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￥ 0.00 Topoisomerase
| Catalog No. | Inhibitor Name | Topoisomerase | Topo I | Topo II | Topo IV | Other |
|---|---|---|---|---|---|---|
| A10174 | Camptothecin | ** | ||||
| A10939 | Topotecan HCl | **** | ||||
| A10465 | Idarubicin HCl | *** | Multicellular spheroids | |||
| A10194 | Daunorubicin HCl | *** | ||||
| A11999 | Betulinic acid | ** | HIV-1,Aminopeptidase N | |||
| A11861 | Flumequine | * | ||||
| A14403 | Doxorubicin | |||||
| A10373 | Etoposide | |||||
| A10478 | Irinotecan | |||||
| A10345 | Epirubicin HCl | |||||
| A10596 | Mitoxantrone HCl | |||||
| A10609 | Moxifloxacin HCl | |||||
| A10479 | Irinotecan HCl Trihydrate | |||||
| A12011 | SN-38 | |||||
| A10071 | Amonafide | |||||
| A10907 | Teniposide | |||||
| A10419 | Gatifloxacin | |||||
| A10426 | Genistein | EGFR | ||||
| A10595 | Mitoxantrone | |||||
| A10735 | Pirarubicin | |||||
| A10041 | Adriamycin | |||||
| A10557 | Marbofloxacin | |||||
| A10666 | Ofloxacin | |||||
| A10740 | Podophyllotoxin | |||||
| A12663 | Amrubicin | |||||
| A13059 | Beta-Lapachone | IDO1 |
Notes:
1.Hover mouse over "" to view the IC50 value.(A few compounds have proven potency but without published IC50 data.)
2.For more details about the compound, click on the product name of your interest.
3.The higher the number of "" is, the more potent the inhibitor or activator is.
4."" refers to compounds which do inhibitory effects on the related isoform, but without specific value.
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Amrubicin
Catalog No. A12663 -
Gatifloxacin
Catalog No. A10419 DNA gyrase/topoisomerase IV 抑制剂Gatifloxacin是一种氟喹诺酮类抗生素，可抑制细菌dna回旋酶(IC50 = 0.109 ng/ml)和拓扑异构酶iv(IC50 = 13.8 ng/ml)。 了解更多 -
Ofloxacin (DL8280)
Catalog No. A10666 -
Ametantrone
Catalog No. A12569 topoisomerase II 抑制剂Ametantrone (AM)是一种合成的9,10-蒽二酮，在位置1和4上带有两个（羟乙基氨基）乙基氨基残基，以及其他蒽醌和蒽环类化合物。 了解更多 -
TAS 103 2HCl
Catalog No. A14141 -
Nemorubicin
Catalog No. A14363 Topoisomerase II 抑制剂Nemorubicin是一种抗癌药物，IC50值为0.08 uM。它对抗烷化剂，拓扑异构酶II抑制剂和铂衍生物具有抗性的肿瘤具有活性。它主要通过抑制拓扑异构酶I起作用。 了解更多 -
Voreloxin Hydrochloride
Catalog No. A15280 -
Levofloxacin hydrate
Catalog No. A16167 topoisomerase II IV 抑制剂Levofloxacin hydrate是广谱的第三代氟喹诺酮类抗生素，是具有抗菌活性的氧氟沙星的旋光性L-异构体。 了解更多 -
Clinafloxacin
Catalog No. A16458 DNA gyrase and topoisomerase IV 抑制剂Clinafloxacin是一种氟喹诺酮，可双重抑制肺炎链球菌中的DNA促旋酶和拓扑异构酶IV。 了解更多 -
Pixantrone
Catalog No. A13022 -
Topotecan
Catalog No. A16815 -
MAC glucuronide α-hydroxy lactone-linked SN-38
Catalog No. A18407 Topoisomerase I inhibitorMAC glucuronide α-hydroxy lactone-linked SN-38 (Topoisomerase I inhibitor) is a stabilized lactone MAC glucuronide α-hydroxy lactone-linked SN-38 drug linker. 了解更多 -
Top1 inhibitor 1
Catalog No. A13304 human topoisomerase I (Top1) inhibitorTop1 inhibitor 1 (compound 28) is a potent human topoisomerase I (Top1) inhibitor with an IC50 value of 29 nM. 了解更多 -
Norfloxacin (Norxacin)
Catalog No. A10652 -
Marbofloxacin
Catalog No. A10557 -
Topotecan HCl (Hycamtin)
Catalog No. A10939 -
Irinotecan HCl Trihydrate (Campto)
Catalog No. A10479 Topoisomerase 抑制剂Irinotecan (CPT 11)是喜树碱家族的一种化合物，是参与细胞DNA复制和转录的拓扑异构酶1的抑制剂。 了解更多 -
Adriamycin
