Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C14H14O3 |
| Molecular Weight | 230.2592 |
| 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)C(O)=O
InChI
InChIKey=CMWTZPSULFXXJA-SECBINFHSA-N
InChI=1S/C14H14O3/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10/h3-9H,1-2H3,(H,15,16)/t9-/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Stereoselective (S)- and (R)-naproxen glucuronosyl transferases of rat liver. | 1991 Mar-Apr |
|
| Simultaneous determination of (R)- and (S)-naproxen and (R)- and (S)-6-O-desmethylnaproxen by high-performance liquid chromatography on a Chiral-AGP column. | 1992 Jun 10 |
|
| Enantiomeric separation of R,S-naproxen by conventional and nano-liquid chromatography with methyl-beta-cyclodextrin as a mobile phase additive. | 2001 Jul 27 |
|
| Methotrexate-induced optic neuropathy. | 2002 Dec |
|
| Occurrence and behavior of the chiral anti-inflammatory drug naproxen in an aquatic environment. | 2014 Dec |
Patents
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| Code System | Code | Type | Description | ||
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245-966-6
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23979-41-1
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1457436
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169118
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DTXSID00904711
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admin on Sat Dec 16 08:34:59 GMT 2023 , Edited by admin on Sat Dec 16 08:34:59 GMT 2023
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484XV9323P
Created by
admin on Sat Dec 16 08:34:59 GMT 2023 , Edited by admin on Sat Dec 16 08:34:59 GMT 2023
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SUBSTANCE RECORD
