EC Number |
Inhibitors |
Structure |
---|
2.7.7.31 | (1R,2S)-1-(6-aminopurin-9-yl)-2-(Hydroxymethyl)cyclopentane |
- |
|
2.7.7.31 | (E)-5-(2-bromovinyl)-2'-deoxyuridine 5'-triphosphate |
- |
|
2.7.7.31 | 1,10-phenanthroline |
not m-isomer |
|
2.7.7.31 | 2',3'-dideoxyadenosine |
inhibition is stronger with (dA)12-18 as primer than with heat denatured DNA, substrate ATP, 50% inhibition at 0.006 mM |
|
2.7.7.31 | 2',3'-dideoxycytidine |
inhibition is stronger with (dA)12-18 as primer than with heat denatured DNA, substrate CTP, 50% inhibition at 0.002 mM |
|
2.7.7.31 | 2',3'-dideoxyguanosine |
inhibition is stronger with (dA)12-18 as primer than with heat denatured DNA, substrate GTP, 50% inhibition at 0.005 mM |
|
2.7.7.31 | 2',3'-dideoxythymidine |
inhibition is stronger with (dA)12-18 as primer than with heat denatured DNA, substrate TTP, 50% inhibition at 0.020 mM |
|
2.7.7.31 | 2',3'-dideoxythymidine 5'-triphosphate |
- |
|
2.7.7.31 | 2,2'-dipyridyl |
- |
|
2.7.7.31 | 3'-azido-TTP |
- |
|