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TG4103
10-Hydroxy Camptothecin has shown promising activity against a range of tumour types. This CPT derivative causes cell toxicity by stabilizing a ternary complex between the nuclear enzyme topoisomerase I (topo I) and double-stranded DNA, leading to single and double strand breaks. TopoGEN provides this reagent as a control poison/inhibitor of topoisomerase I.
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TG4104
9-Amino-20-(R,S)-camptothecin (also known as 9-amino campthecin) is an analogue of camptothecin.  Like other CPT congeners, it shows some promising activity against a range of tumor types.  This compound causes cell toxicity by stabilizing a ternary complex between the nuclear enzyme topoisomerase I (topo I) and double-stranded DNA, leading to single and double strand breaks.  TopoGEN provides this reagent as a control poison/inhibitor of topoisomerase I.
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TG4102
20(S)camptothecin has shown promising activity against a range of tumour types.  This CPT derivative causes cell toxicity by stabilizing a ternary complex between the nuclear enzyme topoisomerase I (topo I) and double-stranded DNA, leading to single and double strand breaks.  TopoGEN provides this reagent as a control poison/inhibitor of topoisomerase I.
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TG4110
Camptothecin is a topo I poison that both inhibits enzyme activity and stabilizes formation of topo I cleavage complexes (Hsiang et al J. Biol. Chem. 260:14873-14878, 1985).  TopoGEN provides this reagent as a control inhibitor/poison of topoisomerase I.  
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TG4100
Hycamtin (topotecan hydrochloride) is a semi-synthetic derivative of camptothecin and is an anti-tumor drug that targets topo I and is a topo I poison (induces cleavage complexes).
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