task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(CS)Nc1ccccn1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c([C@@H](C[NH3+])CCOc2ccc(cc2)OC)ccc(Br)c1
### Response:
COc1ccc(OCC[C@H](C[NH3+])c2ccc(Br)cc2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN1CCc2nc3sc(C(=O)Nc4ccc5c(c4)OCO5)c(N)c3cc2C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCO[C@H]1C[C@@H](NC(=O)C(=O)Nc2ccc3[nH]ccc3c2)C12CCC2
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@@H]1(C(N2C[C@@H](CCC2)c2nc(on2)C)=O)COc2ccccc12
### Response:
Cc1nc([C@@H]2CCCN(C(=O)[C@@H]3COc4ccccc43)C2)no1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(C(=O)NC[C@H](c2ccco2)N2CCOCC2)cc1OC
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(C(=O)N2C[C@H](CCC2)CCc2ccc(F)cc2)c([nH]cc1)=O
### Response:
O=C(c1ccc[nH]c1=O)N1CCC[C@H](CCc2ccc(F)cc2)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc(OC)cc1
Fragment 2: [1*]C(=O)[C@@H]1CCN([10*])C1=O
### Response:
COc1ccc(NC(=O)[C@@H]2CCN(c3ccc(F)cc3C)C2=O)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cccs1
Fragment 2: [5*]N1C[C@H](C)c2ccccc21
### Response:
C[C@H]1CN(C(=O)C(=O)NCCc2cccs2)c2ccccc21 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC(C)n1ncnc1C[C@@H](O)c1ccc(Cl)cn1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(N2CCN(C(=O)C3CCCC3)[C@@H](C)C2=O)c(OC)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[O-][N+](c1c(Oc2ccc(cc2)C#N)ccc(c1)S(N1CCCCCC1)(=O)=O)=O
### Response:
N#Cc1ccc(Oc2ccc(S(=O)(=O)N3CCCCCC3)cc2[N+](=O)[O-])cc1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
COc1cc(OC)cc([C@H]2Nc3nonc3NC3=C2C(=O)CCC3)c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
Cc1cc(C)c(NNC(=O)[C@H](C)OCC(F)(F)F)c(C)c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CCN(C(=O)c1c(F)ccc(N)c1F)c1ccc(F)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C(OCCC(=O)Nc2ccc(OC(C)C)c(c2)C)CCOC1
### Response:
Cc1cc(NC(=O)CCOC2CCOCC2)ccc1OC(C)C |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COc1ccccc1CN(CCO)C(=O)N[C@H]1CCC[C@@H](C2CC2)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(OC)c(OC)c1
Fragment 2: [14*]c1cc([14*])n2nc([14*])cc2n1
### Response:
COc1ccc(-c2cc(C(F)(F)F)n3nc(C(=O)[O-])cc3n2)cc1OC |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C(c1ccc([C@@H]2CCCN2C(=O)[C@@H]2C=CC=N2)s1)N1CCSCC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCC
Fragment 2: [4*]Cc1ccccc1
### Response:
CCCN(Cc1cnc2ncccn12)[C@H]1CCC[NH+](Cc2ccccc2)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](CCc1ccccc1)Oc1cccnc1[N+](=O)[O-]
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(COc1ccc(C(=O)c2ccccc2)cc1)Nc1c(n(nc1C)C)C
### Response:
Cc1nn(C)c(C)c1NC(=O)COc1ccc(C(=O)c2ccccc2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cc(N2CCCCC2)cc(=O)o1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cscc1[C@H](O)c1cccc(F)c1F
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@H]([4*])C
Fragment 2: [5*]N1CC(=O)Nc2ccccc21
### Response:
Cc1csc(S[C@H](C)C(=O)N2CC(=O)Nc3ccccc32)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccccc1Cl
Fragment 2: [5*]Nc1c([16*])c(=O)c2ccccc2n1CC
### Response:
CCn1c(NC(=O)c2ccccc2Cl)c(-c2ccccc2)c(=O)c2ccccc21 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCCC[C@H]([NH2+]CCC)c1cc(F)c(C)cc1F
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(N[C@@H]2CCC[C@@H]2C#N)cc(c(Cl)cc1)Br
### Response:
N#C[C@H]1CCC[C@H]1Nc1ccc(Cl)c(Br)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(Br)cc1CNc1cnn(C(C)(C)C)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1ccc(C2(C[NH2+]Cc3cc[nH]c3)CCOCC2)cc1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC[C@H](C)NC(=O)CN1CCN(C(=O)Nc2cccc3cnccc23)CC1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
Cc1cc(OCC(=O)Oc2ccccc2C)ccc1Cl
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](O)CSc1nc2c(c(=O)n(C)c(=O)n2C)n1Cc1ccccc1Cl
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)(C)OC(=O)N1CCC[C@H](C(=O)N[C@H](C(=O)[O-])c2ccccc2)C1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CCN[5*]
Fragment 2: [8*]CCC
### Response:
CCC[C@H]1C[C@@H]1NC(=O)CCNC(=O)c1ccco1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCc1nn(C)cc1CNC(=O)NCC(C)(C)Cc1ccccc1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCCC[C@H](CC)[C@H]1OC[C@@H](C[NH+]2CCCCC2)O1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CC[NH+]2CCCC[C@@H]2C1
