research use only
Cat.No.S1837
| Related Targets | CXCR Nrf2 Mitophagy LRRK2 ULK FKBP Heme Oxygenase cGAS LC3 Cell wall |
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| Other Autophagy Inhibitors | Resveratrol (trans-Resveratrol) Spautin-1 PIK-III DC661 Lys05 Autophinib Spermidine SMER28 EN6 QX77 |
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In vitro |
DMSO
: 15 mg/mL
(47.88 mM)
Water : Insoluble Ethanol : Insoluble |
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In vivo |
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Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
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| Molecular Weight | 313.28 | Formula | C16H12FN3O3 |
Storage (From the date of receipt) | |
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| CAS No. | 31430-15-6 | Download SDF | Storage of Stock Solutions |
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| Synonyms | Flumoxanal, NSC 313680 | Smiles | COC(=O)NC1=NC2=C(N1)C=C(C=C2)C(=O)C3=CC=C(C=C3)F | ||
| Targets/IC50/Ki |
Atg4B
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| In vitro |
Flubendazole results in morphological changes included contraction of the soma region, formation of blebs on the tegument, rostellar disorganization, loss of hooks and destruction of microtriches in Echinococcus granulosus. This compound have a bicyclic ring system in which a benzene has been fused to the -4 and -5 positions of the heterocycle (imidazole). It and Albendazole shows similar potency in affecting rat embryonic development in vitro, inducing retardation of growth and dysmorphogenic effects at concentrations ≥0.5 μg/mL.
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| In vivo |
Flubendazole (6.32 mg/kg/day) initially induces an arrest of embryonic development followed by a generalized cell death that leads to 100% embryolethality by gestation day (GD) 12.5. This compound (3.46 mg/kg/day) markedly reduces embryonic development by GD 12.5 without causing cell death. This chemical in olive oil causes a statistically significant increase in embryolethality at doses of 7.83 mg/kg per day and higher, with complete resorption in all dams at 31.33 mg/kg per day in rats. This treatment causes a slight increase of metyrapone and daunorubicin activities in hepatic as well as intestinal cytosol in birds. It also leads to statistically significant inhibition of intestinal GST activity. The treatment leads to slight but significant inhibition (decrease to 69%) of 7-ethoxyresorufin activity in hepatic microsomes.
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References |
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