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Details

Stereochemistry ACHIRAL
Molecular Formula C21H28ClNO
Molecular Weight 345.906
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of UR-144 N-(5-CHLOROPENTYL) ANALOG

SMILES

CC1(C)C(C(=O)C2=CN(CCCCCCl)C3=C2C=CC=C3)C1(C)C

InChI

InChIKey=CKIOITGXSRFWIS-UHFFFAOYSA-N
InChI=1S/C21H28ClNO/c1-20(2)19(21(20,3)4)18(24)16-14-23(13-9-5-8-12-22)17-11-7-6-10-15(16)17/h6-7,10-11,14,19H,5,8-9,12-13H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C21H28ClNO
Molecular Weight 345.906
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

UR-144 N-(5-chloropentyl) analog differs from UR-144 by having a chlorine atom on the terminal carbon of the alkyl group, this compound belongs to the class of synthetic cannabinoid. But this compound is not included in the Schedules to the CDSA (Controlled Drugs and Substances Act) and is not a controlled substance. The biological activities of this compound have not been characterized. This product is intended for forensic and research applications.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
UR-144 in products sold via the Internet: identification of related compounds and characterization of pyrolysis products.
2013-08
Indol-3-ylcycloalkyl ketones: effects of N1 substituted indole side chain variations on CB(2) cannabinoid receptor activity.
2010-01-14
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 23:13:44 GMT 2025
Edited
by admin
on Mon Mar 31 23:13:44 GMT 2025
Record UNII
120SQ2FIK4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHANONE, (1-(5-CHLOROPENTYL)-1H-INDOL-3-YL)(2,2,3,3-TETRAMETHYLCYCLOPROPYL)-
Preferred Name English
UR-144 N-(5-CHLOROPENTYL) ANALOG
Common Name English
Code System Code Type Description
CAS
1445577-42-3
Created by admin on Mon Mar 31 23:13:44 GMT 2025 , Edited by admin on Mon Mar 31 23:13:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID501014174
Created by admin on Mon Mar 31 23:13:44 GMT 2025 , Edited by admin on Mon Mar 31 23:13:44 GMT 2025
PRIMARY
FDA UNII
120SQ2FIK4
Created by admin on Mon Mar 31 23:13:44 GMT 2025 , Edited by admin on Mon Mar 31 23:13:44 GMT 2025
PRIMARY
PUBCHEM
90464183
Created by admin on Mon Mar 31 23:13:44 GMT 2025 , Edited by admin on Mon Mar 31 23:13:44 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY