DE69426423T2 - NEUE HEMMER VON URIDINPHOSPHORYLASE (UrdPase) UND DIHYDROURACILDEHYDROGENASE (DHUDase) - Google Patents
NEUE HEMMER VON URIDINPHOSPHORYLASE (UrdPase) UND DIHYDROURACILDEHYDROGENASE (DHUDase)Info
- Publication number
- DE69426423T2 DE69426423T2 DE69426423T DE69426423T DE69426423T2 DE 69426423 T2 DE69426423 T2 DE 69426423T2 DE 69426423 T DE69426423 T DE 69426423T DE 69426423 T DE69426423 T DE 69426423T DE 69426423 T2 DE69426423 T2 DE 69426423T2
- Authority
- DE
- Germany
- Prior art keywords
- phenylthio
- phenylselenenyl
- hydroxyethoxy
- pyrimidine
- methyl
- 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
- 108010019092 Uridine phosphorylase Proteins 0.000 title claims abstract description 61
- 102000006405 Uridine phosphorylase Human genes 0.000 title description 57
- 239000003112 inhibitor Substances 0.000 title description 50
- 108010088106 Dihydrouracil Dehydrogenase (NAD+) Proteins 0.000 title description 43
- 102100022334 Dihydropyrimidine dehydrogenase [NADP(+)] Human genes 0.000 title description 41
- 150000001875 compounds Chemical class 0.000 claims abstract description 91
- 102000004190 Enzymes Human genes 0.000 claims abstract description 37
- 108090000790 Enzymes Proteins 0.000 claims abstract description 37
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 35
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 27
- 238000011282 treatment Methods 0.000 claims abstract description 24
- -1 methoxy, benzyl Chemical group 0.000 claims abstract description 19
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims abstract description 15
- 230000001580 bacterial effect Effects 0.000 claims abstract description 15
- 230000003612 virological effect Effects 0.000 claims abstract description 15
- 230000002538 fungal effect Effects 0.000 claims abstract description 14
- 208000035143 Bacterial infection Diseases 0.000 claims abstract description 12
- 206010017533 Fungal infection Diseases 0.000 claims abstract description 12
- 208000031888 Mycoses Diseases 0.000 claims abstract description 12
- 208000030852 Parasitic disease Diseases 0.000 claims abstract description 12
- 208000036142 Viral infection Diseases 0.000 claims abstract description 12
- 208000022362 bacterial infectious disease Diseases 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 12
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 7
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 4
- 125000001544 thienyl group Chemical group 0.000 claims abstract description 4
- 229960002949 fluorouracil Drugs 0.000 claims description 25
- 201000011510 cancer Diseases 0.000 claims description 23
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 claims description 21
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 claims description 18
- 239000000047 product Substances 0.000 claims description 17
- HBOMLICNUCNMMY-XLPZGREQSA-N zidovudine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](N=[N+]=[N-])C1 HBOMLICNUCNMMY-XLPZGREQSA-N 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 13
- 231100000419 toxicity Toxicity 0.000 claims description 12
- 230000001988 toxicity Effects 0.000 claims description 12
- 229940035893 uracil Drugs 0.000 claims description 11
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 claims description 10
- 230000001575 pathological effect Effects 0.000 claims description 8
