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Details

Stereochemistry RACEMIC
Molecular Formula C26H34N2O
Molecular Weight 390.561
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AM-1248

SMILES

CN1CCCCC1CN2C=C(C(=O)C34CC5CC(CC(C5)C3)C4)C6=C2C=CC=C6

InChI

InChIKey=JRECAXBHMULNJQ-UHFFFAOYSA-N
InChI=1S/C26H34N2O/c1-27-9-5-4-6-21(27)16-28-17-23(22-7-2-3-8-24(22)28)25(29)26-13-18-10-19(14-26)12-20(11-18)15-26/h2-3,7-8,17-21H,4-6,9-16H2,1H3

HIDE SMILES / InChI

Molecular Formula C26H34N2O
Molecular Weight 390.561
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P21554|||Q5UB37
Gene ID: 1268.0
Gene Symbol: CNR1
Target Organism: Homo sapiens (Human)
11.93 nM [Ki]
Target ID: P34972
Gene ID: 1269.0
Gene Symbol: CNR2
Target Organism: Homo sapiens (Human)
4.804 nM [Ki]
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:40:49 UTC 2023
Edited
by admin
on Sat Dec 16 10:40:49 UTC 2023
Record UNII
5EX9HEF4HK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AM-1248
Common Name English
(1-((1-METHYLPIPERIDIN-2-YL)METHYL)-1H-INDOL-3-YL)(ADAMANTAN-1-YL)METHANONE
Systematic Name English
(1-((1-METHYL-2-PIPERIDINYL)METHYL)-1H-INDOL-3-YL)TRICYCLO(3.3.1.13,7)DEC-1-YLMETHANONE
Systematic Name English
METHANONE, (1-((1-METHYL-2-PIPERIDINYL)METHYL)-1H-INDOL-3-YL)TRICYCLO(3.3.1.13,7)DEC-1-YL-
Systematic Name English
1-((N-METHYL-2-PIPERIDINYL)METHYL)-3-(1-ADAMANTANECARBONYL)-1H-INDOLE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-AM-1248
Created by admin on Sat Dec 16 10:40:49 UTC 2023 , Edited by admin on Sat Dec 16 10:40:49 UTC 2023
Code System Code Type Description
PUBCHEM
10293794
Created by admin on Sat Dec 16 10:40:49 UTC 2023 , Edited by admin on Sat Dec 16 10:40:49 UTC 2023
PRIMARY
EPA CompTox
DTXSID101017326
Created by admin on Sat Dec 16 10:40:49 UTC 2023 , Edited by admin on Sat Dec 16 10:40:49 UTC 2023
PRIMARY
CAS
335160-66-2
Created by admin on Sat Dec 16 10:40:49 UTC 2023 , Edited by admin on Sat Dec 16 10:40:49 UTC 2023
PRIMARY
FDA UNII
5EX9HEF4HK
Created by admin on Sat Dec 16 10:40:49 UTC 2023 , Edited by admin on Sat Dec 16 10:40:49 UTC 2023
PRIMARY
WIKIPEDIA
AM-1248
Created by admin on Sat Dec 16 10:40:49 UTC 2023 , Edited by admin on Sat Dec 16 10:40:49 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY