P-AMINOPHENOL HYDROCHLORIDE - Inxight Drugs

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P-AMINOPHENOL HYDROCHLORIDE IWL2N22RFY Possibly Marketed Outside US Source: SALON CODE Glam Hair Color Glam Brown by Daolcosmetic Co.,ltd Source URL: https://www.drugbank.ca/drugs/DB14144 First approved in 2013 Source: BEAUTIFUL WOMANS HAIR LOVES COLORFUL BUBBLES HAIR DYE 5N NATURAL BROWN by Modlina Cosmetics Co., Ltd Source URL: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2b4e78e6-19cb-4d12-b069-52607d883334 P-AMINOPHENOL HYDROCHLORIDE IWL2N22RFY Possibly Marketed Outside US Source: SALON CODE Glam Hair Color Glam Brown by Daolcosmetic Co.,ltd Source URL: https://www.drugbank.ca/drugs/DB14144 First approved in 2013 Source: BEAUTIFUL WOMANS HAIR LOVES COLORFUL BUBBLES HAIR DYE 5N NATURAL BROWN by Modlina Cosmetics Co., Ltd Source URL: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=2b4e78e6-19cb-4d12-b069-52607d883334

Details

Stereochemistry ACHIRAL
Molecular Formula C6H7NO.ClH
Molecular Weight 145.587
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0
SHOW SMILES / InChI Structure of P-AMINOPHENOL HYDROCHLORIDE SHOW STEREO... HIDE STEREO...
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SMILES

Cl.NC1=CC=C(O)C=C1

InChI

InChIKey=RVGOBWDGAVAVPJ-UHFFFAOYSA-N InChI=1S/C6H7NO.ClH/c7-5-1-3-6(8)4-2-5;/h1-4,8H,7H2;1H HIDE SMILES / InChI
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C6H7NO
Molecular Weight 109.1259
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/18811827 | https://www.ncbi.nlm.nih.gov/pubmed/1713494 | (1994) Conjugation-Dependent Carcinogenicity and Toxicity of Foreign Compounds, page 189, retrieved from: https://books.google.ru/books?id=rzJRFA-GePgC | https://www.ncbi.nlm.nih.gov/pubmed/23393911 | https://www.ewg.org/skindeep/ingredient/704384/P-AMINOPHENOL/#.Wm3JS65l-pp

p-Aminophenol is an active metabolite of paracetamol. p-Aminophenol is conjugated with arachidonic acid by fatty acid amide hydrolase to form AM404. AM404 exerts effect through cannabinoid receptors. p- Aminophenol is a nephrotoxic metabolite of paracetamol and phenacetin. It causes acute renal proximal tubular necrosis after administration to rats. p-Aminophenol may cause skin sensitization, dermatitis. p-Aminophenol is a synthetic dye used in hair coloring.

Approval Year

2013589 Targets

Targets

Primary TargetPharmacologyConditionPotency
Arylamine N-acetyltransferase 14Target ID: CHEMBL5101Sources: https://www.ncbi.nlm.nih.gov/pubmed/10692486 Substrate661
Arylamine N-acetyltransferase 14Target ID: CHEMBL5101Sources: https://www.ncbi.nlm.nih.gov/pubmed/10692486 Substrate661
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Unknown2596
PubMed

PubMed

TitleDatePubMed
A new dynamic electrochemical transduction mechanism for interdigitated array microelectrodes. 2004-12 15570369
Degradation of 4-nitrophenol by the lignin-degrading basidiomycete Phanerochaete chrysosporium. 2004-12 15448939
Reactions of arylamine and aminophenol derivatives, and riboflavin with organic radicals. 2004-11 15621695
Toxic effects of aminophenols on aquatic life using the zebrafish embryo test and the comet assay. 2004-10 15389326
Microchip capillary electrophoresis with a boron-doped diamond electrochemical detector for analysis of aromatic amines. 2004-09 15349943
Pharmacophore based synthesis of 3-chloroquinoxaline-2-carboxamides as serotonin3 (5-HT3) receptor antagonist. 2004-09 15340227
Poly(dimethylsiloxane) microchip capillary electrophoresis with electrochemical detection for rapid measurement of acetaminophen and its hydrolysate. 2004-08 15221194
The measurement of alkaline phosphatase at nanomolar concentration within 70 s using a disposable microelectrochemical transistor. 2004-08 15219247
The demonstration of an enhanced microelectrochemical transistor for measurements in neutral solution at low analyte concentration. 2004-08 15219241
Spectrophotometric determination of paracetamol with microwave assisted alkaline hydrolysis. 2004-07 15248961
Scanning electrochemical microscopy of quinoprotein glucose dehydrogenase. 2004-06-01 15167795
Hair dye contact allergy: quantitative exposure assessment of selected products and clinical cases. 2004-06 15274724
Bead-based immunoassays with microelectrode detection. 2004-06 15118802
Bead-based electrochemical immunoassay for bacteriophage MS2. 2004-05-15 15144178
Microbead-based electrochemical immunoassay with interdigitated array electrodes. 2004-05-15 15113686
Synthesis and biological activity of novel retinamide and retinoate derivatives. 2004-05 15133197
Hapten-directed targeting to single-chain antibody receptors. 2004-05 15044963
Toxicity and human health risk of hair dyes. 2004-04 15019177
Flow injection determination of p-aminophenol at trace level using inhibited luminol-dimethylsulfoxide-NaOH-EDTA chemiluminescence. 2004-03-25 15644248
Electrical detection of viral DNA using ultramicroelectrode arrays. 2004-02-01 14750864
Express detection of nonylphenol in water samples by fluorescence polarization immunoassay. 2004-02 14673557
Electric chips for rapid detection and quantification of nucleic acids. 2004-01-15 14683637
[Kinetics and mechanism of aniline oxidation with chlorine dioxide in water]. 2004-01 15330430
Effect of unlabeled helper probes on detection of an RNA target by bead-based sandwich hybridization. 2004-01 14740494
Automated spectrophotometric assay for urine p-aminophenol by an oxidative coupling reaction. 2004 15487710
Kinetics of aniline oxidation with chlorine dioxide. 2004 15137646
Toxicological detection of the new designer drug 1-(4-methoxyphenyl)piperazine and its metabolites in urine and differentiation from an intake of structurally related medicaments using gas chromatography-mass spectrometry. 2003-12-25 14643514
Oxidation-reduction potential as a control variable for the anaerobic stage during anaerobic-aerobic p-nitrophenol degradation. 2003-12-06 14656162
First enantiospecific total synthesis of the antitubercular marine natural product pseudopteroxazole. Revision of assigned stereochemistry. 2003-11-05 14583045
Enzyme-amplified electrochemical detection of DNA using electrocatalysis of ferrocenyl-tethered dendrimer. 2003-11-01 14588003
A potential biomarker of kidney damage identified by proteomics: preliminary findings. 2003-08-29 12944177
Determination of 4-aminophenol impurities in multicomponent analgesic preparations by HPLC with amperometric detection. 2003-08-08 12899997
Synthesis and activity of novel benzoxazole derivatives of mannopeptimycin glycopeptide antibiotics. 2003-08-04 12852976
Immobilized enzyme-linked DNA-hybridization assay with electrochemical detection for Cryptosporidium parvum hsp70 mRNA. 2003-08-01 14572058
Evolution of catabolic pathways for synthetic compounds: bacterial pathways for degradation of 2,4-dinitrotoluene and nitrobenzene. 2003-08 12750857
Enhancement of antioxidant activity of p-alkylaminophenols by alkyl chain elongation. 2003-07-31 12837535
Continuous biotransformation and removal of nitrophenols under denitrifying conditions. 2003-07 12767298
Validation of a method for quantification of ketobemidone in human plasma with liquid chromatography-tandem mass spectrometry. 2003-06-15 12742125
Unbiased spectrophotometric method for estimating phenol or o-cresol in unknown water samples. 2003-06 12732922
Generation of ligand conformations in continuum solvent consistent with protein active site topology: application to thrombin. 2003-04-10 12672230
Metalloantimalarials: targeting of P. falciparum strains with novel iron(III) and gallium(III) complexes of an amine phenol ligand. 2003-04-07 12665363
Sorption and diffusion of phenols onto well-defined ordered nanoporous monolithic silicas. 2003-04-01 12742049
The use of thermal lensing for the determination of pyrogens. 2003-04 12733016
Reversible and irreversible inhibitory activity of succinic and maleic acid derivatives on acetylcholinesterase. 2003-04 12694883
Dlf complexes with uniform coordination geometry: structural and magnetic properties of an LnNi2 core supported by a heptadentate amine phenol ligand. 2003-03-10 12611525
Synthesis of 11C-amides using [11C]carbon monoxide and in situ activated amines by palladium-mediated carboxaminations. 2003-02-07 12926257
Immobilizing a single pybox ligand onto a library of solid supports. 2003 14761160
[Research into simultaneous spectrophotometric determination of components in cough syrup by principal component regression method]. 2002-06 12938324
Renal PGE2 production in the human and rat following phenacetin, acetaminophen and p-aminophenol. 2002 14632321
Effects of alternative carbon sources on biological transformation of nitrophenols. 2002 12688587
Patents

