Nav1.7-IN-3

目录号: A13626

voltage-gated sodium channel Nav1.7 inhibitor

Nav1.7-IN-3

Nav1.7-IN-3 Chemical Structure

CAS NO. 1788872-06-9

Nav1.7-IN-3 is a selective, orally bioavailable voltage-gated sodium channel Nav1.7 inhibitor with an IC50 of 8 nM. Pain relief. Limited CNS penetration.

库存: 现货

规格 价格 数量
1 mg
¥ 3,200.00
5 mg
¥ 9,600.00
10 mg
¥ 16,000.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

产品详情

Nav1.7-IN-3 is a selective, orally bioavailable voltage-gated sodium channel Nav1.7 inhibitor with an IC50 of 8 nM. Pain relief. Limited CNS penetration.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 23.2 mL 116.02 mL 232.05 mL
0.5 mM 4.64 mL 23.2 mL 46.41 mL
1 mM 2.32 mL 11.6 mL 23.2 mL
5 mM 0.46 mL 2.32 mL 4.64 mL

*The above data is based on the productmolecular weight 430.95. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

目录号 A13626
作用机制 Inhibitor (抑制剂)
M. Wt 430.95
Formula C17H20ClFN4O2S2
Purity >99%
Storage

Store lyophilized at -20ºC, keep desiccated.
In lyophilized form, the chemical is stable for 36 months.
In solution, store at -20ºC and use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

CAS No. 1788872-06-9
SMILES FC1=C(S(=O)(NC2=NC=CS2)=O)C=C(Cl)C(NCC34CCCN3CCC4)=C1

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