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9L09

SARS-CoV-2 C-RTC with 13-TP

これはPDB形式変換不可エントリーです。
9L09 の概要
エントリーDOI10.2210/pdb9l09/pdb
EMDBエントリー62692
分子名称RNA-directed RNA polymerase nsp12, Non-structural protein 8, Non-structural protein 7, ... (8 entities in total)
機能のキーワードsars-cov-2 c-rtc, viral protein/rna, viral protein-rna complex
由来する生物種Severe acute respiratory syndrome coronavirus 2
詳細
タンパク質・核酸の鎖数6
化学式量合計167022.57
構造登録者
Huang, Y.C.,Liang, L.,Liu, Y.X.,Yan, L.M.,Lou, Z.Y.,Rao, Z.H. (登録日: 2024-12-12, 公開日: 2025-03-19, 最終更新日: 2025-03-26)
主引用文献Liang, L.,Meng, Y.,Chang, X.,Li, E.,Huang, Y.,Yan, L.,Lou, Z.,Peng, Y.,Zhu, B.,Yu, W.,Chang, J.
Discovery of a 2'-a-Fluoro-2'-b-C-(fluoromethyl) Purine Nucleotide Prodrug as a Potential Oral Anti-SARS-CoV-2 Agent
J Med Chem, 68:1994-2007, 2025
Cited by
PubMed Abstract: A novel 2'-α-fluoro-2'-β--(fluoromethyl) purine nucleoside phosphoramidate prodrug has been designed and synthesized to treat SARS-CoV-2 infection. The SARS-CoV-2 central replication transcription complex (C-RTC, nsp12-nsp7-nsp8) catalyzed in vitro RNA synthesis was effectively inhibited by the corresponding bioactive nucleoside triphosphate (). The cryo-electron microscopy structure of the C-RTC: complex was also determined. Compound exhibited potent in vitro antiviral activity against the SARS-CoV-2 20SF107 strain (EC = 0.56 ± 0.06 μM) and the Omicron BA.5 variant (EC = 0.96 ± 0.23 μM) with low cytotoxicity. Furthermore, it was well tolerated in rats at doses of up to 2000 mg/kg, and a single oral dose of this prodrug at 40 mg/kg led to high levels of in the target organ lungs of rats with a long half-life. These findings support the further development of compound as an orally available antiviral agent for the treatment of SARS-CoV-2 infection.
PubMed: 39804580
DOI: 10.1021/acs.jmedchem.4c02769
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.9 Å)
構造検証レポート
Validation report summary of 9l09
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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