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1191911-27-9

CZC-54252

CAS: 1191911-27-9

Molecular Formula: C22H25ClN6O4S

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1191911-27-9 - Names and Identifiers

Name CZC-54252
Synonyms CS-1730
CZC54252
CZC 54252
CZC-54252
CZC 54252 hydrochloride
N-(2-(5-chloro-2-(2-methoxy-4-morpholinophenylamino)pyrimidin-4-ylamino)phenyl)methanesulfonamide
Methanesulfonamide, N-[2-[[5-chloro-2-[[2-methoxy-4-(4-morpholinyl)phenyl]amino]-4-pyrimidinyl]amino]phenyl]-
N-[2-[[5-Chloro-2-[[2-methoxy-4-(4-morpholinyl)phenyl]amino]-4-pyrimidinyl]amino]phenyl]methanesulfonamide hydrochloride
CAS 1191911-27-9

1191911-27-9 - Physico-chemical Properties

Molecular FormulaC22H25ClN6O4S
Molar Mass504.99
Density1.452±0.06 g/cm3(Predicted)
Boling Point718.1±70.0 °C(Predicted)
Solubility DMSO: 21 mg/mL
pKa8.50±0.10(Predicted)
Storage ConditionKeep in dark place,Inert atmosphere,Store in freezer, under -20°C
In vitro study CZC-54252 inhibits the activity of recombinant human wild-type LRRK2 with an IC 50 ranging from ~1 to ~5 nM. The G2019S mutant is inhibited with an IC 50 ranging from ~2 to ~7 nM in a TF-FRET assay. In addition, they are screened against a kinase panel of 185 kinases and exhibited good selectivity. G2019S LRRK2-induced human neuronal injury is attenuated by CZC-54252 with an EC 50 of ~1 nM and fully reversed to wild-type levels by CZC-54252 at concentration of 1.6 nM.

1191911-27-9 - Preparation solution concentration reference

 1mg5mg10mg
1 mM1.98 ml9.901 ml19.802 ml
5 mM0.396 ml1.98 ml3.96 ml
10 mM0.198 ml0.99 ml1.98 ml
5 mM0.04 ml0.198 ml0.396 ml
Last Update:2024-01-02 23:10:35

1191911-27-9 - Reference Information

biological activity CZC-54252 is an effective LRRK2 inhibitor with IC50 of 1.28 nM and 1.85 nM for human wild type LRRK2 and G2019S LRRK2 respectively.
target TargetValue LRRK2 (WT) (Cell-free say) 1.28 nM LRRK2 (G2019S) (Cell-free say) 1.85 nM
TargetValue
LRRK2 (WT) (Cell-free assay) 1.28 nM
LRRK2 (G2019S) (Cell-free assay) 1.85 nM
in vitro study CZC-54252 inhibits the activity of recombinant human wild-type LRRK2 with an IC 50 ranging from ~ 1 to ~ 5 nM. The G2019S mutant is inhibited with an IC 50 ranging from ~ 2 to ~ 7 nM in a TF-FRET say. In addition, they are screened against a kinase panel of 185 kinases and exhibited good selectivity. G2019S LRRK2-induced human neuronal injury is attenuated by CZC-54252 with an EC 50 of ~ 1 nM and fully reversed to wild-type levels by CZC-54252 at concentration of 1.6 nM.
Last Update:2024-04-09 15:16:38
1191911-27-9
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Shanghai Macklin Biochemical Co., Ltd
Featured ProductsSpot supply
Product Name: CZC-54252 Visit Supplier Webpage Request for quotation
CAS: 1191911-27-9
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328 Click to send a QQ message
WhatsApp: +86-18821248368
Shanghai Amole Biotechnology Co., Ltd.
Spot supply
Product Name: CZC-54252 Request for quotation
CAS: 1191911-27-9
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365 Click to send a QQ message
Wechat: 18916960931
SHANGHAI ACMEC BIOCHEMICAL TECHNOLOGY CO., LTD.
Spot supply
Product Name: CZC-54252 Visit Supplier Webpage Request for quotation
CAS: 1191911-27-9
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922 Click to send a QQ message
Wechat: 18621343501
WhatsApp: +86-18621343501
MedChemExpress (MCE)
Spot supply
Product Name: CZC-54252 Visit Supplier Webpage Request for quotation
CAS: 1191911-27-9
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: CZC-54252 Visit Supplier Webpage Request for quotation
CAS: 1191911-27-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
View History
1191911-27-9
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