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Edotecarin is a potent topoisomerase I inhibitor. It can decrease single-strand DNA cleavage (IC50: 50 nM).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $2,570 | 3-6 months | 3-6 months | |
| 50 mg | $3,380 | 3-6 months | 3-6 months | |
| 100 mg | $4,600 | 3-6 months | 3-6 months |
| Description | Edotecarin is a potent topoisomerase I inhibitor. It can decrease single-strand DNA cleavage (IC50: 50 nM). |
| Targets&IC50 | Topo I:50 nM, PKC:160 μM |
| In vitro | Edotecarin (0.6 μmol/L) increases the formation of DNA-protein complexes in a time-dependent manner, in the presence of human colon cancer cells labeled with 3Hthymidine [1]. |
| In vivo | Edotecarin significantly delays tumor growth, achieving a delay of 10.45 days at a dosage of 3 mg/kg and extending up to 24.83 days at 100 mg/kg. It enhances survival by 83% in mice with D-456MG glioma intracranial tumors and exhibits potent antimetastatic properties [1]. Additionally, combining edotecarin with irinotecan elevates its in vivo antitumor efficacy beyond that observed with either compound individually [2]. |
| Synonyms | PF 804950, J 107088 |
| Molecular Weight | 608.55 |
| Formula | C29H28N4O11 |
| Cas No. | 174402-32-5 |
| Smiles | O=C1C2=C3C(N(C=4C3=CC=C(O)C4)[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)=C6C(=C2C(=O)N1NC(CO)CO)C=7C(N6)=CC(O)=CC7 |
| Relative Density. | 1.96g/cm3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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