1. Signaling Pathways
  2. Metabolic Enzyme/Protease
  3. Aminoacyl-tRNA Synthetase

Aminoacyl-tRNA Synthetase (氨酰-tRNA合成酶)

tRNA Synthetase, aaRS

Aminoacyl-tRNA synthetases (AARSs) are the enzymes that catalyze the aminoacylation reaction by covalently linking an amino acid to its cognate tRNA in the first step of protein translation. In mammals, AARSs usually exist in free form or in the form of a multi-tRNA synthetase complex (MSC), and the latter consists of eight AARSs and three non-enzymatic AARS-interacting multi-functional proteins (AIMP1/p43, AIMP2/p38, and AIMP3/p18).

AARSs are responsible for the proper pairing of codons on mRNA with amino acids. AARSs are also involved in RNA splicing, transcriptional regulation, translation, and other aspects of cellular homeostasis. Study of these enzymes is of great interest to the researchers due to its pivotal role in the growth and survival of an organism. AARSs are one of the leading targets for developing novel anti-infective agents. Further, unfolding the interesting structural and functional aspects of these enzymes in the last few years has qualified them as a potential drug target against various diseases.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-147674
    Isoleucyl tRNA synthetase-IN-2 Inhibitor
    Isoleucyl tRNA synthetase-IN-2 (化合物 36a) 是一种有效、选择性的靶向异亮基 tRNA 合成酶 (IleRS) 的抑制剂,其 Ki,app 值为 114 nM。
    Isoleucyl tRNA synthetase-IN-2
  • HY-161800
    Aminoacyl tRNA synthetase-IN-3 Inhibitor
    Aminoacyl tRNA synthetase-IN-3 (compound 36K3) 是一种针对 Plasmodium falciparum (疟原虫) 的赖氨酸 tRNA 合成酶 (PfLysRS) 的抑制剂 (IC50=59.2 nM),通过占据 PfLysRS 的 ATP 结合位点和 L-赖氨酸结合位点,从而抑制 PfLysRS 的活性。Aminoacyl tRNA synthetase-IN-3 可用于抗疟疾药物的开发。
    Aminoacyl tRNA synthetase-IN-3
  • HY-161799
    LysRs-IN-3 Inhibitor
    LysRs-IN-3 (compound 36) 是一种基于 ASP3026 (HY-13326) 的疟原虫 (Plasmodium) 赖氨酸 tRNA 合成酶 (Lysine tRNA synthetase) 的抑制剂,对疟原虫 (特别是恶性疟原虫) 生长的抑制效果比 ASP3026 (HY-13326) 高出七倍以上。LysRs-IN-3 可用于抗疟药物的开发。
    LysRs-IN-3
  • HY-159103
    LeuRS-IN-2 Inhibitor
    LeuRS-IN-2 (Compound 9) 在单磷酸腺苷 (AMP) 存在下是一种 Wolbachia Leucyl-tRNA synthetase (LeuRS) 抑制剂,其 EC50 值为 6 nM,有效抑制致病性宿主的生长。LeuRS-IN-2 形成腺苷加合物,抑制蛋白质合成,有望用于破坏微生物群的新抗菌剂的研究。
    LeuRS-IN-2
  • HY-12479B
    Epetraborole (R-mandelate) Inhibitor
    Epetraborole R-mandelate 是一种新型的亮氨酰-tRNA 合成酶 (LeuRS) 抑制剂 (IC50=0.31 μM),从而抑制蛋白质的合成。Epetraborole R-mandelate 可用于耐多药的革兰氏阴性病原体感染的研究。
    Epetraborole (R-mandelate)
  • HY-161797
    Antibacterial agent 227 Inhibitor
    Antibacterial agent 227 (Compd 29) 是一种 ThrRS (Seryl-tRNA synthetase,丝氨酰-tRNA 合成酶) 抑制剂。 Antibacterial agent 227 对浮游菌和生物膜培养的金黄色葡萄球菌 (Staphylococcus aureus 25923) 的生长具有显著的抑制作用,最低抑菌浓度 (MIC) 为 32 µg/ml。Antibacterial agent 227 有望作为对多药耐药生物膜形成的金黄色葡萄球菌菌株的有效防腐剂。
    Antibacterial agent 227
  • HY-103280
    LysRs-IN-1 Inhibitor 98.64%
    LysRs-IN-1 是赖氨酸-tRNA 合成酶 (LysRs) 的抑制剂。
    LysRs-IN-1
  • HY-108900A
    Leu-AMS R enantiomer
    Leu-AMS R enantiomer 是 Leu-AMS 的 R 对映体。 Leu-AMS 是亮氨酰-tRNA 合成酶 (LRS) 的有效抑制剂并抑制细菌的生长。
    Leu-AMS R enantiomer
目录号 产品名 / 同用名 应用 反应物种