JP4767850B2 - グルカゴン様ペプチド(glp)−1化合物またはメラノコルチン4受容体(mc4)アゴニストペプチドの経口デリバリーのための化合物、方法および製剤 - Google Patents
グルカゴン様ペプチド(glp)−1化合物またはメラノコルチン4受容体(mc4)アゴニストペプチドの経口デリバリーのための化合物、方法および製剤 Download PDFInfo
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- JP4767850B2 JP4767850B2 JP2006523865A JP2006523865A JP4767850B2 JP 4767850 B2 JP4767850 B2 JP 4767850B2 JP 2006523865 A JP2006523865 A JP 2006523865A JP 2006523865 A JP2006523865 A JP 2006523865A JP 4767850 B2 JP4767850 B2 JP 4767850B2
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- methyl ester
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 84
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- 239000000556 agonist Substances 0.000 title claims abstract description 13
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- 238000000034 method Methods 0.000 title abstract description 30
- 238000009472 formulation Methods 0.000 title abstract description 19
- 102000004196 processed proteins & peptides Human genes 0.000 title description 6
- 108010088406 Glucagon-Like Peptides Proteins 0.000 title 2
- 102000001796 Melanocortin 4 receptors Human genes 0.000 title 2
- 108010021436 Type 4 Melanocortin Receptor Proteins 0.000 title 2
- -1 GLP-1 compound Chemical class 0.000 claims abstract description 79
- 101710198884 GATA-type zinc finger protein 1 Proteins 0.000 claims abstract description 9
- 102100025101 GATA-type zinc finger protein 1 Human genes 0.000 claims abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 65
- 150000003839 salts Chemical class 0.000 claims description 21
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 229960001639 penicillamine Drugs 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 claims description 2
- 101800004266 Glucagon-like peptide 1(7-37) Proteins 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 179
- 235000019439 ethyl acetate Nutrition 0.000 description 177
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 168
- 239000000243 solution Substances 0.000 description 159
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 122
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 99
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- 239000000284 extract Substances 0.000 description 88
- 239000002904 solvent Substances 0.000 description 80
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- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 51
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 45
- 239000007787 solid Substances 0.000 description 45
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- 238000010992 reflux Methods 0.000 description 42
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- 239000011734 sodium Substances 0.000 description 38
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 38
- 239000013543 active substance Substances 0.000 description 36
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- 229910052938 sodium sulfate Inorganic materials 0.000 description 34
- 235000011152 sodium sulphate Nutrition 0.000 description 34
- 239000002253 acid Substances 0.000 description 33
- 239000012044 organic layer Substances 0.000 description 32
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 31
- 150000001721 carbon Chemical group 0.000 description 31
- 238000001819 mass spectrum Methods 0.000 description 24
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 22
