task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(C[NH+]2CCC(c3nnc(Cn4cncn4)n3C)CC2)s1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cn1cc(C(=O)NCCc2ccccc2)c(C(=O)[O-])n1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
COS(=O)(=O)c1ccc(Cl)c2ccccc12
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc2oc(=O)cc(CN3CCC4(CC3)NC(=O)N(C)C4=O)c2cc1C
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1csc(c1)C(=O)N(C)CC(=O)O[C@H]1C[C@H](CCC1)OC
### Response:
CO[C@H]1CCC[C@@H](OC(=O)CN(C)C(=O)c2cccs2)C1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
C[C@H](CO)[C@H](C)Nc1nccc(OCc2ccccc2)n1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a halide group?
O=C1C[C@@H](NC2=NS(=O)(=O)c3ccccc32)CN1CC(F)(F)F
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amide group?
C[C@@H]1CC[C@@H]([NH+](CC(=O)N(C)C)CC(F)(F)F)C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
CCNc1nnc(SCCS(=O)(=O)c2ccc(Br)cc2)s1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(=O)(Nc1ccccc1C(=O)N)[C@H]1C(=CN=N1)I
### Response:
NC(=O)c1ccccc1NC(=O)[C@@H]1N=NC=C1I |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(C)(C)c1nn(c(C(=O)N[C@H](c2ncccc2)c2ccccc2)c1)C
### Response:
CC(C)c1cc(C(=O)N[C@@H](c2ccccc2)c2ccccn2)n(C)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cccc(C)c1OCC(=O)NCCc1c[nH]c2ccccc12
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC[C@H]([NH2+]C)[C@@H]1CCc2cccnc21
Fragment 2: [3*]Oc1ccccc1
### Response:
C[NH2+][C@@H](CCOc1ccccc1)[C@@H]1CCc2cccnc21 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1N(CCc2c1cn[nH]2)C(/C=C/SCc1occc1)=O
### Response:
O=C(/C=C/SCc1ccco1)N1CCc2[nH]ncc2C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc(N[5*])nn1
Fragment 2: [4*][C@@H](COC)C(C)C
### Response:
COC[C@H](Nc1ccc(C(=O)N(C)C)nn1)C(C)C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCC
Fragment 2: [5*][NH2+][C@@]1([15*])CC[C@@H]([15*])C1
### Response:
CCC[NH2+][C@@]1(C(=O)[O-])CC[C@@H](N2CC[NH+](C)CC2)C1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
Cc1ccccc1NC(=O)c1nnc([C@@H]2CCCN(S(=O)(=O)c3ccc(F)c(Cl)c3)C2)s1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(CCO[C@H](C)C1)[C@H](c1c(Cl)cccc1F)CNC(=O)N[C@H]1[C@@H](C)C1
### Response:
C[C@@H]1CN([C@@H](CNC(=O)N[C@@H]2C[C@@H]2C)c2c(F)cccc2Cl)CCO1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N#C/C(=C\c1cc(O)c(OC)cc1)S(=O)(c1ccc(cc1)C)=O
### Response:
COc1ccc(/C=C(\C#N)S(=O)(=O)c2ccc(C)cc2)cc1O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(CC)C(=O)[C@@H](C)NS(=O)(=O)c1cccc(Br)c1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1cnc(F)c(C(=O)[O-])c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(S(=O)(=O)NCC2CC[NH2+]CC2)sc1Br
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C(C(N2CCN(CC2)c2ccccc2)=O)CCN(S(=O)(Cc2ccccc2Cl)=O)C1
### Response:
O=C(C1CCN(S(=O)(=O)Cc2ccccc2Cl)CC1)N1CCN(c2ccccc2)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O1CCC[C@H]1CNC(c1/c(=[NH+]/c2cc(F)c(OC)cc2)oc2c(cccc2c1)OC)=O
### Response:
COc1ccc(/[NH+]=c2\oc3c(OC)cccc3cc2C(=O)NC[C@@H]2CCCO2)cc1F |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC[NH+](CCNC(=O)N[C@H]1CC(=O)N(C(C)(C)C)C1)C(C)C
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccccc1F
Fragment 2: [4*]Cc1ccc2c(c1)OCO2
### Response:
O=C(COc1ccccc1F)N1CCN(Cc2ccc3c(c2)OCO3)CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)c1ccc(NC(=O)CSc2ncc(C(F)(F)F)cc2Cl)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NC(=O)N[C@@H](CC(=O)NNC(=O)c1ccc2c(c1)OCO2)c1ccccc1Cl
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CC(C)CCNC(=O)c1cccc(S(=O)(=O)N[C@@H]2CCCNC2=O)c1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cn(c(c(n1-c1c(cccc1C)C)=O)=O)Cc1onc(n1)-c1cc(F)ccc1
### Response:
Cc1cccc(C)c1-n1ccn(Cc2nc(-c3cccc(F)c3)no2)c(=O)c1=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccccc1[C@H]1CCCN(C(=O)c2cnc(-c3cccnc3)nc2)C1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@@H](C(=O)N1CCN(c2cc(Cl)ccc2C)CC1)n1nc(C)n2c(cc3occc32)c1=O
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH+](C)[C@H]1CC[C@@H](NC(=O)N2CCC(NC(=O)c3ccccc3F)CC2)C1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
ClCc1nc2cccnc2n1CCc1cccs1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CN(Cc1ccno1)Cc1c(C(=O)N2CC[NH+](C3CCCCC3)CC2)nc2ccccn12
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CC=C
Fragment 2: [4*]CCc1ccccc1
### Response:
C=CCn1c(N2CC[NH+](CCc3ccccc3)CC2)nc2c1c(=O)[nH]c(=O)n2C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC[NH+](CC(=O)NC)Cc1c[nH]nc1-c1cccnc1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
COc1ccc2[nH]cc(CC(=O)Nc3cccc(N(C)C(C)=O)c3)c2c1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1cnccn1)N1CCCC[C@@H]1[C@H]1CCCC[C@@H]1O
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Cc1cccc(NC(=S)NNC(=O)c2ccncc2)c1C
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(C(=O)[C@@H](C)S[C@H](C)[C@@H](C)O)c(C)n1Cc1ccco1
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1ccc2c(c1)sc(=S)n2CN1C[C@H](C)O[C@@H](C)C1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCCC
Fragment 2: [4*]CCC
### Response:
CCCNC(=O)N1[C@@H](C(=O)[O-])CC[C@H]2CCCC[C@@H]21 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(c1c(=O)n2c(n(c1C)CC(=O)N1CCCC[C@@H]1C)nc(-c1ccc(cc1)C)n2)c1ccccc1
### Response:
Cc1ccc(-c2nc3n(CC(=O)N4CCCC[C@@H]4C)c(C)c(Cc4ccccc4)c(=O)n3n2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1cccc1[C@H](CNC(=O)C(=O)Nc1ccc(Cl)cc1)[NH+]1CCOCC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
FC(F)(c1cc([C@H]2CN(C(c3nc(ncc3)C)=O)CCC2)n[nH]1)F
### Response:
Cc1nccc(C(=O)N2CCC[C@@H](c3cc(C(F)(F)F)[nH]n3)C2)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nc(COc2ccc(F)cc2)sc1C(=O)Nc1ccc2c(c1)NC(=O)[C@H](C)O2
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](Oc1ccccc1F)C(=O)NNC(=O)c1ccc(Cl)c(Cl)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccccc1CN(C(=S)Nc1ccc(Cl)cc1C)C1CC[NH+](C)CC1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
N#CCc1ccc(NC(=O)[C@@H]2CC(=O)N(CC3CC3)C2)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12nc(C3CC[NH+](Cc4ccco4)CC3)oc2ccc(c1)Cl
### Response:
Clc1ccc2oc(C3CC[NH+](Cc4ccco4)CC3)nc2c1 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
O=C1N[C@@](Cc2ccccc2)(c2ccccc2)C(=O)N1Cc1ccc([N+](=O)[O-])cc1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [11*]Sc1nnc([14*])n1C
Fragment 2: [5*]Nc1ccc([16*])cc1
### Response:
CN(C)c1ccc(NC(=O)CSc2nnc(-c3cccnc3)n2C)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C[C@@H](C[NH+](CC)CC)CN1Cc1c(O)cc(OC)cc1
### Response:
CC[NH+](CC)C[C@@H]1CCN(Cc2ccc(OC)cc2O)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCOC(=O)c1ccc(NS(=O)(=O)c2cc(Cl)ccc2Cl)cc1
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](SCCOc1cccc(Cl)c1)C(N)=O
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cc(Cl)c(C)cc1NCC(=O)Nc1cc(OC)c([N+](=O)[O-])cc1C
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CNC(=O)[C@@H]1CCCN(S(=O)(=O)c2c(C)nn(CC(=O)NC(C)(C)C)c2C)C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NC[C@H]1C[C@@H](O)C[NH+]1Cc1ccccc1)c1n[nH]c2c1CCCC2
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CN1C(=O)c2cccc(NC(=O)Cc3ccc(F)cc3)c2C1=O
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)C[8*]
Fragment 2: [5*]NCc1ccccc1[16*]
### Response:
CC(C)[NH+](C)Cc1ccccc1CNC(=O)N(C)Cc1ccc(F)cc1F |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1([C@H](C(=O)OCC(=O)Nc2cc(Cl)ccc2)CC)ccccc1
### Response:
CC[C@@H](C(=O)OCC(=O)Nc1cccc(Cl)c1)c1ccccc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CNC(=O)c1ccc(Cl)c(NC(=O)[C@H]2C=C[C@@H]([NH3+])C2)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc2nc(C)cc(C(=O)N(C)Cc3ccccc3)c2c1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCn1c(S[C@@H](C)C(=O)N[C@@H](C)c2ccccc2)nc2ccc(Br)cc2c1=O
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1nnnn1[C@H]1CC(=O)[C@@H]2OC[C@H]1O2
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCn1c(SCC(=O)N(C)C2CCOCC2)nnc1-c1ccco1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(C([C@@H](CCC1)[NH2+][C@H]1CCCc2c1cnn2C)=O)CC(F)(F)F
