DE60115265T2 - Zusammensetzungen und verfahren zur verwendung achiraler analoge von cc-1065 und den duocarmycinen - Google Patents
Zusammensetzungen und verfahren zur verwendung achiraler analoge von cc-1065 und den duocarmycinen Download PDFInfo
- Publication number
- DE60115265T2 DE60115265T2 DE60115265T DE60115265T DE60115265T2 DE 60115265 T2 DE60115265 T2 DE 60115265T2 DE 60115265 T DE60115265 T DE 60115265T DE 60115265 T DE60115265 T DE 60115265T DE 60115265 T2 DE60115265 T2 DE 60115265T2
- Authority
- DE
- Germany
- Prior art keywords
- carboxamido
- chloroethyl
- mmol
- phenol
- solution
- 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.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 13
- 239000000203 mixture Substances 0.000 title description 60
- UOWVMDUEMSNCAV-WYENRQIDSA-N rachelmycin Chemical class C1([C@]23C[C@@H]2CN1C(=O)C=1NC=2C(OC)=C(O)C4=C(C=2C=1)CCN4C(=O)C1=CC=2C=4CCN(C=4C(O)=C(C=2N1)OC)C(N)=O)=CC(=O)C1=C3C(C)=CN1 UOWVMDUEMSNCAV-WYENRQIDSA-N 0.000 title description 26
- 239000011230 binding agent Substances 0.000 claims abstract description 11
- 239000002168 alkylating agent Substances 0.000 claims abstract description 9
- 229940100198 alkylating agent Drugs 0.000 claims abstract description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims abstract description 4
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000001453 quaternary ammonium group Chemical group 0.000 claims abstract description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims abstract description 4
- -1 iodine, mercapto Chemical group 0.000 claims description 153
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 119
- 150000001875 compounds Chemical class 0.000 claims description 112
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims description 105
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 82
- 239000000460 chlorine Substances 0.000 claims description 80
- 229910052757 nitrogen Inorganic materials 0.000 claims description 45
- 206010028980 Neoplasm Diseases 0.000 claims description 43
- 201000011510 cancer Diseases 0.000 claims description 36
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 30
- 239000003814 drug Substances 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 229940079593 drug Drugs 0.000 claims description 25
- 239000001257 hydrogen Substances 0.000 claims description 25
- 238000011282 treatment Methods 0.000 claims description 17
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 15
- 238000002360 preparation method Methods 0.000 claims description 15
- 238000000338 in vitro Methods 0.000 claims description 11
- 125000004042 4-aminobutyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])N([H])[H] 0.000 claims description 10
- 108091028043 Nucleic acid sequence Proteins 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 125000005999 2-bromoethyl group Chemical group 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- KPUSFGRUUAWOOZ-UHFFFAOYSA-N n-[2-(2-chloroethyl)-5-hydroxyphenyl]-5-nitro-1h-indole-2-carboxamide Chemical compound OC1=CC=C(CCCl)C(NC(=O)C=2NC3=CC=C(C=C3C=2)[N+]([O-])=O)=C1 KPUSFGRUUAWOOZ-UHFFFAOYSA-N 0.000 claims description 6
- MNFPZBOQEWMBOK-UHFFFAOYSA-N AS-I-145 Chemical compound C1=CC=CC2=C(CCCl)C(NC(=O)C3=CC=4C=C(C(=C(OC)C=4N3)OC)OC)=CC(N)=C21 MNFPZBOQEWMBOK-UHFFFAOYSA-N 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
- GZWGRILFCUPLRU-UHFFFAOYSA-N 4-(butanoylamino)-n-[5-[[2-(2-chloroethyl)-4-hydroxyphenyl]carbamoyl]-1-methylpyrrol-3-yl]-1-methylpyrrole-2-carboxamide Chemical compound CN1C=C(NC(=O)CCC)C=C1C(=O)NC1=CN(C)C(C(=O)NC=2C(=CC(O)=CC=2)CCCl)=C1 GZWGRILFCUPLRU-UHFFFAOYSA-N 0.000 claims description 4
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- APDRQENAZGXECT-UHFFFAOYSA-N n-[5-amino-2-(2-chloroethyl)phenyl]-5,6,7-trimethoxy-1h-indole-2-carboxamide Chemical compound N1C=2C(OC)=C(OC)C(OC)=CC=2C=C1C(=O)NC1=CC(N)=CC=C1CCCl APDRQENAZGXECT-UHFFFAOYSA-N 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 3
- HBYWDESRMFTSDA-UHFFFAOYSA-N n-[4-amino-1-(2-chloroethyl)naphthalen-2-yl]-5-methoxy-1h-indole-2-carboxamide Chemical compound C1=CC=CC2=C(CCCl)C(NC(=O)C=3NC4=CC=C(C=C4C=3)OC)=CC(N)=C21 HBYWDESRMFTSDA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- LRXLMJDKROGRPQ-UHFFFAOYSA-N butyl n-[4-(2-chloroethyl)-3-nitronaphthalen-1-yl]carbamate Chemical compound C1=CC=C2C(NC(=O)OCCCC)=CC([N+]([O-])=O)=C(CCCl)C2=C1 LRXLMJDKROGRPQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052740 iodine Chemical group 0.000 claims description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
- 230000008685 targeting Effects 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 239000011630 iodine Chemical group 0.000 claims 1
- MXUGFYRNNNMOSQ-UHFFFAOYSA-N n-[2-(2-chloroethyl)-5-hydroxyphenyl]-5,6,7-trimethoxy-1h-indole-2-carboxamide Chemical compound N1C=2C(OC)=C(OC)C(OC)=CC=2C=C1C(=O)NC1=CC(O)=CC=C1CCCl MXUGFYRNNNMOSQ-UHFFFAOYSA-N 0.000 claims 1
- 229960005532 CC-1065 Drugs 0.000 abstract description 58
- 229960005501 duocarmycin Drugs 0.000 abstract description 27
- 229930184221 duocarmycin Natural products 0.000 abstract description 26
- 230000003993 interaction Effects 0.000 abstract description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract description 12
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract description 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract description 5
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract description 4
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract description 3
- VQAFBYLFRCCWNB-GOSISDBHSA-N n-[2-[(1s)-1-(chloromethyl)-5-hydroxy-9-methyl-1,2-dihydrobenzo[e]indole-3-carbonyl]imidazo[1,2-a]pyridin-6-yl]-4-hydroxybenzamide Chemical compound C1([C@H](CCl)C2)=C3C(C)=CC=CC3=C(O)C=C1N2C(=O)C(N=C1C=C2)=CN1C=C2NC(=O)C1=CC=C(O)C=C1 VQAFBYLFRCCWNB-GOSISDBHSA-N 0.000 abstract description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 297
- 239000000243 solution Substances 0.000 description 268
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 262
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 173
- 239000007787 solid Substances 0.000 description 107
- 238000005160 1H NMR spectroscopy Methods 0.000 description 91
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 84
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 84
- 235000019439 ethyl acetate Nutrition 0.000 description 84
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 79
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 74
- 230000002829 reductive effect Effects 0.000 description 71
- 108020004414 DNA Proteins 0.000 description 68
- 239000000725 suspension Substances 0.000 description 68
- 239000012044 organic layer Substances 0.000 description 67
- 210000004027 cell Anatomy 0.000 description 65
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 64
- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 64
- 238000004809 thin layer chromatography Methods 0.000 description 63
- 238000006243 chemical reaction Methods 0.000 description 58
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 51
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 50
- 239000011541 reaction mixture Substances 0.000 description 49
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 48
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 47
- 239000000741 silica gel Substances 0.000 description 45
- 229910002027 silica gel Inorganic materials 0.000 description 45
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 43
- 229920006395 saturated elastomer Polymers 0.000 description 40
- 239000011734 sodium Substances 0.000 description 40
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 39
- 239000002904 solvent Substances 0.000 description 39
- 239000003921 oil Substances 0.000 description 38
- 235000019198 oils Nutrition 0.000 description 38
- 239000010457 zeolite Substances 0.000 description 38
- VQNATVDKACXKTF-XELLLNAOSA-N duocarmycin Chemical compound COC1=C(OC)C(OC)=C2NC(C(=O)N3C4=CC(=O)C5=C([C@@]64C[C@@H]6C3)C=C(N5)C(=O)OC)=CC2=C1 VQNATVDKACXKTF-XELLLNAOSA-N 0.000 description 37