Catalog No. A10041 topoisomerase II 抑制剂Adriamycin是一种蒽环类抗生素，它通过插入DNA起作用，而最严重的副作用是危及生命的心脏损害。它通常用于治疗多种癌症，包括血液系统恶性肿瘤，多种类型的癌症和软组织肉瘤。 了解更多 -
Cerubidine (Daunorubicin HCl, Rubidomycin HCl)
Catalog No. A10194 Topoisomerase 抑制剂Cerubidine (Daunorubicin HCl,Rubidomycin HCl)通过插入和抑制大分子生物合成与DNA相互作用。这抑制了拓扑异构酶II的进程，该酶使DNA中的超螺旋松弛以进行转录。 了解更多 -
Camptothecin
Catalog No. A10174 -
Epirubicin HCl
Catalog No. A10345 Topoisomerase II 抑制剂Epirubicin HCl是一种可透过细胞的蒽环类抗肿瘤抗生素。它用于抑制拓扑异构酶II和DNA解旋酶活性。 了解更多 -
Balofloxacin
Catalog No. A11658 Topoisomerase 抑制剂Balofloxacin是一种喹诺酮类抗生素。Balofloxacin的杀菌作用源于对细菌DNA合成所需的酶DNA促旋酶的干扰。Balofloxacin对革兰氏阴性菌有效。它还对革兰氏阳性细菌（包括MRSA和肺炎链球菌）具有增强的活性。 了解更多 -
Sarafloxacin HCl
Catalog No. A11659 Topoisomerase 抑制剂Sarafloxacin hydrochloride是氟喹诺酮类抗菌剂。抑制细菌DNA促旋酶（拓扑异构酶）。 了解更多 -
Flumequine
Catalog No. A11861 Topoisomerase II 抑制剂Flumequine是一种合成化学抗生素，可在回旋酶/拓扑异构酶水平上影响哺乳动物染色体和DNA的解链。抑制拓扑异构酶II， IC50为15 μM。 了解更多 -
Pirarubicin
Catalog No. A10735 Topoisomerase II 抑制剂Pirarubicin是蒽环类抗肿瘤阿霉素的类似物。插入DNA中并与Topo II（拓扑异构酶II）相互作用并抑制DNA复制。 了解更多 -
(S)-10-Hydroxycamptothecin
Catalog No. A11997 Topoisomerase(S)-10-Hydroxycamptothecin是喜树碱衍生物，它通过在染色体DNA中产生链断裂并诱导细胞凋亡来抑制DNA拓扑异构酶。 了解更多 -
Amsacrine hydrochloride
Catalog No. A17707 antineoplastic agentAmsacrine hydrochloride (m-AMSA hydrochloride; acridinyl anisidide hydrochloride) is an inhibitor of topoisomerase II, and acts as an antineoplastic agent which can intercalates into the DNA of tumor cells. 了解更多 -
Pirarubicin Hydrochloride
Catalog No. A18037 topoisomerase II inhibitorPirarubicin Hydrochloride is an anthracycline antibiotics, acts as a topoisomerase II inhibitor, and is a widely used for treatment of various cancers, in particular, solid tumors. 了解更多 -
Gepotidacin
Catalog No. A21086 topoisomerase II inhibitorGepotidacin (GSK2140944) is a novel triazaacenaphthylene bacterial type II topoisomerase inhibitor. 了解更多 -
Karenitecin
Catalog No. A21156 topoisomerase I inhibitorKarenitecin (Cositecan) is a topoisomerase I inhibitor, with potent anti-cancer activity. 了解更多 -
Edotecarin
Catalog No. A21233 Topoisomerase I inhibitorEdotecarin is a potent inhibitor of topoisomerase I that can induces single-strand DNA cleavage, with IC50 of 50 nM. 了解更多 -
Exatecan Mesylate
Catalog No. A21515 DNA topoisomerase I inhibitorExatecan Mesylate is a DNA topoisomerase I inhibitor, with an IC50 of 2.2 μM (0.975 μg/mL), and can be used in cancer research. 了解更多 -
Daunorubicin
Catalog No. A21903 topoisomerase II inhibitorDaunorubicin (Daunomycin; RP 13057; Rubidomycin) is a topoisomerase II inhibitor with potent antineoplastic activities. 了解更多 -
9-amino-CPT
Catalog No. A12540 Topoisomerase I inhibitor9-Aminocamptothecin is a topoisomerase I inhibitor with potent anticancer activity. 了解更多 -
Epirubicin
Catalog No. A12409 Topoisomerase 抑制剂Epirubicin是一种细胞可渗透的抗肿瘤抗生素。阿霉素的立体异构体，其心脏毒性降低。表柔比星的抗肿瘤作用是通过靶向和抑制Topo II（拓扑异构酶II）来介导的。 了解更多 -
MAC glucuronide phenol-linked SN-38
Catalog No. A18403 DNA topoisomerase I inhibitorMAC glucuronide phenol-linked SN-38 is a pH-susceptible lactone MAC glucuronide phenol-linked SN-38 (DNA topoisomerase I inhibitor) drug linker. MAC glucuronide phenol-linked SN-38 is cytotoxic across L540cy cells and Ramos cells with IC50 values of 113 and 67 ng/mL, respectively. 了解更多
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