task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Clc1ccc(C2([NH2+]C3CCCC3)CCOCC2)cc1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
N#CC(C#N)[C@@H](CC(=O)c1ccc(Cl)cc1)c1cccs1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
COc1ccc(SCC(=O)c2ccc(C)c(C)c2)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@H]1CCCC[C@H]1CC
Fragment 2: [9*]n1c(N)nc2c(OC)ncnc21
### Response:
CC[C@@H]1CCCC[C@@H]1n1c(N)nc2c(OC)ncnc21 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
CCc1nn(C)cc1C(=O)N(C)CC(=O)Nc1cccc(C)n1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cn1c(-c2ccco2)nn(C[NH+](C)CCc2ccccc2)c1=S
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
CCNC(=O)[C@H]1CCCN(C(=O)C=C(C2CC2)C2CC2)C1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Brc1ccc2nc(C[C@@H]3CCC[NH2+]C3)sc2c1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
O=C(C[C@@H](c1ccc(F)cc1)c1ccco1)NCc1ccco1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1N(C(C)(C)CC1)C(NCCc1cc(C(N)=O)ccc1)=O
### Response:
CC1(C)CCCN1C(=O)NCCc1cccc(C(N)=O)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCc1nc2ccccc2n1CC
Fragment 2: [1*]C(=O)C[8*]
### Response:
CCn1c(CNC(=O)Cc2cccc(OC)c2)nc2ccccc21 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH+]1CCN(C(C)(C)C(=O)NCC(C)(C)c2ccc(Cl)cc2)CC1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)N2CC[C@H](C)[C@@H](O)C2)cc1OCC(F)F
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(CC(=O)N2CCN(S(=O)(=O)c3ccc4c(c3)sc(=O)n4C)CC2)cc1OC
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1c(=O)/c(=C/c2ccc(F)c(F)c2)s/c1=C(/C#N)C(=O)NC
Fragment 2: [16*]c1ccccc1
### Response:
CNC(=O)/C(C#N)=c1\s/c(=C\c2ccc(F)c(F)c2)c(=O)n1-c1ccccc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(Nc1c(C#N)cccc1)[C@H](C)OC(=O)c1ccc2c(nnn2CC)c1
### Response:
CCn1nnc2cc(C(=O)O[C@@H](C)C(=O)Nc3ccccc3C#N)ccc21 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1c2ccccc2C(=O)c2c1cc(F)c1ccccc21
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC[C@@H]([NH2+][C@H](C)c1cc(Cl)cc(Cl)c1)c1c(C)noc1C
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H](O)CC(C)(C)CNC(=O)/C=C/c1cccnc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
O=C(Nc1ccccc1)c1cc(Br)cn(Cc2cccc(C(F)(F)F)c2)c1=O
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc(F)c(Cl)c1
Fragment 2: [5*]N1C[C@@H](C)NC(=O)c2ccc(F)cc21
### Response:
C[C@@H]1CN(C(=O)c2ccc(F)c(Cl)c2)c2cc(F)ccc2C(=O)N1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@@H]1CCC[C@]([15*])(NC)C1
Fragment 2: [4*]CCC
### Response:
CCCN1CC[NH+]([C@@H]2CCC[C@@](NC)(C(N)=O)C2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)(C)OC(=O)C1CCC(Nc2ccc([N+](=O)[O-])nc2)CC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cc(C)c(NC(=O)c2cc3ccccc3n2C)c(C)c1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@]12CC[C@H]3[C@H](CC[C@@]4(O)C[C@@H](O)CC[C@]34CO)[C@@]13CC[C@@H]2[C@@H]1CC(=O)O[C@@H]1O3
### Response:
4 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CN(CC[NH+](C)C)C(=O)C[C@H]1COCCN1C(=O)c1ccc2[nH]nnc2c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[S@](=O)[C@H]1CCCC[C@@H]1NC(=O)NC1CCC2(CC1)OCCO2
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
C[C@@]1(NC(=O)c2ccc(Cl)cc2)CCS(=O)(=O)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C/C([O-])=N/c1ncn[nH]1
Fragment 2: [9*]n1cnc2c(C)cccc2c1=O
### Response:
Cc1cccc2c(=O)n(C/C([O-])=N/c3ncn[nH]3)cnc12 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cc(S(=O)(=O)N[5*])ccc1C
Fragment 2: [4*]Cc1ccccc1
### Response:
CC[C@H](C)NC(=O)c1cc(S(=O)(=O)NCc2ccccc2)ccc1C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NNC(=O)c1ccc2c(c1)OCCO2)c1ccoc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1cccc(c1N[C@H]1CCC[C@@H](C)C1)C#N
### Response:
C[C@@H]1CCC[C@H](Nc2ncccc2C#N)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCc1cc(C(=O)N[C@H](C)c2ccccc2)c2c(C3CC3)nn(-c3ccc(F)cc3)c2n1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N([5*])[C@H]1CCSC1
Fragment 2: [4*]C[C@@H]1CCCO1
### Response:
[NH3+]C[C@H]1CC[C@@H](C(=O)N(C[C@@H]2CCCO2)[C@H]2CCSC2)O1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(CSc1nc2ccccc2o1)Nc1onc2c1CSC2
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC(=O)N1N=C(c2ccc(Br)cc2)C[C@@H]1c1ccccc1O
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH+](C1CCSCC1)[C@H]1CCN(c2ccccc2)C1=O
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](C(=O)N1CCN(c2cccc[nH+]2)CC1)N1CCOC(C)(C)C1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
N#Cc1nc(/C=C/c2ccc(F)cc2)oc1N1CCN(C(=O)c2cccc(F)c2)CC1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cccc(F)c1
Fragment 2: [3*]OC(C)(C)C
### Response:
CC(C)(C)OC(=O)[C@@H](C(=O)[O-])[C@@H]([NH3+])Cc1cccc(F)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1c(Cl)cc(Cl)cc1Br
Fragment 2: [3*]OCC(=O)NNC([6*])=O
### Response:
O=C(COc1c(Cl)cc(Cl)cc1Br)NNC(=O)c1ccc([N+](=O)[O-])cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CN(CC(=O)N2N=C(C[C@@H]2c2cccs2)c2cccs2)CCN1C(=O)COC
### Response:
COCC(=O)N1CCN(CC(=O)N2N=C(c3cccs3)C[C@@H]2c2cccs2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccccc1N(C)S(=O)(=O)c1cccc2ccccc12
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1
Fragment 2: [5*]Nc1cccc(Cl)c1
### Response:
COc1ccc(N2C(=O)CC[C@@H](C(=O)Nc3cccc(Cl)c3)[C@@H]2c2ccc(F)cc2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cncc(NC(=O)C2CCN(C(=O)Nc3ccccc3)CC2)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)(C)CNC(=O)NCCc1csc(N2CCCC2)n1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1CN(c2ccc(CNC(=O)CCOc3ccccc3)c[nH+]2)CCO1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(Nc1c(C)cccc1CC)Cc1c(noc1C)C
### Response:
CCc1cccc(C)c1NC(=O)Cc1c(C)noc1C |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCS(=O)(=O)c1ccc(Cl)cc1C(=O)N(C)CC(F)(F)F
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccco1
Fragment 2: [13*][C@H]1CCCN1S(=O)(=O)N1CCC(OC)CC1
### Response:
COC1CCN(S(=O)(=O)N2CCC[C@@H]2c2ccco2)CC1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CS(=O)(=O)[C@@H]1CCC[C@@H]([NH2+]CCc2cccs2)C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1ncc(C(=O)N2CCC(c3cc4n(n3)[C@@H](C(F)(F)F)C[C@@H](C)N4)CC2)cn1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCn1nc(C)nc1C
Fragment 2: [5*]NS(=O)(=O)c1ccccc1
### Response:
Cc1nc(C)n(CCNS(=O)(=O)c2ccccc2)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(c1cc(C(=O)Nc2ccc(Cl)cc2)ccc1)S(c1ccc(cc1)OC)(=O)=O
### Response:
COc1ccc(S(=O)(=O)Nc2cccc(C(=O)Nc3ccc(Cl)cc3)c2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCN1C(=O)c2cccc3c(NC(=O)c4ccn(C)n4)ccc1c23
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CCC(=O)N1CCN(CCc2nc(-c3ccccc3)no2)CC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1cn2cc(C)ccc2[nH+]1
Fragment 2: [5*]N1CCN([5*])CC1
### Response:
Cc1ccc2[nH+]c(CN3CCN(S(=O)(=O)c4cc(C)sc4C)CC3)cn2c1 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
C/C=C/C[C@]1(C(=O)[O-])CCN(C(=O)OC(C)(C)C)C1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@]12CCC(=O)N1[C@@H](C(=O)Nc1nc(-c3ccccc3Cl)cs1)CS2
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(C1=CCCCO1)N1CCC2(CCCCC2)C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC(CC1)[NH+](CC(N1[C@H]2CCCC[C@H]2OCC1)=O)CC(N)=O
### Response:
NC(=O)C[NH+](CC(=O)N1CCO[C@@H]2CCCC[C@@H]21)C1CCCC1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COc1cc(NC(=O)c2cccnc2Cl)ccc1-c1cc2ccccc2oc1=O
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[8*]
Fragment 2: [16*]c1cccc(OC)c1
### Response:
CC[C@@H]1Oc2ccc(NC(=O)Cc3ccc(F)cc3)cc2CN(Cc2cccc(OC)c2)C1=O |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
CCC/C(C)=C\C(=O)C1CCC(=O)CC1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCCN(CC1CC1)c1cc2c(cc1Cl)[C@@H](N)C(=O)N2
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC[C@H](C)Cn1c(CCCl)nc2c(C)nn(C)c21
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH2+]C(C)(C)C(=O)N[C@H]1CCCCC[C@@H]1C(=O)[O-]
