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

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ID Name Adduct Structure m/z RT CCS SMI Type Z Ref CCS Type CCS method
CCSBASE_719366fff5638e0180bc13054fc14d2e N-(2-Methylphenyl)-3-oxobutanamide [M-H]- 190.0873 0.77 144.29 CC1=CC=CC=C1NC(=O)CC(=O)C None -1 1 TW polyala
CCSBASE_0c18f9a59cba50311117c88a4b5eeead 2-Isopropyl-6-methyl-4-pyrimidone [M-H]- 151.0877 0.74 139.68 CC1=CC(=O)NC(=N1)C(C)C None -1 1 TW polyala
CCSBASE_ec3ee723f279ded1eec22548736f5626 2-Isopropyl-6-methyl-4-pyrimidone [M+H]+ 153.1023 0.71 133.52 CC1=CC(=O)NC(=N1)C(C)C   None 1 1 TW polyala
CCSBASE_e08d2d9fa0773a2d4b259a044b6b9586 2-Methoxyaniline hydrochloride [M+H]+ 124.0757 0.67 127.49 COC1=CC=CC=C1N None 1 1 TW polyala
CCSBASE_f57954ccfe0f482a245d36559e8bbba8 Felbamate [M+Na]+ 261.0846 0.73 156.38 C1=CC=C(C=C1)C(COC(=O)N)COC(=O)N   Benzenoids 1 1 TW polyala
CCSBASE_0369e49d117e1b7d95284a42361e15e8 Ciprofloxacin [M+H]+ 332.1405 0.71 172.2 C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)O Benzenoids 1 1 TW polyala
CCSBASE_2c268ecf0427bf60e5bc42eb6f5de8ea Ciprofloxacin [M+H]+ 332.1405 0.71 183.78 C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)O Benzenoids 1 1 TW polyala
CCSBASE_b8db0f7d0d8e58d8b620684c4ac2f335 Ciprofloxacin [M+H-H2O]+ 314.13 0.71 170.37 C1CC1N2C=C(C(=O)C3=CC(=C(C=C32)N4CCNCC4)F)C(=O)O Benzenoids 1 1 TW polyala
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