Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C14H16O2 |
| Molecular Weight | 216.2756 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=CC=C(C=C2C=C1)[C@H](C)CO
InChI
InChIKey=LTRANDSQVZFZDG-SNVBAGLBSA-N
InChI=1S/C14H16O2/c1-10(9-15)11-3-4-13-8-14(16-2)6-5-12(13)7-11/h3-8,10,15H,9H2,1-2H3/t10-/m1/s1
| Molecular Formula | C14H16O2 |
| Molecular Weight | 216.2756 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26042491
Both enantiomers of naproxen (6-methoxy-α-methyl-2-naphthaleneacetic acid) and naproxol (6-methoxy-β-2-naphthaleneethanol), and their racemic mixtures, inhibited the radicle growth of R. sativus at a concentration of 1mM
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:39:48 GMT 2025
by
admin
on
Wed Apr 02 09:39:48 GMT 2025
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| Record UNII |
33S398GAY6
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C257
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C83990
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33S398GAY6
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2978
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |