BERGAPTOL
BERGAPTOL Basic information
- Product Name:
- BERGAPTOL
- Synonyms:
-
- 4-HYDROXYPSORALEN
- BERGAPTOL
- BERGAPTOL hplc
- BERGAPTOL WITH HPLC
- 4-Hydroxy-7H-furo[3,2-g][1]benzopyran-7-one
- 4-Hydroxybergapten
- 5-Hydroxy-6,7-furanocouMarin
- NSC 341958
- CAS:
- 486-60-2
- MF:
- C11H6O4
- MW:
- 202.16
- Product Categories:
-
- Heterocycles
- Inhibitors
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Coumarins
- Miscellaneous
- Aromatics
- Mol File:
- 486-60-2.mol
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BERGAPTOL Chemical Properties
- Melting point:
- 287-290°C
- Boiling point:
- 311.9±11.0 °C(Predicted)
- Density
- 1.526±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,2-8°C
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 6.80±0.20(Predicted)
- color
- Pale Beige to Pale Brown
- BRN
- 190104
- LogP
- 1.405 (est)
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Safety Information
- Hazard Codes
- Xn
- Risk Statements
- 22-36
- Safety Statements
- 22-24/25-26
- WGK Germany
- 3
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BERGAPTOL Usage And Synthesis
Uses
A hydroxylated psoralen that acts as a potent inhibitors of debenzylation activity of CYP3A4 enzyme with an IC50 value of 24.92 and 42.93 μM, respectively. Recent studies suggest that it may have antiproliferative and anticancer properties.
Definition
ChEBI: Bergaptol is a member of psoralens and a 5-hydroxyfurocoumarin. It is a conjugate acid of a bergaptol(1-).
in vivo
Bergaptol (10-40 mg/kg, i.p., once a day for two weeks) improves the cognitive impairment in LPS-treated mice[4].
| Animal Model: | LPS (40 μg/kg, i.c.v.)-treated mice[4] |
| Dosage: | 10-40 mg/kg |
| Administration: | i.p., once a day for two week |
| Result: | Reduced LPS-induced fixation and cleavage of neuronal nuclei in the CA1 region of the hippocampus (H&E staining). Increasead the dendritic spine density of mice. Inhibited LPS-induced neuroinflammation. |
target
CYP3A4
IC 50
CYP3
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