LY2228820

p38 MAP kinase (MAPK) inhibitor
概要
LY2228820 is a trisubstituted imidazole derivative and a potent inhibitor of the α- and β-isoforms of p38 MAP kinase (MAPK) in vitro (IC₅₀ = 5.3 and 3.2 nM, respectively) with anti-inflammatory and anti-neoplastic activities (Campbell et al.). This product is supplied as the dimesylate salt of the molecule.


MAINTENANCE AND SELF-RENEWAL
· Combined with other small molecule inhibitors such as Rapamycin (Catalog #73362) and SR1 (Catalog #72342; Li et al.) or SB203580 (Catalog #72222), Vx702, and BIRB-796 (Catalog #72682), enhances the self-renewal of cord blood-derived hematopoietic stem cells (Baudet et al.).

CANCER RESEARCH
· By inhibiting p38 MAPK, which is highly expressed in human cancers, LY2228820 is potent and selective at inhibiting tumor growth in animal models of a variety of human cancers (Campbell et al.).
Alternative Names
Ralimetinib Mesylate; LSN2322600
Cell Type
Cancer Cells and Cell Lines, Hematopoietic Stem and Progenitor Cells
Species
Human, Mouse, Rat, Non-Human Primate, Other
Application
Maintenance
Area of Interest
Cancer Research, Stem Cell Biology
CAS Number
862507-23-1
Chemical Formula
C₂₄H₂₉FN₆ • 2CH₃SO₃H
Molecular Weight
612.7 g/mol
Purity
≥ 98%
Pathway
p38 MAPK
Target
p38 MAPK
技术资料
Document Type 产品名称 Catalog # Lot # 语言
Product Information Sheet LY2228820 (Dimesylate) 74162, 74164 All English
Safety Data Sheet LY2228820 (Dimesylate) 74162, 74164 All English
数据及文献
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