Topoisomerase Inhibitors

Topoisomerase Inhibitors (17)

water-soluble

Cat.No. Product Name Information Product Citations Customer Reviews
S1208 Doxorubicin (Adriamycin) Doxorubicin (Adriamycin) is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis.
S1225 Etoposide (VP-16) Etoposide is a semisynthetic derivative of podophyllotoxin, which inhibits DNA synthesis via topoisomerase II inhibition activity.
S1231 Topotecan HCl Topotecan (Hycamtin, NSC 609699) is a topoisomerase I inhibitor for MCF-7 Luc cells and DU-145 Luc cells with IC50 of 13 nM and 2 nM, respectively.
S1288 Camptothecin Camptothecin (Camptohecine, 20-(S)-Camptothecin, CPT, NSC100880) is a specific inhibitor of DNA topoisomerase I (Topo I) with IC50 of 0.68 μM.
S1198 Irinotecan Irinotecan (Camptosar, Campto, CPT-11) is a topoisomerase I inhibitor for LoVo cells and HT-29 cells with IC50 of 15.8 μM and 5.17 μM, respectively.
S4908 SN-38 SN-38 is an active metabolite of CPT-11 that inhibits DNA topoisomerase I.
S1223 Epirubicin HCl Epirubicin HCl, a semisynthetic L-arabino derivative of doxorubicin, is an antineoplastic agent by inhibiting Topoisomerase.
S2217 Irinotecan HCl Trihydrate (Campto) Irinotecan prevents DNA from unwinding by inhibition of topoisomerase 1.
S3181 Flumequine Flumequine is a synthetic chemotherapeutic antibiotic, inhibiting topoisomerase II with IC50 of 15 μM.
S1889 Mitoxantrone Mitoxantrone is a type II topoisomerase inhibitor with IC50 of 2.0 μM, 0.42 mM for HepG2 and MCF-7/wt cells, respectively
S1463 Ofloxacin (Floxin) Ofloxacin is a synthetic broad-spectrum antimicrobial agent.
S1465 Moxifloxacin HCl Moxifloxacin(Avelox, Avalox) is a fourth generation synthetic fluoroquinolone antibacterial agent.
S1393 Pirarubicin Pirarubicin is an anthracycline agent.
S1367 Amonafide Amonafide (NSC-308847) is a selective topoisomerase II inhibitor.
S1327 Ellagic acid Ellagic acid has antiproliferative and antioxidant property.
S1342 Genistein Genistein, a phytoestrogen found in soy products, is a highly specific inhibitor of protein tyrosine kinase (PTK) which blocks the mitogenic effect mediated by EGF on NIH-3T3 cells with IC50 of 12μM or by insulin with IC50 of 19 μM.
S1228 Idarubicin HCl Idarubicin HCl (Idamycin, Zavedos, 4-demethoxydaunorubicin) is a hydrochloride salt form of Idarubicin which is an anthracycline antibiotic and a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells with IC50 of 3.3 ng/mL.
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