Methylophiopogonanone B
Methylophiopogonanone B Basic information
- Product Name:
- Methylophiopogonanone B
- Synonyms:
-
- (3R)-2,3-Dihydro-5,7-dihydroxy-3-[(4-methoxyphenyl)methyl]-6,8-dimethyl-4H-1-benzopyran-4-one
- Methylophiopogonanone B
- NE-IV
- R-Methylophiopogonanone B
- Methylophiopogonanone B(R-Methylophiopogonanone B)
- 8-Methylophiopogonanone B
- 3-(4'-methoxy-benzyl)-5,7-dihydroxy-6,8-dimethyl-chroman-4-one
- (3R)-5,7-Dihydroxy-3-(4-methoxybenzyl)-6,8-dimethyl-2,3-dihydro-4 H-chromen-4-one
- CAS:
- 74805-91-7
- MF:
- C19H20O5
- MW:
- 328.36
- Mol File:
- 74805-91-7.mol
Methylophiopogonanone B Chemical Properties
- Boiling point:
- 554.5±49.0 °C(Predicted)
- Density
- 1.285
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- solubility
- Soluble in acetone, chloroform and methanol;
- form
- powder
- pka
- 8.24±0.40(Predicted)
- color
- Light yellow
- Water Solubility
- insoluble in water
Methylophiopogonanone B Usage And Synthesis
Description
Methylophiopogonanone B (MO‑B), which belongs to a group of homoisoflavonoids, present in Ophiopogon japonicus, has been identified as an active component with antioxidative and anti‑tumor properties.
Chemical Properties
Methylophiopogonanone B is soluble in methanol, ethanol, DMSO and other organic solvents, and is derived from the fibrous root of Ophiopogon japonicus.
Uses
Methylophiopogonanone B has the effect of enhancing protease activity and regulating cytoskeleton remodeling.
Synthesis
Methylophiopogonanone B was synthesized from 2,4,6-trihydroxy-3,5-dimethylacetophenone in 57% yield.
References
[1] M. FUJII. First synthesis of racemic methylophiopogonanone B and its inhibitory activity of hypoxia-inducible factor-1α[J]. Heterocycles, 2009, 78 1: 207-212. DOI:10.3987/COM-08-11517.
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