Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C16H18O8 |
| Molecular Weight | 338.3093 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@@H]1C[C@@](O)(C[C@@H](OC(=O)\C=C/C2=CC=C(O)C=C2)[C@H]1O)C(O)=O
InChI
InChIKey=BMRSEYFENKXDIS-ZARITIHLSA-N
InChI=1S/C16H18O8/c17-10-4-1-9(2-5-10)3-6-13(19)24-12-8-16(23,15(21)22)7-11(18)14(12)20/h1-6,11-12,14,17-18,20,23H,7-8H2,(H,21,22)/b6-3-/t11-,12-,14+,16-/m1/s1
| Molecular Formula | C16H18O8 |
| Molecular Weight | 338.3093 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 1 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/25569513
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25569513
China is one of the most important centers of diversity for Eriobotrya japonica Lindl. in the world. 3-p-coumaroylquinincacid (3-p-CoQA) was identified and quantified in the peel and pulp of the cultivars tested, this compound possessed relatively higher antioxidant activity, and may be excellent sources of phytochemicals and natural antioxidants.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:50:22 GMT 2025
by
admin
on
Mon Mar 31 22:50:22 GMT 2025
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| Record UNII |
8P26AP250B
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| Record Status |
Validated (UNII)
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| Record Version |
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admin on Mon Mar 31 22:50:22 GMT 2025 , Edited by admin on Mon Mar 31 22:50:22 GMT 2025
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