Flavor compounds

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Name SMILES Flavor type Data resource
taraxacin CC1=CC(=O)C2=C(C)CC3OC(=O)C(C)=C3C=C12 Bitter PlantMolecularTasteDB, PhytoMolecularTasteDB
ACHILLIN CC1=CC(=O)C2=C(C)CC[C@@H]3[C@H](OC(=O)[C@@H]3C)[C@@H]12 Bitter BitterSweet
carpesialactone CC1=CC(=O)C2C(C)CCC3C(C)C(=O)OC3C12 Bitter PlantMolecularTasteDB
Homocamfin CC1=CC(=O)CC(C(C)C)C1 Bitter BitterSweet, BitterDB, ChemTasteDB
bruceine G CC1=CC(=O)CC2(C)C1C(O)C1OC(=O)C(O)C3C4(C)OCC13C2C(O)C4O Bitter PlantMolecularTasteDB
shinjulactone B CC1=CC(=O)OC1C1(C)CC2OC(=O)CC3C(C)C(=O)C(O)=C1C23CO Bitter PlantMolecularTasteDB
dioscorine CC1=CC(=O)OC2(C1)CC1CCC2CN1C Bitter PlantMolecularTasteDB
Eurycomalactone CC1=CC(=O)[C@@H](O)[C@@]2(C)[C@H]1CC(=O)[C@@]1(C)[C@H]3C(=O)O[C@H]([C@@H]3C)[C@H](O)[C@H]21 Bitter BitterSweet
Klaineanone CC1=CC(=O)[C@@H](O)[C@@]2(C)[C@H]1C[C@H]1OC(=O)C[C@H]3[C@@H](C)[C@@H](O)[C@H](O)[C@H]2[C@]31C Bitter BitterSweet
Chaparrinone CC1=CC(=O)[C@@H](O)[C@@]2(C)[C@H]1C[C@H]1OC(=O)C[C@H]3[C@@H](C)[C@@H](O)[C@]4(O)OC[C@@]31[C@@H]24 Bitter BitterSweet
Isocyclogeraniol CC1=CC(C)C(CO)C(C)C1 Bitter BitterSweet
bruceine E CC1=CC(O)C(O)C2(C)C1CC1OC(=O)C(O)C3(O)C4(C)OCC13C2C(O)C4O Bitter PlantMolecularTasteDB
glaucarubol CC1=CC(O)C(O)C2(C)C1CC1OC(=O)C(O)C3C(C)C(O)C4(O)OCC13C42 Bitter PlantMolecularTasteDB
chaparrin CC1=CC(O)C(O)C2(C)C1CC1OC(=O)CC3C(C)C(O)C4(O)OCC13C42 Bitter PlantMolecularTasteDB
Germacradien-6,11-dihydroxy-8,12-olide CC1=CC(O)C2C(CC(C)=CCC1)OC(=O)C2(C)O Bitter Natural_TAS2R_agonists, ChemTasteDB
casteloside B CC1=CC(OC2OC(CO)C(O)C(O)C2O)C(O)C2(C)C1CC1OC(=O)C(O)C3C(C)C(O)C4(O)OCC13C42 Bitter PlantMolecularTasteDB
casteloside A CC1=CC(OC2OC(CO)C(O)C(O)C2O)C(O)C2(C)C1CC1OC(=O)CC3C(C)C(O)C4(O)OCC13C42 Bitter PlantMolecularTasteDB
Acesulfame K CC1=CC([O-])=NS(=O)(=O)O1.[K+] Bitter BitterDB
Absinthin CC1=CC2C3C4C(=C(C)C3C13C1OC(=O)C(C)C1CCC(C)(O)C23)C1OC(=O)C(C)C1CCC4(C)O Bitter Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, ChemTasteDB
2-Methylbicyclo[2.2.2]octa-2,5-diene CC1=CC2C=CC1CC2 Bitter ChemTasteDB
11,13-dihydrotaraxinic acid 1-O-beta-D-glucopiranoside CC1=CC2OC(=O)C(C)C2CCC(C(=O)OC2C(O)C(O)OC(CO)C2O)=CCC1 Bitter PlantMolecularTasteDB
1-Isopropyl-4-methyl CC1=CC=C(C(C)C)CC1 Bitter ChemTasteDB, Off-flavor, FlavorDB, AromaDB, PlantMolecularTasteDB, BitterDB, Flavornet, BitterSweet
Terpinyl isovalerate CC1=CCC(C(C)(C)OC(=O)CC(C)C)CC1 Bitter ChemTasteDB, FlavorDB, PlantMolecularTasteDB, BitterDB, BitterSweet
alpha-Terpinyl anthranilate CC1=CCC(C(C)(C)OC(=O)c2ccccc2N)CC1 Bitter ChemTasteDB, FlavorDB, BitterDB, BitterSweet
Terpinyl formate CC1=CCC(C(C)(C)OC=O)CC1 Bitter ChemTasteDB, FlavorDB, BitterDB, BitterSweet
p-Mentha-1,4-diene CC1=CCC(C(C)C)=CC1 Bitter ChemTasteDB, Food Flavor Laboratory, Off-flavor, FlavorDB, AromaDB, PlantMolecularTasteDB, BitterDB, Flavornet
3-beta-hydroxypelenolide CC1=CCC(O)C(C)CC2OC(=O)C(C)C2CC1 Bitter PlantMolecularTasteDB
Arborescin CC1=CCC23OC2(C)CCC2C(C)C(=O)OC2C13 Bitter ChemTasteDB, Natural_TAS2R_agonists, PlantMolecularTasteDB, BitterDB, BitterSweet
3-Methyl-5,6-dihydro-2H-pyran CC1=CCCOC1 Bitter ChemTasteDB
3,6-Dihydro-4-methyl-2H-pyran CC1=CCOCC1 Bitter ChemTasteDB