PD 089828
CAS No. 179343-17-0
PD 089828 ( PD-089828; PD089828 )
Catalog No. M23806 CAS No. 179343-17-0
PD 089828 is a competitive inhibitor of the receptor tyrosine kinases FGFR1, PDGFRβ, and EGFR (IC50s = 0.15, 1.76, and 5.47 μM, respectively) and a noncompetitive inhibitor of the nonreceptor tyrosine kinase c-Src (IC50 = 0.18 μM)
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 65 | In Stock |
|
10MG | 110 | In Stock |
|
25MG | 237 | In Stock |
|
50MG | 354 | In Stock |
|
100MG | 518 | In Stock |
|
500MG | 1098 | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NamePD 089828
-
NoteResearch use only, not for human use.
-
Brief DescriptionPD 089828 is a competitive inhibitor of the receptor tyrosine kinases FGFR1, PDGFRβ, and EGFR (IC50s = 0.15, 1.76, and 5.47 μM, respectively) and a noncompetitive inhibitor of the nonreceptor tyrosine kinase c-Src (IC50 = 0.18 μM)
-
DescriptionPD 089828 is a competitive inhibitor of the receptor tyrosine kinases FGFR1, PDGFRβ, and EGFR (IC50s = 0.15, 1.76, and 5.47 μM, respectively) and a noncompetitive inhibitor of the nonreceptor tyrosine kinase c-Src (IC50 = 0.18 μM)
-
SynonymsPD-089828; PD089828
-
PathwayAngiogenesis
-
TargetEGFR
-
RecptorEGFR;FGFR1;PDGFRβ
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number179343-17-0
-
Formula Weight405.3
-
Molecular FormulaC18H18Cl2N6O
-
Purity>98% (HPLC)
-
SolubilityDMSO:2.5 mM
-
SMILESCC(C)(C)NC(=O)NC1=C(C=C2C=NC(=NC2=N1)N)C3=C(C=CC=C3Cl)Cl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Dahring TK, et al. Inhibition of growth factor-mediated tyrosine phosphorylation in vascular smooth muscle by PD 089828, a new synthetic protein tyrosine kinase inhibitor. J Pharmacol Exp Ther. 1997 Jun;281(3):1446-56.
molnova catalog
related products
-
Pyrotinib
Pyrotinib (SHR-1258)is a potent and selective EGFR/HER2 dual inhibitor with IC50 of 13/38 nM, respectively.
-
AG 99
AG-99 is an inhibitor of EGFR kinase (IC50: 10 μM in the human epidermoid carcinoma cell line A431).
-
Theliatinib
Theliatinib a potent and highly selective EGFR inhibitor with anti-tumor activity. Ki of 0.05 nM for wild type EGFR and IC50s of 3 and 22 nM for EGFR and EGFR T790M/L858R mutant respectively.