KR20200038987A - 약제학적 조성물 - Google Patents
약제학적 조성물 Download PDFInfo
- Publication number
- KR20200038987A KR20200038987A KR1020207007099A KR20207007099A KR20200038987A KR 20200038987 A KR20200038987 A KR 20200038987A KR 1020207007099 A KR1020207007099 A KR 1020207007099A KR 20207007099 A KR20207007099 A KR 20207007099A KR 20200038987 A KR20200038987 A KR 20200038987A
- Authority
- KR
- South Korea
- Prior art keywords
- phenyl
- aminomethyl
- ethyl
- ethoxy
- benzylcarbamoyl
- 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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- 125000000217 alkyl group Chemical group 0.000 claims description 71
- 238000002347 injection Methods 0.000 claims description 47
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- 125000003118 aryl group Chemical group 0.000 claims description 39
- 102000003827 Plasma Kallikrein Human genes 0.000 claims description 38
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- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 claims description 9
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
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- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 6
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- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 6
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- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 5
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- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 4
- HDDOGAGGUYGJLQ-FTJBHMTQSA-N 3-amino-n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-(1,3-thiazol-4-yl)propan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]thiophene-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1N=CSC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=C(N)C=CS1 HDDOGAGGUYGJLQ-FTJBHMTQSA-N 0.000 claims description 4
- YIVHOQIKHMTVRG-UHFFFAOYSA-N 3-methyl-1h-pyrrole-2-carboxylic acid Chemical compound CC=1C=CNC=1C(O)=O YIVHOQIKHMTVRG-UHFFFAOYSA-N 0.000 claims description 4
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- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 4
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- 229910019142 PO4 Inorganic materials 0.000 claims description 4
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- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 4
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- UCIXIQRCAGGOJY-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 UCIXIQRCAGGOJY-AJQTZOPKSA-N 0.000 claims description 4
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- CYVSDXJVCZURLD-IHLOFXLRSA-N 3-amino-n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(1-benzothiophen-3-yl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]thiophene-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C2=CC=CC=C2SC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=C(N)C=CS1 CYVSDXJVCZURLD-IHLOFXLRSA-N 0.000 claims description 2
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- NKONHEXDLBKQFF-URLMMPGGSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-methyl-1,3-thiazole-5-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=C(C)N=CS1 NKONHEXDLBKQFF-URLMMPGGSA-N 0.000 claims description 2
- PQYXYUJVSKCKFL-JHOUSYSJSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-methylbenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(C)C=C1 PQYXYUJVSKCKFL-JHOUSYSJSA-N 0.000 claims description 2
- XKUREAYXZXNALY-XZWHSSHBSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-5,6-dichloropyridine-3-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CN=C(Cl)C(Cl)=C1 XKUREAYXZXNALY-XZWHSSHBSA-N 0.000 claims description 2
- AWZDEIQJFXSYJV-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-6-methylpyridine-3-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(C)N=C1 AWZDEIQJFXSYJV-AJQTZOPKSA-N 0.000 claims description 2
- ZBMHBTNVTBWRGV-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]cyclohexanecarboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1CCCCC1 ZBMHBTNVTBWRGV-AJQTZOPKSA-N 0.000 claims description 2
- KXEHMWWWSGDRNZ-URLMMPGGSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]furan-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CO1 KXEHMWWWSGDRNZ-URLMMPGGSA-N 0.000 claims description 2
- TYYQIBDJBZYMOH-MPQUPPDSSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]naphthalene-1-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC2=CC=CC=C12 TYYQIBDJBZYMOH-MPQUPPDSSA-N 0.000 claims description 2
- LOIWWQRBLCDGHA-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=N1 LOIWWQRBLCDGHA-IOWSJCHKSA-N 0.000 claims description 2
- NBUOOLFOHRYQNL-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-3-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CN=C1 NBUOOLFOHRYQNL-IOWSJCHKSA-N 0.000 claims description 2
- KUPKLNUHJXRSMI-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-4-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=NC=C1 KUPKLNUHJXRSMI-IOWSJCHKSA-N 0.000 claims description 2
- GCFLQXXLUPHFNT-XZWHSSHBSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]thiophene-3-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CSC=C1 GCFLQXXLUPHFNT-XZWHSSHBSA-N 0.000 claims description 2
