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_fe40326c0aabb08be30fca6b9fd5a08f Adriamycin hydrochloride [M+Na]+ 566.1633 0.79 228.54 CC1C(C(CC(O1)OC2CC(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)CO)O)N)O Phenylpropanoids and polyketides 1 1 TW polyala
CCSBASE_d85e7bc3496c5b9958dc7adfe583f9b3 Adriamycin hydrochloride [M-H]- 542.1668 0.76 223.95 CC1C(C(CC(O1)OC2CC(CC3=C2C(=C4C(=C3O)C(=O)C5=C(C4=O)C(=CC=C5)OC)O)(C(=O)CO)O)N)O Phenylpropanoids and polyketides -1 1 TW polyala
CCSBASE_ea90152cfab6d4183000c55457c3c9cc Furazolidone [M+Na]+ 248.0278 0.74 152.62 C1COC(=O)N1N=CC2=CC=C(O2)[N+](=O)[O-] Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_d2d4075c4376d2697d0c11f9e55875a2 Furazolidone [M-H]- 224.0313 0.7 152.64 C1COC(=O)N1N=CC2=CC=C(O2)[N+](=O)[O-] Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_df46fc4d847d27dbfb53ffc82374dd64 Mosapride citrate [M+H]+ 422.1641 0.78 194.02 CCOC1=CC(=C(C=C1C(=O)NCC2CN(CCO2)CC3=CC=C(C=C3)F)Cl)N Organic acids and derivatives 1 1 TW polyala
CCSBASE_69a4e8e9d26bb2e5f0fbbfd1d2209850 Mosapride citrate [M+Na]+ 444.1461 0.78 207.2 CCOC1=CC(=C(C=C1C(=O)NCC2CN(CCO2)CC3=CC=C(C=C3)F)Cl)N Organic acids and derivatives 1 1 TW polyala
CCSBASE_dd1bebc68a5251b4902483a61112839e Mosapride citrate [M-H]- 420.1495 0.74 202.2 CCOC1=CC(=C(C=C1C(=O)NCC2CN(CCO2)CC3=CC=C(C=C3)F)Cl)N Organic acids and derivatives -1 1 TW polyala
CCSBASE_f9a6efeaa57dc5b644512ac0690500cc N,N-Diethyl-m-toluidine [M+H]+ 164.1434 0.76 138.77 CCN(CC)C1=CC=CC(=C1)C Benzenoids 1 1 TW polyala
CCSBASE_e741580710f12ac6af1205c23652c3c0 Thiazopyr [M+H]+ 397.1004 0.95 180.77 CC(C)CC1=C(C(=NC(=C1C(=O)OC)C(F)F)C(F)(F)F)C2=NCCS2 Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_6f7f1b6790f1dbbf4100cdf6e94cf2d4 Thiazopyr [M+H-H2O]+ 379.0899 0.95 177.39 CC(C)CC1=C(C(=NC(=C1C(=O)OC)C(F)F)C(F)(F)F)C2=NCCS2 Organoheterocyclic compounds 1 1 TW polyala
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