Flavor compounds

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Name SMILES Flavor type Data resource
Isometheptene mucate CNC(C)CCC=C(C)C.O=C(O)C(O)C(O)C(O)C(O)C(=O)O Bitter BitterSweet, BitterDB, ChemTasteDB
Methamphetamine hydrochloride CNC(C)Cc1ccccc1.Cl Bitter BitterSweet, BitterDB, ChemTasteDB
Vancomycin CNC(CC(C)C)C(=O)NC1C(=O)NC(CC(N)=O)C(=O)NC2C(=O)NC3C(=O)NC(C(=O)NC(C(=O)O)c4cc(O)cc(O)c4-c4cc3ccc4O)C(O)c3ccc(c(Cl)c3)Oc3cc2cc(c3OC2OC(CO)C(O)C(O)C2OC2CC(C)(N)C(O)C(C)O2)Oc2ccc(cc2Cl)C1O Bitter BitterDB, ChemTasteDB
N-Methylthiourea CNC(N)=S Bitter BitterSweet, BitterDB, ChemTasteDB
Streptomycin CNC1C(OC2C(OC3C(O)C(O)C(N=C(N)N)C(O)C3N=C(N)N)OC(C)C2(O)C=O)OC(CO)C(O)C1O Bitter BitterSweet, BitterDB, ChemTasteDB
Cyclexedrine hydrochloride CNCC(C)C1CCCCC1.Cl Bitter BitterSweet, BitterDB, ChemTasteDB
Phenylephrine hydrochloride CNCC(O)c1cccc(O)c1.Cl Bitter BitterSweet, BitterDB, ChemTasteDB
norcassaidine CNCCOC(=O)/C=C1\CCC2C(C(O)CC3C(C)(C)C(O)CCC23C)C1C Bitter PlantMolecularTasteDB
norcassamidine CNCCOC(=O)C=C1CCC2C(C(O)CC3C(C)(C(=O)OC)CCCC23C)C1C Bitter PlantMolecularTasteDB
pseudoephedrine CN[C@@H](C)[C@@H](O)c1ccccc1 Bitter PhytoMolecularTasteDB
Compound X COC(=O)C(C)C1CC(OC(C)=O)C2C(C1)C(=O)OC1CCC(C)(C)C(COC(C)=O)C12CO Bitter ChemTasteDB
3-Amino-4-[(1-methoxy-4-methyl-1-oxopentan-2-yl)amino]-4-oxobutanoic acid COC(=O)C(CC(C)C)NC(=O)C(N)CC(=O)O Bitter ChemTasteDB
3-Amino-3-[(6-amino-1-methoxy-1-oxohexan-2-yl)carbamoyl]propanoic acid COC(=O)C(CCCCN)NC(=O)C(N)CC(=O)O Bitter ChemTasteDB
Suosan-aspartame hybrid 34 COC(=O)C(NC(=O)C(CC(=O)O)NC(=S)Nc1ccc(C#N)cc1)C(=O)OC1C2(C)CCC(C2)C1(C)C Bitter ChemTasteDB
yadanzioside L COC(=O)C12OCC34C(CC5C(C)=C(OC6OC(CO)C(O)C(O)C6O)C(=O)CC5(C)C3C(O)C1O)OC(=O)C(OC(=O)C=C(C)C(C)(C)O)C24 Bitter PlantMolecularTasteDB
yadanzioside I COC(=O)C12OCC34C(CC5C(C)=C(OC6OC(CO)C(O)C(O)C6O)C(=O)CC5(C)C3C(O)C1O)OC(=O)C(OC(C)=O)C24 Bitter PlantMolecularTasteDB
bruceine Q COC(=O)C12OCC34C(CC5C(C)=CC(=O)C(O)C5(C)C3C(O)C1O)OC(=O)C(OC(=O)C(O)C(O)C(O)C(O)C(C)CO)C24O Bitter PlantMolecularTasteDB
yadanzioside J COC(=O)C12OCC34C(CC5C(C)C(=O)C(OC6OC(CO)C(O)C(O)C6O)=CC5(C)C3C(O)C1O)OC(=O)C(OC(=O)CC(C)(C)O)C24 Bitter PlantMolecularTasteDB
yadanzioside F COC(=O)C12OCC34C(CC5C(C)C(=O)C(OC6OC(CO)C(O)C(O)C6O)=CC5(C)C3C(O)C1O)OC(=O)C(OC(C)=O)C24 Bitter PlantMolecularTasteDB
tinophyllone COC(=O)C1=CC(=O)CC2C1(C)CCC1C(=O)OC(c3ccoc3)CC12C Bitter PlantMolecularTasteDB
borapetol B COC(=O)C1=CC(O)CC2C3(C)CC(c4ccoc4)OC(=O)C3CC(O)C12C Bitter PlantMolecularTasteDB
borapetoside B COC(=O)C1=CC(O)CC2C3(C)CC(c4ccoc4)OC(=O)C3CC(OC3OC(CO)C(O)C(O)C3O)C12C Bitter PlantMolecularTasteDB
tinocrisposide COC(=O)C1=CCCC2C3(C)CC(c4ccoc4)OC(=O)C3CC(OC3OC(CO)C(O)C(O)C3O)C12C Bitter PlantMolecularTasteDB
10-acetoxyoleuropein COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C(=CCOC(C)=O)C1CC(=O)OCCc1ccc(O)c(O)c1 Bitter PlantMolecularTasteDB
10-acetoxyligustroside COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C(=CCOC(C)=O)C1CC(=O)OCCc1ccc(O)cc1 Bitter PlantMolecularTasteDB
Verbenalin COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C(C)CC(=O)C12 Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB
gardenoside COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C1C=CC2(O)CO Bitter PlantMolecularTasteDB
plumieride COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C1C=CC21C=C(C(C)O)C(=O)O1 Bitter PlantMolecularTasteDB
loganin COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C2C1CC(O)C2C Bitter PlantMolecularTasteDB
raubasine COC(=O)C1=CO[C@@H](C)[C@H]2CN3CCc4c([nH]c5ccccc45)[C@@H]3C[C@H]12 Bitter PhytoMolecularTasteDB