Description：

Flavopiridol HCl competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM in cell-free assays. It is 7.5-fold more selective for CDK1/2/4/6 than CDK7. Flavopiridol is initially found to inhibit EGFR and PKA. Phase 1/2.

Chemical Information：

Molecular Weight (MW)		438.3
Formula		C21H20ClNO5.HCl
CAS No.		131740-09-5
Solubility (25°C) *	DMSO	88 mg/mL (200.77 mM)
	Water	Insoluble
	Alcohol	Insoluble

Preparing Stock Solutions

Concentration Volume (DMSO) Mass	1 mg	5 mg	10 mg
1 mM	2.2815 mL	11.4077 mL	22.8154 mL
5 mM	0.4563 mL	2.2815 mL	4.5631 mL
10 mM	0.2282 mL	1.1408 mL	2.2815 mL
50 mM	0.0456 mL	0.2282 mL	0.4563 mL

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