task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH2+][C@@H](C)[C@H]([8*])C
Fragment 2: [15*]C1CCCC1
### Response:
COc1ccc([C@H](C)[C@H](C)[NH2+]C[C@H](O)C2CCCC2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COCc1cc(CNC(=O)N2CCC[C@@H]2c2c(C)n[nH]c2C)ccc1F
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC(=O)Nc1ccc(S(=O)(=O)N2CC[C@@H](C)[C@H](O)C2)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C[C@H]2OCCN([C@@H]2CC1)C(c1cc(c(C)o1)S(=O)(N(C)C)=O)=O
### Response:
Cc1oc(C(=O)N2CCO[C@@H]3CCCC[C@H]32)cc1S(=O)(=O)N(C)C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cccs1
Fragment 2: [8*]CC[C@@H]([8*])C[NH2+]C
### Response:
C[NH2+]C[C@@H](CCc1cccs1)c1ccccc1Br |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@H](C)c1c(C)noc1C
Fragment 2: [5*]Nc1ccc2n[nH]c(=O)n2n1
### Response:
Cc1noc(C)c1[C@@H](C)Nc1ccc2n[nH]c(=O)n2n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1nc(C)c2c(n1)CC(C)(C)CC2=O
Fragment 2: [5*]N1CCCC1
### Response:
Cc1nc(N2CCCC2)nc2c1C(=O)CC(C)(C)C2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)[C@H]1Oc2c(c(=O)oc3ccccc23)[C@H]1c1ccc(OC)c(OC)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[S@@](=O)c1ccc(C[NH+]2CCC(OC[C@H]3CCCO3)CC2)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccccn1
Fragment 2: [5*]Nc1c[nH]nc1[14*]
### Response:
Cc1cccc(C(=O)Nc2c[nH]nc2-c2ccccn2)c1O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[C@@H]1C[C@@](c2ccccc2)([C@@H](C[NH3+])CO)CCO1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCn1c([C@H](C)NCc2cc3ccccc3[nH]c2=O)nc2ccccc21
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccc(-c2noc(CNc3ccc(C(=O)N4C[C@H](C)O[C@@H](C)C4)cc3)n2)c1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COCCNC1(C#N)CN(C(=O)OC(C)(C)C)C1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CC(C)(C)NC(=O)CCCN1C(=O)[C@@H]2CC[C@](C)(C1=O)C2(C)C
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
O=C(Cc1cccc2ccccc12)NCCOc1ccc2c(c1)OCO2
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc(CS(=O)(=O)N2CCC[C@H](C(=O)Nc3ccc(Cl)c(C(F)(F)F)c3)C2)c1
### Response:
O=C(Nc1ccc(Cl)c(C(F)(F)F)c1)[C@H]1CCCN(S(=O)(=O)Cc2ccccc2)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(NC(=O)C(=O)NCc2ccccc2C)c(Cl)c1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C#CCN(CC(=O)[O-])C(=O)N(CCC)CC1CC1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccc([16*])c1
Fragment 2: [16*]c1ccoc1
### Response:
CCOc1ccc(NC(=O)c2cccc(-c3ccoc3)c2)c(C(N)=O)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1CN(C(=O)c2ccc(C3SCCS3)cc2)CCN1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@@H](C)NC(=O)N1CCC[C@H](c2nc(-c3cccc(F)c3)no2)C1
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
COc1cc(C)c(NC(=O)c2cc(C)no2)cc1OC
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC(C)(C)OC(=O)N1C[C@H](OCc2ccc3ccccc3c2)C[C@H]1C(=O)[O-]
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
COC(=O)[C@H]1CCCC[C@@H]1NC(=O)c1cc(Cl)c(Cl)n1C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@@H]1CCC[NH2+]C1
Fragment 2: [3*]OCC
### Response:
CCOCCCC(=O)N[C@H](C)[C@@H]1CCC[NH2+]C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[NH+](C)CC(C)(C)CN1CCN(c2nc(-c3ccccc3)no2)CC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C([O-])CC1CC[NH+](C[C@@H]2Cc3ccccc32)CC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Nc1c(C(=O)NCc2ccccc2Cl)sc2nc(-c3cccs3)ccc12
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C([NH2+][C@H](c1occc1C)C)c1cc(-c2n[nH]cn2)ccc1
### Response:
Cc1ccoc1[C@H](C)[NH2+]Cc1cccc(-c2nc[nH]n2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [6*]C(N)=O
Fragment 2: [5*]NCC[8*]
### Response:
Cc1cc(C)c(CCNC(=O)COc2ccc(C(N)=O)cc2)c(C)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N([5*])CC
Fragment 2: [4*]Cc1ccnc(/C(N)=N/O)c1
### Response:
CCN(Cc1ccnc(/C(N)=N/O)c1)Cc1ccccn1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[NH+]1CC[C@H](N(C)C(=O)c2cnc(-c3ccsc3)s2)[C@H](C)C1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@@H]([NH3+])CN(C(=O)/C=C/c2cccs2)C1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(S(=O)(=O)NCCC(=O)Nc2nnc(C(C)(C)C)s2)cc1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1c2cc3c(C(C)(C)C)coc3cc2OC(=O)[C@H]1CCC(=O)NCCc1c[nH+]c[nH]1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CO[C@H](C)c1noc([C@@H]([NH3+])CCS(C)(=O)=O)n1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1cccc(Nc2ncccc2C(=O)Nc2ccc(Br)cc2)c1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccn1-c1sc2c(ccc(c2)C([O-])=O)n1
### Response:
O=C([O-])c1ccc2nc(-n3cccc3)sc2c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(O)cc1
Fragment 2: [9*]n1cc(C)cn1
### Response:
Cc1cnn(CCCCC[NH+]2CCN(c3ccc(O)cc3)CC2)c1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
COCCNC(=O)COc1ccc(-c2nn(C)c(=O)c3ccccc23)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=[N+]([O-])c1ccc(/C=C\C(N(CC[NH+](C)C)c2sc3cccc(c3n2)F)=O)cc1
### Response:
C[NH+](C)CCN(C(=O)/C=C\c1ccc([N+](=O)[O-])cc1)c1nc2c(F)cccc2s1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccccc1[S@@](=O)CCC(=O)NCc1ccc(F)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CNC(=O)/C(C#N)=C1/S[C@H](Cc2cccc([N+](=O)[O-])c2)C(=O)N1c1ccccc1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc(C([1*])=O)cc1
Fragment 2: [3*]OC(C)(C)C
### Response:
COc1ccccc1N(C)C(=O)c1ccc(C(=O)OC(C)(C)C)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(NC(=O)C(=O)N[C@@H]2CCN(CC(F)(F)F)C2)cc1F
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(=O)C[C@@H]1CCCCCN1C(=O)c1cccnc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCc1cc(C(N)=O)c(NC(=O)c2ccnn2C)s1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CN(c2c(C[NH+](C)[C@@H](C)C(Nc3c(Cl)cc(cc3)[N+](=O)[O-])=O)cccc2)CCC1
### Response:
C[C@@H](C(=O)Nc1ccc([N+](=O)[O-])cc1Cl)[NH+](C)Cc1ccccc1N1CCCCC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*]N1CCN([5*])CC1
### Response:
C=CCNC(=O)CN1CCN(c2nc(C)nc3sc4c(c23)CCCC4)CC1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
Cc1ccc(C(=O)Nc2c(C(=O)Nc3ccc4c(c3)OCO4)oc3ccccc23)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCOCC1
Fragment 2: [14*]c1cccc[nH+]1
