Semaxanib
CAS No. 194413-58-6
Semaxanib ( SU5416 )
Catalog No. M13045 CAS No. 194413-58-6
Semaxanib (SU5416) is a potent and selective VEGFR(Flk-1/KDR) inhibitor with IC50 of 1.23 μM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 37 | In Stock |
|
| 10MG | 30 | In Stock |
|
| 25MG | 48 | In Stock |
|
| 50MG | 71 | In Stock |
|
| 100MG | 111 | In Stock |
|
| 200MG | 174 | In Stock |
|
| 500MG | 341 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameSemaxanib
-
NoteResearch use only, not for human use.
-
Brief DescriptionSemaxanib (SU5416) is a potent and selective VEGFR(Flk-1/KDR) inhibitor with IC50 of 1.23 μM.
-
DescriptionSemaxanib (SU5416) is a potent and selective VEGFR(Flk-1/KDR) inhibitor with IC50 of 1.23 μM, 20-fold more selective for VEGFR than PDGFRβ, lack of activity against EGFR, InsR and FGFR. Phase 3.
-
In Vitro——
-
In Vivo——
-
SynonymsSU5416
-
PathwayAngiogenesis
-
TargetVEGFR
-
RecptorVEGFR2/Flk1
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number194413-58-6
-
Formula Weight238.28
-
Molecular FormulaC15H14N2O
-
Purity>98% (HPLC)
-
SolubilityEthanol: 2 mg/mL (8.39 mM); DMSO: 22 mg/mL (92.32 mM)
-
SMILESCC1=CC(=C(N1)/C=C\2/C3=CC=CC=C3NC2=O)C
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
Sulfatinib (b)
Sulfatinib (HMPL-012) is a potent, multi-targeted tyrosine kinase inhibitor of VEGFR-1/2/3, FGFR1, CSF1R with IC50 of 2/24/1 nM, 15 nM, 4 nM, respectively.
-
Lariciresinol
Lariciresinol is an enterolignan precursor, it possesses fungicidal activities by disrupting the fungal plasma membrane and therapeutic potential as a novel antifungal agent for the treatment of fungal infectious diseases in humans. Dietary lariciresinol can attenuate mammary tumor growth and reduce blood vessel density in human MCF-7 breast cancer xenografts and carcinogen-induced mammary tumors in rats.
-
Motesanib diphosphat...
A potent, orally bioavailable, multikinase inhibitor inhibitor of VEGFR1/2/3, PDGFR and c-Kit with IC50 of 2-6 nM, 84 nM and 8 nM, respectively.
Cart
sales@molnova.com