MW 570.7 Da. Potent and selective inhibitor of the Parkinson's disease kinase LRRK2. Benzodiazepine based derivative. Inhibits both G2019S mutant and wild-type LRRK2 kinase activity (IC50 values are 6 and 13 nM respectively). Causes dephosphorylation, ubiquitination and degradation of LRRK2. Inhibits IFN-γ-induced monocyte maturation in vitro.
대체 명칭 보기
AURA17, Beta-interferon, Dardarin, Fibroblast interferon, Hypothetical protein FLJ35932, IFB, IFF, IFN-beta, IFNB 1, IFNB_HUMAN, Interferon beta, Interferon beta 1 fibroblast, Interferon beta precursor, LRRK2_HUMAN, Leucine rich repeat kinase 2, Leucine-rich repeat serine/threonine-protein kinase 2, MGC96956, PARK 8, RIPK7, ROCO 2, STK33_HUMAN, Serine threonine kinase 33, Serine/threonine kinase 33, Serine/threonine-protein kinase 33, augmented in rheumatoid arthritis 17, leucine rich repeat serine threonine protein kinase 2
- Chemical Structure
Supplier Data
Chemical Structure - LRRK2-IN-1, LRRK2 inhibitor (AB254524)
2D chemical structure image of ab254524, LRRK2-IN-1, LRRK2 inhibitor
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Biological function summary
Interferon beta participates in antiviral defense by inducing the expression of interferon-stimulated genes. It does not form part of a complex but interacts directly with its receptor IFNAR. In contrast STK33 and LRRK2 function as part of larger kinase complexes. STK33's role remains less clear often linked to serine/threonine phosphorylation involved in survival pathways. LRRK2 frequently referred to in literature for its full name leucine-rich repeat kinase 2 heavily contributes to autophagy and apoptosis regulatory processes.
Pathways
Interferon beta mainly involves itself in the JAK-STAT signaling pathway that regulates immune response. This pathway influences not only immune cell activation but also gene expression critical for viral defense. STK33 associates with pathways relevant to cell growth intersecting with kinases like mTOR. LRRK2 takes part in the MAPK/ERK pathway related to inflammatory responses alongside proteins such as Rab GTPases. LRRK2 inhibitors demonstrate potential in modulating these pathways for therapeutic advances.
Product promise
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