首页 工具
登录
购物车

搜索结果

Search Results for " pi hydrolysis "

如果没找到您满意的产品或者您对产品有其他要求,可以联系我们专业顾问为您提供针对性的合理建议。     QQ咨询       网站留言咨询

提交您的定制咨询

点击图片重新获取验证码
Cat. No. Product Name Target Signaling Pathways
T29126 VU0360172

VU-0360172,VU 0360172

GluR Neuroscience
VU0360172 是 mGlu5 受体的正变构调节剂(EC50 = 16 nM;Ki = 195 nM)。
T6941 PI-1840

PI 1840

PARP; Proteasome Chromatin/Epigenetic; DNA Damage/DNA Repair; Proteases/Proteasome; Ubiquitination
PI-1840 是一种高效的、选择性的蛋白酶体chymotrypsin-like (CT-L)抑制剂,IC50=27nM。
T2370 AC-55541

AOB2796

Proteasome; Protease-activated Receptor GPCR/G Protein; Proteases/Proteasome; Ubiquitination
AC-55541 (AOB2796) 是高选择性的蛋白酶激活受体 2(PAR2)激动剂,pEC50为6.7。它在 PI 水解测定和 Ca2+动态测定中的pEC50值为 5.9 和 6.6,在体内表现出伤害感受器活性。
T15818 LY367385

FXR Metabolism
LY367385 is a highly effective and selective mGluR1a antagonist. LY367385 has neuroprotective, anticonvulsant, and antiepileptic effects. Compared with > 100 μM for mGlu5a, LY367385 has an IC50 of 8.8 μM for inhibits of quisqualate-induced phosphoinositide (PI) hydrolysis.
T39406 (±)-LY367385

(±)-LY367385

(±)-LY367385 is the racemic form of LY367385, and LY367385 is a highly potent and selective mGluR1a antagonist. LY367385 exhibits a high inhibitory activity against quisqualate-induced phosphoinositide (PI) hydrolysis, with an IC50 value of 8.8 μM. In contrast, its inhibitory activity against mGlu5a is greater than 100 μM.
T60355 LY367385 hydrochloride

LY367385 hydrochloride 是一种高效且选择性的mGluR1a 拮抗剂,抑制喹喹啉诱导的磷酸肌醇水解的IC50值为 8.8 μM,而对 mGlu5a 的IC50值大于 100 μM。LY367385 hydrochloride 具有神经保护,抗惊厥和抗癫痫作用。
T37030 PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt)

PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt)

The phosphatidylinositol (PtdIns) phosphates represent a small percentage of total membrane phospholipids. However, they play a critical role in the generation and transmission of cellular signals. PtdIns-(4)-P1 (1,2-dioctanoyl) is a synthetic analog of natural phosphatidylinositol (PtdIns) featuring C8:0 fatty acids at the sn-1 and sn-2 positions. The compound contains the same inositol and diacylglycerol (DAG) stereochemistry as the natural compound. PtdIns-(4)-P1 can be phosphorylated to di- ...
T36937 PtdIns-(1,2-dioctanoyl) (sodium salt)

The phosphatidylinositol (PtdIns) phosphates represent a small percentage of total membrane phospholipids. However, they play a critical role in the generation and transmission of cellular signals. PtdIns-(1,2-dioctanoyl) is a synthetic analog of natural phosphatidylinositol (PtdIns) containing C8:0 fatty acids at the sn-1 and sn-2 positions. The compound features the same inositol and diacyl glycerol (DAG) stereochemistry as that of the natural compound. The short fatty acid chains of this anal...

化合物

VU0360172
Cat.No: T29126
Synonym: VU-0360172,VU 0360172
Target: GluR
PI-1840
Cat.No: T6941
Synonym: PI 1840
Target: PARP, Proteasome
AC-55541
Cat.No: T2370
Synonym: AOB2796
Target: Proteasome, Protease-activated Receptor
LY367385
Cat.No: T15818
Synonym:
Target: FXR
(±)-LY367385
Cat.No: T39406
Synonym: (±)-LY367385
Target:
LY367385 hydrochloride
Cat.No: T60355
Synonym:
Target:
PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt)
Cat.No: T37030
Synonym: PtdIns-(4)-P1 (1,2-dioctanoyl) (ammonium salt)
Target:
PtdIns-(1,2-dioctanoyl) (sodium salt)
Cat.No: T36937
Synonym:
Target:
TargetMol Loading
联系我们
400-820-0310

上海市静安区江场三路238号8楼