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
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
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: Q01959 Gene ID: 6531.0 Gene Symbol: SLC6A3 Target Organism: Homo sapiens (Human) Sources: http://bioreagent.bertinpharma.com/pr783/nitracaine |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
PubMed
Title | Date | PubMed |
---|---|---|
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 Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27185541
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 | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
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 | ||
---|---|---|---|---|---|
|
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
|
PRIMARY | |||
|
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
|
PRIMARY | |||
|
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 | |||
|
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 | |||
|
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
|
PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)