP2016545920A JP2016545920A JP2017507915A5 JP 2017507915 A5 JP2017507915 A5 JP 2017507915A5 JP 2016545920 A JP2016545920 A JP 2016545920A JP 2016545920 A JP2016545920 A JP 2016545920A JP 2017507915 A5 JP2017507915 A5 JP 2017507915A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- furan
- hydroxyformamido
- heptanamido
- carbamoyl
- 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.)
- Ceased
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- -1 —CO 2 H Chemical group 0.000 claims 63
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 59
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 26
- 150000001875 compounds Chemical class 0.000 claims 23
- AEDIXYWIVPYNBI-UHFFFAOYSA-N heptanamide Chemical compound CCCCCCC(N)=O AEDIXYWIVPYNBI-UHFFFAOYSA-N 0.000 claims 19
- 150000003839 salts Chemical class 0.000 claims 19
- KDGKTJGPFXIBEB-UHFFFAOYSA-N n-hydroxyformamide Chemical compound ONC=O KDGKTJGPFXIBEB-UHFFFAOYSA-N 0.000 claims 18
- 239000002253 acid Substances 0.000 claims 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 15
- TVFIYRKPCACCNL-UHFFFAOYSA-N furan-2-carboxamide Chemical compound NC(=O)C1=CC=CO1 TVFIYRKPCACCNL-UHFFFAOYSA-N 0.000 claims 14
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 13
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims 12
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 10
- ICJNEJGCTNSQEN-UYAOXDASSA-N CCCCC[C@H]([C@@H](CC)N(C=O)O)C(NCNC(C1=C(C2=CC(C(O)=O)=CC=C2)OC=C1)=O)=O Chemical compound CCCCC[C@H]([C@@H](CC)N(C=O)O)C(NCNC(C1=C(C2=CC(C(O)=O)=CC=C2)OC=C1)=O)=O ICJNEJGCTNSQEN-UYAOXDASSA-N 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 8
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 4
- 102000004152 Bone morphogenetic protein 1 Human genes 0.000 claims 3
- 108090000654 Bone morphogenetic protein 1 Proteins 0.000 claims 3
- 101000637851 Homo sapiens Tolloid-like protein 1 Proteins 0.000 claims 3
- 101000637850 Homo sapiens Tolloid-like protein 2 Proteins 0.000 claims 3
- 102100031996 Tolloid-like protein 1 Human genes 0.000 claims 3
- 102100031997 Tolloid-like protein 2 Human genes 0.000 claims 3
- 230000000694 effects Effects 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 230000037390 scarring Effects 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- JNIYNIYDWZGBOX-UHFFFAOYSA-N 2-[5-[[2-[[formyl(hydroxy)amino]methyl]heptanoylamino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound ON(C=O)CC(C(=O)NCNC(=O)C1=CC=C(O1)C1=C(C(=O)O)C=CC=C1)CCCCC JNIYNIYDWZGBOX-UHFFFAOYSA-N 0.000 claims 2
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 2
- 201000009794 Idiopathic Pulmonary Fibrosis Diseases 0.000 claims 2
- LOMBIJYMBPCNPY-YLJYHZDGSA-N ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=C(OC=C1)C1=CC=C(C(C(=O)O)=C1)C(=O)O)CCCCC Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=C(OC=C1)C1=CC=C(C(C(=O)O)=C1)C(=O)O)CCCCC LOMBIJYMBPCNPY-YLJYHZDGSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 208000020832 chronic kidney disease Diseases 0.000 claims 2
