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_26e57e370d3435cf0024712b707d94f3 Amrinone [M-H]- 186.0673 0.67 143.11 C1=CN=CC=C1C2=CNC(=O)C(=C2)N Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_08b19b7f16d2e2d317648b8ceb1a3bc3 Phenacetin [M+H-H2O]+ 162.0914 0.84 136.48 CCOC1=CC=C(C=C1)NC(=O)C Benzenoids 1 1 TW polyala
CCSBASE_d74db5afcacd65fd29477e23dd7ce938 Strychnine [M+H]+ 335.1754 0.77 172.14 C1CN2CC3=CCOC4CC(=O)N5C6C4C3CC2C61C7=CC=CC=C75 Alkaloids and derivatives 1 1 TW polyala
CCSBASE_718a142cbfcf00e2f9fdabdf07fc99a9 Piragliatin [M+H]+ 422.0936 0.84 201.19 CS(=O)(=O)C1=C(C=C(C=C1)C(CC2CCC(=O)C2)C(=O)NC3=NC=CN=C3)Cl Benzenoids 1 1 TW polyala
CCSBASE_a1d717369effa8c72204c451c7241248 Piragliatin [M+H-H2O]+ 404.0831 0.84 191.13 CS(=O)(=O)C1=C(C=C(C=C1)C(CC2CCC(=O)C2)C(=O)NC3=NC=CN=C3)Cl Benzenoids 1 1 TW polyala
CCSBASE_068a1916ec1ba50a188e23a3acc3b529 Piragliatin [M+Na]+ 444.0755 0.84 199.38 CS(=O)(=O)C1=C(C=C(C=C1)C(CC2CCC(=O)C2)C(=O)NC3=NC=CN=C3)Cl Benzenoids 1 1 TW polyala
CCSBASE_a5a438247e481101e245165d04b71bf6 Piragliatin [M-H]- 420.079 0.76 203.59 CS(=O)(=O)C1=C(C=C(C=C1)C(CC2CCC(=O)C2)C(=O)NC3=NC=CN=C3)Cl Benzenoids -1 1 TW polyala
CCSBASE_3f39b10c9831b34f664f43d7e07e5af7 Azathioprine [M+H]+ 278.0455 0.78 155.65 CN1C=NC(=C1SC2=NC=NC3=C2NC=N3)[N+](=O)[O-] Organosulfur compounds 1 1 TW polyala
CCSBASE_a121993b4ababccc32d6804a995f5e78 Azathioprine [M+Na]+ 300.0274 0.78 167.82 CN1C=NC(=C1SC2=NC=NC3=C2NC=N3)[N+](=O)[O-] Organosulfur compounds 1 1 TW polyala
CCSBASE_607b113388c0fe6b370f5130a8e71e80 Azathioprine [M-H]- 276.0309 0.72 156.1 CN1C=NC(=C1SC2=NC=NC3=C2NC=N3)[N+](=O)[O-] Organosulfur compounds -1 1 TW polyala
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