### Response:
CCCn1c(CN2CCN(c3cccc[nH+]3)CC2)nc2cc(S(=O)(=O)N3CCOCC3)ccc21 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Fc1cccc(-c2nc(-c3ccc4c(c3)nnn4C3CCCC3)no2)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C(=C\c1ccccc1)/CSc1nnc(-c2ccncc2)o1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(C(=O)NC(=S)NNC(=O)Cn2ccc3ccccc32)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(C(=O)N2C[C@H]3[C@@H](C2)[C@H]2CCCC[NH+]2C3)ccc2N(C(CC)=O)CCc2c1
### Response:
CCC(=O)N1CCc2cc(C(=O)N3C[C@@H]4C[NH+]5CCCC[C@@H]5[C@@H]4C3)ccc21 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(=C\c1ccccc1)/c1c(-c2oc(C)nn2)cccc1
### Response:
Cc1nnc(-c2ccccc2/C=C/c2ccccc2)o1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccccc1
Fragment 2: [4*]C[C@@H]1CCN([5*])C1
### Response:
CC[C@@H](Cc1ccccc1)[NH2+]C[C@@H]1CCN(S(C)(=O)=O)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1cccnc1)N1CCN(C[C@H](O)c2ccccc2)CC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CC[C@@H](CSC)N(C)C(=O)N[C@@H]1CCCn2nc(COC)nc21
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
COc1ccc([C@@H](NC(=O)C(=O)Nc2ccc(Cl)cc2)C(C)C)cc1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(NC(=O)C(=O)N[C@@H](C)c2ccccc2Br)no1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](CCc1ccccc1)NC(=O)NCc1ccccc1F
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nc(C)c(C(=O)N2CC[C@@H]3[C@@H](CCC(=O)N3CCCCO)C2)o1
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCNS(=O)(=O)[C@@H]1CCN(C(=O)c2cccc(OC3CCCC3)c2)C1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1(C2CCCC2)c(=O)c2n(C)c3c(cccc3)c2c(c1)C(N1CCN(CC1)C)=O
### Response:
CN1CCN(C(=O)c2cn(C3CCCC3)c(=O)c3c2c2ccccc2n3C)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(N[C@@H](C2CC2)C)ccc(F)cc1I
### Response:
C[C@@H](Nc1ccc(F)cc1I)C1CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc([16*])cc1
Fragment 2: [5*]N[C@H](C)CO
### Response:
C[C@H](CO)NC(=O)C(=O)Nc1ccc(-c2cn3ccsc3n2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1cccc(N2C[C@H](C(=O)Nc3nc4c(s3)COCC4)CC2=O)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1nn(cc1-c1cc(C(N[C@@H](C)COc2ccc(cc2)Cl)=O)c2c(cccc2)n1)C
### Response:
C[C@@H](COc1ccc(Cl)cc1)NC(=O)c1cc(-c2cnn(C)c2)nc2ccccc12 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CC[C@@H](CO)C1
Fragment 2: [16*]c1ccccc1
### Response:
Cn1cc(C(=O)N2CC[C@@H](CO)C2)c(-c2ccccc2)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cnc([14*])o1
Fragment 2: [1*]C(=O)CC[8*]
### Response:
Cc1ccnc(NC(=O)CCc2ncc(-c3ccc(Cl)cc3)o2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]Oc1ccc([16*])c(F)c1
Fragment 2: [4*]Cc1cc(Cl)c2c(c1)OCCO2
### Response:
CC(=O)c1ccc(OCc2cc(Cl)c3c(c2)OCCO3)cc1F |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [15*][C@H]1CCOC1
### Response:
CCOc1ccc(F)c(C(=O)Nc2ccccc2O[C@H]2CCOC2)c1F |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12sc(c(C)c1ccc(n2)C(F)(F)F)C(N(C1CCCC1)C1CC1)=O
### Response:
Cc1c(C(=O)N(C2CCCC2)C2CC2)sc2nc(C(F)(F)F)ccc12 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCn1nnnc1CN(C)[C@H](C)c1cccc(S(N)(=O)=O)c1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC(=O)C[C@@H]1CCCN1C(=O)c1ccc2c(c1)COC2
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(CCOc1ccc(Cl)cc1)C
### Response:
CCCCOc1ccc(Cl)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]Oc1cccc(C)c1C
Fragment 2: [16*]c1cccc(C)c1C
### Response:
Cc1cccc(OC[C@@H](O)CN2CC[NH+](C)CC2)c1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [12*]S(=O)(=O)c1c[nH]c2nccc(Cl)c12
Fragment 2: [5*]N1CCCC[C@@H]1C1OCCO1
### Response:
O=S(=O)(c1c[nH]c2nccc(Cl)c12)N1CCCC[C@@H]1C1OCCO1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(c(ccc1)Cl)[C@@H](NC(CN(S(=O)(c1ccc2c(c1)OCCO2)=O)C)=O)C
### Response:
C[C@H](NC(=O)CN(C)S(=O)(=O)c1ccc2c(c1)OCCO2)c1ccccc1Cl |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O(Cc1nc2scc(n2c(c1)=O)C)C(C(c1ccccc1)c1ccccc1)=O
### Response:
Cc1csc2nc(COC(=O)C(c3ccccc3)c3ccccc3)cc(=O)n12 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(CC(N)=S)cc1
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC(CC)N(CCOC)C(=O)[C@H]1CC[NH2+][C@@H]1C
### Response:
5 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)c1cc(C(=O)NC[C@](C)(O)CN2CCOCC2)c2ccccc2n1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(N1CCC(CC1)C(OCC)=O)c1cccnc1[S-]
### Response:
CCOC(=O)C1CCN(C(=O)c2cccnc2[S-])CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CN([5*])C
Fragment 2: [1*]C(=O)c1ccc(F)cc1
### Response:
COC(=O)c1ccccc1NC(=O)CN(C)C(=O)c1ccc(F)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC1=C[C@@H]([C@@H]2NN=C3SC(c4ccccc4)=NN32)N=N1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(c(c2CC[NH+](C)Cc2s1)CNC(NCC(C)C)=O)-n1cccc1
### Response:
CC(C)CNC(=O)NCc1c(-n2cccc2)sc2c1CC[NH+](C)C2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(C)(C)O
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cn1cccc(C(F)(F)F)c1=O)N1CCC[C@@H]2CCCC[C@@H]21
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc2ccccc2c1
Fragment 2: [4*]Cc1ccncc1
### Response:
c1ccc2cc(NCc3ccncc3)ccc2c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [13*][C@@H]1[NH+]=C(c2cccc(OC)c2)NC1=S
Fragment 2: [16*]c1ccccc1
### Response:
COc1cccc(C2=[NH+][C@@H](c3ccccc3)C(=S)N2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(C=O)cc1OC
Fragment 2: [4*]CCC
### Response:
CCCOc1ccc(C=O)cc1OC |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1nc(CC)ns1
Fragment 2: [3*]Oc1ccc(C=O)cc1Cl
### Response:
CCc1nsc(Oc2ccc(C=O)cc2Cl)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCN([5*])CC1
Fragment 2: [1*]C(=O)c1cccc(OC)c1
### Response:
COc1cccc(C(=O)Nc2c(C(=O)N3CCN(c4ccccc4OC)CC3)oc3ccccc23)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cn1cnc2c(nnn2-c2ccc(F)cc2)c1=O)N1CCN(c2ccccc2)CC1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)[C@H](NC(=O)C[NH+]1CCN(CC(=O)N2CCCCC2)CC1)c1ccccc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](NC(=O)Nc1ccccc1)C(=O)N[C@H](C)c1ccc(OC(F)F)cc1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Cc1cc(NC(=O)c2csc(Nc3cccnc3)n2)no1
### Response:
Yes |
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