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_9e722e7a87a4104258dfd4651217a64c N,N-Dimethyl-N-benzyl-N-octadecylammonium chloride [M]+ 388.3938 1.0 223.2 CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 Benzenoids 1 1 TW polyala
CCSBASE_e75e25c43a7d9ed7cb80e752ee375a91 Arotinoid acid [M+H-H2O]+ 331.2057 0.78 172.57 CC(=CC1=CC=C(C=C1)C(=O)O)C2=CC3=C(C=C2)C(CCC3(C)C)(C)C Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_b48a82a7bf92cec2e448507187a50589 4'-Chloro-2',5'-dimethoxyacetoacetanilide [M+H]+ 272.0684 0.78 158.5 CC(=O)CC(=O)NC1=CC(=C(C=C1OC)Cl)OC Benzenoids 1 1 TW polyala
CCSBASE_5b1eece04bf2dc86261af08e94f93734 4'-Chloro-2',5'-dimethoxyacetoacetanilide [M+H-H2O]+ 254.0579 0.78 157.23 CC(=O)CC(=O)NC1=CC(=C(C=C1OC)Cl)OC Benzenoids 1 1 TW polyala
CCSBASE_2d333c8e78b7fbac2258513597d72f2b 4'-Chloro-2',5'-dimethoxyacetoacetanilide [M+Na]+ 294.0504 0.78 168.13 CC(=O)CC(=O)NC1=CC(=C(C=C1OC)Cl)OC Benzenoids 1 1 TW polyala
CCSBASE_b0ce1c5c2f8acbf659dd6bcc430cb3dc Minocycline hydrochloride [M+H]+ 458.1922 0.71 205.66 CN(C)C1C2CC3CC4=C(C=CC(=C4C(=C3C(=O)C2(C(=C(C1=O)C(=O)N)O)O)O)O)N(C)C Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_c99f04f23ea90bb8e8b69c2deae18b23 Minocycline hydrochloride [M+K]+ 496.1481 0.71 214.78 CN(C)C1C2CC3CC4=C(C=CC(=C4C(=C3C(=O)C2(C(=C(C1=O)C(=O)N)O)O)O)O)N(C)C Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_06170bd38f66688b56f6279ff8447db1 Minocycline hydrochloride [M+Na]+ 480.1741 0.71 213.69 CN(C)C1C2CC3CC4=C(C=CC(=C4C(=C3C(=O)C2(C(=C(C1=O)C(=O)N)O)O)O)O)N(C)C Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_3bd833662e19571d3506bcbdb502ef4e 5,5'-Bi-2-benzofuran-1,1',3,3'-tetrone [M+H]+ 295.0237 0.74 166.14 C1=CC2=C(C=C1C3=CC4=C(C=C3)C(=O)OC4=O)C(=O)OC2=O Organic acids and derivatives 1 1 TW polyala
CCSBASE_b09424cd1243fafd4af6ee827b6484e4 alpha-Terthiophene [M+H]+ 248.9861 1.02 145.97 C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3 Organoheterocyclic compounds 1 1 TW polyala
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