task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)C[C@H](NC(=O)C[C@H]1OCCc2ccccc21)C1CC1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[S@](=O)[C@H]1CCCC[C@@H]1NC(=O)[C@@H]1CCOc2ccccc21
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCO[C@H](C)C1
Fragment 2: [1*]C(=O)C[4*]
### Response:
C[C@@H]1CN(C2CC[NH+](CC(=O)Nc3ccccc3)CC2)CCO1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CCN(c1ccc(C(=O)N(C)C)cc1)S(C)(=O)=O
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*]Nc1cc([14*])no1
### Response:
CCCC1=NC(SCC(=O)Nc2cc(C(C)(C)C)no2)=NC(=O)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)[C@@H]1CCCN1Cc1ccccc1OCC(F)(F)F
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NCCCN1CCCC1=O)c1cc2scnc2[nH]1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@H]1CCS(=O)(=O)C1
Fragment 2: [5*]N1CCN([5*])CC1
### Response:
O=C([C@H]1CCS(=O)(=O)C1)N1CCN(Cc2ccon2)CC1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H]1CCC=C2C[C@H]3OC(=O)[C@H](C[NH+]4CCN(C(=O)c5ccco5)CC4)[C@H]3[C@H](O)[C@@]21C
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C1C[C@@H](CCN1C)C(N[C@@H](CCc1ccc(OC(C)C)cc1)C)=O
### Response:
CC(C)Oc1ccc(CC[C@@H](C)NC(=O)[C@@H]2CCN(C)C(=O)C2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1[nH]c2c(C)ccc(C)c2c1CC(=O)N(C)CCCc1cnn(C)c1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
C=C[C@H]1C[NH+]2CC[C@@H]1C[C@@H]2CNC(=O)C1CCCCC1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCOC(=O)c1cnn([C@@H]2CCCN(C(=O)NC[C@H](C)c3ccsc3)C2)c1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)C[C@H](CNC(=O)c1ccc(O)cc1O)C(=O)[O-]
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
O=C(Nc1ccccc1N1CCCCC1)[C@@H]1CC(c2ccc(Cl)s2)=NO1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(NC[C@H]1CCCCN1c1ncnc2c1oc1ccccc12)c1ccccc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@H](C)n1cc(I)cn1
Fragment 2: [3*]OCC
### Response:
CCO[C@H](C)n1cc(I)cn1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cccn2cc(CC(N)=S)[nH+]c12
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(F)c(F)ccc1[C@H](N[C@@H](c1ccc(-n2cncc2)cc1)C)COC
### Response:
COC[C@@H](N[C@H](C)c1ccc(-n2ccnc2)cc1)c1ccc(F)c(F)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC[C@H](O1)c1nnc(NC(=O)c2cc3c(cccc3)cc2OC)o1
### Response:
COc1cc2ccccc2cc1C(=O)Nc1nnc([C@@H]2CCCO2)o1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Brc1ccc(cc1)OCCOC(=O)c1cc[n+](cc1)[O-]
### Response:
O=C(OCCOc1ccc(Br)cc1)c1cc[n+]([O-])cc1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C1Nc2ccccc2C[C@@H]1CCC(=O)N1CCc2ccc(Cl)cc2C1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
CCC(=O)Oc1cccc([N+](=O)[O-])c1C
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1nc(C)c(C)o1
Fragment 2: [1*]C(=O)C([1*])=O
### Response:
Cc1nc(-c2cccc(NC(=O)C(=O)N[C@@H](C)[C@@H]3CCCO3)c2)oc1C |
functional_group | ### Instruction:
Does the molecule contain a halide group?
