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_0bea8a1019b73f0fec5fa98a23153c4f 3-Methylbenzoic acid [M-H]- 135.0451 0.82 133.66 CC1=CC(=CC=C1)C(=O)O None -1 1 TW polyala
CCSBASE_58927d1e17f968ee64df2e8689a4ccdc C.I. Solvent Yellow 56 [M+H]+ 254.1652 1.02 164.64 CCN(CC)C1=CC=C(C=C1)N=NC2=CC=CC=C2   None 1 1 TW polyala
CCSBASE_01857eadc899f9427eaba7561525cab1 (3aR)-(+)-Sclareolide [M+H]+ 251.2006 0.98 162.37 C[C@]12CCCC([C@@H]1CC[C@@]3([C@@H]2CC(=O)O3)C)(C)C   None 1 1 TW polyala
CCSBASE_f0ee8680bb6ec6a10323076295769b27 (3aR)-(+)-Sclareolide [M+H-H2O]+ 233.1901 0.97 154.48 C[C@]12CCCC([C@@H]1CC[C@@]3([C@@H]2CC(=O)O3)C)(C)C   None 1 1 TW polyala
CCSBASE_05ec2c4239b7f05c7a0179feea1a0e86 (3aR)-(+)-Sclareolide [M+Na]+ 273.1825 0.97 178.16 C[C@]12CCCC([C@@H]1CC[C@@]3([C@@H]2CC(=O)O3)C)(C)C   None 1 1 TW polyala
CCSBASE_a791b80da5bc30b919575ea4e166bca5 Atorvastatin calcium [M+H-H2O]+ 541.2498 0.86 213.54 CC(C)C1=C(C(=C(N1CC[C@H](C[C@H](CC(=O)[O-])O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_c862db79e1aef7ac76ed175c982a98bd Atorvastatin calcium [M+H-H2O]+ 541.2498 0.86 222.68 CC(C)C1=C(C(=C(N1CC[C@H](C[C@H](CC(=O)[O-])O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_d11ba4175447368ef8e2dc3121d4e3b6 Atorvastatin calcium [M+Na]+ 581.2422 0.85 227.61 CC(C)C1=C(C(=C(N1CC[C@H](C[C@H](CC(=O)[O-])O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_adcae1d229c6bc3aea0c74f5a1d6c1e9 Atorvastatin calcium [M-H]- 557.2457 0.88 229.98 CC(C)C1=C(C(=C(N1CCC(CC(CC(=O)[O-])O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_91f4c3e9884b80608c1d9dbb010038be CJ-013610 [M+H]+ 394.1584 0.73 194.61 CC1=NC=CN1C2=CC=C(C=C2)SC3=CC=CC(=C3)C4(CCOCC4)C(=O)N Organoheterocyclic compounds 1 1 TW polyala
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