task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
functional_group | ### Instruction:
Does the molecule contain a nitro group?
C[C@H](OC(=O)c1ccccc1OC1CCC1)c1nccs1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(Cl)cc1/N=C(\[S-])Nc1cccc(C)c1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCC
Fragment 2: [4*]Cc1cccnc1N[5*]
### Response:
CCCNc1ncccc1C[NH+]1C[C@@H](C)[C@@H](C)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(N[C@@H]1CCS(=O)(=O)C1)c1ccc(OC2CCCCC2)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(C[NH+]1C[C@H]2CC[C@@H]1CN(C(=O)C1CCC1)C2)NCCc1ccccc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1cc(/C=C(\C#N)C(=O)Nc2cccc([N+](=O)[O-])c2)c(Br)cc1O
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(ccc1NC(NC1CC1)=O)[C@@H](C)NC(NC1CC1)=O
### Response:
C[C@@H](NC(=O)NC1CC1)c1ccc(NC(=O)NC2CC2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCN1CCN(C(=O)c2n[nH]c(C(C)C)n2)C[C@H]1C
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1cccc(C(=O)N(C)[C@H](C)c2ccccc2F)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(Cl)cc(c1[C@@H]1CC(=O)NC2=NC(=NC([C@@H]12)=O)SC)Cl
### Response:
CSC1=NC(=O)[C@@H]2C(=N1)NC(=O)C[C@H]2c1ccc(Cl)cc1Cl |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COc1ccc(O)c(C[NH2+][C@@H]2CCOc3c(OC)cccc32)c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(C)cc(N2CC[C@H](NC(=O)c3sccc3C)C2=O)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C([O-])c1ccc(C[C@H]2SC(=O)N(c3ccccc3)C2=O)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
O=C([O-])[C@H]1C=C[C@H](NS(=O)(=O)c2ccc3c(c2)CCO3)C1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)c1ccc(NC(=O)N(C)[C@H](C)c2ccc(-n3cncn3)cc2)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(CNC(c2cc([N-]S(=O)(=O)CC3CCC3)ccc2)=O)ccccc1
### Response:
O=C(NCc1ccccc1)c1cccc([N-]S(=O)(=O)CC2CCC2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(OC)cc1OC
Fragment 2: [5*]Nc1nc([14*])cs1
### Response:
COc1ccc(-c2csc(NC(=O)Cc3ccc(SC)cc3)n2)c(OC)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(C)(OC(NC[C@]1(CCCC[C@@H]1C)NC(C1C[C@@H](O[C@H](C)C1)C)=O)=O)C
### Response:
C[C@@H]1CC(C(=O)N[C@]2(CNC(=O)OC(C)(C)C)CCCC[C@@H]2C)C[C@H](C)O1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(CC(=O)Nc2ccnc(N(C)C)n2)s1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
CCC[C@H](CC(=O)OC)NC(=O)c1ccc(C#N)[n-]1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCc1cc2c(=O)n(-c3cccc(Cl)c3)c(=O)n(CC(=O)Nc3ccccc3C(=O)OC)c2s1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [1*]C(=O)c1ccc(N[5*])cc1
### Response:
CCOC(=O)[C@@H]1CCCN(C(=O)c2ccc(NC(=O)Cc3ccccc3)cc2)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(ccco1)C[NH+]1Cc2c3c(ccc2OC1)c(CCC)cc(=O)o3
### Response:
CCCc1cc(=O)oc2c3c(ccc12)OC[NH+](Cc1ccco1)C3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(nc(c1)OCC(F)F)CNC(=O)NC[C@@]1(C)CCCO1
### Response:
C[C@]1(CNC(=O)NCc2cccc(OCC(F)F)n2)CCCO1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCOC(=O)[C@@H](C#N)c1c(F)c(F)c(Br)c(F)c1F
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(C(=O)OCc2cc(-c3ccc4c(c3)O[C@H](C)C4)on2)no1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1cccc(N[5*])c1
Fragment 2: [16*]c1ccc(OC)c(F)c1
### Response:
COc1ccc([C@H](C)[NH2+]Cc2cccc(NC(=O)N(C)C)c2)cc1F |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Nc1c(C(=O)N[C@@H](CO)c2ccccc2F)cccc1[N+](=O)[O-]
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1C[C@@H](NC(=O)NCCc2ccc(O)cc2)CN1c1ccccc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Cc1nc2n(cc(s2)C)c1C[NH+](Cc1ccccc1)CC1(O)CCOCC1
### Response:
Cc1cn2c(C[NH+](Cc3ccccc3)CC3(O)CCOCC3)c(C)nc2s1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COc1cc(F)cc(C[NH2+]Cc2cccnc2)c1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C[C@@H](CC)N(c1[nH+]ccc([C@@H](O)C)c1)CC
### Response:
CC[C@H](C)N(CC)c1cc([C@H](C)O)cc[nH+]1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(S(=O)(=O)NCCc2cc(N(C)C)nc(-c3ccccn3)n2)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C(=O)CSc1nnc(-c2ccccc2F)n1C)[C@H]1CCCc2ccccc21
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CCc1ccc([C@@H]2C[C@H](C)CCN2c2ncc([N+](=O)[O-])c(N)n2)o1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amine group?
C[C@@H](OC(=O)c1ccc(N2CCOCC2)c(F)c1)C1CCOCC1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccccc1C
Fragment 2: [5*]N1C([S-])=C(C#N)C(=O)N[C@H]1[13*]
### Response:
COc1cccc([C@@H]2NC(=O)C(C#N)=C([S-])N2c2ccccc2C)c1 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
Cc1ccccc1NC(=O)c1cccc(S(=O)(=O)N(C)c2cccc(Cl)c2)c1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C([7*])C#N
Fragment 2: [5*]Nc1cccc([N+](=O)[O-])c1
### Response:
COc1cccc(/C=C(\C#N)C(=O)Nc2cccc([N+](=O)[O-])c2)c1OC |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(c1ccc(cc1)C(N1CC[C@](F)(C1)C(OC)=O)=O)N(CC)CC
### Response:
CCN(CC)C(=O)c1ccc(C(=O)N2CC[C@@](F)(C(=O)OC)C2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCc1nn(C)c(C[C@]2(C[NH3+])CCCC(C)(C)[C@@H]2O)c1Cl
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1cncn1
Fragment 2: [5*]N1CCC[C@H]([15*])C1
### Response:
O=C([C@H]1CCOc2ccccc21)N1CCC[C@H](n2cncn2)C1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CNC(=O)[C@@H]1CCCN(C(=O)Nc2nn(-c3ccccc3Cl)cc2C)C1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1nc([C@@H]2CCCO2)sc1NC(=O)C(C)(C)C
### Response:
CC(C)(C)C(=O)Nc1nnc([C@@H]2CCCO2)s1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc(OC)cc1
Fragment 2: [1*]C(=O)[C@@H]1CC(=O)N(N2CCN(C)CC2)/C(=N/c2ccccc2)S1
### Response:
COc1ccc(NC(=O)[C@@H]2CC(=O)N(N3CCN(C)CC3)/C(=N/c3ccccc3)S2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Cc1nc2n(n1)C[C@@H](Nc1nc3c(cnn3C(C)(C)C)c(=O)[nH]1)CC2
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc2c(C)nc(Nc3nc(C)cc(C)n3)nc2c1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
Cn1cc(CN2CCN(c3ccc(Cl)c(Cl)c3)CC2)cn1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)C1(N(C)Cc2c[nH]nc2-c2ccc(C)cc2)CCCC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(ccc(Cl)cc1)[C@H](C[NH2+]CC)Cc1scc(n1)C
### Response:
CC[NH2+]C[C@H](Cc1nc(C)cs1)c1ccc(Cl)cc1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CN(c1ccccc1)S(=O)(=O)c1ccc2c(c1)C(C)(C)C(=O)N2
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[8*]
Fragment 2: [5*]Nc1ccc(Cl)cc1F
### Response:
COc1ccc2[nH]cc(CC(=O)Nc3ccc(Cl)cc3F)c2c1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
Cc1ccc(Nc2nc(NCCN3CCOCC3)nc3c2cnn3C)cc1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C/C(=N\Nc1nc(C)cc(C)n1)c1ccc(C#N)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C=C(C)CN(CC)C(=O)[C@H](C)N1CCN(C(=O)C2CCCC2)CC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
C[C@H](CO)[C@@H](C)NC(=O)Nc1cc(-c2ccccc2)on1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)CN(C(=O)Nc1ccc2c(c1)oc(=O)n2C)C1CC1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(C(=O)NC[C@H](CCO)c1ccccc1)[C@@H]1CCCC1(C)C
### Response:
CC1(C)CCC[C@H]1NC(=O)NC[C@H](CCO)c1ccccc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C([O-])CCc1cc2n(n1)CCCN(c1ccc(C(=O)N3CCCC3)cn1)C2
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(C[NH+]1CCC(C(=O)[O-])CC1)Nc1ccccc1Oc1ccccc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cccc(NC(=O)COc2cccc3ccc(N4CCCC4)nc23)c1C
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC[C@@H](C)NC(=O)CSc1ccc2c(c1)OCCO2
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(Oc2ccccc2F)c(F)cc1[N+](=O)[O-]
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(cc(C[NH2+][C@@H](C)c2cscc2)sc1)C([O-])=O
### Response:
C[C@H]([NH2+]Cc1cc(C(=O)[O-])cs1)c1ccsc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(=O)(NCc1occc1)[C@H]1[C@@H](c2ccc(cc2)C)Nn2c(C)nnc2S1
### Response:
Cc1ccc([C@H]2Nn3c(C)nnc3S[C@H]2C(=O)NCc2ccco2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CN1C(SCC2[NH+]=c3ccccc3=[NH+]2)=NN[C@H]1c1cccc(NC(=O)c2ccccc2F)c1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CCOC(=O)[C@@H]1CCCN(C(=O)c2c(-c3c(Cl)cccc3Cl)noc2C)C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
C[C@@H]1CN([C@H](C(N)=O)c2ccc(F)cc2)CCN1Cc1[nH+]ccn1C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C/C=C/CS
Fragment 2: [5*][NH+]1CC[C@@H](C)C1
### Response:
C[C@@H]1CC[NH+](C/C=C/CS)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Clc1cc(c(cc1)OC)Cn1c(nc2c1cccc2)CS(C)(=O)=O
### Response:
COc1ccc(Cl)cc1Cn1c(CS(C)(=O)=O)nc2ccccc21 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(ccc(C)cc1)-c1nc(cs1)CC(OC[C@@H]1CC(N(C1)C1CC1)=O)=O
### Response:
Cc1ccc(-c2nc(CC(=O)OC[C@@H]3CC(=O)N(C4CC4)C3)cs2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1n[nH]c(C)c1NC(=O)NC1(c2ccc(F)cc2F)CCOCC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1n(C)ncc1-c1nc(C(N[C@H](c2cc3c(cc2)OCC(=O)N3)C)=O)cs1
### Response:
C[C@H](NC(=O)c1csc(-c2cnn(C)c2)n1)c1ccc2c(c1)NC(=O)CO2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)CCC(=O)c1ccc(OC)c(OC)c1
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC1C(C1CC1)C(=O)Oc1cc2nccnc2cc1
### Response:
O=C(Oc1ccc2nccnc2c1)C(C1CC1)C1CC1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
O=[N+]([O-])c1ccc(S(=O)(=O)N2CCN(CCO)CC2)cc1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@](Nc1ccc(C(N)=O)nn1)(C(=O)[O-])c1ccccc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(oc(cc1)C[NH2+][C@H](COC)c1ccc(F)c(c1)F)CO
### Response:
COC[C@@H]([NH2+]Cc1ccc(CO)o1)c1ccc(F)c(F)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(N(C1CC1)c1nc(cs1)C)c1ccc(cc1)CNC(C)=O
### Response:
CC(=O)NCc1ccc(C(=O)N(c2nc(C)cs2)C2CC2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COCCN(Cc1ccccc1)C(=O)c1ccc(-c2ccc3c(c2)OCCO3)s1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CC(=O)OC
Fragment 2: [9*]n1c2ccc(OC)cc2c2nc(C)sc21
### Response:
COC(=O)Cn1c2ccc(OC)cc2c2nc(C)sc21 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)[C@H]1CCC[C@](CO)([NH2+]C)C1
Fragment 2: [15*][C@@H]1CCCN(C)C1
### Response:
C[NH2+][C@@]1(CO)CCC[C@H](N(C)[C@@H]2CCCN(C)C2)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(OC(=O)NC[C@@H]1CCC[NH+](CN2CCCCC2=O)C1)(C)C
### Response:
CC(C)(C)OC(=O)NC[C@@H]1CCC[NH+](CN2CCCCC2=O)C1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COc1ccc2cnn(CC(=O)Nc3cccnc3)c(=O)c2c1OC
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](CO)CSCC(=O)N[C@@H](C)c1ccc(F)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cc2c(cc1[16*])n(CC)c(=O)n2CC
Fragment 2: [1*]C(=O)N[5*]
### Response:
CCn1c(=O)n(CC)c2cc(N3CCCCC3)c(NC(=O)Nc3cc(C)ccc3C)cc21 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CC(=O)Nc1ccc(S(=O)(=O)Nc2ccc3c(c2)CC(=O)N3C)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
C[C@H]([NH2+]CC(C)(C)C[C@@H](C)O)c1cnccn1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1nc(=O)c2c([nH]1)NC1=C(C(=O)CC(C)(C)C1)[C@H]2c1cc(OC)ccc1OC
Fragment 2: [16*]c1ccccc1
### Response:
COc1ccc(OC)c([C@@H]2C3=C(CC(C)(C)CC3=O)Nc3[nH]c(-c4ccccc4)nc(=O)c32)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccs1
Fragment 2: [1*]C(=O)CN([5*])C
### Response:
CO[C@H]1CCC[C@@H](OC(=O)CN(C)C(=O)c2cccs2)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O[C@@H]1CCCC[C@H]1c1ccc(Cl)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(F)ccc(SCCC(=O)Nc2c(N(C)C)cccc2)c1
### Response:
CN(C)c1ccccc1NC(=O)CCSc1ccc(F)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C(CCN(C(c2nn(c(=O)cc2)C)=O)C1)Oc1c(C)cccc1C
### Response:
Cc1cccc(C)c1OC1CCN(C(=O)c2ccc(=O)n(C)n2)CC1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC(=O)c1cccc(NC(=O)C(=O)NCc2ccc(Cl)cc2)c1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(CCNC(=O)[C@@H]2CCC[NH+](C)C2)on1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC(=O)c1ccccc1OCCCCN1C[C@H](C)O[C@@H](C)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCc1ccccc1
Fragment 2: [5*]N(C)S(=O)(=O)c1cncc(F)c1
### Response:
CN(CCc1ccccc1)S(=O)(=O)c1cncc(F)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1cccc(C(C)(C)C[NH2+]C2CC[NH+](CC=C(C)C)CC2)c1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H](N[C@@H]1CCc2ccccc21)C(=O)Nc1ccc(Cl)cn1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(C(=O)N[C@@H](C)CCC2CCCC2)cc1[N-]S(C)(=O)=O
### Response:
4 |
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