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471-66-9

471-66-9 Structure

471-66-9 Structure
IdentificationBack Directory
[Name]

ALPHA-BOSWELLIC ACID
[CAS]

471-66-9
[Synonyms]

α-BoswellicAci
α-Boswellic acid
A-BOSWELLIC ACID
BOSWELLIC ACID, A-
ALPHA-BOSWELLIC ACID
A-ALPHA-BOSWELLIC ACID
BOSWELLIC ACID, a-(SH)
boswellic acid extract
Boswelia Serrata extract
alpha-Boswellic acid, >98%
Boswellic Acid,a-Boswellic Acid
3α-hydroxyolean-12-en-24-oic Acid
3alpha-Hydroxy-12-oleanen-24-oic acid
Boswellin Extract/beta-boswellic acid
(4R)-3α-Hydroxyolean-12-en-24-oic acid
alpha-Boswellic acid (α-Boswellic acid)
(3α,4β)-3-Hydroxyolean-12-en-23-oic Acid
(3alpha)-3-hydroxyolean-12-en-24-oic acid
(18β)-3α-Hydroxygermanica-12-ene-24-oic acid
Olean-12-en-23-oicacid, 3-hydroxy-, (3a,4b)-
Olean-12-en-23-oic acid, 3-hydroxy-, (3α,4β)-
α-Boswellic acid, 98%, from Boswellia carterii Birdw.
[Molecular Formula]

C30H48O3
[MDL Number]

MFCD03788779
[MOL File]

471-66-9.mol
[Molecular Weight]

456.7
Chemical PropertiesBack Directory
[Melting point ]

289℃
[Boiling point ]

552.7±50.0 °C(Predicted)
[density ]

1.10±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

4.50±0.70(Predicted)
[color ]

White to Off-White
[Water Solubility ]

practically insoluble in water
[BRN ]

3074442
[LogP]

9.430 (est)
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

29181990
Hazard InformationBack Directory
[Uses]

ALPHA-BOSWELLIC ACID is the principal constitutents of frankincense (olibanum). A specific, nonredox inhibitor of 5-lipoxygenase used to treat inflammation.
[in vivo]

alpha-Boswellic acid (3 or 10 mg/kg, intraperitoneal injection) decreases epidermal thickening, mast cell count and dermal infiltration in BALB/c mice induced by 2, 4-dinitrochlorobenzene[1].
alpha-Boswellic acid (200 mg/kg, gavage) has a protective effect on ethanol-induced gastric injury in rats[2].

Animal Model:2,4-Dinitrochlorobenzene-Induced Atopic-like Dermatitis in BALB/c Mice[1]
Dosage:3 or 10 mg/kg
Administration:i.p.
Result:Reduced the severity of the AD-like symptoms.
Attenuated the increase in ear thickness and decreased cutaneous TEWL in DNCB-treated mice.
Animal Model:Ethanol-induced gastric injury in rats[2]
Dosage:200 mg/kg
Administration:i.g.
Result:Reduced injuries associated with the administration of ethanol, gastric juice acidity and the formation of MDA and increased CAT activity and SOD activity and the level of NO and PGE-2 in a dose-depended manner.
Increased the expression of both Nrf2 and HO-1.
[target]

NO | PGE | Nrf2 | HO-1 | ROS
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