metaxalone
group of stereoisomers
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metaxalone
Summary
metaxalone is a group of stereoisomers[1]. metaxalone draws 195 Wikipedia views per month (group_of_stereoisomers category, ranking #115 of 1,063).[2]
Key Facts
- metaxalone's instance of is recorded as group of stereoisomers[3].
- metaxalone's chemical structure is recorded as Metaxalone.svg[4].
- metaxalone's CAS Registry Number is recorded as 1665-48-1[5].
- metaxalone's EC number is recorded as 216-777-6[6].
- metaxalone's canonical SMILES is recorded as CC1=CC(=CC(=C1)OCC2CNC(=O)O2)C[7].
- metaxalone's InChI is recorded as InChI=1S/C12H15NO3/c1-8-3-9(2)5-10(4-8)15-7-11-6-13-12(14)16-11/h3-5,11H,6-7H2,1-2H3,(H,13,14)[8].
- metaxalone's InChIKey is recorded as IMWZZHHPURKASS-UHFFFAOYSA-N[9].
- metaxalone's chemical formula is recorded as C₁₂H₁₅NO₃[10].
- metaxalone's subclass of is recorded as chemical compound[11].
- metaxalone's has use is recorded as medication[12].
- metaxalone's Commons category is recorded as Metaxalone[13].
- metaxalone's MeSH descriptor ID is recorded as C011301[14].
- metaxalone's ChEMBL ID is recorded as CHEMBL1079604[15].
- metaxalone's Guide to Pharmacology Ligand ID is recorded as 7609[16].
- metaxalone's Freebase ID is recorded as /m/08t5w8[17].
- metaxalone's UNII is recorded as 1NMA9J598Y[18].
- metaxalone's ChemSpider ID is recorded as 14709[19].
- metaxalone's ChemSpider ID is recorded as 21240662[20].
- metaxalone's PubChem CID is recorded as 15459[21].
- metaxalone's KEGG ID is recorded as C07934[22].
- metaxalone's KEGG ID is recorded as D00773[23].
- metaxalone's ChEBI ID is recorded as 6797[24].
- metaxalone's found in taxon is recorded as Caenorhabditis elegans[25].
- metaxalone's DrugBank ID is recorded as DB00660[26].
- metaxalone's Human Metabolome Database ID is recorded as HMDB0014798[27].
Why It Matters
metaxalone draws 195 Wikipedia views per month (group_of_stereoisomers category, ranking #115 of 1,063).[2] metaxalone has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28]