- Velpatasvir
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- $0.00 / 100mg
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2025-02-13
- CAS:377049-84-7
- Min. Order: 10mg
- Purity: 95
- Supply Ability: 100000
- Velpatasvir
-
- $0.00 / 100g
-
2025-02-12
- CAS:1377049-84-7
- Min. Order: 1g
- Purity: 98%-102%
- Supply Ability: 10 KGS
- Velpatasvir
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- $100.00 / 25kg
-
2025-02-12
- CAS:1377049-84-7
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 50000KG/month
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| Velpatasvir Basic information |
Product Name: | Velpatasvir | Synonyms: | Velpatasvir;velpatasvir(GS-5816);methyl ((2s)-1-((2s,5s)-2-(9-(2-((2s,4s)-1-((2r)-2-((methoxycarbonyl)amino)-2-phenylacetyl)-4-(methoxymethyl)pyrrolidin-2-yl)-1h-imidazol-5-yl)-1,11-dihydroisochromeno(4',3':6,7)naphtho(1,2-d)imidazol-2-yl)-5-methylpyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl)carbamate;Velpatasvir API;Unifiram (DM-232);Methyl [(2S)-1-[(2S,5S)-2-[9-[2-[(2S,4S)-1-[(2R)-2-[(methoxycarbonyl)amino]-2-phenylacetyl]-4-(methoxymethyl)pyrrolidin-2-yl]-1H-imidazol-5-yl]-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl]-5-methylpyrrolidin-1-yl]-3-methyl-1-oxobutan-2-y;MFCD28411371;Product:Velpatasvir | CAS: | 1377049-84-7 | MF: | C49H54N8O8 | MW: | 883 | EINECS: | 1592732-453-0 | Product Categories: | 1377049-84-7 | Mol File: | 1377049-84-7.mol |  |
| Velpatasvir Chemical Properties |
Melting point | >170oC (dec.) | density | 1.314±0.06 g/cm3(Predicted) | storage temp. | -20°C | solubility | Soluble in DMSO (>25 mg/ml) | form | solid | pka | 10.75±0.46(Predicted) | color | Pale yellow | Stability: | Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months. |
| Velpatasvir Usage And Synthesis |
Description | Velpatasvir (1377049-84-7) is an extremely potent pan-genotypic hepatitis C virus (HCV) NS5A inhibitor.1 It is a component of Epclusa? and Vosevi?, two clinically useful medications with 98% and 97%, respectively, cure rates for HCV.? It displayed EC50’s for GTs 1-4, 6a ranging from 6-16 pM, GT5a at 75 pM, and GT6e at 130 pM. Velpatasvir also displayed an excellent barrier to viral resistance. It has been shown in silico, that velpatasvir binds to the SARS-CoV-2 spike protein and may be a potential therapeutic.2 | Uses | Velpatasvir is a NS5A inhibitor in patients with hepatitis C (HCV) infection. | Definition | ChEBI: Velpatasvir is a complex organic heteropentacyclic compound that is a hepatitis C virus nonstructural protein 5A inhibitor used in combination with sofosbuvir (under the brand name Epclusa) for treatment of patients with chronic hepatitis C of all six major genotypes. It has a role as an antiviral drug and a hepatitis C virus nonstructural protein 5A inhibitor. It is an organic heteropentacyclic compound, a N-acylpyrrolidine, a L-valine derivative, a carbamate ester, a member of imidazoles, a ring assembly and an ether. | Brand name | Epclusa, Sofosvel, Velpanat (all in combination with sofosbuvir) | References | Link et al. (2019), Discovery of velpatasvir (GS-5816): A potent pan-genotypic HCV NS5A inhibitor in the single-tablet regimens Vosevi? and Epclusa?; Bioorg. Med. Chem. Lett., 29 2415
Kadioglu et al. (2020), Identification of novel compounds against three targets of SARS CoV-2 coronavirus by combined virtual screening and supervised machine learning; Comput. Biol. Med. 133 104359 |
| Velpatasvir Preparation Products And Raw materials |
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