task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CN(C(=O)c2ccccc2C#N)C[C@@]1(O)C1CC1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H](NC(=O)N(C)C[C@@H]1CCOC1)C(C)(C)C[NH+](C)C
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCOC(=O)c1oc2cc3sc(N(C)C)nc3cc2c1C
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cc(C)cc(F)c1
Fragment 2: [5*]N1CCN([5*])CC1
### Response:
Cc1ccc(CC(=O)N2CCN(C(=O)c3cc(C)cc(F)c3)CC2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(C)cc1NC(=O)CSc1cc(N2CCN(c3ccc(F)cc3)CC2)ncn1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(Cn2ncc(c2)Cl)CCN(CC1)Cc1onc(n1)-c1c(C)cccc1
### Response:
Cc1ccccc1-c1noc(CN2CCN(Cn3cc(Cl)cn3)CC2)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nc(CC(=O)N2C[C@H](C(N)=O)CC[C@H]2C)cs1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1ccc2[nH]ccc2c1)N1CCC[C@](O)(C[NH+]2CCCC2)C1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cnn(C)c1
Fragment 2: [14*]c1nc(Br)cn2ccnc12
### Response:
Cn1cc(Nc2nc(Br)cn3ccnc23)cn1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CCc1cccc(NC(=O)CCC(=O)c2ccc(Cl)cc2)c1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(C[C@@H]1[NH2+][C@@H]2CCCC[C@@H]2NC1=O)Nc1ccccc1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [6*]C(=O)NNS(=O)(=O)c1ccc([16*])cc1
Fragment 2: [15*]C1CCCCC1
### Response:
O=C(NNS(=O)(=O)c1ccc(C2CCCCC2)cc1)c1cccc(O)c1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
C[C@@H]1CC(=O)[C@@]2(C)[C@@H]3CC[C@@H]4CC(=O)CC[C@@H]4C3=CC[C@@H]2S1(=O)=O
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(sc(cc1)Cl)[C@H](C)NC(=O)N1CCN(C(=O)[C@@H]2[C@H](C2)C)CC1
### Response:
C[C@H](NC(=O)N1CCN(C(=O)[C@H]2C[C@@H]2C)CC1)c1ccc(Cl)s1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(CNc2nc(N3CCN(c4cccc[nH+]4)CC3)[nH+]c3ccccc23)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc([16*])cc1
Fragment 2: [1*]C(=O)C1CC[NH+]([5*])CC1
### Response:
CC(C)[NH+]1CCC(C(=O)N[C@H](C)c2ccc(OCC(F)(F)F)cc2)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@H](O)[C@H](C)CC[NH+]1[C@H](C(Nc1cccc(c1)OC)=O)c1ccccc1
### Response:
COc1cccc(NC(=O)[C@H](c2ccccc2)[NH+]2CC[C@@H](C)[C@@H](O)C2)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)c1ccc(COc2nnc(-c3ccccc3)o2)cc1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccc(C[NH+](C)Cc2ccc(C(=O)NN)cn2)n1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC[C@](C)(NC(=O)COc1ccccc1C)C(=O)OC
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NCc1cccs1)N[C@H](c1ccc(F)cc1)C1CCC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C(COc1ccc(Cl)cc1Cl)Nc1nnc(-c2ccc(C(F)(F)F)cc2)o1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCOC(=O)CCN1C(=O)/C(=C/c2ccc([N+](=O)[O-])cc2)SC1=S
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCOC(=O)Nc1cc(Cl)ccc1OC
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC1[C@@H]([NH2+]C)Cc1nc([C@@H](OC)C)no1
### Response:
C[NH2+][C@@H](Cc1nc([C@H](C)OC)no1)C1CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@@H](C(=O)N1CCC(CC1)C)(Sc1nnc(n1CC)-c1ccncc1)C
### Response:
CCn1c(S[C@H](C)C(=O)N2CCC(C)CC2)nnc1-c1ccncc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(CC)c(NC([C@@H]([NH+]2CCN(CC(F)(F)F)CCC2)C)=O)c1C
### Response:
CCc1cccc(C)c1NC(=O)[C@H](C)[NH+]1CCCN(CC(F)(F)F)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@H]1(c2ccc(F)cc2CC1)NC(=O)N[C@H](CO)c1ccc(c(F)c1)Cl
### Response:
O=C(N[C@H]1CCc2cc(F)ccc21)N[C@H](CO)c1ccc(Cl)c(F)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(Nc1ccon1)c1cc(S(=O)(=O)N2CCOCC2)cs1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
Cc1ccccc1OCc1ccc(C[NH2+]C2CC2)cn1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CCn1c(CNc2cccc(C)c2)nc2ccccc21
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NC(=O)Nc1ccc(C(=O)N[C@@H]2C[C@H]3C[C@@H]2[C@H]2CCC[C@H]32)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@](C)([C@@H]([NH2+]C)C1CCC(C)CC1)N1CCOCC1
