Skip to main content
. Author manuscript; available in PMC: 2021 Jun 15.
Published in final edited form as: Ecotoxicol Environ Saf. 2020 Apr 1;196:110533. doi: 10.1016/j.ecoenv.2020.110533

Table 2.

Cross reactivity of the obtained mAb with 1-NAP related compounds (n=3)

Compound Structure IC50 (ng/mL) CR (%)a
1-naphthol graphic file with name nihms-1581387-t0005.jpg 12.5 100
2-naphthol graphic file with name nihms-1581387-t0006.jpg 1005.0 1.2
Carbaryl graphic file with name nihms-1581387-t0007.jpg 300.7 4.2
1, 3-dihydroxy naphthalene graphic file with name nihms-1581387-t0008.jpg 178.0 6.9
1, 4-dihydroxy naphthalene graphic file with name nihms-1581387-t0009.jpg 200.7 6.2
1, 5-dihydroxy naphthalene graphic file with name nihms-1581387-t0010.jpg 87.4 14.3
1, 6-dihydroxy naphthalene graphic file with name nihms-1581387-t0011.jpg 502.8 2.5
1, 7-dihydroxy naphthalen graphic file with name nihms-1581387-t0012.jpg 881.7 1.4
1, 8-dihydroxy naphthalene graphic file with name nihms-1581387-t0013.jpg 4303.4 0.3
2, 6-dihydroxy naphthalene graphic file with name nihms-1581387-t0014.jpg 2839.7 0.4
a

CR, cross-reactivity. The percentage of CR was calculated using the following equation: CR (%) =[IC50 (NAP)/IC50 (cross-reactant)] × 100.