Fig. 1 · Structure

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BMS-345541

Cat. No. A12559 CAS 445430-58-0

IKK2/IKK1 inhibitor

BMS-345541 is a highly selective inhibitor of the catalytic subunits of IKK-2 and IKK-1 with IC50 of 0.3 μM and 4 μM

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Biological Activity

Target & Activity

Target Activity Value
IKK2 (Cell-free assay) 0.3 μM
IKK1 (Cell-free assay) 4 μM

Cellular Effect

Cell Line Activity Value Description Reference
A549 IC50 5.6 μM Cytotoxicity against human A549 cells measured after 72 hrs by MTT assay [PMID: 27886548]
A549 IC50 8.6 μM Cytotoxicity against human A549 cells assessed as reduction in cell viability after 72 hrs by MTT assay [PMID: 29655083]
Jurkat CC50 100 μM Cytotoxicity against Jurkat cells by Alamar blue assay [PMID: 17540562]
L02 IC50 15.3 μM Cytotoxicity against human HL7702 cells assessed as reduction in cell viability after 72 hrs by MTT assay [PMID: 29655083]
Lewis lung carcinoma cell line IC50 4.8 μM Cytotoxicity against mouse LLC cells measured after 72 hrs by MTT assay [PMID: 27886548]
NCI-H1650 IC50 19.9 μM Cytotoxicity against human NCI-H1650 cells measured after 72 hrs by MTT assay [PMID: 27886548]
NCI-H1650 IC50 9.3 μM Cytotoxicity against human NCI-H1650 cells assessed as reduction in cell viability after 72 hrs by MTT assay [PMID: 29655083]
NCI-H1975 IC50 8 μM Cytotoxicity against human NCI-H1975 cells assessed as reduction in cell viability after 72 hrs by MTT assay [PMID: 29655083]
NCI-H460 IC50 2.8 μM Cytotoxicity against human H460 cells assessed as reduction in cell viability after 72 hrs by MTT assay [PMID: 29655083]
PBMC IC50 1000 nM Antiinflammatory activity in human PBMC assessed as inhibition of LPS-induced TNFalpha release treated for 5 mins before LPS challenge measured after 6 hrs by ELISA [PMID: 21087862]

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 445430-58-0
Applications IKK2/IKK1 inhibitor
Formula C14H17N5
Molecular Weight 255.32
SMILES
CC1=CC2=C(C=C1)N=C(C3=NC=C(N23)C)NCCN

Storage & Solubility

In Vitro Solubility

Reported Solubility

SolventReported Solubility
DMSO 8 mg/mL (31.32 mM)
Water Insoluble
Ethanol Insoluble

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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