Fumarranol
Fumarranol, a Fumagillin (HY-B0751) analogue, is a selective type 2 methionine aminopeptidase (MetAP2) inhibitor with a human IC50 of 3.2 μM. Fumarranol inhibits proliferation of bovine aortic endothelial cells and inhibits angiogenesis in a mouse matrigel plug model. Fumarranol can be used for the researches of cancer, diabetic retinopathy, age-related macular degeneration.
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- CAS No.: 912569-37-0
- 화학식: C16H24O4
- 분자량:280.36
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
All VEGFR Isoforms
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Biological Activity
제품 설명
IC50 & Target
[1]|
MetAp2 3.2 μM (IC50) |
In Vitro
Fumarranol (0-100 μM) selectively inhibits recombinant hMetAP2 enzymatic activity with an IC50 of 3.2 μM, and does not inhibit hMetAP1 at 100 μM[1].
Fumarranol inhibits bovine aortic endothelial cell proliferation with an IC50 of 34 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
- Human pluripotent stem cell endothelial-cell differentiation
- Vascular/Branching Fractal Analysis
- Endothelial Tube Formation Assay
- Matrigel/ECM Transwell Invasion Assay
- Endothelial Cell Migration/Angiogenic Sprouting Assay
- Cell Viability Determination by MTT Colorimetric Assay
- Matrigel Transwell/Boyden Chamber Invasion Assay
Chemical Information
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CAS No. 912569-37-0
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분자량 280.36
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화학식 C16H24O4
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SMILES
O(C)[C@]12[C@](CO)([C@]1([C@]3(C)[C@@H](CC=C(C)C)O3)[H])CCC2=O
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)