Flavor compounds

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Name SMILES Flavor type Data resource
Crispolide C=C1C(=O)OC2C1CC=C1CC(C)(CCC1OO)C2O Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Epizaluzanin C C=C1C(=O)OC2C1CCC(=C)C1CC(O)C(=C)C12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Zaluzanin D C=C1C(=O)OC2C1CCC(=C)C1CC(OC(C)=O)C(=C)C12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
dehydrocostuslactone C=C1C(=O)OC2C1CCC(=C)C1CCC(=C)C12 Bitter AromaDB, PlantMolecularTasteDB
Vulgarolid C=C1C(=O)OC2C1CCC(=O)CC1(C)CCC(O)OC21 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
chrysartemin B C=C1C(=O)OC2C1CCC(C)(O)C13OC1C1OC1(C)C23 Bitter PlantMolecularTasteDB
deoxylactucin C=C1C(=O)OC2C1CCC(C)=C1C(=O)C=C(CO)C12 Bitter PlantMolecularTasteDB
8-Deoxylactucin-15-sulphate C=C1C(=O)OC2C1CCC(C)=C1C(=O)C=C(COS(=O)(=O)[O-])C12 Bitter PlantMolecularTasteDB, ChemTasteDB
(-)-Parthenolide C=C1C(=O)OC2C1CCC(C)=CCCC1(C)OC21 Bitter ChemTasteDB, PhytoMolecularTasteDB, Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB
Parthenin C=C1C(=O)OC2C1CCC(C)C1(O)C=CC(=O)C21C Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Artecalin C=C1C(=O)OC2C1CCC1(C)C(O)CC(=O)C(C)C21 Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Santamarine C=C1C(=O)OC2C1CCC1(C)C(O)CC=C(C)C21 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
tanacetin C=C1C(=O)OC2C1CCC1(C)C(O)CCC(=C)C21O Bitter PlantMolecularTasteDB
Arglabin C=C1C(=O)OC2C1CCC1(C)OC13CC=C(C)C23 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Lactucin C=C1C(=O)OC2C3C(CO)=CC(=O)C3=C(C)CC(O)C12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Lactupicrin C=C1C(=O)OC2C3C(CO)=CC(=O)C3=C(C)CC(OC(=O)Cc3ccc(O)cc3)C12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Lactucin-15-oxalate C=C1C(=O)OC2C3C(COC(=O)C(=O)O)=CC(=O)C3=C(C)CC(O)C12 Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Lactucopicrin-15-oxalate C=C1C(=O)OC2C3C(COC(=O)C(=O)O)=CC(=O)C3=C(C)CC(OC(=O)Cc3ccc(O)cc3)C12 Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Lactucopicrin C=C1C(=O)OC2C3C(COC(=O)Cc4ccc(O)cc4)=CC(=O)C3=C(C)CC(O)C12 Bitter BitterDB, ChemTasteDB
Nobilin C=C1C(=O)OC2C=C(C)C(O)CC=C(C)CC(OC(=O)C(C)=CC)C12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Tatridin A C=C1C(=O)OC2C=C(C)C(O)CCC(C)=CC(O)C12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Tatridn A acetate C=C1C(=O)OC2C=C(C)C(OC(C)=O)CCC(C)=CC(OC(C)=O)C12 Bitter ChemTasteDB
taraxinic acid 1???-O-beta-D-glucopyranoside C=C1C(=O)OC2C=C(C)CCC=C(C(=O)OC3OC(CO)C(O)C(O)C3O)CCC12 Bitter PlantMolecularTasteDB
Costunolide C=C1C(=O)OC2C=C(C)CCC=C(C)CCC12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
arctiopicrin C=C1C(=O)OC2C=C(CO)CCC=C(C)CC(OC(=O)C(C)CO)C12 Bitter PlantMolecularTasteDB
Umbellifolide C=C1C(=O)OC2CC(C)(CCCC(C)=O)C(=O)CC12 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
scabiolide C=C1C(=O)OC2CC(C)=CCCC(COC(C)=O)=CC(OC(=O)C(C)(O)CO)C12 Bitter PlantMolecularTasteDB
Speciformin acetate C=C1C(=O)OC2CC(C)=CCCC3(C)OC3C(OC(C)=O)C12 Bitter Natural_TAS2R_agonists, ChemTasteDB
gafrinin C=C1C(=O)OC2CC(C)C(C(O)CC(C)OC(C)=O)=CCC12 Bitter PlantMolecularTasteDB
Helenalin C=C1C(=O)OC2CC(C)C3C=CC(=O)C3(C)C(O)C12 Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB