: Homatropine Methylbromide 是一种毒蕈碱受体 AChR 拮抗剂,抑制 WKY-E 和 SHR-E ,IC50分别为 162.5 和 170.3 nM。体外活性: Homatropine [14C]methylbromide在
receptor agonist. It has anti-anxiety activity.体内活性: [14C]CP-409,092(P.O.; 100 mg/kg; ) treatment, the total recovery is 89.1
measured in ion-leaky vesicles in the presence of 1 mM potassium. Soraprazan also effectively inhibits dibutyryl
hydrochloride (L-NAME HCl) 是NOS 抑制剂(IC50:70 μM)。细胞实验: rMC-1 cells are incubated in 5 or 25 mM glucose, with or without l-NAME
medium and stimulated with 1 μM human insulin and 1 μM liver X receptor (LXR) agonist T0901317 in the presence
reaction.体外活性: Fructosyl-lysine (100 μM; 1 hour) contains a carbohydrate moiety and appears to be phosphorylated, it can
for Reference)激酶实验: [14C]-monosaccharide uptake inhibition experiments: Stable cell lines over-expressing hSGLT-1, -2, -4, -5
酶 A: 胆固醇酰基转移酶 (ACAT) 抑制剂,对 ACAT1和 ACAT2的 IC50分别为 24 和 9.2 µM。Avasimibe 在前列腺癌中有研究的价值。细胞实验: For foam cell formation
) consisted of 0.1 mg microsomes, 0.25% BSA and 40 PM [14C]oleoyl CoA in buffer A. To avoid the effects of endogenous
DL-TBOATargetMol美国生化试剂,可用于动物细胞实验Product IntroductionBioactivity英文名: DL-TBOA描述: DL-TBOA inhibited [14C] glutamate uptake
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