Fig. 1 · Structure

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IIIM-290

CDK inhibitor

IIIM-290 is a potent and oral CDK inhibitor with IC50s of 90 and 94 nM for CDK2/A and CDK9/T1.

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Biological Activity

Target & Activity

Target Activity Value
CDK2/A IC50 90 nM
CDK9/T1 IC50 94 nM

Cellular Effect

Cell Line Activity Value Description Reference
786-0 GI50 6 μM Growth inhibition of human 786-0 cells after 48 hrs by MTT assay [PMID: 29370702]
A-431 GI50 8 μM Growth inhibition of human A431 cells after 48 hrs by MTT assay [PMID: 29370702]
A549 GI50 4 μM Growth inhibition of human A549 cells after 48 hrs by MTT assay [PMID: 29370702]
BT-549 GI50 5 μM Growth inhibition of human BT549 cells after 48 hrs by MTT assay [PMID: 29370702]
Caco-2 GI50 7 μM Growth inhibition of human Caco2 cells after 48 hrs by MTT assay [PMID: 29370702]
COLO 205 GI50 7 μM Growth inhibition of human COLO205 cells after 48 hrs by MTT assay [PMID: 29370702]
DU-145 GI50 5 μM Growth inhibition of human DU145 cells after 48 hrs by MTT assay [PMID: 29370702]
HCT-116 GI50 5 μM Growth inhibition of human HCT116 cells after 48 hrs by MTT assay [PMID: 29370702]
HEK293 IC50 > 50 μM Inhibition of [3H]-astemizole binding to human ERG expressed in HEK293 cell membranes by scintillation counting method [PMID: 29370702]
HEK293 GI50 22 μM Growth inhibition of human HEK293 cells after 48 hrs by MTT assay [PMID: 29370702]
HL-60 GI50 0.9 μM Growth inhibition of human HL60 cells after 48 hrs by MTT assay [PMID: 29370702]
HOP-62 GI50 7 μM Growth inhibition of human HOP62 cells after 48 hrs by MTT assay [PMID: 29370702]
HOP-92 GI50 3 μM Growth inhibition of human HOP92 cells after 48 hrs by MTT assay [PMID: 29370702]
LOX IMVI GI50 4 μM Growth inhibition of human LOXIMVI cells after 48 hrs by MTT assay [PMID: 29370702]
MCF7 GI50 4 μM Growth inhibition of human MCF7 cells after 48 hrs by MTT assay [PMID: 29370702]
MDA-MB-231 GI50 4 μM Growth inhibition of human MDA-MB-231 cells after 48 hrs by MTT assay [PMID: 29370702]
MDA-MB-468 GI50 4 μM Growth inhibition of human MDA-MB-468 cells after 48 hrs by MTT assay [PMID: 29370702]
MIA PaCa-2 GI50 1 μM Growth inhibition of human MIAPaCa2 cells after 48 hrs by MTT assay [PMID: 29370702]
MOLT-4 GI50 0.5 μM Growth inhibition of human MOLT4 cells after 48 hrs by MTT assay [PMID: 29370702]
NCI-H226 GI50 4 μM Growth inhibition of human NCI-H226 cells after 48 hrs by MTT assay [PMID: 29370702]
NCI-H522 GI50 5 μM Growth inhibition of human NCI-H522 cells after 48 hrs by MTT assay [PMID: 29370702]

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 2213468-64-3
Applications CDK inhibitor
Formula C23H21Cl2NO5
Molecular Weight 462.32
SMILES
OC1=C2C(OC(/C=C/C3=C(Cl)C=CC=C3Cl)=CC2=O)=C([C@]4([H])[C@H](O)CN(C)CC4)C(O)=C1

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

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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