Fig. 1 · Structure

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AT7519 HCl

Cat. No. A11313 CAS 902135-91-5

CDK inhibitor

AT7519 is an inhibitor of multiple cyclin-dependent kinases (CDKs), which may result in cell cycle arrest, induction of apoptosis, and inhibition of tumor cell proliferation.

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Biological Activity

Target & Activity

Target Activity Value
CDK9/CyclinT IC50 <10nM
CDK5/p35 IC50 13nM
CDK2/CyclinA IC50 47nM
GSK-3β IC50 89nM
CDK4/CyclinD1 IC50 100nM
CDK6/CyclinD3 IC50 170nM
CDK1/CyclinB IC50 210nM
CDK3/CyclinE IC50 360nM
PI3Kβ IC50 >1μM
PLK3 IC50 >1μM
RET IC50 >1μM
SGK IC50 >1μM
TrkB IC50 >1μM
JAK2 IC50 >1μM
CDK7/CyclinH/MAT1 IC50 2.4μM
SAPK2A(p38α) IC50 >10μM
p70S6K IC50 >10μM
PDGFR IC50 >10μM
PDK-1 IC50 >10μM
PKBβ IC50 >10μM
VEGFR1 IC50 >10μM
AuroraA IC50 >10μM
c-Abl IC50 >10μM
c-Src IC50 >10μM
Chk1 IC50 >10μM
EGFR IC50 >10μM
FGFR3 IC50 >10μM
IR IC50 >10μM
JNK2 IC50 >10μM
MAPK1 IC50 >10μM
MEK1 IC50 >10μM
Met IC50 >10μM

32 targets · Scroll to view more

Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 902135-91-5
Applications CDK inhibitor
Formula C16H17Cl2N5O2.HCl
Molecular Weight 418.7
Synonyms AT 7519
SMILES
C1CNCCC1NC(=O)C2=C(C=NN2)NC(=O)C3=C(C=CC=C3Cl)Cl.Cl

Storage & Solubility

In Vitro Solubility

Reported Solubility

SolventReported Solubility
DMSO Warmed: 49 mg/mL (117.03 mM)
Water Warmed: 40 mg/mL (95.53 mM)
Ethanol Warmed: 26 mg/mL (62.09 mM)

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.

In Vivo Preparation

Concentration
28 mg/mL
Vehicle
Saline

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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