task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N1[C@@H](CCC1)C(O[C@@H]1CCC[C@H](OC)C1)=O)(C(C)C)=O
### Response:
CO[C@H]1CCC[C@@H](OC(=O)[C@@H]2CCCN2C(=O)C(C)C)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C([O-])C12C[C@H]3C[C@@H](C1)CC(n1cc([N+](=O)[O-])cn1)(C3)C2
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC[C@@H](C)NC(=O)[C@H]1CSCN1C(=O)[C@H]1SCCc2sccc21
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COCC[C@H](NC(=O)N1CCN2C(=O)NC[C@H]2C1)C(=O)[O-]
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(-c2oc(C(=O)Nc3cc(S(=O)(N)=O)c(OC)cc3)cc2)ccc(Cl)cc1
### Response:
COc1ccc(NC(=O)c2ccc(-c3ccc(Cl)cc3)o2)cc1S(N)(=O)=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1ccc(CNC(=O)N[C@@H](CC)c2ccncc2)cc1C
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccccc1N1C[C@H]2C[C@@H]1C[NH2+]2
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(=O)Nc1cccc(NC(=O)c2cccc(C(F)(F)F)c2)c1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
CCCCN(C)c1ncnc(Nc2cccnc2Cl)c1[N+](=O)[O-]
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
S([C@H](C(C)C)C(=O)N[C@@H](c1ccccc1)C)c1nc(C(F)(F)F)ccn1
### Response:
CC(C)[C@@H](Sc1nccc(C(F)(F)F)n1)C(=O)N[C@H](C)c1ccccc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[NH+](CC)C(C)(C)[C@@H](O)c1cc(F)ccc1F
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccc(Cl)s1
Fragment 2: [16*]c1ccccc1
### Response:
C[C@H](NC(=O)[C@H](Cc1ccccc1)n1cnnn1)c1ccc(Cl)s1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCN(CCN1CCCc2ccccc21)[C@@H]1CCS(=O)(=O)C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
S(c1nnc(Cc2nc(sc2)C)o1)[C@@H](C(NCC(C)C)=O)C
### Response:
Cc1nc(Cc2nnc(S[C@H](C)C(=O)NCC(C)C)o2)cs1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](CNC(=O)N1CCN(S(C)(=O)=O)CC1)N1CCOCC1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CCc1nc(CCSC)n(CCc2ccccc2)n1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
Cc1nc(-c2ccc(F)cc2)sc1[C@H](C)N[C@H]1CCCS(=O)(=O)C1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cc(Br)ccc1NC(=O)[C@@H](C)[NH+](C)Cc1cccs1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc2c(c1)-c1onc(C(=O)N[C@H](C)C(C)C)c1CC2
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(cc(cc1)N(C)C)CN/C(N1CCC(CC1)OCC)=[NH+]/C
### Response:
CCOC1CCN(/C(NCc2cccc(N(C)C)c2)=[NH+]\C)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccccc1Cl
Fragment 2: [5*]NCc1ccc([16*])cc1
### Response:
O=C(NCc1ccc(N2CCOCC2)cc1)Nc1ccccc1Cl |
functional_group | ### Instruction:
Does the molecule contain a ether group?
Cc1ccn2/c(=N/C(=O)c3cccc(C[NH+]4CCCC4)c3)[nH]nc2c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCCOCc1ccccc1CNC(=O)[C@H]1C[C@H]2CC[C@@H]1C2
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@@H]1(CCc2c(cc(cc21)Cl)Cl)[NH2+][C@H](CC)CO
### Response:
CC[C@H](CO)[NH2+][C@H]1CCc2c(Cl)cc(Cl)cc21 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CCOC(=O)c1c(NC(=O)c2cc(Cl)ccc2OC)sc2c1CCS(=O)(=O)C2
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H]1CCCN(C(=O)C2C(C)(C)C2(C)C)[C@@H]1C[NH3+]
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N)([C@@H]1C[C@@H](CN1C(=O)OCCO)O)=O
### Response:
NC(=O)[C@@H]1C[C@H](O)CN1C(=O)OCCO |
functional_group | ### Instruction:
Does the molecule contain a halide group?
C=CCN(C(=O)Cc1csc(-c2ccccc2Cl)n1)[C@H]1CCS(=O)(=O)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1nc([14*])c([14*])s1
Fragment 2: [16*]c1ccccc1
### Response:
COc1ccccc1OCC(=O)Nc1nc(-c2ccccc2)c(C(C)=O)s1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC1CCCCC1
Fragment 2: [1*]C(=O)c1cc2cc(Cl)cnc2[nH]1
### Response:
O=C(NC1CCCCC1)C1CCN(C(=O)c2cc3cc(Cl)cnc3[nH]2)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(-c2ccc(cc2)[C@H](C)NS(=O)(CCC(C)(C)C)=O)cncc1
### Response:
C[C@H](NS(=O)(=O)CCC(C)(C)C)c1ccc(-c2cccnc2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@@H]1Cc2ccccc2S1
Fragment 2: [5*]N(C)CC[NH2+]C
### Response:
C[NH2+]CCN(C)C(=O)[C@@H]1Cc2ccccc2S1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CCOc1ccccc1CN1CCC[C@@H](c2nnc(Cn3ccnc3)n2C)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ccccc1
Fragment 2: [7*]C1SC(N2CCCCC2)=NC1=O
### Response:
O=C1N=C(N2CCCCC2)S/C1=C\c1ccc(OCc2ccccc2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
C[C@H](OC(=O)[C@@H]1C[C@H]2CC[C@@H]1O2)c1ccc(Cl)s1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCC[C@@H]1CCC[C@H]1NC(=O)NCCNC(C)=O
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Nc1cccc(Cl)c1)Nc1nc(C(=O)N2CCCC2)cs1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[NH2+]1[C@@H](C(=O)[O-])CS[C@@H]1[C@@H](C)c1ccccc1
### Response:
C[C@@H](c1ccccc1)[C@@H]1[NH2+][C@@H](C(=O)[O-])CS1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*]Nc1ccc(F)c([N+](=O)[O-])c1
### Response:
Cc1ccc(NC(=O)CSCC(=O)Nc2ccc(F)c([N+](=O)[O-])c2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1nc(SCC(=O)NCc2nc(-c3cccs3)n[nH]2)c(C#N)c(C)c1C
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1N(CCOC1)C(=O)N1CC[NH+](CC1)CC(Nc1cc(ccc1Cl)Cl)=O
### Response:
O=C(C[NH+]1CCN(C(=O)N2CCOCC2)CC1)Nc1cc(Cl)ccc1Cl |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccccc1N1CC[C@H](NC(NNC(=O)CCCc2ccccc2)=O)C1=O
### Response:
O=C(CCCc1ccccc1)NNC(=O)N[C@H]1CCN(c2ccccc2)C1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(C)c([C@H](O)[C@H]2C[NH+](C)CCN2C)c1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC(C)c1cc(C(=O)N(c2ccc(O)cc2)S(=O)(=O)c2ccccc2)n[nH]1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(-n2nc(C)c3c2C[C@H](c2cc(OC)c(OC)c(OC)c2)CC3=O)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@@H]1CCCOC1
Fragment 2: [1*]C(=O)CC[8*]
### Response:
CCS(=O)(=O)CCN(C)C(=O)CC[C@@H]1CCCOC1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
C[C@@H](C1CC1)[NH+](CC(=O)Nc1nccs1)C1CC1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@H](Sc1cc(C)c2cccc(C)c2n1)C(=O)Nc1nc2ccc(S(N)(=O)=O)cc2s1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH2+][C@@H]1CC[C@@H](C)C[C@H]1CN(C)C[C@@H]1CCC[NH+]1C
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(C(NCCN2C(=O)CCC2=O)=O)[C@H](CCC1)c1cccc(Cl)c1
### Response:
O=C1CCC(=O)N1CCNC(=O)N1CCC[C@@H]1c1cccc(Cl)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1(SC(=[NH+]C1)N1CCN(CC1)Cc1ncccc1C(F)(F)F)(C)C
### Response:
CC1(C)C[NH+]=C(N2CCN(Cc3ncccc3C(F)(F)F)CC2)S1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1c(C(=O)N2CCO[C@@H](C)C2)cnn1-c1cccc(Cl)c1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCO[C@@H]1CCCN(c2ccc(S(N)(=O)=O)c(N)c2)C1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@]1(c2ccc(Cl)c(Cl)c2)NC(=O)N(Cc2cccc(F)c2F)C1=O
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)(C)[C@H]1CCC2=C3C(=O)N=C(CCC(=O)N4CCCCCC4)N=C3S[C@H]2C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O(C)CC[C@H]([NH2+][C@H]([C@@H](c1cc(F)c(cc1)F)O)C)C
### Response:
COCC[C@@H](C)[NH2+][C@@H](C)[C@H](O)c1ccc(F)c(F)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1nc([14*])cs1
Fragment 2: [1*]C(=O)C[8*]
### Response:
CC(=O)Nc1nc(CC(=O)NCc2cccnc2)cs1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COCc1ccc(C[NH+]2CCC([C@@H](O)C(=O)OC)CC2)o1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*]Nc1ccc([16*])cc1
### Response:
NC(=O)c1ccc(NCC(=O)Nc2ccc(N3CCCC3)cc2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CCC
Fragment 2: [14*]c1nc([S-])c2c3c(sc2n1)CCCC3
### Response:
CCCc1nc([S-])c2c3c(sc2n1)CCCC3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C1C[C@@H]([NH2+]Cc2cccnc2)C(=O)N1c1ccc(Cl)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CSC[C@@H]1CCN(c2cc[nH+]c(CN3CCN(C(C)=O)CC3)c2)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[NH+]1CCC[C@@H](CNC(=O)c2cc(Cl)ccc2OC(F)F)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C/[NH+]=C(/NCCS(C)(=O)=O)N1C[C@H](C)C[C@@H](C)C1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
C[NH2+]C[C@H](C)C(=O)N1CCc2cc(C(=O)[O-])ccc21
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
C[NH2+]CCOc1c(C)cc(C)cc1Br
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@H](C)(n1ncc(c1C1CC1)C(=O)NC1CC[NH+](CC(N)=O)CC1)CC
### Response:
CC[C@@H](C)n1ncc(C(=O)NC2CC[NH+](CC(N)=O)CC2)c1C1CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1
Fragment 2: [5*]N(C)C[8*]
### Response:
COCCN1C[C@@H](C(=O)N(C)Cc2ccc(F)cc2)CC1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
N#CCc1ccc(OC[C@@H](O)C[NH+]2CCc3cncnc3C2)cc1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@@H](n2c(nc3c2cc(C)cc3)CCCl)CCCO1
### Response:
Cc1ccc2nc(CCCl)n([C@H]3CCCOC3)c2c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC[S@](=O)[C@H]1CCCC[C@@H]1NC(=O)[C@@H]1CCOc2ccccc21
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](N1CCN(Cc2cccc(-c3ccncc3)c2)CC1)C(F)(F)F
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Cc1ccc([C@@H](C)NC(=O)N[C@@H](CCO)c2cccs2)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COc1ccc(CNC(=O)c2csc(NC(C)C)n2)cc1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [11*]S[C@H]1CC(=O)c2ccccc2C1=O
Fragment 2: [4*]CCC(=O)[O-]
### Response:
O=C([O-])CCS[C@H]1CC(=O)c2ccccc2C1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(C(=O)C2=C([O-])C(=O)N(Cc3ccco3)[C@H]2c2ccccc2[N+](=O)[O-])cc1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
COc1ccc(OCCNC(=O)N[C@H](C)c2cn(C)nc2C)cc1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cn1c(=O)n(C)c2cc(C(=O)N3CCC[C@@H](n4nc(-c5ccco5)ccc4=O)C3)ccc21
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C=CC[NH+](CC(=O)[O-])[C@H](C)c1ccc(F)cc1O
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(N2C=C(C[NH+](C)CC3N=CC=N3)[C@@H](c3ccc(F)cc3)N2)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
NC(=O)c1nc(-c2cc(Br)ccc2F)nc2c1[nH]c(=O)n2-c1ccc(F)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(c(OC)cccc1)-n1c2c(c(-c3ccccc3)c1)c(SCC)ncn2
### Response:
CCSc1ncnc2c1c(-c1ccccc1)cn2-c1ccccc1OC |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCS(=O)(=O)N1C[C@H](C)C[C@H](C)C1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(C)C(=O)Nc1ccc(cc1)C1(C(N(C)C)=O)CCCCC1
### Response:
CC(C)C(=O)Nc1ccc(C2(C(=O)N(C)C)CCCCC2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cccc(/C=C(\C[NH2+]C(C)C)C(C)C)c1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(C)n2cc(CSC3=NC(=O)CC(N)=N3)nc2n1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)CS(=O)(=O)[N-]c1ccc(Br)c(C)n1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CN(C(=O)[C@H]1NC(=O)N1CCC[C@@H](C1)CCO)c1c(F)cccc1F
### Response:
O=C(N[C@H]1CCN(c2c(F)cccc2F)C1=O)N1CCC[C@H](CCO)C1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CC(C)c1cccc2c1OCC[C@H]2[NH2+]C[C@H]1CN2CCN1CC2
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(C(=O)N[C@H]2CCCC[C@H]2C(C)(C)C)cc1OC
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Fc1cccc(c1)/C(=C\C(O[C@@H](C)CC#C)=O)C
### Response:
C#CC[C@H](C)OC(=O)/C=C(/C)c1cccc(F)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cccc(N2CCN(C(=O)Cc3cccc(OCC#N)c3)CC2)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(nc(OC)ccc1C(=O)N1CCC(CN2C(CCC2)=O)CC1)OC
### Response:
COc1ccc(C(=O)N2CCC(CN3CCCC3=O)CC2)c(OC)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[N+](=O)([O-])c1cnc(N/N=C\c2ccc(cc2)O[C@@H](CC)C)cc1
### Response:
CC[C@@H](C)Oc1ccc(/C=N\Nc2ccc([N+](=O)[O-])cn2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(CC[C@@H]1CCCO1)Nc1ccccc1COc1ccccc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1cc(Br)c(C[NH2+][C@@H](C)c2ccc(F)cc2)cc1OC
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@@H]2CCCC[C@@H]2[NH+]1CC(=O)Nc1ccc(C(=O)N(C)C)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(CNC(=O)COc2cccnc2[N+](=O)[O-])cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [8*]C(F)(F)F
### Response:
Nc1nc(SCC(=O)Nc2cccc(C(F)(F)F)c2)[nH]c(=O)c1NC(=O)c1ccc(F)c(F)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(-c2nnc([C@@H](C)OC(=O)c3cc(S(N)(=O)=O)ccc3C)o2)cc1
### Response:
2 |
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