task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1cnc(Oc2ccccc2)cn1)N1CCC[C@H]1c1cccc(F)c1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
O=C(CSc1cccc(C(F)(F)F)c1)N1CCN(S(=O)(=O)c2cccs2)CC1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)[C@H](C)CNC(=O)Nc1c(C)cccc1C(C)C
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(C(=O)N[C@@H]2C[C@@H]([NH+](C)C)CC2)CCN(CC1)Cc1ccncc1
### Response:
C[NH+](C)[C@H]1CC[C@H](NC(=O)N2CCN(Cc3ccncc3)CC2)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1csc([C@H](C)NC(=O)CCC[NH+]2CCCCC2)n1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccccn1
Fragment 2: [4*]Cc1cnc([14*])nc1
### Response:
COCC(=O)N1CCCN(Cc2cnc(-c3ccccn3)nc2)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1CC1
Fragment 2: [5*]N(C)C[8*]
### Response:
CN(Cc1nnc(C2CC2)n1C)C(=O)c1ccc(Cl)cn1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1CCCCC1
Fragment 2: [5*]Nc1ccnn1[9*]
### Response:
CN(C)C(=O)CCNC(=O)C(=O)Nc1ccnn1C1CCCCC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(c1cnccc1)(=O)NCCNC(=O)NCc1cn(-c2ccccc2)nc1
### Response:
O=C(NCCNC(=O)c1cccnc1)NCc1cnn(-c2ccccc2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cc([14*])[nH]n1
Fragment 2: [16*]c1ccccc1
### Response:
Cc1ccsc1C(=O)N1CCCN(c2cc(-c3ccccc3)n[nH]2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1ccc(N2C(=O)C[C@H](SCC(=O)Nc3cccc(Cl)c3C)C2=O)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC1[C@@H]2CC3C[C@H]1CC(O)(C3)C2
Fragment 2: [1*]C(=O)c1ccc(Cl)cc1
### Response:
O=C(NC1[C@@H]2CC3C[C@H]1CC(O)(C3)C2)c1ccc(Cl)cc1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
NC(=O)c1ccc(NC(=O)c2cccc(NC(=O)c3ccc(Br)o3)c2)nn1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CN[5*]
Fragment 2: [1*]C(=O)c1cc([14*])on1
### Response:
CC(C)(C)NC(=O)CNC(=O)c1cc(-c2ccc(Cl)s2)on1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCCC[8*]
Fragment 2: [1*]C(=O)C[4*]
### Response:
C[C@H]1CCCC[NH+]1CC(=O)NCCCc1ccccc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1c(=O)[nH]c2ccccc21
Fragment 2: [1*]C(=O)CN([5*])C
### Response:
CC(C)NC(=O)CN(C)C(=O)Cn1c(=O)[nH]c2ccccc21 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
C=Cc1cccc(C[NH+]2CC[C@H](CNC(=O)CO)C2)c1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
COC1CCN([C@H](C(=O)NC2CC2)c2ccccc2)CC1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a ether group?
Cc1n[nH]c(C)c1[C@H]1CCC[NH+]1CC(=O)N(C)[C@@H](C)CC(C)C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC1CC1
Fragment 2: [1*]C(=O)c1ccc[nH]1
### Response:
O=C(NC1CC1)[C@@H]1CCC[NH+](C2CCN(C(=O)c3ccc[nH]3)CC2)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CSc1cccc(NC(=O)C(=O)NC[C@@H](c2ccc(F)cc2)N2CC[NH+](C)CC2)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(-c2cc(C(=O)Nc3c(C)n(C)n(-c4ccccc4)c3=O)c3ccccc3n2)o1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)c1ccc(CN(C)Cc2cc(=O)n(C)c(=O)n2C)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OC(F)(F)F
Fragment 2: [13*][C@H]1CSCCS1
### Response:
C[NH2+][C@H](Cc1ccc(OC(F)(F)F)cc1)[C@H]1CSCCS1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
Cc1cc(F)cc([C@](C)(O)[C@@H]2CCC[NH2+]C2)c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CNC(=O)C[C@H](C[NH3+])N(C)C(C)C
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccccc1C
Fragment 2: [9*]n1nc([14*])oc1=S
### Response:
Cc1ccccc1-c1nn(CN2CCCc3ccc(S(C)(=O)=O)cc32)c(=S)o1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC[C@H](Cc1ccc(C)cc1)N(C)C(=O)Cc1nc2nc(C)cc(C)n2n1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
Cc1nn(-c2ccccc2F)c2ncc3c(c12)C(=O)N(c1ccc(C(C)C)cc1)C3=O
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N1CCN(CC1)c1cc(n2nc(sc2n1)-c1ccccc1)=O)(=O)c1cccc(c1)C
### Response:
Cc1cccc(C(=O)N2CCN(c3cc(=O)n4nc(-c5ccccc5)sc4n3)CC2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*][C@H](C[NH3+])S(=O)(=O)c1ccc(F)cc1
Fragment 2: [16*]c1ccc(C)cc1
### Response:
Cc1ccc([C@H](C[NH3+])S(=O)(=O)c2ccc(F)cc2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)[C@H]1C[C@@H]1C(=O)N[C@@H](c1cccc(C(F)(F)F)c1)C1CC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC([NH+]2CCC(CC2)N(C)C(=O)[C@H]2C[C@@H](CCC2)C)CCO1
### Response:
C[C@@H]1CCC[C@@H](C(=O)N(C)C2CC[NH+](C3CCOCC3)CC2)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1c(Cl)cccc1-n1ncnc1-c1ccc(F)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CN(c2nccc(CN3CC[NH+]4CCC[C@@H]4C3)n2)C[C@@H](C)O1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
COc1ccc([C@H](C)Nc2ccc(C(N)=O)nn2)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C(/C=C/c1ccco1)NNC(=O)Cc1cccc2ccccc12
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
C/C=C(\C)[C@H]1C(C)=C[C@H]2CC[C@@H](OS(=O)(=O)[O-])[C@@H](C)[C@H]2[C@H]1/C=C/C=C/C(=O)[O-]
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CC(=O)[O-]
Fragment 2: [3*]OCCN[5*]
### Response:
O=C([O-])COCCNC(=O)C1CCCC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1SCC[NH+](C[C@@H](COCCC23CC4CC(C3)CC(C2)C4)O)C1
### Response:
O[C@H](COCCC12CC3CC(CC(C3)C1)C2)C[NH+]1CCSCC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H](CCc1ccc2c(c1)OCO2)[NH2+][C@@H](CO)c1ccccc1F
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1c[nH]nc1[C@@H](NC(Nc1cccnc1-n1nccc1)=O)C
### Response:
C[C@H](NC(=O)Nc1cccnc1-n1cccn1)c1nc[nH]n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nn(C)c(C)c1[C@H](OC(=O)c1cnn(C(C)C)c1C)C(F)(F)F
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cn1c(N)[n+](CC(=O)c2cccs2)c2ccccc21
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC1(C)CCC(C[NH3+])([C@H](O)c2cccc(F)c2F)CC1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CCCCN(CC)C(=O)C[NH+](C)[C@@H]1CCS(=O)(=O)C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1ccnc(NC(=O)CN(C)c2cc(C)c3ccccc3[nH+]2)c1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1nc(C[NH+]2CCC(CNC(=O)N[C@@H]3CC[C@H]([NH+](C)C)C3)CC2)oc1C
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1sc2c(c1C(=O)N1CCN(C(=O)CCC3CCCC3)CC1)CCCC2)c1cccnc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOCc1ccc(C(=O)N2CCC(O)(Cn3cc[nH+]c3C)CC2)cc1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
C[NH+](C)Cc1nc(-c2c(Cl)cccc2Cl)no1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1[nH]c2ccccc2c1-c1csc(NC(=O)c2cncn2-c2ccc(F)cc2)n1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1cc(Cl)c(C)cc1NC(=O)c1cc([N+](=O)[O-])ccc1OC
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C1([C@@H]([8*])O)CCCC1
Fragment 2: [8*][C@H](O)c1cc(F)cc(F)c1
### Response:
O[C@H](c1cc(F)cc(F)c1)C1([NH+]2CCCCC2)CCCC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(-c2nnc(S[C@@H](C)c3ccc(F)cc3)o2)cc1OC
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccc(C(=O)Nc2ccc(NC=C3C(=O)OC(C)(C)OC3=O)cc2)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1nn(CCO)c(C)c1C[NH2+]C[C@@H]1CCS(=O)(=O)C1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)c1cccc(NCc2ccc(N3CCC(CO)CC3)cc2)n1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cc1ccsc1[C@@H](O)C1(c2ccccc2)CCC1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CCN(C(=O)Nc2ccccc2N2CCCCCC2)C[C@@H]1O
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CCC1(CNC(=O)NC[C@H](c2cccs2)[NH+]2CCCC2)CC1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC[C@@H]1[C@@H](C)CCCN1C(=O)c1cc2c(cc1O)OCO2
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
o1c(C)c(c(C)n1)CCC(=O)Nc1nc(cs1)-c1cc2CC(Nc2cc1)=O
### Response:
Cc1noc(C)c1CCC(=O)Nc1nc(-c2ccc3c(c2)CC(=O)N3)cs1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc([N+]([O-])=O)c(OCC)cc1N1CCSCC1
### Response:
CCOc1cc(N2CCSCC2)ccc1[N+](=O)[O-] |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H](CC(=O)NN)Sc1ccncc1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(OCC1(C)COC1)Cc1c2cc(c(C)cc2oc1)C
### Response:
Cc1cc2occ(CC(=O)OCC3(C)COC3)c2cc1C |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
Cc1cc(C)n(CC(=O)N2CCC([C@H](O)Cc3ccccc3)CC2)c(=O)n1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(C(=O)COc2ccc3c(c2)OCCO3)c(C)n1Cc1ccccc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](C[NH2+]C1CCCCC1)C(N)=O
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CS(=O)(c1cccc(c1[N+]([O-])=O)N[C@H](c1ccccc1Cl)C)=O
### Response:
C[C@H](Nc1cccc(S(C)(=O)=O)c1[N+](=O)[O-])c1ccccc1Cl |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CCOc1ccc(NC(=O)N(C)Cc2csc(Br)c2)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1nccn1C
Fragment 2: [5*]N([5*])S(=O)(=O)c1cc(Cl)ccc1Cl
### Response:
Cn1ccnc1CN(C1CC1)S(=O)(=O)c1cc(Cl)ccc1Cl |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
S=C(Nc1ccccc1Cl)N1CCCC[C@H]1c1cccnc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CSCc1cc(NC(=O)CN2CCCOC2=O)ccc1Cl
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c2OCOc2cc(/C=C2\Oc3c(C2=O)ccc(OCC(N[C@H](CO)C)=O)c3)c1
### Response:
C[C@@H](CO)NC(=O)COc1ccc2c(c1)O/C(=C\c1ccc3c(c1)OCO3)C2=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(OC)c([C@@H]2C[C@H](C(=O)N3CCC4(CC3)OCCO4)N(C)S(=O)(=O)N2)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@H](Cc1ccc(C)cc1)N(C)C(=O)Cc1nc2nc(C)cc(C)n2n1
### Response:
4 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC1(C)C[NH+](C[C@@H](O)COCc2ccco2)C1(C)C
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH+]1CCCCC1
Fragment 2: [4*]C[C@H]([4*])C
### Response:
Cc1cc(N[C@H](C)C[NH+]2CCCCC2)[nH+]cc1N |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C([O-])c1cc(C2CC2)nc2c(-c3ccc(Cl)cc3)cnn12
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][N-]c1ccc([16*])cc1
Fragment 2: [12*]S(=O)(=O)c1cc(F)ccc1F
### Response:
O=S(=O)([N-]c1ccc(-c2ccc3nncn3n2)cc1)c1cc(F)ccc1F |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CSCCN1C(=O)Cl
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cscc1C[NH2+][C@H]1CS[C@H](C)C1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(C(C)C)ccc(cc1)[C@@H]1[C@@H](/C([O-])=C(/C#N)C(=O)NC(C)C)C1
### Response:
CC(C)NC(=O)/C(C#N)=C(/[O-])[C@H]1C[C@@H]1c1ccc(C(C)C)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NCC1CCOCC1)[C@H]1CC(C(c2ccccc2)c2ccccc2)=NO1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@H]1(CN(S(=O)(=O)c2cccc(c2)C(NCCOc2ccccc2)=O)C[C@H](C1)C)C
### Response:
C[C@H]1C[C@H](C)CN(S(=O)(=O)c2cccc(C(=O)NCCOc3ccccc3)c2)C1 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
CCN(C[C@H]1CCOC1)C(=O)c1cc(C)n(-c2ccc(OC)cc2)n1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
s1c(Cl)c(CSc2ncccc2)nn1
### Response:
Clc1snnc1CSc1ccccn1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Clc1ccnc(C[NH+]2CCC(C[NH+]3CCCC3)CC2)c1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C1=C(C)Nc2nnnn2[C@H]1c1ccc(F)c(F)c1
Fragment 2: [3*]OC(C)(C)C
### Response:
CC1=C(C(=O)OC(C)(C)C)[C@H](c2ccc(F)c(F)c2)n2nnnc2N1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)[C@H]1CC[NH+](CC)C[C@H]1C
Fragment 2: [1*]C(=O)[C@@H]1Cc2cc(C)c(C)cc2O1
### Response:
CC[NH+]1CC[C@H](N(C)C(=O)[C@@H]2Cc3cc(C)c(C)cc3O2)[C@H](C)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NS(=O)(=O)C[C@@H]1CCCN(C(=O)CCc2ccccc2Cl)C1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H]([8*])CC
Fragment 2: [3*]Oc1cccc(Cl)c1
### Response:
CC[C@H](Oc1cccc(Cl)c1)C(=O)N[C@H](CC)c1ccc(C)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12c([O-])n[nH]c(c1c(ccc2)N[C@@H]1CC[NH2+]C1)=O
### Response:
O=c1[nH]nc([O-])c2cccc(N[C@@H]3CC[NH2+]C3)c12 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H]([8*])c1ccccc1
Fragment 2: [5*]N[C@H]([8*])C1CCCC1
### Response:
O=C(NCc1nnc2n1CCCCC2)N[C@H](c1ccccc1)C1CCCC1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CCc1c(Cl)cc(N)c(O)c1Cl
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C=CCN(Cc1ccc(C#N)cc1)[C@H]1CCN(CC(F)(F)F)C1=O
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
C[C@@H]1CCO[C@H]1C(=O)Nc1nc2c(cc1C#N)CCC2
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccc2ccccc2n1
Fragment 2: [16*]c1ccc(SC)cc1
### Response:
CSc1ccc([C@H](Cl)Cc2ccc3ccccc3n2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]Cc1nnc(S[11*])n1C
Fragment 2: [11*]Sc1nnc([14*])n1C
### Response:
Cc1nc2c(C)cccn2c(=O)c1Cc1nnc(SCC(=O)NC(C)C)n1C |
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