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 201000006938 muscular dystrophy Diseases 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 206010053219 non-alcoholic steatohepatitis Diseases 0.000 claims 2
- 125000004043 oxo group Chemical group O=* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000006413 ring segment Chemical group 0.000 claims 2
- 239000001384 succinic acid Substances 0.000 claims 2
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 2
- RBBYBZRCJCSVLZ-XPWALMASSA-N (2S)-2-[[2-[2-ethoxy-4-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]acetyl]amino]butanedioic acid Chemical compound CCCCC[C@H]([C@@H](CC)N(O)C=O)C(=O)NCNC(=O)C1=CC=C(O1)C1=CC(OCC)=C(CC(=O)N[C@@H](CC(O)=O)C(O)=O)C=C1 RBBYBZRCJCSVLZ-XPWALMASSA-N 0.000 claims 1
- OOYCZSDPTUAUHM-IEZKXTBUSA-N (2S)-2-[[4-[5-[[[(2R,3R)-2-[2-(2,4-difluorophenyl)ethyl]-3-[formyl(hydroxy)amino]pentanoyl]amino]methylcarbamoyl]furan-2-yl]-2-ethoxybenzoyl]amino]butanedioic acid Chemical compound FC1=C(C=CC(=C1)F)CC[C@@H](C(=O)NCNC(=O)C1=CC=C(O1)C1=CC(=C(C(=O)N[C@H](C(=O)O)CC(=O)O)C=C1)OCC)[C@@H](CC)N(C=O)O OOYCZSDPTUAUHM-IEZKXTBUSA-N 0.000 claims 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 1
- AZCVVKKSIGSIBN-NHCUHLMSSA-N 1-[4-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]cyclopropane-1-carboxylic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C1=CC=C(C=C1)C1(CC1)C(=O)O)CCCCC AZCVVKKSIGSIBN-NHCUHLMSSA-N 0.000 claims 1
- OJDWWBUOFLCESN-CYBMUJFWSA-N 2,6-difluoro-3-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound FC1=C(C(=O)O)C(=CC=C1C=1OC(=CC=1)C(NCNC([C@H](CCCCC)CN(C=O)O)=O)=O)F OJDWWBUOFLCESN-CYBMUJFWSA-N 0.000 claims 1
- UWJMRCZZRINSHA-NHCUHLMSSA-N 2-[3-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]-2-methylpropanoic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C=C(C=CC1)C(C(=O)O)(C)C)CCCCC UWJMRCZZRINSHA-NHCUHLMSSA-N 0.000 claims 1
- NKGCXRHPXKPRGE-GOSISDBHSA-N 2-[3-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]acetic acid Chemical compound ON(C=O)C[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C=C(C=CC=1)CC(=O)O)CCCCC NKGCXRHPXKPRGE-GOSISDBHSA-N 0.000 claims 1
- OJYJMDRAFRSACC-LRTDYKAYSA-N 2-[3-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]propanoic acid Chemical compound ON(C=O)C[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C=C(C=CC1)C(C(=O)O)C)CCCCC OJYJMDRAFRSACC-LRTDYKAYSA-N 0.000 claims 1
- KLWCQQLVUFBCSJ-NHCUHLMSSA-N 2-[3-ethoxy-5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]-2,2-difluoroacetic acid Chemical compound C(C)OC=1C=C(C=C(C1)C=1OC(=CC1)C(NCNC([C@H](CCCCC)[C@@H](CC)N(C=O)O)=O)=O)C(C(=O)O)(F)F KLWCQQLVUFBCSJ-NHCUHLMSSA-N 0.000 claims 1
