Flavor compounds

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Name SMILES Flavor type Data resource
beta-carotene CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)CCCC2(C)C)C(C)(C)CCC1 Bitter PlantMolecularTasteDB
Picrocrocin CC1=C(C=O)C(C)(C)CC(OC2OC(CO)C(O)C(O)C2O)C1 Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB
picrocrocin CC1=C(C=O)C(C)(C)C[C@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C1 Bitter PhytoMolecularTasteDB
phlomisoside II CC1=C(CCc2ccoc2)C2(C)CCC(OC3OC(CO)C(O)C(O)C3OC3OC(CO)C(O)C(O)C3O)C(C)(C)C2CC1 Bitter PlantMolecularTasteDB
castelanolide CC1=C(O)C(=O)C2C3(C)C(CC4C(C)CC(O)C(O)C42C)OC(=O)CC13 Bitter PlantMolecularTasteDB
Artabsin CC1=C2C(=CC1)C(C)(O)CCC1C(C)C(=O)OC21 Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
11,13-Dihydrolactucin CC1=C2C(=O)C=C(CO)C2C2OC(=O)C(C)C2C(O)C1 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
11,13-dihydrolactucopicrin CC1=C2C(=O)C=C(CO)C2C2OC(=O)C(C)C2C(OC(=O)Cc2ccc(O)cc2)C1 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB
11ß,13-dihydrolactucin-8-O-sulfate CC1=C2C(=O)C=C(CO)C2C2OC(=O)C(C)C2C(OS(=O)(=O)O)C1 Bitter PlantMolecularTasteDB
11(S),13-dihydro-8-deoxylactucin CC1=C2C(=O)C=C(CO)C2C2OC(=O)C(C)C2CC1 Bitter PlantMolecularTasteDB
cichorioside B CC1=C2C(=O)C=C(COC3OC(CO)C(O)C(O)C3O)C2C2OC(=O)C(C)C2C(O)C1 Bitter PlantMolecularTasteDB
merolimonol CC1=C2C(O)C(=O)OC3CC4C(C)(C)OC5CC(=O)OCC54C(CC1)C23C Bitter PlantMolecularTasteDB
geigerin CC1=C2C(O)C3C(CC(C)C2CC1=O)OC(=O)C3C Bitter PlantMolecularTasteDB
Artemisin CC1=C2C3OC(=O)C(C)C3C(O)CC2(C)C=CC1=O Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB
anabsin CC1=C2C3OC(=O)C(C)C3CCC(C)(O)C2C2C3C(O)C4(C)OC5(C)CCC6C(C)C(=O)OC6C4(C12)C35 Bitter PlantMolecularTasteDB
anabsinthin CC1=C2C3OC(=O)C(C)C3CCC(C)(O)C2C2C3CC4(C)OC5(C)CCC6C(C)C(=O)OC6C4(C12)C35 Bitter PlantMolecularTasteDB
Taurin, taurine CC1=C2C3OC(=O)C(C)C3CCC2(C)C(=O)CC1 Bitter Natural_TAS2R_agonists
Dihydro taurin CC1=C2C3OC(=O)C(C)C3CCC2(C)C(O)CC1 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
?±-Santonin, (-)-form CC1=C2C3OC(=O)C(C)C3CCC2(C)C=CC1=O Bitter ChemTasteDB, Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, BitterSweet
casteloside C CC1=C2CC3OC(=O)CC4C(C)C(O)C5(OC6OC(CO)C(O)C(O)C6O)OCC34C5C2(C)C(O)C(O)C1 Bitter PlantMolecularTasteDB
santonin CC1=C2[C@H]3OC(=O)[C@@H](C)[C@@H]3CC[C@@]2(C)C=CC1=O Bitter PhytoMolecularTasteDB
yadanziolide A CC1=CC(=O)C(O)C2(C)C1CC1OC(=O)C(O)C3(O)C4(CO)OCC13C2C(O)C4O Bitter PlantMolecularTasteDB
klaineanone CC1=CC(=O)C(O)C2(C)C1CC1OC(=O)CC3C(C)C(O)C(O)C2C13C Bitter PlantMolecularTasteDB
shinjulactone G CC1=CC(=O)C(O)C2(C)C1CC1OC(=O)CC3C(C)C(O)C(O)C2C13CO Bitter PlantMolecularTasteDB
chaparrinone CC1=CC(=O)C(O)C2(C)C1CC1OC(=O)CC3C(C)C(O)C4(O)OCC13C42 Bitter PlantMolecularTasteDB
shinjudilactone CC1=CC(=O)C(O)C2(C)C1CC1OC(=O)CC3C(C)C4(O)C(=O)OCC13C42 Bitter PlantMolecularTasteDB
shinjulactone M CC1=CC(=O)C(O)C2(C)C1CC1OC(=O)CC3C(O)(CO)C(O)C4(O)OCC13C42 Bitter PlantMolecularTasteDB
shinjulactone F CC1=CC(=O)C2(O)OC3=C4C5(CO)C(CC1C42C)OC(=O)CC5C(C)C3=O Bitter PlantMolecularTasteDB
desacetylmatricarin CC1=CC(=O)C2=C(C)CC(O)C3C(C)C(=O)OC3C12 Bitter PlantMolecularTasteDB
8-deacetylmatricarin-8-O-sulfate CC1=CC(=O)C2=C(C)CC(OS(=O)(=O)O)C3C(C)C(=O)OC3C12 Bitter PlantMolecularTasteDB