Leucettinib-92

Leucettinib-92
Item number Size Datasheet Manual SDS Delivery time Quantity Price
AG-MR-C0049-M001 1 mg - -

3 - 9 business days*

132.00€
AG-MR-C0049-M005 5 mg - -

3 - 9 business days*

440.00€
AG-MR-C0049-M025 25 mg - -

3 - 9 business days*

1,320.00€
 
Potent inhibitor of DYRK1A (IC50=1.2nM), DYRK1B (IC50=1.8nM), DYRK3 (IC50=19.3nM) and CLK2... more
Product information "Leucettinib-92"
Potent inhibitor of DYRK1A (IC50=1.2nM), DYRK1B (IC50=1.8nM), DYRK3 (IC50=19.3nM) and CLK2 (IC50=0.6nM) [1]. Inhibits the phosphorylation of Tau at Thr212 and cyclin D1 at Thr286. Corrects cognitive deficits in animal models of Down syndrome. iso-Leucettinib-92 (Prod. No. AG-MR-C0050) is a kinase-inactive isomer and should be used as a negative control together with this compound.
Keywords: LCTB-92, (Z)-2-((Adamantan-1-yl)amino)-5-(benzo[d]thiazol-6-ylmethylene)-3,5-dihydro-4H-imidazol-4-one
Supplier: AdipoGen Life Sciences
Supplier-Nr: AG-MR-C0049

Properties

Application: CLK2/DYRK1 inhibitor
MW: 378,5 D
Formula: C21H22N4OS
Format: Solid

Database Information

CAS : 2732859-57-1| Matching products
KEGG ID : K08823 | Matching products

Handling & Safety

Storage: -20°C
Shipping: +20°C (International: +20°C)
Signal Word: Warning
GHS Hazard Pictograms:
H Phrases: H319
P Phrases: P280, P305, P351, P338
Caution
Our products are for laboratory research use only: Not for administration to humans!
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