N-FormylcytisineCAS# 53007-06-0 |
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| Cas No. | 53007-06-0 | SDF | Download SDF |
| PubChem ID | 179619 | Appearance | Powder |
| Formula | C12H14N2O2 | M.Wt | 218.3 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | (1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-diene-11-carbaldehyde | ||
| SMILES | C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O | ||
| Standard InChIKey | PCYQRXYBKKZUSR-VHSXEESVSA-N | ||
| Standard InChI | InChI=1S/C12H14N2O2/c15-8-13-5-9-4-10(7-13)11-2-1-3-12(16)14(11)6-9/h1-3,8-10H,4-7H2/t9-,10+/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-Formylcytisine Dilution Calculator
N-Formylcytisine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 4.5809 mL | 22.9043 mL | 45.8085 mL | 91.617 mL | 114.5213 mL |
| 5 mM | 0.9162 mL | 4.5809 mL | 9.1617 mL | 18.3234 mL | 22.9043 mL |
| 10 mM | 0.4581 mL | 2.2904 mL | 4.5809 mL | 9.1617 mL | 11.4521 mL |
| 50 mM | 0.0916 mL | 0.4581 mL | 0.9162 mL | 1.8323 mL | 2.2904 mL |
| 100 mM | 0.0458 mL | 0.229 mL | 0.4581 mL | 0.9162 mL | 1.1452 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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A new cytisine-type alkaloid from the stem bark of Maackia amurensis.[Pubmed:20835948]
Nat Prod Res. 2010 Oct;24(16):1499-502.
One new cytisine-type alkaloid, [(3-hydroxy-6-pyridinyl)-methyl]-cytisine (1), was isolated from the stem bark of Maackia amurensis, together with five known alkaloids: cytisine, N-Formylcytisine, N-(3-oxobutyl)cytisine, (-)-epibaptifoline and N-methylcytisine. The structure of 1 was elucidated based on spectral methods (IR, CD, 1D and 2D NMR, HR-ESI-MS and EI-MS).
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.
A phytochemical study of the quinolizidine alkaloids from Genista tenera by gas chromatography-mass spectrometry.[Pubmed:16042152]
Phytochem Anal. 2005 Jul-Aug;16(4):264-6.
Gas chromatography coupled with mass spectrometry has been used to analyse the alkaloids present in the aerial parts of Genista tenera. Anagyrine, cytisine, N-Formylcytisine, N-methylcytisine and lupanine were the major compounds, the last two alkaloids being known for their hypoglycaemic activity. Dehydrocytisine, 5,6-dehydrolupanine, rhombifoline, aphylline and thermopsine were the minor alkaloids. The characterisation of the constituents was based on comparison of their Kovats retention indexes and electron impact-mass spectrometric data recorded on-line with those of reference compounds and literature data.
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.
