(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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Silybin B
Silybin B is an effective inhibitor of raloxifene 4 '- and 6-glucosalylation, an effective anti-fibrinogenic and anti-oligomeric component of Silymarin, with free radical scavenging activity of 1, 1-diphenyl-2-pyridinyl hydrazine (DPPH), and a protective effect against cisplatin-induced neurotoxicity by alleviating DNA damage and apoptosis.
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pTH (28-48) (human)
pTH (28-48) (human) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development.
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DEAC, SE
DEAC, SE can be used for relevant research in the field of life sciences. Its product number is T64949 and CAS number is 139346-57-9.
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