- KFSPSGWABMNFIY-UHFFFAOYSA-N 1-(2-hydroxyethoxymethyl)-5-phenylselanylpyrimidine-2,4-dione Chemical compound O=C1NC(=O)N(COCCO)C=C1[Se]C1=CC=CC=C1 KFSPSGWABMNFIY-UHFFFAOYSA-N 0.000 claims description 7
- YWWZCHLUQSHMCL-UHFFFAOYSA-N diphenyl diselenide Chemical compound C=1C=CC=CC=1[Se][Se]C1=CC=CC=C1 YWWZCHLUQSHMCL-UHFFFAOYSA-N 0.000 claims description 6
- XRECTZIEBJDKEO-UHFFFAOYSA-N flucytosine Chemical compound NC1=NC(=O)NC=C1F XRECTZIEBJDKEO-UHFFFAOYSA-N 0.000 claims description 6
- 229960004413 flucytosine Drugs 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- YWJXYUXIPSIOGG-UHFFFAOYSA-N 1-((2-hydroxyethoxy)methyl)-5-(phenylthio)pyrimidine-2,4(1h,3h)-dione Chemical compound O=C1NC(=O)N(COCCO)C=C1SC1=CC=CC=C1 YWJXYUXIPSIOGG-UHFFFAOYSA-N 0.000 claims description 5
- UTKBQCBAMCEBTL-UHFFFAOYSA-N 1-(2-hydroxyethoxymethyl)-5-phenylsulfanyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1N(COCCO)C(=O)NC(=O)C1SC1=CC=CC=C1 UTKBQCBAMCEBTL-UHFFFAOYSA-N 0.000 claims description 5
- OUAPULXYUWUOHW-UHFFFAOYSA-N 1-(ethoxymethyl)-5-fluoropyrimidine-2,4-dione Chemical compound CCOCN1C=C(F)C(=O)NC1=O OUAPULXYUWUOHW-UHFFFAOYSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- PMRHGPAHIQRUBY-UHFFFAOYSA-N 2,4-bis(phenylmethoxy)-5-phenylselanylpyrimidine Chemical compound C=1C=CC=CC=1COC(N=C1OCC=2C=CC=CC=2)=NC=C1[Se]C1=CC=CC=C1 PMRHGPAHIQRUBY-UHFFFAOYSA-N 0.000 claims description 4
- KFRZFMXZIDRZJI-UHFFFAOYSA-N 5-phenylselanyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1NC(=O)NC(=O)C1[Se]C1=CC=CC=C1 KFRZFMXZIDRZJI-UHFFFAOYSA-N 0.000 claims description 4
- KRPWRQUISWCMBL-UHFFFAOYSA-N 5-phenylsulfanyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1NC(=O)NC(=O)C1SC1=CC=CC=C1 KRPWRQUISWCMBL-UHFFFAOYSA-N 0.000 claims description 4
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 claims description 4
- ZWAOHEXOSAUJHY-ZIYNGMLESA-N doxifluridine Chemical compound O[C@@H]1[C@H](O)[C@@H](C)O[C@H]1N1C(=O)NC(=O)C(F)=C1 ZWAOHEXOSAUJHY-ZIYNGMLESA-N 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims description 4
- GQERGAYPZWJSAF-UHFFFAOYSA-N 1-(2-hydroxyethoxymethyl)-5-phenylselanyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1N(COCCO)C(=O)NC(=O)C1[Se]C1=CC=CC=C1 GQERGAYPZWJSAF-UHFFFAOYSA-N 0.000 claims description 3
- ZSNNBSPEFVIUDS-SHYZEUOFSA-N 1-[(2r,4s,5s)-4-azido-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione Chemical compound C1[C@H](N=[N+]=[N-])[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C=C1 ZSNNBSPEFVIUDS-SHYZEUOFSA-N 0.000 claims description 3
- XXJGBENTLXFVFI-UHFFFAOYSA-N 1-amino-methylene Chemical compound N[CH2] XXJGBENTLXFVFI-UHFFFAOYSA-N 0.000 claims description 3
- DVGDDZUHRSIGQR-UHFFFAOYSA-N 2,4-bis(phenylmethoxy)-5-phenylsulfanylpyrimidine Chemical compound C=1C=CC=CC=1COC(N=C1OCC=2C=CC=CC=2)=NC=C1SC1=CC=CC=C1 DVGDDZUHRSIGQR-UHFFFAOYSA-N 0.000 claims description 3
- JTEGQNOMFQHVDC-RQJHMYQMSA-N 4-amino-1-[(2s,5r)-2-(hydroxymethyl)-1,3-oxathiolan-5-yl]pyrimidin-2-one Chemical compound O=C1N=C(N)C=CN1[C@@H]1O[C@H](CO)SC1 JTEGQNOMFQHVDC-RQJHMYQMSA-N 0.000 claims description 3
- ZEGGHGSNGZPEHQ-UHFFFAOYSA-N 5-phenylselanyl-1h-pyrimidine-2,4-dione Chemical compound O=C1NC(=O)NC=C1[Se]C1=CC=CC=C1 ZEGGHGSNGZPEHQ-UHFFFAOYSA-N 0.000 claims description 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 3
- UXCAQJAQSWSNPQ-XLPZGREQSA-N Alovudine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](F)C1 UXCAQJAQSWSNPQ-XLPZGREQSA-N 0.000 claims description 3
- XQSPYNMVSIKCOC-NTSWFWBYSA-N Emtricitabine Chemical compound C1=C(F)C(N)=NC(=O)N1[C@H]1O[C@@H](CO)SC1 XQSPYNMVSIKCOC-NTSWFWBYSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 3
- 230000004962 physiological condition Effects 0.000 claims description 3
- 239000007858 starting material Substances 0.000 claims description 3
- PJFNWHZWZAJIND-UHFFFAOYSA-N 1-(ethoxymethyl)-5-phenylselanylpyrimidine-2,4-dione Chemical compound O=C1NC(=O)N(COCC)C=C1[Se]C1=CC=CC=C1 PJFNWHZWZAJIND-UHFFFAOYSA-N 0.000 claims description 2
- QBEIABZPRBJOFU-CAHLUQPWSA-N 4-amino-5-fluoro-1-[(2r,5s)-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one Chemical compound C1=C(F)C(N)=NC(=O)N1[C@@H]1O[C@H](CO)CC1 QBEIABZPRBJOFU-CAHLUQPWSA-N 0.000 claims description 2
- LQLQRFGHAALLLE-UHFFFAOYSA-N 5-bromouracil Chemical compound BrC1=CNC(=O)NC1=O LQLQRFGHAALLLE-UHFFFAOYSA-N 0.000 claims description 2
- 229910019213 POCl3 Inorganic materials 0.000 claims description 2
- 238000003776 cleavage reaction Methods 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
- 230000007017 scission Effects 0.000 claims description 2
- LFQULJPVXNYWAG-UHFFFAOYSA-N sodium;phenylmethanolate Chemical compound [Na]OCC1=CC=CC=C1 LFQULJPVXNYWAG-UHFFFAOYSA-N 0.000 claims description 2
- 230000002194 synthesizing effect Effects 0.000 claims description 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 3
- 150000005700 bromopyrimidines Chemical class 0.000 claims 2
- ALJMTFKADFATPR-UHFFFAOYSA-N 1-(ethoxymethyl)-5-phenylselanyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1N(COCC)C(=O)NC(=O)C1[Se]C1=CC=CC=C1 ALJMTFKADFATPR-UHFFFAOYSA-N 0.000 claims 1
- OBLYJXPGYXRQKK-UHFFFAOYSA-N 4-phenylpyrimidine-2-selenol Chemical compound C1(=CC=CC=C1)C1=NC(=NC=C1)[SeH] OBLYJXPGYXRQKK-UHFFFAOYSA-N 0.000 claims 1
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- 229910052711 selenium Inorganic materials 0.000 abstract 1
- DRTQHJPVMGBUCF-XVFCMESISA-N Uridine Chemical class O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-XVFCMESISA-N 0.000 description 95
- DRTQHJPVMGBUCF-PSQAKQOGSA-N beta-L-uridine Natural products O[C@H]1[C@@H](O)[C@H](CO)O[C@@H]1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-PSQAKQOGSA-N 0.000 description 47
- DRTQHJPVMGBUCF-UHFFFAOYSA-N uracil arabinoside Natural products OC1C(O)C(CO)OC1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-UHFFFAOYSA-N 0.000 description 47
- 229940045145 uridine Drugs 0.000 description 47
- 150000003230 pyrimidines Chemical class 0.000 description 22
- 230000015572 biosynthetic process Effects 0.000 description 19
- 230000001965 increasing effect Effects 0.000 description 14
- 238000003786 synthesis reaction Methods 0.000 description 14
- CSRZQMIRAZTJOY-UHFFFAOYSA-N trimethylsilyl iodide Chemical compound C[Si](C)(C)I CSRZQMIRAZTJOY-UHFFFAOYSA-N 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
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- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical class C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 239000000367 immunologic factor Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000007972 injectable composition Substances 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 229940079322 interferon Drugs 0.000 description 1
- 230000037041 intracellular level Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 1
- 238000006138 lithiation reaction Methods 0.000 description 1
- 230000008818 liver damage Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000036210 malignancy Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 1
- 230000003278 mimic effect Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 238000007040 multi-step synthesis reaction Methods 0.000 description 1
- 210000004165 myocardium Anatomy 0.000 description 1
- 230000007135 neurotoxicity Effects 0.000 description 1
- 231100000228 neurotoxicity Toxicity 0.000 description 1
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 1
- 230000036963 noncompetitive effect Effects 0.000 description 1
- 229940127073 nucleoside analogue Drugs 0.000 description 1
- 108010009099 nucleoside phosphorylase Proteins 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000007968 orange flavor Substances 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 229960003742 phenol Drugs 0.000 description 1
- 208000001297 phlebitis Diseases 0.000 description 1
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 description 1
- 231100000683 possible toxicity Toxicity 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 238000002731 protein assay Methods 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000004147 pyrimidine metabolism Effects 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 238000011146 sterile filtration Methods 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 230000009747 swallowing Effects 0.000 description 1
- WFWLQNSHRPWKFK-ZCFIWIBFSA-N tegafur Chemical compound O=C1NC(=O)C(F)=CN1[C@@H]1OCCC1 WFWLQNSHRPWKFK-ZCFIWIBFSA-N 0.000 description 1
- 229960001674 tegafur Drugs 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000004797 therapeutic response Effects 0.000 description 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
- 229940033663 thimerosal Drugs 0.000 description 1
- 230000036967 uncompetitive effect Effects 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000009777 vacuum freeze-drying Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 230000029812 viral genome replication Effects 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 239000009637 wintergreen oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/60—Three or more oxygen or sulfur atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/146,838 US5476855A (en) | 1993-11-02 | 1993-11-02 | Enzyme inhibitors, their synthesis and methods for use |
| PCT/US1994/011173 WO1995012400A1 (en) | 1993-11-02 | 1994-09-30 | Novel enzyme inhibitors, their synthesis, and methods for use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69426423D1 DE69426423D1 (de) | 2001-01-18 |
| DE69426423T2 true DE69426423T2 (de) | 2001-07-12 |
Family
ID=22519188
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69426423T Expired - Lifetime DE69426423T2 (de) | 1993-11-02 | 1994-09-30 | NEUE HEMMER VON URIDINPHOSPHORYLASE (UrdPase) UND DIHYDROURACILDEHYDROGENASE (DHUDase) |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US5476855A (https=) |
| EP (1) | EP0725641B1 (https=) |
| JP (1) | JP3621102B2 (https=) |
| AT (1) | ATE198046T1 (https=) |
| AU (1) | AU699914B2 (https=) |
| DE (1) | DE69426423T2 (https=) |
| ES (1) | ES2155093T3 (https=) |
| PT (1) | PT725641E (https=) |
