Ethyl ganoderate JCAS# 1189555-95-0 |
2D Structure
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 1189555-95-0 | SDF | Download SDF |
PubChem ID | 102004717 | Appearance | Powder |
Formula | C32H46O7 | M.Wt | 542.7 |
Type of Compound | Triterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | ethyl (2R)-6-[(10S,13R,14R,15S,17R)-15-hydroxy-4,4,10,13,14-pentamethyl-3,7,11-trioxo-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxoheptanoate | ||
SMILES | CCOC(=O)C(C)CC(=O)CC(C)C1CC(C2(C1(CC(=O)C3=C2C(=O)CC4C3(CCC(=O)C4(C)C)C)C)C)O | ||
Standard InChIKey | MOGCKMACSLYDKK-DLBHLBNGSA-N | ||
Standard InChI | InChI=1S/C32H46O7/c1-9-39-28(38)18(3)13-19(33)12-17(2)20-14-25(37)32(8)27-21(34)15-23-29(4,5)24(36)10-11-30(23,6)26(27)22(35)16-31(20,32)7/h17-18,20,23,25,37H,9-16H2,1-8H3/t17?,18-,20-,23?,25+,30+,31-,32+/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. |
Description | Standard reference |
Structure Identification | Helvetica Chimica Acta.2009 Aug;92(8):1586–1593.Lanostanoids Isolated from Ganoderma lucidum Mycelium Cultured by Submerged Fermentation.[Reference: WebLink]
|
Ethyl ganoderate J Dilution Calculator
Ethyl ganoderate J Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.8426 mL | 9.2132 mL | 18.4264 mL | 36.8528 mL | 46.066 mL |
5 mM | 0.3685 mL | 1.8426 mL | 3.6853 mL | 7.3706 mL | 9.2132 mL |
10 mM | 0.1843 mL | 0.9213 mL | 1.8426 mL | 3.6853 mL | 4.6066 mL |
50 mM | 0.0369 mL | 0.1843 mL | 0.3685 mL | 0.7371 mL | 0.9213 mL |
100 mM | 0.0184 mL | 0.0921 mL | 0.1843 mL | 0.3685 mL | 0.4607 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. |
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
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- (S,S)-2,6-Bis(4-isopropyl-2-oxazolin-2-yl)pyridine
Catalog No.:BCC8402
CAS No.:118949-61-4
- 1,3-Dihydroxy-4-methoxy-10-methylacridin-9(10H)-one
Catalog No.:BCN1605
CAS No.:1189362-86-4
- 5-(3-Hydroxypropyl)-7-methoxybenzofuran
Catalog No.:BCN1606
CAS No.:118930-92-0
- Balanophonin
Catalog No.:BCN6072
CAS No.:118916-57-7
- Denudaquinol
Catalog No.:BCN8035
CAS No.:1189105-40-5
- Lettowienolide
Catalog No.:BCN8038
CAS No.:1189105-39-2
- Fmoc-D-Allo-Ile-OH
Catalog No.:BCC3508
CAS No.:118904-37-3
- Alstoyunine E
Catalog No.:BCN4782
CAS No.:1188932-15-1
- CEP-32496
Catalog No.:BCC1079
CAS No.:1188910-76-0
- KN-93 Phosphate
Catalog No.:BCC5638
CAS No.:1188890-41-6
- ABT 702 dihydrochloride
Catalog No.:BCC5905
CAS No.:1188890-28-9
- NBQX
Catalog No.:BCC6624
CAS No.:118876-58-7
- Mephedrone hydrochloride
Catalog No.:BCC6183
CAS No.:1189726-22-4
- Fumitremorgin C
Catalog No.:BCC7507
CAS No.:118974-02-0
- 1-O-Deacetyl-2alpha-hydroxykhayanolide E
Catalog No.:BCN1604
CAS No.:1189801-51-1
- Viscumneoside III
Catalog No.:BCN7698
CAS No.:118985-27-6
- 8-Amino-2-naphthalenesulfonic acid
Catalog No.:BCC8783
CAS No.:119-28-8
- Methyl salicylate
Catalog No.:BCN5372
CAS No.:119-36-8
- 7-Anilino-4-hydroxy-2-naphthalenesulfonic acid
Catalog No.:BCC8777
CAS No.:119-40-4
- p-Anisoin
Catalog No.:BCC9113
CAS No.:119-52-8
- Benzoin
Catalog No.:BCC8854
CAS No.:119-53-9
- Benzophenone
Catalog No.:BCC8859
CAS No.:119-61-9
- 2-Carboxybenzaldehyde
Catalog No.:BCN2274
CAS No.:119-67-5
- 5-Amino-2-naphthalenesulfonic acid
Catalog No.:BCC8732
CAS No.:119-79-9
Lanostanoids Isolated from Ganoderma lucidum Mycelium Cultured by Submerged Fermentation.
Helvetica Chimica Acta.2009 Aug;92(8):1586–1593.
Three new lanostane triterpene acids, 3-O-acetylganoderic acid B (1), 8β,9α-dihydroganoderic acid C (3), and 3-O-acetylganoderic acid K (4), as well as two new lanostane triterpene acid ethyl esters, ethyl 3-O-acetylganoderate B (2) and Ethyl ganoderate J (5), were isolated and characterized from Ganoderma lucidum mycelia which was cultured by submerged fermentation method. Their structures were elucidated on the basis of spectroscopic methods. In addition, the identification of two known lanostane triterpene acid methyl esters, methyl O-acetyl ganoderate C and methyl 3,7,11,15,23-pentaoxo-lanost-8-en-26-oate were identified by comparison of the NMR data with those reported in the literature.