Flavor compounds

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Name SMILES Flavor type Data resource
Dehydrotricyclolupone C=C(C)C1CC23C(=O)C(C(=O)CC(C)C)=C(O)C(CC=C(C)C)(CC2C1(C)C)C3=O Bitter BitterDB, ChemTasteDB
Coriamyrtin C=C(C)C1[C@H]2C[C@]3(C)[C@]4(CO4)[C@H]4O[C@H]4[C@]3(O)[C@@H]1C(=O)O2 Bitter BitterSweet
cayaponoside B C=C(C)C=CC(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
N-(2-methylprop-2-enylidene)hydroxylamine C=C(C)C=NO Bitter ChemTasteDB
Rhodinyl acetate C=C(C)CCCC(C)CCOC(C)=O Bitter ChemTasteDB, FlavorDB, BitterDB, BitterSweet
Xanthohumol N C=C(C)CCc1c(O)cc(OC)c(C(=O)C=Cc2ccc(O)cc2)c1O Bitter BitterDB, ChemTasteDB
Dihydrooridonin tetraacetate C=C(C)OC12OCC3(C(OC(C)=O)CCC(C)(C)C3C1OC(C)=O)C1CCC3C(C)C(=O)C12C3OC(C)=O Bitter ChemTasteDB
NOOTKATONE C=C(C)[C@@H]1CCC2=CC(=O)C[C@@H](C)[C@]2(C)C1 Bitter BitterSweet, Flavornet
Tricyclodehydroisohumulone C=C(C)[C@H]1C[C@]23C([O-])=C(C(=O)CC(C)C)C(=O)[C@@]2(O)C(=O)C[C@@H]3C1(C)C Bitter BitterSweet
rotenoid C=C(C)[C@H]1Cc2c(ccc3c2O[C@@H]2COc4cc(OC)c(OC)cc4[C@@H]2C3=O)O1 Bitter PhytoMolecularTasteDB
Picrotoxinin C=C(C)[C@H]1[C@@H]2C(=O)O[C@H]1[C@H]1OC(=O)[C@@]34O[C@@H]3C[C@]2(O)[C@@]14C Bitter BitterSweet
joazeiroside A C=C(CC1OC2(O)C(C3CCC4C5(C)CCC(OC6OC(CO)C(O)C(O)C6O)C(C)(C)C5CCC4(C)C3(C)C2O)C1(C)O)C(C)C Bitter PlantMolecularTasteDB
Dehydrocyanaropicrin C=C(CO)C(=O)OC1CC(=C)C2CC(=O)C(=C)C2C2OC(=O)C(=C)C12 Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Cynaropicrin C=C(CO)C(=O)OC1CC(=C)C2CC(O)C(=C)C2C2OC(=O)C(=C)C12 Bitter ChemTasteDB, Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, BitterSweet
hydroxyvernolide C=C(CO)C(=O)OC1CC23OC2CCC(=CC2OC(=O)C(=C)C21)COC3O Bitter PlantMolecularTasteDB
Hydroxyvernolide C=C(CO)C(=O)O[C@H]1C[C@@]23O[C@@H]2CC/C(=C/[C@H]2OC(=O)C(=C)[C@H]12)CO[C@H]3O Bitter BitterSweet
tamarindienal C=C(O)/C=C/C(=O)C=O.CC(=O)/C=C/C(=O)C=O Bitter PhytoMolecularTasteDB
Oridonin C=C1C(=O)C23C(O)C1CCC2C12COC3(O)C(O)C1C(C)(C)CCC2O Bitter PlantMolecularTasteDB, ChemTasteDB
isodomedin C=C1C(=O)C23C(O)CC4C(C)(C)C(OC(C)=O)CC(O)C4(C)C2CCC1C3O Bitter PlantMolecularTasteDB
umbrosin B C=C1C(=O)C23C(O)CC4C(C)(C)CC(=O)CC4(C)C2CCC1C3O Bitter PlantMolecularTasteDB
umbrosin A C=C1C(=O)C23C(O)CC4C(C)(C)CC(O)CC4(C)C2CCC1C3O Bitter PlantMolecularTasteDB
kamebanin C=C1C(=O)C23C(O)CC4C(C)(C)CCC(O)C4(C)C2CCC1C3O Bitter PlantMolecularTasteDB
Nodosin C=C1C(=O)C23CC1CC(O)C2C12COC(O)C1C(C)(C)CCC2OC3=O Bitter PlantMolecularTasteDB, ChemTasteDB
Shikokianin C=C1C(=O)C23CC1CC(OC(C)=O)C2C12COC3(O)C(O)C1C(C)(C)CCC2OC(C)=O Bitter PlantMolecularTasteDB, ChemTasteDB
Enmein C=C1C(=O)C23CC1CCC2C12COC(O)C1C(C)(C)C(O)CC2OC3=O Bitter PlantMolecularTasteDB, ChemTasteDB
Enmein-3-acetate C=C1C(=O)C23CC1CCC2C12COC(O)C1C(C)(C)C(OC(C)=O)CC2OC3=O Bitter PlantMolecularTasteDB, ChemTasteDB
Rabdosianone I C=C1C(=O)C23CC1CCC2C12COC3(O)C(O)C1C(C)(C)C=CC2=O Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Compound 857 C=C1C(=O)C23CCC4C(C)(C)CC(OOC5OC(CO)C(O)C(O)C5O)CC4(C)C2CCC1C3 Bitter ChemTasteDB
1,2,2???,3???-Tetrahydrovernodalin C=C1C(=O)OC2C1C(OC(=O)C(C)CO)CC1(CC)COC(=O)C(=C)C21 Bitter PlantMolecularTasteDB