task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC[C@@H]1[C@@H](C)CCCN1C(=O)c1ccc(OC)nn1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1c(/N=C/c2ccc(O)c(O)c2)[nH+]c2ccccc21
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[C@@H](C)CC(C)C
Fragment 2: [16*]c1cc[nH+]cc1
### Response:
CC(C)C[C@H](C)CC(=O)NCC1CCN(c2cc[nH+]cc2)CC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C([O-])[C@@H]1C[C@H]1c1cccc(F)c1F
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCC[NH2+]CC[NH+](C)CC(C)(C)O
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NS(=O)(=O)c1cc(Cl)ccc1OC
Fragment 2: [1*]C(=O)[C@H]([4*])C
### Response:
COc1ccc(Cl)cc1S(=O)(=O)N[C@H](C)C(=O)NCc1ccc2c(c1)OCO2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CNC(=O)[C@H](C)Nc1ccc(C(F)(F)F)cc1C(=O)[O-]
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a halide group?
Cc1cccc(/C=C/C(=O)c2cncc(F)c2)c1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COC[C@@H](NC(=O)c1ccccc1C(F)(F)F)c1ccc(F)c(F)c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc([C@@H]2CC(=O)C3=C(C2)Nc2[nH]nc(O)c2[C@H]3c2ccc(Br)cc2)cc1OC
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
c1ccc([C@@H]2C[C@H]2C[NH2+]Cc2nc3c(s2)CCC3)cc1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1cc(Cl)cc(Cl)c1)C1CCN(S(=O)(=O)/C=C/c2ccccc2)CC1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]Oc1ccc(OC)cc1
Fragment 2: [5*]N1CC([15*])C1
### Response:
COc1ccc(OCC(=O)N2CC(OCc3ccc(Cl)cc3)C2)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c2S/C(=C/C(=O)N[C@H](c3ccccc3)C)C(Nc2ccc1)=O
### Response:
C[C@H](NC(=O)/C=C1/Sc2ccccc2NC1=O)c1ccccc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C[C@H]1CCOCCN1C(=O)NCc1cnc(-n2cncc2)cc1
### Response:
C[C@H]1CCOCCN1C(=O)NCc1ccc(-n2ccnc2)nc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(Nc1ccc(-c2cc[nH]n2)cc1)N[C@@H]1CCN(c2ccccc2)C1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H](C(=O)[O-])C(C)C
Fragment 2: [4*][C@@H](C(=O)[O-])C(C)C
### Response:
Cc1ccc(NC(=O)N[C@@H](C(=O)[O-])C(C)C)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1ccnc(NC(=O)c2ccc(SCc3ccccc3)cc2)c1=O
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc2c(ccc(c2)OCC(N(C2CC2)CC2=CC3[C@@H](C=C2)N=CC=3)=O)cc1
### Response:
O=C(COc1ccc2ccccc2c1)N(CC1=CC2=CC=N[C@@H]2C=C1)C1CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cc(/C=N/NCCO)cc(OC)c1O
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](C(=O)[O-])[NH+]1CCc2ccccc2C1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CCOc1c(OC(COc2c(cc(C)cc2)C)=O)cccc1
### Response:
CCOc1ccccc1OC(=O)COc1ccc(C)cc1C |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)c1cc(Br)ccc1NC(=O)c1ccc(Br)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(-c2nnc(CN3CCC[C@H]3Cc3cccc(F)c3)o2)c(C)o1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COc1cc(OC)cc([C@H]2Nc3nonc3NC3=C2C(=O)CCC3)c1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CC(=O)[O-]
Fragment 2: [9*]n1c(CC)cc2ccccc2c1=O
### Response:
CCc1cc2ccccc2c(=O)n1CC(=O)[O-] |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@@H](N[C@@H](CO)c2cc(F)c(F)c(F)c2)C[NH+]1C1CC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(c1nc(N2CCN(C(C[NH+]3CCC(C)CC3)=O)CC2)cc(n1)C)C
### Response:
Cc1cc(N2CCN(C(=O)C[NH+]3CCC(C)CC3)CC2)nc(C(C)C)n1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C(CNC(=O)c1ccc2c(c1)OCO2)Nc1ccccc1N1CCCC1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amine group?
