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 |
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| 10MG | ¥2356 | 有现货 |
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| 25MG | ¥3934 | 有现货 |
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| 50MG | ¥5468 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥1729 | 有现货 |
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生物学信息
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产品名称Pafuramidine
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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
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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。
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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.
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体外实验——
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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.
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同义词——
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通路Microbiology/Virology
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靶点Parasite
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受体Parasite | Antibiotic
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研究领域——
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适应症——
化学信息
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CAS Number186953-56-0
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分子量364.4
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分子式C20H20N4O3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 33.33 mg/mL (91.47 mM; 超声助溶 )
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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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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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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