- CSOOXMLPHMLROL-NHCUHLMSSA-N 2-[4-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]-2-methylpropanoic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C1=CC=C(C=C1)C(C(=O)O)(C)C)CCCCC CSOOXMLPHMLROL-NHCUHLMSSA-N 0.000 claims 1
- OOQSODFEUOWYPX-WOJBJXKFSA-N 2-[4-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]acetic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C1=CC=C(C=C1)CC(=O)O)CCCCC OOQSODFEUOWYPX-WOJBJXKFSA-N 0.000 claims 1
- JNIYNIYDWZGBOX-OAHLLOKOSA-N 2-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound ON(C=O)C[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C1=C(C(=O)O)C=CC=C1)CCCCC JNIYNIYDWZGBOX-OAHLLOKOSA-N 0.000 claims 1
- VOIDFWWWMVOASZ-DNQXCXABSA-N 2-[[3-ethoxy-5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]phenyl]methyl-methylamino]acetic acid Chemical compound C(C)OC=1C=C(CN(CC(=O)O)C)C=C(C1)C=1OC(=CC1)C(NCNC([C@H](CCCCC)[C@@H](CC)N(C=O)O)=O)=O VOIDFWWWMVOASZ-DNQXCXABSA-N 0.000 claims 1
- XUYXGZGYBSPCEY-ILBGXUMGSA-N 2-[carboxymethyl-[2-ethoxy-4-[5-[[[(2R,3R)-3-[formyl(hydroxy)amino]-2-(2-phenylethyl)pentanoyl]amino]methylcarbamoyl]furan-2-yl]benzoyl]amino]acetic acid Chemical compound C(C)OC1=C(C(=O)N(CC(=O)O)CC(=O)O)C=CC(=C1)C=1OC(=CC1)C(NCNC([C@@H]([C@@H](CC)N(C=O)O)CCC1=CC=CC=C1)=O)=O XUYXGZGYBSPCEY-ILBGXUMGSA-N 0.000 claims 1
- GKBOXHJWFVZMHR-AOYPEHQESA-N 2-[carboxymethyl-[3-[5-[[[(2R,3R)-2-[2-(2,4-difluorophenyl)ethyl]-3-[formyl(hydroxy)amino]pentanoyl]amino]methylcarbamoyl]furan-2-yl]-5-ethoxybenzoyl]amino]acetic acid Chemical compound FC1=C(CC[C@@H](C(=O)NCNC(=O)C2=CC=C(O2)C=2C=C(C(=O)N(CC(=O)O)CC(=O)O)C=C(C=2)OCC)[C@@H](CC)N(C=O)O)C=CC(=C1)F GKBOXHJWFVZMHR-AOYPEHQESA-N 0.000 claims 1
- YEDIUVJCFVQHFT-DHIUTWEWSA-N 2-[carboxymethyl-[3-ethoxy-5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoyl]amino]acetic acid Chemical compound C(C)OC=1C=C(C(=O)N(CC(=O)O)CC(=O)O)C=C(C1)C=1OC(=CC1)C(NCNC([C@H](CCCCC)[C@@H](CC)N(C=O)O)=O)=O YEDIUVJCFVQHFT-DHIUTWEWSA-N 0.000 claims 1
- FEGGHDNFYOHIAS-OAHLLOKOSA-N 2-amino-5-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound NC1=C(C(=O)O)C=C(C=C1)C=1OC(=CC1)C(NCNC([C@H](CCCCC)CN(C=O)O)=O)=O FEGGHDNFYOHIAS-OAHLLOKOSA-N 0.000 claims 1
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- JAYZKDJRODJAHD-CQSZACIVSA-N 2-fluoro-3-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound FC1=C(C(=O)O)C=CC=C1C=1OC(=CC=1)C(NCNC([C@H](CCCCC)CN(C=O)O)=O)=O JAYZKDJRODJAHD-CQSZACIVSA-N 0.000 claims 1
- VFQLAARGYVURHL-UHFFFAOYSA-N 2-fluoro-5-[5-[[2-[[formyl(hydroxy)amino]methyl]heptanoylamino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound CCCCCC(CN(O)C=O)C(=O)NCNC(=O)c1ccc(o1)-c1ccc(F)c(c1)C(O)=O VFQLAARGYVURHL-UHFFFAOYSA-N 0.000 claims 1
- VFQLAARGYVURHL-OAHLLOKOSA-N 2-fluoro-5-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound FC1=C(C(=O)O)C=C(C=C1)C=1OC(=CC=1)C(NCNC([C@H](CCCCC)CN(C=O)O)=O)=O VFQLAARGYVURHL-OAHLLOKOSA-N 0.000 claims 1
- 125000004924 2-naphthylethyl group Chemical group C1=C(C=CC2=CC=CC=C12)CC* 0.000 claims 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 1
