1.0 2010-04-08 22:06:45 UTC 2025-11-18 22:59:33 UTC FDB005596 Lipoxygenase Lipoxygenase, also known as bw-755c, is a member of the class of compounds known as trifluoromethylbenzenes. Trifluoromethylbenzenes are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups. Lipoxygenase is practically insoluble (in water) and a very strong basic compound (based on its pKa). Lipoxygenase can be found in soy bean, which makes lipoxygenase a potential biomarker for the consumption of this food product. Lipoxygenases (EC 1.13.11.-) are a family of (non-heme), iron-containing enzymes most of which catalyze the dioxygenation of polyunsaturated fatty acids in lipids containing a cis,cis-1,4- pentadiene into cell signaling agents that serve diverse roles as autocrine signals that regulate the function of their parent cells, paracrine signals that regulate the function of nearby cells, and endocrine signals that regulate the function of distant cells . C10H10F3N3 229.2017 229.08268195 1-[3-(trifluoromethyl)phenyl]-4,5-dihydro-1H-pyrazol-3-amine 1-[3-(trifluoromethyl)phenyl]-4,5-dihydropyrazol-3-amine NC1=NN(CC1)C1=CC=CC(=C1)C(F)(F)F InChI=1S/C10H10F3N3/c11-10(12,13)7-2-1-3-8(6-7)16-5-4-9(14)15-16/h1-3,6H,4-5H2,(H2,14,15) CPXGGWXJNQSFEP-UHFFFAOYSA-N belongs to the class of organic compounds known as trifluoromethylbenzenes. These are organofluorine compounds that contain a benzene ring substituted with one or more trifluoromethyl groups. Trifluoromethylbenzenes Organic compounds Benzenoids Benzene and substituted derivatives Trifluoromethylbenzenes Aromatic heteromonocyclic compounds Alkyl fluorides Amidines Amidrazones Azacyclic compounds Hydrazones Hydrocarbon derivatives Imidolactams Organofluorides Organopnictogen compounds Pyrazolines Alkyl fluoride Alkyl halide Amidine Aromatic heteromonocyclic compound Azacycle Carboxylic acid amidrazone Hydrazone Hydrocarbon derivative Imidolactam Organic nitrogen compound Organofluoride Organohalogen compound Organoheterocyclic compound Organonitrogen compound Organopnictogen compound Pyrazoline Trifluoromethylbenzene logp 2.02 ALOGPS logs -2.68 ALOGPS solubility 4.74e-01 g/l ALOGPS logp 2 ChemAxon pka_strongest_basic 8.45 ChemAxon iupac 1-[3-(trifluoromethyl)phenyl]-4,5-dihydro-1H-pyrazol-3-amine ChemAxon average_mass 229.2017 ChemAxon mono_mass 229.08268195 ChemAxon smiles NC1=NN(CC1)C1=CC=CC(=C1)C(F)(F)F ChemAxon formula C10H10F3N3 ChemAxon inchi InChI=1S/C10H10F3N3/c11-10(12,13)7-2-1-3-8(6-7)16-5-4-9(14)15-16/h1-3,6H,4-5H2,(H2,14,15) ChemAxon inchikey CPXGGWXJNQSFEP-UHFFFAOYSA-N ChemAxon polar_surface_area 41.62 ChemAxon refractivity 64.24 ChemAxon polarizability 20.25 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 3 ChemAxon donor_count 1 ChemAxon physiological_charge 1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 111562 Specdb::CMs 124819 Specdb::MsMs 44517 Specdb::MsMs 44518 Specdb::MsMs 44519 Specdb::MsMs 139842 Specdb::MsMs 139843 Specdb::MsMs 139844 Specdb::MsMs 3409598 Specdb::MsMs 3409599 Specdb::MsMs 3409600 Specdb::MsMs 3409601 Specdb::MsMs 3409602 Specdb::MsMs 3409603 35856 Soy bean Type 1 specific Glycine max 3847