- SJQWETDPGAMVES-JSOSNVBQSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-2-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-chlorobenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1N=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(Cl)C=C1 SJQWETDPGAMVES-JSOSNVBQSA-N 0.000 claims description 2
- KGASRYBCGZUNAS-ZWXJPIIXSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-2-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-methoxybenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1N=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(OC)C=C1 KGASRYBCGZUNAS-ZWXJPIIXSA-N 0.000 claims description 2
- XTDUCJDRKRNRPM-ZWXJPIIXSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-2-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-methylbenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1N=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(C)C=C1 XTDUCJDRKRNRPM-ZWXJPIIXSA-N 0.000 claims description 2
- BHVUGAWTPFXTSW-JSOSNVBQSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-2-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1N=CC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 BHVUGAWTPFXTSW-JSOSNVBQSA-N 0.000 claims description 2
- GWSFNRAHPBVBJY-RRPNLBNLSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-1,2-oxazole-5-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=NO1 GWSFNRAHPBVBJY-RRPNLBNLSA-N 0.000 claims description 2
- YYYMEQVUGUUKPY-WUFINQPMSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-3-chlorothiophene-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=C(Cl)C=CS1 YYYMEQVUGUUKPY-WUFINQPMSA-N 0.000 claims description 2
- SYHVZEPQLZQVQE-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-3-methylbenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC(C)=C1 SYHVZEPQLZQVQE-AJQTZOPKSA-N 0.000 claims description 2
- VEGWZKIUWVMXBY-URLMMPGGSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-3-methylthiophene-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=C(C)C=CS1 VEGWZKIUWVMXBY-URLMMPGGSA-N 0.000 claims description 2
- COXMDBLAIZHMPI-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-chlorobenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(Cl)C=C1 COXMDBLAIZHMPI-IOWSJCHKSA-N 0.000 claims description 2
- AJYZUIMBRBUFPQ-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-methoxybenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(OC)C=C1 AJYZUIMBRBUFPQ-AJQTZOPKSA-N 0.000 claims description 2
- QLQUHMZRFARDGM-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-4-methylbenzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=C(C)C=C1 QLQUHMZRFARDGM-AJQTZOPKSA-N 0.000 claims description 2
- IOKOMILCLYAEGO-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 IOKOMILCLYAEGO-IOWSJCHKSA-N 0.000 claims description 2
- QICJOCRBSRBUHC-WUFINQPMSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-3-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]thiophene-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=NC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CS1 QICJOCRBSRBUHC-WUFINQPMSA-N 0.000 claims description 2
- MGPOPQVVNMABOI-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-pyridin-4-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=CN=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 MGPOPQVVNMABOI-IOWSJCHKSA-N 0.000 claims description 2
- IBCRPNPROJRPGD-IHLOFXLRSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-thiophen-2-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1SC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 IBCRPNPROJRPGD-IHLOFXLRSA-N 0.000 claims description 2
- DOEHDNHECCZREA-WDYNHAJCSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-1-oxo-3-thiophen-2-ylpropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1SC=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=N1 DOEHDNHECCZREA-WDYNHAJCSA-N 0.000 claims description 2
- XQQTZKDEZFNLED-SAIUNTKASA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(1-benzothiophen-3-yl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C2=CC=CC=C2SC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 XQQTZKDEZFNLED-SAIUNTKASA-N 0.000 claims description 2
- ZLHMUZNFVDTJHM-ZWXJPIIXSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(1-benzothiophen-3-yl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-4-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C2=CC=CC=C2SC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=NC=C1 ZLHMUZNFVDTJHM-ZWXJPIIXSA-N 0.000 claims description 2
- GAEPCQZQRDPARJ-NOCHOARKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(1h-indol-3-yl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 GAEPCQZQRDPARJ-NOCHOARKSA-N 0.000 claims description 2
- SYUQOCGTPPIJGB-ZWXJPIIXSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(2-fluorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C(=CC=CC=1)F)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 SYUQOCGTPPIJGB-ZWXJPIIXSA-N 0.000 claims description 2
- BAAMDLCQQMJQAZ-RRPNLBNLSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(3,4-dichlorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]-3,3,3-trifluoropropanamide Chemical compound C1=CC(OCC)=CC=C1C[C@@H](NC(=O)CC(F)(F)F)C(=O)N[C@H](C(=O)NCC=1C=CC(CN)=CC=1)CC1=CC=C(Cl)C(Cl)=C1 BAAMDLCQQMJQAZ-RRPNLBNLSA-N 0.000 claims description 2
