K 01-162

小分子

K 01-162

K648639-5mg

5mg

≥98%

-20°C储存

超低温冰袋运输

K 01-162 (K162) inhibits the fibril formation of A β peptides and eliminates their neurotoxicity. K 01-162 binds with A β 42 peptide with an EC 50 value of 80 nM. K 01-162 binds directly to AβO with a K D value of 19 μM. K 01-162 is capable of penetrating the brain and can be used for the research of Alzheimer’s disease. In Vitro K 01-162 (1 μM; 24 h) reduces the level of intracellular AβO. K 01-162 (0.78-50 μM; 5 min) blocks the synaptic binding activity of AβO in mouse hippocampal neurons. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: MC65 cell line Concentration: 1 μM Incubation Time: 24 hours Result: Reduced the levels of SDS-stable Aβ trimer and larger aggregates. In Vivo K 01-162 (100 μM; intracerebroventricular infusion 0.25 μL/h for 2 weeks) attenuates amyloid load in vivo. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: 5xFAD mice with cerebral Aβ amyloidosisDosage: 100 μM Administration: Intracerebroventricular infusion; 100 μM 0.25 μL/h; for 2 weeks Result: Caused no apparent toxicity and significantly reduced the amyloid load in hippocampus to\n50% of the mock-treated level. Form:Solid

K 01-162 (K162) 可抑制 A β 肽纤维的形成，并消除其神经毒性。K 01-162 与 A β 42 肽结合的 EC 50 值为 80 nM。K 01-162 与 A βO 直接结合，K D 值为 19 μM。K 01-162 能够穿透

677746-25-7

C15H14BrN

288.18 g/mol

24858056

CN(C)C1=CC2=C(C=C1)C3=C(C2)C=C(C=C3)Br

CN(C)C1=CC2=C(C=C1)C3=C(C2)C=C(C=C3)Br

24858056

DMSO : 14.29 mg/mL (49.59 mM; Need ultrasonic)

0

1

1

287.031 Da

287.031 Da

3.200 Ų

17

0

278

0

1

4.5