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_248a89e30f005fb560b7772241dd8714 Isoproterenol hydrochloride [M+H-H2O]+ 194.1176 0.71 145.47 CC(C)NCC(C1=CC(=C(C=C1)O)O)O Benzenoids 1 1 TW polyala
CCSBASE_53a7778b86eea90238602924747b4522 Isoproterenol hydrochloride [M-H]- 210.1135 0.66 154.99 CC(C)NCC(C1=CC(=C(C=C1)O)O)O Benzenoids -1 1 TW polyala
CCSBASE_16bdc5f1878c8b69e9879c59bc3d70d2 Isoproterenol hydrochloride [M-H-H2O]- 192.1024 0.66 153.95 CC(C)NCC(C1=CC(=C(C=C1)O)O)O Benzenoids -1 1 TW polyala
CCSBASE_891a057368e3c5968a0eef42246cef0e Pentetic acid [M+H]+ 394.1456 0.24 180.25 C(CN(CC(=O)O)CC(=O)O)N(CCN(CC(=O)O)CC(=O)O)CC(=O)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_e96d630adb14450c0ca233bff817d5a5 Pentetic acid [M+K]+ 432.1015 0.25 180.22 C(CN(CC(=O)O)CC(=O)O)N(CCN(CC(=O)O)CC(=O)O)CC(=O)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_5be4795274b59ce42974ade79f07cc8a Pentetic acid [M+Na]+ 416.1276 0.25 177.2 C(CN(CC(=O)O)CC(=O)O)N(CCN(CC(=O)O)CC(=O)O)CC(=O)O Organic acids and derivatives 1 1 TW polyala
CCSBASE_13b5f3115927f7bc9a7ccc6eff1853fa Famotidine [M+H]+ 338.0522 0.73 167.0 C1=C(N=C(S1)N=C(N)N)CSCCC(=NS(=O)(=O)N)N Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_36efb68282818cd12f49f717b73ff270 Famotidine [M+Na]+ 360.0342 0.73 172.26 C1=C(N=C(S1)N=C(N)N)CSCCC(=NS(=O)(=O)N)N Organoheterocyclic compounds 1 1 TW polyala
CCSBASE_5effbd0f8f80c86b320760f71afcf39b Famotidine [M-H]- 336.0376 0.67 169.5 C1=C(N=C(S1)N=C(N)N)CSCCC(=NS(=O)(=O)N)N Organoheterocyclic compounds -1 1 TW polyala
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