4-Epi-isoinuviscolideCAS# 68832-39-3 |
2D Structure
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 68832-39-3 | SDF | Download SDF |
PubChem ID | 53320574 | Appearance | Oily solid |
Formula | C15H20O3 | M.Wt | 248.3 |
Type of Compound | Sesquiterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | (3aS,5aR,8S,8aR,9aR)-8-hydroxy-5,8-dimethyl-1-methylidene-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-2-one | ||
SMILES | CC1=CC2C(CC3C1CCC3(C)O)C(=C)C(=O)O2 | ||
Standard InChIKey | APMKESKZWHNIDJ-PFFFPCNUSA-N | ||
Standard InChI | InChI=1S/C15H20O3/c1-8-6-13-11(9(2)14(16)18-13)7-12-10(8)4-5-15(12,3)17/h6,10-13,17H,2,4-5,7H2,1,3H3/t10-,11+,12+,13-,15-/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. |
Targets | NO |
4-Epi-isoinuviscolide Dilution Calculator
4-Epi-isoinuviscolide Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 4.0274 mL | 20.1369 mL | 40.2739 mL | 80.5477 mL | 100.6847 mL |
5 mM | 0.8055 mL | 4.0274 mL | 8.0548 mL | 16.1095 mL | 20.1369 mL |
10 mM | 0.4027 mL | 2.0137 mL | 4.0274 mL | 8.0548 mL | 10.0685 mL |
50 mM | 0.0805 mL | 0.4027 mL | 0.8055 mL | 1.611 mL | 2.0137 mL |
100 mM | 0.0403 mL | 0.2014 mL | 0.4027 mL | 0.8055 mL | 1.0068 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. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- D-Prolinol(oil)
Catalog No.:BCC2708
CAS No.:68832-13-3
- Retusamine
Catalog No.:BCN2122
CAS No.:6883-16-5
- Sempervirine
Catalog No.:BCN4250
CAS No.:6882-99-1
- Sophoridine
Catalog No.:BCN4249
CAS No.:6882-68-4
- Dihydrochelerythrine
Catalog No.:BCN2273
CAS No.:6880-91-7
- Norfluorocurarine
Catalog No.:BCN4811
CAS No.:6880-54-2
- 6-Acetyl-2,2-dimethylchroman-4-one
Catalog No.:BCN4248
CAS No.:68799-41-7
- 4-Oxobedfordiaic acid
Catalog No.:BCN4247
CAS No.:68799-38-2
- Dipotassium glycyrrhizinate
Catalog No.:BCN8487
CAS No.:68797-35-3
- Dehydroeburicoic acid
Catalog No.:BCN3646
CAS No.:6879-05-6
- Tuberstemonine
Catalog No.:BCN4986
CAS No.:6879-01-2
- Triclabendazole
Catalog No.:BCC4742
CAS No.:68786-66-3
- IWP 12
Catalog No.:BCC5622
CAS No.:688353-45-9
- Xanthohumol I
Catalog No.:BCN8016
CAS No.:688360-06-7
- Xanthohumol L
Catalog No.:BCN8017
CAS No.:688360-15-8
- Astemizole
Catalog No.:BCC7691
CAS No.:68844-77-9
- Boc-D-Tyr(Me)-OH
Catalog No.:BCC2597
CAS No.:68856-96-2
- Fmoc-Val-OH
Catalog No.:BCC3570
CAS No.:68858-20-8
- HMP Linker
Catalog No.:BCC2832
CAS No.:68858-21-9
- 8-O-Methylretusin-7-O-beta-D-glucopyranoside
Catalog No.:BCN7899
CAS No.:68862-13-5
- Otonecine
Catalog No.:BCN2009
CAS No.:6887-34-9
- Eburicol
Catalog No.:BCN4252
CAS No.:6890-88-6
- Guaiacol salicylate
Catalog No.:BCC8327
CAS No.:87-16-1
- H-D-Glu-OH
Catalog No.:BCC2936
CAS No.:6893-26-1
New eudesmane derivatives and other sesquiterpenes from the epigeal parts of Dittrichia graveolens.[Pubmed:18981602]
Chem Pharm Bull (Tokyo). 2008 Nov;56(11):1535-45.
In bioassay-guided searches for novel bioactive natural products from higher plants of the Egyptian flora, two new eudesmane sesquiterpene derivatives, 3alpha-hydroxyilicic acid methyl ester (1) and 2alpha-hydroxy-4-epi-ilicic acid (2), together with 11 known sesquiterpenes were isolated from bioactive fractions of the active epigeal parts extracts of Dittrichia graveolens (L.) GREUTER (Asteraceae) growing in the coastal regions of northwestern Egypt. Four other known sesquiterpene lactones with different carbon skeletons, named 2alpha-hydroxy-2R-xanthalongin (8), 4-Epi-isoinuviscolide (9), 8-epi-helenalin (10), and bigelovin (11), were also isolated for the first time from the same source. The stereochemical structures of the isolated compounds were elucidated on the basis of physical and spectroscopic methods including UV, IR, 1H-, 13C-NMR, distortionless enhancement by polarization transfer, 2D NMR, 1H-1H correlation spectroscopy, 1H-13C heteronuclear single-quantum coherence, 1H-13C heteronuclear multiple-bond connectivity, 1H-1H nuclear Overhauser effect spectroscopy experiments, and high-resolution mass spectrometry, as well as some chemical transformations. The antimicrobial, antiinflammatory, and antipyretic activities of D. graveolens extracts and chromatographic fractions were carried out and the various bioactivities of our findings are discussed.