CAS NO: | 823218-99-1 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | SN 2 is a potent activator ofTRPML3ion channel with anEC50of 1.8 μM[1].SN 2 also acts as a potent inhibitor of Dengue virus 2 (DENV2) and Zika virus (ZIKV)[2]. | ||||||||||||||||
IC50& Target | EC50: 1.8±0.13 μM (TRPML3), >29.9 μM (TRPML1)[1] | ||||||||||||||||
体外研究 (In Vitro) | The conductance of TRPML3 channels is estimate, when activated with 10 μM SN-2 is approximately 10 pS at –80 mV. TRPML3-expressing HEK293 cells are perfused with a series starting with compound alone (in SBS), with compound in ELS, and finally with ELS alone. Two representative compounds, SF-24 and SN-2, are tested. SF-24 is one of the least effective compounds, and SN-2 is one of the most active ones. SN-2 has a similar synergistic effect, also reaching up-to 10-fold enhancement of the combined response when compared with the individual responses, reaching average current densities of up to 3 nA/pF at –80 mV. Dominant negative TRPML3(D458K) is highly effective in eliminating SN-2-induced activity in epidermal melanocytes, suggesting that SN-2 activates a channel that is not responsive in presence of TRPML3(D458K). Such a dominant negative action might be attributed to potential heteromerization of TRPML3(D458K) with an SN-2-responsive channel[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 255.35 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H21NO | ||||||||||||||||
CAS 号 | 823218-99-1 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 100 mg/mL(391.62 mM;Need ultrasonic) 配制储备液
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