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Details

Stereochemistry RACEMIC
Molecular Formula C10H13NO4
Molecular Weight 211.2145
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LISADIMATE

SMILES

NC1=CC=C(C=C1)C(=O)OCC(O)CO

InChI

InChIKey=WHQOKFZWSDOTQP-UHFFFAOYSA-N
InChI=1S/C10H13NO4/c11-8-3-1-7(2-4-8)10(14)15-6-9(13)5-12/h1-4,9,12-13H,5-6,11H2

HIDE SMILES / InChI
Molecular Formula C10H13NO4
Molecular Weight 211.2145
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description

Lisadimate (glyceryl PABA), a substituted aminobenzoate, is a sunscreen with actions similar to those of aminobenzoic acid. It is effective against UVB light. Glyceryl PABA (Escalol 106), present in many popular sunscreens, is a common sensitizer which invariably cross-reacts with benzocaine; it is present in over 400 over-the-counter products. Glyceryl PABA does not appear to cross-react with the sunscreening agents amyl (Escalol 506) and octyl (Escalol 507) dimethyl PABA. Glyceryl PABA, may, on occasion, cross-react with para-aminobenzoic acid (PABA), paraphenylenediamine, aniline, and sulfa drugs. Ironically, the sunscreening agent glyceryl PABA may, itself, act as a photosensitizing agent.

Approval Year

Unknown
139594
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Approved
8429
Unknown

Approved Use

Unknown
Sourcing

Sourcing

Vendor/AggregatorIDURL
3B Scientific (Wuhan) Corp
3B8-01193
http://www.3bsc.com/index/pro_info.php?id=73128
Alfa Chemistry
136-44-7
https://www.alfa-chemistry.com/cas_136-44-7.htm
Alfa Chemistry
29593-08-6
https://www.alfa-chemistry.com/cas_29593-08-6.htm
Aurora Fine Chemicals LLC
A14.111.429
http://online.aurorafinechemicals.com/info?ID=A14.111.429
Aurora Fine Chemicals LLC
A17.949.810
http://online.aurorafinechemicals.com/info?ID=A17.949.810
BLD Pharm
BD01360496
http://www.bldpharm.com/products/29593-08-6.html
ChemMol
49415905
http://www.chemmol.com/chemmol/49415905.html
Chemspace
CSSB00012337706
https://chem-space.com/CSSB00012337706
Parchem
38142
https://www.parchem.com/chemical-supplier-distributor/Glyceryl-PABA-038142.aspx
Sigma-Aldrich
PH011337_ALDRICH
https://www.sigmaaldrich.com/catalog/product/aldrich/ph011337
Smolecule
S533287
http://www.smolecule.com/products/s533287
THE BioTek
bt-273247
https://www.thebiotek.com/product/inhibitors/bt-273247
PubMed

PubMed

TitleDatePubMed
Patents

Patents

JP2011506326A
5

Sample Use Guides

In Vivo Use Guide
Sunscreen products containing lisadimate should be applied 1 to 2 hours before sun exposure.
Route of Administration: Topical
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:24:37 UTC 2023
Edited
by admin
on Sat Dec 16 17:24:37 UTC 2023
Record UNII
A886B5N5IM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LISADIMATE
INN   MART.   USAN  
INN   USAN  
Official Name English
(±)-GLYCEROL 1-(P-AMINOBENZOATE)
Common Name English
GLYCERYL P-AMINOBENZOATE [MI]
Common Name English
LISADIMATE [USAN]
Common Name English
1,2,3-PROPANETRIOL, 1-(4-AMINOBENZOATE), (±)-
Common Name English
GLYCERYL PABA [INCI]
Common Name English
GLYCERYL PABA
INCI  
INCI  
Official Name English
LISADIMATE [MART.]
Common Name English
GLYCERYL P-AMINOBENZOATE
MI  
Common Name English
lisadimate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C851
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
EPA PESTICIDE CODE 9102
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
Code System Code Type Description
USAN
BB-100
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
PUBCHEM
8692
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
INN
6627
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106668
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
SMS_ID
100000082524
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
ECHA (EC/EINECS)
205-244-3
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
MERCK INDEX
m5793
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID8042002
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
EVMPD
SUB08532MIG
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
FDA UNII
A886B5N5IM
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
NCI_THESAURUS
C76109
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
CAS
136-44-7
Created by admin on Sat Dec 16 17:24:37 UTC 2023 , Edited by admin on Sat Dec 16 17:24:37 UTC 2023
PRIMARY
Related Record Type Details
Structure of LISADIMATE, (S)-
ENANTIOMER -> RACEMATE
Structure of LISADIMATE, (R)-
ENANTIOMER -> RACEMATE
Related Record Type Details
Structure of LISADIMATE
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