### Response:
Cn1ncc2c1CCC[C@@H]2[NH2+][C@@H]1CCCN(CC(F)(F)F)C1=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
N#C[C@H](COC(=O)c1cccc(Br)c1)Cc1cccs1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(Br)ccc1NC(=O)[C@@H]1CC=CCC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(=O)cc(OC)c(c2CCN(C(=O)C3(CC3)c3ccccc3)CCn12)C(N(C)Cc1nonc1C)=O
### Response:
COc1cc(=O)n2c(c1C(=O)N(C)Cc1nonc1C)CCN(C(=O)C1(c3ccccc3)CC1)CC2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N(C(C)C)C(=O)c1cnn(c1C(F)F)CC(C)C)[C@H]1CCCCO1
### Response:
CC(C)Cn1ncc(C(=O)N(C[C@H]2CCCCO2)C(C)C)c1C(F)F |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@H](O)COC
Fragment 2: [5*][NH+]1CCC([15*])CC1
### Response:
COC[C@@H](O)C[NH+]1CCC(N[C@@H]2CCCc3ccc(Cl)cc32)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccccc1F
Fragment 2: [1*]C(=O)c1cc(S([12*])(=O)=O)ccc1OC
### Response:
CCN(CC)S(=O)(=O)c1ccc(OC)c(C(=O)Nc2ccccc2F)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](CC(=O)Nc1c(F)cccc1Br)c1ccccc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(-c2cnc3c(c2)CN(C(=O)c2ccc4c(c2)OCCO4)CC3)cc1OC
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCN(C1)C(c1sc2c(c1)c(n(c(n2C)=O)C)=O)=O
### Response:
Cn1c(=O)c2cc(C(=O)N3CCCC3)sc2n(C)c1=O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(c1c(c(on1)CC)CNC(c1c(ccc(SC)c1)[N+]([O-])=O)=O)C
### Response:
CCc1noc(CC)c1CNC(=O)c1cc(SC)ccc1[N+](=O)[O-] |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccccc1N1C[C@H]2C[C@@H]1C[NH2+]2
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CC[C@H]1CCCC[C@H]1N(C)C(=O)c1ccc2c(c1)NC(=O)CN2CC
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
Cc1cc(C)c(S(=O)(=O)Oc2ccc(NC(=O)c3ccco3)cc2)c(C)c1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOC(=O)C1=C(CC)[C@H](C(=O)OCC)C(C)=N1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
O=C(NNc1cccnc1Cl)c1cccn1Cc1ccccc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCC[S@@](=O)C(C)(C)C
Fragment 2: [16*]c1ccccc1C#N
### Response:
CC(C)(C)[S@](=O)CCNC(=O)c1ccccc1Sc1ccccc1C#N |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(Cc1ccncc1)[C@@H]1/C(=N/O)[C@H]2CC[C@@H]1C2
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1nn(C)cc1C(=O)N[C@@H](C)c1c(Cl)ccc(F)c1Cl
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
O=C(c1cc(F)cc(Br)c1)N1CCCC[C@H]1CCO
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(S(=O)(=O)[C@H]2CCCC(C)(C)[C@H]2[NH3+])c(C)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Clc1cccc(CC[NH2+]Cc2cc[nH]c2)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cc1csc(-c2ccccn2)n1)NCC1(c2ccccc2)CC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC[NH+]1C[C@@H](Cn2c(N)nc3c2nccc3C)CC1
### Response:
CC[NH+]1CC[C@H](Cn2c(N)nc3c(C)ccnc32)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C([O-])CCCNS(=O)(=O)c1cc(C(F)(F)F)ccc1Cl
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C(Cn1cnc2c(oc3ccccc32)c1=O)NC(=O)NCc1ccco1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc(OC)c(OC)c1
Fragment 2: [3*]OCc1cc(F)cc2c1O[C@H]([13*])OC2
### Response:
COc1ccc(C(=O)OCc2cc(F)cc3c2O[C@H](c2ccccc2)OC3)cc1OC |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NS(=O)(=O)CCC(=O)[O-]
Fragment 2: [16*]c1ccccc1
### Response:
C[C@H](CNS(=O)(=O)CCC(=O)[O-])c1ccccc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
s1c(ncc1)CCN(C(=O)Nc1cncc2ccccc12)CC
### Response:
CCN(CCc1nccs1)C(=O)Nc1cncc2ccccc12 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCN([5*])CC1
Fragment 2: [1*]C(=O)CCCS(=O)(=O)C[8*]
### Response:
O=C(CCCS(=O)(=O)Cc1ccccc1)N1CCN(c2ccccc2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccccc1CNC(=O)C1(Cc2cc(-c3ccccc3C)no2)CCOCC1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(C2(C(=O)NC[C@](C)(O)c3cccs3)CCOCC2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
NC(=O)CCN1CCN(C(=O)c2cn(C/C=C/c3ccccc3)nn2)CC1
### Response:
No |
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