Catalog No. C4898

Fosmidomycin (sodium salt)

(别名:Fosmidomycin sodium salt; 膦胺霉素钠盐)

革兰氏阴性/阳性抗生素

Fosmidomycin (sodium salt)
规格价格货期数量
5mg
¥3258.00
7-15工作日发货
10mg
¥5310.00
7-15工作日发货
25mg
¥11285.00
7-15工作日发货
CAS号:66508-37-0纯度:98.00%
仅用于科研,不用于诊疗。未经明确授权不得转售。
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产品描述

Fosmidomycin is a specific inhibitor of 1-deoxy-d-xylulose 5-phosphate reductoisomerase (DXP) [1]. Fosmidomycin is an antibiotic originally isolated from bacteria of the genus Streptomyces.

1-deoxy-d-xylulose 5-phosphate reductoisomerase is an enzyme that interconverts DXP and 2-C-methyl-D-erythritol 4-phosphate (MEP) [2].

Fosmidomycin was active against both Gram-negative and Gram-positive bacteria and the human malarial parasite P. falciparum with the IC50 of 290-370 nM[3]. Fosmidomycin inhibited 1-deoxy-d-xylulose 5-phosphate reductoisomerase in an alternative nonmevalonate pathway for terpenoid biosynthesis with IC50 of 8.2 nM [1]. Fosmidomycin has been shown to possess activity against Plasmodium falciparum in vitro and in the mouse model. In patients with acute uncomplicated Plasmodium falciparum malaria, oral administration of 1,200 mg fosmidomycin every 8 h for 7 days was effective in curing uncomplicated Plasmodiumfalciparum malaria in humans [4]. Fosmidomycin was an effective and safe antimalarial drug [4]. The treatment was well tolerated and showed a fast parasite and fever clearance [4].

References:
[1] Kuzuyama T, Shimizu T, Takahashi S, et al.  Fosmidomycin, a specific inhibitor of 1-deoxy-D-xylulose 5-phosphate reductoisomerase in the nonmevalonate pathway for terpenoid biosynthesis[J]. Tetrahedron letters, 1998, 39(43): 7913-7916.
[2] Takahashi S, Kuzuyama T, Watanabe H, et al.  A 1-deoxy-D-xylulose 5-phosphate reductoisomerase catalyzing the formation of 2-C-methyl-D-erythritol 4-phosphate in an alternative nonmevalonate pathway for terpenoid biosynthesis[J]. Proceedings of the National Academy of Sciences, 1998, 95(17): 9879-9884.
[3] Jomaa H, Wiesner J, Sanderbrand S, et al.  Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs[J]. Science, 1999, 285(5433): 1573-1576.
[4] Lell B, Ruangweerayut R, Wiesner J, et al.  Fosmidomycin, a novel chemotherapeutic agent for malaria[J]. Antimicrobial agents and chemotherapy, 2003, 47(2): 735-738.

产品性质

物理外观A crystalline solid
CAS号66508-37-0
分子式C4H9NO5P·Na
分子量205.1
小分子别名Fosmidomycin sodium salt
化学名称P-[3-(formylhydroxyamino)propyl]-phosphonic acid, monosodium salt
溶解度≤5mg/ml in PBS, pH 7.2
SMILES[O-]P(CCCN(C=O)O)(O)=O.[Na+]
存储条件-20°C
运输条件蓝冰

产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)

IC50和靶点

生物活性描述磷霉素钠是一种膦酸和抗疟药;对革兰氏阴性菌和革兰氏阳性菌都有活性。

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