Hericerin A
Hericerin A is an isoindolinone derivative and a selective cytotoxic agent. Hericerin A is isolated from Hericium erinaceus cultured on brown rice. Hericerin A downregulates the phosphorylation of AKT and downregulates c-Myc oncoprotein levels downstream of p-AKT inactivation. Hericerin A induces Apoptosis. Hericerin A exhibits anticancer activity against leukemia. Hericerin A is used in research on acute promyelocytic leukemia, breast cancer, and Helicobacter pylori infection.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- CAS. Nr.: 1629208-29-2
- Formel: C21H29NO4
- Molecular Weight:359.47
-
Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Alle Endogenous Metabolite Isoform-spezifische Produkte anzeigen
More
Biologische Aktivität
Beschreibung
IC50 & Target
[1]|
Fungal Metabolite |
In Vitro
Hericerin A (0.01-100 μM; 72 h) exhibits weak cytotoxicity against HEL-299 cells, inhibiting growth by less than 30% at concentrations up to 50 μM, with an IC50 of 64.61 μM[1].
Hericerin A inhibits proliferation and induces apoptosis in HL-60 leukemia cells with an IC50 of 3.06 μmol/L and in HEL-299 cells with an IC50 of 64.61 μmol/L[4].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:HL-60 human acute promyelocytic leukaemia cells
-
Concentration:0.01-100 μM
-
Incubation Time:72 h
-
Result:Reduced the percentage of viable HL-60 cells with an IC50 value of 3.06 μM.
-
Cell Line:HEL-299 human lung fibroblast cells
-
Concentration:0.01-100 μM
-
Incubation Time:72 h
-
Result:Inhibited the growth of HEL-299 cells by less than 30% at concentrations up to 50 μM with an IC50 value of 64.61 μM.
-
Cell Line:HL-60 cells
-
Concentration:3.06 μM
-
Incubation Time:24 h; 48 h
-
Result:Increased the proportion of sub-G1 fraction (M1) cells to 10.30% at 24 h and 13.49% at 48 h.\nIncreased the number of apoptotic bodies after 24 and 48 h incubation periods.
-
Cell Line:HL-60 cells
-
Concentration:3.06 μM
-
Incubation Time:24 h; 48 h
-
Result:Increased Bax expression and decreased Bcl-2 expression in a time-dependent manner.
Increased active forms of caspase-3 and caused proteolytic cleavage of PARP.
Decreased p-AKT levels and down-regulated c-myc.
- Kinase activity and phosphorylation assays
- Western Blot
- Research Protocol for Infectious Diseases
- Detection of Apoptosis
- TUNEL staining for apoptotic DNA fragmentation
- Annexin V plus membrane-impermeant dye apoptosis staining
- Apoptosis Solutions
- Protocol for Kinase activity and phosphorylation assays
- Breast Cancer Modeling
- Cell Viability Determination by MTT Colorimetric Assay
Chemical Information
-
CAS. Nr. 1629208-29-2
-
Molecular Weight 359.47
-
Formel C21H29NO4
-
SMILES
OC1=C2C(=CC(OC)=C1C/C=C(/CCC=C(C)C)\C)C(=O)N(CCO)C2
-
Structure Classification
-
Initial Source
-
Versand
Room temperature in continental US; may vary elsewhere.
-
Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)