表脸
发表于 2025-3-27 00:17:38
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变白
发表于 2025-3-27 03:10:51
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骚动
发表于 2025-3-27 07:51:43
Onyeka Obioha,Candrice Heath,Pearl E. Grimestimalarial drugs, efficiencies, and challenges. Many parasites depend on kinases for various physiological activities, and these enzymes are easily targeted with drugs provided. By virtue of strong conserved nature of all binding sites from ATP molecules, it is difficult to find Plasmodium kinase in
sacrum
发表于 2025-3-27 13:08:17
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relieve
发表于 2025-3-27 14:18:27
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机密
发表于 2025-3-27 19:29:00
different classes of proteasome inhibitors developed including β-lactones, peptide aldehydes, α′β′ epoxyketone, asparagine ethylene diamines, peptide sulphonyl fluorides, peptide boronates, and cyclic peptides. This chapter also highlights how the proteasome inhibitors are validated through in vitr
越自我
发表于 2025-3-28 01:05:13
acuole, hemoglobin is destroyed progressively by a variety of proteases such as aspartic proteases, cysteine proteases, metalloproteases, and aminopeptidases. As a result, the parasite uses hemoglobin as a supply of amino acids. In this chapter, we will go over the vital role of the food vacuole and
Budget
发表于 2025-3-28 05:15:16
Drug Targets for Plasmodium Falciparum: Historic to Future Perspectives
concise
发表于 2025-3-28 07:41:21
Drug Targets for Plasmodium Falciparum: Historic to Future Perspectives978-981-19-4484-0
恭维
发表于 2025-3-28 12:41:54
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