
CAS 137038-57-4
:(-)-Solenopsin A
Description:
(-)-Solenopsin A is a naturally occurring alkaloid primarily derived from the venom of certain fire ants, particularly those in the Solenopsis genus. This compound is characterized by its complex bicyclic structure, which includes a pyridine ring and a long aliphatic side chain. It exhibits a range of biological activities, including antimicrobial and insecticidal properties, making it of interest in both pharmacological and ecological studies. The stereochemistry of (-)-Solenopsin A is significant, as its specific configuration contributes to its biological effects. Additionally, it has been studied for its potential applications in pest control and as a model for developing new therapeutic agents. The compound is typically analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Overall, (-)-Solenopsin A represents a fascinating example of how natural products can influence both biological systems and potential applications in various fields.
Formula:C17H35N
InChI:InChI=1S/C17H35N/c1-3-4-5-6-7-8-9-10-11-14-17-15-12-13-16(2)18-17/h16-18H,3-15H2,1-2H3/t16-,17-/m1/s1
InChI key:InChIKey=AYJGABFBAYKWDX-IAGOWNOFSA-N
SMILES:C(CCCCCCCCCC)[C@H]1N[C@H](C)CCC1
Synonyms:- (-)-Solenopsin A
- Piperidine, 2-methyl-6-undecyl-, (2R,6R)-
- (2R,6R)-2-Methyl-6-undecylpiperidine
- (-)-Solenopsine A
- Piperidine, 2-methyl-6-undecyl-, (2R-trans)-
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Found 3 products.
Solenopsin
CAS:<p>Solenopsin is used as a research tool in the study of ion channels. It has been shown to inhibit potassium channels and activate calcium channels, which are important for nerve transmission. Solenopsin binds to cell-surface receptors, such as the nicotinic acetylcholine receptor, which causes an influx of calcium ions into cells.</p>Formula:C17H35NPurity:Min. 95%Molecular weight:253.5 g/molSolenopsin
CAS:<p>Solenopsin is an ATP-competitive inhibitor of AKT(IC50 : 10 μM) .</p>Formula:C17H35NPurity:98%Color and Shape:SolidMolecular weight:253.47


