Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H34O9 |
| Molecular Weight | 406.4679 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 9 / 9 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)\C=C\[C@@]2(O)C(C)(C)C[C@H](O)C[C@@]2(C)O
InChI
InChIKey=XZRJEYQBLXDNNU-UWAGUHGBSA-N
InChI=1S/C19H34O9/c1-10(27-16-15(24)14(23)13(22)12(9-20)28-16)5-6-19(26)17(2,3)7-11(21)8-18(19,4)25/h5-6,10-16,20-26H,7-9H2,1-4H3/b6-5+/t10-,11+,12-,13-,14+,15-,16-,18-,19-/m1/s1
| Molecular Formula | C19H34O9 |
| Molecular Weight | 406.4679 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 9 / 9 |
| E/Z Centers | 1 |
| Optical Activity | UNSPECIFIED |
Officinalioside is a new lignan glucoside from Borago officinalis L. Officinalioside showed a moderate DPPH radical scavenging activity (IC50: 41.3 ± 0.25 uM) comparable with that of the standard trolox (16.6 ± 2.2 uM) without any significant cytotoxicity towards human cell line A549 (IC50 > 100 uM).
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:27:45 GMT 2023
by
admin
on
Sat Dec 16 11:27:45 GMT 2023
|
| Record UNII |
1Z3J5831FI
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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1Z3J5831FI
Created by
admin on Sat Dec 16 11:27:45 GMT 2023 , Edited by admin on Sat Dec 16 11:27:45 GMT 2023
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91827066
Created by
admin on Sat Dec 16 11:27:45 GMT 2023 , Edited by admin on Sat Dec 16 11:27:45 GMT 2023
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540528-05-0
Created by
admin on Sat Dec 16 11:27:45 GMT 2023 , Edited by admin on Sat Dec 16 11:27:45 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> CONSTITUENT ALWAYS PRESENT |
Compound was extracted from the dried leaves of N. tabacum (3.5 kg) with 90% EtOH at room temperature and partitioned between EtOAc and H2O.
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