solo para uso en investigación
Cat. No.S6814
| Dianas relacionadas | Integrase Bacterial Antibiotics Anti-infection Fungal COVID-19 Parasite Reverse Transcriptase HIV HCV Protease |
|---|---|
| Otros Antiviral Inhibidores | Moroxydine HCl Aloperine Oleanolic Acid Harringtonine NGI-1 U18666A Aloin B Saikosaponin B2 Lapachol DTNB |
| Líneas celulares | Tipo de ensayo | Concentración | Tiempo de incubación | Formulación | Descripción de la actividad | PMID |
|---|---|---|---|---|---|---|
| HuH7 | Function assay | 10 uM | 24 hrs | Cmax in human HuH7 cells assessed as triphosphate concentration per million cells at 10 uM incubated for 24 hrs measured after washout by LC-MS analysis, Cmax=0.0000176μM | 22446091 | |
| Vero | Antiviral assay | 24 hrs | Antiviral activity against Parainfluenza 3 C 243 infected in african green monkey Vero cells assessed as inhibition of virus induced cytopathic effect after 24 hrs by MTS assay, EC50=1.71μM | 22446091 | ||
| Vero | Antiviral assay | 24 hrs | Antiviral activity against SARS coronavirus Toronto-2 infected in african green monkey Vero cells assessed as inhibition of virus induced cytopathic effect after 24 hrs by MTS assay, EC50=2.24μM | 22446091 | ||
| HuH7 | Antiviral assay | 24 hrs | Antiviral activity against Hepatitis C virus genotype 1b infected in human HuH7 cells assessed as inhibition of virus induced cytopathic effect after 24 hrs by MTS assay, EC50=4.1μM | 22446091 | ||
| Vero E6 | Antiviral assay | 24 hrs | Antiviral activity against Dengue virus type 2 New Guinea C infected in african green monkey Vero E6 cells assessed as inhibition of virus induced cytopathic effect after 24 hrs by MTS assay, EC50=9.46μM | 22446091 | ||
| HeLa | Antiviral assay | 24 hrs | Antiviral activity against Yellow fever virus 17D infected in human HeLa cells assessed as inhibition of virus induced cytopathic effect after 24 hrs by MTS assay, EC50=11μM | 22446091 | ||
| MDCK | Antiviral assay | 24 hrs | Antiviral activity against Influenza A virus H3N2 infected in MDCK cells assessed as inhibition of virus induced cytopathic effect after 24 hrs by MTS assay, EC50=27.9μM | 22446091 | ||
| Hep2 | Antiviral assay | 4 days | Antiviral activity against Respiratory syncytial virus A2 infected in human Hep2 cells assessed as reduction of virus-induced cytopathic effect after 4 days by Cell-Titer Glo assay, EC50=0.53μM | 28124907 | ||
| HMVEC | Antiviral assay | 3 to 4 days | Antiviral activity against GFP-fused Ebolavirus infected in TERT-immortalized HMVEC assessed as reduction in viral replication preincubated with cells followed by viral infection measured after 3 to 4 days by fluorescence assay, EC50=0.78μM | 28124907 | ||
| HuH7 | Antiviral assay | 3 days | Antiviral activity against Hepatitis C virus genotype 1b infected in human HuH7 cells preincubated with cells for 3 days followed by viral infection by luciferase assay, EC50=4.1μM | 28124907 | ||
| HuH7 | Antiviral assay | 3 days | Antiviral activity against Ebolavirus infected in human HuH7 cells after 3 days by end point dilution assay, EC50=1.5μM | 28792763 | ||
| Haga clic para ver más datos experimentales de líneas celulares | ||||||
| Peso molecular | 291.26 | Fórmula | C12H13N5O4 |
Almacenamiento (Desde la fecha de recepción) | 3 years -20°C powder |
|---|---|---|---|---|---|
| Nº CAS | 1191237-69-0 | -- | Almacenamiento de soluciones madre |
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| Sinónimos | N/A | Smiles | C1=C2C(=NC=NN2C(=C1)C3(C(C(C(O3)CO)O)O)C#N)N | ||
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In vitro |
DMSO
: 58 mg/mL
(199.13 mM)
Water : Insoluble Ethanol : Insoluble |
|
In vivo |
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Paso 1: Introduzca la información a continuación (Recomendado: Un animal adicional para tener en cuenta la pérdida durante el experimento)
Paso 2: Introduzca la formulación in vivo (Esto es solo la calculadora, no la formulación. Por favor, contáctenos primero si no hay una formulación in vivo en la sección de Solubilidad.)
Resultados del cálculo:
Concentración de trabajo: mg/ml;
Método para preparar el líquido maestro de DMSO: mg fármaco predissuelto en μL DMSO ( Concentración del líquido maestro mg/mL, Por favor, contáctenos primero si la concentración excede la solubilidad del DMSO del lote del fármaco. )
Método para preparar la formulación in vivo: Tomar μL DMSO líquido maestro, luego añadirμL PEG300, mezclar y clarificar, luego añadirμL Tween 80, mezclar y clarificar, luego añadir μL ddH2O, mezclar y clarificar.
Método para preparar la formulación in vivo: Tomar μL DMSO líquido maestro, luego añadir μL Aceite de maíz, mezclar y clarificar.
Nota: 1. Por favor, asegúrese de que el líquido esté claro antes de añadir el siguiente disolvente.
2. Asegúrese de añadir el (los) disolvente(s) en orden. Debe asegurarse de que la solución obtenida, en la adición anterior, sea una solución clara antes de proceder a añadir el siguiente disolvente. Se pueden utilizar métodos físicos como el vórtice, el ultrasonido o el baño de agua caliente para ayudar a la disolución.
| Targets/IC50/Ki |
FIPV
(Cell-free assay) 0.78 μM(EC50)
|
Referencias |
|---|
(datos de https://clinicaltrials.gov, actualizado el 2024-05-22)
| Número NCT | Reclutamiento | Condiciones | Patrocinador/Colaboradores | Fecha de inicio | Fases |
|---|---|---|---|---|---|
| NCT05996744 | Terminated | COVID-19 |
Gilead Sciences |
December 26 2023 | Phase 2|Phase 3 |
| NCT05715528 | Completed | COVID-19 |
Gilead Sciences |
February 8 2023 | Phase 3 |
| NCT05603143 | Terminated | COVID-19 |
Gilead Sciences |
November 5 2022 | Phase 3 |
| NCT04582266 | Completed | COVID-19 |
National Institute of Allergy and Infectious Diseases (NIAID)|Gilead Sciences |
March 31 2021 | -- |
| NCT04859244 | Completed | COVID-19 |
Copycat Sciences LLC |
January 1 2021 | Phase 1 |
| NCT04539262 | Completed | COVID-19 |
Gilead Sciences |
September 14 2020 | Phase 1|Phase 2 |
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