Oxepinac
CAS No. 55689-65-1
Oxepinac( —— )
Catalog No. M35997 CAS No. 55689-65-1
oxepinac is an effective and well-tolerated compound for the treatment of painful osteoarthritis. oxepinac has no teratogenic effect on mouse and rabbit fetuses in animal experiments.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 235 | In Stock |
|
| 10MG | 335 | In Stock |
|
| 25MG | 511 | In Stock |
|
| 50MG | 671 | In Stock |
|
| 100MG | 905 | In Stock |
|
| 200MG | 1218 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameOxepinac
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NoteResearch use only, not for human use.
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Brief Descriptionoxepinac is an effective and well-tolerated compound for the treatment of painful osteoarthritis. oxepinac has no teratogenic effect on mouse and rabbit fetuses in animal experiments.
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Descriptionoxepinac is an effective and well-tolerated compound for the treatment of painful osteoarthritis. oxepinac has no teratogenic effect on mouse and rabbit fetuses in animal experiments.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number55689-65-1
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Formula Weight268.26
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Molecular FormulaC16H12O4
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Purity>98% (HPLC)
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Solubility——
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SMILESO=C1C=2C(=CC(CC(O)=O)=CC2)OCC=3C1=CC=CC3
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Dehydrozingerone
Dehydrozingerone is a naturally occurring molecule. Dehydrozingerone is a versatile compound that has been extensively studied for its various biochemical and physiological effects.
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Caspase 1 Substrate ...
Ac-YVAD-AMC is an inhibitor for caspase. Ac-YVAD-AMC inhibits bacteria-induced cell death of hypersensitive response (HR) cells.
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Pyrocatechol
Pyrocatechol its sulfonic acid is often present in the urine of many mammals. Small amounts of catechol occur naturally in fruits and vegetables along with the enzyme polyphenol oxidase. Upon mixing the enzyme with the substrate and exposure to oxygen (as when a potato or apple is cut) the colorless catechol oxidizes to reddish-brown benzoquinone derivatives.
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