Patents

JP1004635A4 JP2000026572A3 JP2000103975A6 JP2000248077A3 JP2001183835A3 JP2001192500A3 JP2001342238A3 JP2002088066A3 JP2002533511A3 JP2003128513A3 JP2005029590A6 JP2005082628A3 JP2005306866A3 JP2005527113A4 JP2006008642A3 JP2006028082A3 JP2006278197A3 JP2006321834A3 JP2006523256A8 JP2007084524A3 JP2007308427A4 JP2008214479A3 JP2009263324A5 JP2011529977A3 JP2012500104A108 JP3016599B23 JP4550838B23 JP4728230B25 JP4820369B27 JPH01174526A3 JPH01319528A3 JPH0211551A3 JPH02170862A3 JPH02188556A3 JPH0219368A3 JPH02232224A3 JPH02240138A3 JPH0269448A3 JPH03112946A5 JPH03127762A5 JPH03177419A3 JPH04108824A3 JPH04154860A3 JPH0496924A3 JPH05156007A3 JPH05170902A4 JPH05174621A3 JPH05221937A3 JPH0551450A3 JPH06219999A3 JPH06228303A3 US3079435 A3

Sample Use Guides

In Vivo Use Guide UnknownRoute of Administration: Unknown In Vitro Use Guide Sources: https://www.ncbi.nlm.nih.gov/pubmed/21771276 Concentrations of p-aminophenol from 1 to 100 μg/ml produced significant (p < 0.05) loss of mouse cortical neuron viability at 24 hr compared to the controls.
Substance Class Chemical Created by admin on Mon Mar 31 19:23:46 GMT 2025 Edited by admin on Mon Mar 31 19:23:46 GMT 2025
Record UNII IWL2N22RFY
Record Status Validated (UNII)
Record Version {{v}}
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Name Type Language
P-AMINOPHENOL HYDROCHLORIDE Locators: HSDB Sources:
Common Name English
P-AMINOPHENOL HCL Locators: INCI Naming Organization: INCI Sources:
Preferred Name English
RODOL PC Sources:
Brand Name English
PHENOL, 4-AMINO-, HYDROCHLORIDE Sources:
Systematic Name English
4-AMINOPHENOL HYDROCHLORIDE Source:
Systematic Name English
4-HYDROXYANILINIUM CHLORIDE Sources:
Systematic Name English
FOURRINE 83 Sources:
Brand Name English
P-HYDROXYANILINE HYDROCHLORIDE Sources:
Common Name English
PHENOL, 4-AMINO-, HYDROCHLORIDE (1:1) Sources:
Systematic Name English
P-AMINOPHENOL HYDROCHLORIDE [HSDB] Sources:
Common Name English
Code System Code Type Description
HSDB Source:
2151 Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
MESH Source:
C026729 Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
PUBCHEM Source:
5828 Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
FDA UNII
IWL2N22RFY Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
EPA CompTox Source:
DTXSID6058760 Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
DRUG BANK Source:
DBSALT002745 Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
ECHA (EC/EINECS) Source:
200-122-6 Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
CAS Sources:
51-78-5 Created by admin on Mon Mar 31 19:23:46 GMT 2025 , Edited by admin on Mon Mar 31 19:23:46 GMT 2025 PRIMARY
Related Record Type Details
R7P8FRP05V Structure of p-Aminophenol p-Aminophenol
PARENT -> SALT/SOLVATE
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