83
10
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T67899 |
Topoisomerase II inhibitor 13
|
Topoisomerase | DNA Damage/DNA Repair |
Topoisomerase II inhibitor 13抑制拓扑异构酶II (Topo II),对HL-60衍生的HL-60/MX2癌细胞具有较强的抗Topo II 毒性的抗增殖活性。 | |||
T77650 |
Topoisomerase II inhibitor 14
|
Apoptosis; Antioxidant; Topoisomerase; NO Synthase | Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; oxidation-reduction |
Topoisomerase II inhibitor 14 是一种有效的拓扑异构酶 II 抑制剂,具有抗癌活性和抗氧化活性。Topoisomerase II inhibitor 14 诱导细胞凋亡,并将细胞周期阻滞在 S 期。Topoisomerase II inhibitor 14 可降低 GSH、MDA 和 NO 的量。 | |||
T26046 |
Razoxane
|
Topoisomerase | DNA Damage/DNA Repair |
Razoxane 是拓扑异构酶 II 的有效抑制剂,具有抗血管生成的作用,在肾细胞癌中具有研究价值。 | |||
T60781 |
Topoisomerase II inhibitor 8
|
||
Topoisomerase II inhibitor 8 (化合物 22) 显示出良好的抗增殖活性,并将细胞周期阻滞在 G2/M 期。Topoisomerase II inhibitor 8是拓扑异构酶 II 的有效抑制剂 (IC 50 = 0.52 μM)。 | |||
T63304 |
Topoisomerase II inhibitor 9
|
||
Topoisomerase II inhibitor 9 是 Topo II 抑制剂 (IC50: 0.97 μM),也是 DNA 嵌入剂 (IC50: 43.51 μM),能够在 G2/M 期阻滞 Hep G‐2 细胞周期,诱导细胞凋亡 (apoptosis)。 | |||
T64164 |
Topoisomerase II inhibitor 11
|
||
Topoisomerase II inhibitor 11 (compound 3d) 是一种拓扑异构酶 II (Topoisomerase II) 的有效抑制剂 (IC50: 2.89 μM)。Topoisomerase II inhibitor 11 对肾癌 A498 细胞有 92.46% 的抑制效果 (IC50: 3.5 μM)。Topoisomerase II inhibitor 11 能够将细胞周期阻滞在 G2/M 期,抑制细胞增殖并具有凋亡活性。 | |||
T79506 |
Topoisomerase II inhibitor 15
|
Topoisomerase | DNA Damage/DNA Repair |
TopoisomeraseII inhibitor 15 (compound 2g) 为 TopoisomeraseII 的一种抑制剂,能有效诱导细胞凋亡 (apoptotic) 并对头颈部肿瘤展示出较高选择性。 | |||
T61017 | Topoisomerase II inhibitor 6 | ||
Topoisomerase II inhibitor 6 (Compound 5) 是色胺酮的衍生物。它是一种有效的拓扑异构酶的选择性抑制剂。Topoisomerase II inhibitor 6 在 G2 期阻断 CCRF-CEM 的细胞周期并诱导 DNA 双链断裂。Topoisomerase II inhibitor 6 对不同的肿瘤细胞系具有抗增殖活性,在癌症疾病研究中具有潜力。 | |||
T64047 |
Topoisomerase II inhibitor 10
|
||
Topoisomerase II inhibitor 10 是拓扑异构酶II (topoisomerase II) 的有效抑制剂 (IC50: 7.45 μM)。Topoisomerase II inhibitor 10 对 HepG-2、MCF-7 和 HCT-116 细胞表现出良好的抗增殖作用。Topoisomerase II inhibitor 10 能够将 HepG-2 细胞的细胞周期阻滞在 G2-M 期,并诱导其凋亡 (apoptosis)。 | |||
T72157 |
Topoisomerase II inhibitor 7
|
||
TopoisomeraseII inhibitor 7 (化合物 3a) 作为一种高效的拓扑异构酶IIα亚型抑制剂,展现出3.19 μM的IC50值。其能够诱导细胞周期阻滞与凋亡。 | |||
T63068 | Topoisomerase II inhibitor 5 | ||
Topoisomerase II inhibitor 5 (Compound E24) 是一种 DNAtopoisomerase II 抑制剂,具有抗癌作用。 | |||
T62887 |
Topoisomerase II inhibitor 4
|
||
Topoisomerase II inhibitor 4 (compound E17) 是一种拓扑异构酶 II (Topoisomerase II) 的有效抑制剂。Topoisomerase II inhibitor 4 具有抗肿瘤效果,能够将阻滞细胞周期于 G2/M 期,抑制癌细胞增殖并表现出细胞毒性。 | |||
T61283 |
Topoisomerase II inhibitor 3
|
||
Topoisomerase II inhibitor 3 (Compound 6 h) is an acridone derivative that acts as a Type II DNA topoisomerase (topo II) inhibitor. It specifically inhibits the topo IIα/β subtypes, with an IC50 value of 0.17 μM for topo IIα and 0.23 μM for topo IIβ. This compound elicits significant DNA damage and induces apoptosis by triggering the loss of mitochondrial membrane potential [1]. | |||
T79539 |
Topoisomerase II inhibitor 16
|
Topoisomerase | DNA Damage/DNA Repair |
TopoisomeraseII inhibitor 16(化合物CT3)是一个选择性的、口服活性的、能够穿透血脑屏障的,并对锥虫拓扑异构酶 II(trypanosomaltopoisomeraseII)产生不可逆抑制的化合物,能够稳定DNA双螺旋与酶之间的复合物。该抑制剂在恰加斯病的研究中显示出潜在应用价值。 | |||
T61054 | Type II topoisomerase inhibitor 1 | ||
Type II topoisomerase inhibitor 1 可用于抗菌领域。Type II topoisomerase inhibitor 1 是大肠杆菌DNA 旋转酶的选择性抑制剂,IC50值为 1.7 nM,并能与 Asp73 残基形成氢键。Type II topoisomerase inhibitor 1 抑制拓扑异构酶 IV 的活性,IC50值为 0.98 μM。 | |||
T61045 | Topoisomerase I/II inhibitor 2 | ||
Topoisomerase I/II inhibitor 2 (compound 1a) 可显著抑制小鼠模型中的异种移植肿瘤的生长,可用于肝癌治疗。Topoisomerase I/II inhibitor 2 是一种DNA 拓扑异构酶 I/II 的双重抑制剂。Topoisomerase I/II inhibitor 2 是有效的拓扑异构酶抑制剂,对LM9 细胞和Huh7 细胞的 IC50值分别为 6.83 μM 和9.82 μM 。 | |||
T63360 | DNA topoisomerase II inhibitor 1 | ||
DNA topoisomerase II inhibitor 1 是 DNA 拓扑异构酶 II 的有效抑制剂,能够将细胞周期停滞在亚 G1 期,并诱导细胞凋亡 (apoptosis) ,具有抗增值作用。 | |||
T63526 |
Topoisomerase I/II inhibitor 4
|
||
Topoisomerase I/II inhibitor 4 是有效的拓扑异构酶 I(Topo I) 和 II(Topo II) 双重抑制剂,对细胞增殖、侵袭和迁移,诱导细胞凋亡 (apoptosis) 具有抑制作用,能够用于研究肝癌。 | |||
T61990 | Topoisomerase I/II inhibitor 3 | ||
Topoisomerase I/II inhibitor 3 (化合物7) 是拓扑异构酶 I (Topo I)和 II (Topo II)的有效双抑制剂。 通过抑制 PI3K/Akt/mTOR 信号通路,Topoisomerase I/II inhibitor 3抑制细胞增殖、侵袭和迁移,诱导细胞凋亡(apoptosis)。Topoisomerase I/II inhibitor 3 在肝癌中具有研究价值。 | |||
T27299 |
F-14512 (free base)
F14512,F-14512 |
||
F-14512, a DNA topoisomerase II inhibitor, is used potentially for the treatment of acute myeloid leukemia. | |||
T3481 |
Bimolane
|
Topoisomerase | DNA Damage/DNA Repair |
Bimolane 是一种拓扑异构酶 II 抑制剂。 | |||
T1206 |
Amsacrine
AMSA,m-AMSA,安吖啶,CI-880,acridinyl anisidide |
Potassium Channel; Topoisomerase; Autophagy | Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel |
Amsacrine (AMSA) 是一种抗肿瘤剂,可以嵌入到肿瘤细胞的 DNA 中。它还表达拓扑异构酶抑制剂活性,特异性抑制拓扑异构酶 II。 | |||
T5820 |
Amsacrine hydrochloride
acridinyl anisidide hydrochloride,盐酸胺苯吖啶,m-AMSA hydrochloride |
Topoisomerase; Autophagy | Autophagy; DNA Damage/DNA Repair |
Amsacrine hydrochloride (acridinyl anisidide hydrochloride) 是一种拓扑异构酶 II 抑制剂,用于治疗急性髓细胞性白血病。 | |||
T0158 |
Mitoxantrone dihydrochloride
米托蒽醌二盐酸盐,盐酸米托蒽醌,Mitoxantrone 2HCl,Mitoxantrone hydrochloride,NSC-301739,mitozantrone dihydrochloride |
Topoisomerase; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair |
Mitoxantrone dihydrochloride (NSC-301739) 是一种拓扑异构酶 II 的抑制剂;也可抑制蛋白激酶C (PKC),IC50值为8.5 μM。 | |||
T22456 |
Voreloxin hydrochloride
SNS-595 hydrochloride,Vosaroxin,(3S-反式)-1,4-二氢-7-[3-甲氧基-4-(甲基氨基)-1-吡咯烷基]-4-氧代-1-(2-噻唑基)-1,8-萘啶-3-羧酸单盐酸盐 |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
Voreloxin hydrochloride (SNS-595 hydrochloride) 是一种新型拓扑异构酶 II 抑制剂,能够诱导 DNA 双链断裂,阻滞 G2 期,引起细胞凋亡。 | |||
T26339L |
XR-11576 HCl
XR-11576 HCl(346689-77-8 Free base) |
Topoisomerase | DNA Damage/DNA Repair |
XR-11576 HCl 是一种新型口服活性拓扑异构酶I 和II 双重抑制剂,具有抗肿瘤活性。 | |||
T6628 |
Pirarubicin
吡柔比星,Theprubicin,THP |
Topoisomerase; Antibacterial; Antibiotic; Autophagy | Autophagy; DNA Damage/DNA Repair; Microbiology/Virology |
Pirarubicin (Theprubicin) 是一种蒽环类抗生素,是拓扑异构酶 II 抑制剂,可用于各种癌症的研究。 | |||
T6010 |
Idarubicin hydrochloride
盐酸伊达比星,Idamycin,4-demethoxydaunorubicin (NSC256439, 4-DMDR) HCl,4-Demethoxydaunorubicin hydrochloride,Idarubicin HCl,伊达比星盐酸盐,Zavedos |
Topoisomerase; Antibacterial; Autophagy; Antifungal | Autophagy; DNA Damage/DNA Repair; Microbiology/Virology |
Idarubicin hydrochloride (Zavedos) 是一种蒽环类抗白血病药物,能抑制细菌和酵母菌生长,还抑制拓扑异构酶 II,干扰 DNA 复制和 RNA 转录。 | |||
T68896 |
Daniquidone
NSC 320846,BAY-H 2049 |
Topoisomerase | DNA Damage/DNA Repair |
Daniquidone (Batracylin) 是一种有效的 DNA 拓扑异构酶 I 和 DNA 拓扑异构酶 II 双重抑制剂, 具有细胞毒性和抗增殖活性,可诱导 DNA 断裂,可用于研究肿瘤、免疫系统疾病和淋巴系统疾病。 | |||
T3186 |
NU2058
O6-(Cyclohexylmethyl)guanine,O(6)-Cyclohexylmethylguanine |
Topoisomerase; CDK | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
NU2058 (O(6)-Cyclohexylmethylguanine) 是一种基于鸟嘌呤的 CDK 抑制剂,抑制 CDK2 和 CDK1 的IC50值分别为 17 μM 和 26 μM。它也抑制 DNA 拓扑异构酶 II ATPase 活性,具有抗癌活性。 | |||
T8333 |
Aurintricarboxylic acid
ATA,NSC-4056,NSC4056,金精三羧酸,NSC 4056 |
Apoptosis; P2X Receptor; Influenza Virus; Topoisomerase | Apoptosis; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Aurintricarboxylic acid (NSC-4056) 是高效的αβ-亚甲基-ATP 敏感选择性P2X1Rs 和P2X3Rs 变构拮抗剂。 它是核糖核酸酶和拓扑异构酶 II 的有效抑制剂,可阻止核酸与酶结合。 | |||
T36968 |
ARN-21934
|
Topoisomerase | DNA Damage/DNA Repair |
ARN-21934 是高选择性的人拓扑异构酶 II α 抑制剂,具有血脑屏障通透性。依托泊苷抑制 DNA 松弛的IC50为120 μM,ARN-21934 抑制 DNA 松弛的IC50为 2 μM。ARN-21934具有良好的体内药代动力学特性。 | |||
T11090L1 |
Aldoxorubicin hydrochloride
Aldoxorubicin hydrochloride (1361644-26-9 Free base) |
Topoisomerase | DNA Damage/DNA Repair |
Aldoxorubicin hydrochloride 是 Doxorubicin (DNA 拓扑异构酶 II 抑制剂) 的白蛋白结合前药。Aldoxorubicin hydrochloride 在酸性条件下从白蛋白中释放出来。 Aldoxorubicin hydrochloride 显示出有效的抗肿瘤活性。 | |||
T16522 |
Phenoxodiol
脱氢雌马酚,Dehydroequol,Idronoxil,Haginin E |
Apoptosis; IAP; Caspase; Topoisomerase; p53 | Apoptosis; DNA Damage/DNA Repair; Proteases/Proteasome |
Phenoxodiol (Idronoxil) 是合成genestein 的类似物,激活线粒体caspase 系统,抑制XIAP,使癌细胞对fas 介导的凋亡敏感。它在细胞周期的G1/S 期诱导细胞周期阻滞,通过独立于p53的方式上调p21WAF1。它通过稳定可分裂复合物抑制DNA 拓扑异构酶II,从而阻止DNA 复制。 | |||
T24100 |
GR 122222X
GR122222X,GR-122222X |
||
GR 122222X is an inhibitor of topoisomerase II. | |||
T15586 | Intoplicine | Topoisomerase | DNA Damage/DNA Repair |
Intoplicine is an inhibitor of DNA topoisomerase I and II. | |||
T29168 |
XR-5000
NSC-601316,CRC8805,SN-22995,DACA,CRC-8805 |
||
XR-5000 is a DNA topoisomerase I and II inhibitor. | |||
T69870 |
ICRF-193
|
||
ICRF-193 is a DNA topoisomerase II inhibitor. | |||
T26339 |
XR-11576
MLN-576,MLN 576,MLN576,XR 11576 |
||
XR-11576 is a DNA topoisomerase I and II inhibitor for the treatment of solid tumors. | |||
T23750 |
AQ4
AQ-4,AQ 4 |
||
AQ4 is an inhibitor of topoisomerase II. It is also a DNA intercalator. | |||
T25893 |
NU/ICRF 500
|
||
NU/ICRF 500 is a novel anthracenyl-amino acid catalytic inhibitor of topoisomerase II. | |||
T69871 |
ICRF-196
|
||
ICRF-196 is a Topoisomerase II Inhibitor and antineoplastic agent. | |||
T25776 |
Mansonone F
NSC 113136,NSC113136,NSC-113136 |
||
Mansonone F is a topoisomerase II inhibitor with cytotoxic and topo inhibitory potencies. | |||
T11090 |
MC-DOXHZN
Doxorubicin(6-maleimidocaproyl)hydrazone |
Others | Others |
Mc-doxhzn is a protein-binding prodrug of DOXUbicin (DNA topoisomerase II inhibitor) with acid sensitivity. | |||
T29964 |
Ametantrone Acetate
CI-881 |
||
Ametantrone Acetate is a topoisomerase II inhibitor of anthrapyrazole family, which can lead to DNA covalent crosslinking. | |||
T28521 |
Retelliptine
SR-95325B (diHCl),NSC-D-626717-W,SR-95325A (dimaleate),BD-84 |
||
Retelliptine, a DNA topoisomerase II inhibitor, is used potentially for the treatment of cancer. | |||
T69109 | Ellipticine tartrate | ||
Ellipticine tartrate is a DNA intercalating agent and a DNA topoisomerase II inhibitor. | |||
T68801 |
Ardisin
|
||
Ardisin is a Topoisomerase I and II enzyme inhibitor. Ardisin may have antioxidant effects. | |||
T28944 |
Teloxantrone HCl
PD-113309,Moxantrazole,NSC-355644,CI-937,DuP-937,Teloxantrone |
||
Teloxantrone, a DNA topoisomerase II inhibitor, is used potentially for the treatment of solid tumors. | |||
T11391L |
Gepotidacin
GSK2140944 |
Others | Others |
Gepotidacin is a novel triazaacenaphthylene inhibitor of bacterial type II topoisomerase. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0132 |
Etoposide
VP-16,依托泊苷,依托泊甙,VP-16-213 |
Apoptosis; Mitophagy; Topoisomerase; Antibacterial; Antibiotic; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Microbiology/Virology |
Etoposide (VP-16-213) 是一种拓扑异构酶 II 的抑制剂,通过与拓扑异构酶 II 和 DNA 形成复合物来抑制 DNA 合成 (IC50=60.3 μM)。Etoposide 具有抗肿瘤活性,可以诱导细胞凋亡、自噬。 | |||
T6567 |
Levofloxacin
Levaquin,Cravit,Tavanic,Fluoroquinolone,左氧氟沙星,(-)-Ofloxacin |
Topoisomerase; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Levofloxacin (Fluoroquinolone) 是合成的氟喹诺酮类抗生素,有抑制细菌DNA 旋转酶的超螺旋活性的作用,能阻止DNA 复制。 | |||
T6407 |
β-Lapachone
3,4-二氢-2,2-二甲基-2H-萘并[1,2-B]吡喃-5,6-二酮,Beta-Lapachone,NSC-26326,SL-11001,ARQ-501 |
IDO; Apoptosis; Topoisomerase; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism |
β-Lapachone (ARQ-501) 是一种萘醌类天然产物,是拓扑异构酶 I 抑制剂,通过抑制细胞周期进程来诱导细胞凋亡。 | |||
T1020 |
Doxorubicin hydrochloride
Adriamycin,Doxorubicin (Adriamycin) HCl,Hydroxydaunorubicin hydrochloride,盐酸多柔比星,盐酸阿霉素,NSC 123127 |
Apoptosis; Mitophagy; HBV; HIV Protease; Topoisomerase; Antibacterial; Antibiotic; AMPK; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Doxorubicin hydrochloride (Adriamycin) 属于蒽环类抗生素,是人类 DNA 拓扑异构酶 I/II 抑制剂 (IC50=0.8/2.67 μM)。Doxorubicin hydrochloride 具有细胞毒性和抗肿瘤活性。Doxorubicin hydrochloride 可降低 AMPK 及其下游靶蛋白乙酰辅酶 A 羧化酶的磷酸化,还可诱导凋亡和自噬。 | |||
T25775 | Mansonone E | ||
Mansonone E is a topoisomerase II inhibitor with cytotoxic and topo inhibitory potencies. | |||
TN2861 |
3,27-Dihydroxy-20(29)-lupen-28-oic acid methyl ester
|
Others | Others |
3α, 27-Dihydroxylupen-20(29)-en-28-oic acid methyl ester is a topoisomerase II inhibitor. | |||
TN2915 |
3-Acetoxy-27-hydroxy-20(29)-lupen
3-Acetoxy-27-hydroxy-20(29)-lupen-28-oic acid methyl ester |
Others | Others |
3-Acetoxy-27-hydroxy-20(29)-lupen is an acetyl ester form of 3α, 27-Dihydroxylupen-20(29)-en-28-oic acid methyl ester, which is a topoisomerase II inhibitor. | |||
T10238 |
Aclacinomycin A hydrochloride
盐酸阿柔比星,Aclarubicin hydrochloride |
Proteasome | Proteases/Proteasome; Ubiquitination |
Aclacinomycin A (Aclarubicin) hydrochloride is a fluorescent molecule and the first described non-peptidic inhibitor showing discrete specificity for the CTRL (chymotrypsin-like) activity of the 20S proteasome. Aclacinomycin A hydrochloride is also a dual inhibitor of topoisomerase I and II. | |||
T1456 |
Doxorubicin
Hydroxydaunorubicin,阿霉素,Adriamycin |
Topoisomerase; AMPK | Chromatin/Epigenetic; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
Doxorubicin (Adriamycin) 是一种有细胞毒性的蒽环类抗生素,具有肿瘤化疗作用。它抑制DNA 拓扑异构酶 I 和拓扑异构酶 II,IC50分别为0.8 μM 和2.67 μM,从而抑制 DNA 复制。它下调AMPK 的基础磷酸化以及下游 acetyl-CoA 羧化酶。它诱导凋亡和自噬 。 | |||
TN1875 |
Liriodenine
鹅掌揪碱 |
BCL; Caspase; p53 | Apoptosis; Proteases/Proteasome |
Liriodenine is a potent inhibitor of topoisomerase II (EC 5.99.1.3) both in vivo and in vitro, it has antitumor, antibacterial and antifungal activities, it can suppress ventricular arrhythmias induced by myocardial ischaemia reperfusion, through inhibiti |