Pafuramidine
CAS No. 186953-56-0
Pafuramidine( —— )
Catalog No. M33450 CAS No. 186953-56-0
Pafuramidine (DB289) is an experimental prodrug of the orally active metabolite DB75, a potent antiparasitic compound with anti-malarial activity used in the study of parasitic infections and sleeping sickness.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 149 | Get Quote |
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| 5MG | 235 | Get Quote |
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| 10MG | 357 | Get Quote |
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| 25MG | 578 | Get Quote |
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| 50MG | 812 | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NamePafuramidine
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NoteResearch use only, not for human use.
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Brief DescriptionPafuramidine (DB289) is an experimental prodrug of the orally active metabolite DB75, a potent antiparasitic compound with anti-malarial activity used in the study of parasitic infections and sleeping sickness.
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DescriptionPafuramidine (DB289) is an orally active proagent of Furamidine (HY-110137A). Pafuramidine is a potent anti-parasitic agent, can be used to research trypanosomiasis, Pneumocystis pneumonia and malaria.
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In Vitro——
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In VivoPafuramidine (1-10 mg/kg; p.o.; for 5 or 10 days) cures some trypanosomes-infected monkeys.Pafuramidine (2.5-100 mg/kg; p.o.; for 4 or 5 days) cures some Trypanosoma brucei-infected mice.Animal Model:Vervet monkeys (infected by intravenous injection of 104 trypanosomes) Dosage:1, 3, and 10 mg/kg (group 1/2/3); 10 mg/kg (group 4/5)Administration:p.o.; 5 consecutive days for group 1/2/3 (started on the 7th day postinfection); 10 days for group 4 (started on the 14th day postinfection); 10 days for group 5 (started on the 28th day postinfection). Post-treatment monitoring was maintained for a period of 180 days.Result:Cured all three monkeys in group 3 at 10 mg/kg, and did not recur during the monitoring period.All three monkeys in group 4 became aparasitemic by day 5 of dosing, but only two of three monkeys remained free of blood parasites until 180 days post-treatment monitoring.All three monkeys in group 5 became aparasitemic by day 4 of dosing, but only two of three of monkeys remained free of blood trypanosomes by the end of the 180 days of post-treatment monitoring.Animal Model:Female NMRI mice (infected intraperitoneally with 2 × 104 STIB900 bloodstream forms) Dosage:2.5, 5, 25 and 50 mg/kg Administration:p.o.; for 4 days (started on the 4th day postinfection) Result:Cured all four mice at 25 and 50 mg/kg.Animal Model:Female NMRI mice (infected intraperitoneally with 2 × 104 GVR35 bloodstream forms) Dosage:25, 50 and 100 mg/kg Administration:p.o.; for 5 days (started on the 21st day postinfection) Result:Showed good CNS activity in the GVR35 CNS model, with 3/5 mice cured at 100 mg/kg.
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Synonyms——
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PathwayMicrobiology/Virology
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TargetParasite
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RecptorParasite | Antibiotic
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Research Area——
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Indication——
Chemical Information
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CAS Number186953-56-0
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Formula Weight364.4
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Molecular FormulaC20H20N4O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 33.33 mg/mL (91.47 mM; Ultrasonic )
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SMILESN=C(NOC)C=1C=CC(=CC1)C=2OC(=CC2)C=3C=CC(=CC3)C(=N)NOC
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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
1. Mdachi RE, et al. Efficacy of the novel diamidine compound 2,5-Bis(4-amidinophenyl)- furan-bis-O-Methlylamidoxime (Pafuramidine, DB289) against Trypanosoma brucei rhodesiense infection in vervet monkeys after oral administration. Antimicrob Agents Chemother. 2009 Mar;53(3):953-7.?
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