1.0 2010-04-08 22:05:17 UTC 2019-11-26 02:57:10 UTC FDB002209 Cavipetin A Constituent of the edible mushroom Boletinus cavipes. Cavipetin A is found in mushrooms. Cavipetin A C30H42O8 530.6497 530.28796832 (2E)-4-{[(2E,6E,10E,14E)-16-{[(2E)-3-carboxy-2-methylprop-2-enoyl]oxy}-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]oxy}-3-methyl-4-oxobut-2-enoic acid (2E)-4-{[(2E,6E,10E,14E)-16-{[(2E)-3-carboxy-2-methylprop-2-enoyl]oxy}-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]oxy}-3-methyl-4-oxobut-2-enoic acid 128530-02-9 C\C(CC\C=C(/C)CC\C=C(/C)COC(=O)C(\C)=C\C(O)=O)=C/CC\C(C)=C\COC(=O)C(\C)=C\C(O)=O InChI=1S/C30H42O8/c1-21(12-8-14-23(3)16-17-37-29(35)25(5)18-27(31)32)10-7-11-22(2)13-9-15-24(4)20-38-30(36)26(6)19-28(33)34/h11-12,15-16,18-19H,7-10,13-14,17,20H2,1-6H3,(H,31,32)(H,33,34)/b21-12+,22-11+,23-16+,24-15+,25-18+,26-19+ GUDPQPGYABLCEA-OWQAWYIFSA-N belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle. Acyclic diterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Diterpenoids Aliphatic acyclic compounds Carbonyl compounds Carboxylic acids Enoate esters Fatty acid esters Hydrocarbon derivatives Organic oxides Tetracarboxylic acids and derivatives Acyclic diterpenoid Aliphatic acyclic compound Alpha,beta-unsaturated carboxylic ester Carbonyl group Carboxylic acid Carboxylic acid derivative Carboxylic acid ester Enoate ester Fatty acid ester Fatty acyl Hydrocarbon derivative Organic oxide Organic oxygen compound Organooxygen compound Tetracarboxylic acid or derivatives logp 6.08 ALOGPS logs -6.17 ALOGPS solubility 3.59e-04 g/l ALOGPS melting_point Mp 137-138° logp 7.05 ChemAxon pka_strongest_acidic 3.37 ChemAxon pka_strongest_basic -6.6 ChemAxon iupac (2E)-4-{[(2E,6E,10E,14E)-16-{[(2E)-3-carboxy-2-methylprop-2-enoyl]oxy}-2,6,10,14-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]oxy}-3-methyl-4-oxobut-2-enoic acid ChemAxon average_mass 530.6497 ChemAxon mono_mass 530.28796832 ChemAxon smiles C\C(CC\C=C(/C)CC\C=C(/C)COC(=O)C(\C)=C\C(O)=O)=C/CC\C(C)=C\COC(=O)C(\C)=C\C(O)=O ChemAxon formula C30H42O8 ChemAxon inchi InChI=1S/C30H42O8/c1-21(12-8-14-23(3)16-17-37-29(35)25(5)18-27(31)32)10-7-11-22(2)13-9-15-24(4)20-38-30(36)26(6)19-28(33)34/h11-12,15-16,18-19H,7-10,13-14,17,20H2,1-6H3,(H,31,32)(H,33,34)/b21-12+,22-11+,23-16+,24-15+,25-18+,26-19+ ChemAxon inchikey GUDPQPGYABLCEA-OWQAWYIFSA-N ChemAxon polar_surface_area 127.2 ChemAxon refractivity 151.51 ChemAxon polarizability 60.3 ChemAxon rotatable_bond_count 19 ChemAxon acceptor_count 6 ChemAxon donor_count 2 ChemAxon physiological_charge -2 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 43935 Specdb::MsMs 43936 Specdb::MsMs 43937 Specdb::MsMs 126381 Specdb::MsMs 126382 Specdb::MsMs 126383 Specdb::MsMs 2724020 Specdb::MsMs 2724021 Specdb::MsMs 2724022 Specdb::MsMs 2954622 Specdb::MsMs 2954623 Specdb::MsMs 2954624 Specdb::CMs 24321 Specdb::CMs 41881 Specdb::CMs 200406 Specdb::CMs 200407 Specdb::CMs 200409 Specdb::CMs 200411 Specdb::CMs 200414 Specdb::CMs 281074 HMDB30363 #<Reference:0x000055ce31f357a0> Common mushroom Type 1 specific Agaricus bisporus 5341 Mushrooms Unknown generic Oyster mushroom Type 1 specific Pleurotus ostreatus 5322