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Product details
名称
XL01126
英文名称
XL01126
货号
X658669-1mg
包装规格
1mg
浓度
≥99%
储存温度
-20°C储存
运输条件
超低温冰袋运输
产品介绍
XL01126 is a potent degrader of LRRK2 with DC 50 s of 14 nM (G2019S LRRK2) and 32 nM (WT LRRK2), respectively. XL01126 can cross blood-brain barrier and be used as a degrader probe in Parkinson’s disease research. XL01126 exerts function of study of non-c Appearance:Solid IC50& Target:DC50: 15-72 nM (LRRK2) In Vitro:XL01126 (300 nM; 4 h) exhibits strong degradation performance by forming a positively cooperative ternary complex with E3 ubiquitin ligase ligand VHL and target protein LRRK2. XL01126 (10, 30, 100 nM; 24 h) increases mitophagy in immortalized mouse e In Vivo:XL01126 (30mg/kg; p.o.; single dose) shows oral activity with bioavailable value (F) of 15% and can penetrate the blood brain barrier after either oral or parenteral dosing in mice. Pharmacokinetic property of XL01126 in miceRoute Dose mg/kg) Biological Activity:XL01126 is a potent degrader of LRRK2 with DC 50 s of 14 nM (G2019S LRRK2) and 32 nM (WT LRRK2), respectively. XL01126 can cross blood-brain barrier and be used as a degrader probe in Parkinson’s disease research . XL01126 exerts function of study of non-
分子式
C50H64ClFN10O6S2
分子量
1019.69 g/mol
Smiles
O=C([C@H]1N(C([C@@H](NC(C2(F)CC2)=O)C(C)(SC[C@@H]3CC[C@@H](CN4CCN(C(C5=CC=C(NC6=NC=C(Cl)C(NC)=N6)C(OC)=C5)=O)CC4)CC3)C)=O)C[C@H](O)C1)NCC7=CC=C(C8=C(C)N=CS8)C=C7
溶解性
DMSO : ≥ 100 mg/mL (98.07 mM)
Safety
「No Dangerous Attributes」
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「No upstream and downstream information yet」
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XL01126 1mg

XL01126 1mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 1mg; ≥99%.

item number:X658669-1mg
Product model:1mg
level: 1mg; ≥99%
Lead Time:30days
sold 697 Items
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1mg

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