Home >> Research Area >>Natural Products>>Sesquiterpenoids>> 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

CAS# 59742-11-9

1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

2D Structure

Catalog No. BCN7601----Order now to get a substantial discount!

Product Name & Size Price Stock
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 5mg $960 In Stock
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 10mg Please Inquire In Stock
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 20mg Please Inquire Please Inquire
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 50mg Please Inquire Please Inquire
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 100mg Please Inquire Please Inquire
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 200mg Please Inquire Please Inquire
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 500mg Please Inquire Please Inquire
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane: 1000mg Please Inquire Please Inquire

Quality Control of 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

3D structure

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1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

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Chemical Properties of 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

Cas No. 59742-11-9 SDF Download SDF
PubChem ID 10860539 Appearance Powder
Formula C19H24O5 M.Wt 332.39
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(1S,8S,9S,10S,13R)-6,9,10-trimethyl-2-oxo-4,14-dioxatetracyclo[7.5.0.01,13.03,7]tetradeca-3(7),5-dien-8-yl] 2-methylpropanoate
SMILES CC1CCC2C3(C1(C(C4=C(C3=O)OC=C4C)OC(=O)C(C)C)C)O2
Standard InChIKey WNPQEVZAOIQRLM-MFLGIWNWSA-N
Standard InChI InChI=1S/C19H24O5/c1-9(2)17(21)23-16-13-10(3)8-22-14(13)15(20)19-12(24-19)7-6-11(4)18(16,19)5/h8-9,11-12,16H,6-7H2,1-5H3/t11-,12+,16+,18-,19-/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 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

The roots of Ligularia fischeri.

Biological Activity of 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

Description1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane is a natural product from Ligularia fischeri.

Protocol of 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

Structure Identification
J Nat Prod. 2010 Feb 26;73(2):143-6.

A pair of epimeric spirosesquiterpenes from the roots of Ligularia fischeri.[Pubmed: 20104879 ]


METHODS AND RESULTS:
Two new highly oxygenated spirosesquiterpene lactones, ligulactones A (1) and B (2), and one known sesquiterpenoid, 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane (3), were isolated from the roots of Ligularia fischeri. Their structures and relative configurations were elucidated by 1D and 2D NMR and MS data and by comparison of their NMR data with those of related compounds. Single-crystal X-ray diffraction analyses confirmed their structures.
CONCLUSIONS:
Compounds 1 and 2 are C-7 epimers. A possible biosynthetic process for their formation is proposed. Structure 3 was proposed as the likely parent compound for the two new epimeric sesquiterpenoids.

1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane Dilution Calculator

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1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane Molarity Calculator

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Preparing Stock Solutions of 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.0085 mL 15.0426 mL 30.0851 mL 60.1703 mL 75.2129 mL
5 mM 0.6017 mL 3.0085 mL 6.017 mL 12.0341 mL 15.0426 mL
10 mM 0.3009 mL 1.5043 mL 3.0085 mL 6.017 mL 7.5213 mL
50 mM 0.0602 mL 0.3009 mL 0.6017 mL 1.2034 mL 1.5043 mL
100 mM 0.0301 mL 0.1504 mL 0.3009 mL 0.6017 mL 0.7521 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 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane

A pair of epimeric spirosesquiterpenes from the roots of Ligularia fischeri.[Pubmed:20104879]

J Nat Prod. 2010 Feb 26;73(2):143-6.

Two new highly oxygenated spirosesquiterpene lactones, ligulactones A (1) and B (2), and one known sesquiterpenoid, 1beta,10beta-epoxy-6beta-isobutyryloxy-9-oxo-furanoeremophilane (3), were isolated from the roots of Ligularia fischeri. Their structures and relative configurations were elucidated by 1D and 2D NMR and MS data and by comparison of their NMR data with those of related compounds. Single-crystal X-ray diffraction analyses confirmed their structures. Compounds 1 and 2 are C-7 epimers. A possible biosynthetic process for their formation is proposed. Structure 3 was proposed as the likely parent compound for the two new epimeric sesquiterpenoids.

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