task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1c(=O)oc2ccccc21
Fragment 2: [5*]N[C@@H](C)C[8*]
### Response:
C[C@@H](Cn1c(=O)oc2ccccc21)NC(=O)c1ccccn1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1C(N=NN=1)C(SCC)SCC
### Response:
CCSC(SCC)C1N=NN=N1 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
O=C(Nc1ccc2scnc2c1)c1ccc2c(c1)OCO2
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc([C@@H](C[NH3+])OC(C)C)cc1F
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)[C@]1(F)CCN(C(=O)COc2ccc(C(F)(F)F)cc2)C1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(N2CCN(c3ccc(C(=O)Nc4cccc(C#N)c4)cc3[N+](=O)[O-])CC2)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1COCC[NH+]1CC[C@@]1(CCC(C)C)C[C@H](OCC1)C(C)C
### Response:
CC(C)CC[C@@]1(CC[NH+]2CCOCC2)CCO[C@H](C(C)C)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccco1
Fragment 2: [15*][C@@H]1CC(=O)[C@H]2C(=Nc3ccccc3N3C(=O)c4ccccc4[C@H]23)C1
### Response:
O=C1C[C@@H](c2ccco2)CC2=Nc3ccccc3N3C(=O)c4ccccc4[C@@H]3[C@@H]12 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(NCCc1ccccn1)NC1CCN(C(=O)c2ccoc2)CC1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CN[C@@]1(C(=O)OC)CCC[C@H]([NH+](C)C2CCCCC2)C1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=S1(=O)CC[C@H](Cc2nc(-c3ccccn3)nn2Cc2ccccc2)C1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NC(=O)[C@H]1COCCN1C(=O)c1csc(-c2ccoc2)n1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c2C(=O)NC(c2cc(c1)NC([C@@H]1CCCN1S(=O)(c1ccc(OC)cc1)=O)=O)=O
### Response:
COc1ccc(S(=O)(=O)N2CCC[C@H]2C(=O)Nc2ccc3c(c2)C(=O)NC3=O)cc1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
C[NH+](CCn1c(=O)oc2cccnc21)[C@H]1CCC[C@@H]1S(C)(=O)=O
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1CCCCC1
Fragment 2: [5*]NC1CCCCC1
### Response:
O=C(Nc1nc2ccccc2n1CC[NH+]1CCCCC1)NC1CCCCC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O(C)CC(N[C@H]1CCCc2nc(ncc12)C)=O
### Response:
COCC(=O)N[C@H]1CCCc2nc(C)ncc21 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ccccc1C
Fragment 2: [5*]N([5*])Cc1cc(=O)n2ccccc2[nH+]1
### Response:
COC(=O)CN(Cc1cc(=O)n2ccccc2[nH+]1)Cc1ccccc1C |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(c1ccc(C(C)C)cc1)N(C)C(=O)NCCCn1nccc1
### Response:
CC(C)c1ccc(CN(C)C(=O)NCCCn2cccn2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
NC(=O)[C@@H]1COCCN1C(=O)c1cc2cc(F)ccc2o1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(c(cc(cc1[N+](=O)[O-])Br)/C=N/NC(Cn1c2c(c(c3c1cccc3)=O)cccc2)=O)[O-]
### Response:
O=C(Cn1c2ccccc2c(=O)c2ccccc21)N/N=C/c1cc(Br)cc([N+](=O)[O-])c1[O-] |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C1=C(C)NC(=O)N[C@H]1[13*]
Fragment 2: [16*]c1ccccc1[16*]
### Response:
CC1=C(C(=O)Nc2ccccc2C)[C@H](c2ccccc2C(F)(F)F)NC(=O)N1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
Cc1ccoc1C[NH+]1CC[C@@H](C)[C@H](C)C1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCc1nnc2n1N[C@H](c1ccc(OC)cc1)[C@H](C(=O)Nc1ccc(C)c(Cl)c1)S2
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1ccccc1Cl)[C@H]1CCCN(c2ccc(-n3ccnc3)nn2)C1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=S(=O)(NC[C@@H](c1ccccc1)c1c[nH]c2ccccc12)c1cccs1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC(=O)c1c[nH]c(C(=O)N(C)CCC2CCN(c3cc[nH+]cc3)CC2)c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@H](C)C[NH+]1CCCN(C(=O)c2ccc(Cl)cc2)CC1
### Response:
4 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc2cccc(C(=O)N[C@@H](c3n[nH]c(C)n3)C(C)C)c2n1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cccs1
Fragment 2: [8*]C(C)(C)C
### Response:
Cc1nnc(N2C(=O)C(O)=C(C(=O)c3cccs3)[C@@H]2c2ccc(C(C)(C)C)cc2)s1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
N#CCN1CCN(Cc2cccc(OCc3ccccc3C#N)c2)CC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CCCN(CCO)C(=O)Nc1cccc(OC)c1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CCCN(c2ncnc(N)c2[N+](=O)[O-])C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cnc(-c2cccc(NC(=O)C(=O)N[C@@H]3CCN(c4ccccc4)C3)c2)o1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCC(=O)Nc1cccc(NC(=O)C(=O)N[C@H]2CC[C@@H]([NH+](C)C)C2)c1
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1(c(nnn1)-c1cccc(c1)NC(=O)[C@@H]1[C@@H](C)Oc2c(cccc2)O1)C
### Response:
C[C@H]1Oc2ccccc2O[C@@H]1C(=O)Nc1cccc(-c2nnnn2C)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc([16*])cc1
Fragment 2: [1*]C(=O)c1ccc(N[5*])cc1
### Response:
C[C@H](NC(=O)c1ccc(NC(=O)Nc2ccc(Cl)cc2)cc1)c1ccccc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1nnc(N2CCN(C(=O)Cc3cccc(OC)c3)CC2)c2cccn12
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C1CC[C@H](C(=O)Nc2ccc(F)c(-n3cccc3)c2)CN1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(C(=O)N2Cc3c(nc(s3)NC(=O)[C@@H]3CCCO3)CC2)cc(c(OC)c1OC)OC
### Response:
COc1cc(C(=O)N2CCc3nc(NC(=O)[C@@H]4CCCO4)sc3C2)cc(OC)c1OC |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
FC(F)(F)c1cccc2c1CCCC2
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH+](C)[C@H]1CC[C@H](NC(=O)c2cc(F)ccc2Br)C1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CCCCN(C(=O)c1cc(F)cc(F)c1)[C@H]1CCS(=O)(=O)C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CN(C)C(=O)C1CCN(C(=O)NCc2cn(-c3ccccc3)nn2)CC1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCCN2[C@H]1CO[C@@H](C2)CNC(=O)Nc1cc2oc(C)nc2cc1
### Response:
Cc1nc2ccc(NC(=O)NC[C@@H]3CN4CCCC[C@@H]4CO3)cc2o1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cccs1
Fragment 2: [15*]C1CC[NH+](C)CC1
### Response:
CCC(CC)[C@H](NC(=O)NC1CC[NH+](C)CC1)c1cccs1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(ccc(cc1)-n1nncc1)C(N1CCS(=O)(=O)C(C)(C)C1)=O
### Response:
CC1(C)CN(C(=O)c2ccc(-n3ccnn3)cc2)CCS1(=O)=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=Cc1cc(F)c(OCC(=O)N2CCCCCC2)c(F)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(S(=O)(=O)N2CCN(C(=O)c3ccc(N(C)C)cc3)CC2)cc1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
CCCc1nn(C)c2c1NC(=O)C(CC)(CC)N2
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NS(=O)(=O)c1ccc(CCNC(=O)CCC2=c3ccccc3=[NH+]C2)cc1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C#CCOc1ccccc1/C=C(\C#N)C(=O)[O-]
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OC[C@@H](O)C[NH2+]C
Fragment 2: [16*]c1cccc2ccccc12
### Response:
C[NH2+]C[C@H](O)COc1cccc2ccccc12 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)(CNC(=O)[C@H]1C[C@@H]1c1ccc(F)cc1)NC(=O)OC(C)(C)C
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1CCOCCN1C(=O)NCc1ccc(-n2ccnc2)nc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C(CN2C(=O)CCCC2=O)(CCC1)CS
### Response:
O=C1CCCC(=O)N1CC1(CS)CCCC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CS(=O)(=O)c1ccc(NC(=O)N2C[C@H](O)[C@@H](N3CCOCC3)C2)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(-c2nc3s/c(=C\c4ccco4)c(=O)n3c2-c2ccc(OC)cc2)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(-c2nc(C[NH+]3CCN(Cc4ccc(F)cc4)C(=O)C3)c(C)o2)cc1C
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(-c2nn(-c3ccccc3)cc2C(=O)N[C@@H]2CCCNC2=O)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CS(=O)(=O)c1ccccc1C(=O)Nc1nc(-c2ccc([N+](=O)[O-])cc2)cs1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC(CC[NH+]1Cc1ccc(cc1)O[C@@H](C(=O)OC)C)c1n[nH]c(n1)C
### Response:
COC(=O)[C@@H](C)Oc1ccc(C[NH+]2CCC(c3n[nH]c(C)n3)CC2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1ccc(F)c(F)c1F)c1cc2c(s1)CCC2
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC1(C)[C@H]2OCCC[C@H]2[C@@H]1OC(=O)c1ccc(-c2cscn2)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC(=S)N[C@H]1CCCc2c1cnn2C
Fragment 2: [4*][C@@H](C)c1ccccc1
### Response:
C[C@H](NC(=S)N[C@H]1CCCc2c1cnn2C)c1ccccc1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CCC1=NN(c2cc(F)c(F)c(F)c2)C(=O)C1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCC([15*])CC1
Fragment 2: [14*]c1nc2ccccc2o1
### Response:
O=C(CNC(=O)N1CCC(c2nc3ccccc3o2)CC1)N1CCCCC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OC(F)F
Fragment 2: [7*]C(S[11*])C(=O)[O-]
### Response:
O=C([O-])/C(=C\c1ccc(OC(F)F)cc1)Sc1nnc(-c2ccc(F)cc2)o1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CS[11*]
Fragment 2: [4*]CCS[11*]
### Response:
CCn1cc[nH+]c1[C@@H]1CCCN(C(=O)CSCC[NH+]2CCCC2)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(c(C(C)C)cc2[nH]ncc12)O
### Response:
CC(C)c1cc2[nH]ncc2cc1O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C([NH+]1CCC[C@@H](C1)COC)c1sc2C[C@@H](C)CCc2n1
### Response:
COC[C@H]1CCC[NH+](Cc2nc3c(s2)C[C@@H](C)CC3)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(NC2CC[NH+](CC(S(=O)(C)=O)(C)C)CC2)cccc1
### Response:
CC(C)(C[NH+]1CCC(Nc2ccccc2)CC1)S(C)(=O)=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)c1cccc(-c2cnc(Cl)cc2C(=O)[O-])c1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(NCCNC([C@@H]1C=c2c(=[NH+]1)cccc2)=O)C(N1CCN(c2c(cccc2)OC)CC1)=O
### Response:
COc1ccccc1N1CCN(C(=O)C(=O)NCCNC(=O)[C@@H]2C=c3ccccc3=[NH+]2)CC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1cccc(-c2n[nH]c3c2CN(C(=O)CCc2ccncc2)CC3)c1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*]N1CC[S@@](=O)C(C)(C)C1
### Response:
CC(C)CN1CCO[C@@H](CNC(=O)CN2CC[S@@](=O)C(C)(C)C2)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(F)ccccc1O[C@@H](C)CNC(=O)c1nn(c(cc1)=O)CC
### Response:
CCn1nc(C(=O)NC[C@H](C)Oc2ccccc2F)ccc1=O |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COc1ccc(CNC(=O)N[C@H]2C[C@H](C)N(c3ccccc3)C2=O)cc1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[NH2+][C@H](Cc1ncnn1C)C1([NH+]2CCCC2)CCCC1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1c(C)nc(-n2nc(C)cc2NC(=O)c2ccco2)nc1[O-]
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [4*][C@@H](C)c1ccc(C#N)cc1
### Response:
CCc1cccc(C)c1NC(=O)C[NH+](CC)[C@@H](C)c1ccc(C#N)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCOCC(=O)N[C@@H]1CCCC[C@@H]1OC1CCCC1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccccc1[C@@H](C)CC(=O)N1CCc2ccc([N+](=O)[O-])cc2C1
### Response:
4 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(NCc1ccsc1)c1csc(C#CCO)c1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCSc1nc(=O)c2c([nH]1)NC1=C(C(=O)CC(C)(C)C1)[C@@H]2c1cccc(OC)c1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12c([nH]cc2/C=N/n2c(nnc2C)C)c(ccc1)CC
### Response:
CCc1cccc2c(/C=N/n3c(C)nnc3C)c[nH]c12 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[S@@](=O)[C@@H]1CCC[C@H](NC(=O)N2CCSCC2)C1
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CN1CC[NH+](Cc2cccc(O)c2)CC1)Nc1ccncc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](C(=O)Nc1cccc2ccccc12)[NH+]1CCNC(=O)C1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(CSc1oc2ccccc2n1)N/N=C\c1cc(cc(Br)c1[O-])Br
### Response:
O=C(CSc1nc2ccccc2o1)N/N=C\c1cc(Br)cc(Br)c1[O-] |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@@H]2C[C@H](C1)C[C@H]2CNc1nc(ncc1F)Cl
### Response:
Fc1cnc(Cl)nc1NC[C@@H]1C[C@H]2CC[C@@H]1C2 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
O=C1OC[C@H](Cc2ccccc2)N1CN1CCN(c2ccc(F)cn2)CC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CC([4*])(C)C
Fragment 2: [4*][C@H](C)c1c(C)noc1C
### Response:
Cc1noc(C)c1[C@@H](C)NC(=O)NCC(C)(C)NS(C)(=O)=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@@H]1CCCCN1C(=O)COc1ccc(Br)cc1Br
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1C[C@H]1C(=O)Nc1cccc(C(=O)NCC(C)(C)c2cccs2)c1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@@H]1CCCN1[5*]
Fragment 2: [5*]NCc1ccc([16*])cc1
### Response:
COc1ccccc1Oc1ccc(CNC(=O)[C@@H]2CCCN2C(=O)C2CCCC2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CCCCN(CC)C(=O)CNC(=O)c1ccc2c(c1)OCO2
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC[NH2+]Cc1cncc(N2CCC(C)(CC)CC2)n1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
C/C(=C\c1ccccc1)C(=O)Nc1ccc([N+](=O)[O-])cc1C
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@]1(C(=O)N/N=C/c2cccs2)CC1(Br)Br
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cccc(-c2nc(CC(=O)NC3(C#N)CCCCC3)cs2)c1
### Response:
2 |
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