U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C25H27FN2O
Molecular Weight 390.4931
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 5F-CUMYL-PEGACLONE

SMILES

CC(C)(N1C=CC2=C(C3=CC=CC=C3N2CCCCCF)C1=O)C4=CC=CC=C4

InChI

InChIKey=SMRRORRDOWXERZ-UHFFFAOYSA-N
InChI=1S/C25H27FN2O/c1-25(2,19-11-5-3-6-12-19)28-18-15-22-23(24(28)29)20-13-7-8-14-21(20)27(22)17-10-4-9-16-26/h3,5-8,11-15,18H,4,9-10,16-17H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C25H27FN2O
Molecular Weight 390.4931
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:38:43 UTC 2023
Edited
by admin
on Sat Dec 16 16:38:43 UTC 2023
Record UNII
7S7IFQ9PPG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5F-CUMYL-PEGACLONE
Common Name English
SGT-269
Code English
5-FLUORO CUMYL-PEGACLONE
Common Name English
5-(5-FLUOROPENTYL)-2-(2-PHENYLPROPAN-2-YL)-2,5-DIHYDRO-1H-PYRIDO(4,3-B)INDOL-1-ONE
Systematic Name English
5F-SGT-151
Code English
5-FLUORO SGT-151
Common Name English
Code System Code Type Description
FDA UNII
7S7IFQ9PPG
Created by admin on Sat Dec 16 16:38:43 UTC 2023 , Edited by admin on Sat Dec 16 16:38:43 UTC 2023
PRIMARY
SMS_ID
300000024589
Created by admin on Sat Dec 16 16:38:43 UTC 2023 , Edited by admin on Sat Dec 16 16:38:43 UTC 2023
PRIMARY
PUBCHEM
134818048
Created by admin on Sat Dec 16 16:38:43 UTC 2023 , Edited by admin on Sat Dec 16 16:38:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID301336497
Created by admin on Sat Dec 16 16:38:43 UTC 2023 , Edited by admin on Sat Dec 16 16:38:43 UTC 2023
PRIMARY
CAS
2377403-49-9
Created by admin on Sat Dec 16 16:38:43 UTC 2023 , Edited by admin on Sat Dec 16 16:38:43 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
5F-CUMYL-PEGACLONE acts as a potent full agonist of the CB1 receptor.
Related Record Type Details
ACTIVE MOIETY