NZ551506A - Method and reagent for measuring nitroreductase enzyme activity - Google Patents
Method and reagent for measuring nitroreductase enzyme activityInfo
- Publication number
- NZ551506A NZ551506A NZ551506A NZ55150605A NZ551506A NZ 551506 A NZ551506 A NZ 551506A NZ 551506 A NZ551506 A NZ 551506A NZ 55150605 A NZ55150605 A NZ 55150605A NZ 551506 A NZ551506 A NZ 551506A
- Authority
- NZ
- New Zealand
- Prior art keywords
- nitroreductase
- group
- dye
- cell
- methyl
- Prior art date
Links
- 108020001162 nitroreductase Proteins 0.000 title claims abstract description 84
- 102000004459 Nitroreductase Human genes 0.000 title claims abstract description 74
- 238000000034 method Methods 0.000 title claims abstract description 48
- 230000000694 effects Effects 0.000 title claims abstract description 40
- 239000003153 chemical reaction reagent Substances 0.000 title description 7
- 210000004027 cell Anatomy 0.000 claims abstract description 94
- IHXWECHPYNPJRR-UHFFFAOYSA-N 3-hydroxycyclobut-2-en-1-one Chemical compound OC1=CC(=O)C1 IHXWECHPYNPJRR-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000000203 mixture Substances 0.000 claims abstract description 37
- 230000014509 gene expression Effects 0.000 claims abstract description 24
- 230000008859 change Effects 0.000 claims abstract description 21
- 230000003287 optical effect Effects 0.000 claims abstract description 13
- 238000001727 in vivo Methods 0.000 claims abstract description 7
- 210000005260 human cell Anatomy 0.000 claims abstract description 5
- 238000002156 mixing Methods 0.000 claims abstract description 3
- 108020004707 nucleic acids Proteins 0.000 claims abstract description 3
- 102000039446 nucleic acids Human genes 0.000 claims abstract description 3
- 150000007523 nucleic acids Chemical class 0.000 claims abstract description 3
- 239000000975 dye Substances 0.000 claims description 84
- 150000001875 compounds Chemical class 0.000 claims description 71
- 239000003795 chemical substances by application Substances 0.000 claims description 29
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
- 238000012360 testing method Methods 0.000 claims description 20
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 13
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 9
- 239000005864 Sulphur Substances 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- -1 di-substituted nitrobenzyl Chemical group 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 150000002431 hydrogen Chemical group 0.000 claims description 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 7
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical group O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 claims description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- 238000012216 screening Methods 0.000 claims description 5
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical group O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 1
- 239000000758 substrate Substances 0.000 description 37
- 238000002360 preparation method Methods 0.000 description 29
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 27
- 238000003556 assay Methods 0.000 description 27
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 24
- 239000000047 product Substances 0.000 description 20
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 19
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 17
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 16
- 239000000463 material Substances 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 14
- 239000002609 medium Substances 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 239000007787 solid Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 10
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 10
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 239000012298 atmosphere Substances 0.000 description 9
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 9
- 229910001868 water Inorganic materials 0.000 description 9
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 8
- 108700008625 Reporter Genes Proteins 0.000 description 8
- 229940117389 dichlorobenzene Drugs 0.000 description 8
- 238000001914 filtration Methods 0.000 description 8
- 238000003384 imaging method Methods 0.000 description 8
- 108090000623 proteins and genes Proteins 0.000 description 8
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 8
- 230000001105 regulatory effect Effects 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 230000001413 cellular effect Effects 0.000 description 7
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 7
- 238000003818 flash chromatography Methods 0.000 description 7
- 239000002953 phosphate buffered saline Substances 0.000 description 7
- 238000002390 rotary evaporation Methods 0.000 description 7
- PWEBUXCTKOWPCW-UHFFFAOYSA-N squaric acid Chemical compound OC1=C(O)C(=O)C1=O PWEBUXCTKOWPCW-UHFFFAOYSA-N 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- 210000000805 cytoplasm Anatomy 0.000 description 6
- 238000001840 matrix-assisted laser desorption--ionisation time-of-flight mass spectrometry Methods 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 6
- 238000004007 reversed phase HPLC Methods 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000001890 transfection Methods 0.000 description 6
- 239000000556 agonist Substances 0.000 description 5
- 210000000170 cell membrane Anatomy 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000011534 incubation Methods 0.000 description 5
- 230000000873 masking effect Effects 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 210000002966 serum Anatomy 0.000 description 5
- 210000001519 tissue Anatomy 0.000 description 5
- UOGHZHPESMATDD-UHFFFAOYSA-N 5-methoxy-2,3,3-trimethylindole Chemical compound COC1=CC=C2N=C(C)C(C)(C)C2=C1 UOGHZHPESMATDD-UHFFFAOYSA-N 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 102000004142 Trypsin Human genes 0.000 description 4
- 108090000631 Trypsin Proteins 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000005284 excitation Effects 0.000 description 4
- 239000012528 membrane Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 239000012588 trypsin Substances 0.000 description 4
- 239000013598 vector Substances 0.000 description 4
- OANMSBREGBCZMM-UHFFFAOYSA-M 1-[(3,5-dinitrophenyl)methyl]-2,3,3-trimethylindol-1-ium;iodide Chemical compound [I-].C12=CC=CC=C2C(C)(C)C(C)=[N+]1CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 OANMSBREGBCZMM-UHFFFAOYSA-M 0.000 description 3
- 108020004414 DNA Proteins 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 3
- 229930182816 L-glutamine Natural products 0.000 description 3
- 108010057466 NF-kappa B Proteins 0.000 description 3
- 102000003945 NF-kappa B Human genes 0.000 description 3
- 206010028980 Neoplasm Diseases 0.000 description 3
- 241000700605 Viruses Species 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 244000309466 calf Species 0.000 description 3
- 239000006285 cell suspension Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical group C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
- 230000004807 localization Effects 0.000 description 3
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- 239000012679 serum free medium Substances 0.000 description 3
- 239000003039 volatile agent Substances 0.000 description 3
