All AbMole products are for research use only, cannot be used for human consumption.
SU 5214 is a modulator of tyrosine kinase signal transduction, with IC50 values of 14.8 µM (FLK-1) and 36.7 µM (EGFR), respectively.
| Molecular Weight | 251.28 |
| Formula | C16H13NO2 |
| CAS Number | 186611-04-1 |
| Solubility (25°C) | DMSO 10 mM |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
[3] Hye-Kyung Jung, et al. 2019 Seoul Consensus on Esophageal Achalasia Guidelines
[4] Soyeun Kim, et al. Novel Emerging Therapies for Erectile Dysfunction
| Related VEGFR/PDGFR Products |
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| SU5208
SU5208 inhibits vascular endothelial growth factor receptor-2 (VEGFR2). |
| VEGFR-IN-1
VEGFR-IN-1 is a potent angiogenesis inhibitor with IC50s of 0.02, 0.18, 0.24 7.3, and 7 µM for KDR, Flt-1, c-Kit, EGF-R, and c-Src, respectively. |
| (Z)-Orantinib
(Z)-Orantinib ((Z)-SU6668) is a potent, selective, orally active and ATP competitive inhibitor of Flk‐1/KDR, PDGFRβ, and FGFR1, with IC50s of 2.1, 0.008, and 1.2 µM, respectively. |
| (Rac)-SAR131675
(Rac)-SAR131675 is the racemate of SAR131675. |
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