Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T82935 | AuM1Gly
化合物 AuM1Gly
|
98% |
|
|
AuM1Gly 是拓扑异构酶 I (topoisomerase I) 的抑制剂,对 MDA-MB-231 乳腺癌细胞的增殖产生影响,表现出低纳摩尔范围的 IC50 值。 | ||||
TQ0049 | MC-DOXHZN hydrochloride
MC-DOXHZN盐酸盐
|
480998-12-7 | 98% |
|
MC-DOXHZN hydrochloride is an albumin-binding prodrug of Doxorubicin. Doxorubicin is a DNA topoisomerase II inhibitor. | ||||
TN4172 | Guajadial B
化合物 TN4172
|
1414455-03-0 | 98% |
|
Guajadial B acts as a Top1 catalytic inhibitor and delays Top1 poison-mediated DNA damage. Guajadial B shows cytotoxicities against five human cancer cell lines,... | ||||
T15200 | Edotecarin
化合物 T15200
|
174402-32-5 | 98% |
|
Edotecarin is a potent topoisomerase I inhibitor. It can decrease single-strand DNA cleavage (IC50: 50 nM). | ||||
TN2464 | Eleutherin
红葱醌
|
478-36-4 | 98% |
|
Eleutherin is a natural product from Eleutherine americana | ||||
TN4173 | Guajadial C
化合物 TN4173
|
1529775-02-7 | 98% |
|
Guajadial C acts as a Top1 catalytic inhibitor and can delay Top1 poison-mediated DNA damage. It shows cytotoxicity against five human cancer cell lines. | ||||
TN1889 | Lupalbigenin
化合物Lupalbigenin
|
76754-24-0 | 98% |
|
Lupalbigenin sensitizes detachment-induced cell death in human lung cancer cell through down-regulation of pro-survival proteins. | ||||
TN5190 | Tryprostatin A
化合物 TN5190
|
171864-80-5 | 98% |
|
Tryprostatin A is an inhibitor of breast cancer resistance protein. Tryprostatin A and tryprostatin B are indole alkaloid-based fungal products that inhibit mamm... | ||||
T72153 | Topoisomerase IV inhibitor 1
化合物 Topoisomerase IV inhibitor 1
|
2883403-42-5 | 98% |
|
TopoisomeraseIV inhibitor 2 (compound 7d) 作为DNA拓扑异构酶IV(TOPO IV)抑制剂,展现出高效的活性,其对TOPO IV的IC50值为0.23 μM,而对DNA促旋酶的IC50为0.43 μM。此外,该化合物在抗菌领域同样表现出较强的能力,对金黄色葡萄球菌Nerman菌株... | ||||
T72154 | Topoisomerase IV inhibitor 2
化合物 Topoisomerase IV inhibitor 2
|
2883403-36-7 | 98% |
|
TopoisomeraseIV inhibitor 2 (compound 5d) 是一种 DNA 拓扑异构酶 IV 抑制剂,其对 TOPO IV 和 DNA 促旋酶的 IC50 值分别为 0.35 μM 和 0.55 μM。此化合物显示出针对 Staphylococcus aureus Newman 菌株和 Esche... | ||||
T73421 | CPT-Se3
化合物 CPT-Se3
|
2968315-02-6 | 98% |
|
CPT-Se3为含硒的喜树碱前体活性分子,其杀癌和抗肿瘤效力显著。它通过降低GSH/GSSG比率及总硫醇水平,增加Hep G2细胞中ROS含量,触发癌细胞凋亡。CPT-Se3对HeLa、Hep G2、A549及SMMC-7721细胞线具备显着细胞毒性,IC50值介于2.19-4.7 μM。 | ||||
T73422 | CPT-Se4
化合物 CPT-Se4
|
2968315-03-7 | 98% |
|
CPT-Se4为含硒前体活性分子的喜树碱(CPT)衍生物,对癌细胞具有较高杀伤力和抑制肿瘤生长效果。在降低GSH/GSSG比率和总硫醇的同时,CPT-Se4能够增加Hep G2细胞中的ROS水平,触发癌细胞凋亡。此化合物对HeLa、Hep G2、A549和SMMC-7721细胞系显示出显著的细胞毒性,IC50值范围为2.... | ||||
T74364 | SDOX
化合物 SDOX
|
2921601-78-5 | 98% |
|
SDOX为Doxorubicin的前体药物,通过脂质体递送至肿瘤细胞内,在GSH过量释放条件下,触发DOX释放。该机制在不损害抗癌效果的同时,极大地降低了对正常组织的毒副作用。 | ||||
TN1734 | Heveaflavone
橡胶树双黄酮
|
23132-13-0 | 98% |
|
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。 | ||||
T14703 | Karenitecin
化合物 T14703
|
203923-89-1 | 98% |
|
Karenitecin (Cositecan) is an inhibitor of topoisomerase I. It has potent anti-cancer activity. | ||||
T14953 | Chloroquinoxaline sulfonamide
化合物 T14953
|
97919-22-7 | 98% |
|
Chloroquinoxaline sulfonamide is a topoisomerase II alpha/beta poison. It is used to control coccidiosis in poultry, rabbit, sheep, and cattle. | ||||
T15054 | Daun02
化合物 T15054
|
290304-24-4 | 98% |
|
Daun02 is the topoisomerase inhibitor Daunorubicin prodrug. | ||||
T1456 | Doxorubicin
阿霉素
|
23214-92-8 | 98% |
|
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 。 | ||||
TN5133 | 3',5,5',7-Tetrahydroxy-4',6-dimethoxyflavone
化合物 TN5133
|
125537-92-0 | 98% |
|
5,7,3',5'-tetrahydroxy-6,4'-dimethoxyflavone exhibits anti-HIV-1 activity in the anti-syncytium assay using (∆Tat/rev)MC99 virus and 1A2 cell line system, it sho... | ||||
TN2953 | 3-Hydroxysarpagine
化合物 TN2953
|
857297-90-6 | 98% |
|
3-Hydroxysarpagine是一种天然产物,属于夹竹桃科萝芙木属,其产品编号为 TN2953,CAS号为 857297-90-6。3-Hydroxysarpagine可用作对照参考。 |