O=C(CN1C(=O)/C(=C\c2ccccc2F)SC1=S)N[C@@H]1C=CS(=O)(=O)C1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cccnn1
Fragment 2: [16*]c1ccc(S(=O)(=O)NC)cc1
### Response:
CNS(=O)(=O)c1ccc(CCc2nc(-c3cccnn3)no2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(C(=CN(C)c2ccccc2)S(=O)(=O)c2ccc(C)cc2)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCc1nn(C)cc1NC(=O)C(=O)N1CCN([C@@H](CC)CO)CC1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1nnc2n1CCCC2)N1CC[C@]2(CCCN(CC3CC3)C2=O)C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(cc(cc1)NC(C(C)C)=O)NC(=O)NCCc1c(F)cc(F)cc1
### Response:
CC(C)C(=O)Nc1cccc(NC(=O)NCCc2ccc(F)cc2F)c1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
Cn1nc(Br)c2c(N[C@@H](CO)[C@@H](O)c3ccc([N+](=O)[O-])cc3)ncnc21
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(/C=C2\Oc3c(ccc(O)c3C[NH+]3CCC(C)CC3)C2=O)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
N#Cc1ccc(OCC(=O)Nc2ccccc2N2CCc3ccccc32)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC(=S)N[5*]
Fragment 2: [1*]C(=O)C(C)C
### Response:
CC(C)C(=O)NC(=S)Nc1ccc2oc(-c3ccc(C(C)C)cc3)nc2c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N([5*])C(=S)S
Fragment 2: [4*]C(C)C
### Response:
CC(C)N(C(=S)S)C(C)C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1cnn(C)c1C
Fragment 2: [14*]c1n[nH]c(C)n1
### Response:
Cc1nc(-c2cccc(NCc3cnn(C)c3C)c2)n[nH]1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Nc1nc2ccccc2[nH]1)c1ccc(CS(=O)(=O)c2ccccc2)o1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H]1CCCC[C@@H]1[15*]
Fragment 2: [8*]C(F)(F)F
### Response:
Cc1cccc(C(=O)N[C@@H]2CCCC[C@@H]2C(F)(F)F)n1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(OCc1cc([N+](=O)[O-])cc2c1OCOC2)c1cnc2ccccc2n1
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](C(N)=O)n1c(CCCl)nc2cccnc21
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(NC(CSc2n(-c3c(OC)ccc(C)c3)nnn2)=O)cc(cc1C)C
### Response:
COc1ccc(C)cc1-n1nnnc1SCC(=O)Nc1cc(C)cc(C)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccccc1Cl
Fragment 2: [1*]C(=O)c1nn(C)cc1Cl
### Response:
Cn1cc(Cl)c(C(=O)OCC(=O)Nc2ccccc2Cl)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N1CC[NH+](Cc2ncccc2C)CC1)c1ccc(cc1)Cl
### Response:
Cc1cccnc1C[NH+]1CCN(Cc2ccc(Cl)cc2)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(C)cc(OCCCSC2[NH+]=c3ccccc3=[NH+]2)ccc1
### Response:
Cc1cccc(OCCCSC2[NH+]=c3ccccc3=[NH+]2)c1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cc(C)c(NC(=O)N(C)CC(=O)Nc2cccc(Cl)c2)c(C)c1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O(C)CCN1CCN(CC1=O)C(=O)NC[C@H]([NH+](C)C)c1ccc(cc1)Cl
### Response:
COCCN1CCN(C(=O)NC[C@@H](c2ccc(Cl)cc2)[NH+](C)C)CC1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CNS(=O)(=O)[C@@H]1CCOC[C@@H]1Cc1cccc(F)c1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC[NH2+][C@@H](Cc1ccc(CC)s1)[C@@H]1CSCCS1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
C[C@@H]1CCN(C(=O)C(=O)Nc2cccc3ncccc23)C[C@@H]1O
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N([C@H](C)c1ccccc1)c1c(c(n2c(n1)ccc(c2)C)=O)/C=C1/C(=O)N([C@@H](CC)C)C(S1)=S
### Response:
CC[C@@H](C)N1C(=O)/C(=C/c2c(N[C@H](C)c3ccccc3)nc3ccc(C)cn3c2=O)SC1=S |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N1CCOCC1)(C)(C)[C@H]([NH2+]C)c1ccc(cc1)CCC
### Response:
CCCc1ccc([C@@H]([NH2+]C)C(C)(C)N2CCOCC2)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cnc(OC)c(CN2C(=O)CNC([C@H]2C2CC2)=O)c1
### Response:
COc1ncccc1CN1C(=O)CNC(=O)[C@H]1C1CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCCC(=O)Nc1ccc(C)cc1NC(=O)[C@H]1C=CC[NH2+]1
### Response:
5 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(-n2cnnn2)cc1NC(=O)[C@@H]1C=C[C@@H]([NH3+])C1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [10*]N1CC(=O)N[C@](C)(CC)C1=O
Fragment 2: [8*]Cc1cc(C)c(F)c(C)c1
### Response:
CC[C@@]1(C)NC(=O)CN(Cc2cc(C)c(F)c(C)c2)C1=O |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Fc1cc(F)c(F)c(CN[C@H]2CCc3sc(Cl)cc32)c1F
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(Cl)ccc1NC(=O)CSc1nnc(C(C)C)n1N
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
Cn1cc[nH+]c1C[C@](O)(C[NH3+])C(F)(F)F
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C)c1ccc(NC(=O)[C@@H]2CCC[NH+]2Cc2ccccc2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COc1cccc(C2=[NH+][C@@H](c3ccccc3)C(=S)N2)c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
O=C1[C@H]2CC=CC[C@H]2C(=O)N1c1nc2n(n1)[C@@H](c1ccccc1)C[C@@H](c1ccc(Cl)cc1)N2
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NCC[8*]
Fragment 2: [16*]c1cccc([N+](=O)[O-])c1
### Response:
O=C(NCCc1cccc([N+](=O)[O-])c1)c1cc2occc2[nH]1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cccc([N+](=O)[O-])c1C
Fragment 2: [1*]C(=O)N[5*]
### Response:
Cc1c(NC(=O)N2CCC[C@@H](C)[C@@H]2CO)cccc1[N+](=O)[O-] |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@H](C)[C@H]1CC[C@H]([NH2+]C)C1
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CN(C(=O)CCCn1ccnn1)[C@H](c1ccc(Cl)cc1)C(F)(F)F
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(CC)c1ncnc(Cl)c1[N+](=O)[O-]
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [5*]N[C@H]1CCC[C@@H]1[15*]
### Response:
CCOc1ccccc1O[C@H]1CCC[C@@H]1NC(=O)c1ccc(OC)nc1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
C[C@H]1C[C@@H]1C(=O)N1CCN(CC2=Cc3ccccc3OC2)CC1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc(S([12*])(=O)=O)cc1
Fragment 2: [1*]C(=O)CC
### Response:
CCC(=O)Nc1ccc(S(=O)(=O)N2CC[C@@H](C)[C@H](O)C2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[NH+]([5*])C
Fragment 2: [16*]c1c(O)ccc2ccccc12
### Response:
CC(C)NC(=O)C[NH+](C)Cc1c(O)ccc2ccccc12 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CC(C)[NH2+]Cc1ccc(O[C@@H](C)C(N)=O)cc1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1[nH]c2ccccc2c1[C@@]1(O)C(=O)N(C/C=C/c2ccccc2)c2ccccc21
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccc(-n2c(nc3c(c2=O)cnn3-c2c(cccc2)Cl)-c2ccco2)c1)OC
### Response:
COc1ccc(-n2c(-c3ccco3)nc3c(cnn3-c3ccccc3Cl)c2=O)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@@H]([C@H](CCC1)NC(=O)COC(=O)c1ccc(O)cc1)C
### Response:
C[C@H]1CCCC[C@@H]1NC(=O)COC(=O)c1ccc(O)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [6*]C(C)=O
Fragment 2: [16*]c1cccc(S(=O)(=O)/N=c2\[nH]cccc2[16*])c1
### Response:
CC(=O)c1cccc(S(=O)(=O)/N=c2\[nH]cccc2-c2ccccc2)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H]1C[C@H](C)C[NH+](CCC(=O)Nc2ccc(N3CCCC3=O)cc2)C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(c1ccccc1SC[C@H]1CCCO1)N1CCN([C@@H]2CCS(=O)(=O)C2)CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CC(=O)NNc1cc(C#N)cc(Cl)n1
Fragment 2: [3*]OC(C)C
### Response:
CC(C)Oc1ccccc1CC(=O)NNc1cc(C#N)cc(Cl)n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1c(=O)c(C(=O)N2CCN(c3ccccc3)CC2)nc2cccnc21
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(c1ccc(cc1)/C=C/C(=O)OCC)C(C(C)(F)C)=O
### Response:
CCOC(=O)/C=C/c1ccc(NC(=O)C(C)(C)F)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ccccc1
Fragment 2: [16*]c1c(C)n[nH]c1[O-]
### Response:
Cc1n[nH]c([O-])c1[C@H](c1c(C)[nH][nH]c1=O)[C@H]1CN(Cc2ccccc2)c2ccccc21 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)N(C[C@H]1C[C@@H]1C)C(=O)NCC[NH+]1CCCCC1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(F)cc(C(=O)NCc2cccnc2-n2cccn2)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc([C@@H](NC([C@H](C)Cc2c(C)[nH]nc2C)=O)c2ccc(F)cc2)ccc1
### Response:
Cc1n[nH]c(C)c1C[C@@H](C)C(=O)N[C@H](c1ccccc1)c1ccc(F)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCCNC(=O)[C@@H]1CCCN(c2ccc3nnnn3n2)C1
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
COc1cc([C@H]([NH3+])C(=O)[O-])cc(I)c1OC
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cc([14*])nn1C
Fragment 2: [14*]c1cc([14*])n(C)n1
### Response:
CCCc1cc(NC(=O)N(CC)C2CCCCC2)n(C)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC1CCCCC1
Fragment 2: [1*]C(=O)c1ccc([16*])cc1
### Response:
CN1CCN(S(=O)(=O)Cc2ccc(C(=O)NC3CCCCC3)cc2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc([C@@H](O)[C@H](C)[NH2+][C@H](C)c2ccc(C)s2)cc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CO[C@H](C)C(=O)Oc1ccc(Br)cc1Br
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1Nc2c(c(=O)oc3ccccc23)[C@H](c2cccc([N+](=O)[O-])c2)N1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCN(CC1)c1cc2c(cc1NC(Nc1ccccc1F)=O)n(C)c(n2C)=O
### Response:
Cn1c(=O)n(C)c2cc(N3CCCCC3)c(NC(=O)Nc3ccccc3F)cc21 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)c1ccc(NC(=O)[C@@H]2C[C@@H]2[N+](=O)[O-])s1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH+]1CCCC1
Fragment 2: [16*]c1cccnc1
### Response:
Cn1cc(CNc2cccc(CC[NH+]3CCCC3)c2)c(-c2cccnc2)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Cc1c(nc2n(c1NCCOC1CCCCCC1)ncn2)C
### Response:
Cc1nc2ncnn2c(NCCOC2CCCCCC2)c1C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(-c2nc(CC(=O)NCCS(N)(=O)=O)cs2)o1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
O=C(Nc1ccccc1Cl)C(c1ccccc1)c1ccccc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccn2ccnc2c1
Fragment 2: [5*]N1CCc2c([nH]c3ccccc23)C1
### Response:
O=C(c1ccn2ccnc2c1)N1CCc2c([nH]c3ccccc23)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)n1ncc2cc(C(=O)NC[C@@H](c3cccs3)N3CCOCC3)cnc21
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)(O)CNC(=O)c1c(F)ccc([N+](=O)[O-])c1F
### Response:
3 |
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