Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H6O5 |
Molecular Weight | 170.1195 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC(O)=C(O)C(O)=C1
InChI
InChIKey=LNTHITQWFMADLM-UHFFFAOYSA-N
InChI=1S/C7H6O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,8-10H,(H,11,12)
Molecular Formula | C7H6O5 |
Molecular Weight | 170.1195 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:39:03 UTC 2023
by
admin
on
Fri Dec 15 15:39:03 UTC 2023
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Record UNII |
632XD903SP
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Code | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C275
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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DSLD |
1414 (Number of products:4)
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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NCI_THESAURUS |
C68539
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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Code System | Code | Type | Description | ||
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149-91-7
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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674319
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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205-749-9
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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1311389
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | RxNorm | ||
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CHEMBL288114
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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30778
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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GALLIC ACID
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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2117
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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632XD903SP
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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370
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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632XD903SP
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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100000127361
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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m5645
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | Merck Index | ||
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D005707
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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DTXSID0020650
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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20103
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY | |||
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C63648
Created by
admin on Fri Dec 15 15:39:03 UTC 2023 , Edited by admin on Fri Dec 15 15:39:03 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> CONSTITUENT ALWAYS PRESENT | |||
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PARENT -> CONSTITUENT ALWAYS PRESENT |
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PARENT -> CONSTITUENT ALWAYS PRESENT |
1,1-Diphenyl-2-picrylhydrazyl radical scavenging assay(DPPH) IC50 expressed as ug/mL = 3.7 +/- 0.4.
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SALT/SOLVATE -> PARENT | |||
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SOLVATE->ANHYDROUS | |||
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SALT/SOLVATE -> PARENT | |||
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PARENT -> CONSTITUENT ALWAYS PRESENT |
Gallic acid exhibited a significant free radical scavenging effect against 1,1-diphenyl-2-picryl hydrazine (DPPH) radical generation and had an inhibitory effect on lipid peroxidation, as measured by the level of malondialdehyde (MDA) formation.
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SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
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METABOLITE -> PARENT |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |