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JNJ-7706621

Product Name: JNJ-7706621
CAT#: DEAK-2312-LGZ-6
Package: 5mg/10mg/50mg/100mg/10mM * 1mL in DMSO
Datasheet
443797-96-4.png

Description

JNJ-7706621 is a pan-CDK inhibitor with the highest potency against CDK1/2, with an IC50 of 9 nM/4 nM. Its selectivity for CDK1/2 is 6 times higher than CDK3/4/6 in cell-free assays. It also effectively inhibits Aurora A/B and is inactive against Plk1 and Wee1.

Basic Information

Synonyms: JNJ7706621
Application: CDK/Aurora A/B Inhibitor
CAS Number: 443797-96-4
Formula: C15H12F2N6O3S
Molecular Weight: 394.4
SMILES: C1=CC(=C(C(=C1)F)C(=O)N2C(=NC(=N2)NC3=CC=C(C=C3)S(=O)(=O)N)N)F
Solubility-In vitro: In vitro (25°C):
DMSO: 67 mg/mL (169.89 mM)
Water: Insoluble
Ethanol: Insoluble
Solubility-In vivo: 0.5% methylcellulose+0.2% Tween 80: 13 mg/mL

Target Info

CDK6/cyclinD1: 175 nM (IC50)
CDK2/cyclinE: 3 nM (IC50)
Cdk4/cyclin D1: 253 nM (IC50)
Cdk1/cyclin B: 9 nM (IC50)
cdk2/cyclin A: 4 nM (IC50)
CDK3/Cyclin E: 58 nM (IC50)
Aurora A: 11 nM (IC50)
Aurora B: 15 nM (IC50)
VEGF-R2: 154 nM (IC50)
VEGF-R1: 6400 nM (IC50)
VEGF-R3: 735 nM (IC50)
FGF-R1: 575 nM (IC50)
FGF-R2: 226 nM (IC50)
GSK3β: 254 nM (IC50)

Storage

  • The lyophilized form should be stored at -20°C, in a desiccated environment.
  • In lyophilized form, the chemical remains stable for 36 months.
  • In solution, it should be stored at -20°C and used within 3 months to prevent loss of potency. Aliquoting is recommended to avoid multiple freeze/thaw cycles.

Preparing Stock Solutions

0.1 mM_1 mg: 25.35 mL 0.1 mM_5 mg: 126.77 mL 0.1 mM_10 mg: 253.55 mL 0.5 mM_1 mg: 5.07 mL 0.5 mM_5 mg: 25.35 mL 0.5 mM_10 mg: 50.71 mL 1 mM_1 mg: 2.54 mL 1 mM_5 mg: 12.68 mL 1 mM_10 mg: 25.35 mL 5 mM_1 mg: 0.51 mL 5 mM_5 mg: 2.54 mL 5 mM_10 mg: 5.07 mL

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