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 37
- 239000000706 filtrate Substances 0.000 description 36
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 34
- 150000001412 amines Chemical class 0.000 description 34
- 230000015572 biosynthetic process Effects 0.000 description 34
- 229910052938 sodium sulfate Inorganic materials 0.000 description 34
- 235000011152 sodium sulphate Nutrition 0.000 description 34
- 238000005804 alkylation reaction Methods 0.000 description 33
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 32
- 238000002451 electron ionisation mass spectrometry Methods 0.000 description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 30
- 230000029936 alkylation Effects 0.000 description 30
- 239000011780 sodium chloride Substances 0.000 description 30
- 238000003786 synthesis reaction Methods 0.000 description 30
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 29
- 239000003208 petroleum Substances 0.000 description 28
- 239000012299 nitrogen atmosphere Substances 0.000 description 27
- 239000000047 product Substances 0.000 description 27
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 26
- 238000010992 reflux Methods 0.000 description 26
- 230000000694 effects Effects 0.000 description 23
- 230000005484 gravity Effects 0.000 description 22
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 22
- 229910052763 palladium Inorganic materials 0.000 description 21
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 20
- 238000012360 testing method Methods 0.000 description 19
- 229960005510 duocarmycin SA Drugs 0.000 description 18
- RCCYSVYHULFYHE-UHFFFAOYSA-N pentanediamide Chemical compound NC(=O)CCCC(N)=O RCCYSVYHULFYHE-UHFFFAOYSA-N 0.000 description 18
- VQNATVDKACXKTF-UHFFFAOYSA-N Duocarmycin SA Natural products COC1=C(OC)C(OC)=C2NC(C(=O)N3C4=CC(=O)C5=C(C64CC6C3)C=C(N5)C(=O)OC)=CC2=C1 VQNATVDKACXKTF-UHFFFAOYSA-N 0.000 description 17
- 239000006260 foam Substances 0.000 description 17
- 241000282414 Homo sapiens Species 0.000 description 16
- 238000003556 assay Methods 0.000 description 16
- 230000001472 cytotoxic effect Effects 0.000 description 16
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 16
- 239000012298 atmosphere Substances 0.000 description 15
- 0 *CCc(c(NC(*)=O)c1)ccc1O Chemical compound *CCc(c(NC(*)=O)c1)ccc1O 0.000 description 14
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 14
- BMRNBDRINXHDSQ-UHFFFAOYSA-N 3-amino-4-(2-chloroethyl)phenol Chemical compound NC1=CC(O)=CC=C1CCCl BMRNBDRINXHDSQ-UHFFFAOYSA-N 0.000 description 13
- 230000007118 DNA alkylation Effects 0.000 description 13
- 239000002253 acid Substances 0.000 description 13
- BYRVKDUQDLJUBX-JJCDCTGGSA-N adozelesin Chemical compound C1=CC=C2OC(C(=O)NC=3C=C4C=C(NC4=CC=3)C(=O)N3C[C@H]4C[C@]44C5=C(C(C=C43)=O)NC=C5C)=CC2=C1 BYRVKDUQDLJUBX-JJCDCTGGSA-N 0.000 description 13
- 239000002246 antineoplastic agent Substances 0.000 description 13
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 13
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 13
- 229960003750 ethyl chloride Drugs 0.000 description 13
- 239000002244 precipitate Substances 0.000 description 13
- BWQWNOUXSFIABV-UHFFFAOYSA-N 1-(2-chloroethyl)-2-nitro-4-phenylmethoxybenzene Chemical compound C1=C(CCCl)C([N+](=O)[O-])=CC(OCC=2C=CC=CC=2)=C1 BWQWNOUXSFIABV-UHFFFAOYSA-N 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 12
- 238000000354 decomposition reaction Methods 0.000 description 12
- 239000010410 layer Substances 0.000 description 12
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 12
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 12
- 108010006785 Taq Polymerase Proteins 0.000 description 11
- 229950004955 adozelesin Drugs 0.000 description 11
- 238000004440 column chromatography Methods 0.000 description 11
- 229940125904 compound 1 Drugs 0.000 description 11
- 231100000433 cytotoxic Toxicity 0.000 description 11
- 230000003013 cytotoxicity Effects 0.000 description 11