- MZNWXAJMLAFTSG-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(3,4-dichlorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=C(Cl)C(Cl)=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 MZNWXAJMLAFTSG-AJQTZOPKSA-N 0.000 claims description 2
- ORHWIOJJYJCEEN-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(3,4-dichlorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=C(Cl)C(Cl)=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=N1 ORHWIOJJYJCEEN-IOWSJCHKSA-N 0.000 claims description 2
- OKGHJSOTBPWZDZ-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(3,4-dichlorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-4-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=C(Cl)C(Cl)=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=NC=C1 OKGHJSOTBPWZDZ-IOWSJCHKSA-N 0.000 claims description 2
- GBOFJZGDOGSEJK-URLMMPGGSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(3,4-dichlorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]thiophene-2-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=C(Cl)C(Cl)=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CS1 GBOFJZGDOGSEJK-URLMMPGGSA-N 0.000 claims description 2
- WOXROINLYXJADA-AJQTZOPKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(3,4-difluorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]benzamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=C(F)C(F)=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=CC=C1 WOXROINLYXJADA-AJQTZOPKSA-N 0.000 claims description 2
- UIKVVUURJYWPFD-IOWSJCHKSA-N n-[(2r)-1-[[(2s)-1-[[4-(aminomethyl)phenyl]methylamino]-3-(3,4-difluorophenyl)-1-oxopropan-2-yl]amino]-3-(4-ethoxyphenyl)-1-oxopropan-2-yl]pyridine-4-carboxamide Chemical compound C1=CC(OCC)=CC=C1C[C@H](C(=O)N[C@@H](CC=1C=C(F)C(F)=CC=1)C(=O)NCC=1C=CC(CN)=CC=1)NC(=O)C1=CC=NC=C1 UIKVVUURJYWPFD-IOWSJCHKSA-N 0.000 claims description 2
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- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762544346P | 2017-08-11 | 2017-08-11 | |
| US62/544,346 | 2017-08-11 | ||
| GBGB1713660.7A GB201713660D0 (en) | 2017-08-25 | 2017-08-25 | Pharmaceutical compositions |
| GB1713660.7 | 2017-08-25 | ||
| PCT/GB2018/052292 WO2019030540A1 (en) | 2017-08-11 | 2018-08-13 | PHARMACEUTICAL COMPOSITIONS |
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| SG (1) | SG11202001179YA (enExample) |
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Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201609607D0 (en) | 2016-06-01 | 2016-07-13 | Kalvista Pharmaceuticals Ltd | Polymorphs of N-(3-Fluoro-4-methoxypyridin-2-yl)methyl)-3-(methoxymethyl)-1-({4-((2-oxopy ridin-1-yl)methyl)phenyl}methyl)pyrazole-4-carboxamide and salts |
| GB201719881D0 (en) | 2017-11-29 | 2018-01-10 | Kalvista Pharmaceuticals Ltd | Solid forms of plasma kallikrein inhibitor and salts thereof |
| WO2021028645A1 (en) | 2019-08-09 | 2021-02-18 | Kalvista Pharmaceuticals Limited | Plasma kallikrein inhibitors |
| GB201918994D0 (en) | 2019-12-20 | 2020-02-05 | Kalvista Pharmaceuticals Ltd | Treatments of diabetic macular edema and impaired visual acuity |
| GB2591730A (en) * | 2019-12-09 | 2021-08-11 | Kalvista Pharmaceuticals Ltd | New polymorphs |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20070258976A1 (en) * | 2006-05-04 | 2007-11-08 | Ward Keith W | Combination Therapy for Diseases Involving Angiogenesis |
| GB2494851A (en) * | 2011-07-07 | 2013-03-27 | Kalvista Pharmaceuticals Ltd | Plasma kallikrein inhibitors |
| CA2866232A1 (en) * | 2012-05-25 | 2013-11-28 | Novartis Ag | Aqueous pharmaceutical composition containing a biologic therapeutic agent and guanidine or a guanidine derivative and an injection including the composition |
| GB2510407A (en) * | 2013-02-04 | 2014-08-06 | Kalvista Pharmaceuticals Ltd | Aqueous suspensions of kallikrein inhibitors for parenteral administration |
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2017
- 2017-08-25 GB GBGB1713660.7A patent/GB201713660D0/en not_active Ceased
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2018
- 2018-08-13 TW TW107128107A patent/TW201919600A/zh unknown
- 2018-08-13 US US16/637,953 patent/US20200261383A1/en not_active Abandoned
- 2018-08-13 MA MA049837A patent/MA49837A/fr unknown
- 2018-08-13 SG SG11202001179YA patent/SG11202001179YA/en unknown
- 2018-08-13 CA CA3071772A patent/CA3071772A1/en active Pending
- 2018-08-13 EP EP18758700.1A patent/EP3664780A1/en not_active Withdrawn
- 2018-08-13 KR KR1020207007099A patent/KR20200038987A/ko not_active Ceased
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- 2018-08-13 WO PCT/GB2018/052292 patent/WO2019030540A1/en not_active Ceased
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- 2018-08-13 BR BR112020002325-6A patent/BR112020002325A2/pt not_active IP Right Cessation
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| BR112020002325A2 (pt) | 2020-09-01 |
| CN111032018A (zh) | 2020-04-17 |
| MA49837A (fr) | 2020-06-17 |
| GB201713660D0 (en) | 2017-10-11 |
| EP3664780A1 (en) | 2020-06-17 |
| US20200261383A1 (en) | 2020-08-20 |
| CA3071772A1 (en) | 2019-02-14 |
| WO2019030540A1 (en) | 2019-02-14 |
| AU2018315034A1 (en) | 2020-02-27 |
| SG11202001179YA (en) | 2020-03-30 |
| TW201919600A (zh) | 2019-06-01 |
| JP2020530475A (ja) | 2020-10-22 |
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