- CIYVDOLHZQTJRJ-WOJBJXKFSA-N 3-(2-amino-2-oxoethoxy)-5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound NC(COC=1C=C(C(=O)O)C=C(C=1)C=1OC(=CC=1)C(NCNC([C@H](CCCCC)[C@@H](CC)N(C=O)O)=O)=O)=O CIYVDOLHZQTJRJ-WOJBJXKFSA-N 0.000 claims 1
- OLVGYZQTVBDCLJ-WOJBJXKFSA-N 3-(carboxymethoxy)-5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound C(=O)(O)COC=1C=C(C(=O)O)C=C(C=1)C=1OC(=CC=1)C(NCNC([C@H](CCCCC)[C@@H](CC)N(C=O)O)=O)=O OLVGYZQTVBDCLJ-WOJBJXKFSA-N 0.000 claims 1
- SDTSNZJWXCVNMT-UHFFFAOYSA-N 3-[5-[[2-[[formyl(hydroxy)amino]methyl]heptanoylamino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound CCCCCC(CN(O)C=O)C(=O)NCNC(=O)c1ccc(o1)-c1cccc(c1)C(O)=O SDTSNZJWXCVNMT-UHFFFAOYSA-N 0.000 claims 1
- CCQZNGVTACLZPG-FGZHOGPDSA-N 3-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]-5-propoxybenzoic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C=C(C(=O)O)C=C(C1)OCCC)CCCCC CCQZNGVTACLZPG-FGZHOGPDSA-N 0.000 claims 1
- SDZJEFRAJDSNQW-OAHLLOKOSA-N 3-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]-2-methoxybenzoic acid Chemical compound ON(C=O)C[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C(=C(C(=O)O)C=CC1)OC)CCCCC SDZJEFRAJDSNQW-OAHLLOKOSA-N 0.000 claims 1
- KPVFOUNLQKBYIP-MRXNPFEDSA-N 3-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]-2-methylbenzoic acid Chemical compound ON(C=O)C[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C(=C(C(=O)O)C=CC1)C)CCCCC KPVFOUNLQKBYIP-MRXNPFEDSA-N 0.000 claims 1
- NZZQNOHKPCQKKC-IEBWSBKVSA-N 3-ethoxy-2-fluoro-5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound C(C)OC=1C(=C(C(=O)O)C=C(C=1)C=1OC(=CC=1)C(NCNC([C@H](CCCCC)[C@@H](CC)N(C=O)O)=O)=O)F NZZQNOHKPCQKKC-IEBWSBKVSA-N 0.000 claims 1
- BRHPGJGDRPZCNS-MRXNPFEDSA-N 3-ethoxy-5-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound C(C)OC=1C=C(C(=O)O)C=C(C=1)C=1OC(=CC=1)C(NCNC([C@H](CCCCC)CN(C=O)O)=O)=O BRHPGJGDRPZCNS-MRXNPFEDSA-N 0.000 claims 1
- 125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- OBUCNGYFEHMNAD-QGZVFWFLSA-N 4-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]benzoic acid Chemical compound ON(C=O)C[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C1=CC=C(C(=O)O)C=C1)CCCCC OBUCNGYFEHMNAD-QGZVFWFLSA-N 0.000 claims 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims 1
- MVGYSELXXWZWIN-VQIMIIECSA-N 5-(carboxymethoxy)-3-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]-2-hydroxybenzoic acid Chemical compound C(=O)(O)COC=1C=C(C(=C(C(=O)O)C1)O)C=1OC(=CC1)C(NCNC([C@H](CCCCC)[C@@H](CC)N(C=O)O)=O)=O MVGYSELXXWZWIN-VQIMIIECSA-N 0.000 claims 1
- CYPUWXZJVPSHHD-IEBWSBKVSA-N 5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]-2-methoxybenzoic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C=CC(=C(C(=O)O)C1)OC)CCCCC CYPUWXZJVPSHHD-IEBWSBKVSA-N 0.000 claims 1
