task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccccc1
Fragment 2: [5*]Nc1ncnc2c1CCCCC2
### Response:
CC[C@H](Nc1ncnc2c1CCCCC2)c1ccccc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ccc([N+](=O)[O-])cc1
Fragment 2: [5*][NH+]1CCC[C@H]1[13*]
### Response:
Cc1cccc([C@@H]2CCC[NH+]2Cc2ccc([N+](=O)[O-])cc2)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCNC(=O)c1cccc(CNC(=O)[C@H]2COc3ccccc3C2)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Nc1ccc2oc(CSCCO)nc2c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](CNC(=O)N1CCO[C@H](c2ccccc2)C1)c1ccsc1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CNC(=O)c1nn(CCc2ccccc2)c2c1C[C@@H](N1CCOc3ccc(Cl)cc3C1)CC2
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(COc1ccc(Br)cc1)NC(=S)Nc1ccc(Cl)cc1C(=O)[O-]
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)C[C@H](NC(=O)Nc1ccccc1)C(=O)Nc1nccs1
### Response:
5 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
O=C(COC(=O)c1ccc(Cl)nc1)NC(=O)Nc1ccc2c(c1)OCCO2
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc([C@@H](O)[C@H](C)NC(=O)C[C@H](C)c2cccc(F)c2)cc1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1(=O)N(CC(Nc2c(cccc2C(C)C)C(C)C)=O)C([C@](CC)(N1)c1ccc(Cl)cc1)=O
### Response:
CC[C@]1(c2ccc(Cl)cc2)NC(=O)N(CC(=O)Nc2c(C(C)C)cccc2C(C)C)C1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC1(C)NC(=O)N(CC(=O)NCCc2cn3ccccc3[nH+]2)C1=O
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ncc(C)s1
Fragment 2: [5*]N[C@H]([8*])C
### Response:
Cc1cnc([C@H](C)NC(=O)N[C@@H](C)c2ccc3c(c2)OCO3)s1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [4*]CC(=C)C
### Response:
C=C(C)CN(CC)C(=O)CS/C(N)=N/c1ccccc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C=CCCC[C@@H](C)[NH+]1CCC(NC(=O)c2ccoc2C)CC1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
NC(=O)C1CC[NH+](C/C=C/c2ccccc2)CC1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1nncs1
Fragment 2: [1*]C(=O)c1ccc([16*])cc1
### Response:
O=C(Nc1nncs1)c1ccc(N2CCCCC2=O)cc1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CC[C@H]([NH2+][C@@H](C)c1ccccc1N(C)C)c1c(C)noc1C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]COC
Fragment 2: [3*]Oc1ccc(N[5*])cn1
### Response:
COCc1cc(C(=O)Nc2ccc(Oc3ccc(C)cc3)nc2)no1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cc(=O)oc2cc(OC)ccc12
Fragment 2: [8*]Cn1nc([14*])oc1=O
### Response:
COc1ccc2c(Cn3nc(-c4ccco4)oc3=O)cc(=O)oc2c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [7*]Cc1ccco1
Fragment 2: [3*]OCC1=NC(=O)C2=C3CCCC[C@H]3SC2=N1
### Response:
O=C(/C=C/c1ccco1)OCC1=NC(=O)C2=C3CCCC[C@H]3SC2=N1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CN(CCN1Cc1ccccc1C)c1n(cc[nH+]1)C
### Response:
Cc1ccccc1CN1CCN(c2[nH+]ccn2C)CC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H]1CN(C(=O)C2CCN(S(=O)(=O)c3ccc(Cl)c(C(F)(F)F)c3)CC2)C[C@H](C)O1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CCNC(=O)[C@@H](n1c2ncc(cc2nc1[C@@H](C)Cl)C)C
### Response:
CCNC(=O)[C@H](C)n1c([C@@H](C)Cl)nc2cc(C)cnc21 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C=CCNC(=O)c1ccc(NC(=O)Cn2ncc3ccccc3c2=O)cc1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
O=C(Nc1ccc(C(F)(F)F)cc1)c1ccc(NCc2ccccc2)nc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
FC(F)(c1ccc(c(c1)[N+](=O)[O-])NC[C@H]([NH+](C)C)c1ccco1)F
### Response:
C[NH+](C)[C@@H](CNc1ccc(C(F)(F)F)cc1[N+](=O)[O-])c1ccco1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [1*]C(=O)N[5*]
### Response:
Cc1cccc(NC(=O)NCC(=O)Nc2cc(C)ccc2F)c1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
COc1ccc(-n2nc(C)c3c2C[C@H](c2cc(OC)c(OC)c(OC)c2)CC3=O)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COc1ccc(CCl)cc1OCc1nccs1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nnc(=O)[nH]c1N/N=C/c1cccc(OC(C)C)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@@H](C)[C@@H](O)CSc1cccc(Br)c1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CCC1CC1
Fragment 2: [8*]CCC1([15*])CCC([15*])CC1
### Response:
CCCCC1CCC(CCC2CC2)(C(=O)[O-])CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1CCN(C(=O)NCCc2nnc3n2CCCCC3)[C@@H](C)C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(cc(-c2ccccc2)on1)C[S@](Cc1oc(C)cn1)=O
### Response:
Cc1cnc(C[S@](=O)Cc2cc(-c3ccccc3)on2)o1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(CCn1cnc2c([nH]c3ccc(F)cc32)c1=O)NC1CCCC1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*]Nc1cnn([9*])c1
### Response:
COCCn1cc(NC(=O)CSc2nc(C)c(C)c(C)c2C#N)cn1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(S(=O)(=O)N(C)CC(=O)NCc2ccc(C)cc2)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(=O)(Nc1c(Cl)c(ccc1)C)N1CCN(CC1)C(=O)CC1CCCCC1
### Response:
Cc1cccc(NC(=O)N2CCN(C(=O)CC3CCCCC3)CC2)c1Cl |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(C)c(N(C)C(=O)c2cnc(N3CCOCC3)c3ccccc23)c1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [11*]S[C@@H]1CCCc2ccccc21
Fragment 2: [8*]CCC(N)=O
### Response:
Cn1c(CCC(N)=O)nnc1S[C@@H]1CCCc2ccccc21 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C=CCC[C@@H]([NH2+][C@@H](C)c1ccc(F)cn1)c1ccccc1
### Response:
5 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc(C)cc1
Fragment 2: [5*]Nc1ccc2c(c1)OCO2
### Response:
Cc1ccc(C(=O)Nc2c(C(=O)Nc3ccc4c(c3)OCO4)oc3ccccc23)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C#CCNC(=O)c1cnn(-c2ccc(F)cc2)c1CC
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1c[nH+]c(NCCC(=O)Nc2nccs2)nc1N(C)C
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H]1[C@@H](C)CCC[C@H]1NC(=O)C(=O)Nc1ccc(Oc2cccnc2)nc1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12ccccc2NC(=O)C(C)(C)N1C([C@@H](SCc1cc(ccc1OCC)C(C)=O)C)=O
### Response:
CCOc1ccc(C(C)=O)cc1CS[C@@H](C)C(=O)N1c2ccccc2NC(=O)C1(C)C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)N(CCC#N)CC2CC2)c(Cl)c1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@@H](C[C@H]([NH+]2CCCC2(C)C)C1)[NH2+]CC
### Response:
CC[NH2+][C@H]1CC[C@@H]([NH+]2CCCC2(C)C)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
S=C(n1nc(c2[C@H]3[C@@H](Cc21)C3(C)C)C)NC
### Response:
CNC(=S)n1nc(C)c2c1C[C@@H]1[C@H]2C1(C)C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@@H]1CC[C@]2(C)[C@@H](CC[C@@H](O)[C@H]2[15*])[C@]1(C)CO
Fragment 2: [5*]Nc1ccccc1
### Response:
C[C@]1(CO)[C@@H]2CC[C@@H](O)[C@@H](CC(=O)N3CCCC3)[C@]2(C)CC[C@H]1OC(=O)Nc1ccccc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cccc(CNC(=O)NCc2ncoc2C)n1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(/c1cn(Cc2ccc(F)cc2)c2ccccc12)=C(\C#N)C(Nc1ccccc1)=O
### Response:
N#C/C(=C/c1cn(Cc2ccc(F)cc2)c2ccccc12)C(=O)Nc1ccccc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C[NH+](CC(=O)N(CC)Cc1sc(Br)cc1)CC([O-])=O
### Response:
CCN(Cc1ccc(Br)s1)C(=O)C[NH+](C)CC(=O)[O-] |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1ccc(CCNC(=O)NCCC(=O)N(C)C)cc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@@H](CN[C@H](C)c1cnc2cc(C)nn2c1C)[NH+]1CCc2ccccc2C1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CS(=O)C[8*]
Fragment 2: [14*]c1nc(C)cs1
### Response:
Cc1csc(C[S@](=O)Cc2csc(-c3ccccc3F)n2)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Cc1c(C(=O)N2CCN([C@H](C#N)C(C)C)CC2)c(C)n(n1)CCC
### Response:
CCCn1nc(C)c(C(=O)N2CCN([C@H](C#N)C(C)C)CC2)c1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@H]([8*])O
Fragment 2: [15*]C1CCOCC1
### Response:
CC1(C)CC[C@H](NC(=O)NC[C@@H](O)C2CCOCC2)c2ccccc21 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1COCCN1c1cc(c(cc1)NS(=O)(=O)c1ccccc1C)C(=O)[O-]
### Response:
Cc1ccccc1S(=O)(=O)Nc1ccc(N2CCOCC2)cc1C(=O)[O-] |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COCCNC(=O)N1CCC[C@@H](c2nnc(C(=O)Nc3cccc(Cl)c3)s2)C1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@H]2C[C@H]([C@@H]3[C@@H]2CCC3)[C@H]1[NH2+][C@H](CO)C
### Response:
C[C@@H](CO)[NH2+][C@H]1C[C@H]2C[C@@H]1[C@H]1CCC[C@H]21 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)c1ccc(NC(=O)c2n[nH]c(C(C)C)n2)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(ccc(cc1)OC)NC([C@H](NC(c1ccc(cc1)Cl)=O)CC(C)C)=O
### Response:
COc1ccc(NC(=O)[C@@H](CC(C)C)NC(=O)c2ccc(Cl)cc2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCN([5*])CC1
Fragment 2: [1*]C(=O)C(C)C
### Response:
CC(C)C(=O)N1CCN(S(=O)(=O)c2cccc(Br)c2)CC1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
C[C@H](NC(=O)Nc1cnc(C(C)(C)C)nc1)C(=O)NC(C)(C)C
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(CCc1ccccc1)/N=C1/S[C@H]2CS(=O)(=O)C[C@H]2N1c1ccccc1Cl
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
O=C1N[C@@H](c2cccc3c2OCO3)N2CCCC[C@H]12
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [10*]N1CCC[C@@H]([15*])C1=O
Fragment 2: [14*]c1ccn(C)n1
### Response:
Cc1ccc2c(c1C)[C@@H](N[C@@H]1CCCN(c3ccn(C)n3)C1=O)CCO2 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
CC(C)=C1[C@H]2CC[C@@H]1[C@H]1C(=O)N(NC(=O)COc3ccc(Cl)c(C)c3)C(=O)[C@@H]12
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)[C@@]1(NC2CCCC2)CCCS[C@H]1C
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
N#Cc1ccc(C(=O)NCC(=O)N2CCC[C@H]3CCC[C@@H]32)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH+](Cc1csc(-c2ccccc2)n1)C[C@H]1CCOC1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COCCCN(C(=O)[C@H]1CC=CCC1)[C@@H]1CCS(=O)(=O)C1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](O)Cn1c([C@H]2CCC[NH2+]2)nc2cc(C(F)(F)F)ccc21
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCN1C(=O)[C@@H](CC(=O)Nc2cccc(OC)c2)S/C1=N\S(=O)(=O)c1ccc(Cl)s1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)C[8*]
Fragment 2: [4*]Cc1cccnc1C
### Response:
Cc1ncccc1CN(C)Cc1ncnn1C |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1csc2[nH+]c(CN3CCC[C@@H](C(=O)Nc4cnccn4)C3)cc(=O)n12
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COc1ccc(S[C@H](C)C(=O)N(C)c2cccnc2N(C)C)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CN(C(=O)c1ccn(C)n1)[C@H](Cc1ccccc1)C1CCN(C(=O)C2=CCCC2)CC1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N/C=C1\C(=O)NC(=S)N([10*])C1=O
Fragment 2: [16*]c1ccccc1F
### Response:
Cc1c(N/C=C2\C(=O)NC(=S)N(c3ccccc3F)C2=O)c(=O)n(-c2ccccc2)n1C |
functional_group | ### Instruction:
Does the molecule contain a ether group?
COc1cc(CNC(=O)c2occc2Br)ccn1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(-n2ccnc2)c(C(=O)N2CCN(C(=O)[C@@H]3C[C@@H]3C)CC2)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc([C@@H](C)N[C@@H](c2nc(C3CC3)no2)C(C)C)o1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC[NH2+][C@H]1CCC[C@@H](N2CC[C@H]([NH+](C)C)C2)C1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C(=O)c1ccsc1)[C@@H](Cc1ccccc1)C1CCN(C(=O)c2ccc[n+]([O-])c2)CC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOC(=O)[C@]1(C)[NH2+][C@@H](c2ccc(C(C)C)cc2)[C@H]2C(=O)N(CC)C(=O)[C@@H]21
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1(c(Cl)c(CO)c(n1)CCC)-c1ncncc1
### Response:
CCCc1nn(-c2ccncn2)c(Cl)c1CO |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@@H]([C@@H]1C(=O)N1CC(C)(C)[S@](=O)CC1)c1c(Cl)cccc1
### Response:
CC1(C)CN(C(=O)[C@@H]2C[C@@H]2c2ccccc2Cl)CC[S@]1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(COc1ccc([N+](=O)[O-])cc1Cl)NC1CCCCCCC1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(NCCS(=O)(=O)c1ccccc1)N1CCC[C@@H]2CCC[C@@H]21
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C=CCn1c(SCC(=O)c2c[nH]c3ccccc23)nc2scc(C3CC3)c2c1=O
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C(c1cnc([C@H]2CCCO2)s1)N1CCOc2c(Cl)cccc21
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCOC(=O)C1CC[NH+](Cc2oc(CO)cc(=O)c2[O-])CC1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(C)(CN1C[C@H](OCC1)CNC(=O)N1CCN(C([C@H]2C[C@H]2C)=O)CC1)C
### Response:
CC(C)CN1CCO[C@H](CNC(=O)N2CCN(C(=O)[C@H]3C[C@H]3C)CC2)C1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
C[C@H]1CCC[C@]2(CC[NH2+]C[C@@H]2c2cccc(Br)c2)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccccc1
Fragment 2: [16*]c1cc(Br)cc2cccnc12
### Response:
Cc1ccc(C(=O)Nc2ccccc2)cc1S(=O)(=O)Nc1cc(Br)cc2cccnc12 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
C[C@H](CCc1ccccc1)NC(=O)N1CCC[C@H](CN2CCOCC2)C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C(NCC[C@H](O)c1ccccc1)Nc1ccccc1N1CCCC1=O
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a ester group?
CCCS(=O)(=O)CC(=O)N[C@@H](C)Cc1c(Cl)cccc1Cl
### Response:
No |
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