morusin
morusin Basic information
- Product Name:
- morusin
- Synonyms:
-
- Moracin
- 2-(2,4-Dihydroxyphenyl)-3-(3-methyl-2-butenyl)-5-hydroxy-8,8-dimethyl-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one
- 2-(2,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-3-(3-methyl-2-butenyl)-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one
- Mulberrochromene
- 2-(2,4-Dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-3-(3-methyl-2-buten-1-yl)-4H,8H-benzo[1,2-b:3,4-b']dipyran-4-one
- 4H,8H-Benzo(1,2-B:3,4-B')dipyran-4-one,2-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-diMethyl-3-(3-Methyl-2-butenyl)
- Morusin(Mulberrochromene)
- morusin 62596-29-6
- CAS:
- 62596-29-6
- MF:
- C25H24O6
- MW:
- 420.45
- EINECS:
- 300-006-7
- Product Categories:
-
- chemical reagent
- pharmaceutical intermediate
- phytochemical
- reference standards from Chinese medicinal herbs (TCM).
- standardized herbal extract
- Mol File:
- 62596-29-6.mol
morusin Chemical Properties
- Melting point:
- 232-235℃
- Boiling point:
- 656.7±55.0 °C(Predicted)
- Density
- 1.303
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- solubility
- DMF: 20mg/mL; DMF:PBS (pH 7.2) (1:3): 0.25mg/mL; DMSO: 10mg/mL; Ethanol: 15mg/mL
- form
- powder
- pka
- 6.55±0.60(Predicted)
- color
- Beige-orange
- Stability:
- Light Sensitive
morusin Usage And Synthesis
Chemical Properties
Soluble in DMSO, hot methanol, insoluble in petroleum ether, chloroform. Derived from the root bark of Morous alba L., family Moraceae, with the yellowish brown rough skin removed.
Uses
Morusin is an inhibitor of human cervical cancer stem cell growth, attenuating NF-kB activity, and initiating apoptosis.
Definition
ChEBI: An extended flavonoid that is flavone substituted by hydroxy groups at positions 5, 2' and 4', a prenyl group at position 3 and a 2,2-dimethyl pyran group across positions 7 and 8.
in vivo
Morusin retards the growth of breast cancer significantly. Mean tumor weight of the control mice is 1.14±0.30 g, and those of the mice administrated with 5 and 10 mg/kg of morusin are 0.61±0.23 and 0.41±0.10 g, respectively, tumor inhibitory rates are 46.5 %, and 64.1 %, respectively[1].
IC 50
p65; STAT3
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