Dehydrovomifoliol

CAS# 39763-33-2

Dehydrovomifoliol

Catalog No. BCN7562----Order now to get a substantial discount!

Product Name & Size Price Stock
Dehydrovomifoliol: 5mg $748 In Stock
Dehydrovomifoliol: 10mg Please Inquire In Stock
Dehydrovomifoliol: 20mg Please Inquire Please Inquire
Dehydrovomifoliol: 50mg Please Inquire Please Inquire
Dehydrovomifoliol: 100mg Please Inquire Please Inquire
Dehydrovomifoliol: 200mg Please Inquire Please Inquire
Dehydrovomifoliol: 500mg Please Inquire Please Inquire
Dehydrovomifoliol: 1000mg Please Inquire Please Inquire

Quality Control of Dehydrovomifoliol

Number of papers citing our products

Chemical structure

Dehydrovomifoliol

3D structure

Chemical Properties of Dehydrovomifoliol

Cas No. 39763-33-2 SDF Download SDF
PubChem ID 688492 Appearance Oil
Formula C13H18O3 M.Wt 222.28
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (4S)-4-hydroxy-3,5,5-trimethyl-4-[(E)-3-oxobut-1-enyl]cyclohex-2-en-1-one
SMILES CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C
Standard InChIKey JJRYPZMXNLLZFH-URWSZGRFSA-N
Standard InChI InChI=1S/C13H18O3/c1-9-7-11(15)8-12(3,4)13(9,16)6-5-10(2)14/h5-7,16H,8H2,1-4H3/b6-5+/t13-/m1/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 Dehydrovomifoliol

The whole plant of Solanum lyratum.

Biological Activity of Dehydrovomifoliol

Description1. Dehydrovomifoliol could be a marker of Polish heather honey. 2. Dehydrovomifoliol exhibits moderate acetylcholinesterase (AChE) inhibitory activities. 3. Dehydrovomifoliol shows significant cytotoxic activities against three human cancer cell lines, namely, HONE-1 nasopharyngeal, KB oral epidermoid carcinoma, and HT29 colorectal carcinoma cells, and the IC(50) values in the range 3.7-8.1 microM.
TargetsAChR

Dehydrovomifoliol Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
 
 
 
C1
V1
C2
V2

calculate

Dehydrovomifoliol Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Dehydrovomifoliol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4988 mL 22.4942 mL 44.9883 mL 89.9766 mL 112.4708 mL
5 mM 0.8998 mL 4.4988 mL 8.9977 mL 17.9953 mL 22.4942 mL
10 mM 0.4499 mL 2.2494 mL 4.4988 mL 8.9977 mL 11.2471 mL
50 mM 0.09 mL 0.4499 mL 0.8998 mL 1.7995 mL 2.2494 mL
100 mM 0.045 mL 0.2249 mL 0.4499 mL 0.8998 mL 1.1247 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.

Organizitions Citing Our Products recently

 
 
 

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
TsingHua University
The University of Michigan
The University of Michigan
Miami University
Miami University
DRURY University
DRURY University
Jilin University
Jilin University
Fudan University
Fudan University
Wuhan University
Wuhan University
Sun Yat-sen University
Sun Yat-sen University
Universite de Paris
Universite de Paris
Deemed University
Deemed University
Auckland University
Auckland University
The University of Tokyo
The University of Tokyo
Korea University
Korea University
Featured Products
New Products
 

References on Dehydrovomifoliol

Chemometrics as a tool of origin determination of Polish monofloral and multifloral honeys.[Pubmed:24641200]

J Agric Food Chem. 2014 Apr 2;62(13):2973-81.

The aim of this study was to evaluate the application of chemometrics studies to determine the botanical origin of Polish monofloral honeys using NMR spectroscopy. Aqueous extracts of six kinds of honeys, namely, heather (Calluna vulgaris L.), buckwheat (Fagopyrum esculentum L), lime (Tilia L), rape (Brassica napus L. var. napus), acacia (Acacia Mill.), and multifloral ones, were analyzed. Multivariate chemometric data analysis was performed using principal component analysis (PCA) and orthogonal partial least-squares discriminant analysis (OPLS-DA). Chemometric analysis supported by pollen analysis revealed the incorrect classification of acacia honeys by the producers. Characteristic motives for each honey were identified, which allowed chemical profiles of tested honeys to be built. Thus, phenylacetic acid and Dehydrovomifoliol (4-hydroxy-4-[3-oxo-1-butenyl]-3,5,5-trimethylcyclohex-2-en-1-one) were proposed to be markers of Polish heather honey. Formic acid and tyrosine were found to be the most characteristic compounds of buckwheat honey, whereas 4-(1-hydroxy-1-methylethyl)cyclohexane-1,3-dienecarboxylic acid was confirmed as a marker of lime honey.

Two new sesquiterpenoids from Solanum lyratum with cytotoxic activities.[Pubmed:19336938]

Chem Pharm Bull (Tokyo). 2009 Apr;57(4):408-10.

Two new sesquiterpenoids, lyratol C (1) and lyratol D (2), together with two known sesquiterpenoids, Dehydrovomifoliol (3) and blumenol A (4), were isolated from the whole plant of Solanum lyratum. Their structures were established by spectroscopic analyses. In vitro, the four compounds showed significant cytotoxic activities against three human cancer cell lines, namely, HONE-1 nasopharyngeal, KB oral epidermoid carcinoma, and HT29 colorectal carcinoma cells, and gave IC(50) values in the range 3.7-8.1 microM.

Anticholinesterase and antioxidant constituents from Gloiopeltis furcata.[Pubmed:20823607]

Chem Pharm Bull (Tokyo). 2010 Sep;58(9):1236-9.

Activity-directed isolation of the ethyl acetate, methylene chloride and n-hexane fractions of Gloiopeltis furcata resulted in the isolation of 18 compounds. Their structures were elucidated as 2-(3-hydroxy-5-oxotetrahydrofuran-3-yl)acetic acid (1), glutaric acid (2), succinic acid (3), nicotinic acid (4), (E)-4-hydroxyhex-2-enoic acid (5), cholesterol (6), 7-hydroxycholesterol (7), uridine (8), glycerol (9), 5-(hydroxymethyl)-2-methoxybenzene-1,3-diol (10), (5E,7E)-9-oxodeca-5,7-dienoic acid (11), (Z)-3-ethylidene-4-methylpyrrolidine-2,5-dione (12), Dehydrovomifoliol (13), loliolide (14), cholesteryl stearate (15), palmitic acid (16), cis-5,8,11,14,17-eicosapentaenoic acid (17) and alpha-linolenic acid (18) on the basis of spectroscopic and chemical evidences. Their anticholinesterase and antioxidant activities were evaluated via inhibitory activities on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) as well as scavenging activities on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical and peroxynitrite (ONOO(-)). All isolated compounds (1-18) exhibited moderate AChE inhibitory activities with IC(50) values ranging from 1.14-12.50 microg/ml, whereas 1, 7, 9, 17, and 18 showed mild BChE inhibitory activities with IC(50) values ranging from 5.57-15.89 microg/ml. Although most of the compounds isolated were lacking the scavenging activity on DPPH radical and ONOO(-), 5 and 10 showed good DPPH radical scavenging activity, and 5, 10, and 16 showed potent ONOO(-) scavenging activity.

Keywords:

Dehydrovomifoliol,39763-33-2,Natural Products, buy Dehydrovomifoliol , Dehydrovomifoliol supplier , purchase Dehydrovomifoliol , Dehydrovomifoliol cost , Dehydrovomifoliol manufacturer , order Dehydrovomifoliol , high purity Dehydrovomifoliol

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: