task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC1=C([C@H](c2cccc([N+](=O)[O-])c2)c2c(C)n[nH]c2[O-])[C@@H](O)N=N1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCc1ccccc1NC(=O)[C@@H](Cc1ccccc1)N1C(=O)[C@@H]2[C@H](C1=O)[C@H]1C=C[C@@H]2C1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CN(C(CN(C([C@@H]1CC[C@H]2[C@@H]([NH2+]1)CCCC2)=O)CC)=O)C
### Response:
CCN(CC(=O)N(C)C)C(=O)[C@@H]1CC[C@@H]2CCCC[C@@H]2[NH2+]1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(c(cc1OC)CCl)OCc1cccc(OC)c1
### Response:
COc1cccc(COc2ccc(OC)cc2CCl)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccnc([C@H]2CCCN2S(=O)(=O)c2cn[nH]c2)n1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
c1ccc(-c2cc(N3C[C@@H]4[C@H](C3)[C@H]3CC[C@@H]4O3)c3ccccc3[nH+]2)cc1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
O=C1CSC(=S)N1CCN1C(=O)CSC1=S
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(N[C@@H](CC)C)c1c(n(Cc2ccc3OCOc3c2)c2nc3ccccc3nc21)N
### Response:
CC[C@@H](C)NC(=O)c1c(N)n(Cc2ccc3c(c2)OCO3)c2nc3ccccc3nc12 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(N[C@@H]1CCC[C@@H]([C@@H]1C)C)CCC(=O)N[C@H]1[C@H](C)[C@@H](C)CCC1
### Response:
C[C@@H]1[C@@H](C)CCC[C@H]1NC(=O)CCC(=O)N[C@@H]1CCC[C@H](C)[C@@H]1C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cc(CN2CCN(c3ccc(F)cc3)CC2)cc(OC)c1O
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)(C[NH+]1CCC(Nc2ccccc2)CC1)S(C)(=O)=O
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@H]1(CN(CCO1)Cc1ccccc1N1CCN(CC1)C(C)=O)C(N)=O
### Response:
CC(=O)N1CCN(c2ccccc2CN2CCO[C@H](C(N)=O)C2)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@@H]([4*])C
Fragment 2: [8*][C@H](C)S[11*]
### Response:
CCCCNC(=O)[C@H](C)S[C@@H](C)c1ccc(F)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(NC(=O)c2ccc(SC(F)F)cc2)c(C(N)=O)cc1F
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCn1cc(C[NH+]2CCC(CN3C[C@@H](C)O[C@@H](C)C3)CC2)cn1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CN(C)c1ccc(CCCNC(=O)N[C@H]2CCC[C@@H]2CO)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)c1cccc(OCC(=O)N(C)Cc2ccccc2O)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](C[NH2+][C@@H]1CCc2c(Br)cccc21)Cn1cc[nH+]c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(=O)[nH]c(-c2ccc(NCc3ccccc3C)nc2)n1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1cccc(OC)c1OC
Fragment 2: [5*]Nc1cc(OC)c(OC)cc1C
### Response:
COc1cc(C)c(NCc2cccc(OC)c2OC)cc1OC |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)S(=O)(=O)c1cc2c(cc1NC(=O)CCC1CCCC1)n(C)c(=O)n2C
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](C(=O)N[C@H]1c2ccccc2C[C@H]1O)c1ccc(Cl)s1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(C[NH2+]C(C)(C)C)cc1OCc1nccs1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
C[C@H](NC(=O)N1CCCN(c2ncccc2C#N)CC1)C(C)(C)C[NH+](C)C
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(=O)Nc1ccc(-c2nnc(o2)SCC(OC)=O)cc1
### Response:
COC(=O)CSc1nnc(-c2ccc(NC(C)=O)cc2)o1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)C[8*]
Fragment 2: [1*]C(=O)N([5*])C
### Response:
CN(Cc1ccc(Cl)cc1)C(=O)NC1CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC(CC)N(C)S(=O)(=O)c1ccc(C)c(C(=O)OC)c1
### Response:
5 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cc2ccccc2o/c1=[NH+]\c1ccccc1F
Fragment 2: [5*]Nc1ccccn1
### Response:
O=C(Nc1ccccn1)c1cc2ccccc2o/c1=[NH+]\c1ccccc1F |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
OC[C@@H](NC(Nc1cn(CCC)nc1)=O)c1ccc(cc1)Cl
### Response:
CCCn1cc(NC(=O)N[C@H](CO)c2ccc(Cl)cc2)cn1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COc1ccc(-c2cc(C(=O)N[C@H]3CCCc4c3cnn4Cc3ccccc3)no2)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(C(c1ccc(-n2nncc2)cc1)=O)CCCOC
### Response:
COCCCNC(=O)c1ccc(-n2ccnn2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
COc1ccc(CCn2c(-c3cccc([N+](=O)[O-])c3)nc3c(c(=O)c4ccccc4n3C)c2=O)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC[N+]1(C[C@@H](O)CO[C@@H]2C[C@H](C)CC(C)(C)C2)CCOCC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cccs1
Fragment 2: [4*]CCC
### Response:
CCC[NH+]1CCC(N(C)Cc2c[nH]nc2-c2cccs2)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cccn(C)c1=O
Fragment 2: [5*]N1CCC[C@@H](CC)C1
### Response:
CC[C@@H]1CCCN(C(=O)C(=O)Nc2cccn(C)c2=O)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1c(N2C(=O)/C(=C\c3ccc4c(c3)C[C@@H](C)O4)SC2=S)c(=O)n(-c2ccccc2)n1C
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCN(C(=O)CCN1C(=O)[C@@H]2[C@H](C1=O)[C@H]1CC[C@@H]2O1)c1ccc(C)cc1C
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@H]1CC2(CCCC2)Oc2ccccc21
Fragment 2: [1*]C(=O)c1cn(C)nc1CC
### Response:
CCc1nn(C)cc1C(=O)N[C@H]1CC2(CCCC2)Oc2ccccc21 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(OC)c([C@@H](C)NC(=O)[C@@H](C)Nc2ccc3c(c2)CCO3)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(OCc1ccc([N+](=O)[O-])cc1)C1(c2ccccc2)CCOCC1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Nc1cc(N)nc(SCCn2c(=O)oc3cccnc32)n1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC1(C[NH2+]C2CC(c3ccccc3Cl)C2)COC1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)N1C(=O)C[C@@H](NC(=O)c2cc(Br)c[nH]2)C1=O
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC1CC[NH+]([5*])CC1
Fragment 2: [4*][C@H](C)C(N)=O
### Response:
Cc1occc1C(=O)NC1CC[NH+]([C@H](C)C(N)=O)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=S(=O)(NCC1(N2CCOCC2)CCCCC1)C1=Cc2ccccc2CC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
O=C(Nc1ccc(C(=O)OC[C@@H]2CCC[NH+]3CCCC[C@@H]23)cc1)c1ccc([N+](=O)[O-])cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(C)nc(SCc2c(C(=O)N3C[C@H](CCC3)C)nnn2-c2ccc(cc2)Cl)nc1C
### Response:
Cc1cc(C)nc(SCc2c(C(=O)N3CCC[C@H](C)C3)nnn2-c2ccc(Cl)cc2)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1[nH]c2ccccc2c1[C@H](C(=O)[O-])N1CCOCC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(NCc2c(F)ccc(c2)C#N)ccc(S(N(CC)CC)(=O)=O)cc1
### Response:
CCN(CC)S(=O)(=O)c1ccc(NCc2cc(C#N)ccc2F)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1nc2ccccc2s1
Fragment 2: [15*]C1CCCC1
### Response:
C[C@H](Cc1nc2ccccc2s1)N1CC[NH+](C2CCCC2)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [9*]n1nc([14*])ccc1=O
### Response:
CCOC(=O)c1nc(Cn2nc(-c3ccc(C)cc3)ccc2=O)no1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [7*]C1SC(=S)N([10*])C1=O
Fragment 2: [7*]Cc1ccc(F)cc1
### Response:
Cc1ccc(NC(=O)CCN2C(=O)/C(=C/c3ccc(F)cc3)SC2=S)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(c1noc(C)n1)[NH+]1CCC[C@@H](Nc2nn3c(s2)nc(C)c3)C1
### Response:
Cc1cn2nc(N[C@@H]3CCC[NH+](Cc4noc(C)n4)C3)sc2n1 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
Cc1cnc(NC(=O)Cn2nc(C)c3ccccc3c2=O)s1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(NC(=O)Cn1c2c(nn1)cccc2)CN1C(=O)CSC1=O
### Response:
O=C(Cn1nnc2ccccc21)NCCN1C(=O)CSC1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCC[C@H](NC(=O)c1ccnc(C2CCCC2)n1)C(=O)OC
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(ccc1)C[NH2+][C@@H](C([O-])=O)CC(=O)Nc1cc(cc(c1)C)C
### Response:
Cc1cc(C)cc(NC(=O)C[C@@H]([NH2+]Cc2ccccc2)C(=O)[O-])c1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
Cc1ccc(C)n1CCN1CC[NH+](C2CCC(c3ccc(O)cc3)CC2)CC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCC[8*]
Fragment 2: [1*]C(=O)c1cc(=O)c(OC)co1
### Response:
COc1cccc(CCNC(=O)c2cc(=O)c(OC)co2)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc([C@H](CNC(=O)c2sc(-c3ccccn3)nc2C)[NH+](C)C)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)(CNC(=O)CC[C@@H]1NC(=O)NC1=O)[NH+]1CCc2ccccc2C1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@H](c2ccc(F)cc2)CN1C(=O)NCCNC(=O)c1cccnc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [10*]N1C(=O)C[C@H](C)C1=O
Fragment 2: [5*]N1CCN([5*])CC1
### Response:
C[C@H]1CC(=O)N(c2ccc(N3CCN(c4ccccc4)CC3)c([N+](=O)[O-])c2)C1=O |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COC(=O)c1ccc(C)c(NC(=O)N2CCC[C@H]2c2cccc(OC)c2)c1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc2c1o/c(c(C(Nc1cccc(n1)C)=O)c2)=[NH+]\c1ccc(c(F)c1)F
### Response:
Cc1cccc(NC(=O)c2cc3ccccc3o/c2=[NH+]\c2ccc(F)c(F)c2)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c([C@H](O)C[NH2+][C@@H](C2CCCC2)C)ccnc1
### Response:
C[C@@H]([NH2+]C[C@@H](O)c1ccncc1)C1CCCC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccc(OCC(=O)NC[C@H](C[C@H](C)O)C)c1)Cl
### Response:
C[C@H](CNC(=O)COc1ccc(Cl)cc1)C[C@H](C)O |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1cc(=O)n2cc(C)ccc2n1
Fragment 2: [5*][NH+]1CCC[C@@H]1[13*]
### Response:
Cc1ccc2nc(C[NH+]3CCC[C@@H]3C(=O)[O-])cc(=O)n2c1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CCOC(=O)C1CCN(c2nc(-c3ccc4c(c3)OCO4)c3c(N)n(C)nc3n2)CC1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1noc(C)c1CN(C)C(=O)c1cccc(C[S@](C)=O)c1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CC[4*]
Fragment 2: [5*]N[C@@H]1CCCc2ccccc21
### Response:
CC(=O)Nc1ccc(S(=O)(=O)NCCC(=O)N[C@@H]2CCCc3ccccc32)cc1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CCC(=O)N[C@@H]1CCCN(C(=O)N[C@H](C)C2CCCCC2)C1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nc(N2CCOCC2)sc1C(=O)NNC(=O)c1ccc(F)c(F)c1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*][C@H](C)O
Fragment 2: [5*][NH+]1CCC[C@H]([15*])C1
### Response:
C[C@H](O)[C@H]1CCC[NH+](CC(=O)NNC(=O)c2ccccc2)C1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
COc1ccccc1Cn1c([C@@H](C)O)nc2ccccc21
