Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C8H15NO.ClH |
| Molecular Weight | 177.672 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(=O)C[C@H]1CCCCN1
InChI
InChIKey=FMOKUKPRJSMPOI-DDWIOCJRSA-N
InChI=1S/C8H15NO.ClH/c1-7(10)6-8-4-2-3-5-9-8;/h8-9H,2-6H2,1H3;1H/t8-;/m1./s1
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 |
|
| 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
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6152-82-5
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111159
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DTXSID10977077
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228-167-7
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90YI67H3XJ
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SUBSTANCE RECORD