ArgentinineCAS# 16625-57-3 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 16625-57-3 | SDF | Download SDF |
| PubChem ID | 10085878 | Appearance | Oil |
| Formula | C19H21NO2 | M.Wt | 295.4 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 1-[2-(dimethylamino)ethyl]-4-methoxyphenanthren-3-ol | ||
| SMILES | CN(C)CCC1=CC(=C(C2=C1C=CC3=CC=CC=C32)OC)O | ||
| Standard InChIKey | HCXNUWJYBNHDAE-UHFFFAOYSA-N | ||
| 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. Argentinine exhibits significant activity against Trypanosoma cruzi. |
| Targets | Antifection |
Argentinine Dilution Calculator
Argentinine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 3.3852 mL | 16.9262 mL | 33.8524 mL | 67.7048 mL | 84.631 mL |
| 5 mM | 0.677 mL | 3.3852 mL | 6.7705 mL | 13.541 mL | 16.9262 mL |
| 10 mM | 0.3385 mL | 1.6926 mL | 3.3852 mL | 6.7705 mL | 8.4631 mL |
| 50 mM | 0.0677 mL | 0.3385 mL | 0.677 mL | 1.3541 mL | 1.6926 mL |
| 100 mM | 0.0339 mL | 0.1693 mL | 0.3385 mL | 0.677 mL | 0.8463 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
- Bathophenanthroline
Catalog No.:BCC8840
CAS No.:1662-01-7
- CCT251545
Catalog No.:BCC6487
CAS No.:1661839-45-7
- Ginkgolic acid C15:0
Catalog No.:BCN2483
CAS No.:16611-84-0
- 3,4-O-dimethylcedrusin
Catalog No.:BCN8211
CAS No.:166021-14-3
- Cyclogrifolin
Catalog No.:BCN7547
CAS No.:1660156-04-6
- Z-Thr-OBzl
Catalog No.:BCC2737
CAS No.:16597-50-5
- (-)-Tetramisole
Catalog No.:BCC4670
CAS No.:16595-80-5
- Calystegine A5
Catalog No.:BCN1887
CAS No.:165905-26-0
- Naltrexone
Catalog No.:BCC1783
CAS No.:16590-41-3
- 1-Hydroxy-N-methylacridone
Catalog No.:BCN7551
CAS No.:16584-54-6
- Eperezolid
Catalog No.:BCC5177
CAS No.:165800-04-4
- Linezolid
Catalog No.:BCC2496
CAS No.:165800-03-3
- Taberdivarine H
Catalog No.:BCN6958
CAS No.:1662688-34-7
- 9-O-Feruloyl-5,5'-dimethoxylariciresinol
Catalog No.:BCN1535
CAS No.:166322-14-1
- m-Nitrohydrocinnamic acid
Catalog No.:BCC9048
CAS No.:1664-57-9
- 1H-Pyrido[3,4-b]indole-1,3 4(2H,9H)-trione
Catalog No.:BCN7913
CAS No.:16641-79-5
- p-Nitrohydrocinnamic acid
Catalog No.:BCC9124
CAS No.:16642-79-8
- trans-4-(Trifluoromethyl)cinnamic acid
Catalog No.:BCN1534
CAS No.:16642-92-5
- Metaxalone
Catalog No.:BCC5223
CAS No.:1665-48-1
- Avasimibe
Catalog No.:BCC2274
CAS No.:166518-60-1
- H-Tyr(Bzl)-OH
Catalog No.:BCC3130
CAS No.:16652-64-5
- H-Pro-OBzl.HCl
Catalog No.:BCC3021
CAS No.:16652-71-4
- H-Val-OBzl.TosOH
Catalog No.:BCC3140
CAS No.:16652-76-9
- Eurycarpin A
Catalog No.:BCN4693
CAS No.:166547-20-2
New aporphine alkaloids from guatteria foliosa.[Pubmed:7964785]
J Nat Prod. 1994 Jul;57(7):890-5.
Four new alkaloids were obtained from Guatteria foliosa, namely, the noraporphines (-)-3-methoxyputerine [1] and (+)-norguattevaline [2], the more highly oxidized (+)-3-methoxyguattescidine [3], and the oxoaporphine 3-methoxyoxoputerine [4]. Among several other known alkaloids also found in this same plant, (-)-3-hydroxynornuciferine, (-)-isoguattouregidine, and Argentinine exhibited significant activity against Trypanosoma cruzi.
A new dehydroaporphine alkaloid from Papaver fugax.[Pubmed:15143838]
Nat Prod Res. 2004 Jun;18(3):265-8.
A new dehydroaporphine alkaloid (-)-6a,7-dehydrofloripavidine has been isolated from the aerial parts of Papaver fugax Poir. (Papaveraceae) collected from Erzurum (Eastern Anatolia). (-)-Floripavidine (aporphine) and (-)-mecambrine (proaporphine) were isolated as major alkaloids. Other bases present were (+)-salutaridine (promorphinane) and Argentinine (phenanthrene). The presence of Argentinine has been shown for the first time in the Papaveraceae.
Chromone and phenanthrene alkaloids from Dennettia tripetala.[Pubmed:12499602]
Chem Pharm Bull (Tokyo). 2002 Dec;50(12):1613-5.
Dennettine, a new 2,6-dimethoxychromone and three known phenanthrene alkaloids (uvariopsine, stephenanthrine and Argentinine) in addition to the phenolic and known compound vanillin were isolated from the roots of Dennettia tripetala. Their structures were determined by physical and spectroscopical one dimensional (1D) and 2D-NMR analysis, including heteronuclear multiple bond correlation and nuclear Overhauser enhancement spectroscopy.
