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Details

Stereochemistry ACHIRAL
Molecular Formula C23H30N2O2
Molecular Weight 366.4965
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AC-90179

SMILES

COC1=CC=C(CC(=O)N(CC2=CC=C(C)C=C2)C3CCN(C)CC3)C=C1

InChI

InChIKey=AHGNJBSTWQOSAB-UHFFFAOYSA-N
InChI=1S/C23H30N2O2/c1-18-4-6-20(7-5-18)17-25(21-12-14-24(2)15-13-21)23(26)16-19-8-10-22(27-3)11-9-19/h4-11,21H,12-17H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C23H30N2O2
Molecular Weight 366.4965
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacological characterization of AC-90179 [2-(4-methoxyphenyl)-N-(4-methyl-benzyl)-N-(1-methyl-piperidin-4-yl)-acetamide hydrochloride]: a selective serotonin 2A receptor inverse agonist.
2004-09
Characterization of LY344864 as a pharmacological tool to study 5-HT1F receptors: binding affinities, brain penetration and activity in the neurogenic dural inflammation model of migraine.
1997
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:54:48 GMT 2025
Edited
by admin
on Mon Mar 31 21:54:48 GMT 2025
Record UNII
H0EVX3PS4B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-(4-METHOXYPHENYL)-N-(4-METHYLBENZYL)-N-(1-METHYLPIPERIDIN-4-YL)ACETAMIDE
Preferred Name English
AC-90179
Common Name English
BENZENEACETAMIDE, 4-METHOXY-N-((4-METHYLPHENYL)METHYL)-N-(1-METHYL-4-PIPERIDINYL)-
Systematic Name English
Code System Code Type Description
CAS
359878-17-4
Created by admin on Mon Mar 31 21:54:48 GMT 2025 , Edited by admin on Mon Mar 31 21:54:48 GMT 2025
PRIMARY
PUBCHEM
9799308
Created by admin on Mon Mar 31 21:54:48 GMT 2025 , Edited by admin on Mon Mar 31 21:54:48 GMT 2025
PRIMARY
MESH
C492669
Created by admin on Mon Mar 31 21:54:48 GMT 2025 , Edited by admin on Mon Mar 31 21:54:48 GMT 2025
PRIMARY
FDA UNII
H0EVX3PS4B
Created by admin on Mon Mar 31 21:54:48 GMT 2025 , Edited by admin on Mon Mar 31 21:54:48 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY