| Size | Price | Stock |
|---|---|---|
| 500mg | $50 | In-stock |
| 1g | $80 | In-stock |
| 5g | $108 | In-stock |
| 10g | $180 | In-stock |
| 50 g | Get quote | |
| 100 g | Get quote | |
| We match the lowest price on market. | ||
We offer a substantial discount on larger orders, please inquire via [email protected]
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Inquiry for price and availability only. Please place your order via our email or fax.
| Cat. No. : | HY-B0391 |
| M.Wt: | 392.49 |
| Formula: | C24H28N2O3 |
| Purity: | >98 % |
| Solubility: | H2O : < 0.1 mg/mL;DMSO : 33.33 mg/mL (ultrasonic) |
Naftopidil (KT-611) is is a selective alpha1-adrenoceptor antagonist, with Kis of 3.7 nM, 20 nM and 1.2 nM for the cloned human α1a-, α1b- and α1d-adrenoceptor subtypes, respectively. Naftopidil has antiproliferative effects. Naftopidil can be used for the research of prostate hyperplasia[1][2].
IC50 & Target:α1-adrenoceptor[1]
In Vitro: Naftopidil suppresses human prostate tumor growth by altering interactions between tumor cells and stroma[2].
Naftopidil (10 μM for PCa cells, 0.1-10 μM for PrSC; 3 days) shows growth inhibitory effects on PCa cells and PrSC[2].
Naftopidil (50 μM for E9 cells, 25 μM for PrSC; 48 hours) increases the level of cell-cycle regulatory protein p27 in E9 cells, but not PrSC[2].
In Vivo: Naftopidil (10 mg/kg; p.o; daily; for 28 days) decreases microvessel density (MVD) in E9+PrSC tumors mice model[2].
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