task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
functional_group | ### Instruction:
Does the molecule contain a amide group?
CCCn1nc(C(=O)Nc2cncc3ccccc23)ccc1=O
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)[C@@H]1OCC[C@H]1CNC(=O)N1C[C@H]2CCCC[C@H]2C1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1SCCC[C@H]1N[C@@H]1CC[NH+]2CCCC[C@H]12
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1nccs1
Fragment 2: [4*]Cc1ccc(C[4*])o1
### Response:
FC(F)SCc1ccc(CN2CCC[C@@H](c3nccs3)C2)o1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(COc1ccccc1-c1ccccc1)O[C@@H]1CCS(=O)(=O)C1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)C[C@](C)(O)C[NH2+][C@H]1CCOC2(CCCC2)C1
### Response:
5 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH2+]CC[8*]
Fragment 2: [5*][NH2+][C@H](C)C[8*]
### Response:
CCc1nncn1CC[NH2+][C@H](C)Cn1c[nH+]c(C)c1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [1*]C(=O)[C@]12C(=C(c3ccccc3)O[C@@H]3C=CCC[C@H]31)C(=O)C(=O)N2[10*]
### Response:
CCOC(=O)[C@]12C(=C(c3ccccc3)O[C@@H]3C=CCC[C@H]31)C(=O)C(=O)N2c1ccccc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCCCNC(=O)NC[C@@H]1CCC[NH+](C)[C@@H]1c1cccs1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(c1ccc(C[NH2+]CC2(CC2)c2ccccc2)cc1)C(=O)C
### Response:
CC(=O)Nc1ccc(C[NH2+]CC2(c3ccccc3)CC2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
N#Cc1ccc(NC(=O)C(=O)NCc2cn3ccsc3n2)cc1Cl
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Fc1ccc([C@H](C)N(C)C(=O)NCC2CC2)cc1
### Response:
C[C@@H](c1ccc(F)cc1)N(C)C(=O)NCC1CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@H]1CC(=O)N([10*])C1
Fragment 2: [15*]C1CCCCCC1
### Response:
Cc1cc(=O)c(C(=O)N[C@H]2CC(=O)N(C3CCCCCC3)C2)c(C)[nH]1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc2oc([C@@H](C)NC(=O)NCc3ncoc3C)c(C)c2c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
o1nc(nc1[C@@H](C(C)C)NC([C@@H](c1cscc1)C)=O)-c1ccncc1
### Response:
CC(C)[C@@H](NC(=O)[C@H](C)c1ccsc1)c1nc(-c2ccncc2)no1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [1*]C(=O)c1sc2nc([14*])c3c(c2c1N)CC(C)(C)OC3
### Response:
CCOC(=O)c1sc2nc(C(C)C)c3c(c2c1N)CC(C)(C)OC3 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
COC(=O)[C@@H](C)SCc1nc2scc(-c3ccccc3)c2c(=O)[nH]1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C[C@]2(OCC[C@H](C2)[NH2+][C@@H](C(CC)CC)C)CO1
### Response:
CCC(CC)[C@@H](C)[NH2+][C@@H]1CCO[C@]2(CCOC2)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[S@]1(=O)C(C)(C)CN(CC1)CC(=O)c1cc(C)n(c1C)CC
### Response:
CCn1c(C)cc(C(=O)CN2CC[S@](=O)C(C)(C)C2)c1C |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(N[C@@H](C)CC)CCNC(NCc1cccc(C)n1)=O
### Response:
CC[C@H](C)NC(=O)CCNC(=O)NCc1cccc(C)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(NC(=O)N2CCCN(c3nccs3)CC2)no1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1nnc([14*])o1
Fragment 2: [5*]NC[C@H]1CCCC[NH+]1[5*]
### Response:
Cc1ccc(-c2nnc(C[NH+]3CCCC[C@@H]3CNC(=O)OC(C)(C)C)o2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H]1CCC[NH+](Cc2csc(NC(=O)c3cn(Cc4ccccc4)nn3)n2)C1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
O[C@H](CSc1nnc(-c2c[nH]c3ccccc23)n1C1CC1)CN1CCOCC1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCCCc1ccc(NC(=O)[C@H](C)[NH+]2CCC(O)(C(F)(F)F)CC2)cc1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
Cc1cc(C)c2c(c1)NC(=O)[C@@]2(O)CC(=O)c1cccs1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a ether group?
Cc1nc(C)c([C@@H](C)[NH2+][C@H]2CC(C)(C)OC2(C)C)s1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12n(c(=O)cc([nH+]1)CN(Cc1occc1)c1ccc(C)cc1)cccc2
### Response:
Cc1ccc(N(Cc2cc(=O)n3ccccc3[nH+]2)Cc2ccco2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](Nc1cc(F)cc(F)c1)c1cc(F)ccc1O
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1([15*])CCCC1
Fragment 2: [6*]C(=O)[C@H]([8*])C#N
### Response:
Cc1csc([C@H](C#N)C(=O)C2(Cc3cccc(Cl)c3)CCCC2)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1OCC[C@H]1C(=O)Nc1ccccc1C#CCCO
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(C)CCC1N=C2C(C(=O)N=1)=C1CCCC[C@@H]1S2
### Response:
CCCCC1=NC(=O)C2=C3CCCC[C@@H]3SC2=N1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(COc1c(Cl)cc(Cl)cc1Br)NNC(=O)c1ccc([N+](=O)[O-])cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(cc(C)c(NC(C2C[C@H](C)O[C@H](C2)C)=O)c1)OCCOC
### Response:
COCCOc1ccc(NC(=O)C2C[C@H](C)O[C@@H](C)C2)c(C)c1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
C[C@@H](SC1CCCCC1)C(=O)NC(=O)NC1CCCC1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O(CCOC(C)C)C(=O)C=C1CCSCC1
### Response:
CC(C)OCCOC(=O)C=C1CCSCC1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Cc1ccc(SCC(=O)Nc2c(C(C)C)cccc2C(C)C)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12ccc(cc2CCC(=O)N1CCC)NC(N[C@@H]1C(C)(C)[C@@H]2[C@H]1CCO2)=O
### Response:
CCCN1C(=O)CCc2cc(NC(=O)N[C@H]3[C@@H]4CCO[C@@H]4C3(C)C)ccc21 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1ccc(S(=O)(=O)NCC[C@@H](O)c2ccccc2)cc1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@@H](C)n1nccc1NC(=O)C(=O)N1CCc2cc(F)ccc2C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(-n2c(C[NH+](CCC)CC(NC)=O)nnn2)cccc1
### Response:
CCC[NH+](CC(=O)NC)Cc1nnnn1-c1ccccc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(CSc1nncn1-c1ccccc1F)N1CCN(CC(=O)N2CCCC2)CC1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(CNC(=O)C1CCCC1)Nc1nc(C[NH+]2CCCCCC2)cs1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(Cl)cccc(c1)NC(N[C@H](CCC(OCC)=O)C)=O
### Response:
CCOC(=O)CC[C@H](C)NC(=O)Nc1cccc(Cl)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCOCC1
Fragment 2: [1*]C(=O)c1ccc(CC)cc1
### Response:
CCc1ccc(C(=O)Nc2ccc(OC)c(S(=O)(=O)N3CCOCC3)c2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C)c1ncccc1C(=O)N(Cc1ccccc1C(F)(F)F)C1CC1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O[C@H](C[C@H]1CCC[NH+]1Cc1cnc(-c2cccs2)s1)c1ccco1
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=S(=O)(NCc1ccon1)c1sccc1Br
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccccc1OCC[NH+]1CCC(CC(=O)[O-])CC1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
O=C(c1c[nH]c(=O)[nH]1)N1CCC[C@@H](c2nc(-c3cccs3)cc(C(F)(F)F)n2)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [1*]C(=O)C1CCN([5*])CC1
### Response:
CCOc1ccc([C@H]2CCCN2C(=O)C2CCN(C(N)=O)CC2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CS(=O)(=O)/N=C(\[O-])CC(C)C
Fragment 2: [16*]c1ccc([N+](=O)[O-])cc1
### Response:
CC(C)C/C([O-])=N/S(=O)(=O)Cc1ccc([N+](=O)[O-])cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCS[C@H]1CC[C@@H]([NH+](C)Cc2c(Cl)nc3sccn23)C1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CNC(=O)c1cccc(NS(=O)(=O)c2cccc(F)c2)c1C
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CCn1cnc2ccccc2c1=O)N(CC(F)(F)F)C1CCOCC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cc1nc(C(=O)N[C@H](C)c2ccccc2)no1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amide group?
C[C@@H](NC(=O)[C@H]1CC=CCC1)c1ccc(F)c(F)c1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C([C@H]1CN(C[C@@H](CC)CS)CCO1)C
### Response:
CC[C@@H](CS)CN1CCO[C@@H](CC)C1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC(C)COc1ccc([C@H](C)[NH2+]C2C[C@H](C)O[C@@H](C)C2)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12n(cccc1C)c(=O)c1cc(C(=O)OCC)c(=NC(=O)c3occc3)n(c1n2)C[C@@H]1OCCC1
### Response:
CCOC(=O)c1cc2c(=O)n3cccc(C)c3nc2n(C[C@H]2CCCO2)c1=NC(=O)c1ccco1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
Cc1nn(C)c2ncc(NC(=O)c3ccc(C(=O)OC(C)(C)C)cc3)cc12
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc2NC3=C([C@H](Nc2cc1)c1ccc(OC(CC)=O)cc1)C(=O)CC(C)(C3)C
### Response:
CCC(=O)Oc1ccc([C@H]2Nc3ccccc3NC3=C2C(=O)CC(C)(C)C3)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(C)=O
Fragment 2: [5*]N([5*])CC
### Response:
CCN(C(C)=O)c1nc(CN2C[C@@H](C)O[C@H](c3ccccc3)C2)cs1 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
Cc1cc2cc(CCNC(=O)c3ccccc3[N+](=O)[O-])c(=O)[nH]c2cc1C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@@H]([8*])O
Fragment 2: [6*]C(N)=O
### Response:
NC(=O)[C@H]1COCCN1C[C@H](O)c1c(F)cccc1F |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(OC(C)(C)C)ccc(cc1)C(N1CCN(CC1)C(C1CCCC1)=O)=O
### Response:
CC(C)(C)Oc1ccc(C(=O)N2CCN(C(=O)C3CCCC3)CC2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC[C@H](C)COc1c(F)cc(C[NH3+])cc1F
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[NH+]1([C@@H]2CCC[C@H]([NH2+]C)C2)[C@H](CCC1)C
### Response:
C[NH2+][C@H]1CCC[C@@H]([NH+]2CCC[C@@H]2C)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O1[C@@H]2CCC[C@@H](NC(N[C@@H](c3oc(CC)cc3)COC)=O)[C@H]2CC1
### Response:
CCc1ccc([C@@H](COC)NC(=O)N[C@@H]2CCC[C@H]3OCC[C@H]23)o1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CN(C)c1ccc(CCNC(=O)NC[C@@H]2CCC[C@@H]2O)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1cn(c([C@@H]2CCCN(C2)C(=O)NCCc2ccc(cc2)OC)n1)C
### Response:
COc1ccc(CCNC(=O)N2CCC[C@@H](c3nncn3C)C2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC[C@@H](C)C[C@H](C)NC(=O)Cc1c(C)noc1Cl
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
Cc1csc(CC(=O)N2CCN(c3nc(C(F)(F)F)nc4ccccc34)CC2)n1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](NC(=O)c1ccc(Cl)cc1F)c1ccc(N)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(NC(c1ccc(o1)Br)=O)C(CNC(C1CCCCC1)=O)=O
### Response:
O=C(CNC(=O)C1CCCCC1)NNC(=O)c1ccc(Br)o1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@@H](C)c1ccc(C#N)cc1
Fragment 2: [5*]N([5*])CC
### Response:
CCN(C(=O)c1cccc2cc[nH]c12)[C@@H](C)c1ccc(C#N)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@@H](Nc1cnc(cc1)[N+](=O)[O-])(CC(C)(OC)C)C
### Response:
COC(C)(C)C[C@H](C)Nc1ccc([N+](=O)[O-])nc1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C(N[C@H]1CC[NH2+]C1)[C@H]1CC=CCC1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cccc2c(=O)c(C(=O)Nc3ccc(NC(C)=O)cc3)cn(C)c12
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccccc1C
Fragment 2: [4*]Cc1nnc([14*])o1
### Response:
Cc1ccccc1-c1nnc(CSc2nnc(N)s2)o1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)c1c(NC(=O)C(C)(C)C)sc2c1CCN(Cc1ccccc1)C2
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(nn(CN2CCN(CC2)C(OCC)=O)c(n1C)=S)-c1occc1
### Response:
CCOC(=O)N1CCN(Cn2nc(-c3ccco3)n(C)c2=S)CC1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
COc1ccc(OCC(=O)N/N=C\[C@H]2CC=CCC2)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
C[C@@H](c1ccccn1)N(C)C(=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@](O)(CNc1ccc(C#N)cc1F)c1ccco1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1ccc([C@@H](C)N[C@H]2CCN(CC(F)(F)F)C2=O)c(OC)c1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Clc1ccc(-c2ccc(-c3ccccc3)cc2)nn1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [13*][C@@H]1CCCO1
Fragment 2: [16*]c1ccc(Cl)c2ccccc12
### Response:
[NH3+][C@@H](CC[C@@H]1CCCO1)c1ccc(Cl)c2ccccc12 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NCCC1=c2ccccc2=[NH+]C1)Nc1nc2ccccc2s1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NCCc1ccc(Cl)cc1Cl)c1ccccc1O
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)(C)c1cc[n+](C2=C([O-])C(=[OH+])N(Nc3ccccc3)C2=O)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](C[NH+]1CCCCC1)NC(=O)c1cccs1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=S(=O)(c1ccc(CNc2nc3ccccc3o2)cc1)N1CCCCC1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc2C[C@H]([C@@H](O)c2cc1OC)[NH+]1CCC[C@@H](C1)OCC
### Response:
CCO[C@H]1CCC[NH+]([C@@H]2Cc3ccc(OC)cc3[C@@H]2O)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC1(C)CC(=O)C([C@H]2[C@H]3C(=O)CC(C)(C)C[C@H]3O[C@H]2Cc2ccccc2)=C([O-])C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@@H]1(CCCN(C([C@H](C)Cn2c(ncc2)C)=O)C1)n1nc(ccc1=O)-c1sccc1
### Response:
Cc1nccn1C[C@@H](C)C(=O)N1CCC[C@H](n2nc(-c3cccs3)ccc2=O)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C1OCCN1c1ccc(NS(=O)(=O)CCc2ccccc2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COCCOc1ccccc1N1CCN(C(=O)[C@H]2CCCc3ccccc32)CC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC[4*]
Fragment 2: [1*]C(=O)NCC[4*]
### Response:
N#Cc1ccc(OCCNC(=O)N2CC[NH+](C3CCCC3)CC2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NS(=O)(=O)CC
Fragment 2: [11*]Sc1cc(C)c2ccccc2n1
### Response:
CCS(=O)(=O)NCCSc1cc(C)c2ccccc2n1 |
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