Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H19NO4 |
| Molecular Weight | 313.3478 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(O)C=CC(\C=C\C(=O)NCCC2=CC=C(O)C=C2)=C1
InChI
InChIKey=NPNNKDMSXVRADT-WEVVVXLNSA-N
InChI=1S/C18H19NO4/c1-23-17-12-14(4-8-16(17)21)5-9-18(22)19-11-10-13-2-6-15(20)7-3-13/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)/b9-5+
| Molecular Formula | C18H19NO4 |
| Molecular Weight | 313.3478 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Antioxidant and lipophilic constituents of Tinospora crispa. | 1998 Jun |
|
| Quantitative determination of liriodenine and moupinamide in five species of Mollinedia by high performance liquid chromatography. | 2001 Jul-Aug |
|
| Elucidation of Characteristic Sulfur-Fumigated Markers and Chemical Transformation Mechanism for Quality Control of Achyranthes bidentate Blume Using Metabolome and Sulfur Dioxide Residue Analysis. | 2018 |
|
| Nature is the best source of anti-inflammatory drugs: indexing natural products for their anti-inflammatory bioactivity. | 2018 Jan |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:52:45 GMT 2023
by
admin
on
Sat Dec 16 08:52:45 GMT 2023
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| Record UNII |
WC99S6JM5Y
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| Record Status |
Validated (UNII)
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| Record Version |
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5280537
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WC99S6JM5Y
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DTXSID30904143
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17818
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66648-43-9
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65646-26-6
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NON-SPECIFIC STEREOCHEMISTRY |
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|---|---|---|---|---|
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A 70% aq. acetone extract prepared from the leaves of N. tabacum was partitioned between EtOAc and H2O. TMV infection inhibition activity of compound 18.2 ? 2.5%.
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PARENT -> CONSTITUENT ALWAYS PRESENT |
270 uM IC50 vs in vitro prostaglandin synthesis
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PARENT -> CONSTITUENT ALWAYS PRESENT |
Amide
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