Dicoumarol – 1 g

Brand:
Cayman
CAS:
66-76-2
Storage:
-20
UN-No:
De Minimis - 2811 / 6.1

Dicoumarol is a competitive inhibitor of NADH:quinone oxidoreductase (NQO1) with IC50 values of 2.6 and 404 nM in the absence and presence of 2 μM BSA, respectively.{38128} It has antiproliferative activity against MIA PaCa-2 pancreas and HCT116 colon carcinoma cells (IC50s = 52 and 19 μM, respectively, after a 96 hour incubation). Dicoumarol inhibits stress-activated protein kinase (SAPK) in HEK293 cells (IC50 = 19-33 μM) at a point upstream of MEKK1 and downstream of TNF receptor-associated factor 2 (TRAF2), and it inhibits TNF-α and LPS-induced NF-κB activation in HeLa cells.{38129} It also has antiproliferative activity against FL5.12 lymphocytic and MCF-7 breast carcinoma cells (100 μM) by suppressing JNK activation.{38130}  

 

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SKU: 20764 - Category:

Description

A competitive NQO1 inhibitor; inhibits recombinant hNQO1 (IC50s =2.6 and 404 nM in the absence and presence of 2 μM BSA, respectively); has antiproliferative activity against MIA PaCa-2 pancreas and HCT116 colon carcinoma cell lines (IC50s = 52 and 19 μM, respectively); inhibits SAPK activity in HEK293 cells (IC50 = 19-33 μM); inhibits TNF-α and LPS-induced NF-κB activation; has antiproliferative activity against FL5.12 lymphocytic and MCF-7 breast carcinoma cells (100 μM)


Formal name: 3,3′-methylenebis[4-hydroxy-2H-1-benzopyran-2-one

Synonyms:  NSC 17860|NSC 221570|NSC 41834

Molecular weight: 336.3

CAS: 66-76-2

Purity: ≥98%

Formulation: A crystalline solid


Product Type|Biochemicals|Kinase Inhibitors|RAS/RAF/MEK/ERK/MAPK||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Product Type|Biochemicals|Small Molecule Inhibitors|TNF-α/NF-κB Signaling||Research Area|Cancer|Cell Signaling|JNK Signaling||Research Area|Cancer|Cell Signaling|NF-κB Signaling||Research Area|Cancer|Transcription Factors|NF-κB||Research Area|Immunology & Inflammation