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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H15N
Molecular Weight 173.2542
Optical Activity UNSPECIFIED
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
Sigma-2 receptor ligands potentiate conventional chemotherapies and improve survival in models of pancreatic adenocarcinoma.
2009-03-26
New benzomorphan derivatives of MPCB as MOP and KOP receptor ligands.
2007-11
NIH 11082 produces anti-depressant-like activity in the mouse tail-suspension test through a delta-opioid receptor mechanism of action.
2007-07-02
Stereoselective synthesis of benzomorphan derivatives with perpivaloylated galactose as the chiral auxiliary.
2006-04-10
Bremazocine: a kappa-opioid agonist with potent analgesic and other pharmacologic properties.
2005
Kappa-opioid receptor model in a phospholipid bilayer: molecular dynamics simulation.
2002-10-24
8-Carboxamidocyclazocine: a long-acting, novel benzomorphan.
2002-07
Specific kappa opioid receptor agonists.
2001-05-12
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:23:48 GMT 2025
Edited
by admin
on Mon Mar 31 22:23:48 GMT 2025
Record UNII
43RTW43622
Record Status Validated (UNII)
Record Version
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Name Type Language
(-)-6,7-BENZOMORPHAN
Preferred Name English
6,7-BENZOMORPHAN, (-)-
Common Name English
2,6-METHANO-3-BENZAZOCINE, 1,2,3,4,5,6-HEXAHYDRO-, (2R,6S)-
Systematic Name English
Code System Code Type Description
FDA UNII
43RTW43622
Created by admin on Mon Mar 31 22:23:48 GMT 2025 , Edited by admin on Mon Mar 31 22:23:48 GMT 2025
PRIMARY
PUBCHEM
52921323
Created by admin on Mon Mar 31 22:23:48 GMT 2025 , Edited by admin on Mon Mar 31 22:23:48 GMT 2025
PRIMARY
CAS
18715-91-8
Created by admin on Mon Mar 31 22:23:48 GMT 2025 , Edited by admin on Mon Mar 31 22:23:48 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER