M50054
CAS No. 54135-60-3
M50054( Apoptosis Inhibitor )
Catalog No. M27486 CAS No. 54135-60-3
Apoptosis Inhibitor was a novel inhibitor of programmed cell death associate with caspase-3 inhibition.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 50 | Get Quote |
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| 10MG | 71 | Get Quote |
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| 25MG | 146 | Get Quote |
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| 50MG | 219 | Get Quote |
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| 100MG | 322 | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameM50054
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NoteResearch use only, not for human use.
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Brief DescriptionApoptosis Inhibitor was a novel inhibitor of programmed cell death associate with caspase-3 inhibition.
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DescriptionApoptosis Inhibitor was a novel inhibitor of programmed cell death associate with caspase-3 inhibition.(In Vitro):Apoptosis Inhibitor was identified as a novel inhibitor of apoptosis (programmed cell death) using an in vitro cell death assay system induced in human Fas-expressing WC8 cells by soluble human Fas ligand.
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In VitroM50054 inhibits the caspase-3 activation by Etoposide in a dose-dependent manner. The IC50 value of M50054 against Etoposide-induced caspase-3 activation of U937 cells is 79 μg/mL. However, M50054 does not directly inhibit the enzymatic activity of caspase-3 at all concentrations up to 1000 μg/mL.M50054 (1-300 μg/mL) inhibits soluble human Fas ligand-induced cell death of human Fas-expressing WC8 cells in a dose-dependent manner, and the IC50 of 67 μg/mL.M50054 (30-300 μg/mL) inhibits the death of U937 cells induced by etoposide (10 μg/mL) in a dose-dependent manner, and the IC50 value of M50054 against Etoposide-induced cell death of U937 cells is 130 μg/mL. The IC50 value of M50054 against etoposide-induced DNA fragmentation of U937 cells was 54 μg/mL. Cell Proliferation Assay Cell Line:Human Fas-expressing WC8 cells Concentration:1, 3, 10, 30, 100, 300 μg/mL Incubation Time:Pre-incubated for 30 min Result:Inhibited soluble human Fas ligand-induced cell death of human Fas-expressing WC8 cells in a dose-dependent manner, and the IC50 of 67 μg/mL.
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In VivoM50054 (10-300 mg/kg; oral administration 30 min before anti-Fas antibody injection) inhibits the elevation of alanine aminotransferase and aspartate aminotransferase in a dose-dependent manner.M50054 (topical treatment; given daily beginning on day 5 after birth and ending on day 14) significantly improves alopecia (hair loss) symptoms. Animal Model:Female BALB/c miceDosage:10, 30, 100 or 300 mg/kg Administration:Orally administered in a volume of 10 mL/kg Result:Inhibited the elevation of alanine aminotransferase and aspartate aminotransferase in a dose-dependent manner. Significantly improved these parameters at doses of 100 mg/kg and 300 mg/kg.Animal Model:Five-day-old SD rats Dosage:Administration:Topically applied to the head and back of 5-day-old rats once daily for 10 days Result:Alopecia scores significantly decreased throughout the entire observation period compared with the control group.
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SynonymsApoptosis Inhibitor
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PathwayApoptosis
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TargetCaspase
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RecptorCYP1A2|CYP2B6
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Research Area——
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Indication——
Chemical Information
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CAS Number54135-60-3
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Formula Weight236.26
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Molecular FormulaC13H16O4
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C(CCC1)C(CC(C(CCC2)=O)C2=O)C1=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.L E Korhonen, et al. New potent and selective cytochrome P450 2B6 (CYP2B6) inhibitors based on three-dimensional quantitative structure-activity relationship (3D-QSAR) analysis. Br J Pharmacol. 2007 Apr;150(7):932-42.
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