1.0 2010-04-08 22:11:18 UTC 2025-11-19 00:47:07 UTC FDB014494 Momordicin I Constituent of leaves and vines of Momordica charantia (bitter melon). Momordicin I is found in bitter gourd and fruits. (+)-Momordicine I Momordicin I Momordicine I C30H48O4 472.6997 472.355260024 5,9-dihydroxy-14-(4-hydroxy-6-methylhept-5-en-2-yl)-6,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-1-carbaldehyde 5,9-dihydroxy-14-(4-hydroxy-6-methylhept-5-en-2-yl)-6,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-1-carbaldehyde 91590-76-0 CC(CC(O)C=C(C)C)C1CCC2(C)C3C(O)C=C4C(CCC(O)C4(C)C)C3(CCC12C)C=O InChI=1S/C30H48O4/c1-18(2)14-20(32)15-19(3)21-10-11-29(7)26-24(33)16-23-22(8-9-25(34)27(23,4)5)30(26,17-31)13-12-28(21,29)6/h14,16-17,19-22,24-26,32-34H,8-13,15H2,1-7H3 QBXNBPFTVLJTMK-UHFFFAOYSA-N belongs to the class of organic compounds known as cucurbitacins. These are polycyclic compounds containing the tetracyclic cucurbitane nucleus skeleton, 19-(10->9b)-abeo-10alanost-5-ene (also known as 9b-methyl-19-nor lanosta-5-ene), with a variety of oxygenation functionalities at different positions. Cucurbitacins Organic compounds Lipids and lipid-like molecules Steroids and steroid derivatives Cucurbitacins Aliphatic homopolycyclic compounds 3-hydroxy delta-5-steroids 7-hydroxysteroids Aldehydes Cyclic alcohols and derivatives Delta-5-steroids Hydrocarbon derivatives Organic oxides Secondary alcohols Triterpenoids 23-hydroxysteroid 3-hydroxy-delta-5-steroid 3-hydroxysteroid 7-hydroxysteroid Alcohol Aldehyde Aliphatic homopolycyclic compound Carbonyl group Cucurbitacin skeleton Cyclic alcohol Delta-5-steroid Hydrocarbon derivative Hydroxysteroid Organic oxide Organic oxygen compound Organooxygen compound Secondary alcohol Triterpenoid logp 4.41 ALOGPS logs -4.81 ALOGPS solubility 7.37e-03 g/l ALOGPS melting_point Mp 125-128° logp 4.4 ChemAxon pka_strongest_acidic 14.52 ChemAxon pka_strongest_basic -0.74 ChemAxon iupac 5,9-dihydroxy-14-(4-hydroxy-6-methylhept-5-en-2-yl)-6,6,11,15-tetramethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-1-carbaldehyde ChemAxon average_mass 472.6997 ChemAxon mono_mass 472.355260024 ChemAxon smiles CC(CC(O)C=C(C)C)C1CCC2(C)C3C(O)C=C4C(CCC(O)C4(C)C)C3(CCC12C)C=O ChemAxon formula C30H48O4 ChemAxon inchi InChI=1S/C30H48O4/c1-18(2)14-20(32)15-19(3)21-10-11-29(7)26-24(33)16-23-22(8-9-25(34)27(23,4)5)30(26,17-31)13-12-28(21,29)6/h14,16-17,19-22,24-26,32-34H,8-13,15H2,1-7H3 ChemAxon inchikey QBXNBPFTVLJTMK-UHFFFAOYSA-N ChemAxon polar_surface_area 77.76 ChemAxon refractivity 138.56 ChemAxon polarizability 56.34 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 4 ChemAxon donor_count 3 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 21373 Specdb::CMs 44544 Specdb::CMs 131107 Specdb::CMs 138841 Specdb::MsMs 79578 Specdb::MsMs 79579 Specdb::MsMs 79580 Specdb::MsMs 140211 Specdb::MsMs 140212 Specdb::MsMs 140213 Specdb::MsMs 2269189 Specdb::MsMs 2269190 Specdb::MsMs 2269191 Specdb::MsMs 3073230 Specdb::MsMs 3073231 Specdb::MsMs 3073232 HMDB35758 #<Reference:0x000055ce32339608> Bitter gourd Type 1 specific Momordica charantia 3673 Fruits Unknown generic