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc2c(c1)OCCO2
Fragment 2: [3*]OC(F)F
### Response:
C[C@H](NC(=O)CN1C(=O)N[C@@](C)(c2ccc(OC(F)F)cc2)C1=O)c1ccc2c(c1)OCCO2 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
Cc1ccc(/C=C/C(=O)NC2CCN(C(=O)CC(C)C)CC2)o1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC[C@@H](CC)CCO
Fragment 2: [1*]C(=O)c1ccnc(F)c1
### Response:
CC[C@@H](CCO)CNC(=O)c1ccnc(F)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1CCCN(C(=O)C2CC[NH+](C[C@@H](O)c3ccc(F)cc3F)CC2)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC1=NC2(CC[NH+](C[C@@H](O)COc3ccccc3)CC2)N=C1c1cccc(C(F)(F)F)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1cc(N2CCN(Cc3ccccc3)CC2)ncn1)c1cccc2ccccc12
### Response:
5 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCN(CC)S(=O)(=O)c1ccc(C(=O)[O-])o1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(S(=O)(=O)CC(NCc2ccccc2OC)=O)[n+](cc1)[O-]
### Response:
COc1ccccc1CNC(=O)CS(=O)(=O)c1cccc[n+]1[O-] |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@H](N(C(=O)CCC)CCC1)C(N1CC[C@H](C1)CSc1ccccc1)=O
### Response:
CCCC(=O)N1CCCC[C@H]1C(=O)N1CC[C@@H](CSc2ccccc2)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CN(C)c1cc(C(=O)N2CCC[C@@H]2c2cnn(C)c2)ccn1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(NC(=O)C)cc(c(O)c1)NC(=O)C
### Response:
CC(=O)Nc1ccc(O)c(NC(C)=O)c1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
Cc1ccc(S(=O)(=O)N2C[C@H](O)C[C@H]2C(=O)OCc2cccc3cccnc23)cc1C
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(N)[C@@H](C[NH2+]C1CCCCC1)C
### Response:
C[C@H](C[NH2+]C1CCCCC1)C(N)=O |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccnc([14*])n1
Fragment 2: [5*]N1CCC[C@H]([15*])C1
### Response:
COCc1nccc([C@H]2CCCN(Cc3nnc(C)o3)C2)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)(C)c1cc[n+](C2=C([O-])C(=[OH+])N(Nc3ccccc3)C2=O)cc1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C(C)(C)C
Fragment 2: [5*]Nc1sc2c(c1C#N)CC[C@@H]([15*])C2
### Response:
Cc1cc(C(=O)Nc2sc3c(c2C#N)CC[C@@H](C(C)(C)C)C3)no1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccs1
Fragment 2: [5*]Nc1nc2c(s1)CN([5*])CC2
### Response:
COc1cc(C(=O)N2CCc3nc(NC(=O)c4cccs4)sc3C2)cc(OC)c1OC |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][N-]S(=O)(=O)N([5*])C
Fragment 2: [16*]c1cc(OC)ccc1Cl
### Response:
CCCCN(C)S(=O)(=O)[N-]c1cc(OC)ccc1Cl |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc([C@@H]([NH2+]CCn2cc([N+](=O)[O-])cn2)C2CC2)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CC[C@@H]1NC(=O)N(Cc2ccc3c(c2)OCO3)C1=O)N1CCN(c2ccccc2)CC1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C)c1ccc(CN2CCC[C@H](CN3CCOCC3)C2)cc1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(CNC(=O)Cc1ccc[nH]1)NCCc1ccccc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NNS(=O)(=O)c1ccc(F)c(Cl)c1)c1ccc(COc2ccccc2)o1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCNC(=O)[C@H]1CCCN(C(=O)C=C(C2CC2)C2CC2)C1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)([C@H](O)c1ccc(Cl)s1)[NH+]1CCCC1
### Response:
3 |
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