Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H10O9 |
| Molecular Weight | 322.2238 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC(OC(=O)C2=CC(O)=C(O)C(O)=C2)=C(O)C(O)=C1
InChI
InChIKey=COVFEVWNJUOYRL-UHFFFAOYSA-N
InChI=1S/C14H10O9/c15-7-2-6(3-8(16)11(7)18)14(22)23-10-4-5(13(20)21)1-9(17)12(10)19/h1-4,15-19H,(H,20,21)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Differential inhibition of reverse transcriptase and various DNA polymerases by digallic acid and its derivatives. | 1990 Sep-Oct |
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| Cytotoxic effects of digalloyl dimer procyanidins in human cancer cell lines. | 2008 Dec |
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| Inhibition of Ca2+-activated Cl- channels by gallotannins as a possible molecular basis for health benefits of red wine and green tea. | 2010 Nov |
|
| Functional swapping between transmembrane proteins TMEM16A and TMEM16F. | 2014 Mar 14 |
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208-624-7
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m4442
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30814
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536-08-3
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59263
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341
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404KO0584X
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DTXSID50871747
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DIGALLIC ACID
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admin on Fri Dec 15 19:05:21 GMT 2023 , Edited by admin on Fri Dec 15 19:05:21 GMT 2023
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C067648
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admin on Fri Dec 15 19:05:21 GMT 2023 , Edited by admin on Fri Dec 15 19:05:21 GMT 2023
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SUBSTANCE RECORD
