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SCIO-469

SIGMA/SML3008 - ≥98% (HPLC)

Synonym: 2-(6-Chloro-5-((2R,5S)-4-(4-fluorobenzyl)-2,5-dimethylpiperazine-1-carbonyl)-1-methyl-1H-indol-3-yl)-N,N-dimethyl-2-oxoacetamide; 6-Chloro-5-[[(2R,5S)-4-[(4-fluorophenyl)methyl]-2,5-dimethyl-1-piperazinyl]carbonyl]-N,N,1-trimethyl-a-oxo-1H-indole-3-acetamide; SCIO 469; SCIO469; Scios 469; Scios-469; Scios469; Talmapimod

CAS Number: 309913-83-5
Empirical Formula (Hill Notation): C27H30ClFN4O3
Molecular Weight: 513.00
MDL Number: MFCD11973651
Linear Formula: C27H30ClFN4O3
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML3008-5MG 5 mg
$143.00
1/EA
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45-SML3008-25MG 25 mg
$572.00
1/EA
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assay ≥98% (HPLC)
color white to beige
form powder
Quality Level 100 
SMILES string O=C(C(C1=CN(C2=C1C=C(C(Cl)=C2)C(N3[C@@H](CN([C@H](C3)C)CC4=CC=C(C=C4)F)C)=O)C)=O)N(C)C
solubility DMSO: 2 mg/mL, clear
storage temp. 2-8°C
Biochem/physiol Actions: SCIO-469 (Talmapimod) is an orally active, potent and selective mitogen-activated protein kinase (MAPK) p38alpha (p38α, MAPK14) inhibitor (IC50 = 9 nM; 10-fold over p38β, >2000-fold over 20 other kinases) with no significant affinity toward a panel of 70 enzymes and receptors. SCIO-469 inhibits multiple myeloma (MM) growth in mice in vivo (150 or 450 mg/kg powder diet; 5T2MM and 5T33MM) and augments proteasome inhibitor in a murine plasmacytoma model of MM (0.2 mg bortezomib/kg i.v. twice weekly with 30 mg SCIO-469/kg b.i.d. p.o.; RPMI8226).
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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