3-Epiglochidiol

CAS# 29028-10-2

3-Epiglochidiol

Catalog No. BCN5193----Order now to get a substantial discount!

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Quality Control of 3-Epiglochidiol

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Chemical structure

3-Epiglochidiol

3D structure

Chemical Properties of 3-Epiglochidiol

Cas No. 29028-10-2 SDF Download SDF
PubChem ID 488250 Appearance Powder
Formula C30H50O2 M.Wt 442.7
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1R,3aR,5aR,5bR,7aS,9S,11R,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol
SMILES CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C
Standard InChIKey SWEUJTWPRYKNNX-AXLUDCLJSA-N
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 3-Epiglochidiol

The herbs of Glochidion puberum L.

Biological Activity of 3-Epiglochidiol

DescriptionStandard reference

Protocol of 3-Epiglochidiol

Structure Identification
Journal of Chemical & Pharmaceutical Research;2014, 6(5): 990.

Chemical constituents of the aerial parts of Cynanchum chinense R. Br.[Reference: WebLink]


METHODS AND RESULTS:
Fifteen compounds were obtained from 95% aqueous ethanol extract of Cynanchum chinenseR. Br.and elucidated as 3-Epiglochidiol(01), (+)-medioresinol(02), kaempferol-3-O- α-L-rahmnoside(03), catechin(04), 3β-hydroxyolean-12-en-29-oic acid(05), 6-hydroxy-4-(4-hydroxy-3- methoxyphenyl)-3-hydroxymethyl-7-methoxy3,4-dihydro-2-naphthaldehyde(06), detetrahydroconidendrin(07), kaempferol(08), 3-hydroxy-4-methoxybenzoic acid(09), epigallocatechin(10),2β,22β-dihydroxyo -lean-12-en-29-oic acid(11), epicatechin(12), p-hydrobenzoic acid(13).
CONCLUSIONS:
Compounds 01, 05 and 11 were obtained from this genus, and compounds 01, 02, 04, 05-07, 10-11 and 12 were isolated from this plant for the first time.

3-Epiglochidiol Dilution Calculator

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3-Epiglochidiol Molarity Calculator

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Preparing Stock Solutions of 3-Epiglochidiol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.2589 mL 11.2943 mL 22.5887 mL 45.1773 mL 56.4717 mL
5 mM 0.4518 mL 2.2589 mL 4.5177 mL 9.0355 mL 11.2943 mL
10 mM 0.2259 mL 1.1294 mL 2.2589 mL 4.5177 mL 5.6472 mL
50 mM 0.0452 mL 0.2259 mL 0.4518 mL 0.9035 mL 1.1294 mL
100 mM 0.0226 mL 0.1129 mL 0.2259 mL 0.4518 mL 0.5647 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 3-Epiglochidiol

Chemical constituents of the aerial parts of Cynanchum chinense R. Br.

Journal of Chemical & Pharmaceutical Research;2014, 6(5): 990.

Fifteen compounds were obtained from 95% aqueous ethanol extract of Cynanchum chinenseR. Br.and elucidated as 3-Epiglochidiol(01), (+)-medioresinol(02), kaempferol-3-O- α-L-rahmnoside(03), catechin(04), 3β-hydroxyolean-12-en-29-oic acid(05), 6-hydroxy-4-(4-hydroxy-3- methoxyphenyl)-3-hydroxymethyl-7-methoxy3,4-dihydro-2-naphthaldehyde(06), detetrahydroconidendrin(07), kaempferol(08), 3-hydroxy-4-methoxybenzoic acid(09), epigallocatechin(10),2β,22β-dihydroxyo -lean-12-en-29-oic acid(11), epicatechin(12), p-hydrobenzoic acid(13). Compounds 01, 05 and 11 were obtained from this genus, and compounds 01, 02, 04, 05-07, 10-11 and 12 were isolated from this plant for the first time.

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