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PU-H71

Chemical Structure : PU-H71

CAS No.: 873436-91-0

PU-H71 (Zelavespib, NSC 750424)

Catalog No.: PC-72710Not For Human Use, Lab Use Only.

PU-H71 (Zelavespib, NSC 750424) is a potent and selective inhibitor of Hsp90 (Heat shock protein 90) with IC50 of 51 nM in MDA-MB-468 cells.

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25 mg $128 In stock
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100 mg $358 In stock
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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

PU-H71 (Zelavespib, NSC 750424) is a potent and selective inhibitor of Hsp90 (Heat shock protein 90) with IC50 of 51 nM in MDA-MB-468 cells.
PU-H71 inhibits cell growth in a range of breast cancer cell lines with IC50 values of 17, 31, 65, 87 and 140 nM for SKBr3, MCF-7, MDA-MB-468, HCC-1806 and MDA-MB-231 cells, respectively.
PU-H71 inhibits cell proliferation and induce apoptosis in triple-negative breast cancer (TNBC) cells.
PU-H71 demonstrated anti-lymphoma activity and showed synergistic effect with dual PI3K/mTOR inhibition in vitro and in vivo.

Physicochemical Properties

M.Wt 512.37
Formula C18H21IN6O2S
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

100 mM in DMSO (51.2 mg/mL)

Chemical Name/SMILES

8-((6-Iodobenzo[d][1,3]dioxol-5-yl)thio)-9-(3-(isopropylamino)propyl)-9H-purin-6-amine

References

1. Huazhong He, et al. J Med Chem. 2006 Jan 12;49(1):381-90.

2. Eloisi Caldas-Lopes, et al. Proc Natl Acad Sci U S A. 2009 May 19;106(20):8368-73.

3. Carmel T Chan, et al. Cancer Res. 2008 Jan 1;68(1):216-26.

4. Giulino-Roth L, et al. Mol Cancer Ther. 2017 Sep;16(9):1779-1790.

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