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Lrrk2 Inhibitor

Lrrk2 Inhibitor Suppliers list
Company Name: ApexBio Technology  
Tel: + 1-832-696-8203
Email: sales@apexbt.com
Products Intro: Cas:1234480-84-2
ProductName:LRRK2-IN-1
Brand:apexbt | Product Number:A3558
Company Name: Axon Medchem LLC  
Tel: 703 - 9861
Email: info@axonmedchem.com
Products Intro: Cas:1234480-84-2
ProductName:LRRK2-IN-1
Brand:Axon Medchem | Product Number:Axon2493 | Purity:99%
Company Name: Abcam Limited  
Tel: 021-2070050 400921018
Email: us.orders@abcam.com
Products Intro: Cas:1234480-84-2
ProductName:LRRK2-IN-1, LRRK2 inhibitor
Company Name: career henan chemical co
Tel: +86-0371-86658258
Email: factory@coreychem.com
Products Intro: Cas:1234480-84-2
ProductName:LRRK2-IN-1
Purity: Min98% HPLC | Package: 1KG
Company Name: Aladdin Scientific
Tel:
Email: tp@aladdinsci.com
Products Intro: Cas:1234480-84-2
ProductName:LRRK2-IN-1
Purity: 98% | Package: $71.9/5mg;$118.9/10mg;$267.9/25mg;$434.9/50mg;$761.9/100mg;Bulk package | CustNote: 98%

Lrrk2 Inhibitor manufacturers

  • LRRK2-IN-1
  • LRRK2-IN-1 pictures
  • $60.00
  • 2026-09-10
  • CAS:1234480-84-2
  • Purity: 98.82%
  • Supply Ability: 10g
  • LRRK2-IN-1
  • LRRK2-IN-1 pictures
  • $1.00
  • 2019-12-24
  • CAS:1234480-84-2
  • Min. Order: 1KG
  • Purity: Min98% HPLC
Lrrk2 Inhibitor Basic information
Product Name:Lrrk2 Inhibitor
Synonyms:5,11-Dihydro-2-[[2-methoxy-4-[[4-(4-methyl-1-piperazinyl)-1-piperidinyl]carbonyl]phenyl]amino]-5,11-dimethyl-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one;LRRK2-IN-1;LRRK2-TN-1;CS-642;LRRK2-IN-1; LRRK2 INHIBITOR;2-((2-Methoxy-4-(4-(4-methylpiperazin-1-yl)piperidine-1-carbonyl)phenyl)-amino)-5,11-dimethyl-;6H-Pyrimido[4,5-b][1,4]benzodiazepin-6-one, 5,11-dihydro-2-[[2-methoxy-4-[[4-(4-methyl-1-piperazinyl)-1-piperidinyl]carbonyl]phenyl]amino]-5,11-dimethyl-;LRRK2-IN-1 USP/EP/BP
CAS:1234480-84-2
MF:C31H38N8O3
MW:570.69
EINECS:
Product Categories:Inhibitors
Mol File:1234480-84-2.mol
Lrrk2 Inhibitor Structure
Lrrk2 Inhibitor Chemical Properties
Boiling point 787.8±70.0 °C(Predicted)
density 1.278
storage temp. Store at -20°C
solubility ≥28.55 mg/mL in DMSO; insoluble in H2O; ≥57.2 mg/mL in EtOH
form solid
pka8.14±0.42(Predicted)
color Light yellow to yellow
InChIKeyIWMCPJZTADUIFX-UHFFFAOYSA-N
SMILESCN1CCN(CC1)C2CCN(CC2)C(=O)C3=CC(=C(C=C3)NC4=NC=C5C(=N4)N(C6=CC=CC=C6C(=O)N5C)C)OC
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
Lrrk2 Inhibitor Usage And Synthesis
DescriptionLeucine-rich repeat kinase 2 (LRRK2) is an enzyme that interacts with parkin, a ligase that is part of the ubiquitin-proteasome system that mediates the targeting of proteins for degradation. Loss of function of the parkin protein leads to dopaminergic cell death. The development of Parkinson''s disease has been strongly associated with mutations in the LRRK2 gene that lead to increased kinase activity. LRRK2-IN-1 is a potent inhibitor of LRRK2 that inhibits both wild-type and G2019S mutant LRRK2 (IC50s = 13 and 6 nM, respectively). It is selective for LRRK2 over a large panel of other kinases. LRRK2-IN-1 treatment causes dephosphorylation of LRRK2, leading to its dissociation from 14-3-3 proteins, ubiquitination, and degradation. Inhibitors of LRRK2, including LRRK2-IN-1, stimulate macroautophagy in H4 neuroglioma cells.
UsesLRRK2-IN-1 is a benzodiazepine based derivative and is known as a selective inhibitor of the Parkinson''s disease kinase LRRK2.
DefinitionChEBI: LRRK2-IN-1 is a member of the class of pyrimidobenzodiazepines that is 5,11-dimethylpyrimido[4,5-b][1,4]benzodiazepin-6-one carrying at C-2 on the pyrimidine ring a 4-[(4-methylpiperazin-1-yl)piperidine-1-carbonyl]-2-methoxyanilino substituent. It is an inhibitor of the Parkinson's disease kinase LRRK2. It has a role as an EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor and an antineoplastic agent. It is a N-acylpiperidine, a N-alkylpiperazine, an aromatic ether, a pyrimidobenzodiazepine, an aromatic amine, a secondary amino compound and a tertiary amino compound.
in vivo

LRRK2-IN-1 (100 mg/kg, i.p.) induces dephosphorylation of LRRK2 in the kidney of the mice[2]. Peritumoral injection of LRRK2-IN-1 (100 mg/kg) results in a significant decrease in tumor volume and weight of AsPC-1 tumor xenografts[4].

storageStore at -20°C
References[1] XIANMING DENG. Characterization of a selective inhibitor of the Parkinson”s disease kinase LRRK2[J]. Nature chemical biology, 2011, 7 4: 203-205. DOI: 10.1038/nchembio.538
[2] JING ZHAO. LRRK2 dephosphorylation increases its ubiquitination.[J]. Biochemical Journal, 2015, 469 1: 107-120. DOI: 10.1042/bj20141305
[3] CLAUDIA MANZONI . Inhibition of LRRK2 kinase activity stimulates macroautophagy[J]. Biochimica et biophysica acta. Molecular cell research, 2013, 1833 12: Pages 2900-2910. DOI: 10.1016/j.bbamcr.2013.07.020
[4] ALAVI M V. Tau phosphorylation and OPA1 proteolysis are unrelated events: Implications for Alzheimer’s Disease[J]. Biochimica et biophysica acta. Molecular cell research, 2021, 1868 12: Article 119116. DOI: 10.1016/j.bbamcr.2021.119116
Lrrk2 Inhibitor Preparation Products And Raw materials
Tag:Lrrk2 Inhibitor(1234480-84-2) Related Product Information
AX15910 Benzamide, 4-[(9-cyclopentyl-6,7,8,9-tetrahydro-5,8-dimethyl-6-oxo-5H-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-N-(1-methyl-4-piperidinyl)- LRRK2-IN-1 BI 2536 2-[[2-Ethoxy-4-(4-hydroxy-1-piperidinyl)phenyl]amino]-5,11-dihydro-5,11-dimethyl-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one JWG-071