KR900007867A - 레닌-억제 아미노디올 유도체 - Google Patents
레닌-억제 아미노디올 유도체 Download PDFInfo
- Publication number
- KR900007867A KR900007867A KR1019890017025A KR890017025A KR900007867A KR 900007867 A KR900007867 A KR 900007867A KR 1019890017025 A KR1019890017025 A KR 1019890017025A KR 890017025 A KR890017025 A KR 890017025A KR 900007867 A KR900007867 A KR 900007867A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- group
- radical
- substituted
- thienyl
- 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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- 102100028255 Renin Human genes 0.000 title 1
- 108090000783 Renin Proteins 0.000 title 1
- 230000002401 inhibitory effect Effects 0.000 title 1
- -1 pyridine radical Chemical class 0.000 claims 97
- 150000003254 radicals Chemical class 0.000 claims 20
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 16
- 239000001257 hydrogen Substances 0.000 claims 11
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 150000001875 compounds Chemical class 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 6
- IDIDJDIHTAOVLG-VKHMYHEASA-N S-methylcysteine Chemical compound CSC[C@H](N)C(O)=O IDIDJDIHTAOVLG-VKHMYHEASA-N 0.000 claims 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 6
- 229910052801 chlorine Inorganic materials 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims 5
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical group C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims 4
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- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 claims 4
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 4
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- 229910005965 SO 2 Inorganic materials 0.000 claims 4
- 235000004279 alanine Nutrition 0.000 claims 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
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- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 4
- BVAUMRCGVHUWOZ-ZETCQYMHSA-N (2s)-2-(cyclohexylazaniumyl)propanoate Chemical compound OC(=O)[C@H](C)NC1CCCCC1 BVAUMRCGVHUWOZ-ZETCQYMHSA-N 0.000 claims 3
- RWLSBXBFZHDHHX-VIFPVBQESA-N (2s)-2-(naphthalen-2-ylamino)propanoic acid Chemical compound C1=CC=CC2=CC(N[C@@H](C)C(O)=O)=CC=C21 RWLSBXBFZHDHHX-VIFPVBQESA-N 0.000 claims 3
- CNMAQBJBWQQZFZ-LURJTMIESA-N (2s)-2-(pyridin-2-ylamino)propanoic acid Chemical compound OC(=O)[C@H](C)NC1=CC=CC=N1 CNMAQBJBWQQZFZ-LURJTMIESA-N 0.000 claims 3
- VOIZSAUUYAGTMS-LURJTMIESA-N (2s)-2-amino-3-thiophen-3-ylpropanoic acid Chemical compound OC(=O)[C@@H](N)CC=1C=CSC=1 VOIZSAUUYAGTMS-LURJTMIESA-N 0.000 claims 3
- WAMWSIDTKSNDCU-ZETCQYMHSA-N (2s)-2-azaniumyl-2-cyclohexylacetate Chemical compound OC(=O)[C@@H](N)C1CCCCC1 WAMWSIDTKSNDCU-ZETCQYMHSA-N 0.000 claims 3
- SNZIFNXFAFKRKT-NSHDSACASA-N (2s)-2-azaniumyl-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]propanoate Chemical compound CC(C)(C)OC1=CC=C(C[C@H]([NH3+])C([O-])=O)C=C1 SNZIFNXFAFKRKT-NSHDSACASA-N 0.000 claims 3
- BWKMGYQJPOAASG-UHFFFAOYSA-N 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid Chemical compound C1=CC=C2CNC(C(=O)O)CC2=C1 BWKMGYQJPOAASG-UHFFFAOYSA-N 0.000 claims 3
- ZNLAHAOCFKBYRH-UHFFFAOYSA-N 1,4-dioxane-2,3-dione Chemical compound O=C1OCCOC1=O ZNLAHAOCFKBYRH-UHFFFAOYSA-N 0.000 claims 3
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- GTVVZTAFGPQSPC-UHFFFAOYSA-N 4-nitrophenylalanine Chemical compound OC(=O)C(N)CC1=CC=C([N+]([O-])=O)C=C1 GTVVZTAFGPQSPC-UHFFFAOYSA-N 0.000 claims 3
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 3
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- 125000005915 C6-C14 aryl group Chemical group 0.000 claims 3
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- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 claims 3
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims 3
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 claims 3
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 3
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 claims 3
- JTTHKOPSMAVJFE-VIFPVBQESA-N L-homophenylalanine Chemical compound OC(=O)[C@@H](N)CCC1=CC=CC=C1 JTTHKOPSMAVJFE-VIFPVBQESA-N 0.000 claims 3
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- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims 3
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- KAFHLONDOVSENM-HNNXBMFYSA-N O-Benzyl-L-tyrosine Chemical compound C1=CC(C[C@H](N)C(O)=O)=CC=C1OCC1=CC=CC=C1 KAFHLONDOVSENM-HNNXBMFYSA-N 0.000 claims 3
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- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 claims 3
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- 150000005840 aryl radicals Chemical class 0.000 claims 3
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- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims 3
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 3
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- WTKYBFQVZPCGAO-LURJTMIESA-N (2s)-2-(pyridin-3-ylamino)propanoic acid Chemical compound OC(=O)[C@H](C)NC1=CC=CN=C1 WTKYBFQVZPCGAO-LURJTMIESA-N 0.000 claims 2
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- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
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- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
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- 125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 2
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- IYKLZBIWFXPUCS-VIFPVBQESA-N (2s)-2-(naphthalen-1-ylamino)propanoic acid Chemical compound C1=CC=C2C(N[C@@H](C)C(O)=O)=CC=CC2=C1 IYKLZBIWFXPUCS-VIFPVBQESA-N 0.000 claims 1
- ZAFNLUPTKPOREL-LURJTMIESA-N (2s)-2-amino-3-(furan-3-yl)propanoic acid Chemical compound OC(=O)[C@@H](N)CC=1C=COC=1 ZAFNLUPTKPOREL-LURJTMIESA-N 0.000 claims 1
- GNUCLSFLDHLOBV-ZBHICJROSA-N (2s)-2-amino-3-hydroxy-3-thiophen-2-ylpropanoic acid Chemical compound OC(=O)[C@@H](N)C(O)C1=CC=CS1 GNUCLSFLDHLOBV-ZBHICJROSA-N 0.000 claims 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 claims 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical compound C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 claims 1
- ILROLYQPRYHHFG-UHFFFAOYSA-N 1-$l^{1}-oxidanylprop-2-en-1-one Chemical group [O]C(=O)C=C ILROLYQPRYHHFG-UHFFFAOYSA-N 0.000 claims 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims 1
- WGCYRFWNGRMRJA-UHFFFAOYSA-N 1-ethylpiperazine Chemical compound CCN1CCNCC1 WGCYRFWNGRMRJA-UHFFFAOYSA-N 0.000 claims 1
- SOQXOGOPSSWYCB-UHFFFAOYSA-N 2-amino-4-thiophen-3-ylbutanoic acid Chemical compound OC(=O)C(N)CCC=1C=CSC=1 SOQXOGOPSSWYCB-UHFFFAOYSA-N 0.000 claims 1
- 125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 claims 1
- BJRGNJZOJQHLGE-UHFFFAOYSA-N 2-cyclohexylidene-1,3-dioxolane Chemical group O1CCOC1=C1CCCCC1 BJRGNJZOJQHLGE-UHFFFAOYSA-N 0.000 claims 1
- NYCRCTMDYITATC-UHFFFAOYSA-N 2-fluorophenylalanine Chemical compound OC(=O)C(N)CC1=CC=CC=C1F NYCRCTMDYITATC-UHFFFAOYSA-N 0.000 claims 1
- QUGOBTBFBNXICO-UHFFFAOYSA-N 2-thiophen-2-ylbutanoic acid Chemical compound CCC(C(O)=O)C1=CC=CS1 QUGOBTBFBNXICO-UHFFFAOYSA-N 0.000 claims 1
- XWHHYOYVRVGJJY-QMMMGPOBSA-N 4-fluoro-L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(F)C=C1 XWHHYOYVRVGJJY-QMMMGPOBSA-N 0.000 claims 1
- 241000283690 Bos taurus Species 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Divinylene sulfide Natural products C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 0.000 claims 1
- DEFJQIDDEAULHB-IMJSIDKUSA-N L-alanyl-L-alanine Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(O)=O DEFJQIDDEAULHB-IMJSIDKUSA-N 0.000 claims 1
- ZGUNAGUHMKGQNY-ZETCQYMHSA-N L-alpha-phenylglycine zwitterion Chemical compound OC(=O)[C@@H](N)C1=CC=CC=C1 ZGUNAGUHMKGQNY-ZETCQYMHSA-N 0.000 claims 1
- 108010056243 alanylalanine Proteins 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims 1
- 150000003857 carboxamides Chemical class 0.000 claims 1
- 239000003638 chemical reducing agent Substances 0.000 claims 1
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- MHUWZNTUIIFHAS-CLFAGFIQSA-N dioleoyl phosphatidic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COP(O)(O)=O)OC(=O)CCCCCCC\C=C/CCCCCCCC MHUWZNTUIIFHAS-CLFAGFIQSA-N 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 125000003588 lysine group Chemical group [H]N([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 claims 1
- VWHRYODZTDMVSS-QMMMGPOBSA-N m-fluoro-L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC(F)=C1 VWHRYODZTDMVSS-QMMMGPOBSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000004372 methylthioethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])* 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 125000006606 n-butoxy group Chemical group 0.000 claims 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims 1
- 229930192474 thiophene Natural products 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0202—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-X-X-C(=0)-, X being an optionally substituted carbon atom or a heteroatom, e.g. beta-amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0205—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)3-C(=0)-, e.g. statine or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0207—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)4-C(=0), e.g. 'isosters', replacing two amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Description
