task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
functional_group | ### Instruction:
Does the molecule contain a amide group?
CC(C)(C)NC(=O)CNC(=O)Nc1cnn(CC(F)F)c1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
Cc1ccnc(C[C@@H](C)O)c1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CNC(=O)[C@@H](C)C[NH+](C)C1CCC(C)(c2ccccc2)CC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
COc1ccc(C[C@@H](Cl)C2C(C)(C)C2(C)C)cc1OC
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Cn1c2c(cc(cc2)C(N2CCCC[C@H](C2)SCC)=O)nc1
### Response:
CCS[C@@H]1CCCCN(C(=O)c2ccc3c(c2)ncn3C)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C(C)(C)C
Fragment 2: [5*]Nc1ccc(C)c(C)c1
### Response:
Cc1ccc(NCc2nnc(C(C)(C)C)o2)cc1C |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H](CNc1ccc([N+](=O)[O-])cc1)NS(=O)(=O)c1ccc2ccccc2c1
### Response:
0 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
N#Cc1ccc(-c2noc(CCC(=O)c3ccc(F)cc3)n2)nc1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)c1ccc(F)c(NC(=O)c2cccnc2SC)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C([C@@H](O)COCc1occc1)[NH+]1C(C)(C(C)(C1)C)C
### Response:
CC1(C)C[NH+](C[C@@H](O)COCc2ccco2)C1(C)C |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1S(=O)(C[C@@H]2[C@H]1S/C(N2c1ccc(cc1)C(C)C)=N\C(CCc1ccccc1)=O)=O
### Response:
CC(C)c1ccc(N2/C(=N/C(=O)CCc3ccccc3)S[C@H]3CS(=O)(=O)C[C@H]32)cc1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CCC[C@@]1(C=O)NC(=O)NC1=O
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCOCC1
Fragment 2: [1*]C(=O)[C@H]([4*])C
### Response:
C[C@H](C(=O)N1CCOCC1)[NH+]1CCN(Cc2ccc3c(c2)OCO3)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC[NH+](CCn2cc(NC(=O)Nc3cc(OC)cc(F)c3)cn2)CC1
### Response:
COc1cc(F)cc(NC(=O)Nc2cnn(CC[NH+]3CCCCC3)c2)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccc(OCC(=O)NNC(=O)NC2CC[NH+](C)CC2)c1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C)C(=O)c1cccc(NC(=O)C[NH2+]C2CCCCC2)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H](NC(=O)/C(C#N)=C/c1ccc(-n2cccn2)cc1)c1ccccc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(NC(C(=O)N2C[C@H](O)[C@@H](CC2)C)=O)c2c(nccc2)ccc1
### Response:
C[C@@H]1CCN(C(=O)C(=O)Nc2cccc3ncccc23)C[C@@H]1O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1c(Cl)cc(C[NH+]2CCC(N3CCCCC3=O)CC2)cc1OC
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1nc(C[NH+](C)[C@H](C)c2ccc(C(=O)[O-])o2)cs1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC[C@H](c1ccccc1)[C@@](C)(O)C(=O)[O-]
### Response:
6 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
O=c1c2ncccc2n(Cc2ccc(Cl)cc2Cl)c(=O)n1Cc1ccccn1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NCC1CC1)C1([NH2+]Cc2cnn(-c3ccccc3)c2)CCCC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
C[C@@H]1C[C@H]([NH2+][C@@H]2C[C@@H]2C2CCCCC2)CN1C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CC[4*]
Fragment 2: [5*]NS(=O)(=O)c1cccc2nsnc12
### Response:
Cc1cccc(N2CCN(C(=O)CCNS(=O)(=O)c3cccc4nsnc34)C[C@H]2C)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc2nc(N=C3NCN([C@@H]4CCCC[C@H]4C)CN3)nc(C)c2c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cn1ccc(=O)[nH]c1=O)NC[C@H]1CCOC1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccn([9*])n1
Fragment 2: [15*]C1CCCC1
### Response:
C[C@H](CNC(=O)c1ccn(C2CCCC2)n1)c1nc(-c2ccccc2)no1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
