ChemicalBook--->CAS DataBase List--->62687-22-3

62687-22-3

62687-22-3 Structure

62687-22-3 Structure
IdentificationBack Directory
[Name]

handelin
[CAS]

62687-22-3
[Synonyms]

handelin
Yejuhualactone
HANDELIN; YEJUHUALACTONE
6,6'-dihydroxy-6,6',9,9'-tetramethyl-3'-methylene-2,2'-dioxo-2',3a,3',3a',4,5,5',6,6a,6',7,9a,9b,9',9a',9b'-hexadecahydro-4'H-spiro[azuleno[4,5-b]furan-3,10'-[6a,9]ethanoazuleno[4,5-b]furan]-5-yl acetate
Spiro[azuleno[4,5-b]furan-3(2H),10'-[4H-6a,9]ethanoazuleno[4,5-b]furan]-2,2'(3'H)-dione, 4-(acetyloxy)-3a,3'a,4,5,5',6,6',6a,7,9',9a,9'a,9b,9'b-tetradecahydro-6,6'-dihydroxy-6,6',9,9'-tetramethyl-3'-methylene-, (3R,3aR,3'aS,4S,6R,6'R,6aR,6'aR,9'R,9aR,9'aS,9bR,9'bS)-
[Molecular Formula]

C32H40O8
[MDL Number]

MFCD11656142
[MOL File]

62687-22-3.mol
[Molecular Weight]

552.66
Chemical PropertiesBack Directory
[Boiling point ]

731.0±60.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3 (20 ºC 760 Torr)
[form ]

Solid
[pka]

14.34±0.70(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Handelin is a guaianolide dimer from Chrysanthemum boreale that has potent anti-inflammatory activity by down-regulating NF-κB signaling and pro-inflammatory cytokine production[1].
[Definition]

ChEBI: Handelin is a sesterterpenoid.
[in vivo]

Handelin (Compound 1; 10-20 mg/kg; oral administration; for 30 mintues; male Sprague-Dawley rats) treatment inhibits acute inflammation in carrageenan-induced paw edema model. The serum level of IL-1β is also inhibited by Handelin in a carrageenan-induced paw edema model [1].

Animal Model:Male Sprague-Dawley (SD) rats (150-170 g, 5 weeks old) injected with carrageenan[1]
Dosage:10 mg/kg, 20 mg/kg
Administration:Oral administration; for 30 mintues
Result:Inhibited acute inflammation in carrageenan-induced paw. The serum level of IL-1β was also inhibited.
[References]

[1] Y Pyee, et al. Suppression of inflammatory responses by handelin, a guaianolide dimer from Chrysanthemum boreale, via downregulation of NF-κB signaling and pro-inflammatory cytokine production. J Nat Prod. 2014 Apr 25;77(4):917-24. DOI:10.1021/np4009877
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