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LY2409881 hydrochloride

SIGMA/SML2943 - ≥98% (HPLC)

Synonym: 2-{5-Chloro-2-[3-(4-methylpiperazin-1-yl)propylamino]-pyrimidin-4-yl}benzo[b]thiophene-4-carboxylic acid cyclopropylamide hydrochloride; LY 2409881 hydrochloride; LY-2409881 hydrochloride; N-Cyclopropyl-2-[5-Chloro-2-[[3-(4-methylpiperazin-1-yl)propyl]amino]pyrimidin-4-yl]benzo[b]thiophene-4-carboxamide hydrochloride

Empirical Formula (Hill Notation): C24H29ClN6OS · xHCl
Molecular Weight: 485.04 (free base basis)
MDL Number: MFCD28900675
Linear Formula: C24H29ClN6OS · xHCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML2943-5MG 5 mg
$166.00
1/EA
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45-SML2943-25MG 25 mg
$314.00
1/EA
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assay ≥98% (HPLC)
color white to beige
form powder
Quality Level 100 
solubility H2O: 2 mg/mL, clear
storage condition desiccated
storage temp. −20°C
Biochem/physiol Actions: LY2409881 is a potent IκΒ kinase β (IKK2, IKKβ, IKKbeta) inhibitor (IC50 = 30 nM) that effectively inhibits 10 ng/mL TNFα-induced IκB phosphorylation in LY10 DLBCL cells (by >95%; 10 μM) and exhibits good selectivity by kinase profiling among more than 300 kinases (>10-fold selectivity). LY2409881 enhances TNFα cytotoxicity in SKOV3 ovarian cancer cultures (~20% survival with 316 nM LY2409881 & 10 ng/mL TNFα in 72 hrs; 100% survival with LY2409881 or TNFα alone) by blocking NF-κB antiapoptotic signal activation without affecting TRADD & FADD proapoptotic pathway induction. When administered in vivo, LY2409881 is shown to suppress LY10 xenograft-derived tumor growth in mice (50-200 mg/kg, twice weekly ip.).
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. −20°C
UNSPSC 12352200

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