| WO (1) | WO1995012400A1 (https=) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5476855A (en) * | 1993-11-02 | 1995-12-19 | Mahmoud H. el Kouni | Enzyme inhibitors, their synthesis and methods for use |
| EP0748316B1 (en) * | 1994-02-28 | 2002-05-08 | Sunkyong Industries Co., Ltd. | Pyrimidine acyclonucleoside derivatives |
| US5811073A (en) * | 1995-06-19 | 1998-09-22 | President And Fellows Of Harvard College | Method for radioisotopic detection and localization of inflammation in a host |
| US5719132A (en) * | 1996-06-27 | 1998-02-17 | Bristol-Myers Squibb Company | Compositions and methods of treating HIV with d4T, 5-fluorouracil/tegafur, and uracil |
| US6306909B1 (en) | 1997-03-12 | 2001-10-23 | Queen's University At Kingston | Anti-epileptogenic agents |
| US6177437B1 (en) * | 1998-09-04 | 2001-01-23 | University Of Massachusetts Medical Center | Inhibitors of Herpes Simplex virus uracil-DNA glycosylase |
| WO2001055119A2 (en) * | 2000-01-25 | 2001-08-02 | Neurocrine Biosciences, Inc. | Gonadotropin-releasing hormone receptor antagonists and methods relating thereto |
| US7501429B2 (en) * | 2001-04-11 | 2009-03-10 | Queen's University At Kingston | Pyrimidine compounds as anti-ictogenic and/or anti-epileptogenic agents |
| JP2004536071A (ja) * | 2001-05-25 | 2004-12-02 | クイーンズ ユニバーシティ アット キングストン | 複素環ベータアミノ酸およびそれらの抗癲癇誘発剤としての使用 |
| US8592421B2 (en) * | 2003-08-04 | 2013-11-26 | Valery Khazhmuratovich Zhilov | Cyclic bioisosters of purine system derivatives and a pharmaceutical composition based thereon |
| JP2008521930A (ja) * | 2004-12-03 | 2008-06-26 | アドヘレックス テクノロジーズ， インコーポレイテッド | ５−ｆｕおよび５−ｆｕプロドラッグと併用してｄｐｄ阻害物質を投与するための方法 |
| US20100158967A1 (en) * | 2005-05-24 | 2010-06-24 | Ted Reid | Selenium-based biocidal formulations and methods of use thereof |
| WO2007008293A2 (en) * | 2005-05-24 | 2007-01-18 | Selenium, Ltd. | Selenium-based biocidal formulations and methods of use thereof |
| US20100158966A1 (en) * | 2005-05-24 | 2010-06-24 | Ted Reid | Selenium-based biocidal formulations and methods of use thereof |
| US9370187B2 (en) | 2005-05-24 | 2016-06-21 | Selenium, Ltd. | Selenium-based biocidal formulations and methods of use thereof |
| WO2007024863A2 (en) * | 2005-08-22 | 2007-03-01 | Melior Discovery, Inc. | Methods and formulations for modulating lyn kinase activity and treating related disorders |
| BRPI0807928A2 (pt) * | 2007-02-20 | 2014-07-08 | Melior Pharmaceuticals I Inc | Métodos para identificar um ativador de lyn quinase, e para tratar diabetes em um humano, kit, e, composição |
| CA2693809A1 (en) * | 2007-07-23 | 2009-01-29 | Melior Discovery, Inc. | Methods of activating irs-1 and akt |
| CN102014919B (zh) | 2008-03-03 | 2015-02-25 | 托斯克公司 | 减少毒性的甲氨蝶呤佐剂及其使用方法 |
| US8552184B2 (en) * | 2008-07-03 | 2013-10-08 | Melior Pharmaceuticals I, Inc. | Compounds and methods for treating disorders related to glucose metabolism |
| WO2010080086A1 (en) * | 2009-01-12 | 2010-07-15 | Selenium, Ltd. | Anti-microbial orthodontic compositions and appliances and methods of production and use thereof |
| JP2013508293A (ja) * | 2009-10-14 | 2013-03-07 | アドヘレックス テクノロジーズ， インコーポレイテッド | ５−ｆｕ又はそのプロドラッグと、ｄｐｄ阻害剤との組合せに付随した神経毒性の処置 |
| US20130158055A1 (en) | 2010-05-28 | 2013-06-20 | Andrew G. Reaume | Prevention Of Pancreatic Beta Cell Degeneration |
| KR102634575B1 (ko) | 2017-04-10 | 2024-02-06 | 멜리어 파마슈티칼스 아이, 인코포레이티드 | 지방세포의 처리 |
| US11446303B2 (en) | 2019-06-21 | 2022-09-20 | Tosk, Inc. | Uridine phosphorylase (UPase) inhibitors for treatment of liver conditions |
| WO2025260023A1 (en) * | 2024-06-14 | 2025-12-18 | Spiral Therapeutics, Inc. | Methods of treating otic disorders |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3755295A (en) * | 1969-10-24 | 1973-08-28 | Syntex Corp | 1-(2-amino-2-deoxy-{62 -d-ribofuranosyl) pyrimidines and derivatives thereof |
| US3687931A (en) * | 1970-03-19 | 1972-08-29 | Syntex Corp | Halogenated purine and pyrimidine nucleosides and process therefor |
| JPS5738774A (en) * | 1980-08-19 | 1982-03-03 | Chugai Pharmaceut Co Ltd | Uracil derivative and its preparation |
| US4868187A (en) * | 1980-09-16 | 1989-09-19 | Syntex (U.S.A.) Inc. | Anti-viral N-substituted pyrimidines |
| US4613604A (en) * | 1985-07-31 | 1986-09-23 | Brown University Research Foundation | Hydroxymethyl derivatives of 5-benzylacyclouridine and 5-benzoyloxybenzylacyclouridine and their use as potentiators for 5-fluoro-2'-deoxyuridine |
| WO1989009213A1 (fr) * | 1988-03-31 | 1989-10-05 | Mitsubishi Kasei Corporation | Derives de nucleoside de pyrimidine acyclique substitue en 6 et agents antiviraux contenant ces composes en tant qu'ingredients actifs |
| US5077280A (en) * | 1988-04-12 | 1991-12-31 | Brown University Research Foundation | Treatment of viral infections |
| EP0449726B1 (en) * | 1990-03-29 | 1997-06-11 | Mitsubishi Chemical Corporation | Pyrimidine nucleoside derivative and antiviral agent containing the derivative as active ingredient |
| US5141943A (en) * | 1990-04-12 | 1992-08-25 | Brown University Research Foundation | 5-benzyl barbiturate derivatives |
| US5476855A (en) * | 1993-11-02 | 1995-12-19 | Mahmoud H. el Kouni | Enzyme inhibitors, their synthesis and methods for use |
| KR0151811B1 (ko) * | 1993-12-21 | 1998-10-15 | 강박광 | 신규한 항바이러스성 2,4-피리미딘디온 유도체 및 그의 제조방법 |
-
1993
- 1993-11-02 US US08/146,838 patent/US5476855A/en not_active Ceased
-
1994
- 1994-09-30 AT AT94929398T patent/ATE198046T1/de not_active IP Right Cessation
- 1994-09-30 JP JP51321195A patent/JP3621102B2/ja not_active Expired - Fee Related
- 1994-09-30 AU AU78476/94A patent/AU699914B2/en not_active Ceased
- 1994-09-30 ES ES94929398T patent/ES2155093T3/es not_active Expired - Lifetime
- 1994-09-30 WO PCT/US1994/011173 patent/WO1995012400A1/en not_active Ceased
- 1994-09-30 EP EP94929398A patent/EP0725641B1/en not_active Expired - Lifetime
- 1994-09-30 PT PT94929398T patent/PT725641E/pt unknown
- 1994-09-30 DE DE69426423T patent/DE69426423T2/de not_active Expired - Lifetime
-
1995
- 1995-06-06 US US08/466,470 patent/US5721241A/en not_active Expired - Lifetime
-
1997
- 1997-12-01 US US08/980,629 patent/USRE37623E1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP0725641A1 (en) | 1996-08-14 |
| JPH09507054A (ja) | 1997-07-15 |
| AU7847694A (en) | 1995-05-23 |
| DE69426423D1 (de) | 2001-01-18 |
| PT725641E (pt) | 2001-05-31 |
| EP0725641A4 (https=) | 1996-09-04 |
| ES2155093T3 (es) | 2001-05-01 |
| JP3621102B2 (ja) | 2005-02-16 |
| US5476855A (en) | 1995-12-19 |
| WO1995012400A1 (en) | 1995-05-11 |
| ATE198046T1 (de) | 2000-12-15 |
| AU699914B2 (en) | 1998-12-17 |
| US5721241A (en) | 1998-02-24 |
| EP0725641B1 (en) | 2000-12-13 |
| USRE37623E1 (en) | 2002-04-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |