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CZC-54252 hydrochloride

Catalog No. T39202   CAS 1784253-05-9

CZC-54252 hydrochloride is a selective inhibitor of LRRK2 with IC50s of 1.85 nM and 1.28 nM for wild-type and G2019S LRRK2. CZC-54252 hydrochloride has a neuroprotective activity and attenuates G2019S LRRK2-induced human neuronal injury with an EC50 of 1 nM.

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CZC-54252 hydrochloride Chemical Structure
CZC-54252 hydrochloride, CAS 1784253-05-9
Pack Size Availability Price/USD Quantity
1 mg In stock $ 39.00
2 mg In stock $ 55.00
5 mg In stock $ 91.00
10 mg In stock $ 143.00
25 mg In stock $ 279.00
50 mg In stock $ 497.00
100 mg In stock $ 728.00
1 mL * 10 mM (in DMSO) In stock $ 119.00
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Purity: 98.21%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description CZC-54252 hydrochloride is a selective inhibitor of LRRK2 with IC50s of 1.85 nM and 1.28 nM for wild-type and G2019S LRRK2. CZC-54252 hydrochloride has a neuroprotective activity and attenuates G2019S LRRK2-induced human neuronal injury with an EC50 of 1 nM.
Targets&IC50 LRRK2 (wild-type):1.28 nM (IC50), LRRK2 (G2019S):1.85 nM (IC50)
In vitro CZC-54252 hydrochloride(1.6 nM) fully reverses G2019S LRRK2-induced human neuronal injury to wild-type levels. CZC-54252 hydrochloride inhibits the recombinant human wild-type LRRK2 with an IC50 ranging from 1 to 5 nM. CZC-54252 hydrochloride inhibits the G2019S mutant with an IC50 ranging from 2 to 7 nM in a TF-FRET assay[2].
Molecular Weight 541.45
Formula C22H26Cl2N6O4S
CAS No. 1784253-05-9

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 30 mg/mL (55.41 mM), Sonication and heating to 60℃ are recommended.

TargetMolReferences and Literature

1. Nigel Ramsden, et al. Chemoproteomics-based design of potent LRRK2-selective lead compounds that attenuate Parkinson's disease-related toxicity in human neurons. ACS Chem Biol. 2011 Oct 21;6(10):1021-8. 2. Ramsden N, et al. Chemoproteomics-based design of potent LRRK2-selective lead compounds that attenuate Parkinson's disease-related toxicity in human neurons. ACS Chem Biol. 2011 Oct 21;6(10):1021-8.

Related compound libraries

This product is contained In the following compound libraries:
Inhibitor Library Kinase Inhibitor Library Bioactive Compounds Library Max Bioactive Compound Library

Related Products

Related compounds with same targets
LRRK2 inhibitor 1 BIX 02565 IKK 16 URMC-099 HG-10-102-01 GSK2578215A PF-06454589 EB-42486

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Keywords

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