NAPHTHO[1,2-D]THIAZOL-2-AMINE

NAPHTHO[1,2-D]THIAZOL-2-AMINE

中文名称NAPHTHO[1,2-D]THIAZOL-2-AMINE
中文同义词萘并[1,2-D]噻唑-2-胺;化合物SKA-31;SKA-31,K CA 3.1和K CA 2通道激活剂
英文名称2-AMINO-BETA-NAPHTHOTHIAZOLE
英文同义词NAPHTHO[1,2-D][1,3]THIAZOL-2-AMINE;NAPHTHO[1,2-D]THIAZOL-2-YLAMINE;2-AMINO-BETA-NAPHTHOTHIAZOLE;2-AMINO-NAPHTHO[1,2-D]THIAZOLE;2-AMINONAPHTHO-1,2-THIAZOLE;AKOS BBS-00006561;IFLAB-BB F1386-0401;LABOTEST-BB LT00154570
CAS号40172-65-4
分子式C11H8N2S
分子量200.26
EINECS号254-822-1
相关类别合成;有机化工原料;BENZOTHIAZOLE
Mol文件40172-65-4.mol
结构式NAPHTHO[1,2-D]THIAZOL-2-AMINE 结构式

NAPHTHO[1,2-D]THIAZOL-2-AMINE 性质

熔点184-188°C
沸点417.1±28.0 °C(Predicted)
密度1.403±0.06 g/cm3(Predicted)
储存条件Keep in dark place,Sealed in dry,2-8°C
溶解度二甲基亚砜:≥30mg/mL
形态固体
酸度系数(pKa)3.50±0.30(Predicted)
颜色米白色
稳定性供货时可稳定保存 1 年。 DMSO 溶液可在 -20°C 下保存长达 2 个月。
CAS 数据库40172-65-4(CAS DataBase Reference)
EPA化学物质信息Naphtho[1,2-d]thiazol-2-amine (40172-65-4)

NAPHTHO[1,2-D]THIAZOL-2-AMINE 用途与合成方法

SKA-31 是钾离子通道 (potassium channel) 激活剂,作用于 KCa3.1,KCa2.2,KCa2.1 和 KCa2.3 的 EC50 值分别为 260 nM,1.9 μM,2.9 μM,2.9 μM,能增强内皮源性超极化因子反应,降低血压。

EC50: 2.9 μM (KCa2.1), 1.9 μM (KCa2.2), 2.9 μM (KCa2.3), 260 nM (KCa3.1)

SKA-31 activates KCa2/3 channels more potently than PK 26124, and is more selective over other Ion channels.
SKA-31 reduces cell viability with IC 50s of 5.3 μM , 46.9 μM in HCT-116 cells and HCT-8 cells, respectively.
SKA-31 (5.3 μM; 0-96 hours) reduces HCT-116 cells proliferation when added at time zero at 5.3 μM.
SKA-31 triggers apoptosis in HCT-116 cells at 5 μM, and the effect is smaller in HCT-8 cells at 45 μM.
SKA-31 increases the percentage of cells in G0/G1 phase in HCT-116 and HCT-8 cell lines at 5 μM and 45 μM, respectively.
SKA-31 further activates Caspase 3 and reduces Akt phosphorylation induced by CDDP.
SKA-31 has a synergic effect with CDDP also on the inhibition of HCT-116 cell proliferation.

Cell Viability Assay

Cell Line: HCT-116 cells, HCT-8 cells
Concentration:
Incubation Time: 24 hours
Result: Reduced cell viability with IC 50s of 5.3 μM , 46.9 μM in HCT-116 and HCT-8, respectively.

Cell Proliferation Assay

Cell Line: HCT-116 cells
Concentration: 5.3 μM
Incubation Time: 0-96 hours
Result: Reduced HCT-116 cells proliferation when added at time zero at IC 50S value.

Apoptosis Analysis

Cell Line: HCT-116 cells, HCT-8 cells
Concentration: 5 μM (HCT-116 cells), 45 μM (HCT-8 cells)
Incubation Time: 24 hours
Result: Triggered apoptosis in HCT-116 cells, and the effect was smaller in HCT-8 cells.

Cell Cycle Analysis

Cell Line: HCT-116 cells, HCT-8 cells
Concentration: 5 μM (HCT-116), 45 μM (HCT-8)
Incubation Time: 24 hours
Result: Increased the percentage of cells in G0/G1 phase in HCT-116 and HCT-8 cell lines.

Western Blot Analysis

Cell Line: HCT-116 cells
Concentration:
Incubation Time: 24 hours
Result: Further activated Caspase 3 and reduced Akt phosphorylation when co-treatment with CDDP in HCT-116 cells.

SKA-31 is not acutely toxic and has good pharmacokinetic properties.
SKA-31 potentiates native KCa3.1 and KCa2.3 in murine carotid endothelium with EC 50 values of 225 nM and 1.6 μM for KCa3.1 and KCa2.3, respectively.
SKA-31 stimulates KCa3.1 and KCa2.3 in vascular endothelial cells and increases acetylcholine-induced endothelium-derived hyperpolarizing factor (EDHF) -mediated vasodilation.
SKA-31 potentiates EDHF-type vasodilations and lowers blood pressure in mice. Injections of SKA-31 (1-30 mg/kg; i.p.) lower MAP over 24 hours in normotensive wild-type mice but not in KCa3.1(-/-) mice (-/-).

Animal Model: 16-25 weeks mice
Dosage: 1 mg/kg, 10 mg/kg, and 30 mg/kg
Administration: Intraperitoneal injection
Result: Lower MAP over 24 hours in normotensive wild-type mice but not in KCa3.1(-/-) mice (-/-).

安全信息

危险品标志Xn
危险类别码20/21/22-36/37/38-36-22
安全说明22-36/37/39-26

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2024/04/30HY-111655NAPHTHO[1,2-D]THIAZOL-2-AMINE
SKA-31
40172-65-45mg600元
2024/04/30HY-111655NAPHTHO[1,2-D]THIAZOL-2-AMINE
SKA-31
40172-65-410mg1000元

NAPHTHO[1,2-D]THIAZOL-2-AMINE 上下游产品信息

"NAPHTHO[1,2-D]THIAZOL-2-AMINE"相关产品信息
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