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Réf. CatalogueS6626
| Lignées cellulaires | Type dessai | Concentration | Temps dincubation | Formulation | Description de lactivité | PMID |
|---|---|---|---|---|---|---|
| insect cells | Function assay | Inhibition of human recombinant DHODH expressed in baculovirus infected insect cells using dihydroorotate as substrate in presence of quinone by dichlorophenol-indophenol dye based assay, IC50=0.01μM | 27994748 | |||
| A549 | Antiviral assay | Antiviral activity against Yellow fever virus infected in human A549 cells assessed as reduction in virus replication, EC50=0.078μM | 31557612 | |||
| A549 | Antiviral assay | Antiviral activity against West Nile virus infected in human A549 cells assessed as reduction in virus replication, EC50=0.078μM | 31557612 | |||
| A549 | Antiviral assay | Antiviral activity against Dengue virus infected in human A549 cells assessed as reduction in virus replication, EC50=0.078μM | 31557612 | |||
| A549 | Antiviral assay | Antiviral activity against Western equine encephalomyelitis virus infected in human A549 cells assessed as reduction in virus replication, EC50=0.078μM | 31557612 | |||
| A549 | Antiviral assay | Antiviral activity against Vesicular stomatitis virus infected in human A549 cells assessed as reduction in virus replication, EC50=0.078μM | 31557612 | |||
| Jurkat | Antiproliferative assay | 72 hrs | Inhibition of cell proliferation of human Jurkat cells incubated for 72 hrs by Celltiter-Glo assay, IC50=0.2μM | 26079043 | ||
| MDCK | Antiviral assay | 48 hrs | Antiviral activity against VSV infected in MDCK cells assessed as inhibition of VSV replication after 48 hrs by plaque assay, EC50=0.3μM | 23930152 | ||
| MDCK | Antiviral assay | 48 hrs | Antiviral activity against influenza A virus A/WSN/33 (H0N1) infected in MDCK cells after 48 hrs by plaque assay, EC50=0.46μM | 23930152 | ||
| HL60 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human HL60 cells after 72 hrs by MTT assay, IC50=0.544μM | 29727569 | ||
| HCT116 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human HCT116 cells over-expressing DHODH after 72 hrs by MTT assay, IC50=0.679μM | 29727569 | ||
| Jurkat T | Antiproliferative assay | 72 hrs | Antiproliferative activity against human Jurkat T cells assessed as DNA content after 72 hrs by Hoechst 33258 dye-based fluorescence assay, IC50=0.91μM | 29939742 | ||
| Jurkat T | Antiproliferative assay | 72 hrs | Antiproliferative activity against human Jurkat T cells assessed as DNA content after 72 hrs by Hoechst 33258 dye based fluorometric method, IC50=0.93μM | 28235702 | ||
| MIAPaCa2 | Antiproliferative assay | 72 hrs | Antiproliferative activity against human MIAPaCa2 cells after 72 hrs by MTT assay, IC50=1.69μM | 29727569 | ||
| Jurkat T | Cytotoxicity assay | 72 hrs | Cytotoxicity against human Jurkat T cells assessed as compound concentration required to induce up to 30% cell death after 72 hrs by Hoechst 33258 dye based fluorometric method, Activity=45μM | 28235702 | ||
| Jurkat T | Cytotoxicity assay | 72 hrs | Cytotoxicity against human Jurkat T cells assessed as compound concentration required to induce =>30% cell death after 72 hrs by CellTox green assay, Activity=48.2μM | 29939742 | ||
| HCT116 | Growth inhibition assay | 72 hrs | Growth inhibition of human HCT116 cells over-expressing DHODH at 2 times antiproliferative IC50 after 72 hrs in absence of uridine by MTT assay | 29727569 | ||
| HCT116 | Cytostatic activity assay | 10 uM | 24 hrs | Cytostatic activity against human HCT116 cells assessed as reduction in colony forming at 10 uM after 24 hrs by crystal violet staining based assay | 29727569 | |
| HCT116 | Cytostatic activity assay | 10 uM | 7 days | Cytostatic activity against human HCT116 cells assessed as reduction in colony forming at 10 uM after 7 days by crystal violet staining based assay | 29727569 | |
| U937 | Antiproliferative assay | 0.01 to 10 uM | 3 days | Antiproliferative activity against CFSE-labeled human U937 cells at 0.01 to 10 uM after 3 days by propidium iodide staining-based flow cytometry | 29939742 | |
