1227358-55-5
Chemical Structure
Meloxicam-d3-1
- CAS No.: 1227358-55-5
- Formula:C14H10D3N3O4S2
- Molecular Weight:354.42
IUPAC Name: 4-hydroxy-2-methyl-N-(5-(methyl-d3)thiazol-2-yl)-2H-benzo[e][1,2]thiazine-3-carboxamide 1,1-dioxide
InChIKey: ZRVUJXDFFKFLMG-FIBGUPNXSA-N
SMILES: OC(C1=CC=CC=C12)=C(C(NC3=NC=C(S3)C([2H])([2H])[2H])=O)N(C)S2(=O)=O
Biological Activity: Meloxicam-d3-1 is the deuterium labeled Meloxicam. Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 µM and 36.6 µM for COX-2 and COX-1, respectively.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Meloxicam-d3-1 | 98.0% | Meloxicam-d3-1 is the deuterium labeled Meloxicam. Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 µM and 36.6 µM for COX-2 and COX-1, respectively. | ||||||||||||||||||||
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Meloxicam (Standard) | 99.89% | Meloxicam (Standard) is the analytical standard of Meloxicam. This product is intended for research and analytical applications. Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 μM and 36.6 μM for COX-2 and COX-1, respectively. | ||||||||||||||||||||
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Meloxicam-d3 | 99.55% | Meloxicam-d3 is deuterium labeled Meloxicam. Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 μM and 36.6 μM for COX-2 and COX-1, respectively. | ||||||||||||||||||||
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Meloxicam-13C,d3 | Meloxicam-13C,d3 is deuterium labeled Meloxicam. Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 µM and 36.6 µM for COX-2 and COX-1, respectively. | |||||||||||||||||||||
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Meloxicam-13C6 | Meloxicam-13C6 is 13C6-labeled Meloxicam (HY-B0261). Meloxicam is a non-steroidal antiinflammatory agent, inhibits COX activity, with IC50s of 0.49 μM and 36.6 μM for COX-2 and COX-1, respectively. | |||||||||||||||||||||
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Meloxicam | 99.59% | Meloxicam is a non-steroidal antiinflammatory agent that can pass through the blood-brain barrier, inhibits COX activity, with IC50s of 0.49 μM and 36.6 μM for COX-2 and COX-1, respectively. | ||||||||||||||||||||
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