1.0 2010-04-08 22:10:36 UTC 2019-11-26 03:08:11 UTC FDB013246 Protoleucomelone Constituent of the kurukawa mushroom (Boletopsis leucomelas) (edibility not reported). Protoleucomelone is found in mushrooms. 3,4,2',3',5',6',4"-Hepataacetoxy-p-terphenyl BL I Protoleucomelone C30H24O13 592.5038 592.121690854 3,6,11,12-tetrakis(acetyloxy)-5-[4-(acetyloxy)phenyl]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),2,4,6,9,11-hexaen-4-yl acetate 3,6,11,12-tetrakis(acetyloxy)-5-[4-(acetyloxy)phenyl]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),2,4,6,9,11-hexaen-4-yl acetate 112209-51-5 CC(=O)OC1=CC=C(C=C1)C1=C(OC(C)=O)C(OC(C)=O)=C2C(OC3=CC(OC(C)=O)=C(OC(C)=O)C=C23)=C1OC(C)=O InChI=1S/C30H24O13/c1-13(31)37-20-9-7-19(8-10-20)25-27(40-16(4)34)29(42-18(6)36)26-21-11-23(38-14(2)32)24(39-15(3)33)12-22(21)43-30(26)28(25)41-17(5)35/h7-12H,1-6H3 LSEKLPKUWRDLKY-UHFFFAOYSA-N belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups. Hexacarboxylic acids and derivatives Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Hexacarboxylic acids and derivatives Aromatic heteropolycyclic compounds Carbonyl compounds Carboxylic acid esters Dibenzofurans Furans Heteroaromatic compounds Hydrocarbon derivatives Organic oxides Oxacyclic compounds Phenol esters Phenoxy compounds Phenylbenzofurans Aromatic heteropolycyclic compound Benzenoid Benzofuran Carbonyl group Carboxylic acid ester Dibenzofuran Furan Heteroaromatic compound Hexacarboxylic acid or derivatives Hydrocarbon derivative Monocyclic benzene moiety Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Phenol ester Phenoxy compound Phenylbenzofuran logp 4.29 ALOGPS logs -4.71 ALOGPS solubility 1.15e-02 g/l ALOGPS melting_point Mp 203-204° logp 2.44 ChemAxon pka_strongest_basic -3.9 ChemAxon iupac 3,6,11,12-tetrakis(acetyloxy)-5-[4-(acetyloxy)phenyl]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),2,4,6,9,11-hexaen-4-yl acetate ChemAxon average_mass 592.5038 ChemAxon mono_mass 592.121690854 ChemAxon smiles CC(=O)OC1=CC=C(C=C1)C1=C(OC(C)=O)C(OC(C)=O)=C2C(OC3=CC(OC(C)=O)=C(OC(C)=O)C=C23)=C1OC(C)=O ChemAxon formula C30H24O13 ChemAxon inchi InChI=1S/C30H24O13/c1-13(31)37-20-9-7-19(8-10-20)25-27(40-16(4)34)29(42-18(6)36)26-21-11-23(38-14(2)32)24(39-15(3)33)12-22(21)43-30(26)28(25)41-17(5)35/h7-12H,1-6H3 ChemAxon inchikey LSEKLPKUWRDLKY-UHFFFAOYSA-N ChemAxon polar_surface_area 170.94 ChemAxon refractivity 143.16 ChemAxon polarizability 59.62 ChemAxon rotatable_bond_count 13 ChemAxon acceptor_count 6 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 11887 Specdb::MsMs 52707 Specdb::MsMs 52708 Specdb::MsMs 52709 Specdb::MsMs 113652 Specdb::MsMs 113653 Specdb::MsMs 113654 Specdb::MsMs 2727418 Specdb::MsMs 2727419 Specdb::MsMs 2727420 Specdb::MsMs 2978072 Specdb::MsMs 2978073 Specdb::MsMs 2978074 HMDB34711 #<Reference:0x000055ce304e5ad0> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322