| THP1 | Antiproliferative assay | 0.01 to 10 uM | 3 days | Antiproliferative activity against CFSE-labeled human THP1 cells at 0.01 to 10 uM after 3 days by propidium iodide staining-based flow cytometry | 29939742 | |
| U937 | Function assay | 0.1 to 10 uM | up to 4 days | Induction of myeloid differentiation in human U937 cells assessed as increase in CD11b expression level at 0.1 to 10 uM up to 4 days by propidium iodide staining-based flow cytometry | 29939742 | |
| THP1 | Function assay | 0.1 to 10 uM | up to 5 days | Induction of myeloid differentiation in human THP1 cells assessed as increase in CD11b expression level at 0.1 to 10 uM up to 5 days by propidium iodide staining-based flow cytometry | 29939742 | |
| THP1 | Function assay | 0.1 to 10 uM | up to 5 days | Induction of myeloid differentiation in human THP1 cells assessed as increase in CD14 expression level at 0.1 to 10 uM up to 5 days by propidium iodide staining-based flow cytometry | 29939742 | |
| Cliquez pour voir plus de données expérimentales sur la lignée cellulaire | ||||||
| Poids moléculaire | 375.37 | Formule | C23H15F2NO2 |
Stockage (À compter de la date de réception) | 3 years -20°C powder |
|---|---|---|---|---|---|
| N° CAS | 96187-53-0 | -- | Stockage des solutions mères |
|
|
| Synonymes | DUP785, NSC 368390 | Smiles | CC1=C(C2=C(C=CC(=C2)F)N=C1C3=CC=C(C=C3)C4=CC=CC=C4F)C(=O)O | ||
|
In vitro |
DMSO
: 37 mg/mL
(98.56 mM)
Water : Insoluble Ethanol : Insoluble |
|
In vivo |
|||||
Étape 1 : Saisir les informations ci-dessous (Recommandé : Un animal supplémentaire pour tenir compte des pertes pendant lexpérience)
Étape 2 : Saisir la formulation in vivo (Ceci est seulement le calculateur, pas la formulation. Veuillez nous contacter dabord sil ny a pas de formulation in vivo dans la section Solubilité.)
Résultats du calcul :
Concentration de travail : mg/ml;
Méthode de préparation du liquide maître DMSO : mg médicament prédissous dans μL DMSO ( Concentration du liquide maître mg/mL, Veuillez nous contacter dabord si la concentration dépasse la solubilité du DMSO du lot de médicament. )
Méthode de préparation de la formulation in vivo : Prendre μL DMSO liquide maître, puis ajouterμL PEG300, mélanger et clarifier, puis ajouterμL Tween 80, mélanger et clarifier, puis ajouter μL ddH2O, mélanger et clarifier.
Méthode de préparation de la formulation in vivo : Prendre μL DMSO liquide maître, puis ajouter μL Huile de maïs, mélanger et clarifier.
Note : 1. Veuillez vous assurer que le liquide est clair avant dajouter le solvant suivant.
2. Assurez-vous dajouter le(s) solvant(s) dans lordre. Vous devez vous assurer que la solution obtenue, lors de lajout précédent, est une solution claire avant de procéder à lajout du solvant suivant. Des méthodes physiques telles que le vortex, les ultrasons ou le bain-marie chaud peuvent être utilisées pour faciliter la dissolution.
| Targets/IC50/Ki |
DHODH
20 nM
|
|---|---|
| In vitro |
Le Brequinar sodique (BQR) réduit les niveaux de PyN dans les cellules T stimulées par la Con A et inhibe la prolifération cellulaire à de faibles concentrations, ce qui peut être inversé par l'uridine. Cependant, l'uridine est incapable d'inverser les effets de fortes concentrations de BQR. Le BQR possède la capacité d'inhiber la phosphorylation de la tyrosine. |
| In vivo |
Le Brequinar sodique (BQR) induit une anémie par inhibition de l'activité de la DHO-DHase et de la synthèse de novo des pyrimidines in vivo. La co-administration de BQR avec de l'uridine prévient l'anémie. |
Références |
|
(données du https://clinicaltrials.gov, mis à jour le 2024-05-22)
| Numéro NCT | Recrutement | Conditions | Promoteur/Collaborateurs | Date de début | Phases |
|---|---|---|---|---|---|
| NCT03760666 | Terminated | Acute Myeloid Leukemia |
Clear Creek Bio Inc. |
December 20 2018 | Phase 1|Phase 2 |
Tel: +1-832-582-8158 Ext:3
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