107
25
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T31011 |
Coralyne chloride
|
Topoisomerase | DNA Damage/DNA Repair |
Coralyne chloride 是一种具有强抗癌活性的原小檗碱。它可用于制备 Coralyne 衍生物,是一种基于荧光 DNA 的分子整流剂,通过位点特异性插入构建成 DNA 双链体。它可作为一种拓扑异构酶 I 毒性分子,诱导拓扑异构酶 I 介导 DNA 裂解。 | |||
T80968 |
Topoisomerase I inhibitor 10
|
Topoisomerase | DNA Damage/DNA Repair |
TopoisomeraseI inhibitor 10 (compound 13)为一种抗利什曼原虫活性药物,特别针对L. donovani promastigotes的leishmanial topoisomerase IB表现出抑制作用,IC50值为27.91 μM。 | |||
T62094 | Topoisomerase I inhibitor 6 | ||
Topoisomerase I inhibitor 6 (Compound 3) 是一种 Topoisomerase I 的有效抑制剂,可以捕获 DNA-Top1 裂解复合物,在非癌细胞系中具有较小的细胞毒性。Topoisomerase I inhibitor 6 对癌症疾病表现出潜在的研究价值。 | |||
T60766 |
Topoisomerase I inhibitor 3
|
||
Topoisomerase I inhibitor 3 (Compound ZML-14) 诱导 HepG2 细胞凋亡,并在 G2/M 期阻滞细胞周期。Topoisomerase I inhibitor 3 是与拓扑异构酶 I-DNA 复合物相互作用的拓扑异构酶 I 抑制剂。 | |||
T61717 |
Topoisomerase I inhibitor 4
|
||
Topoisomerase I inhibitor 4 (compound 7a) is a potent inhibitor of topoisomerase I activity. It effectively inhibits the proliferation of various cancer cell lines including HepG2, A549, MCF-7, and HeLa, with IC50 values of 1.20 μM, 2.09 μM, 1.56 μM, and 1.92 μM, respectively. Thus, Topoisomerase I inhibitor 4 holds promise for cancer research applications [1]. | |||
T60617 |
Topoisomerase I inhibitor 2
|
||
Topoisomerase I inhibitor 2 是一种高度选择性的DNA 拓扑异构酶 I(Top1) 抑制剂,可抑制Top1活性并导致 DNA 损伤。Topoisomerase I inhibitor 2 阻断 G2/M 期并诱导细胞凋亡,具有抗肿瘤作用。 | |||
T62002 |
Topoisomerase I inhibitor 7
|
||
Topoisomerase I inhibitor 7 (Compound 8) 是有效的Topoisomerase I 抑制剂。Topoisomerase I inhibitor 7 显著抑制肿瘤生长(高达 79%)。在接受 P388 淋巴瘤移植的小鼠模型中,Topoisomerase I inhibitor 7延长了小鼠寿命(153%)。 | |||
T61501 |
Topoisomerase I inhibitor 5
|
||
Topoisomerase I inhibitor 5 is an efficient inhibitor of topoisomerase I, with an IC50 value. It effectively disrupts DNA and inhibits the activity of topoisomerase I. Moreover, it can induce apoptosis in MCF-7 cells and arrest the cell cycle at the G1 phase. Topoisomerase I inhibitor 5 also exhibits potency in reversing P-gp-mediated resistance to Adriamycin [1]. | |||
T62225 |
Topoisomerase I inhibitor 8
|
||
Topoisomerase I inhibitor 8 是一种喜树碱六环类似物,也是 topoisomerase I 的强效抑制剂,对肿瘤细胞有毒性。 | |||
T80967 |
Topoisomerase I inhibitor 9
|
Topoisomerase | DNA Damage/DNA Repair |
TopoisomeraseI inhibitor 9 (compound 3d) 是针对leishmanial topoisomerase IB的抑制剂,具有针对L. donovani promastigotes的抗利什曼原虫活性,其IC50值为34.81 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 。 | |||
