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Pafuramidine

CAS No. 186953-56-0

Pafuramidine ( —— )

产品货号. M33450 CAS No. 186953-56-0

Pafuramidine (DB289) 是一种具有口服活性的 Furamidine (HY-110137A) 前体。Pafuramidine 是一种有效的抗寄生虫剂,可用于锥虫病、肺囊虫肺炎和疟疾的研究。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1568 有现货
10MG ¥2356 有现货
25MG ¥3934 有现货
50MG ¥5468 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥1729 有现货

生物学信息

  • 产品名称
    Pafuramidine
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Pafuramidine (DB289) 是一种具有口服活性的 Furamidine (HY-110137A) 前体。Pafuramidine 是一种有效的抗寄生虫剂,可用于锥虫病、肺囊虫肺炎和疟疾的研究。
  • 产品描述
    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.
  • 体外实验
    ——
  • 体内实验
    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.
  • 同义词
    ——
  • 通路
    Microbiology/Virology
  • 靶点
    Parasite
  • 受体
    Parasite | Antibiotic
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    186953-56-0
  • 分子量
    364.4
  • 分子式
    C20H20N4O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO 中的溶解度 : 33.33 mg/mL (91.47 mM; 超声助溶 )
  • SMILES
    N=C(NOC)C=1C=CC(=CC1)C=2OC(=CC2)C=3C=CC(=CC3)C(=N)NOC
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

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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