NC(=O)CN(Cc1ccccc1N)C(=O)N[C@H]1CCOC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
COC(=O)c1c(cccc1)NC(=O)c1ccc(cc1OC)OC
### Response:
COC(=O)c1ccccc1NC(=O)c1ccc(OC)cc1OC |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)c1c(C)nn2c1ncc1c(=O)n(N3CC[NH+](C)CC3)ccc12
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CC1(CC)CC1
Fragment 2: [5*]Nc1cnn(C[8*])c1
### Response:
CCC1(CNC(=O)Nc2cnn(C[C@@H]3CCCO3)c2)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [15*]C1CCCC1
### Response:
CC[NH+](CC(=O)Nc1c(C)cccc1C)C1CCCC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC[C@@H](C)NC(=O)Cc1ccc(F)cc1F
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H]1CN(C(=O)CN2CCO[C@H](CC(=O)[O-])C2)CCO1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@]1(c2ccc(Cl)cc2)NC(=O)N(CC(=O)Nc2c(C(C)C)cccc2C(C)C)C1=O
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[O-]/C(COc1cc2c(cc1)CCC2)=N\S(=O)(=O)c1cccnc1
### Response:
O=S(=O)(/N=C(\[O-])COc1ccc2c(c1)CCC2)c1cccnc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc([C@H](C)NC(=O)N2CCc3cc(F)ccc3C2)s1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cnc([14*])o1
Fragment 2: [5*]Nc1ccc([16*])cc1
### Response:
CC(C)c1cnc(-c2ccc(NC(=O)c3cccc4cc[nH]c34)cc2)o1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cc(C)cc(C)c1
Fragment 2: [8*]CS(=O)(=O)[C@H]1CC[C@H]([NH2+]C)[C@@H]1C
### Response:
C[NH2+][C@H]1CC[C@H](S(=O)(=O)Cc2cc(C)cc(C)c2)[C@H]1C |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CC(C)[C@H]([NH2+]Cc1ccc(OC(F)(F)F)cc1)c1ccccn1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*][C@H](O)c1ccc2c(c1)oc(=O)n2CC
Fragment 2: [15*]C1(C)CCCC1
### Response:
CCn1c(=O)oc2cc([C@@H](O)C3(C)CCCC3)ccc21 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CNc1nc2c(s1)C(C)(C)OC2(C)C
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C/C(Nc1ccc(C(=O)[O-])c(O)c1)=C1/C(=O)O[C@H](C)C1=O
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC1CC1
Fragment 2: [16*]c1ccccc1
### Response:
Nc1cc(C(=O)O[C@H](C(=O)NC2CC2)c2ccccc2)ccc1Cl |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[NH+](C)CCN(Cc1cccs1)C(=O)c1cc(-c2ccccc2)[nH]n1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CC(C)[C@@H](CNC(=O)CCS(C)(=O)=O)c1ccccc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(CN2CCC([NH+]3CCC[C@@H](C3)C(=O)N3CCC(CC3)F)CC2)ccn1
### Response:
O=C([C@H]1CCC[NH+](C2CCN(Cc3ccncc3)CC2)C1)N1CCC(F)CC1 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
Cc1cc(N(C)C)ccc1NC(=O)N[C@H]1CCC[C@@H](C(F)(F)F)C1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
FC(F)(F)c1ccccc1OC[C@H]1CO1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc2c(c1)OC[C@H](CNC(=O)CCN1CCCCCC1=O)C2
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
CCOC(=O)N1CCC(NC(=O)N(C)Cc2ccc(C(C)C)cc2)CC1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C=C(C)COc1ccccc1NCC(=O)NC1CCCCC1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(Nc1c(cc(N[C@H](c2ccc3cc(OC)ccc3c2)C)cc1)OC)=O
### Response:
COc1ccc2cc([C@H](C)Nc3ccc(NC(C)=O)c(OC)c3)ccc2c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H]1C[C@@H](C)CN(S(=O)(=O)c2ccc(C(=O)Nc3nnc([C@@H]4CCCO4)o3)cc2)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)c1ccc(OCc2ccc(OC)c(OC)c2Br)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [4*][C@H](C)C12CC3CC(CC(C3)C1)C2
### Response:
CCOc1cc(C[NH2+][C@H](C)C23CC4CC(CC(C4)C2)C3)ccc1OC |
functional_group | ### Instruction:
Does the molecule contain a ether group?
O=C(NCc1ccc(-n2ccnc2)nc1)C(=O)Nc1ccc(-c2ccccc2)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(NC(=O)[C@H]1N(C(=O)C2CC2)CCC1)c1c(OCC2CC2)cccc1
### Response:
O=C(NCc1ccccc1OCC1CC1)[C@@H]1CCCN1C(=O)C1CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(C(=O)[C@@H](C)c1ccc(CC)cc1)Nc1nnc(-c2ccccc2)cc1
### Response:
CCc1ccc([C@H](C)C(=O)NNc2ccc(-c3ccccc3)nn2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc([16*])cc1
Fragment 2: [5*]Nc1ccc(C)cc1O
### Response:
Cc1ccc(NC(=O)c2ccc(CS(C)(=O)=O)cc2)c(O)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O[C@H](CN[C@H]1CCOc2ccc(F)cc21)c1ccccc1Cl
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1c(nc([C@H](c2ccccc2)OC)o1)-c1c(C)ncc2C[NH2+]CCc12
### Response:
CO[C@@H](c1ccccc1)c1nc(-c2c(C)ncc3c2CC[NH2+]C3)no1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
COc1ccc(-c2csc(NC(=O)c3ccc(S(C)(=O)=O)cc3)n2)cc1OC
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(C(C)C)nc(C)c(s1)[C@@H](C)NCCc1nncn1C1CC1
### Response:
Cc1nc(C(C)C)sc1[C@@H](C)NCCc1nncn1C1CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(NS(=O)(=O)CCc2ccccc2)cn1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O[C@@H](CSc1cccc(C(F)(F)F)c1)CN1CCN(c2ccc(F)cc2)CC1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(OCc1nncn1C1CC1)[C@H]1C[C@@H]1c1cccc2ccccc12
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCN([5*])CC1
Fragment 2: [4*]Cc1cc(OC)c(O)c(OC)c1
### Response:
COc1cc(CN2CCN(C(=O)c3cccnc3)CC2)cc(OC)c1O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(/N1C[C@H](C)CCC1)(NC[C@H]1CN(CC1)CC(F)(F)F)=[NH+]/C
### Response:
C/[NH+]=C(/NC[C@@H]1CCN(CC(F)(F)F)C1)N1CCC[C@@H](C)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cccc(Cl)c1
Fragment 2: [10*]N1C(=O)N[C@]([13*])(C)C1=O
### Response:
C[C@@]1(c2cccc(Cl)c2)NC(=O)N(Cc2cc(F)cc3cccnc23)C1=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
N#Cc1nc(/C=C/c2ccc(F)cc2)oc1N1CCN(C(=O)c2cccc(F)c2)CC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
s1cnnc1NC(N[C@H]1CC[NH+]([C@H]1c1ccc(Cl)cc1)C)=O
### Response:
C[NH+]1CC[C@H](NC(=O)Nc2nncs2)[C@@H]1c1ccc(Cl)cc1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
O=C(NCc1ccncc1)c1cc2cc([N+](=O)[O-])ccc2s1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@@H]1CCCC[C@@H]1N[5*]
Fragment 2: [5*]NC[C@@H]1CCCC[C@@H]1N[5*]
### Response:
Cc1ccc(CC(=O)N[C@H]2CCCC[C@H]2CNC(=O)OC(C)(C)C)cc1O |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1nnc(C(F)(F)F)s1)C1CCN(C(=O)C2CC2)CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(Cl)c(Cl)c1
Fragment 2: [1*]C(=O)c1ccc([N+](=O)[O-])cc1Cl
### Response:
N#C[C@@H](NC(=O)c1ccc([N+](=O)[O-])cc1Cl)c1ccc(Cl)c(Cl)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CC[C@H]2CC[C@@H](C1)[NH+]2C
Fragment 2: [5*]Nc1cc([16*])ccc1C
### Response:
Cc1ccc(C(N)=O)cc1NC(=O)N1CC[C@H]2CC[C@@H](C1)[NH+]2C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cc(F)c([16*])c(F)c1
Fragment 2: [8*]CC[NH3+]
### Response:
C[C@H]1CC(Oc2c(F)cc(CC[NH3+])cc2F)C[C@H](C)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(Oc2nc(Cl)ncc2F)cncc1Cl
### Response:
Fc1cnc(Cl)nc1Oc1cncc(Cl)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(cc(c(cc1)C)-n1nnnc1)NC(=O)C(NC[C@@H](c1ccco1)[NH+](C)C)=O
### Response:
Cc1ccc(NC(=O)C(=O)NC[C@@H](c2ccco2)[NH+](C)C)cc1-n1cnnn1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
O=C(c1cccc(OCC(F)F)n1)N1CC[C@@]2(CCOC2)C1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc2c(c1)C(=O)N([C@@H](C)C(=O)N[C@H]1CCCOC1)CC1(CC[NH+](C)CC1)O2
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CCOC(=O)c1sc(NC)nc1C(F)(F)F
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc2c(c(ncn2)NC[C@H](c2ccccc2)N2CCOCC2)cc1
### Response:
c1ccc([C@@H](CNc2ncnc3ccccc23)N2CCOCC2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCc2ccccc21
Fragment 2: [1*]C(=O)[C@@H]([4*])C
### Response:
COc1cccc(Nc2nnc(S[C@@H](C)C(=O)N3CCc4ccccc43)s2)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(CNC(=O)N2CCc3c([nH]c4ccccc34)[C@H]2C)cc1OC
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CC(C)OC(=O)c1cc(-c2ccc(/C=C3/C(=O)N(C)C(=O)N=C3[O-])o2)ccc1Cl
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1
Fragment 2: [10*]N1C(=O)[C@@H]2[C@H](C1=O)[C@@H]1c3ccccc3C=CN1[C@@H]2C#N
### Response:
N#C[C@@H]1[C@@H]2C(=O)N(c3ccc(F)cc3)C(=O)[C@@H]2[C@@H]2c3ccccc3C=CN12 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1cc2c3c([nH]c2cc1S(=O)(=O)N(C)Cc1ccco1)CCCC3=O
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cnn([9*])c1[14*]
Fragment 2: [16*]c1ccc(C)cc1
### Response:
Cc1ccc(N2CCC[C@H](NC(=O)c3cnn(CC(C)C)c3C3CC3)C2=O)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1cccc(NC(=O)[C@@H](C)N2CCN(c3cc(Cl)ncn3)CC2)c1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COc1ccc(-c2n[nH]cc2C[NH+]2CCC[C@H]2c2nc3ccc(F)cc3[nH]2)c(OC)c1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C([C@H]1C=C(C2CC2)N=N1)N(Cc1ccccn1)C[C@@H]1CCCO1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]Cc1ccc(C)cc1
Fragment 2: [14*]c1cccc([14*])n1
### Response:
Cc1ccc(Cc2cccc([C@H]3CCCN3S(=O)(=O)c3cn(C)cn3)n2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(Cc1ccco1)C(=O)COc1ncnc2scc(-c3ccc(F)cc3)c12
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C([O-])[C@@H]1C[C@@H]2CC[C@H]1[NH+]2c1nc[nH+]c2c1CCCCC2
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccc(C(=O)N(C[C@@H]2CCCO2)C[C@H]2CN(C(=O)c3cccs3)CCO2)cc1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
CCCN(CC#N)C(=O)c1cc2c(cc1O)OCO2
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCN1C(=O)/C(=C\c2ccc(OC)c(OC)c2C(=O)[O-])S/C1=N\c1nccs1
### Response:
3 |
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