43210-67-9
Chemical Structure
Fenbendazole
- CAS No.: 43210-67-9
- Formula:C15H13N3O2S
- Molecular Weight:299.35
IUPAC Name: methyl (6-(phenylthio)-1H-benzo[d]imidazol-2-yl)carbamate
InChIKey: HDDSHPAODJUKPD-UHFFFAOYSA-N
SMILES: O=C(OC)NC1=NC2=CC=C(SC3=CC=CC=C3)C=C2N1
Biological Activity: Fenbendazole is an orally active benzimidazole anthelmintic agent, with a broad antiparasitic range. Fenbendazole is a microtubule destabilizing agent and acts on helminthes primarily by binding to tubulin and disrupting the tubulin microtubule equilibrium. Fenbendazole stabilizes the transcriptional activator HIF-1α. Fenbendazole possesses an efficient anti-proliferative activity and induces apoptosis. Fenbendazole causes cell-cycle arrest and mitotic cell death, and has antitumor activity in mice xenografted with wild-type p53[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fenbendazole | 99.94% | Fenbendazole is an orally active benzimidazole anthelmintic agent, with a broad antiparasitic range. Fenbendazole is a microtubule destabilizing agent and acts on helminthes primarily by binding to tubulin and disrupting the tubulin microtubule equilibrium. Fenbendazole stabilizes the transcriptional activator HIF-1α. Fenbendazole possesses an efficient anti-proliferative activity and induces apoptosis. Fenbendazole causes cell-cycle arrest and mitotic cell death, and has antitumor activity in mice xenografted with wild-type p53. | ||||||||||||||||||||
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Fenbendazole (Standard) | 99.90% | Fenbendazole (Standard) is the analytical standard of Fenbendazole. This product is intended for research and analytical applications. Fenbendazole is an orally active benzimidazole anthelmintic agent, with a broad antiparasitic range. Fenbendazole is a microtubule destabilizing agent and acts on helminthes primarily by binding to tubulin and disrupting the tubulin microtubule equilibrium. Fenbendazole stabilizes the transcriptional activator HIF-1α. Fenbendazole possesses an efficient anti-proliferative activity and induces apoptosis. Fenbendazole causes cell-cycle arrest and mitotic cell death, and has antitumor activity in mice xenografted with wild-type p53. | ||||||||||||||||||||
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Fenbendazole-d3 | 99.70% | Fenbendazole-d3 is a deuterium labeled Fenbendazole. Fenbendazole-d3 is a HIF-1α agonist and activates the HIF-1α-related GLUT1 pathway. Fenbendazole is an orally active benzimidazole anthelmintic agent, with a broad antiparasitic range. Fenbendazole is a microtubule destabilizing agent. Fenbendazole causes cell-cycle arrest and mitotic cell death, and has antitumor activity in mice xenografted with wild-type p53. | ||||||||||||||||||||
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Similarity Score 0.87
HY-146600SHydroxyfenbendazole-d3 -
Similarity Score 0.83
HY-B0291Oxfendazole -
Similarity Score 0.81
HY-W011239RFenbendazole sulfone (Standard) -
Similarity Score 0.79
HY-123305S5-Hydroxymebendazole-d3 -
Similarity Score 0.77
HY-17595RMebendazole (Standard) -
Similarity Score 0.76
HY-Z7809Albendazole impurity 4 -
Similarity Score 0.76
HY-17595SMebendazole-d3 -
Similarity Score 0.75
HY-B0223SAlbendazole-d3 -
Similarity Score 0.75
HY-B0291ROxfendazole (Standard) -
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