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ICRF-193

SIGMA/I4659 - apoptosis inducer, arabinosidase substrate

Synonym: meso-4,4′-(3,2-Butanediyl)-bis(2,6-piperazinedione)

CAS Number: 21416-88-6
Empirical Formula (Hill Notation): C12H18N4O4
Molecular Weight: 282.30
MDL Number: MFCD01702964
Linear Formula: C12H18N4O4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-I4659-1MG 1 mg
$366.00
1/EA
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45-I4659-5MG 5 mg
$994.00
1/EA
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assay ≥95%
biological source synthetic (organic)
form powder or flakes
  solid
InChI 1S/C12H18N4O4/c1-7(15-3-9(17)13-10(18)4-15)8(2)16-5-11(19)14-12(20)6-16/h7-8H,3-6H2,1-2H3,(H,13,17,18)(H,14,19,20)/t7-,8+
InChI key OBYGAPWKTPDTAS-OCAPTIKFSA-N
Quality Level 200 
SMILES string C[C@@H]([C@@H](C)N1CC(=O)NC(=O)C1)N2CC(=O)NC(=O)C2
solubility DMSO: 4 mg/mL
storage temp. −20°C
Application: ICRF-193 has been used as a topoisomerase II (TOP2) inhibitor to treat mouse oocytes to investigate the role of TOP2 in meiosis.
Biochem/physiol Actions: ICRF-193 helps in the enhancement of cell cycle without chromosome segregation. It is considered as an important drug for chemo-differentiation therapy against acute promyelocytic leukemia (APL). ICRF-193 serves as an inducer of differentiation between anticancer drugs.
Biochem/physiol Actions: ICRF-193 induces a G2 checkpoint that is associated with an ATR-dependent inhibition of polo-like kinase 1 (plk1) activity and a decrease in cyclin B1 phosphorylation. Induces apoptosis in several cell lines including K562 and Molt-4 cells., ICRF-193 is a topoisomerase II inhibitor, more potent against topoisomerase II-β than topoisomerase II-α, and may in addition cause DNA strand breaks.
General description: ICRF-193 is a bisdiopiperazine derivative. It inhibits topoisomerase II by forming a non-cleavable complex.
Packaging: 1, 5 mg in glass bottle
Purity ≥95%
Storage Temp. −20°C
UNSPSC 12352204

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