Claims (7)
- 일반식(Ⅰ)의 화합물 및 생리적으로 허용되는 염.상기식에서, A는 일반식(Ⅱ)의 라디칼이고, R5는 (C6-C14)-아릴, (C6-C14)-아릴-(C1-C4)-알킬(여기에서, 각각의 아릴 라디칼은 (C1-C6)알킬, 아미노, 모노-또는 디-(C1-C4)알킬아미노, 아미노-(C1-C4)-알킬, 하이드록시-(C1-C4)알킬, 모노-또는 디-(C1-C4)-알킬아미노-(C1-C4)-알킬, 하이드록실, (C1-C4)-알콕시, 할로겐, 포르밀, (C1-C4) 알콕시카보닐, 카복사미도, 모노- 또는 디-(C1-C4)-알킬아미노카보닐 또는 니트로로 구성된 그룹에서 선택된 라디칼 1,2 또는 3개로 치환될 수 있다), 티에닐 또는 티에닐-(C1-C4)-알킬(여기에서, 각각의 티오펜 라디칼은 (C1-C4)-알킬, (C1-C4)-알콕시 또는 할로겐으로 구성된 그룹에서 선택되는 라디칼 1 또는 2개로 치환될 수 있다), 2-, 3- 또는 4-피리딜 또는 2-, 3- 또는 4-피리딜 -(C1-C4)-알킬 (여기에서, 피리딘라디칼은 (C1-C4)-알킬, (C1-C4)-알콕시 또는 할로겐으로 구성된 그룹에서 선택되는 라디칼 1 또는 2개로 치환될 수 있다)이고, E는 CH2그룹 또는 라디칼 NR9이며, R9은 수소 또는 (C1-C4)-알킬 라디칼이고, G는 S, SO, SO2, O, CO 또는 CS로 구성된 그룹에서 선택되는 라디칼이거나 직접 결합을 나타내며, R6는 수소, (C1-C18)-알킬, (C3-C7)-사이클로알킬(이들은 각기 아미노, 하이드록시, 머캅토, 할로겐, (C1-C4)-알콕시, 모노-또는 디-(C1-C4)-알킬아미노, 카복실, (C1-C4)-알콕시카보닐, 페닐-(C1-C4)-알콕시 또는 CONR7R8라디칼로 치환될 수 있다), (C1-C4)-알콕시, (C6-C14)-아릴, (C6-C14)-아릴-(C1-C4)-알킬, (C6-C14)-아릴-(C1-C4)-알콕시(여기에서, 각각의 아릴 라디칼은 상기 R5의 정의에서와 같이 치환될 수 있다), Het 또는 Het-(C1-C4)-알킬(여기에서, Het는 벤젠에 융합되고, 방향족 부분적으로 수소화되거나 완전히 수소화되며, 이형원자로서 N,O,S,NO,SO 또는 SO2로 구성된 그룹에서 선택되는 라디칼 1 또는 2개를 함유하고; (C1-C4)-알킬,(C1-C4)-알콕시, (C1-C4)-알콕시카보닐, 하이드록실, 할로겐, 아미노, 모노- 또는 디-(C1-C4)-알킬아미노, 또는 NR7R8라디칼로 구성된 그룹에서 선택되는 라디칼 1 또는 2개로 치환될 수 있다)이고, R7및 R8은 동일하거나 상이하며, 다른 하나와 독립적으로 수소, (C1-C8)-알킬(이것은 (C1-C4)-알킬아미노, 디-(C1-C4)-알킬아미노, 하이드록실 또는 (C1-C4)-알콕시로 치환될 수 있다), (C3-C7)-사이클로알킬, 머캅토, (C1-C4)알킬티오, 페닐티오, (C1-C4)-알콕시카보닐, 카복실, (C6-C14)-아릴(여기에서, 아릴라디칼은 R5에서와 같이 치환될 수 있다), Het 또는 Het-(C1-C4)-알킬(여기에서, Het는 R6에서 정의한 바와 같다)이거나; R7및 R8가 질소원자와 함께 모노사이클릭은 바이사이클릭이며 환원자가 1 또는 2개의 질소원자를 함유할 수 있고 (C1-C4)-알킬에 의해 치환될 수 있는 5- 내지 12-원환을 생성하며 B는 N말단이 A와 연결되고, C말단이 아미노산의와 연결되는 라디칼을 나타내고, 이때의 아미노산은 페닐알라닌, 히스티딘, 타이로신, 트립토판, 메티오닌, 류신, 이소류신, 아스파라긴, 아스파르트산, β-2-티에닐알라닌, β-3-티에닐알라닌, β-2-푸릴알라닌, β-3-푸릴알라닌, 리실, 오르니틴, 발린, 알라닌, 2,4-디아미노부티르산, 아르기닌, 4-클로로 페닐알라닌, 메티오닌설폰, 메티오닌 설폭사이드, 2-피리딜알라닌, 3-피리딜알라닌, 사이클로헥실알라닌, 사이클로헥실글리신, 임-메틸히스티딘, O-메틸타이로신, O-벤질타이로신, O-3급-부틸타이로신, 페닐글리신, 1-나프틸알라닌, 2-나프틸알라닌, 4-니트로페닐알라닌, 노르발린, β-2-벤조[b]티에닐알라닌, β-3-벤조[b]티에닐알라닌, 2-플루오로페닐알라닌, 3-플루오로페닐알라닌, 4-플루오로페닐알라닌, 노르류신, 시스테인, S-메틸시스테인, 1,2,3,4-테트라하이드로이소-퀴놀린-3-카복실산, 호모페닐알라닌, DOPA, O-디메틸-DOPA, 2-아미노-4-(2-티에닐)부티르산, 벤조디옥솔-5-일-알라닌, N-메틸히스티딘, 2-아미노-4-(3-티에닐)부티르산, 3-(2-티에닐)-세린, (Z)-디하이드로페닐알라닌, (E)-디하이드로페닐알라닌, 디옥솔란-1,3-일-3-알라닌, N-필롤릴알라닌 및 1-, 3-, 또는 4-피라졸릴알라닌으로 구성되는 그룹에서 선택되며, R1은 수소 또는 (C1-C4)알킬이고, R2는 수소, (C1-C8)알킬, (C3-C8)-사이클로알킬(이것은 (C1-C3)-알킬로 치환될 수 있다) 또는 페닐(이것은 (C1-C3)-알콕시, (C1-C3)-알킬, 할로겐, 니트로, 트리플루오로메틸 또는 하이드록실로 구성된 그룹에서 선택되는 라디칼 1 또는 1개로 치환될 수 있다)이며, R3및 R4는 동일하거나 상이하며, 다른 하나와는 독립적으로 수소; (C1-C10)-알킬; (C1-C6)-알카노일; (C6-C9)-사이클로알카노일; 페닐, 페닐(C1-C4)-알킬 또는 벤조일(각각의 경우에서, 방향족 환은 (C1-C4)알킬, (C1-C4)-알콕시, Cl, F, Br, 니트로, 트리플루오로메틸 또는 메틸렌디옥시로 구성된 그룹에서 선택되는 1,2 또는 3개의 라디칼에 의해 임의로 치환된다); (C1-C6)-알카노일 옥시-(C1-C2)-알킬 또는 (C1-C6)-알콕시카보닐옥시-(C1-C2)-알킬 또는이거나, R3및 R4가 산소원자와 함께는 디옥솔라논, 디옥산디온 또는 디옥솔란 환을 형성하며, 디옥솔란환은 (C1-C4)-알킬로 일치환 또는 이치환되거나 (C4-C8)-사이클로알킬렌 또는 페닐에 의해 치환될 수 있으며, D는 Het 라디칼 (R6에서 정의한 바와 같다)이고, m 및 n은 각기 0,1,2,3,4 또는 5이다.
- 제1항에 있어서, A가 일반식(Ⅱ)의 라디칼을 나타내고, R5는 페닐, 2-티에닐, 2-피리딜, 1-나프틸, 페닐-(C1-C4)-알킬, 2-티에닐-(C1-C4)-알킬 2-피리딜-(C1-C4)-알킬 또는 1-나프틸-(C1-C4)-알킬 (이들은 메틸, 에틸, 이소프로필, 3급-부틸, 메톡시, 하이드록시, F, Cl 또는 니트로로 구성된 그룹에서 1,2 또는 3개의 라디칼에 의해 임의로 치환된다)을 나타내며, E는 CH2그룹, -NH-그룹 또는 -N-(CH3)-그룹을 나타내고, G는 S, SO2, O, CO 및 CS로 구성된 그룹에서 선택되는 라디칼이거나 직접결합을 나타내며, R6는 메틸, 에틸, 이소프로필, 3급-부틸, 이소부틸, 2-하이드록시에틸, 2-메톡시에틸, 카복시메틸, 2-카복시에틸, 메톡시카보닐메틸, 메톡시카보닐에틸, 에톡시카보닐메틸, 2-에톡시카보닐에틸, 카바모일메틸, 2-카바모일에틸, 2-아미노에틸, 2-디메틸아미노에틸, 2-모르폴리노에틸, 아미노이소부틸, 2-피페리디노에틸, 아미노프로필, 디메틸아미노프로필, 메틸아미노프로필, 피페리디노프로필, 모르폴리노프로필, 메틸아미노이소부틸, 디메틸아미노이소부틸, 피페리디노이소부틸, 모르폴리노이소부틸, 사이클로포프로필, 사이클로부틸, 사이클로펜틸 또는 사이클로헥실, 페닐, 1-또는 2-나프틸, o-, m- 또는 p-메틸페닐, o-, m- 또는 p-하이드록시페닐 o-, m- 또는 p-아미노페닐, 벤질, 2-페닐에틸 또는 α- 또는 β-나프틸메틸, 비치환되거나 치환된헤테로아릴(예 ; 2- 또는 3-피롤릴, 2-푸릴, 2-티에닐, 2- 또는 4-이미다졸릴, 1-메틸 -2, -4- 또는 -5이미다졸릴, 1,3-티아졸-2-일, 2-, 3- 또는 4-피리딜, 1-옥시도 -2-, -3- 또는 -4-피리디노, 2-피라지닐, 2-, 4- 또는 5-피리미디닐, 2-, 3- 또는 4-퀴놀릴, 1-, 3- 또는 4-이소퀴놀릴 또는 2-벤즈옥사졸릴, 메톡시, 에톡시 또는 n-부톡시이거나, 질소원자 및 경우에 따라 산소원자를 함유하는 5- 또는 6-원환(예; 1-피롤리디닐, 1-피페리디닐 또는 4-모르폴리닐)의 일부로서 아미노이고, R7및 R8은 동일하거나 상이하며, 다른 하나와 독립적으로 수소, 메틸, 에틸, 프로필, 부틸, 이소부틸, 2급-부틸, 3급-부틸, 아미노에틸, 아미노프로필, 메틸아미노에틸, 디메틸아미노프로필, 하이드록시에틸, 메톡시에틸, 사이클로헥실메틸, 머캅토에틸, 메틸티오에틸, 벤질, 1-펜에틸, 2-펜에틸, 2-(3,4-디메톡시)펜에틸, 2-피리딜 메틸 또는 3-피리딜메틸을 나타내며, R7및 R8가 질소원자와 함께는 피롤리딘, 피페리딘, 아제핀, 아족신, 모폴린, 피페라진, 4-메틸피페라진, 4-에틸피페라진, 호모피페라진 또는 티오모폴린 환을 나타내고, B는 페닐알라닌, 히스티딘, 타이로신, 트립토판, 메티오닌, 류신, 이소류신, 아스파라긴, 아스파르트산, β-2-티에닐알라닌, β-3-티에닐알라닌, β-푸릴알라닌, 리신, 오르니틴, 2,4-디아미노부티르산, 아르기닌, 노르발린, 4-클로로페닐알라닌, 메티오닌설폰, 메티오닌 설폭사이드, 2-피리딜알라닌, 3-피리딜알라닌, 