Flavor compounds

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Name SMILES Flavor type Data resource
Diisobutylamine CC(C)CNCC(C)C Bitter BitterSweet, BitterDB, ChemTasteDB
Butethamine m-isomer hydrochloride CC(C)CNCCOC(=O)c1cccc(N)c1.Cl Bitter BitterSweet, BitterDB, ChemTasteDB
Isobutyl salicylate CC(C)COC(=O)c1ccccc1O Bitter ChemTasteDB, BitterDB, FlavorDB
L-leucine CC(C)C[C@H](N)C(=O)O Bitter AromaDB, BitterSweet
Gly-leu, Glycyl-l-leucine, Glycylleucine CC(C)C[C@H](NC(=O)CN)C(=O)O Bitter BitterSweet
Phe-leu, Phenylalanylleucine CC(C)C[C@H](NC(=O)[C@@H](N)Cc1ccccc1)C(=O)O Bitter BitterSweet
Trp-leu CC(C)C[C@H](NC(=O)[C@H](N)Cc1c[nH]c2ccccc12)C(=O)O Bitter BitterSweet
Compound 843 CC(C)N1C(=O)c2ccc([N+](=O)[O-])cc2S1(=O)=O Bitter BitterSweet, ChemTasteDB
Propanolol CC(C)NCC(O)COc1cccc2ccccc12 Bitter BitterDB, ChemTasteDB
Isopropyl alcohol CC(C)O Bitter ChemTasteDB, Off-flavor, FlavorDB, BitterDB, BitterSweet
3-(propan-2-yloxy)-1,2-benzothiazole 1,1-dioxide CC(C)OC1=NS(=O)(=O)c2ccccc21 Bitter BitterSweet, BitterDB, ChemTasteDB
ecboline CC(C)[C@@]1(NC(=O)[C@@H]2C=C3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)CN2C1=O Bitter PhytoMolecularTasteDB
acorone CC(C)[C@H]1C(=O)C[C@H](C)[C@@]12CC[C@@H](C)C(=O)C2 Bitter PhytoMolecularTasteDB
(-)-alpha Thujone CC(C)[C@]12CC(=O)[C@@H](C)[C@H]1C2 Bitter BitterSweet
Carnosol CC(C)c1cc2c(c(O)c1O)C13CCCC(C)(C)C1CC2OC3=O Bitter PlantMolecularTasteDB, BitterDB, ChemTasteDB
Carnosol CC(C)c1cc2c(c(O)c1O)[C@@]13CCCC(C)(C)[C@@H]1C[C@@H]2OC3=O Bitter BitterSweet
4-Isopropylbenzaldehydeoxime CC(C)c1ccc(C=NO)cc1 Bitter BitterSweet, BitterDB, ChemTasteDB
Sodium N-(2-bromo-4-propan-2-ylphenyl)sulfamate CC(C)c1ccc(NS(=O)(=O)[O-])c(Br)c1.[Na+] Bitter ChemTasteDB
Sodium N-[2,6-di(propan-2-yl)phenyl]sulfamate CC(C)c1cccc(C(C)C)c1NS(=O)(=O)[O-].[Na+] Bitter ChemTasteDB
Chonemorphine CC(C1CCC2C3CCC4CC(N)CCC4(C)C3CCC21C)N(C)C Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB
lutein CC(C=CC=C(C)C=CC1=C(C)CC(O)CC1(C)C)=CC=CC=C(C)C=CC=C(C)C=CC1C(C)=CC(O)CC1(C)C Bitter PlantMolecularTasteDB
beta-carotene CC(C=CC=C(C)C=CC1=C(C)CCCC1(C)C)=CC=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C Bitter BitterDB, ChemTasteDB
Ganoderic acid A CC(CC(=O)CC(C)C1CC(O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3O)C(=O)O Bitter BitterSweet, PlantMolecularTasteDB, BitterDB, ChemTasteDB
3-(p-chlorophenylosulfonyl)butanoic acid CC(CC(=O)O)S(=O)(=O)c1ccc(Cl)cc1 Bitter ChemTasteDB
Chlorhexadol CC(CC(C)(C)O)OC(O)C(Cl)(Cl)Cl Bitter BitterSweet, BitterDB, ChemTasteDB
3-Amino-3-[(1-cyclohexylpropan-2-yl)(methyl)carbamoyl]propanoic acid, LL-form CC(CC1CCCCC1)N(C)C(=O)C(N)CC(=O)O Bitter ChemTasteDB
Taurocholic acid CC(CCC(=O)NCCS(=O)(=O)O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CC(O)C12C Bitter Natural_TAS2R_agonists, BitterDB, ChemTasteDB
Dehydrocholic acid CC(CCC(=O)O)C1CCC2C3C(=O)CC4CC(=O)CCC4(C)C3CC(=O)C12C Bitter BitterSweet, BitterDB, ChemTasteDB
Ursodiol CC(CCC(=O)O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CCC12C Bitter BitterDB, ChemTasteDB
brydioside C CC(CCC(O)C(C)(C)OC1OC(COC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O)C1CCC2(C)C3CC=C4C(CCC(OC5OC(CO)C(O)C(O)C5O)C4(C)C)C3(C)C(=O)CC12C Bitter PlantMolecularTasteDB