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Details

Stereochemistry RACEMIC
Molecular Formula C12H15N
Molecular Weight 173.2542
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 6,7-BENZOMORPHAN

SMILES

C1C[C@H]2C[C@H](CC3=CC=CC=C23)N1

InChI

InChIKey=NSLKFRGZLUIUKO-QWRGUYRKSA-N
InChI=1S/C12H15N/c1-2-4-12-9(3-1)7-11-8-10(12)5-6-13-11/h1-4,10-11,13H,5-8H2/t10-,11-/m0/s1

HIDE SMILES / InChI

Molecular Formula C12H15N
Molecular Weight 173.2542
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
8-Carboxamidocyclazocine: a long-acting, novel benzomorphan.
2002 Jul
Kappa-opioid receptor model in a phospholipid bilayer: molecular dynamics simulation.
2002 Oct 24
Bremazocine: a kappa-opioid agonist with potent analgesic and other pharmacologic properties.
2005 Summer
Stereoselective synthesis of benzomorphan derivatives with perpivaloylated galactose as the chiral auxiliary.
2006 Apr 10
NIH 11082 produces anti-depressant-like activity in the mouse tail-suspension test through a delta-opioid receptor mechanism of action.
2007 Jul 2
New benzomorphan derivatives of MPCB as MOP and KOP receptor ligands.
2007 Nov
Sigma-2 receptor ligands potentiate conventional chemotherapies and improve survival in models of pancreatic adenocarcinoma.
2009 Mar 26
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:57:09 GMT 2023
Edited
by admin
on Sat Dec 16 08:57:09 GMT 2023
Record UNII
A8J3S2MS1D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
6,7-BENZOMORPHAN
MI  
Common Name English
(±)-6,7-BENZOMORPHAN
Common Name English
1,2,3,4,5,6-HEXAHYDRO-2,6-METHANO-3-BENZAZOCINE
Systematic Name English
6,7-BENZOMORPHAN [MI]
Common Name English
2-AZABENZO(F)BICYCLO(3.3.1)NONANE
Systematic Name English
(±)-BENZOMORPHAN
Common Name English
2,6-METHANO-3-BENZAZOCINE, 1,2,3,4,5,6-HEXAHYDRO-
Systematic Name English
Code System Code Type Description
FDA UNII
A8J3S2MS1D
Created by admin on Sat Dec 16 08:57:09 GMT 2023 , Edited by admin on Sat Dec 16 08:57:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID80982138
Created by admin on Sat Dec 16 08:57:09 GMT 2023 , Edited by admin on Sat Dec 16 08:57:09 GMT 2023
PRIMARY
MERCK INDEX
m2367
Created by admin on Sat Dec 16 08:57:09 GMT 2023 , Edited by admin on Sat Dec 16 08:57:09 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Benzomorphan
Created by admin on Sat Dec 16 08:57:09 GMT 2023 , Edited by admin on Sat Dec 16 08:57:09 GMT 2023
PRIMARY
CAS
575-19-9
Created by admin on Sat Dec 16 08:57:09 GMT 2023 , Edited by admin on Sat Dec 16 08:57:09 GMT 2023
PRIMARY
PUBCHEM
52921323
Created by admin on Sat Dec 16 08:57:09 GMT 2023 , Edited by admin on Sat Dec 16 08:57:09 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE