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16-O-Acetylpolyporenic acid C

CAS# 2535-06-0

16-O-Acetylpolyporenic acid C

Catalog No. BCN4058----Order now to get a substantial discount!

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16-O-Acetylpolyporenic acid C: 5mg Please Inquire In Stock
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Quality Control of 16-O-Acetylpolyporenic acid C

Number of papers citing our products

Chemical structure

16-O-Acetylpolyporenic acid C

3D structure

Chemical Properties of 16-O-Acetylpolyporenic acid C

Cas No. 2535-06-0 SDF Download SDF
PubChem ID 12019177 Appearance Powder
Formula C33H48O5 M.Wt 524.7
Type of Compound Triterpenoids Storage Desiccate at -20°C
Synonyms 3-Oxo-16alpha-acetoxy-24-methylene-5alpha-lanosta-7,9(11)-dien-21-oic acid
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2R)-2-[(5R,10S,13R,14R,16R,17R)-16-acetyloxy-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl]-6-methyl-5-methylideneheptanoic acid
SMILES CC(C)C(=C)CCC(C1C(CC2(C1(CC=C3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C)OC(=O)C)C(=O)O
Standard InChIKey FPLFOXNTFUNRIC-SJXZRTDNSA-N
Standard InChI InChI=1S/C33H48O5/c1-19(2)20(3)10-11-22(29(36)37)28-25(38-21(4)34)18-33(9)24-12-13-26-30(5,6)27(35)15-16-31(26,7)23(24)14-17-32(28,33)8/h12,14,19,22,25-26,28H,3,10-11,13,15-18H2,1-2,4-9H3,(H,36,37)/t22-,25-,26+,28+,31-,32-,33+/m1/s1
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.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of 16-O-Acetylpolyporenic acid C

The herbs of Daedalea dickinsii

Biological Activity of 16-O-Acetylpolyporenic acid C

DescriptionStandard reference

Protocol of 16-O-Acetylpolyporenic acid C

Structure Identification
Phytochemistry. 2000 Aug;54(8):757-62.

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.
METHODS AND RESULTS:
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.
CONCLUSIONS:
These are the first described triterpene derivatives isolated from this fungus.

16-O-Acetylpolyporenic acid C Dilution Calculator

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16-O-Acetylpolyporenic acid C Molarity Calculator

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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.

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References on 16-O-Acetylpolyporenic acid C

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

Phytochemistry. 2000 Aug;54(8):757-62.

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.

Keywords:

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