Flavor compounds

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Name SMILES Flavor type Data resource
trans-Cyclo(D-Ala-L-Val) CC1NC(=O)C(C(C)C)NC1=O Bitter BitterDB, ChemTasteDB
cis-Cyclo(L-Ala-L-Tyr) CC1NC(=O)C(Cc2ccc(O)cc2)NC1=O Bitter BitterDB, ChemTasteDB
cis-Cyclo(L-Ala-L-Phe) CC1NC(=O)C(Cc2ccccc2)NC1=O Bitter BitterDB, ChemTasteDB
trans-Cyclo(D-Ala-L-Pro) CC1NC(=O)C2CCCN2C1=O Bitter BitterDB, ChemTasteDB
cis-Cyclo(L-Ala-Gly) CC1NC(=O)CNC1=O Bitter BitterDB, ChemTasteDB
pseudocarpaine CC1NC2CCCCCCCC(=O)OC3CCC(CCCCCCCC(=O)OC1CC2)NC3C Bitter PlantMolecularTasteDB
Digitoxin CC1OC(OC2C(O)CC(OC3C(O)CC(OC4CCC5(C)C(CCC6C5CCC5(C)C(C7=CC(=O)OC7)CCC65O)C4)OC3C)OC2C)CC(O)C1O Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Avenacoside A CC1OC(OC2C(OC3CCC4(C)C(=CCC5C4CCC4(C)C5CC5OC6(CCC(C)(COC7OC(CO)C(O)C(O)C7O)O6)C(C)C54)C3)OC(CO)C(OC3OC(CO)C(O)C(O)C3O)C2O)C(O)C(O)C1O Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Avenacoside B CC1OC(OC2C(OC3CCC4(C)C(=CCC5C4CCC4(C)C5CC5OC6(CCC(C)(COC7OC(CO)C(O)C(O)C7O)O6)C(C)C54)C3)OC(CO)C(OC3OC(CO)C(O)C(OC4OC(CO)C(O)C(O)C4O)C3O)C2O)C(O)C(O)C1O Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
alpha-hederin CC1OC(OC2C(OC3CCC4(C)C(CCC5(C)C4CC=C4C6CC(C)(C)CCC6(C(=O)O)CCC45C)C3(C)CO)OCC(O)C2O)C(O)C(O)C1O Bitter PlantMolecularTasteDB
Neoeriocitrin CC1OC(OC2C(Oc3cc(O)c4c(c3)OC(c3ccc(O)c(O)c3)CC4=O)OC(CO)C(O)C2O)C(O)C(O)C1O Bitter BitterSweet, PlantMolecularTasteDB, ChemTasteDB
Naringin CC1OC(OC2C(Oc3cc(O)c4c(c3)OC(c3ccc(O)cc3)CC4=O)OC(CO)C(O)C2O)C(O)C(O)C1O Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB
pinocembrin 7-beta-neohesperidoside CC1OC(OC2C(Oc3cc(O)c4c(c3)OC(c3ccccc3)CC4=O)OC(CO)C(O)C2O)C(O)C(O)C1O Bitter PlantMolecularTasteDB
2S-5-[alpha-L-rhamnopyranosyl-(1??í2)-beta-D-glucopyranosyloxy]naringenin CC1OC(OC2C(Oc3cc(O)cc4c3C(=O)CC(c3ccc(O)cc3)O4)OC(CO)C(O)C2O)C(O)C(O)C1O Bitter PlantMolecularTasteDB
Scillaren CC1OC(OC2C=C3CCC4C(CCC5(C)C(c6ccc(=O)oc6)CCC45O)C3(C)CC2)C(O)C(OC2OC(CO)C(O)C(O)C2O)C1O Bitter BitterSweet, BitterDB, ChemTasteDB
Convallatoxin CC1OC(OC2CCC3(C=O)C4CCC5(C)C(C6=CC(=O)OC6)CCC5(O)C4CCC3(O)C2)C(O)C(O)C1O Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
laserine CC=C(C)C(=O)OC(C)C(OC(=O)C(C)=CC)c1cc(OC)c2c(c1)OCO2 Bitter PlantMolecularTasteDB
laserine oxide CC=C(C)C(=O)OC(c1cc(OC)c2c(c1)OCO2)C(C)OC(=O)C1(C)OC1C Bitter PlantMolecularTasteDB
gymnemic acids CC=C(C)C(=O)OC1C(O)C2(COC(C)=O)C(O)CC3(C)C(=CCC4C5(C)CCC(OC6OC(C(=O)O)C(O)C(O)C6O)C(C)(CO)C5CCC43C)C2CC1(C)C Bitter PlantMolecularTasteDB
vaginatin CC=C(C)C(=O)OC1C=C(C)CCC2(O)C(C(C)C)CC(=O)C12C Bitter PlantMolecularTasteDB
azadirachtin CC=C(C)C(=O)OC1CC(OC(C)=O)C2(C(=O)OC)COC3C2C12COC(O)(C(=O)OC)C2C(C)(C12OC1(C)C1CC2OC2OC=CC21O)C3O Bitter PlantMolecularTasteDB
Aglycon H.g.-12 CC=C(C)C(=O)OC1CC2C(CC=C3CC(O)CCC32C)C2(O)CCC(C(C)=O)C12C Bitter Natural_TAS2R_agonists, BitterDB, ChemTasteDB
Hg-12 CC=C(C)C(=O)OC1CC2C(CC=C3CC(OC4CC(OC)C(OC5CC(OC)C(OC6OC(C)C(O)C(OC)C6O)C(C)O5)C(C)O4)CCC32C)C2(O)CCC(C(C)=O)C12C Bitter BitterDB, ChemTasteDB
nuezhenide CC=C1C(OC2OC(CO)C(O)C(O)C2O)OC=C(C(=O)OC)C1CC(=O)OCC1OC(OCCc2ccc(O)cc2)C(O)C(O)C1O Bitter PlantMolecularTasteDB
Oleuropein CC=C1C(OC2OC(CO)C(O)C(O)C2O)OC=C(C(=O)OC)C1CC(=O)OCCc1ccc(O)c(O)c1 Bitter ChemTasteDB, PhytoMolecularTasteDB, PlantMolecularTasteDB, BitterDB, BitterSweet
ligstroside CC=C1C(OC2OC(CO)C(O)C(O)C2O)OC=C(C(=O)OC)C1CC(=O)OCCc1ccc(O)cc1 Bitter PlantMolecularTasteDB
huperzine A CC=C1C2C=C(C)CC1(N)c1ccc(=O)[nH]c1C2 Bitter PlantMolecularTasteDB
Senecionine CC=C1CC(C)C(C)(O)C(=O)OCC2=CCN3CCC(OC1=O)C23 Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB
retrorsine CC=C1CC(C)C(O)(CO)C(=O)OCC2=CCN3CCC(OC1=O)C23 Bitter PlantMolecularTasteDB
echitamine CC=C1C[N+]2(C)CCC34c5ccccc5NC32C(O)CC1C4(CO)C(=O)OC Bitter PlantMolecularTasteDB, PhytoMolecularTasteDB