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=CC(\C=C\C(=O)NCCC2=CC=C(O)C=C2)=CC=C1O
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
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0002537 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22951040 |
17.36 µM [IC50] | ||
Target ID: CHEMBL3464 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22951040 |
|||
Target ID: WP408 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Nature is the best source of anti-inflammatory drugs: indexing natural products for their anti-inflammatory bioactivity. | 2018-01 |
|
| 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 |
|
| Safety, Efficacy, and Physicochemical Characterization of Tinospora crispa Ointment: A Community-Based Formulation against Pediculus humanus capitis. | 2017-08 |
|
| A new 9,10-dihydrophenanthrene from Dendrobium moniliforme. | 2016 |
|
| [Studies on chemical constituents from branch of Trema angustifolia]. | 2004-03 |
|
| Quantitative determination of liriodenine and moupinamide in five species of Mollinedia by high performance liquid chromatography. | 2001-11-16 |
|
| Antioxidant and lipophilic constituents of Tinospora crispa. | 1998-06 |
|
| Pharmacological studies on Aristolochia papillaris Mast. (Aristolochiaceae). | 1993-10 |
|
| [Studies on the chemical constituents of Annona squamosa]. | 1992 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:21:25 GMT 2025
by
admin
on
Mon Mar 31 22:21:25 GMT 2025
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| Record UNII |
WC99S6JM5Y
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Validated (UNII)
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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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