- 229910004298 SiO 2 Inorganic materials 0.000 description 22
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 21
- 239000000126 substance Substances 0.000 description 21
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 20
- 229920006395 saturated elastomer Polymers 0.000 description 20
- 238000000065 atmospheric pressure chemical ionisation Methods 0.000 description 19
- 239000003921 oil Substances 0.000 description 19
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 16
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- 239000010410 layer Substances 0.000 description 16
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 16
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 15
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 15
- 238000000746 purification Methods 0.000 description 15
- 239000000706 filtrate Substances 0.000 description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 13
- TVQGDYNRXLTQAP-UHFFFAOYSA-N ethyl heptanoate Chemical compound CCCCCCC(=O)OCC TVQGDYNRXLTQAP-UHFFFAOYSA-N 0.000 description 12
- 238000001914 filtration Methods 0.000 description 12
- 230000008569 process Effects 0.000 description 12
- 238000004587 chromatography analysis Methods 0.000 description 11
- 230000007062 hydrolysis Effects 0.000 description 11
- 238000006460 hydrolysis reaction Methods 0.000 description 11
- HNBDRPTVWVGKBR-UHFFFAOYSA-N methyl pentanoate Chemical compound CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 description 11
- 239000011541 reaction mixture Substances 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- XNCNNDVCAUWAIT-UHFFFAOYSA-N Methyl heptanoate Chemical compound CCCCCCC(=O)OC XNCNNDVCAUWAIT-UHFFFAOYSA-N 0.000 description 10
- 239000002274 desiccant Substances 0.000 description 10
- 102400000322 Glucagon-like peptide 1 Human genes 0.000 description 9
- 241000700159 Rattus Species 0.000 description 9
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- DTHNMHAUYICORS-KTKZVXAJSA-N Glucagon-like peptide 1 Chemical group C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 DTHNMHAUYICORS-KTKZVXAJSA-N 0.000 description 8
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
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- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 8
- 229910001873 dinitrogen Inorganic materials 0.000 description 8
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 7
- 239000012043 crude product Substances 0.000 description 7
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- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 6
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- PSHNBYJXNBSZHI-UHFFFAOYSA-N methyl 6-amino-6-oxohexanoate Chemical compound COC(=O)CCCCC(N)=O PSHNBYJXNBSZHI-UHFFFAOYSA-N 0.000 description 6
- 150000004702 methyl esters Chemical class 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 5
- PTGGKLDEZXPCBX-UHFFFAOYSA-N 4-[4-(2-aminophenyl)-1,3-oxazol-2-yl]butanoic acid Chemical compound NC1=CC=CC=C1C1=COC(CCCC(O)=O)=N1 PTGGKLDEZXPCBX-UHFFFAOYSA-N 0.000 description 5
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- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Substances FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 5
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- 125000004494 ethyl ester group Chemical group 0.000 description 5
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 description 5
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- QPIUQLBBCQTWMJ-UHFFFAOYSA-N 1-(5-chloro-2-methoxyphenyl)ethanone Chemical compound COC1=CC=C(Cl)C=C1C(C)=O QPIUQLBBCQTWMJ-UHFFFAOYSA-N 0.000 description 4
- SGXUUCSRVVSMGK-UHFFFAOYSA-N 2-bromo-1-(2-nitrophenyl)ethanone Chemical compound [O-][N+](=O)C1=CC=CC=C1C(=O)CBr SGXUUCSRVVSMGK-UHFFFAOYSA-N 0.000 description 4
- LKMDYDGPEROASV-UHFFFAOYSA-N 2-bromo-1-(5-chloro-2-methoxyphenyl)ethanone Chemical compound COC1=CC=C(Cl)C=C1C(=O)CBr LKMDYDGPEROASV-UHFFFAOYSA-N 0.000 description 4
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 4
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
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- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 4
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- 235000019341 magnesium sulphate Nutrition 0.000 description 4
- WGWCCCBSMGNFOE-UHFFFAOYSA-N methyl 5-amino-5-oxopentanoate Chemical compound COC(=O)CCCC(N)=O WGWCCCBSMGNFOE-UHFFFAOYSA-N 0.000 description 4
- JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
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- UFOVULIWACVAAC-UHFFFAOYSA-N 1-ethynyl-2-methoxybenzene Chemical compound COC1=CC=CC=C1C#C UFOVULIWACVAAC-UHFFFAOYSA-N 0.000 description 3
- FGRJGVWULZKYIR-UHFFFAOYSA-N 1-o-methyl 8-o-phenacyl octanedioate Chemical compound COC(=O)CCCCCCC(=O)OCC(=O)C1=CC=CC=C1 FGRJGVWULZKYIR-UHFFFAOYSA-N 0.000 description 3
- IEPFZGYUZLDRNQ-UHFFFAOYSA-N 5-[3-(2-methoxyphenyl)-1,2,4-oxadiazol-5-yl]pentanoic acid Chemical compound COC1=CC=CC=C1C1=NOC(CCCCC(O)=O)=N1 IEPFZGYUZLDRNQ-UHFFFAOYSA-N 0.000 description 3
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- 229910015900 BF3 Inorganic materials 0.000 description 3
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- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 3
- ILUJQPXNXACGAN-UHFFFAOYSA-N O-methylsalicylic acid Chemical compound COC1=CC=CC=C1C(O)=O ILUJQPXNXACGAN-UHFFFAOYSA-N 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
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- 229910021529 ammonia Inorganic materials 0.000 description 3
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- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 2
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- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
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- 238000002844 melting Methods 0.000 description 2
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- UTUVQTIFVPMOCQ-UHFFFAOYSA-N methyl 2-(benzenecarbonothioylsulfanyl)acetate Chemical compound COC(=O)CSC(=S)C1=CC=CC=C1 UTUVQTIFVPMOCQ-UHFFFAOYSA-N 0.000 description 2
- VBVMAZHWZFPGPT-UHFFFAOYSA-N methyl 3-[4-(2-nitrophenyl)-1,3-oxazol-2-yl]propanoate Chemical compound O1C(CCC(=O)OC)=NC(C=2C(=CC=CC=2)[N+]([O-])=O)=C1 VBVMAZHWZFPGPT-UHFFFAOYSA-N 0.000 description 2
- MEPGPWOEYRMFBT-UHFFFAOYSA-N methyl 5-[2-(2-methoxyphenyl)-1,3-oxazol-4-yl]pentanoate Chemical compound COC(=O)CCCCC1=COC(C=2C(=CC=CC=2)OC)=N1 MEPGPWOEYRMFBT-UHFFFAOYSA-N 0.000 description 2
- FYJDBTBFSPFPIU-UHFFFAOYSA-N methyl 5-[2-(2-methoxyphenyl)-1,3-oxazol-5-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=CN=C1C1=CC=CC=C1OC FYJDBTBFSPFPIU-UHFFFAOYSA-N 0.000 description 2
- WQFWHQDNLLVTEA-UHFFFAOYSA-N methyl 5-[4-(2-hydroxy-4-methoxyphenyl)-1,3-thiazol-2-yl]pentanoate Chemical compound S1C(CCCCC(=O)OC)=NC(C=2C(=CC(OC)=CC=2)O)=C1 WQFWHQDNLLVTEA-UHFFFAOYSA-N 0.000 description 2
- TVJNYVKMWZMQND-UHFFFAOYSA-N methyl 5-amino-6-oxoheptanoate;hydrochloride Chemical compound Cl.COC(=O)CCCC(N)C(C)=O TVJNYVKMWZMQND-UHFFFAOYSA-N 0.000 description 2
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- ZCWRANGOCUZGAS-UHFFFAOYSA-N methyl 7-(5-phenyl-1,3-oxazol-2-yl)heptanoate Chemical compound O1C(CCCCCCC(=O)OC)=NC=C1C1=CC=CC=C1 ZCWRANGOCUZGAS-UHFFFAOYSA-N 0.000 description 2
- MYHFAKDYNZJORT-UHFFFAOYSA-N methyl 7-[5-(2-methoxyphenyl)-1h-imidazol-2-yl]heptanoate Chemical compound N1C(CCCCCCC(=O)OC)=NC=C1C1=CC=CC=C1OC MYHFAKDYNZJORT-UHFFFAOYSA-N 0.000 description 2
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- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
- RLFNGUOPCOBMQT-UHFFFAOYSA-N methyl 4-[2-(2-hydroxyphenyl)-4-methyl-1,3-oxazol-5-yl]butanoate Chemical compound CC1=C(CCCC(=O)OC)OC(C=2C(=CC=CC=2)O)=N1 RLFNGUOPCOBMQT-UHFFFAOYSA-N 0.000 description 1
- ZKRSMEISOPCWJR-UHFFFAOYSA-N methyl 4-[2-(2-methoxyphenyl)-4-methyl-1,3-oxazol-5-yl]butanoate Chemical compound CC1=C(CCCC(=O)OC)OC(C=2C(=CC=CC=2)OC)=N1 ZKRSMEISOPCWJR-UHFFFAOYSA-N 0.000 description 1
- LNVYZQUPFCGQIR-UHFFFAOYSA-N methyl 4-[2-(2-methoxyphenyl)-4-methyl-1,3-oxazol-5-yl]butanoate;methyl 5-[2-(2-methoxyphenyl)-1,3-oxazol-4-yl]pentanoate Chemical compound COC(=O)CCCCC1=COC(C=2C(=CC=CC=2)OC)=N1.CC1=C(CCCC(=O)OC)OC(C=2C(=CC=CC=2)OC)=N1 LNVYZQUPFCGQIR-UHFFFAOYSA-N 0.000 description 1
- JGTDEHLLRKQPDL-UHFFFAOYSA-N methyl 4-[4-(2-aminophenyl)-1,3-oxazol-2-yl]butanoate Chemical compound O1C(CCCC(=O)OC)=NC(C=2C(=CC=CC=2)N)=C1 JGTDEHLLRKQPDL-UHFFFAOYSA-N 0.000 description 1
- KURANIFHTFDKFI-UHFFFAOYSA-N methyl 4-[5-(2-methoxyphenyl)-1,2-oxazol-3-yl]butanoate Chemical compound O1N=C(CCCC(=O)OC)C=C1C1=CC=CC=C1OC KURANIFHTFDKFI-UHFFFAOYSA-N 0.000 description 1
- HURZMSZDVGMYKJ-UHFFFAOYSA-N methyl 4-amino-4-oxobutanoate Chemical compound COC(=O)CCC(N)=O HURZMSZDVGMYKJ-UHFFFAOYSA-N 0.000 description 1
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- USOBXDYRYQTXSU-UHFFFAOYSA-N methyl 5-[(2-methylpropan-2-yl)oxycarbonylamino]-6-oxoheptanoate Chemical compound COC(CCCC(C(C)=O)NC(=O)OC(C)(C)C)=O USOBXDYRYQTXSU-UHFFFAOYSA-N 0.000 description 1
- INPHCWZJOHCIKJ-UHFFFAOYSA-N methyl 5-[2-(2-hydroxyphenyl)-1,3-thiazol-4-yl]pentanoate Chemical compound COC(=O)CCCCC1=CSC(C=2C(=CC=CC=2)O)=N1 INPHCWZJOHCIKJ-UHFFFAOYSA-N 0.000 description 1
- WXTVYFSMVXSQCQ-UHFFFAOYSA-N methyl 5-[2-(2-methoxyphenyl)-1,3-thiazol-4-yl]pentanoate Chemical compound COC(=O)CCCCC1=CSC(C=2C(=CC=CC=2)OC)=N1 WXTVYFSMVXSQCQ-UHFFFAOYSA-N 0.000 description 1
- INRSTTCJNIPLHS-UHFFFAOYSA-N methyl 5-[3-(2-methoxyphenyl)-1,2,4-oxadiazol-5-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)OC)=N1 INRSTTCJNIPLHS-UHFFFAOYSA-N 0.000 description 1
- LRMCERXWLAUAFQ-UHFFFAOYSA-N methyl 5-[4-(2-acetamidophenyl)-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)NC(C)=O)=C1 LRMCERXWLAUAFQ-UHFFFAOYSA-N 0.000 description 1
- OVTNQEONMLTACH-UHFFFAOYSA-N methyl 5-[4-(2-aminophenyl)-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)N)=C1 OVTNQEONMLTACH-UHFFFAOYSA-N 0.000 description 1
- IKYSLIWYUHLVDS-UHFFFAOYSA-N methyl 5-[4-(2-hydroxyphenyl)-5-methyl-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)O)=C1C IKYSLIWYUHLVDS-UHFFFAOYSA-N 0.000 description 1
- IBJSWQJNHYFNAE-UHFFFAOYSA-N methyl 5-[4-(2-methoxyphenyl)-1,3-thiazol-2-yl]pentanoate Chemical compound S1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)OC)=C1 IBJSWQJNHYFNAE-UHFFFAOYSA-N 0.000 description 1
- CDOKZYRBEFSWPK-UHFFFAOYSA-N methyl 5-[4-(2-methoxyphenyl)-5-methyl-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)OC)=C1C CDOKZYRBEFSWPK-UHFFFAOYSA-N 0.000 description 1
- TXOCYUDKKKHAJF-UHFFFAOYSA-N methyl 5-[4-(2-methoxyphenyl)triazol-1-yl]pentanoate Chemical compound N1=NN(CCCCC(=O)OC)C=C1C1=CC=CC=C1OC TXOCYUDKKKHAJF-UHFFFAOYSA-N 0.000 description 1
- QCHRRTLHPRYLAM-UHFFFAOYSA-N methyl 5-[4-(2-nitrophenyl)-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)[N+]([O-])=O)=C1 QCHRRTLHPRYLAM-UHFFFAOYSA-N 0.000 description 1
- YHGWFBOBQJGTSW-UHFFFAOYSA-N methyl 5-[4-(5-chloro-2-methoxyphenyl)-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=C(Cl)C=2)OC)=C1 YHGWFBOBQJGTSW-UHFFFAOYSA-N 0.000 description 1
- FBYOUVUZIMHBEH-UHFFFAOYSA-N methyl 5-[4-[2-(methanesulfonamido)phenyl]-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)NS(C)(=O)=O)=C1 FBYOUVUZIMHBEH-UHFFFAOYSA-N 0.000 description 1
- PQNBYZLOYZMZPF-UHFFFAOYSA-N methyl 5-[4-[2-(trifluoromethyl)phenyl]-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)C(F)(F)F)=C1 PQNBYZLOYZMZPF-UHFFFAOYSA-N 0.000 description 1
- LQHGNKCWWGGNNM-UHFFFAOYSA-N methyl 5-[4-[2-[(2,2,2-trifluoroacetyl)amino]phenyl]-1,3-oxazol-2-yl]pentanoate Chemical compound O1C(CCCCC(=O)OC)=NC(C=2C(=CC=CC=2)NC(=O)C(F)(F)F)=C1 LQHGNKCWWGGNNM-UHFFFAOYSA-N 0.000 description 1
- MNOHXVBSGSQEPX-UHFFFAOYSA-N methyl 5-[5-(2-methoxyphenyl)triazol-1-yl]pentanoate Chemical compound COC(=O)CCCCN1N=NC=C1C1=CC=CC=C1OC MNOHXVBSGSQEPX-UHFFFAOYSA-N 0.000 description 1
- OQEZMRVNSROGPF-UHFFFAOYSA-N methyl 5-azidopentanoate Chemical compound COC(=O)CCCCN=[N+]=[N-] OQEZMRVNSROGPF-UHFFFAOYSA-N 0.000 description 1
- ZMGNKRJTJWASFK-UHFFFAOYSA-N methyl 5-bromo-6-oxoheptanoate Chemical compound COC(=O)CCCC(Br)C(C)=O ZMGNKRJTJWASFK-UHFFFAOYSA-N 0.000 description 1
- RAVVJKCSZXAIQP-UHFFFAOYSA-N methyl 5-bromopentanoate Chemical compound COC(=O)CCCCBr RAVVJKCSZXAIQP-UHFFFAOYSA-N 0.000 description 1
- HDLGIEZOMYJKAK-UHFFFAOYSA-N methyl 6-chloro-6-oxohexanoate Chemical compound COC(=O)CCCCC(Cl)=O HDLGIEZOMYJKAK-UHFFFAOYSA-N 0.000 description 1
- BSBYQAYWPXHLPQ-UHFFFAOYSA-N methyl 6-oxoheptanoate Chemical compound COC(=O)CCCCC(C)=O BSBYQAYWPXHLPQ-UHFFFAOYSA-N 0.000 description 1
- VPHQMOSJKHBDBS-UHFFFAOYSA-N methyl 7-[(2-methoxybenzoyl)amino]-6-oxoheptanoate Chemical compound COC(=O)CCCCC(=O)CNC(=O)C1=CC=CC=C1OC VPHQMOSJKHBDBS-UHFFFAOYSA-N 0.000 description 1
- BQFAFRPHJLMNTB-UHFFFAOYSA-N methyl 7-[(2-methylpropan-2-yl)oxycarbonylamino]-6-oxoheptanoate Chemical compound COC(CCCCC(CNC(=O)OC(C)(C)C)=O)=O BQFAFRPHJLMNTB-UHFFFAOYSA-N 0.000 description 1
- UKONAOQWOSFIKE-UHFFFAOYSA-N methyl 7-[3-(2-methoxyphenyl)-1,2-oxazol-5-yl]heptanoate Chemical compound O1C(CCCCCCC(=O)OC)=CC(C=2C(=CC=CC=2)OC)=N1 UKONAOQWOSFIKE-UHFFFAOYSA-N 0.000 description 1
- VUTSVZAXFXDYDI-UHFFFAOYSA-N methyl 7-[5-(5-chloro-2-hydroxyphenyl)-1,3-thiazol-2-yl]heptanoate Chemical compound S1C(CCCCCCC(=O)OC)=NC=C1C1=CC(Cl)=CC=C1O VUTSVZAXFXDYDI-UHFFFAOYSA-N 0.000 description 1
- BXRLUWIDTDLHQE-UHFFFAOYSA-N methyl 7-bromoheptanoate Chemical compound COC(=O)CCCCCCBr BXRLUWIDTDLHQE-UHFFFAOYSA-N 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- RQGNSKOYEKUEED-UHFFFAOYSA-N n-(2-ethynylphenyl)acetamide Chemical compound CC(=O)NC1=CC=CC=C1C#C RQGNSKOYEKUEED-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000012585 nuclear overhauser effect spectroscopy experiment Methods 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- LIGACIXOYTUXAW-UHFFFAOYSA-N phenacyl bromide Chemical compound BrCC(=O)C1=CC=CC=C1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 description 1
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
- DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid;trioxomolybdenum Chemical compound O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.OP(O)(O)=O DHRLEVQXOMLTIM-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
- 230000036470 plasma concentration Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- GCYXWQUSHADNBF-AAEALURTSA-N preproglucagon 78-108 Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC=1N=CNC=1)[C@@H](C)O)[C@@H](C)O)C(C)C)C1=CC=CC=C1 GCYXWQUSHADNBF-AAEALURTSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- DSNYFFJTZPIKFZ-UHFFFAOYSA-N propoxybenzene Chemical group CCCOC1=CC=CC=C1 DSNYFFJTZPIKFZ-UHFFFAOYSA-N 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000012056 semi-solid material Substances 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- KZJPVUDYAMEDRM-UHFFFAOYSA-M silver;2,2,2-trifluoroacetate Chemical compound [Ag+].[O-]C(=O)C(F)(F)F KZJPVUDYAMEDRM-UHFFFAOYSA-M 0.000 description 1
- XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical class [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000012453 sprague-dawley rat model Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- YUKQRDCYNOVPGJ-UHFFFAOYSA-N thioacetamide Chemical compound CC(N)=S YUKQRDCYNOVPGJ-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 description 1
- 229940094989 trimethylsilane Drugs 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical class [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 239000011123 type I (borosilicate glass) Substances 0.000 description 1
- 238000000825 ultraviolet detection Methods 0.000 description 1
- 230000009278 visceral effect Effects 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/26—Glucagons
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/24—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Gastroenterology & Hepatology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicinal Preparation (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
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| PCT/US2004/024386 WO2005019184A1 (en) | 2003-08-20 | 2004-08-18 | Compounds, methods and formulations for the oral delivery of a glucagon like peptide (glp)-1 compound or an melanocortin 4 receptor (mc4) agonist peptide |
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| EP (1) | EP1658273B1 (enExample) |
| JP (1) | JP4767850B2 (enExample) |
| AT (1) | ATE350369T1 (enExample) |
| CA (1) | CA2532026C (enExample) |
| DE (1) | DE602004004156T2 (enExample) |
| ES (1) | ES2278346T3 (enExample) |
| WO (1) | WO2005019184A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011207886A (ja) * | 2003-08-20 | 2011-10-20 | Emisphere Technologies Inc | グルカゴン様ペプチド(glp)−1化合物またはメラノコルチン4受容体(mc4)アゴニストペプチドの経口デリバリーのための化合物、方法および製剤 |
