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

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

[H][C@]1(COC(O1)(C2=CC=CC=C2)C3=CC=CC=C3)[C@@]4([H])CCCCN4

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
Stereospecific binding of 3H-phencyclidine in brain membranes.
1982 Jun 21
Characterization of specific sigma opiate/phencyclidine (PCP)-binding sites in the human brain.
1983
Psychotomimetic sigma-ligands, dexoxadrol and phencyclidine block the same presynaptic potassium channel in rat brain.
1988 Sep
Comparison of the effects of the acute administration of dexoxadrol, levoxadrol, MK-801 and phencyclidine on body temperature in the rat.
1989 Aug
Interaction of phencyclidine with voltage-dependent potassium channels in cultured rat hippocampal neurons: comparison with block of the NMDA receptor-ionophore complex.
1989 Nov
Phencyclidine binds to blood platelets with high affinity and specifically inhibits their activation by adrenaline.
1992 Jul 1

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:52 GMT 2023
Edited
by admin
on Fri Dec 15 15:43:52 GMT 2023
Record UNII
811X558HU0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEVOXADROL
INN  
INN  
Official Name English
levoxadrol [INN]
Common Name English
PIPERIDINE, 2-((4R)-2,2-DIPHENYL-1,3-DIOXOLAN-4-YL)-, (2R)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
Code System Code Type Description
CAS
4792-18-1
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
PRIMARY
FDA UNII
811X558HU0
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
PRIMARY
MESH
C005840
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
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PUBCHEM
14208378
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
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INN
1503
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
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NCI_THESAURUS
C66010
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
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EPA CompTox
DTXSID801023588
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
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SMS_ID
100000082305
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
PRIMARY
EVMPD
SUB08496MIG
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
PRIMARY
ChEMBL
CHEMBL306386
Created by admin on Fri Dec 15 15:43:52 GMT 2023 , Edited by admin on Fri Dec 15 15:43:52 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY