Prunasin
Based on 1 publication(s) in Google Scholar
Prunasin is an orally active cyanogenic glucoside and the main metabolite of Amygdalin (HY-N0190). Prunasin can specifically inhibit rat DNA polymerase β (IC50: 98 μM). Prunasin has anti-inflammatory and anti-fibrotic activities. Prunasin can be used in the research of diseases such as liver fibrosis.
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- Reinheit: 99.56%
- CAS. Nr.: 99-18-3
- Formel: C14H17NO6
- Molecular Weight:295.29
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Speicherung:
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
Publications Citing Use of MedChemExpress (MCE) Prunasin
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Biologische Aktivität
|
DNA Polymerase |
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| Jurkat | IC50 |
>100 μg/mL
Compound: 6
|
Cytotoxicity against human Jurkat T cells after 36 hrs by MTT assay
Cytotoxicity against human Jurkat T cells after 36 hrs by MTT assay
|
[PMID: 21546250] |
Prunasin (6.25-100 μM; 22 h) can inhibit the production of NO in RAW264.7 cells and suppress the expression of α-SMA and Col1A1 in JS1 cells[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:JS1 cells
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Concentration:6.25, 12.5, 25, 50 and 100 μM
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Incubation Time:22 h
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Result:Inhibited the mRNA levels of α-SMA and Col1A1.
Pharmacokinetic Analysis in Rats[2]
| Route and Dose (mg/kg) | ke (/min) | T1/2ke (min) | Cmax (ng/mL) | Tmax (min) | AUC0-t (ng•min/mL) | AUC0-∞ (ng•min/mL) | MRT (min) | Vd (mL/kg) | CL (mL/min/kg) | F (%) |
| i.v. 5 | 0.010 | 69.42 | 6926.50 | 2.00 | 207670.12 | 208663.12 | 43.94 | 2469.24 | 25.05 | / |
| p.o. 5 | 0.013 | 63.48 | 2912.06 | 16.00 | 134797.34 | 135731.78 | 46.80 | 3369.66 | 37.02 | 64.91 |