Details
Stereochemistry | RACEMIC |
Molecular Formula | C21H25NO3 |
Molecular Weight | 339.4281 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN1CCCC(C1)OC(=O)C(O)(C2=CC=CC=C2)C3=CC=CC=C3
InChI
InChIKey=OJYOTLHNSMYONM-UHFFFAOYSA-N
InChI=1S/C21H25NO3/c1-2-22-15-9-14-19(16-22)25-20(23)21(24,17-10-5-3-6-11-17)18-12-7-4-8-13-18/h3-8,10-13,19,24H,2,9,14-16H2,1H3
Molecular Formula | C21H25NO3 |
Molecular Weight | 339.4281 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14463342 | https://www.ncbi.nlm.nih.gov/pubmed/13616780
Curator's Comment: The most characteristic psychological
aspects of the JB 318 (N-ethyl-3-piperidyl-benzilate) reaction were self-preoccupation, self-imposed stereotypy of behavior, and a reduced awareness of the environment. The post-JB 318 hypomania was a sort
of emotional rebound phenomenon—a defensive reaction akin to counterphobic
mechanisms which consisted of denial and reaction formation.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1907609 Sources: https://www.ncbi.nlm.nih.gov/pubmed/11087580 |
1.46 nM [Ki] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13192610 |
Primary | Unknown Approved UseUnknown |
||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14463342
N-Ethyl-3-piperidyl benzilate (JB-318) 15 mg were administered orally to 10 medical students
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13791503
Curator's Comment: JB-318* is a JB-318 tritiated derivative.
In order to determine whether perehlorie acid completely extracted
JB-318* from tissues, various amounts (1--10 ug) of JB-318* were added to aqueous homogenates of brain and kidney which were then incubated
at 0 degrees for 1 hour.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:30:36 GMT 2023
by
admin
on
Sat Dec 16 08:30:36 GMT 2023
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Record UNII |
02J52696MZ
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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DEA NO. |
7482
Created by
admin on Sat Dec 16 08:30:36 GMT 2023 , Edited by admin on Sat Dec 16 08:30:36 GMT 2023
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N-Ethyl-3-piperidyl benzilate
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02J52696MZ
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62504
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DTXSID20863199
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524174
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3567-12-2
Created by
admin on Sat Dec 16 08:30:36 GMT 2023 , Edited by admin on Sat Dec 16 08:30:36 GMT 2023
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |