Flavor compounds

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Name SMILES Flavor type Data resource
Nodosinol CC(=O)OC1OCC23C(CCC(C)(C)C12)OC(=O)C12CC(CC(=O)C13)C(C)C2=O Bitter ChemTasteDB
Isobutyl acetate CC(=O)OCC(C)C Bitter ChemTasteDB, FlavorDB, BitterDB, Flavornet
Triacetin CC(=O)OCC(COC(C)=O)OC(C)=O Bitter ChemTasteDB, BitterDB, FlavorDB
Glucose pentaacetate CC(=O)OCC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(C=O)OC(C)=O Bitter BitterSweet, BitterDB, ChemTasteDB
suspensolide A aglycon CC(=O)OCC1(O)C(OC(C)=O)CC2C(CO)=COC(OC(=O)CC(C)C)C21 Bitter PlantMolecularTasteDB
suspensolide A CC(=O)OCC1(O)C(OC(C)=O)CC2C(COC3OC(CO)C(O)C(O)C3O)=COC(OC(=O)CC(C)C)C21 Bitter PlantMolecularTasteDB
Diterpene derivative 3 CC(=O)OCC12C(CCC(C)(C)C1C(=O)O)OC(=O)C13CC(CC(O)C12)C(C)C3=O Bitter BitterSweet, ChemTasteDB
Compound V CC(=O)OCC12C(CCC(C)(C)C1CO)OC(=O)C13CC(CC(O)C12)C(C)C3O Bitter ChemTasteDB
Teumarin CC(=O)OCC12C(O)CC(C)C3(CC(c4ccoc4)OC3=O)C1CC(O)CC21CO1 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
Teuflavin CC(=O)OCC12C(O)CC(C)C3(CC(c4ccoc4)OC3O)C1CCC(=O)C21CO1 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
clerodin CC(=O)OCC12C(OC(C)=O)CC(C)C(C)(C3CC4C=COC4O3)C1CCCC21CO1 Bitter PlantMolecularTasteDB
Teuflavoside CC(=O)OCC1=C2C(OC3OC(CO)C(O)C(O)C3O)CC(C)C3(CC(c4ccoc4)OC3=O)C2CCC1 Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
.alpha.-D-Glucopyranose, pentaacetate CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O Bitter BitterSweet
Sucrose octaacetate CC(=O)OCC1OC(OC2(COC(C)=O)OC(COC(C)=O)C(OC(C)=O)C2OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O Bitter ChemTasteDB, BitterSweet, BitterDB, FlavorDB
amarelloside CC(=O)OCC1OC(OC2C(OC3(COC(=O)c4ccccc4)OC(CO)C(OC(=O)c4ccccc4)C3OC(=O)c3ccccc3)OC(COC(C)=O)C(OC(C)=O)C2OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O Bitter PlantMolecularTasteDB
gentomoside CC(=O)OCC1OC(OC2OC=C3C(=O)OCCC3(O)C2C2CO2)C(OC(C)=O)C(OC(C)=O)C1OC(=O)c1cccc(OC2OC(CO)C(O)C(O)C2O)c1O Bitter PlantMolecularTasteDB
Raffinose undecaacetate CC(=O)OCC1OC(OCC2OC(OC3(COC(C)=O)OC(COC(C)=O)C(OC(C)=O)C3OC(C)=O)C(OC(C)=O)C(OC(C)=O)C2OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O Bitter BitterDB, ChemTasteDB
6''-O-Acetylgenistin CC(=O)OCC1OC(Oc2cc(O)c3c(=O)c(-c4ccc(O)cc4)coc3c2)C(O)C(O)C1O Bitter BitterDB, ChemTasteDB
Geranyl acetate CC(=O)OCC=C(C)CCC=C(C)C Bitter ChemTasteDB, Off-flavor, Riechstoff-Lexikon - Index, FlavorDB, BitterDB, Flavornet, BitterSweet
3891-59-6 CC(=O)OC[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H](C=O)OC(C)=O Bitter BitterSweet
clerodin CC(=O)OC[C@@]12[C@@H](OC(C)=O)C[C@@H](C)[C@](C)([C@@H]3C[C@H]4C=CO[C@H]4O3)[C@H]1CCC[C@]21CO1 Bitter PhytoMolecularTasteDB
Caryoptin CC(=O)OC[C@@]12[C@@H](OC(C)=O)C[C@@H](C)[C@](C)([C@@H]3C[C@H]4C=CO[C@H]4O3)[C@H]1CC[C@@H](OC(C)=O)[C@]21CO1 Bitter BitterSweet
6-Acetylpicropolin CC(=O)OC[C@@]12[C@H](CCC[C@]13CO3)[C@@]1(C[C@@H](c3ccoc3)OC1=O)[C@H](C)C(=O)[C@@H]2OC(C)=O Bitter BitterSweet
Acetylgenistin CC(=O)OC[C@H]1O[C@@H](Oc2cc(O)c3c(=O)c(-c4ccc(O)cc4)coc3c2)[C@H](O)[C@@H](O)[C@@H]1O Bitter BitterSweet
Piperonyl acetate CC(=O)OCc1ccc2c(c1)OCO2 Bitter ChemTasteDB, BitterDB, FlavorDB
nimbinin CC(=O)O[C@@H]1C[C@H]2C(C)(C)C(=O)C=C[C@]2(C)[C@H]2CC[C@@]3(C)[C@H](c4ccoc4)C(=O)[C@H]4O[C@]43[C@]12C Bitter PhytoMolecularTasteDB
Cascarillin CC(=O)O[C@@H]1C[C@]2(C)[C@H](CC[C@@H](O)[C@]2(C)O)[C@@](C=O)(C[C@@H](O)c2ccoc2)[C@@H]1C Bitter BitterSweet
Nomilin CC(=O)O[C@H]1CC(=O)OC(C)(C)[C@@H]2CC(=O)[C@]3(C)[C@H](CC[C@@]4(C)[C@H](c5ccoc5)OC(=O)[C@H]5O[C@]543)[C@@]12C Bitter BitterSweet
taxine CC(=O)O[C@H]1CC2[C@@H](OC(C)=O)C=C3C[C@](C)(C(=O)[C@H](O)C(=C1C)C2(C)C)[C@@H](O)C[C@@H]3OC(=O)[C@H](O)[C@H](c1ccccc1)N(C)C Bitter PhytoMolecularTasteDB
Bufotoxin CC(=O)O[C@H]1C[C@]2(O)C3CC[C@@H]4C[C@@H](OC(=O)CCCCCCC(=O)NC(CCCN=C(N)N)C(=O)O)CC[C@]4(C)C3CC[C@]2(C)[C@H]1c1ccoc(=O)c1 Bitter BitterSweet