Flavor compounds

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Name SMILES Flavor type Data resource
Parillin C[C@H]1CC[C@@]2(OC1)O[C@H]1C[C@H]3[C@@H]4CC[C@@H]5C[C@@H](O[C@@H]6O[C@H](CO[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@@H](O[C@@H]7O[C@@H](C)[C@H](O)[C@@H](O)[C@H]7O)[C@H](O)[C@H]6O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)CC[C@]5(C)[C@H]4CC[C@]3(C)[C@H]1[C@@H]2C Bitter BitterSweet
Tomatine C[C@H]1CC[C@]2(NC1)O[C@H]1C[C@H]3[C@@H]4CC[C@H]5C[C@@H](O[C@@H]6O[C@H](CO)[C@H](O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O[C@@H]8OC[C@@H](O)[C@H](O)[C@H]8O)[C@H]7O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)CC[C@]5(C)[C@H]4CC[C@]3(C)[C@H]1[C@@H]2C Bitter BitterSweet
Cycloheximid, Cycloheximide C[C@H]1C[C@H](C)C(=O)[C@H]([C@H](O)CC2CC(=O)NC(=O)C2)C1 Bitter BitterSweet
digitoxin C[C@H]1O[C@@H](O[C@H]2[C@@H](O)C[C@H](O[C@H]3[C@@H](O)C[C@H](O[C@H]4CC[C@]5(C)[C@H]6CC[C@]7(C)[C@@H](C8=CC(=O)OC8)CC[C@]7(O)[C@@H]6CC[C@@H]5C4)O[C@@H]3C)O[C@@H]2C)C[C@H](O)[C@@H]1O Bitter BitterSweet
conessine C[C@H]1[C@H]2CC[C@H]3[C@@H]4CC=C5C[C@@H](N(C)C)CC[C@]5(C)[C@H]4CC[C@]23CN1C Bitter PhytoMolecularTasteDB
digitonin C[C@H]1[C@H]2[C@@H](O[C@]13CC[C@@H](C)CO3)[C@@H](O)[C@H]1[C@@H]3CC[C@H]4C[C@@H](O[C@@H]5O[C@H](CO)[C@H](O[C@@H]6O[C@H](CO)C(O)[C@H](O[C@@H]7OC[C@@H](O)[C@H](O)[C@H]7O)[C@H]6O[C@@H]6O[C@H](CO)[C@H](O)[C@H](O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@H]6O)[C@H](O)[C@H]5O)[C@H](O)C[C@]4(C)[C@H]3CC[C@@]12C Bitter PhytoMolecularTasteDB
Officinalisnin 1 C[C@H]1[C@H]2[C@H](C[C@H]3[C@@H]4CC[C@@H]5C[C@@H](O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)CC[C@]5(C)[C@H]4CC[C@@]32C)O[C@]1(O)CC[C@@H](C)CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O Bitter BitterSweet
Harpagoside C[C@]1(OC(=O)/C=C/c2ccccc2)C[C@@H](O)[C@]2(O)C=CO[C@@H](O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@H]12 Bitter BitterSweet
Prednisone C[C@]12CC(=O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@@]43C)[C@@H]1CC[C@]2(O)C(=O)CO Bitter BitterSweet
cardenolide C[C@]12CCCCC1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](C3=CC(=O)OC3)CC[C@H]12 Bitter PhytoMolecularTasteDB
Prednisolone C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)C=C[C@@]43C)[C@@H]1CC[C@]2(O)C(=O)CO Bitter BitterSweet
Hydrocortisone C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@]2(O)C(=O)CO Bitter BitterSweet
Pentamethonium bromide C[N+](C)(C)CCCCC[N+](C)(C)C.[Br-].[Br-] Bitter BitterSweet, BitterDB, ChemTasteDB
choline C[N+](C)(C)CCO Bitter PlantMolecularTasteDB, PhytoMolecularTasteDB
Choline chloride C[N+](C)(C)CCO.[Cl-] Bitter BitterDB, ChemTasteDB
Succinylcholine chloride C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C.[Cl-].[Cl-] Bitter BitterSweet, BitterDB, ChemTasteDB
trigonelline C[n+]1cccc(C(=O)[O-])c1 Bitter PlantMolecularTasteDB, PhytoMolecularTasteDB
Propyphenazone Cc1c(C(C)C)c(=O)n(-c2ccccc2)n1C Bitter BitterSweet, BitterDB, ChemTasteDB
Clonixin Cc1c(Cl)cccc1Nc1ncccc1C(=O)O Bitter BitterSweet, BitterDB, ChemTasteDB
Deferiprone Cc1c(O)c(=O)ccn1C Bitter BitterSweet, BitterDB, ChemTasteDB
cayaponoside C5b Cc1c(O)c(OC2OC(CO)C(O)C(O)C2O)cc2c1C=CC1C2(C)C(=O)CC2(C)C(C(C)(O)C(=O)CCC(C)(C)O)C(O)CC12C Bitter PlantMolecularTasteDB
cabenoside A Cc1c(O)c(OC2OC(CO)C(O)C(O)C2O)cc2c1C=CC1C2(C)C(=O)CC2(C)C(C(C)(O)C(O)C=CC(C)(C)O)C(O)CC12C Bitter PlantMolecularTasteDB
cayaponoside C Cc1c(O)c(OC2OC(CO)C(O)C(O)C2O)cc2c1CCC1C2(C)C(=O)CC2(C)C(C(C)(O)C(=O)CCC(C)(C)O)C(O)CC12C Bitter PlantMolecularTasteDB
cayaponoside D Cc1c(O)c(OC2OC(CO)C(O)C(O)C2O)cc2c1CCC1C2(C)C(=O)CC2(C)C(C(C)(O)C(O)C=CC(C)(C)O)C(O)CC12C Bitter PlantMolecularTasteDB
cabenoside B Cc1c(O)c(OC2OC(CO)C(O)C(O)C2OC2OC(CO)C(O)C(O)C2O)cc2c1C=CC1C2(C)C(=O)CC2(C)C(C(C)(O)C(O)C=CC(C)(C)O)C(O)CC12C Bitter PlantMolecularTasteDB
cedrin Cc1c(O)cc2c(c1O)C(=O)C(O)C(c1cc(O)c(O)c(O)c1)O2 Bitter PlantMolecularTasteDB
cedrin Cc1c(O)cc2c(c1O)C(=O)[C@H](O)[C@@H](c1cc(O)c(O)c(O)c1)O2 Bitter PhytoMolecularTasteDB
Methylthiouracil Cc1cc(=O)[nH]c(=S)[nH]1 Bitter BitterSweet, BitterDB, ChemTasteDB
Antipyrine Cc1cc(=O)n(-c2ccccc2)n1C Bitter BitterSweet, BitterDB, ChemTasteDB
4-methylumbelliferone Cc1cc(=O)oc2cc(O)ccc12 Bitter PlantMolecularTasteDB