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Details

Stereochemistry RACEMIC
Molecular Formula C20H22BrN3O
Molecular Weight 400.312
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BRORPHINE

SMILES

CC(N1CCC(CC1)N2C(=O)NC3=C2C=CC=C3)C4=CC=C(Br)C=C4

InChI

InChIKey=CNOFBGYRMCBVLO-UHFFFAOYSA-N
InChI=1S/C20H22BrN3O/c1-14(15-6-8-16(21)9-7-15)23-12-10-17(11-13-23)24-19-5-3-2-4-18(19)22-20(24)25/h2-9,14,17H,10-13H2,1H3,(H,22,25)

HIDE SMILES / InChI

Molecular Formula C20H22BrN3O
Molecular Weight 400.312
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 15:25:23 UTC 2023
Edited
by admin
on Sat Dec 16 15:25:23 UTC 2023
Record UNII
38H2BE6LU4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BRORPHINE
Common Name English
1-(1-(1-(4-BROMOPHENYL)ETHYL)-4-PIPERIDINYL)-1,3-DIHYDRO-2H-BENZIMIDAZOL-2-ONE
Systematic Name English
1-(1-(1-(4-BROMOPHENYL)ETHYL)PIPERIDIN-4-YL)-1,3-DIHYDRO-2H-BENZIMIDAZOL-2-ONE
Systematic Name English
1-(1-(1-(4-BROMOPHENYL)ETHYL)PIPERIDIN-4-YL)-1,3-DIHYDRO-2H-BENZO(D)IMIDAZOL-2-ONE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Brorphine
Created by admin on Sat Dec 16 15:25:23 UTC 2023 , Edited by admin on Sat Dec 16 15:25:23 UTC 2023
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Sat Dec 16 15:25:23 UTC 2023 , Edited by admin on Sat Dec 16 15:25:23 UTC 2023
DEA NO. 9098
Created by admin on Sat Dec 16 15:25:23 UTC 2023 , Edited by admin on Sat Dec 16 15:25:23 UTC 2023
Code System Code Type Description
SMS_ID
300000035019
Created by admin on Sat Dec 16 15:25:23 UTC 2023 , Edited by admin on Sat Dec 16 15:25:23 UTC 2023
PRIMARY
PUBCHEM
145975294
Created by admin on Sat Dec 16 15:25:23 UTC 2023 , Edited by admin on Sat Dec 16 15:25:23 UTC 2023
PRIMARY
FDA UNII
38H2BE6LU4
Created by admin on Sat Dec 16 15:25:23 UTC 2023 , Edited by admin on Sat Dec 16 15:25:23 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY