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Paclitaxel-bromothiophene is a semisynthetic taxane analogue of Paclitaxel. It exhibits potent antiproliferative activity against 4-T1 breast cancer cells, with an IC50 value of 15.18 nM. This compound also shows high binding affinity to C5aR1 (Kd= 19.4 μM). In 4-T1 breast cancer tumor-bearing mice, Paclitaxel-bromothiophene demonstrates excellent antitumor efficacy. It is applicable for breast cancer research.
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| Description | Paclitaxel-bromothiophene is a semisynthetic taxane analogue of Paclitaxel. It exhibits potent antiproliferative activity against 4-T1 breast cancer cells, with an IC50 value of 15.18 nM. This compound also shows high binding affinity to C5aR1 (Kd= 19.4 μM). In 4-T1 breast cancer tumor-bearing mice, Paclitaxel-bromothiophene demonstrates excellent antitumor efficacy. It is applicable for breast cancer research. |
| In vitro | Paclitaxel-bromothiophene (Compound 6v) demonstrates potent antiproliferative activity against 4-T1 breast cancer cells with an IC 50 value of 15.18 nM. It also exhibits high binding affinity to C5aR1 with a K d value of 19.4 μM. |
| In vivo | Paclitaxel-bromothiophene (10-20 mg/kg, intraperitoneal injection, 21 days) exhibits significant tumor inhibition in mice bearing 4-T1 breast cancer tumors. |
| 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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