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[Plasmodium chabudi: enzymatic synthesis of dihydropteroate and its inhibition by sulfonamides].

作者信息

Walter R D, Königk E

出版信息

Z Tropenmed Parasitol. 1971 Sep;22(3):256-9.

PMID:5134866
Abstract
摘要

相似文献

1
[Plasmodium chabudi: enzymatic synthesis of dihydropteroate and its inhibition by sulfonamides].[查氏疟原虫:二氢蝶酸的酶促合成及其被磺胺类药物的抑制作用]
Z Tropenmed Parasitol. 1971 Sep;22(3):256-9.
2
The enzymic synthesis of dihydropteroate and dihydrofolate by Plasmodium berghei.伯氏疟原虫对二氢蝶酸和二氢叶酸的酶促合成。
J Protozool. 1973 Aug;20(3):459-64. doi: 10.1111/j.1550-7408.1973.tb00926.x.
3
Effect of methylation inhibitors on fermentations of S. lincolnensis. Production of N-demethyllincomycin.甲基化抑制剂对林肯链霉菌发酵的影响。N-去甲基林可霉素的产生。
J Antibiot (Tokyo). 1973 Aug;26(8):429-36. doi: 10.7164/antibiotics.26.429.
4
Relation between structure of sulphonamides and inhibition of H2-pteroate synthesis in Escherichia coli.磺胺类药物的结构与大肠杆菌中H2-蝶酸合成抑制之间的关系。
J Pharm Pharmacol. 1974 Apr;26(4):228-34. doi: 10.1111/j.2042-7158.1974.tb09263.x.
5
The enzymatic synthesis of dihydrofolate and dihydropteroate in cell-free preparations from wild-type and sulfonamide-resistant pneumococcus.野生型和磺胺耐药性肺炎球菌无细胞制剂中二氢叶酸和二氢蝶酸的酶促合成。
Biochemistry. 1966 Jan;5(1):67-74. doi: 10.1021/bi00865a010.
6
Inhibition by sulfonamides of the biosynthesis of folic acid.
Int J Lepr Other Mycobact Dis. 1967 Oct-Dec;35(4):580-9.
7
Antagonism of colistin-sulphonamide synergism by para-aminobenzoic acid.对氨基苯甲酸对黏菌素-磺胺协同作用的拮抗作用。
Nature. 1966 Mar 26;209(5030):1357. doi: 10.1038/2091357a0.
8
[Aspects of mitotic pathology due to sulfonamides].[磺胺类药物导致的有丝分裂病理学方面]
G Ital Chemioter. 1972 Jul;19(3):57-62.
9
Sulfonamide structure-activity relationships in a cell-free system. 2. Proof for the formation of a sulfonamide-containing folate analog.无细胞体系中的磺胺类构效关系。2. 含磺胺类叶酸类似物形成的证据。
J Med Chem. 1974 Jan;17(1):23-8. doi: 10.1021/jm00247a006.
10
Synthesis of omega-(4-aminophenylsulfonamido)alkyl disulfides and thiosulfates and their activity against dihydropteroate synthetase from sulfanilamide-resistant Neisseria gonorrhoeae.
J Pharm Sci. 1982 Jul;71(7):799-802. doi: 10.1002/jps.2600710720.

引用本文的文献

1
Active case detection, treatment of falciparum malaria with combined chloroquine and sulphadoxine/pyrimethamine and vivax malaria with chloroquine and molecular markers of anti-malarial resistance in the Republic of Vanuatu.瓦努阿图共和国的活动性病例检测、采用氯喹和磺胺多辛/乙胺嘧啶联合治疗恶性疟和氯喹治疗间日疟以及抗疟药物耐药性的分子标记物。
Malar J. 2010 Apr 6;9:89. doi: 10.1186/1475-2875-9-89.
2
Sulfadoxine resistance in Plasmodium vivax is associated with a specific amino acid in dihydropteroate synthase at the putative sulfadoxine-binding site.间日疟原虫对磺胺多辛的耐药性与二氢蝶酸合酶中假定的磺胺多辛结合位点处的一种特定氨基酸有关。
Antimicrob Agents Chemother. 2004 Jun;48(6):2214-22. doi: 10.1128/AAC.48.6.2214-2222.2004.
3
Cultivation techniques for the erythrocytic stages of malaria parasites.
疟原虫红细胞内期的培养技术
Bull World Health Organ. 1972;47(3):357-73.
4
[Culture technics applicable to erythrocyte stages of paludism parasites].[适用于疟原虫红细胞期的培养技术]
Bull World Health Organ. 1973;48(3):355-72.
5
Biochemistry of Plasmodium (malarial parasites).疟原虫(疟疾病原体)的生物化学
Microbiol Rev. 1979 Dec;43(4):453-95. doi: 10.1128/mr.43.4.453-495.1979.