- HOSZYAKZPYGGQV-UYAOXDASSA-N 5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]-2-methylbenzoic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C=CC(=C(C(=O)O)C1)C)CCCCC HOSZYAKZPYGGQV-UYAOXDASSA-N 0.000 claims 1
- KVJPULCOPXGRLR-QZTJIDSGSA-N 5-[5-[[[(2R)-2-[(1R)-1-[formyl(hydroxy)amino]propyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]pyridine-3-carboxylic acid Chemical compound ON(C=O)[C@H](CC)[C@H](C(=O)NCNC(=O)C1=CC=C(O1)C=1C=NC=C(C(=O)O)C1)CCCCC KVJPULCOPXGRLR-QZTJIDSGSA-N 0.000 claims 1
- KQFXPMDLKBVKFX-OAHLLOKOSA-N 5-[5-[[[(2R)-2-[[formyl(hydroxy)amino]methyl]heptanoyl]amino]methylcarbamoyl]furan-2-yl]-2-hydroxybenzoic acid Chemical compound OC1=C(C(=O)O)C=C(C=C1)C=1OC(=CC=1)C(NCNC([C@H](CCCCC)CN(C=O)O)=O)=O KQFXPMDLKBVKFX-OAHLLOKOSA-N 0.000 claims 1
- 208000009304 Acute Kidney Injury Diseases 0.000 claims 1
- 206010006895 Cachexia Diseases 0.000 claims 1
- 208000029147 Collagen-vascular disease Diseases 0.000 claims 1
- 208000007342 Diabetic Nephropathies Diseases 0.000 claims 1
- 206010016654 Fibrosis Diseases 0.000 claims 1
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| MA39171A1 (fr) * | 2014-01-10 | 2017-07-31 | Glaxosmithkline Intellectual Property (No 2) Ltd | Dérivés d'hydroxy formamide et leur utilisation |
| WO2017006295A1 (en) * | 2015-07-08 | 2017-01-12 | Glaxosmithkline Intellectual Property (No.2) Limited | Hydroxy formamide derivatives and their use |
| JP2018525353A (ja) | 2015-07-09 | 2018-09-06 | グラクソスミスクライン、インテレクチュアル、プロパティー、（ナンバー２）、リミテッドＧｌａｘｏｓｍｉｔｈｋｌｉｎｅ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ （Ｎｏ．２） Ｌｉｍｉｔｅｄ | Ｂｍｐ１、ｔｌｌ１および／またはｔｌｌ２の阻害剤としての使用するための、ｎ−ヒドロキシホルムアミド化合物およびそれらを含んでなる組成物 |
| CN106699604B (zh) * | 2017-01-09 | 2019-01-01 | 四川同晟生物医药有限公司 | 一种沙库比曲及其中间体的制备方法 |
| US9862675B1 (en) * | 2017-07-05 | 2018-01-09 | King Fahd University Of Petroleum And Minerals | Method of N-formylating amines with a phosphonic anhydride |
| BR112021010095A2 (pt) | 2018-11-29 | 2021-09-28 | VenatoRx Pharmaceuticals, Inc. | Composições de combinação que compreendem um inibidor de beta-lactamase e usos das mesmas |
| CN116507638A (zh) * | 2020-07-31 | 2023-07-28 | 葛兰素史密斯克莱知识产权发展有限公司 | 抗原结合蛋白 |
| EP4225321A4 (en) | 2020-10-07 | 2024-11-20 | Venatorx Pharmaceuticals, Inc. | PROCESS FOR BORON-CONTAINING COMPOUNDS |
| CN114230463B (zh) * | 2021-12-28 | 2024-06-21 | 青岛科技大学 | 一种邻羟基苯甲酸苯酯的后处理方法 |
| CN114195638B (zh) * | 2021-12-28 | 2023-07-14 | 青岛科技大学 | 一种邻羟基苯甲酸苯酯的制备方法 |
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| JP2018525353A (ja) | 2015-07-09 | 2018-09-06 | グラクソスミスクライン、インテレクチュアル、プロパティー、（ナンバー２）、リミテッドＧｌａｘｏｓｍｉｔｈｋｌｉｎｅ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ （Ｎｏ．２） Ｌｉｍｉｔｅｄ | Ｂｍｐ１、ｔｌｌ１および／またはｔｌｌ２の阻害剤としての使用するための、ｎ−ヒドロキシホルムアミド化合物およびそれらを含んでなる組成物 |
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2015
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2016
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