Alyxialactone

CAS# 132237-63-9

Alyxialactone

Catalog No. BCN6171----Order now to get a substantial discount!

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Number of papers citing our products

Chemical structure

Alyxialactone

3D structure

Chemical Properties of Alyxialactone

Cas No. 132237-63-9 SDF Download SDF
PubChem ID 14194343 Appearance Powder
Formula C10H16O4 M.Wt 200.2
Type of Compound Iridoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (4R,4aS,6S,7R,7aS)-6-hydroxy-4-(hydroxymethyl)-7-methyl-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-3-one
SMILES CC1C(CC2C1COC(=O)C2CO)O
Standard InChIKey DYRWCEDTDIXFOD-ZEBDFXRSSA-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 Alyxialactone

The herbs of Paederia scandens (Lour.) Merr

Biological Activity of Alyxialactone

DescriptionAlyxialactone is a natural product from Paederia scandens (Lour.) Merr.

Protocol of Alyxialactone

Structure Identification
Phytochemistry,1990,29(10):3197-3199.

Iridolactones fromAlyxia reinwardti[Reference: WebLink]


METHODS AND RESULTS:
Investigation of the leaves ofAlyxia reinwardti led to the isolation of two iridolactones, Alyxialactone and 4-epi-Alyxialactone, whose structures were determined through 2D NMR spectroscopy.

Alyxialactone Dilution Calculator

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Alyxialactone Molarity Calculator

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Preparing Stock Solutions of Alyxialactone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.995 mL 24.975 mL 49.95 mL 99.9001 mL 124.8751 mL
5 mM 0.999 mL 4.995 mL 9.99 mL 19.98 mL 24.975 mL
10 mM 0.4995 mL 2.4975 mL 4.995 mL 9.99 mL 12.4875 mL
50 mM 0.0999 mL 0.4995 mL 0.999 mL 1.998 mL 2.4975 mL
100 mM 0.05 mL 0.2498 mL 0.4995 mL 0.999 mL 1.2488 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 Alyxialactone

Three New Iridoid Derivatives Have Been Isolated from the Stems of Neonauclea reticulata (Havil.) Merr. with Cytotoxic Activity on Hepatocellular Carcinoma Cells.[Pubmed:30205569]

Molecules. 2018 Sep 8;23(9). pii: molecules23092297.

Three new iridoids, namely neonanin A (1), neonanin B (2) and neoretinin A (3), as well as twelve known compounds, 6-hydroxy-7-methyl-1-oxo-4-carbomethoxyoctahydrocyclopenta[c]pyran (4), 4-epi-Alyxialactone (5), loganetin (6), loganin (7), phenylcoumaran-alpha'-aldehyde (8), cleomiscosin A (9), ficusal (10), balanophonin (11), vanillic acid (12), p-coumaric acid (13), cis,trans-abscisic acid (14), and trans,trans-abscisic acid (15) were isolated from the stems of Neonauclea reticulata (Havil.) Merr. These new structures were determined by the detailed analysis of spectroscopic data and comparison with the data of known analogues. Compounds 1(-)13 were evaluated using an in-vitro MTT cytotoxic assay for hepatocellular carcinoma (HCC) cells, and the preliminary results showed that ficusal (10), balanophonin (11), and p-coumaric acid (13) exhibited moderate cytotoxic activity, with EC50 values of 85.36 +/- 4.36, 92.63 +/- 1.41, and 29.18 +/- 3.48 microg/mL against Hep3B cells, respectively.

Non-glycosidic iridoids from Cymbaria mongolica.[Pubmed:11853749]

Phytochemistry. 2002 Mar;59(5):537-42.

Six non-glycosidic iridoids, i.e. (1R,4S,4aS,7S,7aS)-7-hydroxyl-4-hydroxy- methyl-7-methyl-1-methoxyl-1,4,4a,7a-tetrahydrocyclopenta[e]pyran-3-one (1), (1S,4R,4aS,7S,7aS)-7-hydroxyl-4-hydroxymethyl-7-methyl-1-methoxyl-1,4,4a,7a-tetra hydrocyclopenta[e]pyran-3-one (2), (1R,4R,4aS,7S,7aS)-7-hydroxyl-4-hydroxy-methyl-7-methyl-1-methoxyl-1,4,4a,7a-tetr ahydrocyclopenta[e]pyran-3-one (3), (1R, 4R, 4aS, 7aS)-4,7-dihydroxymethyl-1-methoxyl-1,4,4a,7a-tetrahydrocyclopenta-6-ene[e]pyran- 3-one (4), (1R, 4R, 4aS, 7aS)-4,7-dihydroxymethyl-1-hydroxyl-1,4,4a, 7a-tetrahydrocyclopenta-6-ene[e]pyran-3-one (5), (1R, 4S, 4aS, 7aS)-4,7-dihydroxy-methyl-1-methoxyl-1,4,4a,7a-tetrahydrocyclopenta-6-ene[e]pyran -3-one (6), as well as five known non-glycosidic iridoids mussaenin A (7), gardendiol (8), isoboonein (9), 4-epi-Alyxialactone (10) and rehmaglutin D (11) have been isolated from the Chinese medicinal plant Cymbaria mongolica. Their structures were elucidated by spectroscopic methods. These compounds exhibit significant antitumor and antibacterial activity.

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