(E)-AG 556
CAS No. 133550-41-1
(E)-AG 556 ( (E)-Tyrphostin AG 556 )
Catalog No. M27474 CAS No. 133550-41-1
AG 556 is a selective inhibitor of EGFR and blocks LPS-induced TNF-α production.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 42 | Get Quote |
|
10MG | 72 | Get Quote |
|
25MG | 147 | Get Quote |
|
50MG | 222 | Get Quote |
|
100MG | 331 | Get Quote |
|
200MG | 489 | Get Quote |
|
500MG | 777 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product Name(E)-AG 556
-
NoteResearch use only, not for human use.
-
Brief DescriptionAG 556 is a selective inhibitor of EGFR and blocks LPS-induced TNF-α production.
-
DescriptionAG 556 is a selective inhibitor of EGFR and blocks LPS-induced TNF-α production.
-
Synonyms(E)-Tyrphostin AG 556
-
PathwayAngiogenesis
-
TargetEGFR
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number133550-41-1
-
Formula Weight336.4
-
Molecular FormulaC20H20N2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESN#C/C(/C(NCCCCc1ccccc1)=O)=C\c(cc1)cc(O)c1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Qa'dan F, et al. Cinchonain Ib isolated from Eriobotrya japonica induces insulin secretion in vitro and in vivo. J Ethnopharmacol. 2009 Jul 15;124(2):224-7.
molnova catalog
related products
-
RO 46-8443
RO 46-8443 is the first non-peptide endothelin ETB receptor selective antagonist. RO 46-8443 displays up to 2000-fold selectivity for ETB receptors both in terms of binding inhibitory potency and functional inhibition.
-
EGFR-IN-7
EGFR-IN-7 is a selective and potent EGFR kinase inhibitor.TQB3804 displayed potent enzymatic activities for EGFRd746-750/T790M/C797S, EGFRL858R/T790M/C797S, EGFRd746-750/T790M, and EGFRL858R/T790M with IC50 of 0.46, 0.13, 0.26, and 0.19 nM respectively, and has similar enzymatic activity for EGFRWT (IC50 = 1.07) to Osimertinib.
-
EGFR/ErbB2 Inhibitor
EGFR/ErbB2 Inhibitor is a cell-permeable inhibitor of EGFR and c-ErbB2 (IC50s = 20 and 79 nM, respectively)