Problem statement: Answer the multiple-choice question.
Query: Which compound has a -25.662% hERG inhibition at 10uM?
Constraint: You must select none, one or more options from a, b, c, d, or e without using any additional words.
Options:
a.) O=C(NCc1ccc(Cl)cc1)C1CCN(S(=O)(=O)c2cccnc2)CC1
b.) CC1(C)SC2c3ccccc3C(=O)N2[C@@H]1C(=O)NCc1ccco1
c.) O=[N+]([O-])c1ccccc1/C=N/n1c(-c2cccnc2)n[nH]c1=S
d.) CC(C)(C)NS(=O)(=O)c1ccc2c(c1)oc(=O)c1cc(S(=O)(=O)NC(C)(C)C)ccc12
e.) COc1ccc(Oc2nc(SC)nc3ccccc23)cc1
Answer: a. O=C(NCc1ccc(Cl)cc1)C1CCN(S(=O)(=O)c2cccnc2)CC1
{#Task|Problem statement!}: Answer the {#multiple choice|multiple-choice|MCQ!} question.
{#Question|Query!}: Which {#compound|drug!} {#has|exhibits!} a {herg_central_at_10uM#}{herg_central_at_10uM__units} {herg_central_at_10uM__names__noun}?
Constraint: You must select none, one or more options from {%multiple_choice_enum%2-5%aA1} without using any {#other|additional!} words.
Options:
{SMILES%herg_central_at_10uM%}
Answer: {%multiple_choice_result}. {SMILES#}
O=C(NCc1ccc(Cl)cc1)C1CCN(S(=O)(=O)c2cccnc2)CC1
O=C(NCc1ccc(Cl)cc1)C1CCN(S(=O)(=O)c2cccnc2)CC1
N-[(4-chlorophenyl)methyl]-1-pyridin-3-ylsulfonylpiperidine-4-carboxamide