Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H4O4 |
| Molecular Weight | 140.0936 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=COC(=O)C=C1
InChI
InChIKey=ORGPJDKNYMVLFL-UHFFFAOYSA-N
InChI=1S/C6H4O4/c7-5-2-1-4(3-10-5)6(8)9/h1-3H,(H,8,9)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Inhibition of HIV-1 proteinase by non-peptide carboxylates. | 1991 Apr 15 |
|
| Characterization and expression of enzymatically active recombinant filarial prolyl 4-hydroxylase. | 2001 Sep 3 |
|
| Stimulation by caffeic acid, coumalic acid, and corilagin of the germination of resting spores of the clubroot pathogen Plasmodiophora brassicae. | 2003 Jan |
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| Code System | Code | Type | Description | ||
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500-05-0
Created by
admin on Sat Dec 16 04:28:57 GMT 2023 , Edited by admin on Sat Dec 16 04:28:57 GMT 2023
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m3815
Created by
admin on Sat Dec 16 04:28:57 GMT 2023 , Edited by admin on Sat Dec 16 04:28:57 GMT 2023
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22978
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207-899-0
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DTXSID60870569
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admin on Sat Dec 16 04:28:57 GMT 2023 , Edited by admin on Sat Dec 16 04:28:57 GMT 2023
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68141
Created by
admin on Sat Dec 16 04:28:57 GMT 2023 , Edited by admin on Sat Dec 16 04:28:57 GMT 2023
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Coumalic acid
Created by
admin on Sat Dec 16 04:28:57 GMT 2023 , Edited by admin on Sat Dec 16 04:28:57 GMT 2023
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OB1JPY343G
Created by
admin on Sat Dec 16 04:28:57 GMT 2023 , Edited by admin on Sat Dec 16 04:28:57 GMT 2023
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SUBSTANCE RECORD
