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Baimantuoluoside C

CAS# 60124-17-6

Baimantuoluoside C

2D Structure

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Quality Control of Baimantuoluoside C

3D structure

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Baimantuoluoside C

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Chemical Properties of Baimantuoluoside C

Cas No. 60124-17-6 SDF Download SDF
PubChem ID 44576309 Appearance White powder
Formula C28H38O6 M.Wt 470.60
Type of Compound Steroids Storage Desiccate at -20°C
Synonyms Baimantuoluoside C aglycone; 27-Hydroxywithanolide B
Solubility Soluble in chloroform, ethanol and ethyl acetate; insoluble in petroleum ether and water
SMILES CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(CCC4C3C5C(O5)C6(C4(C(=O)C=CC6)C)O)C)CO
Standard InChIKey AWVMHXZWAKRDGG-MEBIVHGNSA-N
Standard InChI InChI=1S/C28H38O6/c1-14-12-20(33-25(31)16(14)13-29)15(2)17-7-8-18-22-19(9-11-26(17,18)3)27(4)21(30)6-5-10-28(27,32)24-23(22)34-24/h5-6,15,17-20,22-24,29,32H,7-13H2,1-4H3/t15-,17+,18-,19-,20+,22-,23-,24-,26+,27-,28-/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 Baimantuoluoside C

The herbs of Physali alkekengi

Protocol of Baimantuoluoside C

Structure Identification
Helvetica Chimica Acta, 2010, 92(7):1315-1323.

Baimantuoluosides A – C, Three New Withanolide Glucosides from the Flower of Datura metel L.[Reference: WebLink]


METHODS AND RESULTS:
In search for bioactive compounds from the flower of Datura metel L., three new withanolide glucosides, namely baimantuoluoside A, baimantuoluoside B, and Baimantuoluoside C (1–3, resp.) were isolated. Enzymatic hydrolysis of 1–3 afforded the corresponding aglycones 1a, 2a, and 3a, respectively.
CONCLUSIONS:
The structures of the new compounds were elucidated as (5α,6α,7α,12β,22R)-5,12-dihydroxy-1,26-dioxo-6,7 : 22,26-diepoxyergosta-2,24-dien-27-yl β-D-glucopyranoside (1), (5α,6α,7α,12α,22R)-5,12-dihydroxy-1,26-dioxo-6,7 : 22,26-diepoxyergosta-2,24-dien-27-yl β-D-glucopyranoside (2), (5α,6α,7α,22R)-5-hydroxy-1,26-dioxo-6,7 : 22,26-diepoxyergosta-2,24-dien-27-yl β-D-glucopyranoside (3) on the basis of chemical and physicochemical evidence, and are further confirmed by the structure determination by X-ray diffraction of withanolide aglycone 1a.

Baimantuoluoside C Dilution Calculator

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Baimantuoluoside C Molarity Calculator

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Preparing Stock Solutions of Baimantuoluoside C

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.1249 mL 10.6247 mL 21.2495 mL 42.4989 mL 53.1237 mL
5 mM 0.425 mL 2.1249 mL 4.2499 mL 8.4998 mL 10.6247 mL
10 mM 0.2125 mL 1.0625 mL 2.1249 mL 4.2499 mL 5.3124 mL
50 mM 0.0425 mL 0.2125 mL 0.425 mL 0.85 mL 1.0625 mL
100 mM 0.0212 mL 0.1062 mL 0.2125 mL 0.425 mL 0.5312 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 Baimantuoluoside C

Baimantuoluosides A – C, Three New Withanolide Glucosides from the Flower of Datura metel L.

Helvetica Chimica Acta, 2010, 92(7):1315-1323.

In search for bioactive compounds from the flower of Datura metel L., three new withanolide glucosides, namely baimantuoluoside A, baimantuoluoside B, and Baimantuoluoside C (1–3, resp.) were isolated. Enzymatic hydrolysis of 1–3 afforded the corresponding aglycones 1a, 2a, and 3a, respectively. The structures of the new compounds were elucidated as (5α,6α,7α,12β,22R)-5,12-dihydroxy-1,26-dioxo-6,7 : 22,26-diepoxyergosta-2,24-dien-27-yl β-D-glucopyranoside (1), (5α,6α,7α,12α,22R)-5,12-dihydroxy-1,26-dioxo-6,7 : 22,26-diepoxyergosta-2,24-dien-27-yl β-D-glucopyranoside (2), (5α,6α,7α,22R)-5-hydroxy-1,26-dioxo-6,7 : 22,26-diepoxyergosta-2,24-dien-27-yl β-D-glucopyranoside (3) on the basis of chemical and physicochemical evidence, and are further confirmed by the structure determination by X-ray diffraction of withanolide aglycone 1a.

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