task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(C(N(C)C)=O)NC(Nc1c(cc(cc1)F)Cl)=O
### Response:
CN(C)C(=O)CNC(=O)Nc1ccc(F)cc1Cl |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[NH3+][C@@H](Cc1cccc(F)c1F)[C@@H]1OC[C@H]2CCCN2C1
### Response:
[NH3+][C@@H](Cc1cccc(F)c1F)[C@H]1CN2CCC[C@@H]2CO1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1noc(C[4*])n1
Fragment 2: [4*]Cc1ccccc1
### Response:
C[NH+]1CCN(Cc2noc(COCc3ccccc3)n2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1cc2c(s1)-c1ccccc1S(=O)(=O)C2)N1CCc2ccccc21
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
C[C@H]1CC[C@H](C(C)(C)c2ccc(Cl)cc2F)[C@H](O)C1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@H](C)C[NH+](CC)Cc1cnc(N2CC[NH+](C)CC2)nc1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1cncn1
Fragment 2: [4*]Cc1ccc([14*])nc1
### Response:
O=C(NCc1ccc(-n2cncn2)nc1)N(C[C@H]1CCOC1)C1CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@@H]2N(C([C@@H]([C@@H]2CC=1)c1ccc(cc1Cl)Cl)=O)O
### Response:
O=C1[C@H](c2ccc(Cl)cc2Cl)[C@@H]2CC=C[C@@H]2N1O |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccnc1C[NH+]1CCN(Cc2ccc(Cl)cc2)CC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CC[C@@H](C(=O)c1ccc(C)cc1)[C@@H]1c2cc(Br)ccc2OC(=O)[C@@H]1C(=O)OC
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
C[C@H]1C[C@H]1C(=O)Nc1cccc(C(=O)N(c2ccc(C#N)cc2)C2CC2)c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@@H](C(=O)NC1CCC(C(=O)OC(C)(C)C)CC1)c1ccccc1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccc(C=O)o1
Fragment 2: [16*]c1ccc(OC)c([N+](=O)[O-])c1
### Response:
COc1ccc(-c2ccc(C=O)o2)cc1[N+](=O)[O-] |
functional_group | ### Instruction:
Does the molecule contain a halide group?
Cc1ccc[nH+]c1N1CCN(C(=O)CCn2nc(C)c(C)c2C)CC1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N([C@H]1C=CS(=O)(=O)C1)(c1ccc(cc1)Cl)C(=O)Cc1ccc(OC)cc1
### Response:
COc1ccc(CC(=O)N(c2ccc(Cl)cc2)[C@H]2C=CS(=O)(=O)C2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@H]1C=C[C@@H]([NH3+])C1
Fragment 2: [5*]NC[C@@H](C)CCO
### Response:
C[C@@H](CCO)CNC(=O)[C@H]1C=C[C@@H]([NH3+])C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1sccc1C
Fragment 2: [8*][C@H](O)c1sccc1C
### Response:
Cc1ccsc1[C@@H](O)C1(c2ccccc2)CCC1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COc1cc(C)c(NC(=O)c2cc(C)no2)cc1OC
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc2c(c1)OCCO2
Fragment 2: [5*]N1CCC([15*])CC1
### Response:
COC(=O)C1CCN(C(=O)C[NH+]2CCC[C@@H]2c2ccc3c(c2)OCCO3)CC1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cccc(NC(=O)c2cc(-c3ccco3)nc3ccccc23)n1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12n(CC=C)c(nc1cccc2)[C@H](C)NC(COc1c(ccc(c1)C)C)=O
### Response:
C=CCn1c([C@H](C)NC(=O)COc2cc(C)ccc2C)nc2ccccc21 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(CCc1cc(Cl)no1)Nc1ccc2occc(=O)c2c1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H]1[C@@H](C(=O)[O-])CCN1C(=O)CCN1C(=O)CCC1=O
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CS(=O)(=O)/N=C(\[O-])CCCSc1ccccc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [13*][C@H]1Nc2c(F)ccc([N+](=O)[O-])c2[C@H]2C=CC[C@H]21
Fragment 2: [16*]c1ccccc1O
### Response:
O=[N+]([O-])c1ccc(F)c2c1[C@H]1C=CC[C@H]1[C@@H](c1ccccc1O)N2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C/C(=N\Nc1ncnc2sc(C)c(C)c12)c1cccc(OC(F)F)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12c(ncn1-c1ccc(cn1)C(Nc1c(OCC)c(Cl)ccc1)=O)cccc2
### Response:
CCOc1c(Cl)cccc1NC(=O)c1ccc(-n2cnc3ccccc32)nc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)C1CCC(C)(C)CC1
Fragment 2: [1*]C(=O)CC(=O)[O-]
### Response:
CN(C(=O)CC(=O)[O-])C1CCC(C)(C)CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC(CC)[S@](=O)CCC(=O)[O-]
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@@H](C)NC(=O)[C@H](C)NC(=O)C1=Cc2cc(OC)ccc2OC1
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Nc1cccc(-c2cc3ccccc3[nH]2)c1)[C@@H]1CCC[NH+](C2CCSCC2)C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(-n2nnnc2SCC(=O)N[C@H]2CCCC[C@H]2C)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(-c2nnc(C3CC[NH+](Cc4ccc5ncccc5c4)CC3)o2)s1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1CCc2sc(C(=O)Nc3cc(F)ccc3F)cc2C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CC[C@@H]1NC(=O)NC1=O)NCc1cn2cc(Cl)ccc2n1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@H]1C(C#N)=C(N)O[C@H]2N=NC(C)=C12
Fragment 2: [16*]c1ccc(OC)c([16*])c1
### Response:
COCc1cc([C@H]2C(C#N)=C(N)O[C@H]3N=NC(C)=C23)ccc1OC |
functional_group | ### Instruction:
Does the molecule contain a ester group?
