Details
Stereochemistry | ACHIRAL |
Molecular Formula | C12H17N |
Molecular Weight | 175.2701 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C(N1CCCCC1)C2=CC=CC=C2
InChI
InChIKey=NZVZVGPYTICZBZ-UHFFFAOYSA-N
InChI=1S/C12H17N/c1-3-7-12(8-4-1)11-13-9-5-2-6-10-13/h1,3-4,7-8H,2,5-6,9-11H2
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Design, synthesis, and structure-activity relationships of a series of 3-[2-(1-benzylpiperidin-4-yl)ethylamino]pyridazine derivatives as acetylcholinesterase inhibitors. | 2001 Aug 16 |
|
[Application of neural networks using the volume learning algorithm for the study of structure-activity relationship in chemical compounds]. | 2001 Jul-Aug |
|
NR2B selective NMDA receptor antagonists. | 2002 |
|
Syntheses and reactivities of disubstituted and trisubstituted fluorous pyridines with high fluorous phase affinities: solid state, liquid crystal, and ionic liquid-phase properties. | 2002 Oct 4 |
|
Quaternary salts of E2020 analogues as acetylcholinesterase inhibitors for the reversal of neuromuscular block. | 2002 Sep 16 |
|
Aromatic amino-acid residues at the active and peripheral anionic sites control the binding of E2020 (Aricept) to cholinesterases. | 2003 Nov |
|
Human acetylcholinesterase inhibitors: electronic-topological and neural network approaches to the structure-activity relationships study. | 2005 May |
|
Zwitterionic (4-benzyl-piperidinium-1-yl-meth-yl)phospho-nate. | 2007 Dec 6 |
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID80183289
Created by
admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
|
PRIMARY | |||
|
220-809-4
Created by
admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
|
PRIMARY | |||
|
7HZE16210B
Created by
admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
|
PRIMARY | |||
|
2905-56-8
Created by
admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
|
PRIMARY | |||
|
76190
Created by
admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD