Topoisomerase

Topoisomerase

货号 产品名 CAS号 信息
FB03999 Voreloxin 175414-77-4 Voreloxin is a naphthyridine analogue with antineoplastic activity and an inhibitor of Topo II.
FB04001 Voreloxin HCl 175519-16-1 Voreloxin HCl is a naphthyridine analogue with antineoplastic activity and an inhibitor of Topo II.
FB10891 Voacamine 3371-85-5 Voacamine, isolated from the plant Tabernaemontana coronaria, is an antiprotozoal agent effective against a large array of trypanosomatid parasites including Indian strain of Leishmania donovani and Brazilian strains of Leishmania amazonensis and Trypanosoma cruzi by inhibiting the relaxation activity of topoisomerase IB.
FB11216 Topoisomerase Inhibitor C14 1082340-21-3 Topoisomerase inhibitor C14 is a 3-fluoro-6-methoxyquinoline derivatives and an inhibitor of bacterial DNA gyrase and topoisomerase IV.
FB10945 Top-Tdp Tri Inhibitor C12 2092927-74-5 Top-Tdp tri inhibitor C12 is one of the first triple inhibitors of human topoisomerase 1, tyrosyl–DNA phohosphodiesterase 1 (Tdp1), and tyrosyl–DNA phosphodiesterase 2 (Tdp2).
FB03996 TAS-103 174634-08-3 TAS-103 is a dual inhibitor of topoisomerase-I (topo-I) and topoisomerase-II (topoII).
FB00655 TAS-103 2HCl 174634-09-4 TAS-103 2HCl is a dual inhibitor of topoisomerase-I (topo-I) and topoisomerase-II (topoII).
FB00648 SW044248 522650-83-5 SW044248 is a noncanonical Top1 inhibitor with a pattern of selective toxicity for NSCLC cells.
FB10613 SN-38 86639-52-3 SN-38 is an active metabolite of CPT-11 that inhibits DNA topoisomerase I, DNA synthesis and causes frequent DNA single-strand breaks.
FB11051 Sabarubicin 211100-13-9 Sabarubicin is a Top II inhibitor with anticancer activity.
FB07157 Pirarubicin HCl 95343-20-7 Pirarubicin HCl is an analogue of the anthracycline anti-neoplastic doxorubicin, which is an inhibitor of Topo II.
FB03346 Pefloxacin Mesylate Dihydrate 149676-40-4 Pefloxacin mesylate, antibacterial agent, can prevent bacterial DNA replication via inhibiting DNA gyrase or topoisomerse.
FB16488 NSC745887 54490-26-5 NSC745887 can effectively inhibit the proliferation of various cancers by trapping DNA-topoisomerase cleavage. NSC745887 reduced the cell survival rate and increased the sub-G1 population in dose- and time-dependent manners in GBM cells. Moreover, NSC745887 increased expression of γH2AX and caused DNA fragmentation leading to DNA damage.NSC745887 caused apoptosis by the caspase-8/9-caspase-3-poly(ADP-ribose) polymerase cascade.
FB10869 NISC-6 2097636-49-0 NISC-6 is a napthalamide-isoselenocyanate compound which acts as a dual Topoisomerase-IIα and Akt pathway inhibitor.
FB17796 Nalidixic acid sodium salt 3374-05-8 Nalidixic acid sodium salt, a quinolone antibiotic, is effective against both gram-positive and gram-negative bacteria. Nalidixic acid acts in a bacteriostatic manner in lower concentrations and is bactericidal in higher concentrations. Nalidixic acid inhibits a subunit of DNA gyrase and topoisomerase IV and reversibly blocks DNA replication in susceptible bacteria.
FB03450 Nadifloxacin 124858-35-1 Nadifloxacin is a fluoroquinolone broad-spectrum antibacterial, working by inhibiting the enzyme DNA gyrase and thus inhibiting the bacterial multiplication.
FB10548 Moxifloxacin HCl 186826-86-8 Moxifloxacin HCl is a fluoroquinolone antibiotic agent.
FB12886 Levofloxacin HCl 177325-13-2 Levofloxacin HCl, a fluoroquinolone antibiotic, is an inhibitor of DNA gyrase and topoisomerase IV.
FB07674 Irinotecan   97682-44-5 Irinotecan is a camptothecin analog prevents DNA from unwinding by inhibition of topoisomerase 1.
FB07698 Irinotecan HCl 100286-90-6 Irinotecan HCl is an inhibitor of topoisomerase 1 that prevents DNA from unwinding.
FB02799 INNO-206 1361644-26-9 INNO-206 is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubicin (DOXO-EMCH) with antineoplastic activity.
FB12027 Indotecan 915303-09-2 Indotecan is a potent topoisomerase 1(Top1) inhibitor with IC50 values of 300, 1200, 560 nM for P388, HCT116, MCF-7 cell lines, respectively.
FB06650 Idarubicin 58957-92-9 Idarubicin is a semisynthetic 4-demethoxy analogue of the antineoplastic anthracycline antibiotic daunorubicin.
FB08592 Idarubicin HCl 57852-57-0 Idarubicin HCl is a HCl 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 in a cell-free assay.
FB07787 Gepotidacin 1075236-89-3 Gepotidacin is a first in class triazaacenaphthylene antibiotic that inhibits bacterial type II DNA replication by inhibiting the activity of bacterial topoisomerase and has in vitro activity against susceptible and drug-resistant pathogens.
FB06178 Genz-644282 529488-28-6 Genz-644282 is a non-camptothecin inhibitor of topoisomerase I with potential antineoplastic activity (IC50=1.2 nM).
FB11205 F14512 866874-63-7 F14512 is a DNA topoisomerase II inhibitor potentially for the treatment of acute myeloid leukemia.
FB03976 Exatecan Mesylate 169869-90-3 Exatecan mesylate is a totally synthetic analogue of the topoisomerase I-inhibitor camptothecin, which was synthesised to impart increased aqueous solubility, greater tumour efficacy, and less toxicity than camptothecin itself.
FB08428 Exatecan 171335-80-1 Exatecan is a totally synthetic analogue of the topoisomerase I-inhibitor camptothecin, which was synthesised to impart increased aqueous solubility, greater tumour efficacy, and less toxicity than camptothecin itself.
FB02434 Etoposide 33419-42-0 Etoposide inhibits DNA synthesis by inhibiting topoisomerase II (IC50 = 60.3 μM).
FB08260 Epirubicin HCl 56390-09-1 Epirubicin HCl, a L-arabino derivative of doxorubicin, can inhibit topoisomerase and used as antineoplastic agent.
FB10052 Ellipticine HCl 5081-48-1 Ellipticine HCl is a potent antineoplastic agent and inhibits DNA topoisomerase II activities.
FB00905 Doxorubicin HCl   25316-40-9 Doxorubicin HCl is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage and apoptosis in tumor cells.
FB03275 DOXO-EMCH 151038-96-9 DOXO-EMCH is a 6-maleimidocaproyl hydrazone derivative of Doxorubicin, is an albumin binding prodrug.
FB07032 Daunorubicin HCl 23541-50-6 Daunorubicin HCl can inhibit both DNA synthesis (Ki = 0.02 μM) and RNA synthesis.
FB06137 Daun02 290304-24-4 Daun02 is converted by β-galactosidase to Daunorubicin, which is a topoisomerase inhibitor, and alsois a daunorubicin b-galactoside prodrug for use in conjunction.
FB09776 Coralyne 6872-73-7 Coralyne is a cytotoxic agent trageting topoisoerase I, used in combinational chemotherapy to improve the effectiveness in combating proliferation of cancer cells.
FB08926 Ciprofloxacin HCl H2O 86393-32-0 Ciprofloxacin HCl is an antibiotic agent and used to treat bacterial infections.
FB19554 Chrysomycin B 83852-56-6 Chrysomycin B is an antibiotic isolated from a strain of Streptomyces. It inhibits topoisomerase II and causes DNA damage in A549 cell line.
FB08157 Campathecin 7689-03-4 Camptothecin is a potent DNA enzyme topoisomerase I (topo I) inhibitor with an IC50 and IC70 of 50 nM and 0.225 μM for breast cancer cell line MDA-MB-231.
FB11748 BNP 1350 203923-89-1 BNP 1350 is a topoisomerase I inhibitor, with potent anti-cancer activity.
FB06171 Amsacrine 51264-14-3 Amsacrine can intercalate into the DNA of tumor cells with antineoplastic activity.
FB02258 Amrubicin HCl 110311-30-3 Amrubicin HCl is a topoisomerase II inhibitor used in the treatment of lung cancer.
FB03871 Alternariol 641-38-3 Alternariol is a mycotoxin, topoisomerase I and II inhibitor and potential ER agonist found in Alternaria.
FB11136 AEZS-108 139570-93-7 AEZS-108 is a peptide agonist of the gonadotropin releasing hormone-1 receptor (GnRH-1R).
FB07330 Aclarubicin 57576-44-0 Aclarubicin is an oligosaccharide anthracycline antineoplastic antibiotic isolated from the bacterium Streptomyces galilaeus.
FB11135 Aclarubicin HCl 75443-99-1 Aclarubicin HCl is the HCl salt of aclarubicin, an oligosaccharide anthracycline antineoplastic antibiotic isolated from the bacterium Streptomyces galilaeus.
FB16109 1,4-Naphthoquinone 130-15-4 A choleretic.
FB05893 3-O-trans-p-Coumaroyltormentic Acid 121064-78-6 3-O-trans-p-Coumaroyltormentic acid, a natural product isolated and purified from the leaves of Eriobotrya japonica calli, induces apoptotic cell death in human leukemia (HL60) via mainly mitochondrial pathway by, at least in part, Topo I inhibition, and may be promising lead compound for developing an effective drug for treatment of leukemia.
FB10669 10-Hydroxycamptothecin 64439-81-2 (±)-10-Hydroxycamptothecin is an inhibitor of topoisomerase I and can affect phosphorylation of histone H1 and H3 with anticancer activity. It can be isolated from camptotheca acuminate.
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