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

Details

Stereochemistry ABSOLUTE
Molecular Formula C24H28FN3O
Molecular Weight 393.497
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-(4-Fluorophenyl)-4-[(6bS,10aR)-2,3,6b,9,10,10a-hexahydro-3-methyl-1H-pyrido[3?,4?:4,5]pyrrolo[1,2,3-de]quinoxalin-8(7H)-yl]-1-butanone

SMILES

CN1CCN2[C@@H]3CCN(CCCC(=O)C4=CC=C(F)C=C4)C[C@@H]3C5=C2C1=CC=C5

InChI

InChIKey=HOIIHACBCFLJET-NHCUHLMSSA-N
InChI=1S/C24H28FN3O/c1-26-14-15-28-21-11-13-27(16-20(21)19-4-2-5-22(26)24(19)28)12-3-6-23(29)17-7-9-18(25)10-8-17/h2,4-5,7-10,20-21H,3,6,11-16H2,1H3/t20-,21-/m1/s1

HIDE SMILES / InChI

Molecular Formula C24H28FN3O
Molecular Weight 393.497
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 20:23:49 GMT 2025
Edited
by admin
on Wed Apr 02 20:23:49 GMT 2025
Record UNII
FR8MDN3MMB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-(4-Fluorophenyl)-4-[(6bS,10aR)-2,3,6b,9,10,10a-hexahydro-3-methyl-1H-pyrido[3?,4?:4,5]pyrrolo[1,2,3-de]quinoxalin-8(7H)-yl]-1-butanone
Systematic Name English
1-(4-fluorophenyl)-4-[(10S,15R)-4-methyl-1,4,12-triazatetracyclo[7.6.1.05,16.010,15]hexadeca-5,7,9(16)-trien-12-yl]butan-1-one
Preferred Name English
1-Butanone, 1-(4-fluorophenyl)-4-[(6bS,10aR)-2,3,6b,9,10,10a-hexahydro-3-methyl-1H-pyrido[3?,4?:4,5]pyrrolo[1,2,3-de]quinoxalin-8(7H)-yl]-
Systematic Name English
Code System Code Type Description
CAS
313368-92-2
Created by admin on Wed Apr 02 20:23:49 GMT 2025 , Edited by admin on Wed Apr 02 20:23:49 GMT 2025
PRIMARY
PUBCHEM
69471377
Created by admin on Wed Apr 02 20:23:49 GMT 2025 , Edited by admin on Wed Apr 02 20:23:49 GMT 2025
PRIMARY
FDA UNII
FR8MDN3MMB
Created by admin on Wed Apr 02 20:23:49 GMT 2025 , Edited by admin on Wed Apr 02 20:23:49 GMT 2025
PRIMARY