3-O-Acetyl-alpha-boswellic acid | CAS:89913-60-0

3-O-Acetyl-alpha-boswellic acid

ChemFaces products have been cited in many studies from excellent and top scientific journals

Product Name	3-O-Acetyl-alpha-boswellic acid
Price:	$338 / 10mg
CAS No.:	89913-60-0
Catalog No.:	CFN90529
Molecular Formula:	C₃₂H₅₀O₄
Molecular Weight:	498.74 g/mol
Purity:	>=98%
Type of Compound:	Triterpenoids
Physical Desc.:	Powder
Source:	The herbs of Boswellia carterii Birdw.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS SDF
Similar structural:	Comparison (Web) (SDF)
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Description:

3-O-Acetyl-alpha-boswellic acid has strong anti-inflammatory activity.

Targets:

PGE | LTB

In vivo:

Cancer Research, 2005 , 65 :176-176.

Inhibitory effects of beta-boswellic acids on 12-O-tetradecanoylphorbol-13-acetate-induced inflammation, expression of pro-inflammatory cytokines, arachidonic acid metabolism, and tumor promotion in mouse skin[Reference: WebLink]

Boswellia serrata extracts have been used for centuries as an herbal medicine for the treatment of inflammation and related diseases in India and China.
METHODS AND RESULTS:
A preparation of Boswellia extract (BE) contains about 35-40% total beta-boswellic acids and further separated and purified by a Phenomenex Synergi MAX-RP 80A column into 6 peaks. Four peaks were identified as beta-boswellic acid, 3-O-acetyl-beta-boswelic acid, 11-keto-beta-boswellic acid and 3-O-acety-11-keto-beta-boswellic acid, respectively. The other 2 peaks were alpha-boswellic acid and 3-O-Acetyl-alpha-boswellic acid . Beta-boswellic acid and its 3 derivatives had strong anti-inflammatory activity in mouse ear edema test. Topical application of TPA (0.8 nmol) onto ears of CD-1 mice once a day for 4-5 days induced persistent inflammation that was corrected with elevated protein levels of pro-inflammatory cytokines as well as formation of PGE2 and LTB4 levels in the mouse ears.
CONCLUSIONS:
Topical application of BE and pure beta-boswellic acid at 30 min before each TPA application once a day for 4 days inhibited TPA-induced persistent inflammation and expression IL-1beta and IL-6 protein levels as well as inhibited formation of LTB4 levels, but not PGE2 levels in mouse ears.

3-O-Acetyl-alpha-boswellic acid Description

Source:	The herbs of Boswellia carterii Birdw.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

J Chromatogr A. 2004 Jan 16;1023(2):277-85.

Characterization of archaeological frankincense by gas chromatography-mass spectrometry.[Pubmed: 14753694]

METHODS AND RESULTS:
A simple gas chromatography-mass spectrometry (GC-MS) method has been developed for the characterization of frankincense in archaeological samples. After trimethylsilylation of the methanolic extract, 15 triterpenoids have been found among the chemical constituents of commercial olibanum (alpha-boswellic acid, 3-O-Acetyl-alpha-boswellic acid , beta-boswellic acid, 3-O-acetyl-beta-boswellic acid, alpha-amyrin, beta-amyrin, lupeol, 3-epi-beta-amyrin, 3-epi-beta-amyrin, 3-epi-lupeol, alpha-amyrenone, beta-amyrenone, lupenone, 3alpha-hydroxy-lup-20(29)-en-24-oic acid and 3-O-acetyl-hydroxy-lup-20(29)-en-24-oic acid). These compounds have been unequivocally identified by retention time and mass spectral comparison with pure standards previously isolated, for the most part, in our laboratory. Within these triterpenes, acid ones, the corresponding O-acetates, and their products of degradation were found to be characteristic of frankincense (Boswellia resin).
CONCLUSIONS:
The presence of these unusual triterpenic compounds in an archaeological resinous sample, recovered during excavations from Dahshour site (Egypt, XIIth Dynasty), enabled us to identify unambiguously frankincense resin among several other materials. Additional chromatographic peaks of this sample were assigned to broad chemical classes using retention time and mass spectra features.

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Triterpenoids Compound Library PGE Inhibitor Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	2.0051 mL	10.0253 mL	20.0505 mL	40.1011 mL	50.1263 mL
5 mM	0.401 mL	2.0051 mL	4.0101 mL	8.0202 mL	10.0253 mL
10 mM	0.2005 mL	1.0025 mL	2.0051 mL	4.0101 mL	5.0126 mL
50 mM	0.0401 mL	0.2005 mL	0.401 mL	0.802 mL	1.0025 mL
100 mM	0.0201 mL	0.1003 mL	0.2005 mL	0.401 mL	0.5013 mL

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CFN90966	Gymnestrogenin	19942-02-0	490.72	C₃₀H₅₀O₅
CFN90961	Gymnemagenin	22467-07-8	506.71	C₃₀H₅₀O₆
CFN90978	21-O-Tigloylgymnemagenin	1581276-63-2	588.81	C₃₅H₅₆O₇
CFN70307	Protoescigenin	20853-07-0	506.7	C₃₀H₅₀O₆
CFN99305	Olean-12-ene-3,24-diol	119318-15-9	442.7	C₃₀H₅₀O₂
CFN97007	Soyasapogenol B	595-15-3	458.7	C₃₀H₅₀O₃
CFN91068	Soyasapogenol C	595-14-2	440.7	C₃₀H₄₈O₂
CFN91069	Soyasapogenol D	65892-76-4	472.8	C₃₁H₅₂O₃
CFN99870	Melilotigenin C	188970-21-0	456.7	C₃₀H₄₈O₃