Cart
sales@molnova.com
SU5204
CAS No. 186611-11-0
SU5204( 3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one )
Catalog No. M22955 CAS No. 186611-11-0
SU5204, an analogue of SU5025, pharmacologically inhibits VEGFR2(IC50s of 4 and 51.5 μM for FLK-1 (VEGFR-2) and HER2).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 30 | In Stock |
|
| 5MG | 28 | In Stock |
|
| 10MG | 42 | In Stock |
|
| 25MG | 75 | In Stock |
|
| 50MG | 110 | In Stock |
|
| 100MG | 177 | In Stock |
|
| 200MG | 259 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSU5204
-
NoteResearch use only, not for human use.
-
Brief DescriptionSU5204, an analogue of SU5025, pharmacologically inhibits VEGFR2(IC50s of 4 and 51.5 μM for FLK-1 (VEGFR-2) and HER2).
-
DescriptionSU5204, an analogue of SU5025, pharmacologically inhibits VEGFR2(IC50s of 4 and 51.5 μM for FLK-1 (VEGFR-2) and HER2).
-
In Vitro——
-
In Vivo——
-
Synonyms3-[(2-Ethoxyphenyl)methylidene]-1H-indol-2-one
-
PathwayAngiogenesis
-
TargetVEGFR
-
RecptorVEGFR2|HER2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number186611-11-0
-
Formula Weight265.31
-
Molecular FormulaC17H15NO2
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (376.92 mM)
-
SMILESO=C1NC2=C(C=CC=C2)/C1=C/C3=CC=CC=C3OCC
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Peng Cho Tang, et al. 3-heteroaryl-2-indolinone compounds for the treatment of disease. US5792783A.
molnova catalog
related products
-
TG 100801
TG 100801 is a dual inhibitor of VEGFr2 and Src family (Src and YES) kinases and is a candidate compound for the treatment of age-related macular degeneration (AMD).
-
Tyrphostin AG1433
Tyrphostin AG1433 is an inhibitor of tyrosine kinases and also a dual inhibitor of PDGFRβ(IC50s = 5.0 μM) and VEGFR-2 (Flk-1/KDR)(IC50s = 9.3 μM).
-
Cabozantinib hydroch...
Cabozantinib (XL184) is a potent pan-tyrosine kinases inhibitor that inhibits VEGFR2, c-Met, Kit, Axl, and Flt4 (IC50s: 0.035, 1.3, 4.6, 7 and 6 nM).
