N-AcetylcytisineCAS# 6018-52-6 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 6018-52-6 | SDF | Download SDF |
| PubChem ID | 927586.0 | Appearance | Powder |
| Formula | C13H16N2O2 | M.Wt | 232.28 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (1R,9S)-11-acetyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one | ||
| SMILES | CC(=O)N1CC2CC(C1)C3=CC=CC(=O)N3C2 | ||
| Standard InChIKey | WCRIKJOQMRFVPX-WDEREUQCSA-N | ||
| Standard InChI | InChI=1S/C13H16N2O2/c1-9(16)14-6-10-5-11(8-14)12-3-2-4-13(17)15(12)7-10/h2-4,10-11H,5-8H2,1H3/t10-,11+/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. |
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| 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. |
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| 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. | ||
N-Acetylcytisine Dilution Calculator
N-Acetylcytisine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.3051 mL | 21.5257 mL | 43.0515 mL | 86.103 mL | 107.6287 mL |
| 5 mM | 0.861 mL | 4.3051 mL | 8.6103 mL | 17.2206 mL | 21.5257 mL |
| 10 mM | 0.4305 mL | 2.1526 mL | 4.3051 mL | 8.6103 mL | 10.7629 mL |
| 50 mM | 0.0861 mL | 0.4305 mL | 0.861 mL | 1.7221 mL | 2.1526 mL |
| 100 mM | 0.0431 mL | 0.2153 mL | 0.4305 mL | 0.861 mL | 1.0763 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. | |||||
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Electron impact mass spectral study of halogenated N-acetyl- and N-propionylcytisines.[Pubmed:21488117]
Rapid Commun Mass Spectrom. 2011 May 15;25(9):1193-7.
(-)-Cytisine and its derivatives, characterised by high affinity to neuronal nicotinic acetylcholine receptors with specificity for the alpha4beta2 subtype, have been shown to be important probes in central nervous system (CNS) research. Electron impact mass spectral (EI-MS) fragmentations of halogenated derivatives of N-Acetylcytisine and N-propionylcytisine have been investigated. Detailed fragmentation pathways have been identified for all significant ions including a few characteristic fragment ions. The principal mass spectral fragmentation routes of iodine and bromine compounds have been determined on the basis of low (EI), high resolution (HRD) and B(2)/E linked scan mass spectra as well as linked scans at constant B/E.
Electron ionization mass spectral study of selected N-amide and N-alkyl derivatives of cytisine.[Pubmed:17370243]
Rapid Commun Mass Spectrom. 2007;21(8):1409-13.
(-)-Cytisine and its derivatives are promising alkaloids in the development of new drugs for the treatment of disorders of the central nervous system (CNS). Electron ionization (EI) mass spectral fragmentations of cytisine (1), N-methylcytisine (2), N-ethylcytisine (3), N-Acetylcytisine (4), N-propionylcytisine (5) and N-benzoylcytisine (6) have been investigated. Detailed fragmentation pathways have been identified for all significant ions, including a few characteristic fragment ions. The principal fragmentation routes of compounds 1-6 have been determined on the basis of EI low-resolution, high-resolution and B2/E linked scans as well as linked scans at constant B/E.
Chemotaxonomy of Portuguese Ulex: quinolizidine alkaloids as taxonomical markers.[Pubmed:16876210]
Phytochemistry. 2006 Sep;67(17):1943-9.
Six species of Portuguese Ulex L. in a total of nineteen populations were studied by GC-EIMS as to their content in quinolizidine alkaloids. Sparteine, beta-isosparteine, jussiaeiine A, N-methylcytisine, cytisine, 5,6-dehydrolupanine, rhombifoline, lupanine, jussiaeiine B, N-formylcytisine, N-Acetylcytisine, anagyrine, jussiaeiine C, jussiaeiine D, pohakuline, baptifoline, and epibaptifoline were detected. Analysis of the chromatograms showed that the chemical profile of all species was mainly composed of N-methylcytisine, cytisine, anagyrine, and jussiaeiines A, B, C and D. Therefore a quantification study of these alkaloids in all the populations studied was done by GC. These data were then submitted to cluster analysis and principal component analysis, which allowed the definition of five chemotypes and the recognition of hybrids. N-methylcytisine, cytisine, and jussiaeiines A, C and D are recognized as markers of this genus in Portugal.
Quinolizidine alkaloid profiles of two taxa of Teline maderensis.[Pubmed:14713148]
Z Naturforsch C J Biosci. 2003 Nov-Dec;58(11-12):776-8.
The alkaloid composition of the aerial parts of two taxa of Teline maderensis was studied by capillary GLC and GLC-MS. N-Methylcytisine was the major alkaloid found in both plants. Contents of cytisine and lupanine were higher in T. maderensis var. paivae while anagyrine content was more pronounced in T. maderensis var. maderensis. The alkaloids dehydrocytisine, N-Acetylcytisine and epibaptifoline appeared only in T. maderensis var. maderensis and N-formylcytisine was identified as a minor constituent in T. maderensis var. paivae, and detected only in trace amounts in the other variety of the plant.
Quinolizidine alkaloids inGenista acanthoclada and its holoparasite,Cuscuta palaestina.[Pubmed:24248948]
J Chem Ecol. 1993 Mar;19(3):441-8.
About 20 quinolizidine alkaloids were identified inGenista acanthoclada by capillary GLC and GLC-MS, such as sparteine, 11,12-dehy-drosparteine, retamine,N-methylcytisine, cytisine, 17-oxosparteine, lupanine,alpha-isolupanine, 5,6-dehydrolupanine, 10-oxosparteine,N-carbomethoxycytisine, 17-oxoretamine,N-formylcytisine,N-Acetylcytisine, and anagyrine. Its phloem-feeding holoparasiteCuscuta palaestina contained alkaloids too, such as sparteine, 11,12-dehydrosparteine, retamine,N-methylcytisine, cytisine, 17-oxosparteine, lupanine,N-carbomethoxycytisine, and anagyrine. Whereas sparteine, retamine, 17-oxosparteine, and cytisine are the main alkaloids ofG. acanthoclada, lupanine, cytisine,N-methylcytisine, and anagyrine are abundant and enriched inC. palaestina. Since these alkaloids figure as antiherbivoral chemical defense compounds inGenista, it is assumed that the parasite can exploit the acquired allelochemicals for its own protection.