### Response:
4 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1CCC[NH+](CCNC(=O)NCc2ccc(Cl)nc2)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cn1ncc2c(=O)n(CCC(=O)N(C[C@@H]3CCOC3)C3CC3)cnc21
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1nc(C)cc1C
Fragment 2: [5*]Nc1ccc([16*])c(OC)c1
### Response:
COc1cc(NC(=O)Cn2nc(C)cc2C)ccc1NC(=O)OC(C)(C)C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [6*]C(=O)CC#N
Fragment 2: [16*]c1ccc(F)cc1F
### Response:
N#CCC(=O)c1ccc(F)cc1F |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCOC(=O)CSc1ncnc2c1sc1nc(CC(C)C)c3c(c12)CCC3
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
O=C(NC1CC1)[C@H](Sc1ccc(C(F)(F)F)cn1)c1ccc(F)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
c1ccc2[nH]c(SC[C@@H]3CC[NH2+]C3)nc2c1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
Cc1cnc([C@@H](C)NC(=O)Nc2ccc([NH+]3CCC(C)CC3)cc2)s1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1nc(N)[nH+]cc1CC
Fragment 2: [4*][C@H](C)c1nnc([14*])o1
### Response:
CCc1c[nH+]c(N)nc1N[C@H](C)c1nnc(C(C)C)o1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1CC[C@@H](C(=O)N2CCC[C@H]2c2cccc3c2OCCO3)N1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[C@H](C)NC(=O)C(=O)Nc1cc(Br)ccc1-n1cccn1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@@H]1CC=CCC1
Fragment 2: [14*]c1ncc([16*])c([14*])n1
### Response:
CC(C)c1ncc(-c2ccncc2)c(C2CCC(CNC(=O)[C@@H]3CC=CCC3)CC2)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1/C(=C/[C@H]2C=NN=C2c2ccccc2)SC(=S)N1Cc1ccccc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](C(=O)OCc1nncn1C1CC1)c1ccc2ccccc2c1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1c(C)cc(CN(C)C(=O)CCC2CCN(C(C)=O)CC2)cc1C
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CC(=O)[C@@H]1CC[C@@H]([NH2+]C2CCC([N+](=O)[O-])CC2)[C@H]([N+](=O)[O-])C1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(CC(=O)NC)c1cncc(C(=O)OC)n1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(c1nc(on1)[C@H]1Cc2[nH+]c[nH]c2CN1)CC(C)C
### Response:
CC(C)CCc1noc([C@H]2Cc3[nH+]c[nH]c3CN2)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
FC(Oc1c(cc(CN(c2ccc3nnc(C)n3n2)C)cc1)OCC)F
### Response:
CCOc1cc(CN(C)c2ccc3nnc(C)n3n2)ccc1OC(F)F |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1cc(N2CC[NH+](C)[C@@]3(CCNC(=O)CC3)C2)nc(OC)n1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(-c2n[nH]cc2CN2CC[C@H](S(=O)(=O)NC3CC3)C2)cc1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCCc1cc(NC(=O)N(C)[C@H]2CCN(c3ccccc3F)C2=O)n(C)n1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1ccc(NC(C)=O)cc1NC(=O)[C@H]1CSc2nccc(=O)n2C1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(-c2csc(SCCO)n2)cc1
### Response:
OCCSc1nc(-c2ccccc2)cs1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1cc2c3c(cccc31)CN(C(=O)Nc1cccc(Cl)c1F)CC2
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(C(=O)Nc2cccc(-c3ccc(OC)nn3)c2)cc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@H]1(CCC[C@@H](C)N1C(=O)c1cc(OC)ccc1)C
### Response:
COc1cccc(C(=O)N2[C@H](C)CCC[C@H]2C)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1
Fragment 2: [14*]c1ccco1
### Response:
COC(=O)[C@@H]1C(=O)N=C(N2CCN(c3ccc(F)cc3)CC2)N[C@@H]1c1ccco1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CCc1ccc(O)cc1)N/N=C\c1cc(Cl)cc(Cl)c1O
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1nc([C@@H]2CCCN(C(=O)c3cc(C(C)C)n[nH]3)C2)nc2c1CCC(=O)N2C
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(=O)Nc1ccc(Nc2ncnc(Oc3ccc(C)c(C)c3)c2[N+](=O)[O-])cc1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(C[C@]2(C(NCC)=O)CCN(C(=O)C)C2)ccc(c1)-c1c(cccc1)OC
### Response:
CCNC(=O)[C@@]1(Cc2ccc(-c3ccccc3OC)cc2)CCN(C(C)=O)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(=O)N1N=C(c2ccccc2[N-]S(C)(=O)=O)C[C@H]1c1ccnc2ccccc12
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccncc1
Fragment 2: [1*]C(=O)c1cnn([9*])c1C
### Response:
CCc1ncsc1NC(=O)c1cnn(-c2ccncc2)c1C |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
Cc1c(Oc2ccc3cn[nH]c3c2)nn2c(C(F)(F)F)nnc2c1C
