Zaltoprofen
CAS No. 74711-43-6
Zaltoprofen( CN 100 | Soleton )
Catalog No. M15848 CAS No. 74711-43-6
Zaltoprofen is an inhibitor of Cox-1 and Cox-2 for treatment of arthritis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 35 | In Stock |
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| 10MG | 32 | In Stock |
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| 25MG | 50 | In Stock |
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| 50MG | 63 | In Stock |
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| 100MG | 86 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 183 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameZaltoprofen
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NoteResearch use only, not for human use.
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Brief DescriptionZaltoprofen is an inhibitor of Cox-1 and Cox-2 for treatment of arthritis.
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DescriptionZaltoprofen is an inhibitor of Cox-1 and Cox-2 for treatment of arthritis.(In Vitro):Zaltoprofen (0.1-10 μM; 15 min) inhibits thromboxane B2 production in human platelets in a dose-dependent manner.Zaltoprofen (0.01-1 μM; 30 min) inhibits prostaglandin E2 production by interleukin-1β-stimulated synovial cells.Zaltoprofen (0.1-1 μM; 5 min) inhibits the bradykinin-induced increase of [Ca2+]i in DRG cells.(In Vivo):Zaltoprofen (5-20 mg/kg; a single p.o.) inhibits bradykinin-induced nociceptive responses in rats.Zaltoprofen (3-30 mg/kg; a single p.o.) inhibits the acetic acid-induced writhing response of mice in a dose-dependent manner.
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In VitroZaltoprofen (0.1-10 μM; 15 min) inhibits thromboxane B2 production in human platelets in a dose-dependent manner.Zaltoprofen (0.01-1 μM; 30 min) inhibits prostaglandin E2 production by interleukin-1β-stimulated synovial cells.Zaltoprofen (0.1-1 μM; 5 min) inhibits the bradykinin-induced increase of [Ca2+]i in DRG cells.
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In VivoZaltoprofen (5-20 mg/kg; a single p.o.) inhibits bradykinin-induced nociceptive responses in rats.Zaltoprofen (3-30 mg/kg; a single p.o.) inhibits the acetic acid-induced writhing response of mice in a dose-dependent manner. Animal Model:Eight-week-old male Wistar rats were injected Bradykinin every 15 min Dosage:5, 10, 20 mg/kg Administration:A single p.o.Result:Inhibited bradykinin-induced nociceptive responses, with an ED50 of 9.7 mg/kg.The duration of analgesic effect was 60-90 min.
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SynonymsCN 100 | Soleton
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PathwayChromatin/Epigenetic
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TargetCOX
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RecptorCOX-1| COX-2
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number74711-43-6
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Formula Weight298.36
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Molecular FormulaC17H14O3S
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Purity>98% (HPLC)
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SolubilityEthanol: 31 mg/mL (103.9 mM); DMSO: 60 mg/mL (201.09 mM)
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SMILESO=C(O)C(C)C1=CC=C(C(C2)=C1)SC3=CC=CC=C3C2=O
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Chemical Name10,11-Dihydro-alpha-methyl-10-oxodibenzo(b,f)thiepin-2-acetic acid
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Tang HB, et al. Neuropharmacology, 2005, 48(7), 1035-1042.
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