N106
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货号：A1231634
N106 是一种新型肌质网钙 ATP 酶 (SERCA2a) SUMO ylation激活剂。N106 直接激活 SUMO -激活酶 E1 连接酶。
N106 化学结构
N106 3D分子结构
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N106 纯度/质量文件 产品仅供科研
货号：A1231634
标准纯度：
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产品说明书
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N106 质控信息
CDC25B-IN-2
✔
Akt
99%+
Clevidipine
✔
97%
Verapamil HCl
✔
99%
Amlodipine
✔
99%
Amlodipine maleate
✔
98%
(+)-cis-Diltiazem HCl
✔
95%
Zegocractin
++
Orai1/STIM1-mediated Ca2+ currents, IC50: 120 nM
99%+
Tanshinone IIA sulfonate sodium
✔
98%
Ulixacaltamide
++
hCaV3.1, IC50: 50 nM
hCaV3.2, IC50: 110 nM
99%+
Dronedarone Hydrochloride
✔
95%
Nitrendipine
+
Calcium channel, IC50: 95 nM
98%
Efonidipine HCl monoethanolate
✔
98%
Cinnarizine
✔
98%
SEA0400
++
ROS,ERK,p38 MAPK
99%+
Fasudil HCl
✔
Rho,PKA
98%
ML-9
✔
Akt,MLCK
99%+
Flunarizine 2HCl
+
Calcium channel, Ki: 68 nM
95%
Lomerizine 2HCl
✔
98%
Efonidipine
✔
98%
Levamlodipine
✔
97%
Nisoldipine
++
L-type Cav1.2, IC50: 10 nM
97%
Isradipine
✔
98%
Lacidipine
✔
98%
Lercanidipine
✔
98%
Loureirin B
✔
Potassium Channel
99%+
Tetracaine HCl
✔
98%
Manidipine
+++
Calcium channel, IC50: 2.6 nM
98%
Manidipine Dihydrochlorid
+++
Calcium channel, IC50: 2.6 nM
98%
Nicardipine
✔
98%
Wilforgine
✔
98+%
Econazole
✔
99%+
Ginsenoside Rd
✔
NF-κB
98%
Fendiline HCl
✔
98+%
Mesaconitine
✔
98%
Tetrandrine
✔
95%
Nifedipine
✔
95%
Nilvadipine
++++
Calcium channel, IC50: 0.03 nM
98%
Barnidipine
++++
[3 H]nitrendipine, Ki: 0.21 nM
95+%
Azelnidipine
✔
97%
Levetiracetam
✔
98%
Nimodipine
✔
95%
Benidipine HCl
✔
98%
Pinaverium bromide
✔
98%
Pranidipine
✔
98%
NP118809
+
N-type Ca2+ channel, IC50: 0.11 μM
L-type calcium channel, IC50: 12.2 μM
98%
Amlodipine Besylate
+++
Calcium channel, IC50: 1.9 nM
97%
Cilnidipine
✔
98%
Cinepazide Maleate
✔
98%
Terfenadine
✔
98%
YM-58483
✔
99%+
Ranolazine
✔
98%
Praeruptorin A
✔
Akt,p38 MAPK
98%
Ranolazine 2HCl
✔
98%
Felodipine
++++
L-type calcium channel, IC50: 0.15 nM
98%
PD173212
+++
N-type Ca2+ channel, IC50: 36 nM
98%
Levamlodipine besylate
✔
97%
Carboxyamidotriazole Orotate
✔
98%
IGS-1.76
✔
98+%
WH-4-023
++++
++++
99%+
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1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多，抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用，但抑制强度暂时没有相关数据。
N106 生物活性
描述
N106 is the first SERCA2a SUMOylation activator. N106 directly activates the SUMO-activating enzyme, E1 ligase. N106 can be used in heart failure research to improve the contractile properties of cultured rat cardiomyocytes. N106 increases cell contractility, ATPase activity of calcium-transient SERCA2a, and SUMOylation within 10 minutes of administration, and these effects last for 24 hours in cardiomyocytes [1]
N106 动物研究
Animal study
When administered intravenously at a dose of 10 mg/kg, N106 has a half-life of 65.4 min and a Cmax of 2.24 μM in a mouse model, with an oral bioavailability of 56% and a half-life (t1/2) of 19 min. In in vivo experiments, N106 increased cardiac SERCA2A SUMOylation and significantly improved ventricular function in heart failure mice[1]
N106 参考文献
N106 实验方案
计算器
摩尔计算器
总药量计算器
工作液计算器
存储液制备
1mg
5mg
10mg
1 mM
5 mM
10 mM
2.82mL
0.56mL
0.28mL
14.11mL
2.82mL
1.41mL
28.22mL
5.64mL
2.82mL
N106 技术信息
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