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Trikamsteroside E

CAS# 952579-37-2

Trikamsteroside E

2D Structure

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Quality Control of Trikamsteroside E

3D structure

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Trikamsteroside E

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Chemical Properties of Trikamsteroside E

Cas No. 952579-37-2 SDF Download SDF
PubChem ID 102086541 Appearance Powder
Formula C48H76O23 M.Wt 1021.10
Type of Compound Steroids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1S,2S,3'S,4S,4'S,5'S,6S,7R,8R,9S,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-7-(hydroxymethyl)-5',9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3',4',16-triol
SMILES CC1COC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)C)CO)C(C1O)O
Standard InChIKey PAUALFMTFPEINK-VZSCNEEOSA-N
Standard InChI InChI=1S/C48H76O23/c1-18-13-65-48(39(59)31(18)54)25(12-49)30-28(71-48)11-24-22-6-5-20-9-21(51)10-29(46(20,4)23(22)7-8-45(24,30)3)67-43-38(36(27(53)15-63-43)68-41-34(57)33(56)26(52)14-62-41)70-42-35(58)37(32(55)19(2)66-42)69-44-40(60)47(61,16-50)17-64-44/h5,18-19,21-44,49-61H,6-17H2,1-4H3/t18-,19-,21+,22+,23-,24-,25-,26+,27-,28-,29+,30-,31-,32-,33-,34+,35+,36-,37+,38+,39-,40-,41-,42-,43-,44-,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 Trikamsteroside E

The herbs of Trillium tschonoskii Maxim.

Trikamsteroside E Dilution Calculator

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Trikamsteroside E Molarity Calculator

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Preparing Stock Solutions of Trikamsteroside E

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 0.9793 mL 4.8967 mL 9.7934 mL 19.5867 mL 24.4834 mL
5 mM 0.1959 mL 0.9793 mL 1.9587 mL 3.9173 mL 4.8967 mL
10 mM 0.0979 mL 0.4897 mL 0.9793 mL 1.9587 mL 2.4483 mL
50 mM 0.0196 mL 0.0979 mL 0.1959 mL 0.3917 mL 0.4897 mL
100 mM 0.0098 mL 0.049 mL 0.0979 mL 0.1959 mL 0.2448 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 Trikamsteroside E

[Chemical Constituents from Roots and Rhizome of Trillium tschonoskii( )].[Pubmed:30132316]

Zhong Yao Cai. 2016 Apr;39(4):770-4.

Objective: To investigate the chemical constituents from the roots and rhizome of Trillium tschonoskii. Methods: The85% methanol elution parts from the roots and rhizome of Trillium tschonoskii were separated and purified by polyamide,silica gel,RPC18,Sephadex LH-20 column chromatography and the preparation of high performance liquid. Chemical structures were identified by MS,1D and 2D-NMR experiment. Results: Ten steroidal saponins compounds were isolated and identified as diosgenin-3-O-alpha-L-rhamnopyranosyl-( 1-->4)-alpha-L-rhamnopyranosyl-( 1-->4)-[alpha-L-rhamnopyranosyl( 1 -->2) ]-beta-D-glucopyranoside( 1),Trikamsteroside E( 2),deoxyTrikamsteroside E( 3),( 23 S,24S,25S)-spirostan-5-ene-1beta,3beta,21,23,24-pentahydroxy-1beta-O-alpha-L-rham nopyranosyl-( 1 -->2)-[O-beta-D-xylopyranosyl( 1-->3) ]-O-alpha-L-pyranarabinoside( 4),trikamsteroside B( 5),27-hydroxy-trikamsteroside B( 6),3-acetyl-pennogenin( 7),dioscoreanoside I( 8),sileneoside G( 9) and intergristerone B( 10). Conclusion: Compounds 8 ~ 10 are isolated from this genus for the first time,compounds 1,3,4,6,7 are isolated from this plant for the first time.

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