C#CCNC(=O)NNc1c(Cl)cc(Cl)cc1Cl
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
Cc1cc(C)c2nc(N3CCN(C(=O)[C@@H]4CCCCN4S(C)(=O)=O)CC3)sc2c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NC(=O)Cn1cc(C(=O)O[C@H]2CCC[C@@H](C(F)(F)F)C2)nn1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)[C@H](Cc1c[nH]c2ccccc12)NS(=O)(=O)c1cccc2nonc12
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]Oc1ccc(C[4*])cc1
Fragment 2: [8*]CCCO
### Response:
C[C@@H](C#N)Oc1ccc(C[NH+]2CCC[C@@H]2CCCO)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccc(c1)CN1[C@@H](C(=O)NCc2n[nH]c(=S)n2C)CCC1=O)C
### Response:
Cc1ccc(CN2C(=O)CC[C@@H]2C(=O)NCc2n[nH]c(=S)n2C)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(n(C)ccn1)COc1c2c(OCC(=O)N2)ccc1
### Response:
Cn1ccnc1COc1cccc2c1NC(=O)CO2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccc(OC[C@H](O)CNC(=O)Nc2c(C)cccc2C)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)(C)NC(=O)c1cccc([N-]S(=O)(=O)c2ccc(F)c(F)c2)c1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1nc(NC(=O)c2ccccc2Cl)sc1Cc1ccccc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCn1nc(CC(C)C)cc1C(=O)N[C@@H]1CCC[NH+](Cc2cccnc2)C1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(ccc1NC(N[C@@H](C)CCCO)=O)Sc1scc(n1)C
### Response:
Cc1csc(Sc2ccc(NC(=O)N[C@@H](C)CCCO)cc2)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@@H]1CSCN1[5*]
Fragment 2: [1*]C(=O)c1ccoc1
### Response:
CC(C)CC[C@@H](C)NC(=O)[C@@H]1CSCN1C(=O)c1ccoc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(=O)NCCCN(C)C(=O)C1C[C@H](C)O[C@@H](C)C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc2c(c(CNC(N3CCN(CC3)c3[nH+]cc(cc3)-c3nc(C)on3)=O)c1)cccc2
### Response:
Cc1nc(-c2ccc(N3CCN(C(=O)NCc4cccc5ccccc45)CC3)[nH+]c2)no1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(noc(c1)C(C)C)NC(Cn1c(cccc1)=O)=O
### Response:
CC(C)c1cc(NC(=O)Cn2ccccc2=O)no1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Cc1n(ncc1C(=O)NC1CCN(c2cc(ccc2)F)CC1)C(C)C
### Response:
Cc1c(C(=O)NC2CCN(c3cccc(F)c3)CC2)cnn1C(C)C |
functional_group | ### Instruction:
Does the molecule contain a ether group?
O=C(c1csc2c1CCCC2)N1CCO[C@H]2CCCC[C@H]21
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(NS(=O)(=O)c2ccccc2[N+](=O)[O-])cc1N1CCCC1=O
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=[PH2][C@H](Cc1ccccc1)c1ccccc1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC(=O)N1CCC(N2CCN(C(=O)c3cccc(F)c3)CC2)CC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
O=C(CSc1ncc(C(F)(F)F)cc1Cl)NCc1ccccc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C([O-])CC1CCN(S(=O)(=O)c2cc[nH]c2)CC1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CN(C(=O)c1cccc(C(F)(F)F)c1F)C1CCCCC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc(C[7*])cc1
Fragment 2: [5*]N1CCC[C@H](CC)C1
### Response:
CC[C@H]1CCCN(C(=O)/C=C/c2ccc(NC(C)=O)cc2)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cc(-c2nnc(CN3CCCCC[C@H]3c3ccco3)o2)c(C)o1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)NNC([6*])=O
Fragment 2: [5*]NCC[8*]
### Response:
CCc1cnc(CCNC(=O)NNC(=O)[C@H]2CCCO2)s1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1CN(Cc2ccc(Cl)cc2Cl)C[C@H](C)O1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(NC(=O)[C@@H](Sc2nnnn2C[C@@H]2CCCO2)C(C)C)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc(c1C#N)CNc1cccc([N+](=O)[O-])c1C
### Response:
Cc1c(NCc2ccccc2C#N)cccc1[N+](=O)[O-] |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12ccccc2N(C(=O)/C=C/C)C[C@@H](C(N1)=O)C
### Response:
C/C=C/C(=O)N1C[C@H](C)C(=O)Nc2ccccc21 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCC(CC)(C(=O)[O-])N1C(=O)[C@@H]2[C@H](C1=O)C2(C)C
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]Cn1c(=O)n([9*])c(=O)c2c1c1cc(C)ccc1n2C
Fragment 2: [16*]c1ccccc1
### Response:
COc1cccc(Cn2c(=O)n(-c3ccccc3)c(=O)c3c2c2cc(C)ccc2n3C)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)CN1CCO[C@@H](CNC(=O)/C=C/c2ccnc(Cl)c2)C1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(-c2occn2)ccc(c(NC(N2CCC[C@@H]2c2ccco2)=O)c1)C
### Response:
Cc1ccc(-c2ncco2)cc1NC(=O)N1CCC[C@@H]1c1ccco1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
NC(=O)Nc1ccc(NC(=O)[C@H]2CCN(c3cc(F)cc(F)c3)C2=O)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CCOC(=O)c1cn(Cc2cccc(C(F)(F)F)c2)c2nc(C)ccc2c1=O
