IsovallesiachotamineCAS# 34384-71-9 |
- Vallesiachotamine
Catalog No.:BCN3548
CAS No.:5523-37-5
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 34384-71-9 | SDF | Download SDF |
| PubChem ID | 6442678 | Appearance | Powder |
| Formula | C21H22N2O3 | M.Wt | 350.4 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | methyl (2S,12bS)-2-[(Z)-1-oxobut-2-en-2-yl]-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate | ||
| SMILES | CC=C(C=O)C1CC2C3=C(CCN2C=C1C(=O)OC)C4=CC=CC=C4N3 | ||
| Standard InChIKey | NTVLUSJWJRSPSM-AHHXMMTISA-N | ||
| Standard InChI | InChI=1S/C21H22N2O3/c1-3-13(12-24)16-10-19-20-15(14-6-4-5-7-18(14)22-20)8-9-23(19)11-17(16)21(25)26-2/h3-7,11-12,16,19,22H,8-10H2,1-2H3/b13-3+/t16-,19-/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. | ||
| Description | Standard reference |
| In vitro | Vallesiachotamine and isovallesiachotamine from the seeds of Strychnos tricalysioides.[Pubmed: 17396774]Planta Med. 1982 May;45(5):28-30.
Turbinatine, a potential key intermediate in the biosynthesis of corynanthean-type indole alkaloids.[Pubmed: 12880329]J Nat Prod. 2003 Jul;66(7):1017-21.
|
| Structure Identification | Nat Prod Commun. 2012 Jun;7(6):731-4.Indole alkaloids from Vinca major and V. minor growing in Turkey.[Pubmed: 22816294]
|
Isovallesiachotamine Dilution Calculator
Isovallesiachotamine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 2.8539 mL | 14.2694 mL | 28.5388 mL | 57.0776 mL | 71.347 mL |
| 5 mM | 0.5708 mL | 2.8539 mL | 5.7078 mL | 11.4155 mL | 14.2694 mL |
| 10 mM | 0.2854 mL | 1.4269 mL | 2.8539 mL | 5.7078 mL | 7.1347 mL |
| 50 mM | 0.0571 mL | 0.2854 mL | 0.5708 mL | 1.1416 mL | 1.4269 mL |
| 100 mM | 0.0285 mL | 0.1427 mL | 0.2854 mL | 0.5708 mL | 0.7135 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
- Acebutolol HCl
Catalog No.:BCC4322
CAS No.:34381-68-5
- CP-673451
Catalog No.:BCC4981
CAS No.:343787-29-1
- Ginsenoside Ro
Catalog No.:BCN5937
CAS No.:34367-04-9
- Isoapetalic acid
Catalog No.:BCN5276
CAS No.:34366-34-2
- NS 3623
Catalog No.:BCC6190
CAS No.:343630-41-1
- NSC697923
Catalog No.:BCC4000
CAS No.:343351-67-7
- Cirsiliol
Catalog No.:BCN6822
CAS No.:34334-69-5
- Benzyl 2,6-dimethoxybenzoate
Catalog No.:BCN3697
CAS No.:34328-54-6
- OXA (17-33)
Catalog No.:BCC6364
CAS No.:343268-91-7
- TCS PrP Inhibitor 13
Catalog No.:BCC5999
CAS No.:34320-83-7
- Chelerythrine
Catalog No.:BCN5275
CAS No.:34316-15-9
- Boc-Abu-OH.DCHA
Catalog No.:BCC3200
CAS No.:27494-48-0
- N-Demethyl-alpha-obscurine
Catalog No.:BCN7362
CAS No.:34399-44-5
- H-D-Pro-OH
Catalog No.:BCC3023
CAS No.:344-25-2
- Betamipron
Catalog No.:BCC8876
CAS No.:3440-28-6
- Boc-D-Glu-OBzl
Catalog No.:BCC3394
CAS No.:34404-30-3
- H-D-Lys(Z)-OH
Catalog No.:BCC2678
CAS No.:34404-32-5
- Boc-Lys(Z)-OSu
Catalog No.:BCC3418
CAS No.:34404-36-9
- 8-Chloroadenosine
Catalog No.:BCC7935
CAS No.:34408-14-5
- Lathyrol
Catalog No.:BCN4963
CAS No.:34420-19-4
- 2,3-dihydrosciadopitysin
Catalog No.:BCN4034
CAS No.:34421-19-7
- Lyoniside
Catalog No.:BCN5277
CAS No.:34425-25-7
- Ikshusterol
Catalog No.:BCN5278
CAS No.:34427-61-7
- Ligularine
Catalog No.:BCN2090
CAS No.:34429-54-4
Indole alkaloids from Vinca major and V. minor growing in Turkey.[Pubmed:22816294]
Nat Prod Commun. 2012 Jun;7(6):731-4.
A new indole alkaloid, 11-hydroxypolyneuridine, was isolated from Vinca major subsp. major L. and the known indole alkaloids vallesiachotamine and Isovallesiachotamine from Vinca minor L. This is the first report on the alkaloids of both Vinca species growing in Turkey; vallesiachotamine and Isovallesiachotamine were isolated from a Vinca species for the first time. V. minor may be considered as a new source for these two alkaloids due to their occurrence in high amount in the aerial parts of the plant. The alkaloid extracts of the two Vinca species were found to have high lipid peroxidation inhibitory and DPPH radical scavenging activities. Anticholinesterase activity of the extracts was also very strong.
Turbinatine, a potential key intermediate in the biosynthesis of corynanthean-type indole alkaloids.[Pubmed:12880329]
J Nat Prod. 2003 Jul;66(7):1017-21.
Extraction of the leaves of Chimarrhis turbinata has led to the isolation of turbinatine (1), a new corynanthean-type indole alkaloid, besides four known indole alkaloids, strictosidine, 5alpha-carboxystrictosidine, vallesiachotamine, and Isovallesiachotamine. The structural determination of 1 was based on 1D and 2D spectroscopic data. An evaluation of the DNA-damaging activities of the isolates was performed by means of a bioassay using mutant strains of Saccharomyces cerevisiae, which indicated these compounds were weakly active.
Vallesiachotamine and isovallesiachotamine from the seeds of Strychnos tricalysioides.[Pubmed:17396774]
Planta Med. 1982 May;45(5):28-30.
The alkaloids vallesiachotamine and Isovallesiachotamine have been isolated from the seeds of Strychnos tricalysioides and identified on the basis of their spectral characteristics. The potential chemotaxonomic significance of these alkaloids is briefly discussed.
