(Rac)-Modipafant
CAS No. 122956-68-7
(Rac)-Modipafant( —— )
Catalog No. M34339 CAS No. 122956-68-7
(Rac)-Modipafantis an orally available and selective platelet-activating factor receptor (PAFR) antagonist that inhibits PAF-induced aggregation of washed platelets in rabbits, and can be used to study arthritis and ischemia/reperfusion (I/R) in the superior mesenteric artery (SMA) of the rat.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 521 | In Stock |
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| 10MG | 752 | In Stock |
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| 25MG | 1159 | In Stock |
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| 50MG | 2213 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name(Rac)-Modipafant
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NoteResearch use only, not for human use.
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Brief Description(Rac)-Modipafantis an orally available and selective platelet-activating factor receptor (PAFR) antagonist that inhibits PAF-induced aggregation of washed platelets in rabbits, and can be used to study arthritis and ischemia/reperfusion (I/R) in the superior mesenteric artery (SMA) of the rat.
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Description(Rac)-Modipafant (UK-74505) is an orally active, selective, long-acting irreversible platelet activating factor receptor (PAFR) antagonist. (Rac)-Modipafant prevents dengue infection.
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In Vitro——
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In Vivo(Rac)-Modipafant (UK-74505) (10 mg/kg; p.o.; twice a day until day 10) prevents Severe Dengue Infection.(Rac)-Modipafant exhibits highly selective, time-dependent inhibition of PAF-induced aggregation of rabbit washed platelets (IC50=26.3 and 1.12 nM after 0.25 and 60 min preincubation, respectively).(Rac)-Modipafant (5-20 mg/kg; p.o.) dose-dependently inhibits the Zymosan -induced articular hyperalgesia.Animal Model:8- to 10-week-old BALB/c mice (DEN-2 strain infected) Dosage:10 mg/kg Administration:P.o.; twice a day (started on days 0, 3, 5, or 7) until day 10 Result:Decreased by approximately 50% the lethality associated with DEN-2 infection.Animal Model:Male BALB/C (8- to 10- week-old) wild-type mice Dosage:5, 10 and 20 mg/kg Administration:P.o.Result:Dose-dependently inhibited the Zymosan -induced articular hyperalgesia.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorPAFR
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Research Area——
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Indication——
Chemical Information
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CAS Number122956-68-7
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Formula Weight605.09
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Molecular FormulaC34H29ClN6O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (82.63 mM; Ultrasonic )
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SMILESO=C(OCC)C1=C(NC(=C(C(=O)NC2=NC=CC=C2)C1C=3C=CC=CC3Cl)C)C=4C=CC(=CC4)N5C(=NC=6C=NC=CC65)C
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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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CRAC intermediate 2
CRAC intermediate 2 is a intermediate compound for CRAC inhibitor synthesis.
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G250.A2
G250.A2
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Cltrinin
Citrinin (NSC 186) is a mycotoxin that causes food contamination and has different toxic effects. Citrinin is an effective oral anticancer agent. Citrinin has various regulatory effects on mouse immune system, including regulating the number of immune cells, inducing apoptosis and autophagy of immune cells, altering toll-like receptor expression and cytokine production. Citrinin can induce oxidative stress and lead to early apoptosis of oocytes. Low doses of Citrinin have neuroprotective effects against glutamate-induced excitotoxicity in rat cortical neurons. In addition, Citrinin also has antibacterial activity.
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