- LSWBGEANPGMYSI-UHFFFAOYSA-M 1,2-dimethyl-6-nitroquinolin-1-ium;iodide Chemical compound [I-].C1=C([N+]([O-])=O)C=CC2=[N+](C)C(C)=CC=C21 LSWBGEANPGMYSI-UHFFFAOYSA-M 0.000 description 2
- HUXJXNSHCKHFIL-UHFFFAOYSA-N 1-(2-bromoethoxy)-2-methoxyethane Chemical compound COCCOCCBr HUXJXNSHCKHFIL-UHFFFAOYSA-N 0.000 description 2
- FFBQMQQSEARMDA-UHFFFAOYSA-M 1-[(3,5-dinitrophenyl)methyl]-5-methoxy-2,3,3-trimethylindol-1-ium;iodide Chemical compound [I-].C=1C(OC)=CC=C2C=1C(C)(C)C(C)=[N+]2CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 FFBQMQQSEARMDA-UHFFFAOYSA-M 0.000 description 2
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 2
- FLHJIAFUWHPJRT-UHFFFAOYSA-N 2,3,3-trimethylindole Chemical compound C1=CC=C2C(C)(C)C(C)=NC2=C1 FLHJIAFUWHPJRT-UHFFFAOYSA-N 0.000 description 2
- DXYYSGDWQCSKKO-UHFFFAOYSA-N 2-methylbenzothiazole Chemical compound C1=CC=C2SC(C)=NC2=C1 DXYYSGDWQCSKKO-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKKJLVBELUTLKV-MZCSYVLQSA-N Deuterated methanol Chemical compound [2H]OC([2H])([2H])[2H] OKKJLVBELUTLKV-MZCSYVLQSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 210000004102 animal cell Anatomy 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 201000011510 cancer Diseases 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000013553 cell monolayer Substances 0.000 description 2
- 239000013058 crude material Substances 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000006911 enzymatic reaction Methods 0.000 description 2
- 238000001952 enzyme assay Methods 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000000799 fluorescence microscopy Methods 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine group Chemical group N1=CCC2=CC=CC=C12 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 230000003834 intracellular effect Effects 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 210000004962 mammalian cell Anatomy 0.000 description 2
- CPRRHERYRRXBRZ-SRVKXCTJSA-N methyl n-[(2s)-1-[[(2s)-1-hydroxy-3-[(3s)-2-oxopyrrolidin-3-yl]propan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]carbamate Chemical group COC(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CO)C[C@@H]1CCNC1=O CPRRHERYRRXBRZ-SRVKXCTJSA-N 0.000 description 2
- 238000010369 molecular cloning Methods 0.000 description 2
- 210000003463 organelle Anatomy 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 230000001935 permeabilising effect Effects 0.000 description 2
- 239000013600 plasmid vector Substances 0.000 description 2
- 238000003752 polymerase chain reaction Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 238000012552 review Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000013518 transcription Methods 0.000 description 2
- 230000035897 transcription Effects 0.000 description 2
- 230000002103 transcriptional effect Effects 0.000 description 2
- 238000010361 transduction Methods 0.000 description 2
- 230000026683 transduction Effects 0.000 description 2
- 230000010474 transient expression Effects 0.000 description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
- 230000003612 virological effect Effects 0.000 description 2
- BRZYSWJRSDMWLG-DJWUNRQOSA-N (2r,3r,4r,5r)-2-[(1s,2s,3r,4s,6r)-4,6-diamino-3-[(2s,3r,4r,5s,6r)-3-amino-4,5-dihydroxy-6-[(1r)-1-hydroxyethyl]oxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-5-methyl-4-(methylamino)oxane-3,5-diol Chemical compound O1C[C@@](O)(C)[C@H](NC)[C@@H](O)[C@H]1O[C@@H]1[C@@H](O)[C@H](O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H]([C@@H](C)O)O2)N)[C@@H](N)C[C@H]1N BRZYSWJRSDMWLG-DJWUNRQOSA-N 0.000 description 1
- FQHCPFMTXFJZJS-UHFFFAOYSA-N (4-methoxyphenyl)hydrazine;hydrochloride Chemical compound Cl.COC1=CC=C(NN)C=C1 FQHCPFMTXFJZJS-UHFFFAOYSA-N 0.000 description 1