- 231100000135 cytotoxicity Toxicity 0.000 description 11
- 238000005481 NMR spectroscopy Methods 0.000 description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- 238000004458 analytical method Methods 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 10
- 238000003818 flash chromatography Methods 0.000 description 10
- 239000000651 prodrug Substances 0.000 description 10
- 229940002612 prodrug Drugs 0.000 description 10
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 10
- TVTJUIAKQFIXCE-HUKYDQBMSA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynyl-1H-purine-6,8-dione Chemical compound NC=1NC(C=2N(C(N(C=2N=1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C)=O TVTJUIAKQFIXCE-HUKYDQBMSA-N 0.000 description 9
- 230000004568 DNA-binding Effects 0.000 description 9
- 229940125851 compound 27 Drugs 0.000 description 9
- 238000001035 drying Methods 0.000 description 9
- 239000000499 gel Substances 0.000 description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 9
- 239000000543 intermediate Substances 0.000 description 9
- AZVARJHZBXHUSO-DZQVEHCYSA-N methyl (1R,4R,12S)-4-methyl-3,7-dioxo-10-(5,6,7-trimethoxy-1H-indole-2-carbonyl)-5,10-diazatetracyclo[7.4.0.01,12.02,6]trideca-2(6),8-diene-4-carboxylate Chemical compound COC1=C(OC)C(OC)=C2NC(C(=O)N3C[C@H]4C[C@]44C5=C(C(C=C43)=O)N[C@@](C5=O)(C)C(=O)OC)=CC2=C1 AZVARJHZBXHUSO-DZQVEHCYSA-N 0.000 description 9
- JZMUJQGIASARGH-UHFFFAOYSA-N 5,6,7-trimethoxy-1h-indole-2-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC2=C1NC(C(O)=O)=C2 JZMUJQGIASARGH-UHFFFAOYSA-N 0.000 description 8
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 8
- 230000004071 biological effect Effects 0.000 description 8
- 239000012267 brine Substances 0.000 description 8
- 229940125782 compound 2 Drugs 0.000 description 8
- 239000012043 crude product Substances 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 229910000027 potassium carbonate Inorganic materials 0.000 description 8
- 239000000523 sample Substances 0.000 description 8
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 8
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 7
- 229930024421 Adenine Natural products 0.000 description 7
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 description 7
- AZVARJHZBXHUSO-UHFFFAOYSA-N Duocarmycin A Natural products COC1=C(OC)C(OC)=C2NC(C(=O)N3CC4CC44C5=C(C(C=C43)=O)NC(C5=O)(C)C(=O)OC)=CC2=C1 AZVARJHZBXHUSO-UHFFFAOYSA-N 0.000 description 7
- 241000699670 Mus sp. Species 0.000 description 7
- 229960000643 adenine Drugs 0.000 description 7
- 230000001093 anti-cancer Effects 0.000 description 7
- 229960005519 duocarmycin A Drugs 0.000 description 7
- 230000012010 growth Effects 0.000 description 7
- 238000001727 in vivo Methods 0.000 description 7
- 238000011534 incubation Methods 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- 238000012746 preparative thin layer chromatography Methods 0.000 description 7
- 238000000746 purification Methods 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- 238000012216 screening Methods 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
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Applications Claiming Priority (3)
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| US66616000A | 2000-09-19 | 2000-09-19 | |
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| PCT/US2001/029160 WO2002030894A2 (en) | 2000-09-19 | 2001-09-19 | Compositions and methods of the use thereof achiral analogues of cc-1065 and the duocarmycins |
Publications (2)
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| DE60115265D1 DE60115265D1 (de) | 2005-12-29 |
| DE60115265T2 true DE60115265T2 (de) | 2006-08-10 |
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| IL289094A (en) | 2019-06-17 | 2022-02-01 | Tagworks Pharmaceuticals B V | Tetrazines for increasing the speed and yield of the "click release" reaction |
| CA3143925A1 (en) | 2019-06-17 | 2020-12-24 | Tagworks Pharmaceuticals B.V. | Compounds for fast and efficient click release |
| JP7337260B2 (ja) * | 2019-08-26 | 2023-09-01 | クッジェ ファーマ カンパニー,リミテッド | インドールカルボキサミド誘導体及びそれを含む薬剤学的組成物 |
| US20250327057A1 (en) | 2021-09-06 | 2025-10-23 | Veraxa Biotech Gmbh | Novel aminoacyl-trna synthetase variants for genetic code expansion in eukaryotes |
| DK4186529T3 (da) | 2021-11-25 | 2025-08-25 | Veraxa Biotech Gmbh | Forbedrede antistof-payload-konjugater (apc) fremstillet ved stedspecifik konjugering ved hjælp af genetisk kodeudvidelse |
| CA3238627A1 (en) | 2021-11-25 | 2023-06-01 | Christine Kohler | Improved antibody-payload conjugates (apcs) prepared by site-specific conjugation utilizing genetic code expansion |
| US20250135011A1 (en) | 2021-12-08 | 2025-05-01 | European Molecular Biology Laboratory | Hydrophilic tetrazine-functionalized payloads for preparation of targeting conjugates |
| EP4314031B1 (en) | 2022-02-15 | 2024-03-13 | Tagworks Pharmaceuticals B.V. | Masked il12 protein |
| KR20250049569A (ko) | 2022-07-15 | 2025-04-11 | 페온 테라퓨틱스 리미티드 | 항체-약물 접합체 |
| WO2024080872A1 (en) | 2022-10-12 | 2024-04-18 | Tagworks Pharmaceuticals B.V. | Strained bicyclononenes |
| CN120569216A (zh) | 2023-01-20 | 2025-08-29 | 巴斯夫欧洲公司 | 稳定型生物聚合物组合物、其制造和用途 |
| AU2024237490A1 (en) | 2023-03-10 | 2025-09-25 | Tagworks Pharmaceuticals B.V. | Trans-cyclooctene with improved t-linker |
| WO2025021929A1 (en) | 2023-07-27 | 2025-01-30 | Veraxa Biotech Gmbh | Hydrophilic trans-cyclooctene (hytco) compounds, constructs and conjugates containing the same |
| WO2025056807A1 (en) | 2023-09-15 | 2025-03-20 | Basf Se | Stabilized biopolymer composition, their manufacture and use |
| WO2025149667A1 (en) | 2024-01-12 | 2025-07-17 | Pheon Therapeutics Ltd | Antibody drug conjugates and uses thereof |
| WO2025174248A1 (en) | 2024-02-16 | 2025-08-21 | Tagworks Pharmaceuticals B.V. | Trans-cyclooctenes with "or gate" release |
Family Cites Families (5)
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|---|---|---|---|---|
| EP0888301B1 (en) * | 1996-03-08 | 2005-08-10 | The Scripps Research Institute | Mcbi analogs of cc-1065 and the duocarmycins |
| US5843937A (en) * | 1996-05-23 | 1998-12-01 | Panorama Research, Inc. | DNA-binding indole derivatives, their prodrugs and immunoconjugates as anticancer agents |
| US6060608A (en) * | 1996-05-31 | 2000-05-09 | The Scripps Research Institute | Analogs of CC-1065 and the duocarmycins |
| NZ503966A (en) * | 1997-10-14 | 2002-10-25 | Scripps Research Inst | iso -CBI and iso -CI analogs of CC-1065 and the duocarmycins |
| JP3045706B1 (ja) * | 1998-09-14 | 2000-05-29 | 科学技術振興事業団 | Dnaの特定塩基配列をアルキル化する化合物及びその合成法 |
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- 2001-09-19 EP EP01973146A patent/EP1320522B8/en not_active Expired - Lifetime
- 2001-09-19 WO PCT/US2001/029160 patent/WO2002030894A2/en not_active Ceased
- 2001-09-19 DE DE60115265T patent/DE60115265T2/de not_active Expired - Lifetime
- 2001-09-19 CN CNB018159346A patent/CN1315805C/zh not_active Expired - Fee Related
- 2001-09-19 DK DK01973146T patent/DK1320522T3/da active
- 2001-09-19 US US09/955,062 patent/US6660742B2/en not_active Expired - Lifetime
- 2001-09-19 ES ES01973146T patent/ES2254492T3/es not_active Expired - Lifetime
- 2001-09-19 JP JP2002534280A patent/JP5010089B2/ja not_active Expired - Fee Related
- 2001-09-19 AT AT01973146T patent/ATE310724T1/de not_active IP Right Cessation
Also Published As
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|---|---|
| EP1320522B8 (en) | 2006-02-01 |
| DE60115265D1 (de) | 2005-12-29 |
| DK1320522T3 (da) | 2006-04-03 |
| WO2002030894A2 (en) | 2002-04-18 |
| CN1315805C (zh) | 2007-05-16 |
| US6660742B2 (en) | 2003-12-09 |
| ATE310724T1 (de) | 2005-12-15 |
| JP5010089B2 (ja) | 2012-08-29 |
| EP1320522B1 (en) | 2005-11-23 |
| US20030073731A1 (en) | 2003-04-17 |
| WO2002030894A3 (en) | 2002-06-20 |
| JP2004511466A (ja) | 2004-04-15 |
| CN1461298A (zh) | 2003-12-10 |
| EP1320522A2 (en) | 2003-06-25 |
| ES2254492T3 (es) | 2006-06-16 |
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