Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H9N2O3S.K |
Molecular Weight | 312.385 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[K+].[O-]S(=O)(=O)C1=CC2=C(C=C1)N=C(N2)C3=CC=CC=C3
InChI
InChIKey=YPSWUECEJGNOLY-UHFFFAOYSA-M
InChI=1S/C13H10N2O3S.K/c16-19(17,18)10-6-7-11-12(8-10)15-13(14-11)9-4-2-1-3-5-9;/h1-8H,(H,14,15)(H,16,17,18);/q;+1/p-1
Molecular Formula | K |
Molecular Weight | 39.0983 |
Charge | 1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C13H9N2O3S |
Molecular Weight | 273.287 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=611798eb-4004-40e8-b7ff-345136253975Curator's Comment: description was created based on several sources, including:
http://www.ncbi.nlm.nih.gov/pubmed/23112351
Sources: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=611798eb-4004-40e8-b7ff-345136253975
Curator's Comment: description was created based on several sources, including:
http://www.ncbi.nlm.nih.gov/pubmed/23112351
Ensulizole (INN) (phenylbenzimidazole sulfonic acid) is a common sunscreen agent. In 1999, the United States Food and Drug Administration regulated that the name ensulizole be used on sunscreen labels in the United States. It is a selective UVB filter, allowing almost all UVA transmission. The scope of UVB is 290 to 340 nanometers whereas the UVA range is 320 to 400 nanometers. For better UVA protection, it must be paired with avobenzone, titanium dioxide, or zinc oxide; outside of the United States it can also be paired with a UV absorber of the Tinosorb or Mexoryl types. Because is water-soluble, it has the characteristic of feeling lighter on skin. As such, it is often used in sunscreen lotions or moisturizers whose aesthetic goal is a non-greasy finish. The free acid is poorly soluble in water, so it is only used as its soluble salts
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: ultraviolet B Sources: http://www.ncbi.nlm.nih.gov/pubmed/23112351 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Preventing | ALOE SUNSCREEN Approved UseUnknown Launch Date2011 |
PubMed
Title | Date | PubMed |
---|---|---|
Comparison of the hanson microette and the Van Kel apparatus for in vitro release testing of topical semisolid formulations. | 2001 Oct |
|
The sunscreen agent 2-phenylbenzimidazole-5-sulfonic acid photosensitizes the formation of oxidized guanines in cellulo after UV-A or UV-B exposure. | 2010 Oct |
|
Quantum chemical investigation and experimental verification on the aquatic photochemistry of the sunscreen 2-phenylbenzimidazole-5-sulfonic acid. | 2010 Oct 1 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:57:02 GMT 2023
by
admin
on
Sat Dec 16 19:57:02 GMT 2023
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Record UNII |
058078A0QS
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Record Status |
Validated (UNII)
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |