Home >> Research Area >>Natural Products>>Diterpenoids>> 14-Deoxy-12-hydroxyandrographolide

14-Deoxy-12-hydroxyandrographolide

CAS# 219721-33-2

14-Deoxy-12-hydroxyandrographolide

2D Structure

Catalog No. BCN4673----Order now to get a substantial discount!

Product Name & Size Price Stock
14-Deoxy-12-hydroxyandrographolide: 5mg $799 In Stock
14-Deoxy-12-hydroxyandrographolide: 10mg Please Inquire In Stock
14-Deoxy-12-hydroxyandrographolide: 20mg Please Inquire Please Inquire
14-Deoxy-12-hydroxyandrographolide: 50mg Please Inquire Please Inquire
14-Deoxy-12-hydroxyandrographolide: 100mg Please Inquire Please Inquire
14-Deoxy-12-hydroxyandrographolide: 200mg Please Inquire Please Inquire
14-Deoxy-12-hydroxyandrographolide: 500mg Please Inquire Please Inquire
14-Deoxy-12-hydroxyandrographolide: 1000mg Please Inquire Please Inquire

Quality Control of 14-Deoxy-12-hydroxyandrographolide

3D structure

Package In Stock

14-Deoxy-12-hydroxyandrographolide

Number of papers citing our products

Chemical Properties of 14-Deoxy-12-hydroxyandrographolide

Cas No. 219721-33-2 SDF Download SDF
PubChem ID 38350572 Appearance Powder
Formula C20H30O5 M.Wt 350.45
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 4-[(1S)-2-[(1R,4aS,5R,6R,8aS)-6-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]-2H-furan-5-one
SMILES CC12CCC(C(C1CCC(=C)C2CC(C3=CCOC3=O)O)(C)CO)O
Standard InChIKey KHQNSSJNIXVKMK-XWIHJEQYSA-N
Standard InChI InChI=1S/C20H30O5/c1-12-4-5-16-19(2,8-6-17(23)20(16,3)11-21)14(12)10-15(22)13-7-9-25-18(13)24/h7,14-17,21-23H,1,4-6,8-11H2,2-3H3/t14-,15+,16+,17-,19+,20+/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 14-Deoxy-12-hydroxyandrographolide

The herbs of Andrographis paniculata (Burm. f.) Nees

Biological Activity of 14-Deoxy-12-hydroxyandrographolide

TargetsAntifection

14-Deoxy-12-hydroxyandrographolide Dilution Calculator

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

calculate

14-Deoxy-12-hydroxyandrographolide Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of 14-Deoxy-12-hydroxyandrographolide

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.8535 mL 14.2674 mL 28.5347 mL 57.0695 mL 71.3369 mL
5 mM 0.5707 mL 2.8535 mL 5.7069 mL 11.4139 mL 14.2674 mL
10 mM 0.2853 mL 1.4267 mL 2.8535 mL 5.7069 mL 7.1337 mL
50 mM 0.0571 mL 0.2853 mL 0.5707 mL 1.1414 mL 1.4267 mL
100 mM 0.0285 mL 0.1427 mL 0.2853 mL 0.5707 mL 0.7134 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 14-Deoxy-12-hydroxyandrographolide

A new diterpene from the leaves of Andrographis paniculata Nees.[Pubmed:22574448]

Nat Prod Commun. 2012 Apr;7(4):485-6.

Phytochemical investigation of the methanolic extract of the leaves of Andrographis paniculata Nees yielded a minor, new diterpene, 21-nor-3,19-isopropylidine-14-deoxy-ent-labda-8(17),13-dien-16,15-olide (1), together with five known labdane type diterpenes, andrographolide 3, 14-deoxyandrographolide 4, 14-Deoxy-12-hydroxyandrographolide 5, 14-deoxy-11,12-dihydroandrographolide 6, neoandrographolide 7, and two acids, cinnamic acid 8, and ferulic acid 9. The chemical structures were established by spectroscopic analyses, including 1D- and 2D-NMR spectroscopic experiments, and on the basis of HR-ESI MS analyses. The methanolic extract of the leaves exhibited moderate antibacterial and antifungal activities at a dose of 200 microg/mL in comparison with the reference standards.

Cardiovascular activity of labdane diterpenes from Andrographis paniculata in isolated rat hearts.[Pubmed:22536026]

J Biomed Biotechnol. 2012;2012:876458.

The dichloromethane (DCM) extract of Andrographis paniculata Nees was tested for cardiovascular activity. The extract significantly reduced coronary perfusion pressure by up to 24.5 +/- 3.0 mm Hg at a 3 mg dose and also reduced heart rate by up to 49.5 +/- 11.4 beats/minute at this dose. Five labdane diterpenes, 14-Deoxy-12-hydroxyandrographolide (1), 14-deoxy-11,12-didehydroandrographolide (2), 14-deoxyandrographolide (3), andrographolide (4), and neoandrographolide (5), were isolated from the aerial parts of this medicinal plant. Bioassay-guided studies using animal model showed that compounds, (2) and (3) were responsible for the coronary vasodilatation. This study also showed that andrographolide (4), the major labdane diterpene in this plant, has minimal effects on the heart.

Keywords:

14-Deoxy-12-hydroxyandrographolide,219721-33-2,Natural Products, buy 14-Deoxy-12-hydroxyandrographolide , 14-Deoxy-12-hydroxyandrographolide supplier , purchase 14-Deoxy-12-hydroxyandrographolide , 14-Deoxy-12-hydroxyandrographolide cost , 14-Deoxy-12-hydroxyandrographolide manufacturer , order 14-Deoxy-12-hydroxyandrographolide , high purity 14-Deoxy-12-hydroxyandrographolide

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: