Valechlorine

CAS# 51771-49-4

Valechlorine

Catalog No. BCN2763----Order now to get a substantial discount!

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

Quality Control of Valechlorine

Number of papers citing our products

Chemical structure

Valechlorine

3D structure

Chemical Properties of Valechlorine

Cas No. 51771-49-4 SDF Download SDF
PubChem ID 71522011 Appearance Oil
Formula C22H31ClO8 M.Wt 458.93
Type of Compound Iridoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(1S,6S,7S,7aS)-4-(acetyloxymethyl)-7-(chloromethyl)-7-hydroxy-1-(3-methylbutanoyloxy)-6,7a-dihydro-1H-cyclopenta[c]pyran-6-yl] 3-methylbutanoate
SMILES CC(C)CC(=O)OC1C=C2C(C1(CCl)O)C(OC=C2COC(=O)C)OC(=O)CC(C)C
Standard InChIKey HHVCVAIASNFMBE-KVJIRVJXSA-N
Standard InChI InChI=1S/C22H31ClO8/c1-12(2)6-18(25)30-17-8-16-15(9-28-14(5)24)10-29-21(20(16)22(17,27)11-23)31-19(26)7-13(3)4/h8,10,12-13,17,20-21,27H,6-7,9,11H2,1-5H3/t17-,20+,21-,22+/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 Valechlorine

The herbs of Valeriana officinalis L.

Biological Activity of Valechlorine

Description1. Valeranone shows antileishmanial and cytotoxic activity.
TargetsAntifection

Valechlorine Dilution Calculator

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

calculate

Valechlorine Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Valechlorine

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.179 mL 10.8949 mL 21.7898 mL 43.5796 mL 54.4745 mL
5 mM 0.4358 mL 2.179 mL 4.358 mL 8.7159 mL 10.8949 mL
10 mM 0.2179 mL 1.0895 mL 2.179 mL 4.358 mL 5.4475 mL
50 mM 0.0436 mL 0.2179 mL 0.4358 mL 0.8716 mL 1.0895 mL
100 mM 0.0218 mL 0.1089 mL 0.2179 mL 0.4358 mL 0.5447 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 Valechlorine

Antileishmanial and cytotoxic compounds from Valeriana wallichii and identification of a novel nepetolactone derivative.

Molecules, 2015, 20(4):5740-53.

The chloroform extract of Valeriana wallichii (V. wallichii) rhizomes was investigated to elucidate the structures responsible for reported antileishmanial activity. Besides bornyl caffeate (1, already been reported by us previously), bioassay-guided fractionation resulted in two additional cinnamic acid derivatives 2-3 with moderate leishmanicidal activity. The structure of a novel nepetolactone derivative 4 having a cinnamic acid moiety was elucidated by means of spectral analysis. To the best of our knowledge villoside aglycone (5) was isolated from this plant for the first time. The bioassay-guided fractionation yielded two new (compounds 6-7) and two known valtrates (compounds 8-9) with leishmanicidal potential against Leishmania major (L. major) promastigotes. In addition, β-bisabolol (10), α-kessyl alcohol (11), valeranone (12), bornyl isovalerate (13) and linarin-2-O-methylbutyrate (14) were identified. This is the first report on the isolation of 4'-demethylpodophyllotoxin (15), podophyllotoxin (16) and pinoresinol (17) in V. wallichii. In total thirteen known and four new compounds were identified from the extract and their cytotoxic and antileishmanial properties were evaluated.

Description

Valechlorine, a autophagy enhancer, breaks down lipid droplets. Valechlorine reduces oleic acid (OA)-induced lipid accumulation in an Atg5-dependent manner.

Keywords:

Valechlorine,51771-49-4,Natural Products, buy Valechlorine , Valechlorine supplier , purchase Valechlorine , Valechlorine cost , Valechlorine manufacturer , order Valechlorine , high purity Valechlorine

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: