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Flavopiridol Hydrochloride

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Category Human immunodeficiency Virus (HIV)
CAS 131740-09-5
Description Flavopiridol hydrochloride competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM. It is 7.5-fold more selective for CDK1/2/4/6 than CDK7. Flavopiridol is initially found to inhibit EGFR and PKA.
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Product Information

Synonyms NSC 649890 HCl; NSC649890 HCl; NSC-649890 HCl
Molecular Weight 438.3
Molecular Formula C21H20ClNO5.HCl
Canonical SMILES CN1CCC(C(C1)O)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4Cl)O)O.Cl
InChI InChI=1S/C21H20ClNO5.ClH/c1-23-7-6-12(17(27)10-23)19-14(24)8-15(25)20-16(26)9-18(28-21(19)20)11-4-2-3-5-13(11)22;/h2-5,8-9,12,17,24-25,27H,6-7,10H2,1H3;1H/t12-,17+;/m0./s1
InChIKey LGMSNQNWOCSPIK-LWHGMNCYSA-N
Boiling Point 603.6°C at 760 mmHg
Melting Point 169.5-170°C
Flash Point 318.8°C
Purity >98%
Solubility In Vitro:
H2O : ≥ 20 mg/mL(45.63 mM)
DMF : 7.69 mg/mL(17.55 mM;Need ultrasonic)
Appearance Light yellow to khaki (Solid)
Storage 4°C, sealed storage, away from moisture
* In solvent :
-80°C, 6 months
-20°C, 1 month (sealed storage, away from moisture)
Complexity 628
Exact Mass 437.0796782
In Vitro Flavopiridol (2 μM) robustly induces a distinct pattern of ER stress in CLL cells that contributes to cell death through IRE1-mediated activation of ASK1 and possibly downstream Caspases. Flavopiridol results in potent upregulation of a number of PRGs in treatments lasting 4-24 h. Flavopiridol has and immediate and long-term effect on the expression of several PRGs. In serum starved cells re-stimulated with serum, flavopiridol also inhibits the expression of these genes, but subsequently, JUNB, GADD45B and EGR1 are upregulated in the presence of flavopirido.
PSA 94.14000
Target CDK; Autophagy; HIV
Vapor Pressure 2.03E-15mmHg at 25°C

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