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| EP1915168A4 (en) | 2005-07-08 | 2010-03-31 | Ipsen Pharma | LIGANDS OF MELANOCORTIN RECEPTORS |
| ES2663916T3 (es) | 2005-07-08 | 2018-04-17 | Ipsen Pharma | Ligandos de los receptores de la melanocortina |
| CA2618628C (en) | 2005-08-18 | 2014-11-18 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate hsp90 activity |
| EP2057112B1 (en) | 2006-08-31 | 2018-12-19 | Emisphere Technologies, Inc. | Compounds and compositions for delivering active agents |
| NZ579403A (en) * | 2007-02-08 | 2012-03-30 | Synta Pharmaceuticals Corp | Triazole compounds that are useful in the treatment of proliferative disorders, such as cancer |
| JP2011518841A (ja) | 2008-04-24 | 2011-06-30 | ニューリンク ジェネティクス, インコーポレイテッド | Ido阻害剤 |
| WO2009139181A1 (ja) | 2008-05-15 | 2009-11-19 | 大正製薬株式会社 | 4員環構造を有する10a-アザライド化合物 |
| WO2011045418A1 (en) * | 2009-10-16 | 2011-04-21 | Dsm Ip Assets B.V. | Azido alkanoic acids and derivatives thereof in feed for reducing methane formation emanating from the digestive activities of ruminants |
| JP6588027B2 (ja) | 2014-10-24 | 2019-10-09 | 武田薬品工業株式会社 | 複素環化合物 |
| MX385777B (es) | 2014-12-24 | 2025-03-04 | Lg Chemical Ltd | Derivado de biarilo como agonista de gpr120. |
| WO2016168388A2 (en) | 2015-04-14 | 2016-10-20 | Palatin Technologies, Inc. | Therapies for obesity, diabetes and related indications |
| CN107163011B (zh) * | 2017-05-27 | 2019-10-01 | 上海应用技术大学 | 3-(3,4,5-三甲氧基苯甲酰)-苯并呋喃类微管蛋白抑制剂及其制备方法和用途 |
| CN113248455A (zh) * | 2021-05-25 | 2021-08-13 | 湖北科技学院 | 一种3,5-二取代异噁唑类衍生物及其合成方法 |
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2004
- 2004-08-18 EP EP04779446A patent/EP1658273B1/en not_active Expired - Lifetime
- 2004-08-18 DE DE602004004156T patent/DE602004004156T2/de not_active Expired - Lifetime
- 2004-08-18 JP JP2006523865A patent/JP4767850B2/ja not_active Expired - Fee Related
- 2004-08-18 WO PCT/US2004/024386 patent/WO2005019184A1/en not_active Ceased
- 2004-08-18 ES ES04779446T patent/ES2278346T3/es not_active Expired - Lifetime
- 2004-08-18 CA CA2532026A patent/CA2532026C/en not_active Expired - Fee Related
- 2004-08-18 US US10/566,342 patent/US7662771B2/en not_active Expired - Lifetime
- 2004-08-18 AT AT04779446T patent/ATE350369T1/de not_active IP Right Cessation
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| JP2001131090A (ja) * | 1997-02-07 | 2001-05-15 | Emisphere Technolgies Inc | 化合物及び活性剤を送達するための組成物 |
| JP2002536400A (ja) * | 1999-02-11 | 2002-10-29 | エミスフェアー・テクノロジーズ・インク | オキサジアゾール化合物及び活性剤をデリバリーするための組成物 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011207886A (ja) * | 2003-08-20 | 2011-10-20 | Emisphere Technologies Inc | グルカゴン様ペプチド(glp)−1化合物またはメラノコルチン4受容体(mc4)アゴニストペプチドの経口デリバリーのための化合物、方法および製剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| ES2278346T3 (es) | 2007-08-01 |
| ATE350369T1 (de) | 2007-01-15 |
| US20100120876A1 (en) | 2010-05-13 |
| WO2005019184A1 (en) | 2005-03-03 |
| CA2532026A1 (en) | 2005-03-03 |
| US8765796B2 (en) | 2014-07-01 |
| US20080214448A1 (en) | 2008-09-04 |
| EP1658273B1 (en) | 2007-01-03 |
| DE602004004156T2 (de) | 2007-10-11 |
| US8552039B2 (en) | 2013-10-08 |
| DE602004004156D1 (de) | 2007-02-15 |
| EP1658273A1 (en) | 2006-05-24 |
| US7662771B2 (en) | 2010-02-16 |
| CA2532026C (en) | 2012-04-17 |
| US20140031287A1 (en) | 2014-01-30 |
| JP2007502816A (ja) | 2007-02-15 |
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