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_4c41aa946a01ae00473cbf7fee468ca6 Sodium octyl sulfate [M-H]- 209.0853 0.91 155.65 CCCCCCCCOS(=O)(=O)[O-] Organic acids and derivatives -1 1 TW polyala
CCSBASE_c57edd1e60a3cd8724bf19701dcac287 SAR115740 [M+H]+ 402.1412 0.91 191.72 C1=CC(=CC(=C1)F)CN2C3=C(C=C(C=C3)F)C=C2C(=O)NC4=CC5=C(C=C4)NC=C5 None 1 1 TW polyala
CCSBASE_939327eb156a7a0f8f0e1447c650dbd9 SAR115740 [M+K]+ 440.0971 0.92 198.17 C1=CC(=CC(=C1)F)CN2C3=C(C=C(C=C3)F)C=C2C(=O)NC4=CC5=C(C=C4)NC=C5 None 1 1 TW polyala
CCSBASE_b0fff16317a8accacd296402abb01e89 SAR115740 [M+Na]+ 424.1232 0.91 197.81 C1=CC(=CC(=C1)F)CN2C3=C(C=C(C=C3)F)C=C2C(=O)NC4=CC5=C(C=C4)NC=C5 None 1 1 TW polyala
CCSBASE_c9dc6a58d6487476889d75796fc4f00c SAR115740 [M-H]- 400.1267 0.88 199.82 C1=CC(=CC(=C1)F)CN2C3=C(C=C(C=C3)F)C=C2C(=O)NC4=CC5=C(C=C4)NC=C5 None -1 1 TW polyala
CCSBASE_5892be92d484815cae5bc735579ded13 1-Phenylurea [M+H]+ 137.0709 0.74 127.64 C1=CC=C(C=C1)NC(=O)N Benzenoids 1 1 TW polyala
CCSBASE_2b485bc27a957edccd5f5623bf1f6dce 1,4-Heptanolide [M+FA-H]- 173.0819 0.74 140.3 CCCC1CCC(=O)O1 Organoheterocyclic compounds -1 1 TW polyala
CCSBASE_e90ecdec786275ec6485b067702455dd Enterolactone [M+H]+ 299.1278 0.8 167.76 C1C(C(C(=O)O1)CC2=CC(=CC=C2)O)CC3=CC(=CC=C3)O Lignans, neolignans and related compounds 1 1 TW polyala
CCSBASE_cf1ad6137551d13992c1461f83b3fc17 Enterolactone [M+H-H2O]+ 281.1173 0.8 162.28 C1C(C(C(=O)O1)CC2=CC(=CC=C2)O)CC3=CC(=CC=C3)O Lignans, neolignans and related compounds 1 1 TW polyala
CCSBASE_b2bfee0b908d962c2e68a5cfa5dd9478 Enterolactone [M+Na]+ 321.1097 0.8 175.73 C1C(C(C(=O)O1)CC2=CC(=CC=C2)O)CC3=CC(=CC=C3)O Lignans, neolignans and related compounds 1 1 TW polyala
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