사이클로헥실알라닌, 사이클로헥실글리신, 임-메틸히스티딘, O-메틸타이로신, O-벤질타이로신, O-3급-부틸-타이로신, 페닐글리신 1-나프틸알라닌, 2-나프틸알라닌, 4-니트로페닐알라닌, 노르류신, 발린, 알라닌, 시스테인, S-메틸시스테인, N-메틸히스티딘, 벤조디올-5-일-알라닌, 1,2,3,4-테트라하이드로이소퀴놀린-3-카복실산 호모페닐알라닌, 2-아미노-4-(2-티에닐)부티르산, (Z)-데하이드로페닐알라닌, (E)-데하이드로페닐알라닌 및 디옥솔란-1,3-일-3-알라닌으로 구성된 그룹에서 선택되는 2가 라디칼이며, R1은 수소 또는 메틸이고, R2는 이소프로필, 페닐 또는 사이클로헥실이며, R3및 R4는 동일하거나 상이하며, 다른 하나와 독립적으로 수소, 아세톡시메틸, 아세톡시에틸, 피발로일옥시메틸, 피발로일옥시에틸, 2,2-디메틸부티릴옥시메틸, 에톡시카보닐옥시메틸, 에톡시카보닐옥시에틸, 3급-부톡시카보닐옥시메틸 또는 3급-부톡시카보닐옥시에틸이고, R3및 R4가 산소원자와 함께는 디옥솔란, 디옥산디온, 디메틸디옥솔란, 페닐디옥솔란 또는 사이클로헥실리덴디옥솔란 환을 형성하며; D는 2-, 3- 또는 4- 피리딘 라디칼, 2-, 4- 또는 5-이미다졸라디칼 또는 2-옥사졸린 라디칼 (여기에서 언급된 헤테로사이클은 각각 (C1-C4)-알킬, 메톡시, 염소, 불소, 브롬 및 CF3로 구성된 그룹에서 선택되는 라디칼 1 또는 2개로 치환될 수 있다)이고, m은 0,1 또는 2이며, n은 0, 1, 2 또는 3인 일반식(Ⅰ)의 화합물 및 이외 생리적으로 허용되는 염.
- 제1항 또는 2항에 있어서, A가 일반식(Ⅱ)의 라디칼을 나타내고, R5는 페닐, 2-티에닐, 2-피리딜, 1-나프틸, 또는 벤질, 2-티에닐메틸, 2-피리딜메틸 또는 1-나프틸메틸(이들은, 하이드록시, 디하이드록시, 메톡시, 디메톡시, F 또는Cl에 의해 임의로 치환된다)을 나타내며, E는 CH2그룹, -NH-그룹 또는 -N-(CH3)-그룹을 나타내고, G는 S, SO2, O, CO 및 CS로 구성된 그룹에서 선택되는 라디칼이며, R6는 메틸, 에틸, 이소프로필, 3급-부틸, 이소부틸, 2-하이드록시에틸, 2-메톡시에틸, 카복시메틸, 1-카복시에틸, 메톡시카보닐메틸, 2-메톡시카보닐에틸, 에톡시카보닐메틸, 2-에톡시카보닐에틸 카바모일메틸, 2-카바모일에틸, 2-아미노에틸, 2-디메틸아미노에틸, 2-모르폴리노에틸, 아미노프로필, 아미노이소부틸, 메틸아미노이소부틸, 디메틸아미노이소부틸, 2-피페리디노에틸, 사이클로프로필, 사이클로부틸, 사이클로펜틸 또는 사이클로헥실, 페닐, 1-또는 2-나프틸, o-, m- 또는 p-메틸페닐, o-, m- 또는 p-하이드록시페닐 o-, m- 또는 p-아미노페닐, 벤질, 2-페닐에틸 또는 α- 또는 β-나프틸메틸, 비치환되거나 치환된 헤테로아릴(예 ; 2- 또는 3-피롤릴, 2-푸릴, 2-티에닐, 2- 또는 4-이미다졸릴, 1-메틸 -2, -4- 또는 -5-이미다졸릴, 1,3-티아졸-2-일, 2-, 3- 또는 4-피리딜, 1-옥시도 -2-, -3- 또는 -4-피리디노, 2-피라지닐, 2-, 4- 또는 5-피리미디닐, 2-, 3- 또는 4-퀴놀릴, 1-, 3- 또는 4-이소퀴놀릴 또는 2-벤즈옥사졸릴, 메톡시, 에톡시 또는 n-부톡시이거나, 질소원자 및 경우에 따라 산소원자를 함유하는 5- 또는 6-원환(예; 1-피롤리디닐, 1-피페리디닐 또는 4-모르폴리닐)의 일부로서 아미노이고, R7및 R8은 동일하거나 상이하며, 다른 하나와 독립적으로 수소, 메틸, 에틸, 프로필, 부틸, 이소부틸, 2급-부틸, 3급-부틸, 하이드록시에틸, 메톡시에틸, 아미노에틸, 아미노프로필, 벤질메틸 또는 피리딜메틸을 나타내며, R7및 R8가 질소원자와 함께는 피롤리딘, 피페리딘, 모폴린 또는 피페라진 환을 나타내고, B는 페닐알라닌, 히스티딘, 타이로신, 트립토판, 메티오닌, 류신, 이소류신, 아스파라긴, 아스파르트산, β-2-티에닐알라닌, β-3-티에닐알라닌, β-2-푸릴알라닌, 리신, 오르니틴, 2,4-디아미노부티르산, 아르기닌, 노르발린, 4-클로로페닐알라닌, 메티오닌설폰, 메티오닌 설폭사이드, 2-피리딜알라닌, 3-피리딜알라닌, 사이클로헥실알라닌, 사이클로헥실글리신, 임-메틸히스티딘, O-메틸타이로신, O-벤질타이로신, O-3급-부틸-타이로신, 페닐글리신 1-나프틸알라닌, 2-나프틸알라닌, 4-니트로페닐알라닌, 노르류신, 발린, 알라닌, 시스테인, S-메틸시스테인, N-메틸히스티딘, 벤조디올-5-일-알라닌, 1,2,3,4-테트라하이드로이소퀴놀린-3-카복실산 호모페닐알라닌, 2-아미노-4-(2-티에닐)부티르산, (Z)-데하이드로페닐알라닌, (E)-데하이드로페닐알라닌 및 디옥솔란-1,3-일-3-알라닌으로 구성된 그룹에서 선택되는 2가 라디칼이며, R1은 수소이고, R2는 이소프로필 또는 사이클로헥실이며, R3및 R4는 동일하거나 상이하며, 다른 하나와 독립적으로 수소, 아세톡시메틸, 아세톡시에틸, 피발로일옥시메틸, 피발로일옥시에틸, 2,2-디메틸부티릴옥시메틸, 에톡시카보닐옥시메틸, 에톡시카보닐옥시에틸, 3급-부톡시카보닐옥시메틸 또는 3급-부톡시카보닐옥시에틸이고, R3및 R4가 산소원자와 함께는 디옥솔란, 디옥산디온, 디메틸디옥솔란, 페닐디옥솔란 또는 사이클로헥실리덴디옥솔란 환을 형성하며, D는 2-, 3- 또는 4- 피리딘 라디칼, 2-, 4- 또는 5-이미다졸라디칼 또는 2-옥사졸린 라디칼 (여기에서 언급된 헤테로사이클은 메틸, 에틸, 프로필, 부틸, 이소부틸, 2급-부틸, 메톡시 및 염소로 구성된 그룹에서 선택되는 라디칼 1 또는 2개로 치환될 수 있다)이고, m은 1이고, n은 0, 1, 2 또는 3인 일반식(Ⅰ)의 화합물 및 이의 생리적으로 허용되는 염.
- 말단 카복실 그룹을 지니는 단편 또는 이의 반응성 유도체를 유리 아미노 그룹을 지니는 적합한 단편과 커플링시키고, 다른 작용그룹을 보호하기 위해 임시로 도입된 보호그룹(들)을 임의로 제거한 후, 생성된 화합물을 이의 생리적으로 허용되는 염으로 임의로 전환시키는 단계를 함유하는, 제1항 내지 3항의 일반식(Ⅰ)의 화합물의 제조방법.
- 제1항 내지 3항중 어느 한 항의 화합물의 약제로서의 용도.
- 고혈압치료를 위한 제1항 내지 3항중 어느 한 항의 화합물의 약제로서의 용도.
