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 |
---|---|---|
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 Mar 1 |
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Self-activating nuclease activity of copper (II) complexes of hydroxyl-rich ligands. | 2006 Jan |
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Carbohydrazones of substituted salicylaldehydes as potential lead compounds for the development of narrow-spectrum antimicrobials. | 2007 Jul-Aug |
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2,3,4-Trihydroxy-benzaldehyde. | 2008 Jul 23 |
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The severity of Puumala hantavirus induced nephropathia epidemica can be better evaluated using plasma interleukin-6 than C-reactive protein determinations. | 2010 May 25 |
|
(E)-N'-(2,3,4-Trihy-droxy-benzyl-idene)-isonicotinohydrazide dihydrate. | 2010 Oct 31 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:21:38 GMT 2023
by
admin
on
Sat Dec 16 19:21:38 GMT 2023
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Record UNII |
7UGV46Q4M2
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Record Status |
Validated (UNII)
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Record Version |
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DTXSID9057684
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22595
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7UGV46Q4M2
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