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| Product | Description | |
|---|---|---|
| Baloxavir marboxil | Baloxavir marboxil (S-033188) is a selective inhibitor of influenza cap-dependent endonuclease. Baloxavir marboxil, a potent antiviral agent, shows activity against influenza A and B virus [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S-033188; RG 6152. CAS No. 1985606-14-1. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg. Product ID: HY-109025. |  |
| 7,8-Difluoro-6,11-dihydrodibenzo[b,e]thiepin-11-ol | 7,8-Difluoro-6,11-dihydrodibenzo[b,e]thiepin-11-ol is an impurity of Baloxavir Marboxil which is an inhibitor of the cap-dependent endonuclease of influenza A and B viruses. Synonyms: 12,13-difluoro-9-thiatricyclo[9.4.0.0(3),?]pentadeca-1(11),3(8),4,6,12,14-hexaen-2-ol; Zofluza intermediate; Baloxavir Marboxil Impurity 7. CAS No. 1985607-83-7. Molecular formula: C14H10F2OS. Mole weight: 264.29. |  |
| Baloxavir | Baloxavir (Baloxavir acid), derived from the proagent Baloxavir marboxil, is a first-in-class, potent and selective cap-dependent endonuclease (CEN) inhibitor within the polymerase PA subunit of influenza A and B viruses. Baloxavir inhibits viral RNA transcription and replication and has potently antiviral activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Baloxavir acid; S-033447. CAS No. 1985605-59-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109025A. | |
| Baloxavir-[d4] | Baloxavir-[d4] is an isotope compound of Baloxavir. Baloxavir marboxil is a first-in-class, one-dose oral medicine with a novel proposed mechanism of action that has demonstrated efficacy in a wide range of influenza viruses, including in vitro activity against oseltamivir-resistant strains and avian strains (H7N9, H5N1) in non-clinical studies. Baloxavir is a polymerase acidic, cap-dependent, endonuclease inhibitor that is indicated for the treatment of acute uncomplicated influenza in patients aged 12 years and older who have been symptomatic for no more than 48 hours. It blocks viral proliferation by binding to one of two endonuclease binding sites, inhibiting the initiation of mRNA synthesis for both influenza A and influenza B strains. Baloxavir can interact with polyvalent cation-containing products, which can decrease its plasma concentration. CAS No. 2415027-80-2. Molecular formula: C24H15D4F2N3O4S. Mole weight: 487.51. | |
| (R)-7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione | (R)-7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione is an impurity of Baloxavir Marboxil which is an inhibitor of the cap-dependent endonuclease of influenza A and B viruses. Synonyms: (12aR)-3,4,12,12a-Tetrahydro-7-(phenylmethoxy)-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione. CAS No. 1985607-70-2. Molecular formula: C17H17N3O4. Mole weight: 327.33. | |
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