- 제1항 내지 3항중 어느 한 항의 화합물을 함유하는 약학적 제제.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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DE3839128A1 (de) * | 1988-11-19 | 1990-05-31 | Hoechst Ag | Renin-hemmende dipeptide, verfahren zu ihrer herstellung, diese enthaltende mittel und deren verwendung |
GB8827308D0 (en) * | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
IE68045B1 (en) * | 1990-05-11 | 1996-05-15 | Abbott Lab | Renin inhibitors |
IE911774A1 (en) * | 1990-06-11 | 1991-12-18 | Akzo Nv | Pyridinylpiperazine derivatives |
CA2018801C (en) * | 1990-06-12 | 2000-08-22 | Pierre Louis Beaulieu | Antiherpes peptide derivatives having a 1,4-dioxo c n-terminus |
DE4021007A1 (de) * | 1990-07-02 | 1992-01-09 | Hoechst Ag | Aminodiol-derivate |
PL294870A1 (ko) * | 1991-06-21 | 1993-02-08 | Hoechst Ag |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3627877A1 (de) * | 1986-07-30 | 1988-02-04 | Hoechst Ag | Renin-hemmende di- und tripeptide, verfahren zu deren herstellung, diese enthaltende mittel und ihre verwendung |
US5032577A (en) * | 1986-12-31 | 1991-07-16 | Abbott Laboratories | Peptidylaminodiols |
EP0309766B1 (en) * | 1987-09-29 | 1998-04-15 | Banyu Pharmaceutical Co., Ltd. | N-acylamino acid derivatives and their use |
IL90184A0 (en) * | 1988-05-09 | 1989-12-15 | Abbott Lab | Functionalized peptidyl aminodiols and-triols |
-
1988
- 1988-11-24 DE DE3839559A patent/DE3839559A1/de not_active Withdrawn
-
1989
- 1989-11-21 ES ES89121499T patent/ES2054989T3/es not_active Expired - Lifetime
- 1989-11-21 AT AT8989121499T patent/ATE104678T1/de active
- 1989-11-21 DE DE58907505T patent/DE58907505D1/de not_active Expired - Fee Related
- 1989-11-21 EP EP89121499A patent/EP0370454B1/de not_active Expired - Lifetime
- 1989-11-22 JP JP1302296A patent/JPH02193968A/ja active Pending
- 1989-11-22 FI FI895568A patent/FI93645C/fi not_active IP Right Cessation
- 1989-11-22 IL IL92405A patent/IL92405A0/xx unknown
- 1989-11-22 NZ NZ231485A patent/NZ231485A/xx unknown
- 1989-11-23 NO NO894663A patent/NO177351C/no unknown
- 1989-11-23 DK DK589589A patent/DK589589A/da not_active Application Discontinuation
- 1989-11-23 PT PT92388A patent/PT92388B/pt not_active IP Right Cessation
- 1989-11-23 PH PH39581A patent/PH27267A/en unknown
- 1989-11-23 KR KR1019890017025A patent/KR900007867A/ko not_active Ceased
- 1989-11-24 ZA ZA898990A patent/ZA898990B/xx unknown
- 1989-11-24 HU HU896173A patent/HU204262B/hu not_active IP Right Cessation
- 1989-11-24 AU AU45475/89A patent/AU628109B2/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
NO894663L (no) | 1990-05-25 |
AU4547589A (en) | 1990-09-13 |
DE3839559A1 (de) | 1990-05-31 |
DK589589A (da) | 1990-05-25 |
NO894663D0 (no) | 1989-11-23 |
HU204262B (en) | 1991-12-30 |
AU628109B2 (en) | 1992-09-10 |
PT92388B (pt) | 1995-07-18 |
HUT52524A (en) | 1990-07-28 |
HU896173D0 (ko) | 1990-02-28 |
NO177351B (no) | 1995-05-22 |
PT92388A (pt) | 1990-05-31 |
FI93645B (fi) | 1995-01-31 |
FI93645C (fi) | 1995-05-10 |
EP0370454B1 (de) | 1994-04-20 |
DE58907505D1 (de) | 1994-05-26 |
FI895568A0 (fi) | 1989-11-22 |
ATE104678T1 (de) | 1994-05-15 |
JPH02193968A (ja) | 1990-07-31 |
ES2054989T3 (es) | 1994-08-16 |
NO177351C (no) | 1995-08-30 |
IL92405A0 (en) | 1990-07-26 |
EP0370454A3 (en) | 1990-10-24 |
ZA898990B (en) | 1990-08-29 |
NZ231485A (en) | 1993-03-26 |
DK589589D0 (da) | 1989-11-23 |
PH27267A (en) | 1993-05-04 |
EP0370454A2 (de) | 1990-05-30 |
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