Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H10O3 |
Molecular Weight | 214.2167 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(C=CC=C1)C(=O)OC2=CC=CC=C2
InChI
InChIKey=ZQBAKBUEJOMQEX-UHFFFAOYSA-N
InChI=1S/C13H10O3/c14-12-9-5-4-8-11(12)13(15)16-10-6-2-1-3-7-10/h1-9,14H
Molecular Formula | C13H10O3 |
Molecular Weight | 214.2167 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionCurator's Comment: Description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/23387858
Curator's Comment: Description was created based on several sources, including
http://www.ncbi.nlm.nih.gov/pubmed/23387858
Phenyl salicylate belongs to the family of hydroxybenzoic acid derivatives. Phenyl salicylate is used as a food additive. Antimycobacterial activity of phenyl salicylates (salols) was studied in connection with antituberculotic activity of salicylic derivatives. Phenyl salicylates are esters. Phenyl salicylates (salols) represent a new group of antimycobacterial compounds. Phenyl salicylate is included in the number of medications, indicated for the treatment of symptoms of irritative voiding, used to relieve the discomfort, pain, frequent urge to urinate, and cramps/spasms of the urinary tract caused by an infection or a medical procedure. Phenyl salicylate works as a pain reliever in these combinations.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL206 Sources: http://www.ncbi.nlm.nih.gov/pubmed/22197706 |
49.78 µM [EC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | PROSED EC Approved UsePROSED EC is indicated for the relief of discomfort of the lower urinary tract caused by hypermotility resulting from inflammation or diagnostic procedures and in the treatment of cystitis, urethritis and trigonitis when caused by organisms which maintain or produce an acid urine and are susceptible to formaldehyde. |
PubMed
Title | Date | PubMed |
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Estrogenic activity of phenolic additives determined by an in vitro yeast bioassay. | 2001 Feb |
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Effect of some ultraviolet light absorbers on photo-stabilization of azadirachtin-A. | 2002 Oct |
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Effect of ultraviolet light absorbers on photostabilization of azadirachtin-A in solution (part: II). | 2003 Jan |
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Viscosity at the dynamic crossover in o-terphenyl and salol under high pressure. | 2004 Jun 18 |
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Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods. | 2006 Nov |
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Mass spectrometric identification of covalent adducts of the skin allergen 2,4-dinitro-1-chlorobenzene and model skin proteins. | 2008 Aug |
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Kinetic evidence for the occurrence of independent ion-exchange processes in the cationic micellar-mediated reaction of piperidine with anionic phenyl salicylate. | 2009 Jun 11 |
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The role of nucleation in vitrification of supercooled liquids. | 2010 Apr 21 |
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Infrared spectroscopy study of structural changes in glass-forming salol. | 2010 Mar |
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Phenyl 3,5-di-tert-butyl-2-hy-droxy-benzoate. | 2010 Nov 24 |
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The estrogenic potential of salicylate esters and their possible risks in foods and cosmetics. | 2012 Mar 7 |
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Simultaneous determination of the UV-filters benzyl salicylate, phenyl salicylate, octyl salicylate, homosalate, 3-(4-methylbenzylidene) camphor and 3-benzylidene camphor in human placental tissue by LC-MS/MS. Assessment of their in vitro endocrine activity. | 2013 Oct 1 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/drp/phenyl-salicylate.html
One tablet of PROSED EC orally 4 times per day followed by liberal fluid intake.
Each tablet of PROSED EC contains: Phenyl Salicylate 36.2 mg
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/24004914
Phenyl Salicylate at 10 uM increased the number of MCF-7 cells by approximately 1.8 fold
Substance Class |
Chemical
Created
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admin
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Edited
Fri Dec 15 16:45:01 UTC 2023
by
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on
Fri Dec 15 16:45:01 UTC 2023
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Record UNII |
28A37T47QO
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
PHENYL SALICYLATE
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WHO-VATC |
QG04BX12
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WHO-ATC |
G04BX12
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NCI_THESAURUS |
C2356
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C75079
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DTXSID6021957
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m8690
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607
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204-259-2
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PHENYL SALICYLATE
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1534209
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28A37T47QO
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CHEMBL1339216
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895808
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C026041
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34918
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3462
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SUB14839MIG
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28A37T47QO
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36122
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DB11071
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8361
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118-55-8
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100000079433
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33406
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Related Record | Type | Details | ||
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ACTIVE MOIETY |