BMS-599626 2HCL(714971-09-2 Free base)

TargetMol
Product Code: TAR-T2610L
Supplier: TargetMol
CodeSizePrice
TAR-T2610L-1mg1mg£140.00
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TAR-T2610L-5mg5mg£193.00
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TAR-T2610L-10mg10mg£310.00
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TAR-T2610L-1mL1 mL * 10 mM (in DMSO)£352.00
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TAR-T2610L-25mg25mg£483.00
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TAR-T2610L-50mg50mg£667.00
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TAR-T2610L-100mg100mg£914.00
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Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20°C

Images

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Further Information

Bioactivity:
BMS-599626 2HCL is a BMS-599626 derivative.BMS-599626 is an orally available and selective dual inhibitor of HER1 and HER2 with IC50s of 20 and 30 nM, respectively.BMS-599626 inhibits tumor cell proliferation and has the potential to increase tumor BMS-599626 inhibits tumor cell proliferation and has the potential to increase tumor response to radiotherapy.
CAS:
1781932-33-9
Molecular Weight:
603.47
Pathway:
Tyrosine Kinase/Adaptors|Angiogenesis|JAK/STAT signaling
Purity:
0.98
SMILES:
O=C(OC[C@@H]1COCCN1)NC2=CN3C(C(NC4=CC=C(N(N=C5)CC6=CC(F)=CC=C6)C5=C4)=NC=N3)=C2C.Cl.Cl
Target:
HER

References

Haluska P, et al. HER receptor signaling confers resistance to the insulin-like growth factor-I receptor inhibitor, BMS-536924. Mol Cancer Ther. 2008;7(9):2589-2598. Wong TW, et al. Preclinical antitumor activity of BMS-599626, a pan-HER kinase inhibitor that inhibits HER1/HER2 homodimer and heterodimer signaling. Clin Cancer Res. 2006;12(20 Pt 1):6186-6193. Torres MA, et al. AC480, formerly BMS-599626, a pan Her inhibitor, enhances radiosensitivity and radioresponse of head and neck squamous cell carcinoma cells in vitro and in vivo. Invest New Drugs. 2011;29(4):554-561.