Home » Cellular Processes » Angiogenesis » EGFR » HDS 029

HDS 029

Cat. No. 2646

Price and Availability

For HDS 029 pricing & availability please select your country from the drop down menu:
Submit

By clicking submit you agree to accept a cookie from Tocris Bioscience. For details, please read our privacy and cookie policy.

Chemical Name: N-(4-[(-3-Chloro-4-fluorophenyl)amino]pyrido[3,4-d]pyrimidin-6-yl-2-butynamide

Biological Activity

Potent inhibitor of the ErbB receptor family (IC₅₀ values are 0.3, 0.5 and 1.1 nM for ErbB1 (EGFR), ErbB4 and ErbB2 respectively). Inhibits EGF-induced erbB1 autophosphorylation in NIH3T3 cells and heregulin-stimulated ErbB autophosphorylation in MDA-MB-453 human breast carcinoma cells (IC₅₀ values are 2.5 and 24 nM respectively).

Technical Data

M.Wt:

355.76

Formula:

C₁₇H₁₁ClFN₅O

Solubility:

Soluble to 25 mM in DMSO

Purity:

>97 %

Storage:

Store at -20°C

CAS No:

881001-19-0

The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.

Resources

Other Information

View R&D Systems' research poster featuring HDS 029

Certificate of Analysis / Safety Data Sheet

Certificate of Analysis: View current batch

Safety Data Sheet: View Safety Data Sheet

References

Klutchko et al (2006) Tyrosine kinase inhibitors. 19. 6-alkynamides of 4-anilinoquinazolines and 4-aniliopyrido[3,4-d]pyrimidines as irreversible inhibitors of the erbB family of tyrosine kinase receptors. J.Med.Chem. 49 1475. PMID: 16480284.

If you know of a relevant citation for this product please let us know.

View Related Products by Target

Angiogenesis EGFR

Growth Factor Receptors Receptor Tyrosine Kinases (RTKs)

Keywords: HDS 029, supplier, Potent, inhibitors, ErbB, receptor, family, Epidermal, Growth, Factors, Receptors, Her, EGFR, Receptor, Tyrosine, Kinases, RTKs, HDS029