1.0 2010-04-08 22:14:51 UTC 2019-11-26 03:18:35 UTC FDB020169 Dictyoquinazol A Alkaloid from the edible mushroom Dictyophora indusiata. Dictyoquinazol A is found in mushrooms. 3-(2-Hydroxymethyl-4-methoxyphenyl)-6-methoxy-4(3H)-quinazolinone C17H16N2O4 312.3199 312.11100701 3-[2-(hydroxymethyl)-4-methoxyphenyl]-6-methoxy-3,4-dihydroquinazolin-4-one 3-[2-(hydroxymethyl)-4-methoxyphenyl]-6-methoxyquinazolin-4-one COC1=CC2=C(C=C1)N=CN(C2=O)C1=CC=C(OC)C=C1CO InChI=1S/C17H16N2O4/c1-22-12-4-6-16(11(7-12)9-20)19-10-18-15-5-3-13(23-2)8-14(15)17(19)21/h3-8,10,20H,9H2,1-2H3 SHUSJJZZTZAKPD-UHFFFAOYSA-N belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring. Quinazolines Organic compounds Organoheterocyclic compounds Diazanaphthalenes Benzodiazines Aromatic heteropolycyclic compounds Alkyl aryl ethers Anisoles Aromatic alcohols Azacyclic compounds Benzyl alcohols Heteroaromatic compounds Hydrocarbon derivatives Lactams Methoxyanilines Methoxybenzenes Organic oxides Organonitrogen compounds Organopnictogen compounds Phenoxy compounds Primary alcohols Pyrimidones Alcohol Alkyl aryl ether Anisole Aromatic alcohol Aromatic heteropolycyclic compound Azacycle Benzenoid Benzyl alcohol Ether Heteroaromatic compound Hydrocarbon derivative Lactam Methoxyaniline Methoxybenzene Monocyclic benzene moiety Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Phenol ether Phenoxy compound Primary alcohol Pyrimidine Pyrimidone Quinazoline logp 1.14 ALOGPS logs -3.23 ALOGPS solubility 1.83e-01 g/l ALOGPS logp 1.52 ChemAxon pka_strongest_acidic 14.66 ChemAxon pka_strongest_basic -0.95 ChemAxon iupac 3-[2-(hydroxymethyl)-4-methoxyphenyl]-6-methoxy-3,4-dihydroquinazolin-4-one ChemAxon average_mass 312.3199 ChemAxon mono_mass 312.11100701 ChemAxon smiles COC1=CC2=C(C=C1)N=CN(C2=O)C1=CC=C(OC)C=C1CO ChemAxon formula C17H16N2O4 ChemAxon inchi InChI=1S/C17H16N2O4/c1-22-12-4-6-16(11(7-12)9-20)19-10-18-15-5-3-13(23-2)8-14(15)17(19)21/h3-8,10,20H,9H2,1-2H3 ChemAxon inchikey SHUSJJZZTZAKPD-UHFFFAOYSA-N ChemAxon polar_surface_area 71.36 ChemAxon refractivity 87.32 ChemAxon polarizability 32.52 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 5 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 9325 Specdb::CMs 46772 Specdb::CMs 157839 Specdb::MsMs 286585 Specdb::MsMs 286586 Specdb::MsMs 286587 Specdb::MsMs 325201 Specdb::MsMs 325202 Specdb::MsMs 325203 Specdb::MsMs 2366938 Specdb::MsMs 2366939 Specdb::MsMs 2366940 Specdb::MsMs 2598235 Specdb::MsMs 2598236 Specdb::MsMs 2598237 HMDB40435 #<Reference:0x000055ce326b88d8> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322