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Details

Stereochemistry ACHIRAL
Molecular Formula C6H5NO3
Molecular Weight 139.1088
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-NITROPHENOL

SMILES

OC1=CC=C(C=C1)[N+]([O-])=O

InChI

InChIKey=BTJIUGUIPKRLHP-UHFFFAOYSA-N
InChI=1S/C6H5NO3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H

HIDE SMILES / InChI

Molecular Formula C6H5NO3
Molecular Weight 139.1088
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Sulfating-activity and stability of cDNA-expressed allozymes of human phenol sulfotransferase, ST1A3*1 ((213)Arg) and ST1A3*2 ((213)His), both of which exist in Japanese as well as Caucasians.
1999 Aug
Cytochrome P450 isoform selectivity in human hepatic theobromine metabolism.
1999 Mar
Sulfation of environmental estrogen-like chemicals by human cytosolic sulfotransferases.
2000 Jan 7
Enzymatic properties, tissue-specific expression, and lysosomal location of two highly homologous rat SULT1C2 sulfotransferases.
2000 May 27
Establishment of a human hepatoma cell line, HLE/2E1, suitable for detection of p450 2E1-related cytotoxicity.
2000 Oct
Oriented antibody immobilization to polystyrene macrocarriers for immunoassay modified with hydrazide derivatives of poly(meth)acrylic acid.
2001
Environmental pesticide exposure in Honduras following hurricane Mitch.
2001
Biotransformation of nitrophenols in upflow anaerobic sludge blanket reactors.
2001 Dec
A novel transverse push-pull microprobe: in vitro characterization and in vivo demonstration of the enzymatic production of adenosine in the spinal cord dorsal horn.
2001 Jan
Nitrophenols in precipitation.
2001 Jan
Sulfur-rich zinc chemistry: new tris(thioimidazolyl)hydroborate ligands and their zinc complex chemistry related to the structure and function of alcohol dehydrogenase.
2001 Jul 30
Trace level determination of phenols as pentafluorobenzyl derivatives by gas chromatography-negative-ion chemical ionization mass spectrometry.
2001 Jun
Identification of multiple constitutive and inducible hepatic cytochrome P450 enzymes in market weight swine.
2001 Jun
Removal of phenols from aqueous streams by the cloud point extraction technique with oxyethylated methyl dodecanoates as surfactants.
2001 Jun 1
Molecular cloning, expression, and characterization of a canine sulfotransferase that is a human ST1B2 ortholog.
2001 Jun 1
Binding and oxidation of alkyl 4-nitrophenyl ethers by rabbit cytochrome P450 1A2: evidence for two binding sites.
2001 Jun 19
Variables in human liver microsome preparation: impact on the kinetics of l-alpha-acetylmethadol (LAAM) n-demethylation and dextromethorphan O-demethylation.
2001 Mar
Degradation of diphenyl ether herbicides by the lignin-degrading basidiomycete Coriolus versicolor.
2001 Nov
Effect of onion consumption by rats on hepatic drug-metabolizing enzymes.
2001 Oct
Kinetic study of the phenolysis of bis(4-nitrophenyl) carbonate, bis(4-nitrophenyl) thionocarbonate, and methyl 4-nitrophenyl thionocarbonate.
2001 Oct 5
Amperometric microbial biosensor for direct determination of organophosphate pesticides using recombinant microorganism with surface expressed organophosphorus hydrolase.
2001 Sep
Theoretical study of the internal rotational barriers in nitrotoluenes, nitrophenols, and nitroanilines.
2002 Jan
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:22:07 GMT 2023
Edited
by admin
on Fri Dec 15 15:22:07 GMT 2023
Record UNII
Y92ZL45L4R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-NITROPHENOL
MART.   MI  
Common Name English
PHENOL, P-NITRO-
Common Name English
4-NITROPHENOL [HSDB]
Common Name English
P-NITROPHENOL [MART.]
Common Name English
NITROPHENOL, P-
Common Name English
PHENOL, 4-NITRO-
Systematic Name English
PARACETAMOL IMPURITY F [EP IMPURITY]
Common Name English
P-NITROPHENOL [MI]
Common Name English
P-HYDROXYNITROBENZENE
Common Name English
4-HYDROXYNITROBENZENE
Systematic Name English
NSC-1317
Code English
4-HYDROXY-1-NITROBENZENE
Systematic Name English
ACETAMINOPHEN RELATED COMPOUND F
USP-RS  
Common Name English
4-NITROPHENOL
HSDB  
Systematic Name English
ACETAMINOPHEN RELATED COMPOUND F [USP-RS]
Common Name English
NIPHEN
Common Name English
1-HYDROXY-4-NITROBENZENE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 56301
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
Code System Code Type Description
CAS
100-02-7
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
MERCK INDEX
m7978
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
4-NITROPHENOL
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
HSDB
1157
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
CHEBI
16836
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
MESH
C024836
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
CHEBI
57917
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
NSC
1317
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
FDA UNII
Y92ZL45L4R
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-811-7
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
PUBCHEM
980
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
RS_ITEM_NUM
1003064
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
DRUG BANK
DB04417
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID0021834
Created by admin on Fri Dec 15 15:22:07 GMT 2023 , Edited by admin on Fri Dec 15 15:22:07 GMT 2023
PRIMARY
Related Record Type Details
METABOLIC ENZYME -> SUBSTRATE