SU 5402 (GMP) is SU 5402 (HY-10407) produced by using GMP guidelines. GMP small molecules work appropriately as an auxiliary reagent for cell therapy manufacture. SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGFRβ, respectively.
For research use only. We do not sell to patients.
- CAS No.: 215543-92-3
- Formula: C17H16N2O3
- Molecular Weight:296.32
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
|
VEGFR2 20 nM (IC50) |
PDGFRβ 510 nM (IC50) |
EGFR 30 nM (IC50) |
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| HUVEC | IC50 |
>50 μM
Compound: 2
|
Evaluated for the inhibition of cell proliferation induced by EGF in HUVEC or NIH3T3 cells
Evaluated for the inhibition of cell proliferation induced by EGF in HUVEC or NIH3T3 cells
|
[PMID: 10893303] |
| HUVEC | IC50 |
0.05 μM
Compound: 2
|
Evaluated for the inhibition of cell proliferation induced by VEGF in HUVEC or NIH3T3 cells
Evaluated for the inhibition of cell proliferation induced by VEGF in HUVEC or NIH3T3 cells
|
[PMID: 10893303] |
| HUVEC | IC50 |
2.8 μM
Compound: 2
|
Evaluated for the inhibition of cell proliferation induced by FGF in HUVEC or NIH3T3 cells
Evaluated for the inhibition of cell proliferation induced by FGF in HUVEC or NIH3T3 cells
|
[PMID: 10893303] |
| HUVEC | IC50 |
28.4 μM
Compound: 2
|
Evaluated for the inhibition of cell proliferation induced by PDGF in HUVEC or NIH3T3 cells
Evaluated for the inhibition of cell proliferation induced by PDGF in HUVEC or NIH3T3 cells
|
[PMID: 10893303] |
| NIH3T3 | IC50 |
10 μM
Compound: SU-5402
|
Inhibition of acidic FGF-stimulated FGFR1 tyrosine autophosphorylation in mouse NIH/3T3 cells by immunoblotting
Inhibition of acidic FGF-stimulated FGFR1 tyrosine autophosphorylation in mouse NIH/3T3 cells by immunoblotting
|
[PMID: 9139660] |
SU 5402 (GMP) (5 μM, added at days 4, 6 and 8 of differentiation) inhibits neural induction from hiPSC as well as hESC (TZ1 hiPSC or H9 hESC), indicating that FGF signaling is required for neural induction[1].
SU 5402 (GMP) (0.8 μM, from day 2 to day 12), together with PD184352 and CHIR99021, enhances the reprogramming efficiency and increases the number of colonies (reprogram MEFs to iPSCs)[2].
SU 5402 (GMP) together with PD184352 and CHIR99021 accelerate differentiation of iPSCs[2].
SU 5402 (GMP) (10 μM, from day 5 to day 17) efficiently differentiates IWR-1 (HY-12238)-treated hiPSCs into retinal pigment epithelium (RPE) progenitors[3].
SU 5402 (GMP) enhances neuronal differentiation efficiency[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 215543-92-3
-
Molecular Weight 296.32
-
Formula C17H16N2O3
-
SMILES
O=C(CCC1=C(NC=C1C)/C=C2C(NC3=C\2C=CC=C3)=O)O
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. Zeng H, et al. Specification of region-specific neurons including forebrain glutamatergic neurons from human induced pluripotent stem cells. PLoS One. 2010 Jul 29;5(7):e11853. [Content Brief]
[2]. Nishihara K, et al. Induced Pluripotent Stem Cells Reprogrammed with Three Inhibitors Show Accelerated Differentiation Potentials with High Levels of 2-Cell Stage Marker Expression. Stem Cell Reports. 2019 Feb 12;12(2):305-318. [Content Brief]
[3]. Ito A, et al. Efficient and robust induction of retinal pigment epithelium cells by tankyrase inhibition regardless of the differentiation propensity of human induced pluripotent stem cells. Biochem Biophys Res Commun. 2021 May 7;552:66-72. [Content Brief]
[4]. Chambers SM, et al. Combined small-molecule inhibition accelerates developmental timing and converts human pluripotent stem cells into nociceptors. Nat Biotechnol. 2012 Jul 1;30(7):715-20. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)