CO[C@]1(C)C[C@H](NC(=O)N2CCOC[C@@H]2C2CC2)C1(C)C
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCNS(=O)(=O)c1ccc(C)c(C(=O)N2CC[S@@](=O)C(C)(C)C2)c1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
COc1cc2c(cc1OC)CN(C(=O)Nc1cc(C)cc(C)c1)CC2
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(CCNC(=O)c1ccc(O)c(Cl)c1)Nc1ccncc1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CSC[C@@H](C)N(C)C(=O)N[C@H]1CCC[NH+](C)C1
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C1CCCCC1)S(=O)(=O)N1CCN(C(=O)c2ccc(Br)s2)CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C(C)(C)C
Fragment 2: [1*]C(=O)C[4*]
### Response:
CC(C)(C)n1ncc2c1CCC[C@H]2NC(=O)CSc1nc2ccccc2o1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cscc1[C@H](Br)c1ccc2[nH]c(=O)c(=O)[nH]c2c1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C(/C=C\c1ccccc1)NCCn1ncc2c(=O)n(Cc3cccc(F)c3)cnc21
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C(C1)c1scc(C[NH2+]Cc2ccc(cc2)N2CCCCCC2)n1
### Response:
c1cc(N2CCCCCC2)ccc1C[NH2+]Cc1csc(C2CC2)n1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1ccc([C@]2(C)NC(=O)N(CC(=O)Nc3cccc(OC(F)(F)F)c3)C2=O)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a ether group?
O=C(Nc1ccc(OC[C@@H]2CCCO2)cc1)N1CCN(C2CCCC2)C(=O)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1csc(N[5*])n1
Fragment 2: [5*]N1C[C@H](C)O[C@@H](C)C1
### Response:
C[C@H]1CN(Cc2csc(NC(=O)[C@@H]3CC(=O)N(C)C3)n2)C[C@H](C)O1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
Cc1ccc([C@@H]([NH2+][C@H]2CCO[C@]3(CCSC3)C2)C2CC2)cc1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1ccccc1O[C@@H]1CCCC[C@@H]1[NH3+]
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CS(=O)(=O)N1CCCN(Cc2ncn(-c3ccccc3)n2)CC1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](Nc1cccc(CN2CCCCC2=O)c1)C(=O)Nc1cccc([N+](=O)[O-])c1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(O)c(-c2nc([C@H]3C[NH+]4CCN3CC4)no2)c1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1nc(N)nc(N)n1
Fragment 2: [11*]Sc1ccc(C)cc1C
### Response:
Cc1ccc(SCc2nc(N)nc(N)n2)c(C)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCN1C(=O)S/C(=C\c2ccc(OCc3ccc([N+](=O)[O-])cc3)c(Cl)c2)C1=O
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
O=C(CSCc1ncn(-c2ccccc2)n1)NCc1cccs1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccc(Cl)s1
Fragment 2: [4*]C1([C@H]([8*])O)CCCC1
### Response:
O[C@@H](c1ccc(Cl)s1)C1([NH+]2CCCC2)CCCC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCc1sc(C)nc1C
Fragment 2: [5*]NC(N[5*])=[NH+]C
### Response:
C/[NH+]=C(/NCCc1sc(C)nc1C)N[C@@H]1CCC[C@H](C(F)(F)F)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(NCc1nnc2n1CCCCC2)c1cncn1-c1ccc(F)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[NH+]1CCC(=NNC(=O)c2cc(-c3ccccc3)nc3ccccc23)CC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
N#C[C@@H]1CCCC[C@H]1OC(=O)CCc1cc(Cl)cs1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[NH+](Cc1ccccc1NC(C)=O)[C@@H]1CCN(c2ccccc2)C1=O
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(CNC(=O)N[C@H]2CCC[C@H](S(=O)(C)=O)C2)c(N(C)C)cc(C)cc1
### Response:
Cc1ccc(CNC(=O)N[C@H]2CCC[C@H](S(C)(=O)=O)C2)c(N(C)C)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@@H](C)O[3*]
Fragment 2: [5*]Nc1ccc([16*])cc1
### Response:
Cc1ccnc2nc(C(=O)O[C@H](C)C(=O)Nc3ccc(Oc4ccccc4)cc3)nn12 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1noc(C)c1[C@@H](C)NC(=O)Nc1ccc(NC(=O)[C@H]2CCCO2)cc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O1CCCC[C@H]1CC[C@H]([NH2+]C)c1c(cc(F)c(c1)C)F
### Response:
C[NH2+][C@@H](CC[C@@H]1CCCCO1)c1cc(C)c(F)cc1F |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC[NH2+]C/C=C/c1cccc(F)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CSc1ccccc1NC(=O)c1cc2n(n1)[C@H](C(F)(F)F)C[C@H](c1ccc3c(c1)OCO3)N2
