1.0 2010-04-08 22:04:45 UTC 2020-02-24 19:10:16 UTC FDB000900 2-Amino-3-methylimidazo[4,5-f]quinoline Isolated from cooked foods, e.g. sardines, beef extract. 2-Amino-3-methylimidazo[4,5-f]quinoline is found in fishes and animal foods. 2-AMINO-3-METHYL-3H-IMIDAZO-[4,5-f]-QUINOLINE 2-amino-3-methyl-3H-imidazo(4,5-f)quinoline 2-amino-3-methylimidazo(4,5-f)- quinoline 2-Amino-3-methylimidazo(4,5-f)-quinoline 2-amino-3-methylimidazo(4,5-f)quinoline 2-amino-3-methylimidazo(4,5-f)quinoline hydrobromide 2-amino-3-methylimidazolo(4,5-f)quinoline 2-AMIQ 3-methyl-3H-imidazo(4,5-f)quinolin-2-amine 3-methyl-3H-imidazo[4,5-f]quinolin-2-amine 3H-Imidazo(4,5-f)quinolin-2-amine, 3-methyl- 3H-Imidazo(4,5-f)quinoline, 2-amino-3-methyl- GIQ IQ LQ N3-IQ C11H10N4 198.2239 198.09054634 3-methyl-3H-imidazo[4,5-f]quinolin-2-amine 3-methylimidazo[4,5-f]quinolin-2-amine 76180-96-6 CN1C(N)=NC2=C1C=CC1=NC=CC=C21 InChI=1S/C11H10N4/c1-15-9-5-4-8-7(3-2-6-13-8)10(9)14-11(15)12/h2-6H,1H3,(H2,12,14) ARZWATDYIYAUTA-UHFFFAOYSA-N belongs to the class of organic compounds known as quinolines and derivatives. Quinolines and derivatives are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. Quinolines and derivatives Organic compounds Organoheterocyclic compounds Quinolines and derivatives Aromatic heteropolycyclic compounds Azacyclic compounds Benzenoids Benzimidazoles Heteroaromatic compounds Hydrocarbon derivatives N-substituted imidazoles Organonitrogen compounds Organopnictogen compounds Pyridines and derivatives Aromatic heteropolycyclic compound Azacycle Azole Benzenoid Benzimidazole Heteroaromatic compound Hydrocarbon derivative Imidazole N-substituted imidazole Organic nitrogen compound Organonitrogen compound Organopnictogen compound Pyridine Quinoline imidazoquinoline logp 1.61 ALOGPS logs -2.45 ALOGPS solubility 7.02e-01 g/l ALOGPS melting_point Mp 300° logp 1.5 ChemAxon pka_strongest_basic 7.59 ChemAxon iupac 3-methyl-3H-imidazo[4,5-f]quinolin-2-amine ChemAxon average_mass 198.2239 ChemAxon mono_mass 198.09054634 ChemAxon smiles CN1C(N)=NC2=C1C=CC1=NC=CC=C21 ChemAxon formula C11H10N4 ChemAxon inchi InChI=1S/C11H10N4/c1-15-9-5-4-8-7(3-2-6-13-8)10(9)14-11(15)12/h2-6H,1H3,(H2,12,14) ChemAxon inchikey ARZWATDYIYAUTA-UHFFFAOYSA-N ChemAxon polar_surface_area 56.73 ChemAxon refractivity 57.96 ChemAxon polarizability 21.26 ChemAxon rotatable_bond_count 0 ChemAxon acceptor_count 3 ChemAxon donor_count 1 ChemAxon physiological_charge 1 ChemAxon formal_charge 0 ChemAxon Specdb::MsIr 3610 Specdb::MsIr 3611 Specdb::MsIr 3612 Specdb::CMs 16886 Specdb::CMs 26889 Specdb::CMs 100425 Specdb::CMs 168597 Specdb::MsMs 13061 Specdb::MsMs 13062 Specdb::MsMs 13063 Specdb::MsMs 19733 Specdb::MsMs 19734 Specdb::MsMs 19735 Specdb::MsMs 440708 Specdb::MsMs 440709 Specdb::MsMs 452590 Specdb::MsMs 452591 Specdb::MsMs 2227127 Specdb::MsMs 2227599 Specdb::MsMs 2229449 Specdb::MsMs 2244758 Specdb::MsMs 2245333 Specdb::MsMs 2246830 Specdb::MsMs 2247478 Specdb::MsMs 2248798 Specdb::MsMs 2249567 Specdb::MsMs 2250876 Specdb::MsMs 2251552 Specdb::MsMs 2376317 Specdb::MsMs 2376318 Specdb::MsMs 2376319 Specdb::MsMs 2562321 HMDB29706 GIQ #<Reference:0x000055ce3202c1e0> Fishes Unknown generic