首页> 外国专利> NOVEL PLASMODIUM FALCIPARUM PROTEASE, ANTIBODIES THEREFOR, PEPTIDE SUBSTRATES SPECIFIC TO SAID PROTEASE, AND THEIR USE AS A MEDICINE AGAINST MALARIA

NOVEL PLASMODIUM FALCIPARUM PROTEASE, ANTIBODIES THEREFOR, PEPTIDE SUBSTRATES SPECIFIC TO SAID PROTEASE, AND THEIR USE AS A MEDICINE AGAINST MALARIA

机译:恶性疟原虫新蛋白酶,其抗体,肽类蛋白酶(特定于所述蛋白酶)及其作为抗疟疾药物的用途

摘要

Utilization as active ingredients in the preparation of a drug against paludism of compounds having formula (I): R1-P1-P2-R2, wherein P1 is in particular a peptidic rest selected amongst TLG, IVG, VLG and SG, or N-methylated analogs thereof or having a D configuration, R1 is particularly H, a protection group for the N-terminal group, or a hydrosolubilizing group, P2 is for example a rest of lysin or arginine, or R2 is particularly -OH, -CH2Cl, the rest of an aliphatic amine, or the rest of an aminated antipaludic drug, it being understood that in the compounds of formula (I), the peptidic bond between at least two acids of the rest P1 and/or between P1 and P2, and/or optionnaly between P1 et R1 and/or between P2 et R2 may be replaced by a pseudo-peptidic bond.
机译:在制备具有式(I)的化合物的paludism的药物中用作活性成分:R1-P1-P2-R2,其中P1特别是选自TLG,IVG,VLG和SG的肽残基,或N-甲基化或其类似物或具有D构型,R1特别是H,N端基的保护基团或加氢基团,P2是例如其余的赖氨酸或精氨酸,或R2特别是-OH,-CH2Cl,其余的脂族胺或其余的胺化抗paludicic药物,应理解在式(I)的化合物中,其余P1的至少两个酸之间和/或P1和P2之间的肽键,和/或者在P1与R1之间和/或在P2与R2之间可以被伪肽键取代。

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