Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H6O4 |
| Molecular Weight | 154.1201 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=CC=C(C=O)C(O)=C1O
InChI
InChIKey=CRPNQSVBEWWHIJ-UHFFFAOYSA-N
InChI=1S/C7H6O4/c8-3-4-1-2-5(9)7(11)6(4)10/h1-3,9-11H
| Molecular Formula | C7H6O4 |
| Molecular Weight | 154.1201 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| (E)-N'-(2,3,4-Trihy-droxy-benzyl-idene)-isonicotinohydrazide dihydrate. | 2010-10-31 |
|
| The severity of Puumala hantavirus induced nephropathia epidemica can be better evaluated using plasma interleukin-6 than C-reactive protein determinations. | 2010-05-25 |
|
| 2,3,4-Trihydroxy-benzaldehyde. | 2008-07-23 |
|
| Carbohydrazones of substituted salicylaldehydes as potential lead compounds for the development of narrow-spectrum antimicrobials. | 2007-10-05 |
|
| Self-activating nuclease activity of copper (II) complexes of hydroxyl-rich ligands. | 2006-01 |
|
| alpha-Glucosidase inhibition of 6-hydroxyflavones. Part 3: Synthesis and evaluation of 2,3,4-trihydroxybenzoyl-containing flavonoid analogs and 6-aminoflavones as alpha-glucosidase inhibitors. | 2005-03-01 |
|
| New non-nucleoside inhibitors of hepatitis C virus RNA-dependent RNA polymerase. | 2004-07 |
|
| Antibacterial activities of phenolic benzaldehydes and benzoic acids against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica. | 2003-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 15:20:36 GMT 2025
by
admin
on
Wed Apr 02 15:20:36 GMT 2025
|
| Record UNII |
7UGV46Q4M2
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| Record Status |
Validated (UNII)
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| Record Version |
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