task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCn1c(C[C@H](O)CCSC)nc2ccccc21
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Fc1ccc(-c2csc(N3CCN(C(=S)NCc4ccccc4)CC3)n2)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
Cc1n[nH]c(C)c1CCC(=O)N(C)Cc1csc2ccccc12
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@H](C)CN(C(=O)C[NH+](CCC#N)CC(C)(C)C)C1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc2c3c1O[C@H]1[C@@H](O)CC=C[C@@]31CC[N+](C)(C)C2
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(=O)Nc1ccc(SCc2nc3ccsc3c(=O)[nH]2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
NC(=O)c1ccc(SCC(=O)Nc2ccc3c(c2)Cc2ccccc2-3)c([N+](=O)[O-])c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
Cc1ccc(N)c(S[C@H]2CC[NH2+]C2)c1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1c(F)cccc1NC(=O)NCc1cnn(-c2ccccc2)c1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1ccccc1NC(=O)[C@]12CC[C@H](c3nc(C#N)c(C#N)nc31)C2(C)C
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(=O)NN=Cc1ccc2c(c1)OCCO2
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCc1nnc2n1CC[NH+]([5*])CC2
Fragment 2: [1*]C(=O)c1ccccn1
### Response:
O=C(NCc1nnc2n1CC[NH+](Cc1cccs1)CC2)c1ccccn1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cccc(C(=O)NCCc2nc(-c3ccccn3)cs2)c1O
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CC(C)[NH+](CC(N)=O)CC(=O)N(C)c1ccc([N+](=O)[O-])cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCOC(=O)c1cc2sccc2n1CC(=O)N1CCc2ccccc21
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(Cc2cccc([C@H]3CCCN3S(=O)(=O)c3cn(C)cn3)n2)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc2nc(SCC([O-])=O)n(c(=O)c12)CCCCC
### Response:
CCCCCn1c(SCC(=O)[O-])nc2ccccc2c1=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cc(Br)c([C@H]2OCC[C@@H]2CO)cc1OC
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C([C@@H]1[C@H](C1)c1ccc(cc1)F)NCC(C)(C)NC(OC(C)(C)C)=O
### Response:
CC(C)(CNC(=O)[C@H]1C[C@@H]1c1ccc(F)cc1)NC(=O)OC(C)(C)C |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(c1c[nH]c2nccc(Cl)c12)N1CC[C@H](c2ccc(F)cc2)C1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[C@@H](C[NH+](C)C)C(=O)[O-]
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C[C@H]1CCCO1
Fragment 2: [8*]CN1C(=O)N=C2S[C@H]([13*])C(C)=C2C1=O
### Response:
CC1=C2C(=O)N(C[C@H]3CCCO3)C(=O)N=C2S[C@@H]1C(=O)[O-] |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
O=C(N[C@H]1CC[NH+](CC2CC2)C1)c1ccc(OCC(F)F)nc1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nc2ccccc2n1CC(=O)N(C)CCC[NH3+]
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
OCCN(Cc1cccnc1)c1cnc2ccccc2n1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H]([8*])CC
Fragment 2: [8*]C(C)(C)C
### Response:
CC[C@@H](NC(=O)C(=O)Nc1cnc(C(C)(C)C)nc1)c1nc(C)cs1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cn1cc(C(=O)NC2CCCCC2)cn1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COCCN1C(=O)C(C#N)=C(C)/C(=C\Nc2ccc(C)c([N+](=O)[O-])c2)C1=O
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(nc1)[C@H](C#N)C(=O)CCC(=O)c1ccc(c(C)c1)C
### Response:
Cc1ccc(C(=O)CCC(=O)[C@@H](C#N)c2ccccn2)cc1C |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1([C@H](C)N[C@H]2C(=O)N(CCC2)c2ccn(n2)C)ccc(cc1)-n1cncc1
### Response:
C[C@H](N[C@@H]1CCCN(c2ccn(C)n2)C1=O)c1ccc(-n2ccnc2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1C[C@@H]2CCCC[C@]21[13*]
Fragment 2: [16*]c1ccccc1
### Response:
COc1ccc(CNC(=O)N2C[C@@H]3CCCC[C@]32c2ccccc2)cc1OC |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)c1nnc([O-])c2c1cnn2-c1ccccc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1c(SCc2ccc(cc2)OC)n(c(c2cc(OC)c(cc12)OC)=O)N
### Response:
COc1ccc(CSc2nc3cc(OC)c(OC)cc3c(=O)n2N)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(-c2csc(-n3c(NC(=O)CC4CCCC4)cnc3C)n2)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)C[C@](C)(O)CNC(=O)CC[C@H](C)O
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](NC(=O)NCC(C)(C)[NH+](C)C)C(=O)N1CCCC[C@H]1C
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC1=NN(C(=O)c2c(I)cnn2C)[C@@](O)(C(F)(F)F)C1
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nc(CC(=O)N2CCC3(CC2)CC(=O)N(C[C@H]2CCCO2)C3)cs1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12ccc(cc1ccc(c2)CNC(/C=C/c1nc2c(nc1)cccc2)=O)OC
### Response:
COc1ccc2cc(CNC(=O)/C=C/c3cnc4ccccc4n3)ccc2c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[8*]
Fragment 2: [16*]c1cccc(O)c1
### Response:
CCN(CC)C(=O)[C@@H]1C[C@@H]([NH3+])CN1C(=O)Cc1cccc(O)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCC[8*]
Fragment 2: [1*]C(=O)C1CCN([5*])CC1
### Response:
O=C(NCCc1ccccc1)C1CCN(C(=O)c2cc3oc(-c4ccccc4)cc3[nH]2)CC1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
C[C@@H]1CCCCN1c1ccc(NC(=S)NC(=O)c2ccco2)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCO[C@@H](C1)C[NH+](C[C@@H](CS)CC)C
### Response:
CC[C@H](CS)C[NH+](C)C[C@@H]1CCCCO1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(c2ccccc21)C/[NH+]=C(/N[C@H]1c2ccccc2OCC1)N
### Response:
N/C(N[C@@H]1CCOc2ccccc21)=[NH+]\Cc1cccc2ccccc12 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NS(=O)(=O)c1cnn(C)c1
Fragment 2: [4*][C@@H](C)c1ccc(C)o1
### Response:
Cc1ccc([C@H](C)NS(=O)(=O)c2cnn(C)c2)o1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccccc1/C=C/C(=O)Nc1cccc(CCC(=O)N(C)C)c1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
CCC[C@@H](CS)C[NH+](C)Cc1ccncc1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(C[NH+](C[C@@H](O)Cn2cccn2)C2CC2)cc1C
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc([16*])cc1
Fragment 2: [5*]Nc1ccc(OC)c(OC)c1
### Response:
C#CCOc1ccc(C(=O)Nc2ccc(OC)c(OC)c2)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccc(OC)c1Cl)C(=O)NC(=S)Nc1c(cc2nn(-c3ccc(cc3)F)nc2c1)C
### Response:
COc1ccc(C(=O)NC(=S)Nc2cc3nn(-c4ccc(F)cc4)nc3cc2C)cc1Cl |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@](N)(C(=O)Nc1cnn(C[C@@H]2CCCO2)c1)C(F)(F)F
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)(C)OC(=O)N1CC[C@H](CCI)C1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC[C@@H](C)NC(=O)C1=NNC(=O)CC1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)c1cc(C)nc(N[C@@H]2CCC[NH+](Cc3cccc(OC)c3)C2)n1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CCOc1cccc(/C=N/c2ccc3c(CCC3)c2)c1O
### Response:
CCOc1cccc(/C=N/c2ccc3c(c2)CCC3)c1O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(C)c(NC(=O)CCN2CC[S@](C(C2)(C)C)=O)c1
### Response:
Cc1ccccc1NC(=O)CCN1CC[S@@](=O)C(C)(C)C1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CN(C)C(=O)c1ccc2c(c1)[C@H]1C=CC[C@H]1[C@@H](c1ccccc1OCc1ccccc1)N2
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CCO[3*]
Fragment 2: [3*]Oc1ccc(C)cc1
### Response:
Cc1ccc(OCCC(=O)NC2COC2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COc1ccc(C(=O)N2CCC(OCc3ccccc3OC)CC2)cn1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccccc1C(=O)Nc1nc2c(s1)CN(C)CC2
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CO[C@@H](CNC(=O)/C=C/c1cccc([N+](=O)[O-])c1)c1ccc(F)cc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1([C@H]2N(C(=O)Nc3cc4CCCc4cc3)CCC2)cc2c(cc1)OCCO2
### Response:
O=C(Nc1ccc2c(c1)CCC2)N1CCC[C@H]1c1ccc2c(c1)OCCO2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(C[NH+]1CCC(C(=O)N2CCCCCC2)CC1)Nc1cccc2ccccc12
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CC[8*]
Fragment 2: [16*]c1ccccc1
### Response:
O=C(CCc1nc(-c2ccccc2)no1)N1CCN(Cc2ccc3c(c2)CCO3)CC1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
[NH3+]C[C@@H](c1ccccc1)[NH+]1CCCCCC1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1ccc(Cl)c(CC)c1NC(=O)C[C@@H]1CCS(=O)(=O)C1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [10*]N1CCCC1=O
Fragment 2: [7*]Cc1ccc([16*])cc1
### Response:
O=C(/C=C/c1ccc(N2CCCC2=O)cc1)NCC(=O)Nc1cccnc1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COCCc1nnc(S[C@@H]2CCCc3ccccc32)n1N
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)c1sc(S(=O)(=O)N2CCC(C(N)=O)CC2)c(C(=O)OC)c1C
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cc2sc(NC(=O)CC(C)C)nc2cc1Cl
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C1=C(c2ccccc2)NC(=O)N[C@H]1[13*]
Fragment 2: [3*]OCC
### Response:
CCOC(=O)C1=C(c2ccccc2)NC(=O)N[C@H]1c1cc(Cl)cc(Cl)c1OC |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1(CCC(=O)NCc2cc(ccc2)F)c2c(cccc2)n(C)c(=O)c1=O
### Response:
Cn1c(=O)c(=O)n(CCC(=O)NCc2cccc(F)c2)c2ccccc21 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CC([6*])=O
Fragment 2: [16*]c1ccc(Cl)cc1[16*]
### Response:
Cc1ccc(C(=O)COc2ccc(Cl)cc2N2C(=O)[C@H]3CCCC[C@@H]3C2=O)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1cc(C(=O)N2CCC[C@H]2Cc2cccc(F)c2)ccc1=O
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Nc1ncc(Cc2cccc(F)c2)c(N)n1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCC[C@H]2CCC[C@@H]21
Fragment 2: [14*]c1ccco1
### Response:
O=C(NC[C@H](c1ccco1)[NH+]1CCCC1)N1CCC[C@H]2CCC[C@@H]21 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@H]1CCC[C@@H]([S@@](=O)CC)C1
Fragment 2: [5*]N[C@H]1CCC[C@@H]([S@@](=O)CC)C1
### Response:
CC[S@](=O)[C@@H]1CCC[C@H](NC(=O)N2CC[C@H](c3ccccc3OC)C2)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1cccc(OC)c1=O
Fragment 2: [1*]C(=O)[C@H]([8*])CC
### Response:
CC[C@H](C(=O)NC(C)(C)C)n1cccc(OC)c1=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOC(=O)NCCCn1c(C)cc2ccccc21
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccccc1[C@@H]1C[NH+](Cc2cc(C(C)=O)cn2C)C[C@H]1C(=O)[O-]
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC[C@@H](C)[NH+](C)CCNC(CC1CCC1)=O
### Response:
CC[C@@H](C)[NH+](C)CCNC(=O)CC1CCC1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
C[C@H]1CCCN(C(=O)CSc2nnc(-c3ccc([N+](=O)[O-])cc3)o2)C1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)(C)NC1=CC(=O)OC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1cccc(C(=O)c2ccc(O)cc2)c1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1[nH+]cn(C[C@@H](C)[NH2+][C@@H](c2cccc(F)c2)c2ccccn2)c1C
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1C(N)=C([C@@H](C2C=1ONC=2C(C)(C)C)c1cccnc1)C#N
### Response:
CC(C)(C)C1=C2C(=NC(N)=C(C#N)[C@@H]2c2cccnc2)ON1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](C(=O)C1=c2ccccc2=[NH+]C1)[NH+]1CCC[C@@H]1[C@@H]1CC=CS1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCN([5*])CC1
Fragment 2: [12*]S(=O)(=O)c1ccc2ccccc2c1
### Response:
CCCCS(=O)(=O)N1CCN(S(=O)(=O)c2ccc3ccccc3c2)CC1 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
O=C1N=C([O-])[C@]2(Cc3cc([N+](=O)[O-])ccc3N3CCOC[C@@H]32)C(=O)N1c1ccc(Cl)cc1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(N2C(SCC(=O)Nc3ccc(Br)cc3)=N[C@@H]3CS(=O)(=O)C[C@H]32)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1nc(-n2ccnc2C#N)ccc1N
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CN(CC#CCNC(=O)CSC1CCCC1)Cc1ccccc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(C[C@@H](C(C)(C(OC)=O)C)CCC1)C(=O)CSCc1cscn1
### Response:
COC(=O)C(C)(C)[C@H]1CCCN(C(=O)CSCc2cscn2)C1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C(NCC#Cc1ccccc1)NC[C@@H]1C[C@@]12CCc1ccccc12
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1nc2sc(C)c(C)c2c(=O)[nH]1
Fragment 2: [11*]Sc1nnc([14*])s1
### Response:
Cc1sc2nc(CSc3nnc(NC4CC4)s3)[nH]c(=O)c2c1C |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Cc1ccc(C)c(C[NH2+][C@H](C)c2ccc(C)c(F)c2)c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cc(NC(=O)C(=O)c2ccc(C(C)(C)C)cc2)n(C)n1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]ON(C[8*])CC(=O)OC
Fragment 2: [16*]c1ccccc1
### Response:
COC(=O)CN(Cc1ccccc1)Oc1ccc(Cl)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC[C@]1(O)CC[C@@H](C)C[C@H]1C
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccc(cc1)-c1nc([nH]c1)SCC(=O)Nc1cccc(Cl)c1
### Response:
O=C(CSc1nc(-c2ccccc2)c[nH]1)Nc1cccc(Cl)c1 |
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