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc([16*])c([N+](=O)[O-])c1
Fragment 2: [4*]Cc1ccc([16*])cc1[N+](=O)[O-]
### Response:
C[NH+](Cc1ccsc1)Cc1ccc(C(N)=O)cc1[N+](=O)[O-] |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1nc([C@@H]2CN3CC[NH+]2CC3)nc([O-])c1F
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC(C)(C)C(=O)N1CCCc2cc(N)ccc21
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CN(C)c1ccc(C(=O)Nc2[nH]ncc2N)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
C=CC[NH+](CC(=O)[O-])[C@@H]1CCC[C@H](C(C)(C)C)CC1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C([O-])c1ccc([C@H]2CCCN(C(=O)c3ccc4[nH]ccc4c3)C2)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(cc1)-n1/c(s/c(=C\c2ccc(c(c2)OC)OC)c1=O)=C(/c1nnc2n1CCCCC2)C#N
### Response:
COc1ccc(/C=c2\s/c(=C(/C#N)c3nnc4n3CCCCC4)n(-c3ccccc3)c2=O)cc1OC |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1c([O-])oc2ccccc2c1=O
Fragment 2: [16*]c1ccccc1
### Response:
CC(=O)[C@@H](O)[C@@H](c1ccccc1)c1c([O-])oc2ccccc2c1=O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(OC)ccc(/C=N/OCc2nc3c4c(n(CC(C)C)c(c4C)C)ncn3n2)c1
### Response:
COc1ccc(/C=N/OCc2nc3c4c(C)c(C)n(CC(C)C)c4ncn3n2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1nc(-c2cc([N+](=O)[O-])ccc2OC)n[nH]1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOCCN(C)S(=O)(=O)c1cc(Cl)ccc1C#N
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)c1cccc(NC(=O)CCn2[nH]c(=O)ccc2=O)c1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1CC[NH+](Cc2cc(=O)c(OCC(=O)NCc3ccco3)co2)CC1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH2+]Cc1ccc(Br)cc1
Fragment 2: [5*][NH2+][C@@H](C)CC(C)(C)OC
### Response:
COC(C)(C)C[C@H](C)[NH2+]Cc1ccc(Br)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH2+]C[C@]1(C)CCCO1
Fragment 2: [4*]C[C@]1(C)CCCO1
### Response:
C[C@@H]([NH2+]C[C@]1(C)CCCO1)C(=O)NC1CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(C)nc([C@@H](CC)NC(Nc2c(Cl)ccc(C#N)c2)=O)no1
### Response:
CC[C@@H](NC(=O)Nc1cc(C#N)ccc1Cl)c1noc(C)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1(C)(C)N(Cc2c(C#N)c(nn2-c2ccccc2)C)CC[NH+](C)C1
### Response:
Cc1nn(-c2ccccc2)c(CN2CC[NH+](C)CC2(C)C)c1C#N |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NC(=O)C[NH+]1CCCN(CC2CCCCC2)CC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CS(=O)(=O)CS(=O)(=O)OCCCl
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CC(C)(C)C
Fragment 2: [16*]c1ccccc1
### Response:
Cc1nn(-c2ccccc2)c(C)c1/C=N/NC(=O)c1n[nH]c2c1C[C@@H](CC(C)(C)C)CC2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@H]([8*])CN[5*]
Fragment 2: [1*]C(=O)C([1*])=O
### Response:
Cn1cccc1[C@H](CNC(=O)C(=O)NCc1ccco1)[NH+]1CCCCCC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H]1[C@H]2CCO[C@@H]2C1(C)C
Fragment 2: [1*]C(=O)CS(=O)(=O)C(C)C
### Response:
CC(C)S(=O)(=O)CC(=O)N[C@@H]1[C@H]2CCO[C@@H]2C1(C)C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CCc1cc(Cl)no1)Nc1ccc2occc(=O)c2c1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(cn(c(c1)C(=O)OC)C)S(=O)(N(C)Cc1cc(ccc1)OC)=O
### Response:
COC(=O)c1cc(S(=O)(=O)N(C)Cc2cccc(OC)c2)cn1C |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[NH+]1CCN(CCOc2ccccc2Cl)CC1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(C[C@H](C)N[C@H](C)c2ccccc2[N+](=O)[O-])n[nH]1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C[C@@H]1[C@H](N(C(NC2CCN(CC2)C(=O)OC(C)C)=O)CCC1)C
### Response:
CC(C)OC(=O)N1CCC(NC(=O)N2CCC[C@H](C)[C@H]2C)CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1cc(CO)c(Br)cc1OCc1ccc(F)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(C[NH2+]C1(c2ccc(Br)cc2)CCOCC1)Nc1ccccc1C(F)(F)F
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
CCc1ccc(-c2nc(N)ccc2[N+](=O)[O-])cc1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC/[NH+]=C(/NCC#Cc1ccccc1)NC[C@@H]1CCO[C@@H]1c1ccccc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C/C=C/C(=O)N[C@@H](Cc1ccc(F)cc1)C(=O)[O-]
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1sc(=O)n(CCC(=O)NNc2ncccc2Cl)c1C
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1C(N)=[NH+]C[C@@H]1[13*]
Fragment 2: [8*]CN=[N+]=[N-]
### Response:
[N-]=[N+]=NC[C@H]1C[NH+]=C(N)N1c1cccc(F)c1 |
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