- INJBXCHXYYOKAF-UHFFFAOYSA-N (4Z)-4-[[1-(5-carboxypentyl)-3,3-dimethylbenzo[g]indol-1-ium-2-yl]methylidene]-2-[(E)-[1-[(3,5-dinitrophenyl)methyl]-3,3-dimethylindol-2-ylidene]methyl]-3-oxocyclobuten-1-olate Chemical compound C12=CC=CC=C2C(C)(C)\C(=C/C=2C(\C(=C/C=3C(C4=C(C5=CC=CC=C5C=C4)[N+]=3CCCCCC(O)=O)(C)C)\C=2[O-])=O)N1CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 INJBXCHXYYOKAF-UHFFFAOYSA-N 0.000 description 1
- JTHSKDDWUNXYIM-UHFFFAOYSA-M 1,2,3-trimethyl-3h-indol-1-ium;iodide Chemical compound [I-].C1=CC=C2C(C)C(C)=[N+](C)C2=C1 JTHSKDDWUNXYIM-UHFFFAOYSA-M 0.000 description 1
- IMINZNDLTTVURA-UHFFFAOYSA-N 1-(iodomethyl)-3,5-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC(CI)=CC([N+]([O-])=O)=C1 IMINZNDLTTVURA-UHFFFAOYSA-N 0.000 description 1
- KSPMXOLMFBUXDT-UHFFFAOYSA-N 1-[(3,5-dinitrophenyl)methyl]-3,3-dimethylindol-1-ium Chemical compound CC1(C)[CH+]N(CC2=CC(=CC(=C2)[N+]([O-])=O)[N+]([O-])=O)C2=CC=CC=C12 KSPMXOLMFBUXDT-UHFFFAOYSA-N 0.000 description 1
- CHZQITPCINTISY-UHFFFAOYSA-M 1-[2-(2-methoxyethoxy)ethyl]-2,3,3-trimethylindol-1-ium;bromide Chemical compound [Br-].C1=CC=C2[N+](CCOCCOC)=C(C)C(C)(C)C2=C1 CHZQITPCINTISY-UHFFFAOYSA-M 0.000 description 1
- WUYMUVBIVVABRN-UHFFFAOYSA-N 1-[[4-[4-amino-5-(3-methoxyphenyl)pyrrolo[2,3-d]pyrimidin-7-yl]phenyl]methyl]piperidin-4-ol Chemical group COC1=CC=CC(C=2C3=C(N)N=CN=C3N(C=3C=CC(CN4CCC(O)CC4)=CC=3)C=2)=C1 WUYMUVBIVVABRN-UHFFFAOYSA-N 0.000 description 1
- NJGSRFQZESCHAA-UHFFFAOYSA-M 1-ethyl-5-methoxy-2,3,3-trimethylindol-1-ium;iodide Chemical compound [I-].COC1=CC=C2[N+](CC)=C(C)C(C)(C)C2=C1 NJGSRFQZESCHAA-UHFFFAOYSA-M 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- AZNKMUGIRVLVAD-UHFFFAOYSA-N 2,3,3-trimethyl-1-(4-sulfobutyl)indol-1-ium-5-sulfonate Chemical compound C1=C(S(O)(=O)=O)C=C2C(C)(C)C(C)=[N+](CCCCS([O-])(=O)=O)C2=C1 AZNKMUGIRVLVAD-UHFFFAOYSA-N 0.000 description 1
- HZTPKMIMXLTOSK-UHFFFAOYSA-N 2-bromohexanoic acid Chemical compound CCCCC(Br)C(O)=O HZTPKMIMXLTOSK-UHFFFAOYSA-N 0.000 description 1
- YAQKYKGFPQPPQE-UHFFFAOYSA-N 2-methyl-6-nitro-1,3-benzothiazole Chemical compound C1=C([N+]([O-])=O)C=C2SC(C)=NC2=C1 YAQKYKGFPQPPQE-UHFFFAOYSA-N 0.000 description 1
- DXDPHHQJZWWAEH-UHFFFAOYSA-N 2-methyl-6-nitroquinoline Chemical compound C1=C([N+]([O-])=O)C=CC2=NC(C)=CC=C21 DXDPHHQJZWWAEH-UHFFFAOYSA-N 0.000 description 1
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 1
- JJTONRSDXLRCIB-UHFFFAOYSA-M 3-ethyl-2-methyl-6-nitro-1,3-benzothiazol-3-ium;iodide Chemical compound [I-].[O-][N+](=O)C1=CC=C2[N+](CC)=C(C)SC2=C1 JJTONRSDXLRCIB-UHFFFAOYSA-M 0.000 description 1
- OOYJYKUIXISCBG-UHFFFAOYSA-N 6-(1,1,2-trimethylbenzo[e]indol-3-ium-3-yl)hexanoic acid;iodide Chemical compound [I-].C1=CC=CC2=C(C(C(C)=[N+]3CCCCCC(O)=O)(C)C)C3=CC=C21 OOYJYKUIXISCBG-UHFFFAOYSA-N 0.000 description 1
- DCUHPQGXEYMLAA-UHFFFAOYSA-N 6-(2,3,3-trimethylindol-1-ium-1-yl)hexanoic acid;iodide Chemical compound [I-].C1=CC=C2C(C)(C)C(C)=[N+](CCCCCC(O)=O)C2=C1 DCUHPQGXEYMLAA-UHFFFAOYSA-N 0.000 description 1
- MXBLNJHSCCLLQV-UHFFFAOYSA-N 6-(2,3-dimethylindol-3-yl)hexanoic acid Chemical compound C1=CC=C2C(CCCCCC(O)=O)(C)C(C)=NC2=C1 MXBLNJHSCCLLQV-UHFFFAOYSA-N 0.000 description 1
- GEYZCYGWDQYAKU-UHFFFAOYSA-N 6-(5-methoxy-2,3,3-trimethylindol-1-ium-1-yl)hexanoic acid;bromide Chemical compound [Br-].COC1=CC=C2[N+](CCCCCC(O)=O)=C(C)C(C)(C)C2=C1 GEYZCYGWDQYAKU-UHFFFAOYSA-N 0.000 description 1
- NVRVNSHHLPQGCU-UHFFFAOYSA-N 6-bromohexanoic acid Chemical compound OC(=O)CCCCCBr NVRVNSHHLPQGCU-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 102000011724 DNA Repair Enzymes Human genes 0.000 description 1
- 108010076525 DNA Repair Enzymes Proteins 0.000 description 1
- 230000005778 DNA damage Effects 0.000 description 1
- 231100000277 DNA damage Toxicity 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 102000003688 G-Protein-Coupled Receptors Human genes 0.000 description 1
- 108090000045 G-Protein-Coupled Receptors Proteins 0.000 description 1
- 108090000604 Hydrolases Proteins 0.000 description 1
- 102000004157 Hydrolases Human genes 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 102000043136 MAP kinase family Human genes 0.000 description 1
- 108091054455 MAP kinase family Proteins 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 108091027981 Response element Proteins 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 108700025695 Suppressor Genes Proteins 0.000 description 1
- 108700012920 TNF Proteins 0.000 description 1
- 108091023040 Transcription factor Proteins 0.000 description 1
- 102000040945 Transcription factor Human genes 0.000 description 1
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 1
- 239000013504 Triton X-100 Substances 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 108060008682 Tumor Necrosis Factor Proteins 0.000 description 1
- 102100040247 Tumor necrosis factor Human genes 0.000 description 1
- YEUPDJCHNCOAHU-UHFFFAOYSA-N [iodo(dinitro)methyl]benzene Chemical compound [N+](=O)([O-])C(C1=CC=CC=C1)([N+](=O)[O-])I YEUPDJCHNCOAHU-UHFFFAOYSA-N 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- NHYXMAKLBXBVEO-UHFFFAOYSA-N bromomethyl acetate Chemical compound CC(=O)OCBr NHYXMAKLBXBVEO-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 238000000423 cell based assay Methods 0.000 description 1
- 239000002771 cell marker Substances 0.000 description 1
- 230000030570 cellular localization Effects 0.000 description 1
- 230000033077 cellular process Effects 0.000 description 1
- 230000036755 cellular response Effects 0.000 description 1
- 230000005754 cellular signaling Effects 0.000 description 1
- 230000004700 cellular uptake Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000002299 complementary DNA Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940125810 compound 20 Drugs 0.000 description 1
- 229940125846 compound 25 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- 230000001086 cytosolic effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000004520 electroporation Methods 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 230000003511 endothelial effect Effects 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 210000002216 heart Anatomy 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 210000002443 helper t lymphocyte Anatomy 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 230000007762 localization of cell Effects 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 210000003470 mitochondria Anatomy 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 1
- BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 239000002773 nucleotide Substances 0.000 description 1
- 125000003729 nucleotide group Chemical group 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- MHYFEEDKONKGEB-UHFFFAOYSA-N oxathiane 2,2-dioxide Chemical compound O=S1(=O)CCCCO1 MHYFEEDKONKGEB-UHFFFAOYSA-N 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 230000022532 regulation of transcription, DNA-dependent Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 238000003571 reporter gene assay Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000012096 transfection reagent Substances 0.000 description 1
- 238000011820 transgenic animal model Methods 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 238000002371 ultraviolet--visible spectrum Methods 0.000 description 1
- 241000701161 unidentified adenovirus Species 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/007—Squaraine dyes
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
