solo para uso en investigación
Cat. No.: S1742
Estructura química
| Dianas relacionadas | Integrase Bacterial Antibiotics Anti-infection Fungal Antiviral COVID-19 Parasite HIV HCV Protease |
|---|---|
| Otros Reverse Transcriptase Inhibidores | Dapivirine (TMC120) Fangchinoline Salicylanilide 3'-Fluoro-3'-deoxythymidine (Alovudine) Ulonivirine Lersivirine (UK-453061) Bifendate 4-Chloro-2-(trifluoroacetyl)aniline hydrochloride Islatravir |
| Líneas celulares | Tipo de ensayo | Concentración | Tiempo de incubación | Formulación | Descripción de la actividad | PMID |
|---|---|---|---|---|---|---|
| CEM-SS cells | Function assay | Antiviral activity against HIV1 RF in CEM-SS cells assessed as inhibition of virus-induced cytopathic effect by XTT assay, EC50=1.5 nM | ||||
| human MT4 cells | Function assay | Antiviral activity against Human immunodeficiency virus 1 subtype C infected in human MT4 cells assessed as reduction in virus induced cytopathicity, EC50=0.00488 μM | ||||
| human Jurkat E6-1 cells | Function assay | 2 days | Antiviral activity against HIV1 Env-pseudovirus infected in human Jurkat E6-1 cells after 2 days by luciferase assay, IC50=0.04 μM | |||
| human C1866 cells | Cytotoxicity assay | 72 h | Cytotoxicity against human C1866 cells after 72 hrs by MTT assay, EC50=0.04943 μM | |||
| human MT2 cells | Function assay | 4 days | Antiviral activity against wild type HIV1 3B infected in human MT2 cells assessed as inhibition of p24 antigen production after 4 days by ELISA, EC50=0.053 μM | |||
| HeLa cells | Function assay | Antiviral activity against wild type HIV1 in HeLa cells by MAGI assay, IC50=0.053 μM | ||||
| 293T cells | Function assay | Inhibition of wild type HIV1 reverse transcriptase in 293T cells, IC50=0.06 μM | ||||
| MDCK2 cells | Function assay | 10 μM | Inhibition of human MRP2 expressed in MDCK2 cells assessed as increase in intracellular CMF fluorescence at 10 uM by CMFDA assay | |||
| Haga clic para ver más datos experimentales de líneas celulares | ||||||
| Peso molecular | 266.3 | Fórmula | C15H14N4O |
Almacenamiento (Desde la fecha de recepción) | |
|---|---|---|---|---|---|
| Nº CAS | 129618-40-2 | Descargar SDF | Almacenamiento de soluciones madre |
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| Sinónimos | NSC 641530,NVP | Smiles | CC1=C2C(=NC=C1)N(C3=C(C=CC=N3)C(=O)N2)C4CC4 | ||
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In vitro |
DMSO
: 53 mg/mL
(199.02 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 |
Reverse transcriptase
|
|---|---|
| In vitro |
Nevirapine (NSC 641530) is a non-nucleoside RT inhibitor with a well-characterized inhibitory activity on RT enzymes of retroviral origin. It is also an effective inhibitor of the endogenous RT in murine and human cell lines. This compound is a highly specific inhibitor of HIV-1 reverse transcriptase (RT) which exhibits an IC50 = 84 nM in enzyme assays and IC50 = 40nM against HIV-1 replication in cell culture. It alters the cleavage specificity of the RNase H, resulting in Nevirapine-induced stimulation of RNase H activity beyond the increase expected from the change in cleavage specificity. It is an inhibitor of only CYP3A4 at concentrations that are well above those of therapeutic relevance (Ki = 270 mM). Its exposure rescues the differentiation block present in acute myeloid leukemia (AML) cell lines and primary blasts from two AML patients, as indicated by morphological, functional and immunophenotypic assays. |
| In vivo |
Nevirapine (NSC 641530) is metabolized to 4-CANVP as a major metabolite in all male animals and in female mice, dogs, and monkeys. 3-OHNVP is a major fecal metabolite in all animals except for the male rat. In the bile of rats, 4-CANVP is a major metabolite along with 12-OHNVP glucuronide. |
Referencias |
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(datos de https://clinicaltrials.gov, actualizado el 2024-05-22)
| Número NCT | Reclutamiento | Condiciones | Patrocinador/Colaboradores | Fecha de inicio | Fases |
|---|---|---|---|---|---|
| NCT05725252 | Completed | Healthy Volunteers |
NVP Healthcare |
May 28 2023 | Phase 1 |
| NCT05354713 | Completed | Healthy Volunteers |
NVP Healthcare |
November 5 2022 | Phase 1 |
| NCT04926727 | Unknown status | Nausea Gravidarum|Vomiting of Pregnancy |
Italfarmaco|Opera CRO a TIGERMED Group Company |
October 4 2021 | -- |
| NCT02738502 | Completed | Maternal-fetal Infection Transmission |
ANRS Emerging Infectious Diseases|Institut National de la Santé Et de la Recherche Médicale France |
July 6 2016 | Phase 2 |
| NCT02383849 | Completed | Low-Birth-Weight Infant|Tuberculosis|HIV |
International Maternal Pediatric Adolescent AIDS Clinical Trials Group|National Institute of Allergy and Infectious Diseases (NIAID)|Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
August 4 2015 | -- |