
CAS 6306-71-4: Lobendazole
Formula:C10H11N3O2
InChI:InChI=1S/C10H11N3O2/c1-2-15-10(14)13-9-11-7-5-3-4-6-8(7)12-9/h3-6H,2H2,1H3,(H2,11,12,13,14)
InChI key:InChIKey=OKOVSTKGUBOSTB-UHFFFAOYSA-N
SMILES:N(C(OCC)=O)C=1NC=2C(N1)=CC=CC2
Synonyms:- 2-((Ethoxycarbonyl)amino)benzimidazole
- 2-Benzimidazolecarbamic acid, ethyl ester
- 2-Benzimidazolecarbamic acid, ethyl ester (8CI)
- 2-Carboethoxyaminobenzimidazole
- Benzimidazol-2-ylcarbamate ethyl ester
- Benzimidazole carbamate d'ethyle
- Benzimidazole carbamate d'ethyle [French]
- Carbamic acid, (2-benzimidazolyl)-, ethyl ester
- Carbamic acid, 1H-benzimidazol-2-yl-, ethyl ester
- Carbamic acid, N-1H-benzimidazol-2-yl-, ethyl ester
- Ethyl 1H-benzimidazol-2-ylcarbamate
- See more synonyms
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Found 5 products.
Ethyl (1H-Benzo[d]imidazol-2-yl)carbamate
CAS:Controlled ProductFormula:C10H11N3O2Color and Shape:NeatMolecular weight:205.21Lobendazole
CAS:Lobendazole is a metabolite of thiophanate.Formula:C10H11N3O2Color and Shape:SolidMolecular weight:205.21N-(1H-Benzimidazol-2-yl)carbamic acid ethyl ester
CAS:N-(1H-Benzimidazol-2-yl)carbamic acid ethyl ester is a biologically active compound that is used as a diluent for hydrophobic drugs. It is also used as an insoluble carrier for drugs that are poorly soluble in water and has been shown to be effective in oral administration in animals. N-(1H-Benzimidazol-2-yl)carbamic acid ethyl ester inhibits the activity of enzymes involved in signal transduction pathways, such as protein kinase C, protein kinase A, and phosphatidylinositol 3-kinase. This drug is a substrate for various enzymes and can be conjugated with other drugs or substances to form new molecules.Formula:C10H11N3O2Purity:Min. 95%Molecular weight:205.21 g/mol