Flavor compounds

Please start searching↓

Name SMILES Flavor type Data resource
cneorin Q CC1(C)CC(C2(C)C=CC(=O)O2)C2(C=C3C(CCC45CC34C(=O)OC5c3ccoc3)OO2)O1 Bitter PlantMolecularTasteDB
loliolide CC1(C)CC(O)CC2(C)OC(=O)C=C12 Bitter PlantMolecularTasteDB
hederagenin CC1(C)CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(CO)C5CCC43C)C2C1 Bitter PlantMolecularTasteDB
3-O-beta-D-glucuronopyranosyl-oleanolic acid CC1(C)CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CCC(OC6OC(C(=O)O)C(O)C(O)C6O)C(C)(C)C5CCC43C)C2C1 Bitter PlantMolecularTasteDB
Momordin Ic CC1(C)CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CCC(OC6OC(C(=O)O)C(O)C(OC7OCC(O)C(O)C7O)C6O)C(C)(C)C5CCC43C)C2C1 Bitter BitterDB, ChemTasteDB
Vitalboside A CC1(C)CCC2(C(=O)O)CCC3(C)C(=CCC4C5(C)CCC(OC6OC(CO)C(O)C(O)C6O)C(C)(C)C5CCC43C)C2C1 Bitter BitterDB, ChemTasteDB
Momordin II CC1(C)CCC2(C(=O)OC3OC(CO)C(O)C(O)C3O)CCC3(C)C(=CCC4C5(C)CCC(OC6OC(C(=O)O)C(O)C(OC7OCC(O)C(O)C7O)C6O)C(C)(C)C5CCC43C)C2C1 Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
quinoside A CC1(C)CCC2(C(=O)OC3OCC(O)C(OC4OC(CO)C(O)C(O)C4O)C3O)CCC3(C)C(=CCC4C5(C)CCC(OC6OC(CO)C(O)C(O)C6O)C(C)(COC6OC(CO)C(O)C(O)C6O)C5CCC43C)C2C1 Bitter PlantMolecularTasteDB
erythrodiol CC1(C)CCC2(CO)CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(C)C5CCC43C)C2C1 Bitter PlantMolecularTasteDB
OLEANOLIC ACID CC1(C)CC[C@]2(C(=O)O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1 Bitter BitterSweet
oleanolic CC1(C)CC[C@]2(C(=O)O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6OC[C@H](O)[C@H](O)[C@H]6O[C@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)C(C)(C)C5CC[C@]43C)[C@H]2C1 Bitter PhytoMolecularTasteDB
arjunetin CC1(C)CC[C@]2(C(=O)O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)C[C@@H](O)[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2[C@@H]1O Bitter PhytoMolecularTasteDB
taraxerol CC1(C)CC[C@]2(C)CC=C3[C@@](C)(CC[C@H]4[C@@]3(C)CC[C@H]3C(C)(C)[C@@H](O)CC[C@@]34C)[C@@H]2C1 Bitter PhytoMolecularTasteDB
gymnemagenin CC1(C)C[C@H]2C3=CC[C@@H]4[C@@]5(C)CC[C@H](O)[C@@](C)(CO)[C@@H]5CC[C@@]4(C)[C@]3(C)C[C@H](O)[C@@]2(CO)[C@@H](O)[C@@H]1O Bitter PhytoMolecularTasteDB
zapoterin CC1(C)OC(=O)C=CC2(C)C1CC(=O)C1(C)C2C(O)CC2(C)C(c3ccoc3)OC(=O)C3OC321 Bitter PlantMolecularTasteDB
Obacunone CC1(C)OC(=O)C=CC2(C)C1CC(=O)C1(C)C2CCC2(C)C(c3ccoc3)OC(=O)C3OC321 Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
tricoccin S13 CC1(C)OC(=O)C=CC2(C)C1CC(O)C1(C)C3=CCC(C4COC(=O)C4)C3(C)CCC21 Bitter PlantMolecularTasteDB
obacunone CC1(C)OC(=O)C=C[C@@]2(C)[C@H]1CC(=O)[C@]1(C)[C@@H]2CC[C@@]2(C)[C@H](c3ccoc3)OC(=O)[C@H]3O[C@]321 Bitter BitterSweet, PhytoMolecularTasteDB
Zapoterin CC1(C)OC(=O)C=C[C@@]2(C)[C@H]1CC(=O)[C@]1(C)[C@@H]2[C@@H](O)C[C@@]2(C)[C@H](c3ccoc3)OC(=O)[C@H]3O[C@]321 Bitter BitterSweet
deacetyl nomilin CC1(C)OC(=O)CC(O)C2(C)C1CC(=O)C1(C)C2CCC2(C)C(c3ccoc3)OC(=O)C3OC321 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB
melianone CC1(C)OC1C1CC(C2CCC3(C)C4=CCC5C(C)(C)C(=O)CCC5(C)C4CCC23C)C(O)O1 Bitter PlantMolecularTasteDB, PhytoMolecularTasteDB
oxypeucedanin CC1(C)OC1COc1c2ccoc2cc2oc(=O)ccc12 Bitter PlantMolecularTasteDB
tricoccin S2 CC1(C)OC2(CC1C1(C)C=CC(O)O1)CC1C(O)(CCC34CC13C(=O)OC4c1ccoc1)O2 Bitter PlantMolecularTasteDB
cneorin F CC1(C)OC2CC(=O)OC2(C)C1CC(=O)CC1=CCCC23CC12C(=O)OC3c1ccoc1 Bitter PlantMolecularTasteDB
tricoccin R9 CC1(C)OC2CC(=O)OC2(C)C1CC(=O)CC1C(=O)CCC23CC12C(=O)OC3c1ccoc1 Bitter PlantMolecularTasteDB
tricoccin S18 CC1(C)OC2CC(=O)OC2(C)C1Cc1cc2c(o1)CCC13CC21C(O)OC3c1ccoc1 Bitter PlantMolecularTasteDB
evodol CC1(C)OC2CC(=O)OCC23C1=C(O)C(=O)C1(C)C3CCC2(C)C(c3ccoc3)OC(=O)C3OC321 Bitter PlantMolecularTasteDB
rutaevin CC1(C)OC2CC(=O)OCC23C1C(=O)C(O)C1(C)C3CCC2(C)C(c3ccoc3)OC(=O)C3OC321 Bitter PlantMolecularTasteDB
limonexic acid CC1(C)OC2CC(=O)OCC23C1CC(=O)C1(C)C3CCC2(C)C(C3=CC(=O)OC3O)OC(=O)C3OC321 Bitter PlantMolecularTasteDB
Limonin CC1(C)OC2CC(=O)OCC23C1CC(=O)C1(C)C3CCC2(C)C(c3ccoc3)OC(=O)C3OC321 Bitter ChemTasteDB, Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, BitterSweet