Fragment 2: [4*][C@@H](CC)[C@@H]([8*])[NH3+]
### Response:
CC[C@@H]([C@H]([NH3+])c1ccccc1)N1CC[NH+]2CCCC[C@@H]2C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CC(C)C
Fragment 2: [9*]n1nnnc1S[11*]
### Response:
CC(C)Cn1nnnc1SCc1cc(=O)n2ccsc2n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O[C@H](c1ccccc1)C(N/N=C/c1cc(c(c(OC)c1)O)Br)=O
### Response:
COc1cc(/C=N/NC(=O)[C@H](O)c2ccccc2)cc(Br)c1O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(=O)Nc1cccc(OCCNC(=O)N2CCOC(C)(C)C2)c1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[NH2+]C[C@]1(c2ccccc2Br)CC[C@@H]1C
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1csc(-c2cccc(CN/C([O-])=N/S(=O)(=O)c3ccccc3)c2)n1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccccc1OCCC(=O)N1CC[C@H](Cc2ccccc2)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cc(C)cc(C2=CCN(C(=O)[C@@H](C)O)CC2)c1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=c1[nH]cnc2cc(NCc3ccc4c(c3)OCCO4)c([N+](=O)[O-])cc12
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(Cn1nc(-c2cc(F)ccc2)nn1)(N[C@@]1(CCS(=O)(C1)=O)C)=O
### Response:
C[C@@]1(NC(=O)Cn2nnc(-c3cccc(F)c3)n2)CCS(=O)(=O)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
N[C@H](c1ccc(C(=O)[O-])cc1Cl)C(F)(F)F
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1([C@H]([NH3+])c2oc(CC)cc2)c(c(cc(Cl)c1)Br)OC
### Response:
CCc1ccc([C@@H]([NH3+])c2cc(Cl)cc(Br)c2OC)o1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
s1c(c(cc1C(Nc1ncc(N)c(c1)C)=O)C)Br
### Response:
Cc1cc(NC(=O)c2cc(C)c(Br)s2)ncc1N |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
COc1ccccc1OC(=O)c1ccc(OCC(C)C)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C([O-])(=O)CC[C@@H](C)NC(c1oc(cc1)C[NH3+])=O
### Response:
C[C@H](CCC(=O)[O-])NC(=O)c1ccc(C[NH3+])o1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(=O)n(CC(=O)NCc2cccs2)n1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH2+][C@@H]([8*])c1ccc(C)cc1
Fragment 2: [4*]Cc1ccc(N[5*])cc1
### Response:
Cc1ccc([C@@H]([NH2+]Cc2ccc(NC(=O)c3ccco3)cc2)C2CC2)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(OC)c(O)ccc1/C=N/NC(=O)Cn1cnc2c(c1=O)cc(s2)-c1ccccc1
### Response:
COc1cc(/C=N/NC(=O)Cn2cnc3sc(-c4ccccc4)cc3c2=O)ccc1O |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc([O-])nc(SCC(=O)N[C@H]2N=C3CCCC[C@@H]3S2)n1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1([C@H]2CN(C)CCO2)nc(c(c(=O)[nH]1)Br)C
### Response:
Cc1nc([C@H]2CN(C)CCO2)[nH]c(=O)c1Br |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCCn1c(N)c(N(C)C(=O)c2ccc3c(c2)OCO3)c(=O)[nH]c1=O
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CN(C(=O)CSc1ccc(Cl)cc1)c1cccc2ncccc12
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Nc1ccccc1C(=O)N1CCCCC1)C(=O)NC1CC1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccsc1
Fragment 2: [15*][C@@H]1[C@@H]2C(=C[C@@H]3CC[C@H]2N3C)C(C#N)=C(N)C1(C#N)C#N
### Response:
CN1[C@@H]2C=C3C(C#N)=C(N)C(C#N)(C#N)[C@H](c4ccsc4)[C@H]3[C@H]1CC2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(NC(=O)c2ccc(Cl)c(S(=O)(=O)N3C[C@@H](C)O[C@@H](C)C3)c2)cc1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O[C@@H]([C@H](c1ccc(c(c1)Cl)Cl)C[NH3+])c1cscc1C
### Response:
Cc1cscc1[C@@H](O)[C@@H](C[NH3+])c1ccc(Cl)c(Cl)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cn1cc[nH+]c1C[C@H](O)Cc1ccc(Br)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(N(C)C)cccc(C(N2CCC(CC2)c2cscc2)=O)c1
### Response:
CN(C)c1cccc(C(=O)N2CCC(c3ccsc3)CC2)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
S1[C@H]2CO[C@@H](C(C)C)CC2=C2C(N(c3ccc(cc3)C)C(N=C21)=S)=O
### Response:
Cc1ccc(N2C(=O)C3=C4C[C@H](C(C)C)OC[C@@H]4SC3=NC2=S)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(c1cc(N2CCC[C@H](CO)C2)ccc1[N+](=O)[O-])N1CCCC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CCOC(=O)[C@H](/C(C)=N/NC(=O)OC)C(C)C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H]1C(=O)Nc2c(c(C)nn2C)[C@H]1c1ccc([16*])c(OC)c1
Fragment 2: [1*]C(=O)c1ccco1
### Response:
COc1cc([C@@H]2c3c(C)nn(C)c3NC(=O)[C@H]2NC(=O)c2ccco2)ccc1OC(F)F |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc2c(c1)=C[C@H](CN(C(=O)COc1ccccc1)c1ccccc1)C(=O)[NH+]=2
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
C[C@H](NC(=O)N1CCN(C(=O)[C@@H]2C[C@@H]2C)CC1)C(C)(C)C[NH+](C)C
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CCOC(=O)[C@@H]1C(=O)CO[C@H]1C
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a amine group?
NC(=O)CSc1ncc2c(n1)-c1ccccc1N(Cc1ccccc1)S2(=O)=O
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(=O)(N1C(=NCC1)SCc1ccc(C)cc1)c1cc(cc(OC)c1)OC
### Response:
COc1cc(OC)cc(C(=O)N2CCN=C2SCc2ccc(C)cc2)c1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CCSc1cncc(N(C)CC(=O)Nc2ccccc2)n1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
O=C(Nc1ccnn1[C@H]1CCCc2ccccc21)C1=NN(Cc2ccc(F)cc2)C(=O)CC1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CCO[C@H]1C[C@H](NC(=O)NCc2ncn(C)n2)C12CCC2
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(NC)COc1cccc(CC(N2C[C@@H](OCC2(C)C)C)=O)c1
### Response:
CNC(=O)COc1cccc(CC(=O)N2C[C@H](C)OCC2(C)C)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1c(C(=O)OC[C@H](C#N)Cc2cccs2)cc(Cl)c1Cl
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cc2ccc(C)cc2nc1C
Fragment 2: [5*]Nc1ccc(=O)n(C)c1
### Response:
Cc1ccc2cc(C(=O)Nc3ccc(=O)n(C)c3)c(C)nc2c1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
Cc1ccc(-c2nn3c(=O)cc(CNC(=O)c4ccc(Cl)cc4)nc3s2)cc1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1Cc2ccccc2N1c1nccc(OCC(=O)[O-])n1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(CCC(=O)N2C(C)(C)C(C)(C2)C)ccc(cc1)OCC
### Response:
CCOc1ccc(CCC(=O)N2CC(C)(C)C2(C)C)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCCS(=O)(=O)N1CCC[C@H](C(=O)Nc2ccc(OCC)cc2)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(NNC(=O)c1cc2ccccc2o1)C(=O)NC1CC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1c2ccccc2CCN1c1c(C[NH3+])cc(F)cc1
### Response:
[NH3+]Cc1cc(F)ccc1N1CCc2ccccc2C1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
C[C@H](OC(=O)CNC(=O)C12CC3CC(CC(C3)C1)C2)C(=O)Nc1ncc(Cl)cc1Cl
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(F)ccc1NC(=O)C1CCN(S(=O)(=O)c2cccnc2)CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C(F)F
Fragment 2: [9*]n1ncc(C[NH3+])c1[14*]
### Response:
Cc1ccc(C)c(-n2ncc(C[NH3+])c2C(F)F)c1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC[C@H]1NC(=O)[C@H](CC)N(Cc2cscc2C)C1=O
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(CN(C)C(c2cnn3c2nc(-c2ccc(cc2)C)cc3C(F)F)=O)cc1
### Response:
Cc1ccc(-c2cc(C(F)F)n3ncc(C(=O)N(C)Cc4ccccc4)c3n2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1ncc(C[NH+](C)Cc2ccc(C)s2)s1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](c1ccccc1)N(C)C(=O)CN1C(=O)CN(c2ccccc2)C1=O
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OC(C)(C)C
Fragment 2: [4*][C@@H](C)c1ccc[nH]1
### Response:
C[C@H](OC[C@@H]1CCCN(C(=O)OC(C)(C)C)C1)c1ccc[nH]1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCn1c([C@@H](C)[NH2+][C@H](C)CCN2CCOCC2)nc2ccccc21
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ccc([16*])cc1
Fragment 2: [6*]C(=O)NC
### Response:
CCN(CCC#N)Cc1ccc(C(=O)NC)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C([C@H]1CC(=O)N(C)C21CCN(C(c1cc(oc1C)C(C)C)=O)CC2)[O-]
### Response:
Cc1oc(C(C)C)cc1C(=O)N1CCC2(CC1)[C@@H](C(=O)[O-])CC(=O)N2C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1ccsc1)N(CCc1cccc(F)c1)C1CC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)[C@H](NC(=O)c1ccc(NC(C)=O)cc1)c1ccc(F)c(F)c1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CCc1cccc(CC)c1NC(=O)C(=O)NCCCO
### Response:
No |
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