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16-O-Acetylpolyporenic acid C

16-O-Acetylpolyporenic acid C

Catalog No. BCN4058
Size Price Stock
20mg $298 In stock
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Quality Control of 16-O-Acetylpolyporenic acid C

Chemical structure

16-O-Acetylpolyporenic acid C

16-O-Acetylpolyporenic acid C Dilution Calculator

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16-O-Acetylpolyporenic acid C Molarity Calculator

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Chemical Properties of 16-O-Acetylpolyporenic acid C

Cas No. 2535-06-0 SDF Download SDF
Chemical Name 2,3,6-trimethylbenzoic acid
SMILES CC1=C(C(=C(C=C1)C)C(=O)O)C
Standard InChIKey JRUKSSBDIZXQDX-UHFFFAOYSA-N
Standard InChI InChI=1S/C10H12O2/c1-6-4-5-7(2)9(8(6)3)10(11)12/h4-5H,1-3H3,(H,11,12)
Type of Compound Triterpenoids Appearance Powder
Formula C33H48O5 M.Wt 524.7
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other courier with RT , or blue ice upon request.

Preparing Stock Solutions of 16-O-Acetylpolyporenic acid C

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.9059 mL 9.5293 mL 19.0585 mL 38.117 mL 47.6463 mL
5 mM 0.3812 mL 1.9059 mL 3.8117 mL 7.6234 mL 9.5293 mL
10 mM 0.1906 mL 0.9529 mL 1.9059 mL 3.8117 mL 4.7646 mL
50 mM 0.0381 mL 0.1906 mL 0.3812 mL 0.7623 mL 0.9529 mL
100 mM 0.0191 mL 0.0953 mL 0.1906 mL 0.3812 mL 0.4765 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

Preparation of 16-O-Acetylpolyporenic acid C

This product is isolated and purified from the herbs of Daedalea dickinsii

References on 16-O-Acetylpolyporenic acid C

Constituents of the fungi Daedalea quercina and Daedaleopsis confragosa var. tricolor.[Pubmed: 11014261]


Phytochemical examination of solvent extracts of the wood-rotting fungi Daedalea quercina and Daedaleopsis confragosa var. tricolor led to the isolation of five new triterpene derivatives and some known fungal constituents. All structures were identified by one- and two-dimensional NMR spectroscopy and mass spectrometry. From Daedalea quercina, the new natural products 16-O-Acetylpolyporenic acid C, 16alpha-acetoxy-24-methylene-3-oxolanost-8-en-21-oic acid, (+)-24-methylene-3,23-dioxolanost-8-en-26-oic acid, (+)-3beta,12beta-dihydroxy-24-methyl-23-oxolanost-8-en-26-oi c acid and 12beta,23-epoxy-3alpha,23-dihydroxy-24-methyllanost-8- en-26-oic acid could be isolated. From Daedaleopsis confragosa var. tricolor, the compounds 3alpha-carboxyacetoxyquercinic acid, 3alpha-carboxyacetoxy-24-methylene-23-oxolanost-8-en-2 6-oic acid and 5alpha,8alpha-epidioxyergosta-6,22-dien-3beta-ol were identified. These are the first described triterpene derivatives isolated from this fungus.

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