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1ccc(-c2nc(C3CC3)no2)cc1)N(Cc1cccs1)C1CC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cc1nc(Cc2ccccc2)sc1C(=O)N1CCC[C@@H]1c1ccncc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc(n1)[C@@H](C(C)C)NC(Nc1c(ccc(C(=O)NC)c1)OC)=O
### Response:
CNC(=O)c1ccc(OC)c(NC(=O)N[C@@H](c2ccccn2)C(C)C)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cc(OC)cc(OC)c1
Fragment 2: [15*]C1(O)CCC2(CC1)OCCO2
### Response:
COc1cc(OC)cc(C2(O)CCC3(CC2)OCCO3)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
OCCC[C@@H](C)[NH2+]Cc1c(nn(C)c1Cl)-c1ccccc1
### Response:
C[C@H](CCCO)[NH2+]Cc1c(-c2ccccc2)nn(C)c1Cl |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)C(C)(C)C[NH2+][C@@H]1C[C@H]1c1ccccc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1N(CCC1(C)C)C(=O)CNC(=O)CCc1ccc(C)cc1
### Response:
Cc1ccc(CCC(=O)NCC(=O)N2CCC(C)(C)C2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COC(=O)[C@H](C)CNC(=O)Nc1cccc(SC(F)F)c1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C1O[C@H](/C=N/c2ccc(C(F)(F)F)cc2)c2ccccc21
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC[NH+](CC)[C@H](C)C(=O)Nc1ccc(F)c(N)c1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
c1ccc(-c2cnc(C[NH2+]C[C@@H]3CCCS3)s2)cc1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)N2CCN(C(=O)[C@H]3CCC(=O)N3)CC2)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C[C@@H]1Cc2ccccc2S1
Fragment 2: [8*]Cn1cc(C[NH3+])c(C)n1
### Response:
Cc1nn(C[C@@H]2Cc3ccccc3S2)cc1C[NH3+] |
functional_group | ### Instruction:
Does the molecule contain a ether group?
COc1cc2c(cc1OC)CN(C(=O)[C@@H]1CCCN(C(=O)c3cn(C)nc3OC)C1)CC2
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COC(=O)c1ccc(C(=O)Nc2nc3ccc(NC(C)=O)cc3s2)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCCCC1n1nc(C[NH2+]Cc2sccc2C)cc1
### Response:
Cc1ccsc1C[NH2+]Cc1ccn(C2CCCCC2)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH+]1CCC[C@@H]1[13*]
Fragment 2: [4*]Cc1cccc([16*])c1
### Response:
Cn1cnnc1[C@H]1CCC[NH+]1Cc1cccc(-c2cccnc2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@@H](CC)CO
Fragment 2: [8*]CC=C
### Response:
C=CCN1C(=O)/C(=C/c2c(N[C@@H](CC)CO)nc3ccccn3c2=O)SC1=S |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)CCNC(=O)N[C@H]2CC[C@H]([NH+](C)C)C2)c(Cl)c1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@@H](C)CN(S(=O)(=O)N2CC[C@H](C(=O)[O-])[C@@H]2C)C1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCc1c(CC)nn(C)c1OC
Fragment 2: [4*]Cc1c(CC)nn(C)c1OC
### Response:
CCc1nn(C)c(OC)c1CNC(=O)NCC[C@@H]1C[C@H]2CC[C@@H]1C2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C[NH+]2C[C@H](C)N(c3cc(cc(c3)C)F)C[C@H]2C1
### Response:
Cc1cc(F)cc(N2C[C@H]3CCC[NH+]3C[C@@H]2C)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(CC[C@H](C[C@H]1C)C)C(/C=C/c1ccc(cc1)C(NC)=O)=O
### Response:
CNC(=O)c1ccc(/C=C/C(=O)N2CC[C@@H](C)C[C@H]2C)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(=O)Nc1ccc(S(=O)(=O)Nc2ccc3c(c2)CCCN3C(=O)c2cccnc2)cc1
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
C[C@H](Sc1nc2cc(Cl)ccc2n1Cc1ccccc1)C(=O)N1CCC(C(N)=O)CC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*][NH+](C)[C@@H]1CCCc2ccccc21
### Response:
C[NH+](CC(=O)NC1(C#N)CCCCCC1)[C@@H]1CCCc2ccccc21 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CN1C2=C(C#N)C(=O)CCN2c2ccccc21
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(OC1(Cc2ccccc2)CCCCC1)C([O-])=O
### Response:
O=C([O-])COC1(Cc2ccccc2)CCCCC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=c1c2cc(F)ccc2nc([S-])n1CCc1c[nH]c2ccccc12
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@H](C)(Sc1n(c(C2CC2)nn1)Cc1occc1)C(=O)Nc1cccc2c1cccn2
### Response:
C[C@@H](Sc1nnc(C2CC2)n1Cc1ccco1)C(=O)Nc1cccc2ncccc12 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1cccc(C(=O)NC(=S)Nc2ccccc2C#N)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=S(=O)(c1ccccc1)C1[C@@H]2CCC[C@H]1C2Cl
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC#N
Fragment 2: [1*]C(=O)C[8*]
### Response:
N#CCOc1cccc(CC(=O)N[C@H]2CCCC[C@@H]2n2cccn2)c1 |
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