Problem statement: Answer the MCQ question.
Query: Which compound exhibits a 4.628\% hERG inhibition at 1uM?
Constraint: You must select none, one or more options from a, b, c, d, or e without using any other words.
Options:
(a) CC1(C(=O)OCc2cc(=O)n3cc(Br)ccc3n2)CC1(Cl)Cl
(b) CC(C)NC(=O)C(C)n1cccc1C(=O)c1ccccc1
(c) Cc1[nH]nc2nc(SCC(=O)NCC3CCCO3)n(-c3ccc(Br)cc3)c(=N)c12
(d) O=C1S/C(=C/c2ccc(N3CCOCC3)o2)C(=O)N1Cc1ccc(F)cc1
(e) O=C(O)c1ccccc1C(=O)N1CCN(c2cccc(Cl)c2)CC1
Answer: c. Cc1[nH]nc2nc(SCC(=O)NCC3CCCO3)n(-c3ccc(Br)cc3)c(=N)c12
{#Task|Problem statement!}: Answer the {#multiple choice|multiple-choice|MCQ!} question.
{#Question|Query!}: Which {#compound|drug!} {#has|exhibits!} a {herg_central_at_1uM#}{herg_central_at_1uM__units} {herg_central_at_1uM__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_1uM%}
Answer: {%multiple_choice_result}. {SMILES#}
Cc1[nH]nc2nc(SCC(=O)NCC3CCCO3)n(-c3ccc(Br)cc3)c(=N)c12
Cc1[nH]nc2nc(SCC(=O)NCC3CCCO3)n(-c3ccc(Br)cc3)c(=N)c12
[C][C][NH1][N][=C][N][=C][Branch1][S][S][C][C][=Branch1][C][=O][N][C][C][C][C][C][O][Ring1][Branch1][N][Branch1][N][C][=C][C][=C][Branch1][C][Br][C][=C][Ring1][#Branch1][C][=Branch1][C][=N][C][=Ring2][Ring1][N][Ring2][Ring1][=Branch2]
2-[[5-(4-bromophenyl)-4-imino-3-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl]sulfanyl]-N-(oxolan-2-ylmethyl)acetamide