Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C8H15NO |
| Molecular Weight | 141.2108 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C[C@H]1CCCCN1
InChI
InChIKey=JEIZLWNUBXHADF-MRVPVSSYSA-N
InChI=1S/C8H15NO/c1-7(10)6-8-4-2-3-5-9-8/h8-9H,2-6H2,1H3/t8-/m1/s1
| Molecular Formula | C8H15NO |
| Molecular Weight | 141.2108 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/13402501
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13402501
Pelletierine is an alkaloid found in the root-bark of the pomegranate tree. There is a little information about the pharmacological application of this compound, but one article describes the anthelminthic activity of pelletierine.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Syntheses of (-)-pelletierine and (-)-homopipecolic acid. | 2012-04-07 |
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| Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid. | 2008-07-04 |
|
| The anthelminthic activity of pelletierine and isopelletierine. | 1956-12 |
Patents
| Substance Class |
Chemical
Created
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E58YT08G4A
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