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Obeldesivir is an antiviral nucleoside analog and a prodrug form of GS-441524 (Cay-30469). It inhibits the replication of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and SARS-CoV-2 ?eta, Gamma, or Omicron variants in infected Vero E6 cells (EC50s = 1.36, 1.127, 0.349, and 0.106 µM, respectively) with a 50% cytotoxicity concentration (CC50) value of 128 µM. Obeldesivir (250 or 500 mg/kg per day) reduces nucleocapsid guide RNA (gRNA) copy number and small-guide RNA (sgRNA) levels in the lungs of, and decreases lung damage in, a KI-hACE2 mouse model of SARS-CoV-2 infection. It reduces the levels of the spike glycoprotein (S protein), also known as the surface glycoprotein, in the lungs of, as well as decreases particle forming units (PFUs) in the lung tissues, reduces lung and spleen inflammation, and prevents viral infection-induced death in, a K18-hACE2 mouse model of SARS-CoV-2 infection when administered at doses of 100 or 250 mg/kg per day.Formal Name: 2-C-(4-aminopyrrolo[2,1-f][1,2,4]triazin-7-yl)-2,5-anhydro-D-altrononitrile, 6-(2-methylpropanoate). CAS Number: 2647441-36-7. Synonyms: ATV006, GS-5245. Molecular Formula: C16H19N5O5. Formula Weight: 361.4. Purity: >98%. Formulation: (Request formulation change), A solid. Solubility: DMSO: Soluble, Methanol: Slightly Soluble, Water: Slightly Soluble. SMILES: N#C[C@@]1(C2=CC=C3N2N=CN=C3N)O[C@@H]([C@H]([C@H]1O)O)COC(C(C)C)=O. InChi Code: InChI=1S/C16H19N5O5/c1-8(2)15(24)25-5-10-12(22)13(23)16(6-17,26-10)11-4-3-9-14(18)19-7-20-21(9)11/h3-4,7-8,10,12-13,22-23H,5H2,1-2H3,(H2,18,19,20)/t10-,12-,13-,16+/m1/s1. InChi Key: YIHPGVCWGSURHO-VSBTWAGUSA-N.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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