Flavor compounds

Please start searching↓

Name SMILES Flavor type Data resource
arvenin II CC(=O)OC(C)(C)CCC(=O)C(C)(O)C1C(O)CC2(C)C3CC=C4C(CC(OC5OC(CO)C(O)C(O)C5O)C(=O)C4(C)C)C3(C)C(=O)CC12C Bitter PlantMolecularTasteDB
cayaponoside A CC(=O)OC(C)(C)CCC(=O)C(C)(O)C1C(O)CC2(C)C3CCc4c(cc(OC5OC(CO)C(O)C(O)C5O)c(O)c4C)C3(C)C(=O)CC12C Bitter PlantMolecularTasteDB
alpha-Methylbenzyl acetate CC(=O)OC(C)c1ccccc1 Bitter ChemTasteDB, BitterDB, FlavorDB
nomilinic acid CC(=O)OC(CC(=O)O)C1(C)C(C(C)(C)O)CC(=O)C2(C)C1CCC1(C)C(c3ccoc3)OC(=O)C3OC312 Bitter PlantMolecularTasteDB
shinjuglycoside C CC(=O)OC1C(=O)C(C)C2CC(=O)OC3CC4C(C)CC(OC5OC(CO)C(O)C(O)C5O)C(=O)C4(C)C1C32C Bitter PlantMolecularTasteDB
glaucin B CC(=O)OC1C(=O)C2(C)C(CCC3(C)C(c4ccoc4)OC(=O)C4OC432)C23COC(=O)CC2OC(C)(C)C13 Bitter PlantMolecularTasteDB
shinjulactone L CC(=O)OC1C(=O)C2C3(C)C(=O)C(O)CC(C)C3CC3OC(=O)CC(C1C)C32C Bitter PlantMolecularTasteDB
condurangin A CC(=O)OC1C(OC(=O)/C=C/c2ccccc2)C2C(CCC3CC(OC4OC(CO)C(OC5OC(CO)C(OC6OC(CO)C(OC7OC(CO)C(OC8OC(CO)C(O)C(O)C8O)C(O)C7O)C(O)C6O)C(O)C5O)C(O)C4O)CCC32C)C2(O)CCC(C(C)=O)C12C Bitter PlantMolecularTasteDB
taccalonolide B CC(=O)OC1C(OC(C)=O)C2(C)C(C(O)C3C2C(C)C=C2OC(=O)C(C)(O)C23C)C2C(O)C(=O)C3CC4OC4C(OC(C)=O)C3(C)C12 Bitter PlantMolecularTasteDB
taccalonolide A CC(=O)OC1C(OC(C)=O)C2(C)C(C(OC(C)=O)C3C2C(C)C=C2OC(=O)C(C)(O)C23C)C2C(O)C(=O)C3CC4OC4C(OC(C)=O)C3(C)C12 Bitter PlantMolecularTasteDB
alpha-caesalpin CC(=O)OC1C2C(Cc3occc3C2(C)O)C2(C)C(=O)CCC(C)(C)C2(O)C1OC(C)=O Bitter PlantMolecularTasteDB
simarolide CC(=O)OC1CC(C)(C(=O)C2COC(=O)C2)C2CC(=O)OC3CC4C(C)CC(O)C(=O)C4(C)C1C32C Bitter PlantMolecularTasteDB
matricarin CC(=O)OC1CC(C)=C2C(=O)C=C(C)C2C2OC(=O)C(C)C12 Bitter PlantMolecularTasteDB
matricin CC(=O)OC1CC(C)=C2C=CC(C)(O)C2C2OC(=O)C(C)C12 Bitter PlantMolecularTasteDB
asclepiadin CC(=O)OC1CC(C)OC2OC3CC4CCC5C(CCC6(C)C(C7=CC(=O)OC7)CCC56O)C4(C=O)CC3OC12O Bitter PlantMolecularTasteDB
toosendanin CC(=O)OC1CC(O)C23COC(O)C1(C)C2CC(O)C1(C)C3C(=O)C(OC(C)=O)C2(C)C(c3ccoc3)CC3OC321 Bitter PlantMolecularTasteDB
lanatoside C CC(=O)OC1CC(OC2C(O)CC(OC3C(O)CC(OC4CCC5(C)C(CCC6C5CC(O)C5(C)C(C7=CC(=O)OC7)CCC65O)C4)OC3C)OC2C)OC(C)C1OC1OC(CO)C(O)C(O)C1O Bitter PlantMolecularTasteDB, FlavorDB
solidagonic acid CC(=O)OC1CC2(C)C(C)=CCCC2C(C)(CCC(C)=CC(=O)O)C1C Bitter PlantMolecularTasteDB
Cascarillin CC(=O)OC1CC2(C)C(CCC(O)C2(C)O)C(C=O)(CC(O)c2ccoc2)C1C Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Bufotoxin CC(=O)OC1CC2(O)C3CCC4CC(OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O)CCC4(C)C3CCC2(C)C1c1ccc(=O)oc1 Bitter ChemTasteDB
Bufotoxin CC(=O)OC1CC2(O)C3CCC4CC(OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O)CCC4(C)C3CCC2(C)C1c1ccoc(=O)c1 Bitter BitterDB
nimbinin CC(=O)OC1CC2C(C)(C)C(=O)C=CC2(C)C2CCC3(C)C(c4ccoc4)C(=O)C4OC43C12C Bitter PlantMolecularTasteDB
Herbolide A CC(=O)OC1CC2C(C=C(C)CCC=C1C)OC(=O)C2C Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
VE-1 CC(=O)OC1CC2C3=CCC4CC(OC5OC(CO)C(O)C(O)C5O)CCC4(C)C3=CCC2(C)C1C1C(O)OC2C1OC(C)C2(O)C(C)C Bitter PlantMolecularTasteDB
Compound VII CC(=O)OC1CC2CC3(C(=O)OC4CCC(C)(C)C5C(OC(C)=O)OCC45C13)C(=O)C2C Bitter ChemTasteDB
Compound XVII CC(=O)OC1CC2CC3(C(O)C2C)C1C12COC3(O)C(O)C1C(C)(C)CCC2OC(C)=O Bitter ChemTasteDB
Pancuronium bromide CC(=O)OC1CC2CCC3C(CCC4(C)C3CC([N+]3(C)CCCCC3)C4OC(C)=O)C2(C)CC1[N+]1(C)CCCCC1.[Br-].[Br-] Bitter BitterSweet, BitterDB, ChemTasteDB
Compound XX CC(=O)OC1CC2OC(=O)C34CC(CCC3C23COC(=O)C3C1(C)C)C(C)C4=O Bitter ChemTasteDB
Sintenin CC(=O)OC1CC=C(C)C(OC(C)=O)CC2C(C=C1C)OC(=O)C2C Bitter ChemTasteDB
glaucanol CC(=O)OC1CCC2(C)C1CCC1(C)C2CCC2C3(C)CCCC(C)(C)C3CCC21C Bitter PlantMolecularTasteDB