Rubroside GCAS# 227597-42-4 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 227597-42-4 | SDF | Download SDF |
PubChem ID | 100966788 | Appearance | Red powder |
Formula | C33H38Cl2N2O9 | M.Wt | 677.58 |
Type of Compound | Miscellaneous | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 2-[(2S,4E)-4-[(2E,4E,6E,8E,10Z,12E,14Z,16E)-11-chloro-17-[(2S,3S,5R)-3-chloro-5-methyloxolan-2-yl]-1-hydroxyheptadeca-2,4,6,8,10,12,14,16-octaenylidene]-3,5-dioxo-1-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]pyrrolidin-2-yl]acetamide | ||
SMILES | CC1CC(C(O1)C=CC=CC=CC(=CC=CC=CC=CC=CC(=C2C(=O)C(N(C2=O)C3C(C(C(CO3)O)O)O)CC(=O)N)O)Cl)Cl | ||
Standard InChIKey | HQSONZSAXNUXGI-RBJMWSPMSA-N | ||
Standard InChI | InChI=1S/C33H38Cl2N2O9/c1-20-17-22(35)26(46-20)16-12-8-7-10-14-21(34)13-9-5-3-2-4-6-11-15-24(38)28-29(41)23(18-27(36)40)37(32(28)44)33-31(43)30(42)25(39)19-45-33/h2-16,20,22-23,25-26,30-31,33,38-39,42-43H,17-19H2,1H3,(H2,36,40)/b3-2+,6-4+,8-7-,9-5+,14-10+,15-11+,16-12+,21-13-,28-24+/t20-,22+,23+,25-,26+,30+,31-,33-/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 | 1. Rubroside G may show antifungal activity against Aspergillus fumigatus and Candida albicans. |
Targets | Antifection |
Rubroside G Dilution Calculator
Rubroside G Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.4758 mL | 7.3792 mL | 14.7584 mL | 29.5168 mL | 36.896 mL |
5 mM | 0.2952 mL | 1.4758 mL | 2.9517 mL | 5.9034 mL | 7.3792 mL |
10 mM | 0.1476 mL | 0.7379 mL | 1.4758 mL | 2.9517 mL | 3.6896 mL |
50 mM | 0.0295 mL | 0.1476 mL | 0.2952 mL | 0.5903 mL | 0.7379 mL |
100 mM | 0.0148 mL | 0.0738 mL | 0.1476 mL | 0.2952 mL | 0.369 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
- Xanthobaccin A
Catalog No.:BCN1864
CAS No.:227596-81-8
- Mucrolidin
Catalog No.:BCN5072
CAS No.:227471-20-7
- (3S,7S)-5,6-Dehydro-4''-de-O-methylcentrolobine
Catalog No.:BCN1481
CAS No.:227289-51-2
- AZ 11645373
Catalog No.:BCC7646
CAS No.:227088-94-0
- 9-Deacetyl-9-benzoyl-10-debenzoyl-4beta,20-epoxytaxchinin A
Catalog No.:BCN7676
CAS No.:227011-48-5
- Hyponine E
Catalog No.:BCC8999
CAS No.:226975-99-1
- 3,6-Dimethoxyapigenin
Catalog No.:BCN4830
CAS No.:22697-65-0
- Emapunil
Catalog No.:BCC5521
CAS No.:226954-04-7
- LB42708
Catalog No.:BCC5344
CAS No.:226929-39-1
- 4-Hydroxy-1,10-secocadin-5-ene-1,10-dione
Catalog No.:BCN6661
CAS No.:226904-40-1
- Lansoprazole sodium
Catalog No.:BCC4298
CAS No.:226904-00-3
- Quercetin-3-O-glucuronide
Catalog No.:BCN3149
CAS No.:22688-79-5
- Rubroside H
Catalog No.:BCN1857
CAS No.:227597-43-5
- (±)-HIP-A
Catalog No.:BCC7294
CAS No.:227619-64-9
- (±)-HIP-B
Catalog No.:BCC7295
CAS No.:227619-65-0
- Ethyl 3-(4-methoxyphenyl)propanoate
Catalog No.:BCN4038
CAS No.:22767-72-2
- Z-D-Trp-OH
Catalog No.:BCC2748
CAS No.:2279-15-4
- EPI-001
Catalog No.:BCC6536
CAS No.:227947-06-0
- Ecdysterone 20,22-monoacetonide
Catalog No.:BCN5073
CAS No.:22798-96-5
- Ecdysterone 2,3:20,22-diacetonide
Catalog No.:BCN5074
CAS No.:22798-98-7
- Ac-D-Trp-OH
Catalog No.:BCC3116
CAS No.:2280-01-5
- 1-Hydroxy-2,3,5-trimethoxyxanthone
Catalog No.:BCN6569
CAS No.:22804-49-5
- 1,2,3,7-Tetramethoxyxanthone
Catalog No.:BCN7519
CAS No.:22804-52-0
- 3-(4-Hydroxy-3,5-dimethoxyphenyl)-1,2-propanediol
Catalog No.:BCN1480
CAS No.:22805-15-8
Rubrosides A−H, New Bioactive Tetramic Acid Glycosides from the Marine Sponge Siliquariaspongia japonica1
J. Org. Chem., 1999, 64 (7):2331–9.
Eight new tetramic acid glycosides named rubrosides A-H(rubroside A,rubroside B, rubroside C, rubroside D, rubroside E, rubroside F, Rubroside G, rubroside H) have been isolated from the marine sponge Siliquariaspongia japonica. Their structures were elucidated on the basis of spectral data as tetramic acid glycosides containing polyenes terminating in a 4-chloro-2-methyltetrahydrofuran ring. The absolute stereochemistry of the furan functionality in the two major metabolites, rubrosides D and F, was determined by the NMR method using chiral anisotropic reagents for tetrahydro-2-furoic acid derived by RuO4 oxidation. The absolute stereochemistry of tetramic acid and of the sugar moieties in all rubrosides was deduced by chiral GC analysis of chemical degradation products. The rubrosides induced numerous large intracellular vacuoles in 3Y1 rat fibroblasts at concentrations of 0.5−1.0 μg/mL, and rubrosides A, C, D, and E were cytotoxic against P388 murine leukemia cells with IC50 values of 0.046−0.21 μg/mL. Most rubrosides show antifungal activity against Aspergillus fumigatus and Candida albicans.