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
5MG 235 Get Quote
10MG 357 Get Quote
25MG 578 Get Quote
50MG 812 Get Quote
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Biological Information

  • Product Name
    Pafuramidine
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    Pafuramidine (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.
  • In Vitro
    ——
  • In Vivo
    Pafuramidine (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.
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    Parasite
  • Recptor
    Parasite | Antibiotic
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    186953-56-0
  • Formula Weight
    364.4
  • Molecular Formula
    C20H20N4O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 33.33 mg/mL (91.47 mM; Ultrasonic )
  • SMILES
    N=C(NOC)C=1C=CC(=CC1)C=2OC(=CC2)C=3C=CC(=CC3)C(=N)NOC
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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