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(/N=C2/C=C([O-])[C@@H](NO)c3ccccc32)cc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1CN(CCn2cc[nH+]c2)CC[C@@H]1[NH3+]
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c2c(ccc1CC)ncc(C#N)c2Nc1cc(OC)ccc1OC
### Response:
CCc1ccc2ncc(C#N)c(Nc3cc(OC)ccc3OC)c2c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH+]1CCC[C@@H]([15*])C1
Fragment 2: [4*]Cc1ccc(Cl)c(F)c1
### Response:
CNC(=O)[C@@H]1CCC[NH+](Cc2ccc(Cl)c(F)c2)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cc([16*])ccc1C
Fragment 2: [5*]NC[C@](C)(O)CCC(C)C
### Response:
CC(=O)Nc1cc(NC(=O)NC[C@](C)(O)CCC(C)C)ccc1C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC1(C)C[C@H]([NH2+]C[C@@H]2CCC[C@@H]2NS(C)(=O)=O)C(C)(C)O1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
[NH3+][C@@H](Cc1cccc(F)c1F)[C@H]1CN2CCC[C@@H]2CO1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCC
Fragment 2: [1*]C(=O)[C@H]1C[NH2+]CCN1[5*]
### Response:
CCNC(=O)[C@H]1C[NH2+]CCN1[C@@H](C)C1(C)CC1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CCc1ccc(C(=O)Nc2ccc(OC)c(S(=O)(=O)N3CCOCC3)c2)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [7*]C1SC(=N)N([10*])C1=O
Fragment 2: [8*]C(F)(F)F
### Response:
N=C1S/C(=C\c2ccc([N+](=O)[O-])cc2)C(=O)N1c1ccccc1C(F)(F)F |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCc1ccc(Cl)cc1
Fragment 2: [1*]C(=O)C(=O)NNC(=O)CC(C)(C)C
### Response:
CC(C)(C)CC(=O)NNC(=O)C(=O)NCc1ccc(Cl)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(=O)n(cc(Cl)c(=O)[nH]1)Cc1nc(COc2ccc(C)cc2)sc1
### Response:
Cc1ccc(OCc2nc(Cn3cc(Cl)c(=O)[nH]c3=O)cs2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1[nH]c2ccccc2c1[C@@H]1c2ccccc2C(=O)N1CC(=O)NCCC(C)C
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCCOc1ccc(N2C[C@H](C)C(=O)NC2=O)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a ether group?
COc1ccc(-c2nnc3sc(NC(=O)COc4cc(C)cc(C)c4)nn23)cc1OC
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@H](c1nc(CC(C)C)no1)N1Cc2ccccc2C1=O
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(ccc1CC)NC(=O)NCC(Nc1ccc(cc1)OC)=O
### Response:
CCc1ccc(NC(=O)NCC(=O)Nc2ccc(OC)cc2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1nc(-c2cccs2)cc1C(=O)NCCc1ccccc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)CC[8*]
Fragment 2: [1*]C(=O)c1nc2c(C)cccn2c1C[4*]
### Response:
Cc1cccn2c(C[NH+]3CCc4sccc4C3)c(C(=O)N(C)CCc3ccccc3)nc12 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(c1cc(cc(c1)OC)OC)N(Cc1occc1)c1sc2c(n1)ccc(c2)F
### Response:
COc1cc(OC)cc(C(=O)N(Cc2ccco2)c2nc3ccc(F)cc3s2)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCN(CC)S(=O)(=O)c1ccc(Cl)c(NC(=O)C2CCC2)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](C[NH+]1CCCCC1)[NH2+][C@@H]1CCCS[C@@H]1C
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C1Nc2c(c(=O)oc3ccccc23)[C@H](c2cccc([N+](=O)[O-])c2)N1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc(c1CNC(NCC)=O)OC
### Response:
CCNC(=O)NCc1ccccc1OC |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(-c2nc(COC(=O)c3cc(C#N)cn3C)no2)cc1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCCCCNC(=O)Nc1ccc(OC(F)F)c2ncccc12
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CC1CC1
Fragment 2: [4*][C@H](C)/C([O-])=N/S(=O)(=O)c1cccc2cc(C)cnc12
### Response:
Cc1cnc2c(S(=O)(=O)/N=C(\[O-])[C@@H](C)OCC3CC3)cccc2c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Clc1ncc(Cl)c(Oc2ccccc2)n1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ncc(CN(C)C(=O)c2ccc(-c3ccco3)[nH]c2=O)s1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)CCOc1ccc(NC(=O)N[C@H]2CCCC[C@@H]2O)cc1
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
[NH3+][C@@H](CC(=O)[O-])c1cccc2ccccc12
### Response:
3 |
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