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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H23NO2
Molecular Weight 309.4021
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEVOXADROL

SMILES

C1OC(O[C@@H]1[C@H]2CCCCN2)(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=HGKAMARNFGKMLC-MOPGFXCFSA-N
InChI=1S/C20H23NO2/c1-3-9-16(10-4-1)20(17-11-5-2-6-12-17)22-15-19(23-20)18-13-7-8-14-21-18/h1-6,9-12,18-19,21H,7-8,13-15H2/t18-,19+/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H23NO2
Molecular Weight 309.4021
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Levoxadrol is an active enantiomer of dexoxadrol.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Phencyclidine binds to blood platelets with high affinity and specifically inhibits their activation by adrenaline.
1992-07-01
Interaction of phencyclidine with voltage-dependent potassium channels in cultured rat hippocampal neurons: comparison with block of the NMDA receptor-ionophore complex.
1989-11
Comparison of the effects of the acute administration of dexoxadrol, levoxadrol, MK-801 and phencyclidine on body temperature in the rat.
1989-08
Psychotomimetic sigma-ligands, dexoxadrol and phencyclidine block the same presynaptic potassium channel in rat brain.
1988-09
Coexpression of N-methyl-D-aspartate and phencyclidine receptors in Xenopus oocytes injected with rat brain mRNA.
1988-05
Effects of phencyclidine, SKF 10,047 and related psychotomimetic agents on N-methyl-D-aspartate receptor mediated synaptic responses in rat hippocampal slices.
1987-07
Characterization of specific sigma opiate/phencyclidine (PCP)-binding sites in the human brain.
1983
Stereospecific binding of 3H-phencyclidine in brain membranes.
1982-06-21

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:06:58 GMT 2025
Edited
by admin
on Mon Mar 31 18:06:58 GMT 2025
Record UNII
811X558HU0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOXADROL
INN  
INN  
Official Name English
PIPERIDINE, 2-((4R)-2,2-DIPHENYL-1,3-DIOXOLAN-4-YL)-, (2R)-
Preferred Name English
levoxadrol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
Code System Code Type Description
CAS
4792-18-1
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
PRIMARY
FDA UNII
811X558HU0
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
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MESH
C005840
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
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PUBCHEM
14208378
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
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INN
1503
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
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NCI_THESAURUS
C66010
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
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EPA CompTox
DTXSID801023588
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
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SMS_ID
100000082305
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
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EVMPD
SUB08496MIG
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
PRIMARY
ChEMBL
CHEMBL306386
Created by admin on Mon Mar 31 18:06:58 GMT 2025 , Edited by admin on Mon Mar 31 18:06:58 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY