Name:
Adduct:
Polarity:
Z:
m/z:
±:
CCS: Ã…
±: %
SMI:

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_f714001cd9e14b8c6c4a3b9b6a97e34b Enterolactone [M-H]- 297.1132 0.78 165.89 C1C(C(C(=O)O1)CC2=CC(=CC=C2)O)CC3=CC(=CC=C3)O Lignans, neolignans and related compounds -1 1 TW polyala
CCSBASE_b0f982ba876b317db1023099405f53d9 (9Z,12R)-12-Hydroxyoctadec-9-enoic acid [M+Na]+ 321.24 1.04 186.7 CCCCCCC(CC=CCCCCCCCC(=O)O)O Lipids and lipid-like molecules 1 1 TW polyala
CCSBASE_3a419d41c852f073b47edffc60d8ef78 (9Z,12R)-12-Hydroxyoctadec-9-enoic acid [M-H]- 297.2435 0.98 181.02 CCCCCCC(CC=CCCCCCCCC(=O)O)O Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_8fed0c887c245f0b7ffac372d01e39eb (9Z,12R)-12-Hydroxyoctadec-9-enoic acid [M-H-H2O]- 279.2324 0.98 180.89 CCCCCCC(CC=CCCCCCCCC(=O)O)O Lipids and lipid-like molecules -1 1 TW polyala
CCSBASE_8fe80e74f292ef83689265653ea61610 Hydrochlorothiazide [M+H]+ 297.9718 0.7 161.13 C1NC2=CC(=C(C=C2S(=O)(=O)N1)S(=O)(=O)N)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_a861aed113ab678e3d2011397cbab882 Hydrochlorothiazide [M+Na]+ 319.9537 0.71 174.71 C1NC2=CC(=C(C=C2S(=O)(=O)N1)S(=O)(=O)N)Cl Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_38890ed9506a78e346e9d02519945302 Perfluorooctanesulfonamide [M-H]- 497.9462 0.9 169.84 C(C(C(C(C(F)(F)S(=O)(=O)N)(F)F)(F)F)(F)F)(C(C(C(F)(F)F)(F)F)(F)F)(F)F Organohalogen compounds -1 1 TW polyala
CCSBASE_4174e1967eab0fdb5d22cbb2649cfae9 2,2'-(Tetradecylimino)diethanol [M+H]+ 302.3054 0.89 194.08 CCCCCCCCCCCCCCN(CCO)CCO Organic nitrogen compounds 1 1 TW polyala
CCSBASE_0adb70eb0cc4e7984f5f02e572bed6b2 2,2'-(Tetradecylimino)diethanol [M+H-H2O]+ 284.2949 0.89 191.61 CCCCCCCCCCCCCCN(CCO)CCO Organic nitrogen compounds 1 1 TW polyala
CCSBASE_e54b5aab8cdec7783c7c250ddae4de71 Deethylatrazine [M+H]+ 188.0697 0.77 139.76 CC(C)NC1=NC(=NC(=N1)N)Cl Organoheterocyclic compounds 1 1 TW polyala
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