- C12Q1/32—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving dehydrogenase
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Immunology (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Biophysics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NZ583956A NZ583956A (en) | 2004-05-28 | 2005-05-24 | Method and reagent for measuring nitroreductase enzyme activity |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0411993.9A GB0411993D0 (en) | 2004-05-28 | 2004-05-28 | Method and reagent for measuring nitroreductase enzyme activity |
| PCT/GB2005/002057 WO2005118839A1 (en) | 2004-05-28 | 2005-05-24 | Method and reagent for measuring nitroreductase enzyme activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ551506A true NZ551506A (en) | 2010-04-30 |
Family
ID=32671256
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ551506A NZ551506A (en) | 2004-05-28 | 2005-05-24 | Method and reagent for measuring nitroreductase enzyme activity |
| NZ583956A NZ583956A (en) | 2004-05-28 | 2005-05-24 | Method and reagent for measuring nitroreductase enzyme activity |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ583956A NZ583956A (en) | 2004-05-28 | 2005-05-24 | Method and reagent for measuring nitroreductase enzyme activity |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US7579140B2 (https=) |
| EP (1) | EP1749103B1 (https=) |
| JP (1) | JP4838239B2 (https=) |
| CN (1) | CN1993477A (https=) |
| AT (1) | ATE553215T1 (https=) |
| AU (1) | AU2005250209B2 (https=) |
| CA (2) | CA2778894C (https=) |
| GB (1) | GB0411993D0 (https=) |
| NZ (2) | NZ551506A (https=) |
| WO (1) | WO2005118839A1 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7767834B2 (en) | 2004-08-13 | 2010-08-03 | Elitech Holding B.V. | Phosphonylated fluorescent dyes and conjugates |
| EP1781675B1 (en) | 2004-08-13 | 2014-03-26 | Epoch Biosciences, Inc. | Phosphonate fluorescent dyes and conjugates |
| GB0505777D0 (en) * | 2005-03-22 | 2005-04-27 | Amersham Biosciences Uk Ltd | Enzyme detection method and reagent |
| GB0800938D0 (en) | 2008-01-18 | 2008-02-27 | Ge Healthcare Uk Ltd | Multiplex cell signalling assay |
| WO2010151592A1 (en) * | 2009-06-23 | 2010-12-29 | Bayer Healthcare Llc | System and apparatus for determining temperatures in a fluid analyte system |
| JP5535664B2 (ja) * | 2010-01-15 | 2014-07-02 | 株式会社Adeka | 色調補正剤、スクアリリウム化合物及び光学フィルター |
| US8828678B2 (en) | 2010-11-16 | 2014-09-09 | Enzo Life Sciences, Inc. | Self-immolative probes for enzyme activity detection |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5039818A (en) * | 1986-02-27 | 1991-08-13 | Syntex (U.S.A.) Inc. | Squaraine dye |
| US5403686A (en) | 1993-09-27 | 1995-04-04 | Eastman Kodak Company | Electrophotographic element and imaging method exhibiting reduced incidence of laser interference patterns |
| JP2000508709A (ja) * | 1996-04-19 | 2000-07-11 | アマーシャム・ファルマシア・バイオテック・ユーケイ・リミテッド | スクアラート染料類および蛍光配列決定法におけるそれらの使用 |
| EP1196398A4 (en) | 1999-07-06 | 2002-11-06 | Surromed Inc | BRIDGED FLUORESCENT DYES, THEIR PRODUCTION AND USE IN DETECTION METHODS |
| GB0002261D0 (en) * | 2000-02-02 | 2000-03-22 | Amersham Pharm Biotech Uk Ltd | Fluorescent detection method & reagent |
| AU2003224912A1 (en) * | 2002-04-10 | 2003-10-27 | Igor Borovoy | Dyes and fluorescent compounds |
-
2004
- 2004-05-28 GB GBGB0411993.9A patent/GB0411993D0/en not_active Ceased
-
2005
- 2005-05-24 CA CA2778894A patent/CA2778894C/en not_active Expired - Fee Related
- 2005-05-24 EP EP05746539A patent/EP1749103B1/en not_active Expired - Lifetime
- 2005-05-24 CA CA2568754A patent/CA2568754C/en not_active Expired - Fee Related
- 2005-05-24 NZ NZ551506A patent/NZ551506A/en not_active IP Right Cessation
- 2005-05-24 JP JP2007514089A patent/JP4838239B2/ja not_active Expired - Fee Related
- 2005-05-24 US US11/569,682 patent/US7579140B2/en not_active Expired - Fee Related
- 2005-05-24 CN CNA200580025476XA patent/CN1993477A/zh active Pending
- 2005-05-24 AU AU2005250209A patent/AU2005250209B2/en not_active Ceased
- 2005-05-24 AT AT05746539T patent/ATE553215T1/de active
- 2005-05-24 NZ NZ583956A patent/NZ583956A/en not_active IP Right Cessation
- 2005-05-24 WO PCT/GB2005/002057 patent/WO2005118839A1/en not_active Ceased
-
2009
- 2009-07-10 US US12/500,730 patent/US8378120B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP1749103B1 (en) | 2012-04-11 |
| ATE553215T1 (de) | 2012-04-15 |
| US20080317674A1 (en) | 2008-12-25 |
| CA2568754C (en) | 2012-08-21 |
| WO2005118839A1 (en) | 2005-12-15 |
| US7579140B2 (en) | 2009-08-25 |
| GB0411993D0 (en) | 2004-06-30 |
| AU2005250209B2 (en) | 2009-07-30 |
| JP2008500828A (ja) | 2008-01-17 |
| EP1749103A1 (en) | 2007-02-07 |
| US20090325209A1 (en) | 2009-12-31 |
| CA2778894A1 (en) | 2005-12-15 |
| CN1993477A (zh) | 2007-07-04 |
| CA2778894C (en) | 2013-12-31 |
| US8378120B2 (en) | 2013-02-19 |
| AU2005250209A1 (en) | 2005-12-15 |
| NZ583956A (en) | 2011-08-26 |
| CA2568754A1 (en) | 2005-12-15 |
| JP4838239B2 (ja) | 2011-12-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Matikonda et al. | Core remodeling leads to long wavelength fluoro-coumarins | |
| US8378120B2 (en) | Method and reagent for measuring nitroreductase enzyme activity | |
| CN100577742C (zh) | 花青染料标记试剂 | |
| EP3489324A1 (en) | Fluorescent probe and preparation method and use thereof | |
| CA2449201C (en) | Acridone derivatives as labels for fluorescence detection of target materials | |
| CA2399368C (en) | Fluorescent detection method and reagent | |
| CN103382313B (zh) | 一种萘酰亚胺荧光染料及其制备和应用 | |
| CN108484622A (zh) | 多信号荧光探针的合成及其同时区分检测Hcy、Cys和GSH的应用 | |
| Bora et al. | Diazaoxatriangulenium: synthesis of reactive derivatives and conjugation to bovine serum albumin | |
| WO2020033681A2 (en) | Silicon-substituted rhodamine dyes and dye conjugates | |
| Resa et al. | New dual fluorescent probe for simultaneous biothiol and phosphate bioimaging | |
| Koren et al. | Evaluation of Ebselen-azadioxatriangulenium as redox-sensitive fluorescent intracellular probe and as indicator within a planar redox optode | |
| Cui et al. | Effect of different substituents on the fluorescence properties of precursors of synthetic GFP analogues and a polarity-sensitive lipid droplet probe with AIE properties for imaging cells and zebrafish | |
| WO2006100417A1 (en) | Enzyme detection method and reagent | |
| US20030211454A1 (en) | Detection reagent | |
| CN116023326B (zh) | 一类氮芳基吡啶菁染料衍生物荧光探针及其制备方法和应用 | |
| EP3143400A1 (en) | Cell tracking reagents and their methods of use | |
| Wang et al. | Unsymmetrical pentamethine cyanines for visualizing physiological acidities from the whole-animal to the cellular scale with pH-responsive deep-red fluorescence | |
| Rong et al. | A bichromophoric squaraine based NIR fluorescent probe for G-quadruplex in living cells | |
| CN115716803A (zh) | 一种萘酰亚胺荧光探针及其在极性和粘度检测中的应用 | |
| Zhao et al. | Functionalized α‐Cyanostilbene Derivatives for Detection of Hypoxia or Proteostasis Imbalance in Live Cells | |
| Ghorpade et al. | N-Functionalized fluorophores: detecting urinary albumin and imaging lipid droplets | |
| CN112341411B (zh) | 一种类罗非昔布衍生物、制备的有机荧光染料骨架及用途 | |
| CN121005688B (zh) | 一种杂环化合物在作为荧光探针中的应用 | |
| CN112898228B (zh) | 基于混合组装的混合聚集体fret探针及其在检测线粒体自噬中的用途 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PSEA | Patent sealed | ||
| RENW | Renewal (renewal fees accepted) | ||
| RENW | Renewal (renewal fees accepted) | ||
| LAPS | Patent lapsed |