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。 | |||
T17731 |
CL2A-SN-38
|
Others | Others |
CL2A-SN-38 是一种药物-接头偶联物,由一种有效的 DNA 拓扑异构酶 I 抑制剂 SN-38 和接头 CL2A 组成,用于制造抗体药物偶联物。它对一系列人类实体瘤类型提供显着和特异性的抗肿瘤作用。 | |||
T21319 |
Gimatecan
LBQ707,STI481 |
Topoisomerase | DNA Damage/DNA Repair |
Gimatecan (STI481) 是一种有效的拓扑异构酶 I (topoisomerase I) 抑制剂。Gimatecan 是一种具有口服活性的喜树碱类似物。具有抗肿瘤活性。 | |||
T60123 |
Chimmitecan
(S)-9-Allyl-10-hydroxycamptothecin,吉米替康 |
Topoisomerase | DNA Damage/DNA Repair |
Chimmitecan ((S)-9-Allyl-10-hydroxycamptothecin) 是一种topoisomerase I 抑制剂,在体内、外表现有效的活性。 | |||
T60200 |
IndiMitecan
LMP776 |
Topoisomerase | DNA Damage/DNA Repair |
IndiMitecan (LMP776) 是一种具有抗癌活性的拓扑异构酶 I(Top1)抑制剂。 | |||
T7187 |
Genz-644282
Genz644282 |
Topoisomerase | DNA Damage/DNA Repair |
Genz-644282 是一种用于癌症治疗的新型非喜树碱拓扑异构酶 I 抑制剂。 | |||
T21319L |
Gimatecan HCl
ST1481 HCL,Gimatecan HCl(292618-32-7 Free base) |
Topoisomerase | DNA Damage/DNA Repair |
Gimatecan HCl (ST1481 HCL) 是一种有效的拓扑异构酶 I (topoisomerase I) 抑制剂。Gimatecan HCl 是一种具有口服活性的喜树碱类似物。具有抗肿瘤活性。 | |||
TQ0088 |
Exatecan Mesylate
依沙替康甲磺酸盐,依喜替康甲磺酸盐,DX8951f |
Topoisomerase | DNA Damage/DNA Repair |
Exatecan Mesylate (DX8951f) 是一种 DNA 拓扑异构酶 I 抑制剂,IC50值为 2.2 μM,可研究癌症。 | |||
T60163 |
Lurtotecan
GI147211,OSI-211 |
Topoisomerase | DNA Damage/DNA Repair |
Lurtotecan (GI147211) 是一种半合成的喜树碱类似物。Lurtotecan 是一种具有抗癌作用的拓扑异构酶I 抑制剂。 | |||
T15168 |
DRF-1042
|
Topoisomerase | DNA Damage/DNA Repair |
DRF-1042 是一种具有口服活性的喜树碱类似物,具有抗癌活性和杀虫活性,抑制 DNA 拓扑异构酶 I (DNA topoisomerase I) ,可用于研究前列腺癌和结肠癌等实体肿瘤。 | |||
T7309 |
TAS-103 dihydrochloride
6-[[2-(二甲基氨基)乙基]氨基]-3-羟基-7H-茚并[2,1-C]喹啉-7-酮二盐酸盐,TAS-103 (dihydrochloride),BMS-247615 dihydrochloride |
Topoisomerase | DNA Damage/DNA Repair |
TAS-103 dihydrochloride (BMS-247615 dihydrochloride) 是可用于癌症研究的一种 DNA 拓扑异构酶 I/II 双重抑制剂。 | |||
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。 | |||
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。 | |||
T7551 |
Belotecan hydrochloride
CKD-602 |
Topoisomerase | DNA Damage/DNA Repair |
Belotecan hydrochloride (CKD-602) 是一种合成的水溶性喜树碱衍生物和拓扑异构酶 I 抑制剂,具有潜在的抗肿瘤活性。 | |||
T6336 |
Amonafide
NSC308847,AS1413,氨萘非特,Nafidimide,AS1413,Quinamed |
Topoisomerase | DNA Damage/DNA Repair |
Amonafide (NSC-308847,AS1413) 是一种拓扑异构酶 II 的抑制剂和 DNA 的嵌入剂,通过拓扑异构酶 II 介导的反应产生蛋白质相关的 DNA 链断裂 | |||
T11872L |
LMP744 hydrochloride
NSC706744 hydrochloride,MJ-III65 hydrochloride |
Topoisomerase | DNA Damage/DNA Repair |
LMP744 hydrochloride (NSC-706744 hydrochloride) 是一种是拓扑异构酶 1 抑制剂,显示出抗肿瘤的活性。 | |||
T71137 |
Simmitecan hydrochloride
|
Topoisomerase | DNA Damage/DNA Repair |
Simmitecan hydrochloride 是一种喜树碱衍生物,是一种拓扑异构酶 I 抑制剂,具有抗癌活性,可用于研究是实体瘤。 | |||
T9088 |
Topovale
ARC111,ARC 111,ARC-111,Topoval |
Topoisomerase | DNA Damage/DNA Repair |
Topovale (ARC111) 是一种有效的拓扑异构酶 I 抑制剂。Topovale 抑制缺氧介导的缺氧诱导因子 1alpha 的积累。 Topovale 对一组癌细胞表现出低 nM 细胞毒性。与 P388 细胞相比,在 CPT 抗性拓扑异构酶 I (TOP1) 缺陷的 P388/CPT45 细胞中,Topovale 细胞毒性和 Topovale 诱导的细胞凋亡减少了 > 100 倍。 | |||
T11249L |
Dxd
Exatecan derivative for ADC,OQM5SD32BQ,UNII-OQM5SD32BQ |
Topoisomerase | DNA Damage/DNA Repair |
Dxd (OQM5SD32BQ) 是一种有效的DNA 拓扑异构酶 I 抑制剂,IC50值为 0.31 μM,用作HER2靶向ADC 的偶联药物。 | |||
T11249 |
Exatecan
依喜替康,DX-8951,DX-8951f |
Topoisomerase | DNA Damage/DNA Repair |
Exatecan (DX-8951f) 是一种 DNA 拓扑异构酶 I (TOP1) 抑制剂,IC50 值为 2.2 μM (0.975 μg/mL)。Exatecan 具有抗肿瘤活性,可用于癌症研究。 | |||
T24610 |
Pegamotecan
Prothecan,PEG-camptothecin,PEG-beta-CPT |
Topoisomerase | DNA Damage/DNA Repair |
Pegamotecan (PEG-camptothecin)是一种拓扑异构酶I(TOP1)抑制剂,具有抗癌活性,它可用于治疗食管癌、非小细胞肺癌和胰腺癌。 | |||
T77584 |
Tubulin inhibitor 35
Tubulin IN 35 |
Apoptosis; Microtubule Associated; Topoisomerase | Apoptosis; Cytoskeletal Signaling; DNA Damage/DNA Repair |
Tubulin inhibitor 35 (Tubulin IN 35) 是一种有效的拓扑异构酶 I 和微管蛋白聚合 的双重抑制剂,具有抗肿瘤活性,对 MGC-803 和 RKO 细胞株的迁移和侵袭有抑制作用,中断细胞周期,诱导凋亡 (apoptosis)。 | |||
T17731L |
CL2A-SN-38 DCA 1279680-68-0(free base)
|
Others | Others |
CL2A-SN-38 DCA 1279680-68-0(free base) 是一种药物-接头偶联物,由有效的 DNA 拓扑异构酶 I 抑制剂 SN-38 和接头 CL2A 组成,用于制造抗体药物偶联物 (ADC)。CL2A-SN-38 由有效的 DNA 拓扑异构酶组成I 抑制剂 SN-38 和接头 CL2A 以制造抗体药物偶联物 (ADC)。 CL2A-SN-38 对一系列人类实体瘤类型提供显着和特异性的抗肿瘤作用。 CL2A 是一种不可切割的复杂 PEG8 和含有三唑的 PABC-肽-mc 接头。 CL2A 可通过 pH 敏感性裂解,产生旁观者效应,并通过二硫键在半胱氨酸残基处结合抗体。 | |||
T15586 | Intoplicine | Topoisomerase | DNA Damage/DNA Repair |
Intoplicine is an inhibitor of DNA topoisomerase I and II. | |||
T11872 |
LMP744
NSC706744,MJ-III65 |
Others | Others |
LMP744 is a DNA intercalator and Topoisomerase I (Top1) inhibitor with antitumor activity. | |||
T27147 |
Deoxynybomycin
|
||
Deoxynybomycin, a selective anti-tumor agent, inhibits topoisomerase I and induces apoptosis. | |||
T24036 |
WJ35435
WJ 35435,WJ-35435 |
||
WJ35435 is a histone deacetylase and topoisomerase I dual inhibitor. | |||
T29168 |
XR-5000
NSC-601316,CRC8805,SN-22995,DACA,CRC-8805 |
||
XR-5000 is a DNA topoisomerase I and II inhibitor. | |||
T13183 |
Top1 inhibitor 1
|
Others | Others |
Top1 inhibitor 1 is a potent inhibitor of human topoisomerase I (Top1)(IC50: 29 nM). | |||
T70445 |
Lurtotecan dihydrochloride
|
||
Lurtotecan dihydrochloride is an antineoplastic (DNA Topoisomerase I 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. | |||
T71185 |
Indotecan hydrochloride
|
||
Indotecan hydrochloride is a novel selective and potent topoisomerase I inhibitor with potential anticancer activitity. | |||
T39373 |
PNU-EDA-Gly5
PNU-EDA-Gly5 |
||
PNU-EDA-Gly5 is a DNA topoisomerase I inhibitor-based oligo-glycine linker-payload used for the synthesis of antibody-drug conjugates (ADCs). It consists of the DNA topoisomerase I inhibitor PNU-159682 and the linker EDA-Gly5. | |||
T12209 |
Netropsin dihydrochloride
|
Others | Others |
Netropsin dihydrochloride is a small-molecule MGB (minor-groove binder), inhibits the catalytic activity of isolated topoisomerase and interferes with the stabilization of the cleavable complexes of topoisomerase II and I in nuclei. | |||
T13191 |
TP3011
CH0793011 |
Others | Others |
TP3011 is a potent topoisomerase I inhibitor equipotent as SN38 and is an active metabolite of CH-0793076. | |||
T40365 | T-2513 | ||
T-2513 is a potent and specific inhibitor of topoisomerase I. It acts by forming covalent bonds with the topoisomerase I-DNA complex, thereby enhancing its stability. This interaction disrupts the normal process of DNA replication and RNA synthesis, ultimately resulting in cellular apoptosis. | |||
T14703 |
Karenitecin
BNP 1350,Cositecan |
Topoisomerase | DNA Damage/DNA Repair |
Karenitecin (Cositecan) is an inhibitor of topoisomerase I. It has potent anti-cancer activity. | |||
T70513 |
NB-506 Free Base
|
||
NB-506 Free Base is an indolocarbazole antitumor agent; a DNA topoisomerase I inhibitor. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1123 |
Camptothecin
NSC-100880,Campathecin,喜树碱,(S)-(+)-Camptothecin,CPT |
Apoptosis; Influenza Virus; Topoisomerase; Antibiotic; Antifungal | Apoptosis; DNA Damage/DNA Repair; Microbiology/Virology |
Camptothecin (CPT) 属于生物碱类天然产物,是一种 DNA 拓扑异构酶 I (Topo I) 的抑制剂 (IC50=679 nM),具有特异性。Camptothecin 具有抗肿瘤活性,可以诱导细胞凋亡。 | |||
TQ0134 |
Podocarpusflavone A
|
Topoisomerase | DNA Damage/DNA Repair |
Podocarpusflavone A is a DNA topoisomerase I inhibitor. It has moderated anti-proliferative activity induce cell apoptosis in MCF-7. | |||
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。 | |||
T3S1957 |
9-amino-CPT
9-氨基喜树碱,Aminocamptothecin,9-amino-2(S)-camptothecin,9-Aminocamptothecin |
Topoisomerase | DNA Damage/DNA Repair |
9-amino-CPT (Aminocamptothecin) 是一种拓扑异构酶I 的抑制剂,具有抗肿瘤活性。 | |||
T5853 |
Rubitecan
RFS 2000,鲁比特康,9-Nitrocamptothecin |
Topoisomerase | DNA Damage/DNA Repair |
Rubitecan (9-Nitrocamptothecin) 是一种与喜树碱相关的半合成药物,具有有效的抗肿瘤和抗病毒特性。它是一种 DNA 拓扑异构酶 I 抑制剂,以浓度依赖性方式抑制 DNA 拓扑异构酶 I 并在无细胞试验中增加超螺旋 DNA 的比例。 | |||
T5784 |
Topotecan
NSC 609669,拓扑替康,SKF 104864A |
Topoisomerase; Autophagy | Autophagy; DNA Damage/DNA Repair |
Topotecan (NSC-609669) 是一种拓扑异构酶 I 抑制剂,通过抑制 DNA 拓扑异构酶起抗肿瘤作用,可用于治疗卵巢癌。 | |||
T2764 |
(S)-10-Hydroxycamptothecin
10-羟喜树碱,10-羟基喜树碱,10-Hydroxycamptothecin,10-HCPT |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
(S)-10-Hydroxycamptothecin (10-HCPT) 是一种从喜树中分离的 DNA 拓扑异构酶 I 抑制剂。它显著诱导细胞凋亡,可研究肝癌、胃癌、结肠癌和白血病。 | |||
TN1917 |
Mauritianin
|
Topoisomerase | DNA Damage/DNA Repair |
Mauritianin 是一种从 Acalypha indica 的花和叶中分离出来的山柰酚苷,是一种拓扑异构酶 I 抑制剂。Mauritianin 具有细胞保护活性。 | |||
T1703 |
SN-38
7-乙基-10-羟基喜树碱,NK012,伊立替康杂质B,SN 38 |
DNA/RNA Synthesis; Topoisomerase; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
SN-38 (NK012) 是 DNA 拓扑异构酶 I (Topo I) 抑制剂 Irinotecan 的活性代谢产物,可以抑制 DNA 和 RNA 合成 (IC50=0.077/1.3 μM)。SN-38 具有抗肿瘤活性,可以诱导细胞自噬。 | |||
T6228 |
Irinotecan
CPT-11,Topotecin,伊立替康,(+)-Irinotecan |
Topoisomerase; Autophagy | Autophagy; DNA Damage/DNA Repair |
Irinotecan (CPT-11) 是喜树碱的衍生物,是一种 DNA 拓扑异构酶 I (Topo I) 的抑制剂。Irinotecan 通过与 Topo I 复合物结合来阻止 DNA 链的重新连接,并导致双链 DNA 断裂和细胞死亡,具有抗肿瘤活性。 | |||
T0486L |
Irinotecan Hydrochloride
盐酸伊立替康,伊立替康盐酸盐,Camptothecin 11 hydrochloride,CPT-11 hydrochloride |
Topoisomerase; Autophagy | Autophagy; DNA Damage/DNA Repair |
Irinotecan Hydrochloride (CPT-11 hydrochloride) 是喜树碱半合成衍生物的盐酸盐,是一种拓扑异构酶 I 抑制剂,可研究结肠癌和直肠癌。 | |||
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。 | |||
TN1037 |
Groenlandicine
|
Topoisomerase | DNA Damage/DNA Repair |
Groenlandicine 是来自黄连的一种原小檗碱生物碱,能诱导拓扑异构酶 I 介导的 DNA 裂解。它对人类重组醛糖还原酶(HRAR)具有中度的抑制作用,IC50值为 154.2 μM。 | |||
T2830 |
Betulinic acid
白桦脂酸,桦木酸,ALS-357,Lupatic acid,Betulic acid |
Apoptosis; Mitophagy; NF-κB; HIV Protease; Topoisomerase; Endogenous Metabolite; Aminopeptidase; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Betulinic acid (ALS-357) 是从白桦树皮中分离出来的一种五环三萜类天然产物,是真核细胞拓扑异构酶 I 的抑制剂,IC50值为 5 μM,具有抗逆转录病毒、抗疟疾、抗癌和抗炎特性。 | |||
T3339 |
Sophoridine
5-Epidihydrosophocarpine,槐定碱,Dihydro-5-episophocarpine |
Apoptosis; Topoisomerase | Apoptosis; DNA Damage/DNA Repair |
Sophoridine (Dihydro-5-episophocarpine) 是一种从豆科植物槐豆斜生植物的叶子中分离出来的喹喔啉生物碱。它是胰腺癌的候选药物,诱导细胞凋亡。 | |||
T16726 |
Rebeccamycin
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Topoisomerase | DNA Damage/DNA Repair |
Rebeccamycin is an antitumor antibiotic+ inhibits DNA topoisomerase I. Rebeccamycin appears to exert its primary antineoplastic effect by poisoning topoisomerase I. It also has a negligible effect on protein kinase C and topoisomerase II. | |||
TN1734 |
Heveaflavone
橡胶树双黄酮 |
Antioxidant; Topoisomerase | DNA Damage/DNA Repair; oxidation-reduction |
Heveaflavone 抑制拓扑异构酶 I 并清除 DPPH 自由基,具有抗增殖和抗氧化作用。 | |||
T14196 |
Alternariol
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Others | Others |
Alternariol (AOH), a mycotoxin synthesized by Alternaria species, displays numerous therapeutic and biological effects, including phytotoxic, cytotoxic, anti-HIV, anti-cancer, and anti-microbial properties. It functions by inhibiting the catalytic activity of topoisomerase I and II enzymes. | |||
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. | |||
TN2105 |
Proscillaridin A
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Topoisomerase | DNA Damage/DNA Repair |
Proscillaridin A 是从Drimia robusta 中提取的一种天然产物。是强力的拓扑异构酶 I 和 II 的抑制剂,IC50值分别为 30 nM 和 100 nM。 | |||
T75655 |
Hippeastrine
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Hippeastrine 是一种活性生物碱,对拓扑异构酶 ITop I 具有良好的剂量依赖性抑制作用,IC50为7.25 μg/mL。具有抗增殖和抗癌活性。 | |||
T72236 |
erythro-Austrobailignan-6
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erythro-Austrobailignan-6 是一种口服活性的抗癌化合物,能够抑制 DNA 拓扑异构酶 I 及 II 的活性,同时诱导细胞凋亡并增加 p38 和 JNK 的磷酸化。 | |||
T1521 |
(±)-10-Hydroxycamptothecin
Hydroxy Camptothecine,10-羟基喜树碱,10-Hydroxycamptothecin |
Topoisomerase | DNA Damage/DNA Repair |
(±)-10-Hydroxycamptothecin (Hydroxy Camptothecine) 是一种从喜树茎木中分离出来的生物碱,抑制拓扑异构酶 I 活性,具有广谱抗肿瘤活性。 | |||
TN4283 | Isodiospyrin | Topoisomerase; Antifection | DNA Damage/DNA Repair; Microbiology/Virology |
Isodiospyrin is a novel human DNA topoisomerase I inhibitor, it exhibits cytotoxic activity to tumor cell lines. Isodiospyrin has antibacterial activity, the minimum inhibitory concentrations (MICs) against Gram-positive bacteria ranged from 0.78 to 50 mi | |||
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 。 |