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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
Structure of PELLETIERINE

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

HIDE SMILES / InChI

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

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.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
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

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:21:44 GMT 2025
Edited
by admin
on Mon Mar 31 22:21:44 GMT 2025
Record UNII
E58YT08G4A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(-)-PELLETIERINE
Preferred Name English
PELLETIERINE
MI  
Common Name English
2-PROPANONE, 1-(2R)-2-PIPERIDINYL-
Systematic Name English
PELLETIERINE [MI]
Common Name English
PUNICINE
Common Name English
(R)-(-)-PELLETIERINE
Common Name English
PELLETIERINE, (-)-
Common Name English
Code System Code Type Description
MERCK INDEX
m8451
Created by admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
PRIMARY Merck Index
CAS
2858-66-4
Created by admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID101014415
Created by admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
PRIMARY
ECHA (EC/EINECS)
220-673-6
Created by admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
PRIMARY
PUBCHEM
3034881
Created by admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
PRIMARY
FDA UNII
E58YT08G4A
Created by admin on Mon Mar 31 22:21:44 GMT 2025 , Edited by admin on Mon Mar 31 22:21:44 GMT 2025
PRIMARY