Flavor compounds

Please start searching↓

Name SMILES Flavor type Data resource
Veatchine C=C1C2CCC3C(CCC4C5(C)CCCC43C3OCCN3C5)(C2)C1O Bitter BitterSweet, BitterDB, ChemTasteDB
Garryine C=C1C2CCC3C(CCC4C5(C)CCCC43CN3CCOC35)(C2)C1O Bitter BitterSweet, BitterDB, ChemTasteDB
Rabdosianone II C=C1C2CCC3C45COC(O)(C(O)C4C(C)(C)C=CC5=O)C3(C2)C1OC(C)=O Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Grosheimin C=C1CC(O)C2C(=C)C(=O)OC2C2C(C)C(=O)CC12 Bitter ChemTasteDB, Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, BitterSweet
suavioside C1 C=C1CC23CCC4C(C)(C(=O)OC5OC(CO)C(O)C(O)C5O)CCCC4(C)C2CCC1(OC1OC(COC(=O)/C=C/c2ccc(O)cc2)C(O)C(O)C1O)C3 Bitter PlantMolecularTasteDB
Stevisalioside A C=C1CC23CCC4C(C)(C(=O)OC5OC(CO)C(OC6OCC(O)C(O)C6O)C(OC(C)=O)C5OC(C)=O)CCCC4(C)C2C(O)C1C(=O)C3 Bitter BitterSweet
suavioside D2 C=C1CC23CCC4C(C)(C(=O)OC5OC(COC(=O)/C=C/c6ccc(O)c(O)c6)C(O)C(O)C5O)CCCC4(C)C2CCC1(OC1OC(CO)C(O)C(O)C1O)C3 Bitter PlantMolecularTasteDB
Tatridin B C=C1CC2OC(=O)C(=C)C2C(O)C=C(C)CCC1O Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Herbolide D C=C1CCC(O)C(C)=CC2OC(=O)C(C)C2CC1O Bitter Natural_TAS2R_agonists
isoridentin C=C1CCC2C(=C)C(=O)OC2C=C(C)C(O)CC1O Bitter PlantMolecularTasteDB
Artemorin C=C1CCC2C(=C)C(=O)OC2C=C(C)CCC1O Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Peroxyartemorin C=C1CCC2C(=C)C(=O)OC2C=C(C)CCC1OO Bitter BitterDB, ChemTasteDB
Andrographolide C=C1CCC2C(C)(CO)C(O)CCC2(C)C1CC=C1C(=O)OCC1O Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
dehydroandrographolide C=C1CCC2C(C)(CO)C(O)CCC2(C)C1CC=C1C=COC1=O Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB
sciadin C=C1CCC2C3(C)CCCC24C(OC3=O)OC(c2ccoc2)CC14 Bitter PlantMolecularTasteDB
beta-caryophyllene C=C1CCC=C(C)CCC2C1CC2(C)C Bitter AromaDB, PlantMolecularTasteDB, FlavorDB
andrograpanin C=C1CC[C@H]2[C@@](C)(CCC[C@@]2(C)CO)[C@@H]1CCC1=CCOC1=O Bitter PhytoMolecularTasteDB
neoandrographolide C=C1CC[C@H]2[C@@](C)(CCC[C@@]2(C)CO[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@@H]1CCC1=CCOC1=O Bitter PhytoMolecularTasteDB
andrographolide C=C1CC[C@H]2[C@@](C)(CC[C@@H](O)[C@@]2(C)CO)[C@@H]1C/C=C1/C(=O)OC[C@H]1O Bitter PhytoMolecularTasteDB
Andrographolide C=C1CC[C@H]2[C@@](C)(CC[C@@H](O)[C@@]2(C)CO)[C@@H]1CC=C1C(=O)OC[C@H]1O Bitter BitterSweet
lettucenin A C=C1CCc2c(C)ccc3c(C=O)c(=O)oc-3c21 Bitter PlantMolecularTasteDB
Tatridin B C=C1C[C@@H]2OC(=O)C(=C)[C@H]2[C@H](O)C=C(C)CC[C@@H]1O Bitter BitterSweet
stevioside C=C1C[C@]23CC[C@@H]4[C@](C)(C(=O)O[C@@H]5O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]5O)CCC[C@]4(C)[C@H]2CC[C@@]1(O[C@@H]1O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]1O[C@@H]1O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]1O)C3 Bitter BitterSweet
ailanthone C=C1[C@@H]2CC(=O)O[C@@H]3C[C@H]4C(C)=CC(=O)[C@@H](O)[C@]4(C)[C@@H]4[C@]23CO[C@@]4(O)[C@@H]1O Bitter BitterSweet, PhytoMolecularTasteDB
atisine C=C1[C@H]2CC[C@@]3(CC[C@H]4[C@@]5(CCC[C@@]4(C)CN4CCOC45)[C@@H]3C2)[C@@H]1O Bitter PhytoMolecularTasteDB
Methacycline Hydrochloride C=C1c2cccc(O)c2C(O)=C2C(=O)C3(O)C(=O)C(=C(N)O)C(=O)C(N(C)C)C3C(O)C12.Cl Bitter BitterSweet
Methacycline hydrochloride C=C1c2cccc(O)c2C(O)=C2C(=O)C3(O)C(O)=C(C(N)=O)C(=O)C(N(C)C)C3C(O)C12.Cl Bitter BitterDB, ChemTasteDB
sclareol C=CC(C)(O)CCC1C(C)(O)CCC2C(C)(C)CCCC21C Bitter AromaDB, PlantMolecularTasteDB, FlavorDB
phlebotricoside C=CC(C)(O)CCC=C(C)C(=O)OCC1OC(Oc2ccc(O)cc2)C(O)C(O)C1O Bitter PlantMolecularTasteDB
Falcarindiol C=CC(O)C#CC#CC(O)C=CCCCCCCC Bitter ChemTasteDB, PhytoMolecularTasteDB, Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB