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Lupeol 3-hydroxyoctadecanoate

CAS# 108885-61-6

Lupeol 3-hydroxyoctadecanoate

2D Structure

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Lupeol 3-hydroxyoctadecanoate

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Chemical Properties of Lupeol 3-hydroxyoctadecanoate

Cas No. 108885-61-6 SDF Download SDF
PubChem ID 131843987 Appearance Powder
Formula C48H84O3 M.Wt 709.2
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,7aR,9S,11aR,11bR,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]chrysen-9-yl] 3-hydroxyoctadecanoate
SMILES CCCCCCCCCCCCCCCC(CC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C)O
Standard InChIKey ISCGWWWBTBITFA-HQBPQUAZSA-N
Standard InChI InChI=1S/C48H84O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-36(49)34-42(50)51-41-28-30-46(7)39(44(41,4)5)27-31-48(9)40(46)25-24-38-43-37(35(2)3)26-29-45(43,6)32-33-47(38,48)8/h36-41,43,49H,2,10-34H2,1,3-9H3/t36?,37-,38+,39-,40+,41-,43+,45+,46-,47+,48+/m0/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 Lupeol 3-hydroxyoctadecanoate

The roots of Biondia hemsleyana.

Biological Activity of Lupeol 3-hydroxyoctadecanoate

DescriptionStandard reference

Protocol of Lupeol 3-hydroxyoctadecanoate

Structure Identification
Chemical Research in Chinese Universities,2003,24(3):436-41.

Chemical Constituents from the Roots of Biondia Hemsleyana[Reference: WebLink]

Nineteen I compounds were isolated from the,ethanol extract of the roots of Biondia hemsleyana (Warb.) Tsiang through. the repeated column chromatography on normal and reversed phase silica gel.
METHODS AND RESULTS:
By the spectroscopic and chemical evidence, their structures were elucidated as alpha-amyrin-3beta-acetate (1), Lupeol 3-hydroxyoctadecanoate (2), lupeol 3, 5-dihydroxyeicosanoate (3), cycloeucalenol (4), 4-methoxy salicylic aldehyde(5), 4-methoxy salicylic acid(6), isovanillin(7), scopoletin(8), isovanillic acid(9), cleomiscosin A (10), 2-hydroxmethyl-5-methoxylphenyl-O-beta-D-glucopyranoside (11), pregn-4-ene-3, 20-dione (12), neridienone (13), daucosterol(14), pregn-5-ene-3beta, 17alpha, 20alpha-triol-20-O-beta-D-canaropyranoside (15), periplogenin-3-O-beta-D-gluco pyranosyl-(1-->4)-beta-D-cymaropyranoside (16), pregn-5-ene-3beta, 20 (S)-diol-3-O-[2-O-acetyl-beta-D-digitalopyranosyl (1-->4)-beta-D-cymaropyranosyl]-20-O-beta-D-glucopyranosyl-(1-->6)-beta- D-glucopyranosyl-(1-->4)-beta-D-digitalo pyranoside(17), pregn-5-ene-3beta, 20(S)-diol-20-O-alpha-D-glucopyranosyl-(1-->6)-beta-D-glucopyranoside(18 , biondianoside C) and pregn-5-ene-3beta, 20(S)-diol-3-O-[beta-D-glucopyranosyl]-20-O-beta-D-glucopyranosyl-(1-->6 )-beta-D-glucopyranoside (19, biondianoside D) respectively.
CONCLUSIONS:
All compounds were isolated from this genus for the first time and 3, 11, 18 and 19 were new compounds among them.

Lupeol 3-hydroxyoctadecanoate Dilution Calculator

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Preparing Stock Solutions of Lupeol 3-hydroxyoctadecanoate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.41 mL 7.0502 mL 14.1004 mL 28.2008 mL 35.251 mL
5 mM 0.282 mL 1.41 mL 2.8201 mL 5.6402 mL 7.0502 mL
10 mM 0.141 mL 0.705 mL 1.41 mL 2.8201 mL 3.5251 mL
50 mM 0.0282 mL 0.141 mL 0.282 mL 0.564 mL 0.705 mL
100 mM 0.0141 mL 0.0705 mL 0.141 mL 0.282 mL 0.3525 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 Lupeol 3-hydroxyoctadecanoate

Chemical Constituents from the Roots of Biondia Hemsleyana

Chemical Research in Chinese Universities,2003,24(3):436-41.

Nineteen I compounds were isolated from the,ethanol extract of the roots of Biondia hemsleyana (Warb.) Tsiang through. the repeated column chromatography on normal and reversed phase silica gel. By the spectroscopic and chemical evidence, their structures were elucidated as alpha-amyrin-3beta-acetate (1), Lupeol 3-hydroxyoctadecanoate (2), lupeol 3, 5-dihydroxyeicosanoate (3), cycloeucalenol (4), 4-methoxy salicylic aldehyde(5), 4-methoxy salicylic acid(6), isovanillin(7), scopoletin(8), isovanillic acid(9), cleomiscosin A (10), 2-hydroxmethyl-5-methoxylphenyl-O-beta-D-glucopyranoside (11), pregn-4-ene-3, 20-dione (12), neridienone (13), daucosterol(14), pregn-5-ene-3beta, 17alpha, 20alpha-triol-20-O-beta-D-canaropyranoside (15), periplogenin-3-O-beta-D-gluco pyranosyl-(1-->4)-beta-D-cymaropyranoside (16), pregn-5-ene-3beta, 20 (S)-diol-3-O-[2-O-acetyl-beta-D-digitalopyranosyl (1-->4)-beta-D-cymaropyranosyl]-20-O-beta-D-glucopyranosyl-(1-->6)-beta- D-glucopyranosyl-(1-->4)-beta-D-digitalo pyranoside(17), pregn-5-ene-3beta, 20(S)-diol-20-O-alpha-D-glucopyranosyl-(1-->6)-beta-D-glucopyranoside(18 , biondianoside C) and pregn-5-ene-3beta, 20(S)-diol-3-O-[beta-D-glucopyranosyl]-20-O-beta-D-glucopyranosyl-(1-->6 )-beta-D-glucopyranoside (19, biondianoside D) respectively. All compounds were isolated from this genus for the first time and 3, 11, 18 and 19 were new compounds among them.

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