| Company Name: |
BOC Sciences |
| Tel: |
16314854226 |
| Email: |
info@bocsci.com |
5Hydroxy Meloxicam manufacturers
|
| | 5Hydroxy Meloxicam Basic information |
| Product Name: | 5Hydroxy Meloxicam | | Synonyms: | 4-Hydroxy-N-[5-(hydroxyMethyl)-2-thiazolyl]-2-Methyl-2H-1,2-benzothiazine-3-carboxaMide 1,1-Dioxide;5'-HydroxyMethyl 5'-DesMethyl MeloxicaM;5'-Hydroxy Meloxicam HCl;Meloxicam Impurity 11;4-Hydroxy-N-(5-(hydroxymethyl)thiazol-2-yl)-2-methyl-2H-benzo[e][1,2]thiazine-3-carboxamide 1,1-dioxide;2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-N-[5-(hydroxymethyl)-2-thiazolyl]-2-methyl-, 1,1-dioxide;Hydroxymeloxicam-13C6;5'-hydroxy Meloxicam | | CAS: | 130262-92-9 | | MF: | C14H13N3O5S2 | | MW: | 367.4 | | EINECS: | | | Product Categories: | Metabolites | | Mol File: | 130262-92-9.mol |  |
| | 5Hydroxy Meloxicam Chemical Properties |
| Melting point | 230-232°C | | storage temp. | -20°C Freezer | | solubility | DMSO (Slightly), Methanol (Slightly, Sonicated) | | form | Solid | | color | Pale Yellow to Yellow |
| | 5Hydroxy Meloxicam Usage And Synthesis |
| Description | 5’-hydroxy Meloxicam is a metabolite of the non-steroidal anti-inflammatory drug (NSAID) meloxicam . It is formed via metabolism of meloxicam primarily by the cytochrome P450 (CYP) isoform CYP2C9 and to a lesser extent by CYP3A4. | | Chemical Properties | Yellow Solid | | Uses | A metabolite of Meloxicam. | | Definition | ChEBI: 5'-hydroxymethyl-5'-desmethylmeloxicam is a benzothiazine. | | References | [1] C CHESNé. Metabolism of Meloxicam in human liver involves cytochromes P4502C9 and 3A4.[J]. Xenobiotica, 1998, 28 1: 1-13. DOI: 10.1080/004982598239704 |
| | 5Hydroxy Meloxicam Preparation Products And Raw materials |
|