1.0 2010-04-08 22:04:56 UTC 2025-11-18 22:30:34 UTC FDB001360 Amasterol Isolated from Amaranthus viridis (calalu). Amasterol is found in green vegetables. Amasterol C28H44O2 412.6478 412.334130652 14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-7,9-dien-5-ol 14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-7,9-dien-5-ol 85643-78-3 CC(C)C(=C)CCC(C)(O)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC12C InChI=1S/C28H44O2/c1-18(2)19(3)11-16-28(6,30)25-10-9-23-22-8-7-20-17-21(29)12-14-26(20,4)24(22)13-15-27(23,25)5/h7-8,18,21,23-25,29-30H,3,9-17H2,1-2,4-6H3 VRCVXRWYXYWACO-UHFFFAOYSA-N belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton. Ergosterols and derivatives Organic compounds Lipids and lipid-like molecules Steroids and steroid derivatives Ergostane steroids Aliphatic homopolycyclic compounds 3-hydroxy delta-5-steroids 3-hydroxy delta-7-steroids Cyclic alcohols and derivatives Delta-5-steroids Delta-7-steroids Hydrocarbon derivatives Secondary alcohols Tertiary alcohols 20-hydroxysteroid 3-hydroxy-delta-5-steroid 3-hydroxy-delta-7-steroid 3-hydroxysteroid Alcohol Aliphatic homopolycyclic compound Cyclic alcohol Delta-5-steroid Delta-7-steroid Ergosterol-skeleton Hydrocarbon derivative Hydroxysteroid Organic oxygen compound Organooxygen compound Secondary alcohol Tertiary alcohol logp 6.35 ALOGPS logs -5.01 ALOGPS solubility 4.06e-03 g/l ALOGPS melting_point Mp 170° logp 5.33 ChemAxon pka_strongest_acidic 18.27 ChemAxon pka_strongest_basic -0.19 ChemAxon iupac 14-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-7,9-dien-5-ol ChemAxon average_mass 412.6478 ChemAxon mono_mass 412.334130652 ChemAxon smiles CC(C)C(=C)CCC(C)(O)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC12C ChemAxon formula C28H44O2 ChemAxon inchi InChI=1S/C28H44O2/c1-18(2)19(3)11-16-28(6,30)25-10-9-23-22-8-7-20-17-21(29)12-14-26(20,4)24(22)13-15-27(23,25)5/h7-8,18,21,23-25,29-30H,3,9-17H2,1-2,4-6H3 ChemAxon inchikey VRCVXRWYXYWACO-UHFFFAOYSA-N ChemAxon polar_surface_area 40.46 ChemAxon refractivity 127.47 ChemAxon polarizability 49.97 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 2 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 16552 Specdb::CMs 41721 Specdb::CMs 149474 Specdb::MsMs 74022 Specdb::MsMs 74023 Specdb::MsMs 74024 Specdb::MsMs 133302 Specdb::MsMs 133303 Specdb::MsMs 133304 Specdb::MsMs 2410333 Specdb::MsMs 2410334 Specdb::MsMs 2410335 Specdb::MsMs 2556075 Specdb::MsMs 2556076 Specdb::MsMs 2556077 HMDB30054 #<Reference:0x000055ce319aa5d8> Green vegetables Unknown generic