1. Cell Cycle/DNA Damage Metabolic Enzyme/Protease
  2. HSP
  3. PU-20F

PU-20F is a Hsp90 inhibitor with an EC50 of 6.8 μM. PU-20F competes with Geldanamycin (HY-15230) for binding to Hsp90 and regulates the function of this molecular chaperone. PU-20F induces the degradation of oncogenic Her2 tyrosine kinase. PU-20F blocks the growth of breast cancer cells. PU-20F can be used in breast cancer-related research.

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PU-20F

PU-20F Chemical Structure

CAS No. : 422508-29-0

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Description

PU-20F is a Hsp90 inhibitor with an EC50 of 6.8 μM. PU-20F competes with Geldanamycin (HY-15230) for binding to Hsp90 and regulates the function of this molecular chaperone. PU-20F induces the degradation of oncogenic Her2 tyrosine kinase. PU-20F blocks the growth of breast cancer cells. PU-20F can be used in breast cancer-related research[1].

IC50 & Target[1]

HSP90

6.8 μM (EC50)

In Vitro

PU-20F (compound 59) competes with geldanamycin for binding to purified Hsp90 protein with an EC50 of 6.8 μM[1].
PU-20F (72 h) inhibits the growth of MCF-7 human breast cancer cells with an IC50 of 23 μM[1].
PU-20F induces degradation of Her2 tyrosine kinase in MCF-7 human breast cancer cells with an IC50 of 20 μM[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

417.44

Formula

C20H24FN5O4

CAS No.
SMILES

FC=1N=C(N)C=2N=C(N(C2N1)CC3OCCC3)CC4=CC(OC)=C(OC)C(OC)=C4

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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PU-20F
Cat. No.:
HY-121706
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