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Details

Stereochemistry ACHIRAL
Molecular Formula C6H6NO6P
Molecular Weight 219.0887
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-NITROPHENYL PHOSPHATE

SMILES

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

InChI

InChIKey=XZKIHKMTEMTJQX-UHFFFAOYSA-N
InChI=1S/C6H6NO6P/c8-7(9)5-1-3-6(4-2-5)13-14(10,11)12/h1-4H,(H2,10,11,12)

HIDE SMILES / InChI

Molecular Formula C6H6NO6P
Molecular Weight 219.0887
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

PubMed

PubMed

TitleDatePubMed
Pestalotiopisorin B, a new isocoumarin derivative from the mangrove endophytic fungus Pestalotiopsis sp. HHL101.
2020-04
Catalytic properties of wheat phytase that favorably degrades long-chain inorganic polyphosphate.
2020-01-01
Kaempferol promotes proliferation, migration and differentiation of MC3T3-E1 cells via up-regulation of microRNA-101.
2019-12
Recyclable metal nanoparticle-immobilized polymer dot on montmorillonite for alkaline phosphatase-based colorimetric sensor with photothermal ablation of Bacteria.
2019-11-15
Calmodulin-Calcineurin Interaction beyond the Calmodulin-Binding Region Contributes to Calcineurin Activation.
2019-10-01
Interleukin-35 stimulates tumor necrosis factor-α activated osteoblasts differentiation through Wnt/β-catenin signaling pathway in rheumatoid arthritis.
2019-10
CdS quantum dots generated in-situ for fluorometric determination of thrombin activity.
2019-08-29
Amplified electrochemical immunoassay for 5-methylcytosine using a nanocomposite prepared from graphene oxide, magnetite nanoparticles and β-cyclodextrin.
2019-07-02
A reanalysis of protein tyrosine phosphatases inhibitory studies using the unnatural substrate analogue p-nitrophenyl phosphate.
2019-05-01
Colorimetric Analysis of Alkaline Phosphatase Activity in S. aureus Biofilm.
2019-04-12
Vibrio cholerae LMWPTP-2 display unique surface charge and grooves around the active site: Indicative of distinctive substrate specificity and scope to design specific inhibitor.
2019-02
Consequences of Heterogeneous Crowding on an Enzymatic Reaction: A Residence Time Monte Carlo Approach.
2019-01-31
Fluorometric determination of pesticides and organophosphates using nanoceria as a phosphatase mimic and an inner filter effect on carbon nanodots.
2019-01-09
Phosphatase-like Activity of Porous Nanorods of CeO2 for the Highly Stabilized Dephosphorylation under Interferences.
2019-01-09
An alkaline phosphatase from Bacillus amyloliquefaciens YP6 of new application in biodegradation of five broad-spectrum organophosphorus pesticides.
2019
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:52:40 GMT 2025
Edited
by admin
on Mon Mar 31 19:52:40 GMT 2025
Record UNII
59NF9TE3BA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-404086
Preferred Name English
4-NITROPHENYL PHOSPHATE
Systematic Name English
P-NITROPHENYL PHOSPHATE
Common Name English
PHENOL, P-NITRO-, DIHYDROGEN PHOSPHATE
Systematic Name English
PHOSPHORIC ACID, P-NITROPHENYL ESTER
Systematic Name English
PHOSPHORIC ACID, MONO(4-NITROPHENYL) ESTER
Systematic Name English
NITROPHENYLPHOSPHATE
Common Name English
4-NITROPHENYL DIHYDROGEN PHOSPHATE
Systematic Name English
MONO(4-NITROPHENYL) PHOSPHATE
Systematic Name English
ALKALINE PHOSPHATASE YELLOW
Common Name English
PHOSPHORIC ACID, MONO(P-NITROPHENYL) ESTER
Systematic Name English
P-NITROPHENOL PHOSPHATE
Common Name English
P-NITROPHENYL DIHYDROGEN PHOSPHATE
Common Name English
Code System Code Type Description
NSC
404086
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
CHEBI
17440
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-353-9
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
DRUG BANK
DB04214
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
CAS
330-13-2
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID60861876
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
FDA UNII
59NF9TE3BA
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
PUBCHEM
378
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
CHEBI
61146
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
MESH
C008644
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
WIKIPEDIA
para-Nitrophenylphosphate
Created by admin on Mon Mar 31 19:52:40 GMT 2025 , Edited by admin on Mon Mar 31 19:52:40 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT