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_f39380f042ccb7ecdf29e18c29b5ec01 Nitrofurantoin [M+Na]+ 261.023 0.74 156.71 C1C(=O)NC(=O)N1N=CC2=CC=C(O2)[N+](=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_aad153dbda7700b7abeda64ebdc2f662 Nitrofurantoin [M-H]- 237.0265 0.69 153.06 C1C(=O)NC(=O)N1N=CC2=CC=C(O2)[N+](=O)[O-] Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_c732eb2f0e68a89dd6af05b65784fba7 Sucrose octaacetate [M+K]+ 717.1639 0.87 234.97 CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C Organic oxygen compounds 1 1 TW polyala
CCSBASE_99760b56bd9ef9c6fa99f10fd309ad84 Carbaryl [M+Na]+ 224.0682 0.88 147.76 CNC(=O)OC1=CC=CC2=CC=CC=C21 Benzenoids 1 1 TW polyala
CCSBASE_9e87a0214875639aa062185a5497e518 Methylene blue [M]+ 284.1216 0.6 163.58 CN(C)C1=CC2=C(C=C1)N=C3C=CC(=[N+](C)C)C=C3S2 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_2c57698ea01a03d2cab88bf6e518cb00 Nicardipine hydrochloride [M+FA-H]- 524.2038 0.73 228.71 CC1=C(C(C(=C(N1)C)C(=O)OCCN(C)CC2=CC=CC=C2)C3=CC(=CC=C3)[N+](=O)[O-])C(=O)OC Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_ecaa0889e2b0e9aa0639fbe7a81cf68e Nicardipine hydrochloride [M+H]+ 480.2129 0.8 210.72 CC1=C(C(C(=C(N1)C)C(=O)OCCN(C)CC2=CC=CC=C2)C3=CC(=CC=C3)[N+](=O)[O-])C(=O)OC Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_562eb648b2185ba2ac1d0af442667fd1 Nicardipine hydrochloride [M+H-H2O]+ 462.2024 0.79 203.17 CC1=C(C(C(=C(N1)C)C(=O)OCCN(C)CC2=CC=CC=C2)C3=CC(=CC=C3)[N+](=O)[O-])C(=O)OC Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_f46266459452ab7d68a65edd899f2d6a Nicardipine hydrochloride [M-H]- 478.1983 0.74 215.44 CC1=C(C(C(=C(N1)C)C(=O)OCCN(C)CC2=CC=CC=C2)C3=CC(=CC=C3)[N+](=O)[O-])C(=O)OC Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_027326e1b7e93f27e81fefc4f733e3a2 Dazomet [M+H]+ 163.0358 1.01 123.57 CN1CN(C(=S)SC1)C Organoheterocyclic compounds 1 1 TW polyala
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