Home >> Research Area >>Natural Products>>Triterpenoids>> Notoginsenoside FP2

Notoginsenoside FP2

CAS# 1004988-75-3

Notoginsenoside FP2

Catalog No. BCN8692----Order now to get a substantial discount!

Product Name & Size Price Stock
Notoginsenoside FP2: 5mg Please Inquire In Stock
Notoginsenoside FP2: 10mg Please Inquire In Stock
Notoginsenoside FP2: 20mg Please Inquire Please Inquire
Notoginsenoside FP2: 50mg Please Inquire Please Inquire
Notoginsenoside FP2: 100mg Please Inquire Please Inquire
Notoginsenoside FP2: 200mg Please Inquire Please Inquire
Notoginsenoside FP2: 500mg Please Inquire Please Inquire
Notoginsenoside FP2: 1000mg Please Inquire Please Inquire

Quality Control of Notoginsenoside FP2

Number of papers citing our products

Chemical structure

Notoginsenoside FP2

3D structure

Chemical Properties of Notoginsenoside FP2

Cas No. 1004988-75-3 SDF Download SDF
PubChem ID 101838198 Appearance Powder
Formula C58H98O26 M.Wt 1211.4
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2R,3S,4S,5R,6S)-2-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2S)-2-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-3-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-en-2-yl]oxyoxane-3,4,5-triol
SMILES CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)OC8C(C(C(C(O8)COC9C(C(C(O9)CO)O)O)O)O)O)C
Standard InChIKey FPMOROOPDIFSMA-HOJZLLFESA-N
Standard InChI InChI=1S/C58H98O26/c1-24(2)10-9-14-58(8,84-51-46(74)41(69)40(68)31(80-51)23-76-49-45(73)39(67)30(21-61)77-49)25-11-16-57(7)35(25)26(62)18-33-55(5)15-13-34(54(3,4)32(55)12-17-56(33,57)6)81-52-47(42(70)37(65)28(19-59)78-52)83-53-48(43(71)38(66)29(20-60)79-53)82-50-44(72)36(64)27(63)22-75-50/h10,25-53,59-74H,9,11-23H2,1-8H3/t25-,26+,27+,28+,29+,30-,31+,32-,33+,34-,35-,36-,37+,38+,39-,40+,41-,42-,43-,44+,45+,46+,47+,48+,49+,50-,51-,52-,53-,55-,56+,57+,58-/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 Notoginsenoside FP2

The roots of Panax notoginseng

Protocol of Notoginsenoside FP2

Structure Identification
Helvetica Chimica Acta, 2008,91(1):60-66.

Two New Dammarane‐Type Bisdesmosides from the Fruit Pedicels of Panax notoginseng.[Reference: WebLink]

Two new dammarane-type triterpenoidal saponins, notoginsenoside FP1 (1) and Notoginsenoside FP2 (2), were isolated from the fruit pedicels of Panax notoginseng, along with 22 known compounds.
METHODS AND RESULTS:
Their structures were elucidated on the basis of spectroscopic evidences and chemical methods. The known compounds were identified as ginsenosides Rg1 (3), Re (4), Rb3 (5), Rc (6), Rd (7), Rb2 (8), Rb1 (9), F2 (10), and F1 (11); as notoginsenosides R1 (12), Fa (13), and Fc (14); as vina-ginsenoside R7 (15); as gypenosides IX (16), XVII (17), and XIII (18), and as chikusetsusaponin-L5 (19), quercetin 3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside (20), kaempferol 3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside (21), benzyl-β-primeveroside (22), (S)-tryptophan (23), and icariside B6 (24). Compounds 15, 19 and 22–24 are reported for the first time from the title plant.

Notoginsenoside FP2 Dilution Calculator

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

calculate

Notoginsenoside FP2 Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Notoginsenoside FP2

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 0.8255 mL 4.1275 mL 8.2549 mL 16.5098 mL 20.6373 mL
5 mM 0.1651 mL 0.8255 mL 1.651 mL 3.302 mL 4.1275 mL
10 mM 0.0825 mL 0.4127 mL 0.8255 mL 1.651 mL 2.0637 mL
50 mM 0.0165 mL 0.0825 mL 0.1651 mL 0.3302 mL 0.4127 mL
100 mM 0.0083 mL 0.0413 mL 0.0825 mL 0.1651 mL 0.2064 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 Notoginsenoside FP2

Two New Dammarane‐Type Bisdesmosides from the Fruit Pedicels of Panax notoginseng.

Helvetica Chimica Acta, 2008,91(1):60-66.

Two new dammarane-type triterpenoidal saponins, notoginsenoside FP1 (1) and Notoginsenoside FP2 (2), were isolated from the fruit pedicels of Panax notoginseng, along with 22 known compounds. Their structures were elucidated on the basis of spectroscopic evidences and chemical methods. The known compounds were identified as ginsenosides Rg1 (3), Re (4), Rb3 (5), Rc (6), Rd (7), Rb2 (8), Rb1 (9), F2 (10), and F1 (11); as notoginsenosides R1 (12), Fa (13), and Fc (14); as vina-ginsenoside R7 (15); as gypenosides IX (16), XVII (17), and XIII (18), and as chikusetsusaponin-L5 (19), quercetin 3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside (20), kaempferol 3-O-β-D-glucopyranosyl-(1→2)-β-D-galactopyranoside (21), benzyl-β-primeveroside (22), (S)-tryptophan (23), and icariside B6 (24). Compounds 15, 19 and 22–24 are reported for the first time from the title plant.

Description

Notoginsenoside FP2, a dammarane-Type Bisdesmoside isolated from the Fruit Pedicels of Panax notoginseng, has potential to treat cardiovascular disease.

Keywords:

Notoginsenoside FP2,1004988-75-3,Natural Products, buy Notoginsenoside FP2 , Notoginsenoside FP2 supplier , purchase Notoginsenoside FP2 , Notoginsenoside FP2 cost , Notoginsenoside FP2 manufacturer , order Notoginsenoside FP2 , high purity Notoginsenoside FP2

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: