ContaminantDB: Ethopropazine hydrochloride

Identification Taxonomy Biological Properties Physical Properties Toxicity Profile Spectra Concentrations Links References XML

Record Information

Version

1.0

Creation Date

2016-05-22 05:06:13 UTC

Update Date

2016-11-09 01:15:46 UTC

Accession Number

CHEM018259

Identification

Common Name

Ethopropazine hydrochloride

Class

Small Molecule

Description

The monohydrochloride salt of profenamine. An antimuscarinic, it is used for the symptomatic treatment of Parkinson's disease.

Contaminant Sources

HMDB Contaminants - Urine
ToxCast & Tox21 Chemicals

Contaminant Type

Not Available

Chemical Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
10-(2-(Diethylamino)propyl)phenothiazine monohydrochloride	ChEBI
Ethopropazine HCL	ChEBI
Ethopropazine hydrochloride	ChEBI
Ethopropazine monohydrochloride	ChEBI
N,N-Diethyl-alpha-methyl-10H-phenothiazine-10-ethylamine hydrochloride	ChEBI
N,N-Diethyl-alpha-methyl-10H-phenothiazine-10-ethylamine monohydrochloride	ChEBI
Profenamine HCL	ChEBI
Profenamine monohydrochloride	ChEBI
Parkin	Kegg
Parsidol	Kegg
N,N-Diethyl-a-methyl-10H-phenothiazine-10-ethylamine hydrochloride	Generator
N,N-Diethyl-α-methyl-10H-phenothiazine-10-ethylamine hydrochloride	Generator
N,N-Diethyl-a-methyl-10H-phenothiazine-10-ethylamine monohydrochloride	Generator
N,N-Diethyl-α-methyl-10H-phenothiazine-10-ethylamine monohydrochloride	Generator
Ethopropazine	MeSH
Lysivane	MeSH
Parsitan	MeSH
Profenamine	MeSH

Chemical Formula

C₁₉H₂₅ClN₂S

Average Molecular Mass

348.933 g/mol

Monoisotopic Mass

348.143 g/mol

CAS Registry Number

1094-08-2

IUPAC Name

diethyl[1-(10H-phenothiazin-10-yl)propan-2-yl]amine hydrochloride

Traditional Name

ethopropazine hydrochloride

SMILES

Cl.CCN(CC)C(C)CN1C2=CC=CC=C2SC2=CC=CC=C12

InChI Identifier

InChI=1S/C19H24N2S.ClH/c1-4-20(5-2)15(3)14-21-16-10-6-8-12-18(16)22-19-13-9-7-11-17(19)21;/h6-13,15H,4-5,14H2,1-3H3;1H

InChI Key

VXPCQISYVPFYRK-UHFFFAOYSA-N

Chemical Taxonomy

Description

belongs to the class of organic compounds known as phenothiazines. These are polycyclic aromatic compounds containing a phenothiazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a para-thiazine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzothiazines

Sub Class

Phenothiazines

Direct Parent

Phenothiazines

Alternative Parents

Substituents

Phenothiazine
Alkyldiarylamine
Diarylthioether
Aryl thioether
Tertiary aliphatic/aromatic amine
Para-thiazine
Benzenoid
Tertiary aliphatic amine
Tertiary amine
Thioether
Azacycle
Hydrocarbon derivative
Amine
Organopnictogen compound
Organic nitrogen compound
Organonitrogen compound
Hydrochloride
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

hydrochloride (CHEBI:31568 )

Biological Properties

Status

Detected and Not Quantified

Origin

Not Available

Cellular Locations

Not Available

Biofluid Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Applications

Not Available

Biological Roles

Not Available

Chemical Roles

Not Available

Physical Properties

State

Not Available

Appearance

Not Available

Experimental Properties

Property	Value
Melting Point	Not Available
Boiling Point	Not Available
Solubility	Not Available

Predicted Properties

Property	Value	Source
Water Solubility	0.0052 g/L	ALOGPS
logP	5.75	ALOGPS
logP	5	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	9.6	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	6.48 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	98 m³·mol⁻¹	ChemAxon
Polarizability	36.24 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	1	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0002-0009000000-428fc01cf04a72556535	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0002-0009000000-428fc01cf04a72556535	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0002-0009000000-428fc01cf04a72556535	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0002-0009000000-79a60dd0eb6af52900f4	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0002-0009000000-79a60dd0eb6af52900f4	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0002-0009000000-79a60dd0eb6af52900f4	Spectrum

Toxicity Profile

Route of Exposure

Not Available

Mechanism of Toxicity

Not Available

Metabolism

Not Available

Toxicity Values

Not Available

Lethal Dose

Not Available

Carcinogenicity (IARC Classification)

Not Available

Uses/Sources

Not Available

Minimum Risk Level

Not Available

Health Effects

Not Available

Symptoms

Not Available

Treatment

Not Available

Concentrations

Not Available

External Links

DrugBank ID

DBSALT000813

HMDB ID

Not Available

FooDB ID

Not Available

Phenol Explorer ID

Not Available

KNApSAcK ID

Not Available

BiGG ID

Not Available

BioCyc ID

Not Available

METLIN ID

Not Available

PDB ID

Not Available

Wikipedia Link

Not Available

Chemspider ID

Not Available

ChEBI ID

31568

PubChem Compound ID

122824

Kegg Compound ID

Not Available

YMDB ID

Not Available

ECMDB ID

Not Available

References

Synthesis Reference

Not Available

MSDS

Not Available

General References

1. https://www.ncbi.nlm.nih.gov/pubmed/?term=12200839

2. https://www.ncbi.nlm.nih.gov/pubmed/?term=13042233

3. https://www.ncbi.nlm.nih.gov/pubmed/?term=29438107

Ethopropazine hydrochloride (CHEM018259)

Structure for CHEM018259: Ethopropazine hydrochloride