Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H39NO |
| Molecular Weight | 345.5619 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCCCC(=O)NCC1=CC=CC=C1
InChI
InChIKey=MLGPKWUKOQAAGI-UHFFFAOYSA-N
InChI=1S/C23H39NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-23(25)24-21-22-18-15-14-16-19-22/h14-16,18-19H,2-13,17,20-21H2,1H3,(H,24,25)
| Molecular Formula | C23H39NO |
| Molecular Weight | 345.5619 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Influence of colour type and previous cultivation on secondary metabolites in hypocotyls and leaves of maca (Lepidium meyenii Walpers). | 2010-04-15 |
|
| Analysis of macamides in samples of Maca (Lepidium meyenii) by HPLC-UV-MS/MS. | 2005-12-01 |
|
| Constituents of Lepidium meyenii 'maca'. | 2002-01 |
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 20:02:58 GMT 2025
by
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Mon Mar 31 20:02:58 GMT 2025
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| Record UNII |
1M5UVS8JUU
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Validated (UNII)
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DTXSID50458532
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140849
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| Related Record | Type | Details | ||
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PARENT -> CONSTITUENT ALWAYS PRESENT |
The structure elucidation of the isolated compound was based primarily on 1D and 2D NMR spectroscopic analyses, including 1H1H COSY, 1H13C HMQC, 1H13C HMBC and 1H1H NOESY experiments, as well as from 1H15N NMR HMBC correlations.
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