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12ccccc1ccc1c2[C@@H](c2c([nH]c(=O)[nH]c2N1)=O)c1cc(OC)c(c(c1)OC)OC
### Response:
COc1cc([C@@H]2c3c([nH]c(=O)[nH]c3=O)Nc3ccc4ccccc4c32)cc(OC)c1OC |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCNC(=O)[C@H](C)N1CCN(CC(=O)NC(C)C)CC1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1CN(CCC(=O)NNC(=O)Cc2ccccc2F)C[C@H](C)O1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C1CCN([5*])CC1
Fragment 2: [1*]C(=O)C(C)C
### Response:
CCc1cc(C#N)c(NC(=O)C2CCN(C(=O)C(C)C)CC2)s1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)CCC(C)C
Fragment 2: [1*]C(=O)N([5*])C
### Response:
CC[S@](=O)[C@@H]1CCCC[C@@H]1NC(=O)N(C)CCC(C)C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@@H](C)CN(C(=O)CCn2cc(C(=O)[O-])cn2)C1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
O=C(CNc1ccc(Cl)cc1F)NC[C@@H]1COc2ccccc2O1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@H](NC(=O)CCOc2ccc(cc2)C=O)c2c(cc(cc2)Cl)C1
### Response:
O=Cc1ccc(OCCC(=O)N[C@H]2CCc3cc(Cl)ccc32)cc1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
COC(=O)/C=C/c1ccc(NCC(=O)N2CCCCC2)c([N+](=O)[O-])c1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H](Cc1cccs1)N(C)C[C@@H]1CCCC[C@@H]1[NH3+]
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C/[NH+]=C(/NCc1ccnn1C)NCC1([NH+]2CCCCC2)CCCCC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCC
Fragment 2: [4*]C(CC)CC
### Response:
CCC[NH2+][C@H]1CC[NH+](C(CC)CC)[C@H](C)[C@@H]1C |
functional_group | ### Instruction:
Does the molecule contain a ester group?
CO[C@@H]1CCC[C@H]1OC(=O)c1ccc(CCNC(N)=O)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(C1CC1)[NH2+][C@@H]1CCCS[C@H]1C
### Response:
C[C@@H]1SCCC[C@H]1[NH2+]CC1CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1nc(C)cs1
Fragment 2: [5*]N1CCn2c(S[11*])nnc21
### Response:
COc1ccc(N2CCn3c(SCC(=O)Nc4nc(C)cs4)nnc32)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CCC[C@@](O)(C[NH2+][C@@H](C)C[C@@H]2CCC[NH2+]2)C1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1C[C@H]([13*])O[C@@H](C)C1
Fragment 2: [16*]c1ccccc1
### Response:
C[C@H]1CN(c2ncccc2S(N)(=O)=O)C[C@H](c2ccccc2)O1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCOCC1
Fragment 2: [1*]C(=O)c1cccnc1[14*]
### Response:
O=C(Nc1ccc(N2CCOCC2)nc1)c1cccnc1N1CCCC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[C@H](NC(=O)C[NH+]1CCCN(S(=O)(=O)c2ccc(F)cc2)CC1)c1ccccc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1nnc(NC(=O)CCn2cncn2)s1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@H]1CCCC[NH+]1CCNC(=O)c1ccc2ccccc2n1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@@H]1CSc2nc(C)c(CC)c(=O)n2C1
Fragment 2: [5*]N([5*])[C@H](C)CC
### Response:
CCc1c(C)nc2n(c1=O)C[C@H](C(=O)N([C@H](C)CC)[C@@H](C)CC)CS2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cccc(C(=O)Nc2ccc(NC=C3C(=O)OC(C)(C)OC3=O)cc2)c1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[NH+]1(C2CCC(C)(CC2)C)CCCC[C@H]1[C@@H]1CC(NC1)=O
### Response:
CC1(C)CCC([NH+]2CCCC[C@H]2[C@H]2CNC(=O)C2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=S(=O)([O-])c1ccc(S(=O)(=O)[O-])c2ccccc12
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
Cc1ccccc1-c1nn2c(=O)cc(N3CCN(C(=O)Nc4ccccc4F)CC3)nc2s1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Nc1ccccc1OC(F)F)N1CCN(C(=O)C2CCCC2)CC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
C[NH+](C)[C@@H]1CCC[C@@H](NC(=O)NCc2cc(=O)[nH]c3ccccc23)C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC[C@H]([NH3+])[C@H](Sc1cc2ccccc2[nH]1)c1cccnc1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc2[nH]c([C@H]3CCCN(C(=O)c4ccnn4C(C)C)C3)c(-c3ccncc3)c2c1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
COc1ccc(-c2ccc(=O)n([C@H](C)C(=O)N3CCN(C=O)CC3)n2)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(Cl)cc(ccc1C(N(C)Cc1c(F)cccc1Cl)=O)[N+](=O)[O-]
### Response:
CN(Cc1c(F)cccc1Cl)C(=O)c1ccc([N+](=O)[O-])cc1Cl |
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