1.0 2010-04-08 22:11:25 UTC 2019-11-26 03:10:38 UTC FDB014710 Momordicoside L Constituent of Momordica charantia (bitter melon). Momordicoside L is found in bitter gourd and fruits. Momordicoside L C36H58O9 634.8403 634.408083454 5-hydroxy-14-[(4E)-6-hydroxy-6-methylhept-4-en-2-yl]-6,6,11,15-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-1-carbaldehyde 5-hydroxy-14-[(4E)-6-hydroxy-6-methylhept-4-en-2-yl]-6,6,11,15-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-1-carbaldehyde 81348-83-6 CC(C\C=C\C(C)(C)O)C1CCC2(C)C3C(OC4OC(CO)C(O)C(O)C4O)C=C4C(CCC(O)C4(C)C)C3(CCC12C)C=O InChI=1S/C36H58O9/c1-20(9-8-13-32(2,3)43)21-12-14-35(7)30-24(44-31-29(42)28(41)27(40)25(18-37)45-31)17-23-22(10-11-26(39)33(23,4)5)36(30,19-38)16-15-34(21,35)6/h8,13,17,19-22,24-31,37,39-43H,9-12,14-16,18H2,1-7H3/b13-8+ BOHOBTRHAFBJOW-MDWZMJQESA-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 heteropolycyclic compounds 3-hydroxy delta-5-steroids Acetals Aldehydes Cyclic alcohols and derivatives Delta-5-steroids Hexoses Hydrocarbon derivatives O-glycosyl compounds Organic oxides Oxacyclic compounds Oxanes Polyols Primary alcohols Secondary alcohols Tertiary alcohols Triterpenoids 25-hydroxysteroid 3-hydroxy-delta-5-steroid 3-hydroxysteroid Acetal Alcohol Aldehyde Aliphatic heteropolycyclic compound Carbonyl group Cucurbitacin skeleton Cyclic alcohol Delta-5-steroid Glycosyl compound Hexose monosaccharide Hydrocarbon derivative Hydroxysteroid Monosaccharide O-glycosyl compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organooxygen compound Oxacycle Oxane Polyol Primary alcohol Secondary alcohol Tertiary alcohol Triterpenoid logp 3.20 ALOGPS logs -4.29 ALOGPS solubility 3.23e-02 g/l ALOGPS melting_point Mp 227-232° logp 2.59 ChemAxon pka_strongest_acidic 12.21 ChemAxon pka_strongest_basic -0.79 ChemAxon iupac 5-hydroxy-14-[(4E)-6-hydroxy-6-methylhept-4-en-2-yl]-6,6,11,15-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-ene-1-carbaldehyde ChemAxon average_mass 634.8403 ChemAxon mono_mass 634.408083454 ChemAxon smiles CC(C\C=C\C(C)(C)O)C1CCC2(C)C3C(OC4OC(CO)C(O)C(O)C4O)C=C4C(CCC(O)C4(C)C)C3(CCC12C)C=O ChemAxon formula C36H58O9 ChemAxon inchi InChI=1S/C36H58O9/c1-20(9-8-13-32(2,3)43)21-12-14-35(7)30-24(44-31-29(42)28(41)27(40)25(18-37)45-31)17-23-22(10-11-26(39)33(23,4)5)36(30,19-38)16-15-34(21,35)6/h8,13,17,19-22,24-31,37,39-43H,9-12,14-16,18H2,1-7H3/b13-8+ ChemAxon inchikey BOHOBTRHAFBJOW-MDWZMJQESA-N ChemAxon polar_surface_area 156.91 ChemAxon refractivity 171.4 ChemAxon polarizability 72.02 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 9 ChemAxon donor_count 6 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 66849 Specdb::MsMs 66850 Specdb::MsMs 66851 Specdb::MsMs 124524 Specdb::MsMs 124525 Specdb::MsMs 124526 Specdb::MsMs 2362622 Specdb::MsMs 2362623 Specdb::MsMs 2362624 Specdb::MsMs 2600522 Specdb::MsMs 2600523 Specdb::MsMs 2600524 Specdb::CMs 23157 Specdb::CMs 592536 Specdb::CMs 592537 Specdb::CMs 592538 Specdb::CMs 592539 Specdb::CMs 592540 Specdb::CMs 592541 Specdb::CMs 592542 Specdb::CMs 592543 Specdb::CMs 592544 Specdb::CMs 592545 Specdb::CMs 592546 Specdb::CMs 592547 Specdb::CMs 592548 Specdb::CMs 592549 Specdb::CMs 592550 Specdb::CMs 592551 Specdb::CMs 592552 Specdb::CMs 592553 Specdb::CMs 592554 Specdb::CMs 592555 Specdb::CMs 592556 Specdb::CMs 592557 Specdb::CMs 592558 Specdb::CMs 592559 HMDB35917 #<Reference:0x000055ce31c4beb8> Bitter gourd Type 1 specific Momordica charantia 3673 Fruits Unknown generic