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Details

Stereochemistry ACHIRAL
Molecular Formula C16H24N2O4
Molecular Weight 308.3728
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NITRACAINE

SMILES

CCN(CC)CC(C)(C)COC(=O)C1=CC=C(C=C1)[N+]([O-])=O

InChI

InChIKey=SPTIETJWCCCJSE-UHFFFAOYSA-N
InChI=1S/C16H24N2O4/c1-5-17(6-2)11-16(3,4)12-22-15(19)13-7-9-14(10-8-13)18(20)21/h7-10H,5-6,11-12H2,1-4H3

HIDE SMILES / InChI
Nitracaine, a new psychoactive substance, a structural analog of the dopamine reuptake inhibitor, dimethocaine; intended for research applications. The physiological and toxicological properties of this compound are still not known.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q01959
Gene ID: 6531.0
Gene Symbol: SLC6A3
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
The syntheses, characterization and in vitro metabolism of nitracaine, methoxypiperamide and mephtetramine.
2014 Jul-Aug
Headspace analysis of new psychoactive substances using a Selective Reagent Ionisation-Time of Flight-Mass Spectrometer.
2014 Mar 1
Identification of in vitro and in vivo human metabolites of the new psychoactive substance nitracaine by liquid chromatography coupled to quadrupole time-of-flight mass spectrometry.
2016 Jul

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Curator's Comment: It was to investigated the in vitro metabolism of nitracaine, using human liver microsome incubations, to evaluate the cytochrome P450 (CYP) enzyme isoforms responsible for the phase-I metabolism and to compare the information from the in vitro experiments with data resulting from an authentic user's urine sample. Accurate mass spectra of metabolites were obtained using liquid chromatography-quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) and were used in the structural identification of metabolites. Two major and three minor phase-I metabolites were identified from the in vitro experiments. The observed phase-I metabolites were formed through N-deethylation, N,N-deethylation, N-hydroxylation, and de-esterification, with CYP2B6 and CYP2C19 being the main enzymes catalyzing their formation.
Unknown
Name Type Language
NITRACAINE
Common Name English
J3.267.868H
Code English
4-NITROBENZOIC ACID 3-(DIETHYLAMINO)-2,2-DIMETHYLPROPYL ESTER
Systematic Name English
P-NITROBENZOIC ACID 2,2-DIMETHYL-3-(DIETHYLAMINO)PROPYL ESTER
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Nitracaine
Created by admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
Code System Code Type Description
FDA UNII
B8ZB08WI9O
Created by admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
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WIKIPEDIA
NITRACAINE
Created by admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
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EPA CompTox
DTXSID301031590
Created by admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
PRIMARY
PUBCHEM
91936940
Created by admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
PRIMARY
CAS
1648893-21-3
Created by admin on Sat Dec 16 11:19:45 GMT 2023 , Edited by admin on Sat Dec 16 11:19:45 GMT 2023
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