Epipterosin L

CAS# 52611-75-3

Epipterosin L

Catalog No. BCN5680----Order now to get a substantial discount!

Product Name & Size Price Stock
Epipterosin L: 5mg $989 In Stock
Epipterosin L: 10mg Please Inquire In Stock
Epipterosin L: 20mg Please Inquire Please Inquire
Epipterosin L: 50mg Please Inquire Please Inquire
Epipterosin L: 100mg Please Inquire Please Inquire
Epipterosin L: 200mg Please Inquire Please Inquire
Epipterosin L: 500mg Please Inquire Please Inquire
Epipterosin L: 1000mg Please Inquire Please Inquire

Quality Control of Epipterosin L

Number of papers citing our products

Chemical structure

Epipterosin L

3D structure

Chemical Properties of Epipterosin L

Cas No. 52611-75-3 SDF Download SDF
PubChem ID 46848746 Appearance Powder
Formula C15H20O4 M.Wt 264.3
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2S,3R)-3-hydroxy-6-(2-hydroxyethyl)-2-(hydroxymethyl)-2,5,7-trimethyl-3H-inden-1-one
SMILES CC1=C(C(=C2C(=C1)C(C(C2=O)(C)CO)O)C)CCO
Standard InChIKey OOAFRMHKOSBPID-HIFRSBDPSA-N
Standard InChI InChI=1S/C15H20O4/c1-8-6-11-12(9(2)10(8)4-5-16)14(19)15(3,7-17)13(11)18/h6,13,16-18H,4-5,7H2,1-3H3/t13-,15+/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 Epipterosin L

The rhizoma of Cibotium barometz (L.) J.Sm.

Protocol of Epipterosin L

Structure Identification
Zhongguo Zhong Yao Za Zhi. 2012 Apr;37(7):946-50.

Sesquiterpenoids of Coniogramme maxima.[Pubmed: 22792795]


METHODS AND RESULTS:
Fifteen compounds were separated by chromatography technique. Their structures were determined by spectral data, including 10 sesquiterpenoids as (3S)-pteroside D (1), Epipterosin L (2), pterosin D (3), onitin (4), pterosin Z (5), onitisin (6), onitisin-glucopyranoside (7), onitin-15-O-beta-D-glucopyranoside (8), (2S,3R)-pterosin-L-2'-O-beta-D-glucopyranoside (9) and (3R)-peterosin D-3-O-beta-D-glucopyranoside (10). The other compounds were uracil (11), 3,4-dihydroxybenzaldehyde (12), 5-hydroxymethyl-2-furancarboxaldehyde (13), beta-sitosterol (14) and daucosterol (15).
CONCLUSIONS:
The above 15 compounds are separated from C. maxima for the first time, including 9 compounds being first separated from genus Coniogramme.

Epipterosin L Dilution Calculator

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

calculate

Epipterosin L Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Epipterosin L

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.7836 mL 18.9179 mL 37.8358 mL 75.6716 mL 94.5895 mL
5 mM 0.7567 mL 3.7836 mL 7.5672 mL 15.1343 mL 18.9179 mL
10 mM 0.3784 mL 1.8918 mL 3.7836 mL 7.5672 mL 9.4589 mL
50 mM 0.0757 mL 0.3784 mL 0.7567 mL 1.5134 mL 1.8918 mL
100 mM 0.0378 mL 0.1892 mL 0.3784 mL 0.7567 mL 0.9459 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 Epipterosin L

[Sesquiterpenoids of Coniogramme maxima].[Pubmed:22792795]

Zhongguo Zhong Yao Za Zhi. 2012 Apr;37(7):946-50.

OBJECTIVE: To study sesquiterpenoids of Coniogramme maxima. METHOD: Chemical constituents were separated by chromatography and their structures were identified according to physicochemical property and spectrum data. RESULT: Fifteen compounds were separated by chromatography technique. Their structures were determined by spectral data, including 10 sesquiterpenoids as (3S)-pteroside D (1), epi-pterosin L (2), pterosin D (3), onitin (4), pterosin Z (5), onitisin (6), onitisin-glucopyranoside (7), onitin-15-O-beta-D-glucopyranoside (8), (2S,3R)-pterosin-L-2'-O-beta-D-glucopyranoside (9) and (3R)-peterosin D-3-O-beta-D-glucopyranoside (10). The other compounds were uracil (11), 3,4-dihydroxybenzaldehyde (12), 5-hydroxymethyl-2-furancarboxaldehyde (13), beta-sitosterol (14) and daucosterol (15). CONCLUSION: The above 15 compounds are separated from C. maxima for the first time, including 9 compounds being first separated from genus Coniogramme.

Keywords:

Epipterosin L,52611-75-3,Natural Products, buy Epipterosin L , Epipterosin L supplier , purchase Epipterosin L , Epipterosin L cost , Epipterosin L manufacturer , order Epipterosin L , high purity Epipterosin L

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: