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morusin

Basic information Safety Supplier Related

morusin Basic information

Product Name:
morusin
Synonyms:
  • 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
  • Morusin?, >99%
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
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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
Major Application
food and beverages
InChI
1S/C25H24O6/c1-13(2)5-7-17-22(29)21-19(28)12-20-16(9-10-25(3,4)31-20)24(21)30-23(17)15-8-6-14(26)11-18(15)27/h5-6,8-12,26-28H,7H2,1-4H3
InChIKey
XFFOMNJIDRDDLQ-UHFFFAOYSA-N
SMILES
[o]1c2c([c](c(c1c4c(cc(cc4)O)O)CC=C(C)C)=O)c(cc3c2C=CC(O3)(C)C)O
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Safety Information

WGK Germany 
WGK 3
Storage Class
11 - Combustible Solids
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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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