task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N[C@@H](CC)C(C)(C)c1ccccc1)(NCc1c(nn(c1)C)CC)=O
### Response:
CCc1nn(C)cc1CNC(=O)N[C@@H](CC)C(C)(C)c1ccccc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(O)[C@](C1CCCCC1)([NH2+]CC(=O)N(CC)[C@@H]1CCS(=O)(C1)=O)C
### Response:
CCN(C(=O)C[NH2+][C@](C)(CO)C1CCCCC1)[C@@H]1CCS(=O)(=O)C1 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
COc1cc(C)c(I)c(C)c1C#N
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC1=NN(c2ccc(C(=O)Nc3cccnc3-n3cccn3)cc2)CC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CS(=O)(=O)CC[C@H]([NH3+])C(=O)N[C@@H]1CONC1=O
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
NC(=O)CN1CCN([C@H]2CC(=O)N(CCc3ccccc3)C2=O)CC1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[NH2+][C@H](C)c1ccn(CC(=O)NC(C)(C)C)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(C(=O)N2CCC[C@H](CCC(=O)NCc3ccc(F)c(F)c3)C2)nc(C)n1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CC(C)n1cc(C(=O)c2ccccc2OCC(=O)Nc2ccc(Cl)c(Cl)c2)cc(C#N)c1=O
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1noc2ncc(NC(=O)C=C3CN(C(=O)OC(C)(C)C)C3)cc12
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(C)(CNC(N[C@@H](C)C(N1CCCC[C@H]1C)=O)=O)[NH+](C)C
### Response:
C[C@H](NC(=O)NCC(C)(C)[NH+](C)C)C(=O)N1CCCC[C@H]1C |
functional_group | ### Instruction:
Does the molecule contain a ester group?
O=C(OCc1nnc(-c2ccc(Cl)cc2)o1)c1cccc(-n2cnnn2)c1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1nc([14*])nc(NN)n1
Fragment 2: [16*]c1cccc(Cl)c1
### Response:
NNc1nc(Nc2cccc(Cl)c2)nc(N2CCOCC2)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC[NH3+]
Fragment 2: [4*]Cc1cc(F)cc(Br)c1
### Response:
[NH3+]CCOCc1cc(F)cc(Br)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@H]1CC[C@@]([15*])([NH2+]C)C1
Fragment 2: [15*]C1CCCCC1
### Response:
C[NH2+][C@]1(C(=O)[O-])CC[C@H](SC2CCCCC2)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cc1c(F)cccc1F)NC[C@H]1CC[C@H](C(=O)[O-])O1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
CC(C)n1cnnc1SCc1csc(-c2ccccc2F)n1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COC(C)(C)C[C@H](C)NC(=O)Nc1ccc(-n2ncn(C)c2=O)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
o1c(nc(n1)CCOC)-c1cc(ccc1)S(CC)(=O)=O
### Response:
CCS(=O)(=O)c1cccc(-c2nc(CCOC)no2)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H](NC(=O)c1cc2c(s1)CS(=O)(=O)C2)C12CC3CC(CC(C3)C1)C2
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC[NH2+][C@H](C)c1cc(F)ccc1Oc1cccnc1C
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(C[NH3+])cc1
Fragment 2: [5*]N1C[C@@H](C)[C@H](C)C1
### Response:
C[C@@H]1CN(c2ccc(C[NH3+])cc2)C[C@H]1C |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
Cc1nc(N2CC[NH+](C)CC2)[nH]c(=O)c1CC#N
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CCc1nnc(NC(=O)[C@H]2CC(=O)C(OCc3ccccc3)=CO2)s1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(C(=O)Nc2ccc(-n3ncn(C)c3=O)cc2)c(C)n1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1ccccc1NC(=O)C(=O)N[C@@H](C)C1CCCCC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1c([C@H]2CCC[NH+]2Cc2cc(C(F)(F)F)ccc2F)cnn1C
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CCC[C@H](O)CNS(=O)(=O)N1CCCCCC1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CSCc1ccnc(NCc2[nH]c(-c3ccccc3)c[nH+]2)c1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CN(S(=O)(=O)c1cc(c(N2CCOCC2)cc1)C(=O)Nc1sc(nn1)C(C)C)C
### Response:
CC(C)c1nnc(NC(=O)c2cc(S(=O)(=O)N(C)C)ccc2N2CCOCC2)s1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC[C@H](C)N/C(N)=[NH+]/C[C@H]1CN2CCCC[C@@H]2CO1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCC
Fragment 2: [1*]C(=O)[C@H]([4*])C
### Response:
CCC[NH+]1CCC(NC(=O)[C@@H](C)Sc2ccccc2Cl)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1ccc([C@H](C)CC(=O)N(C)[C@@H](C)CS(C)(=O)=O)cc1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1c([14*])noc1C
Fragment 2: [5*]N1CCCC[C@@H]1[13*]
### Response:
Cc1onc(-c2ccccc2Cl)c1C(=O)N1CCCC[C@@H]1C(=O)[O-] |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)[C@]1(CC(=O)N2CCOCC2)C(=O)C[C@H]2CC[C@@H]1N2Cc1ccc(F)cc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CC[C@@](C#N)([C@](C)(O)C2(C)CC2)C1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(COC(=O)C1CCN(C(=O)c2ccc(Cl)cc2)CC1)Nc1cccc(F)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1([C@@H](CCCC1)CO)S(c1c(cc(N)cc1C)C)(=O)=O
### Response:
Cc1cc(N)cc(C)c1S(=O)(=O)N1CCCC[C@H]1CO |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccnc1)C(OCC(N1CC(=O)Nc2c1cccc2)=O)=O
### Response:
O=C1CN(C(=O)COC(=O)c2ccncc2)c2ccccc2N1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CC[C@H](C)Cn1c(CCCl)nc2c(C)nn(C)c21
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCS(=O)(=O)c1ccc(C#N)cc1
Fragment 2: [5*]N1CCCc2ccccc21
### Response:
N#Cc1ccc(S(=O)(=O)CCN2CCCc3ccccc32)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cccc(-c2csc(/C(C#N)=C\Nc3ccc(Cl)c(C(F)(F)F)c3)n2)c1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(C(N(CC(C)C)CC(C)C)=O)cc2ccc(OC)cc2oc1=O
### Response:
COc1ccc2cc(C(=O)N(CC(C)C)CC(C)C)c(=O)oc2c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1SC(CN(C1)C(=O)NCc1ccccc1C)(C)C
### Response:
Cc1ccccc1CNC(=O)N1CCSC(C)(C)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCNC(=O)[C@H]1CCCN(C(=O)C=C(C2CC2)C2CC2)C1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccc([16*])c1
Fragment 2: [3*]OCC
### Response:
CCOC(=O)c1cccc(NC2=C(Cl)C(=O)N(Cc3ccccc3)C2=O)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Clc1cc(C[S@]([C@@H](C(=O)NCC(C)C)C)=O)ccc1Cl
### Response:
CC(C)CNC(=O)[C@@H](C)[S@](=O)Cc1ccc(Cl)c(Cl)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C1C(=Cc2ccccc2I)C(=O)c2ccccc21
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(C(=O)Nc2ccc(-n3ccnn3)cc2)c(C(C)(C)C)nn(c1)C
### Response:
Cn1cc(C(=O)Nc2ccc(-n3ccnn3)cc2)c(C(C)(C)C)n1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@@H](NC[C@]1(CCCO1)C)(C[NH3+])c1cc(sc1C)C
### Response:
Cc1cc([C@@H](C[NH3+])NC[C@@]2(C)CCCO2)c(C)s1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@H](C)CSC
Fragment 2: [5*]NS(=O)(=O)c1c(C)cc(C)cc1C
### Response:
CSC[C@@H](C)NS(=O)(=O)c1c(C)cc(C)cc1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccccc1C#N
Fragment 2: [16*]c1ccccc1
### Response:
C[C@H]1C[C@H](NC(=O)COc2ccccc2C#N)CN1c1ccccc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCN1C(=O)C[C@@H]([NH3+])[C@@H]1c1ccccc1C1CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[C@@H]1OC(=O)c2ccccc21
Fragment 2: [5*]NCc1ccccc1C
### Response:
Cc1ccccc1CNC(=O)C[C@@H]1OC(=O)c2ccccc21 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc2nc(SCC(=O)[O-])n(CC(C)C)c(=O)c2[nH]1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC[NH2+][C@@]1(C(=O)[O-])CCC[C@@H](Sc2ncc(C)cn2)C1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(C[NH+]2CCN([C@@H](C)C(=O)NC3CCCC3)CC2)cc1SC
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(c(Cl)nccc1)S(=O)(NCC=C)=O
### Response:
C=CCNS(=O)(=O)c1cccnc1Cl |
functional_group | ### Instruction:
Does the molecule contain a ester group?
O=C(C[C@@H]1CSc2nccc(=O)n21)Nc1ccccn1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1n(ncc1)S(c1cc(Cl)c(OC)cc1Cl)(=O)=O
### Response:
COc1cc(Cl)c(S(=O)(=O)n2cccn2)cc1Cl |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)Cn2c(C)cc(C)c(C#N)c2=O)c(C)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1oc(-c2cccs2)nc1C[S@@](=O)CCO
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCC[NH2+]CC[NH+](C)CC(C)(C)O
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc(F)cc1
Fragment 2: [15*][C@H]1CC[C@@H](CC)C1
### Response:
CC[C@@H]1CC[C@H]([NH+]2CCN(C(=O)c3ccc(F)cc3)CC2)C1 |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
COc1ccc([C@H](C)NC(=O)Cc2ccc(C)cc2)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
[NH3+][C@H](Cc1cccc(O)c1)c1ccccn1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(NCC(C)(O)C)c1c(c([N+](=O)[O-])ccc1F)F
### Response:
CC(C)(O)CNC(=O)c1c(F)ccc([N+](=O)[O-])c1F |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
FC(F)Oc1cccc(c1)C(=O)N1c2ccccc2O[C@@H](C(=O)OC)C1
### Response:
COC(=O)[C@H]1CN(C(=O)c2cccc(OC(F)F)c2)c2ccccc2O1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C=CCNC(=O)[C@H](C)SCc1ccc(-n2cccn2)cc1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C(F)F
Fragment 2: [14*]c1cc([16*])c2c(C)noc2n1
### Response:
CCn1cc(-c2cc(C(F)F)c3c(C)noc3n2)c(C)n1 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
CC(C)OC(=O)N1CCC2(CC1)C[C@H](c1ccccc1)C(=O)N(C)C2
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)Oc1ccc(C(=O)NCc2ccc(S(N)(=O)=O)cc2)cc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1c2nc(SCc3c(Cl)cccc3)nn2[C@H](C(C(=O)OC)=C1C)c1ccncc1
### Response:
COC(=O)C1=C(C)Nc2nc(SCc3ccccc3Cl)nn2[C@H]1c1ccncc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [12*]S(=O)(=O)c1c(F)cccc1Br
Fragment 2: [5*]N1C[C@H]2CC[C@@H]1C2
### Response:
O=S(=O)(c1c(F)cccc1Br)N1C[C@H]2CC[C@@H]1C2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(cccc1C(=O)NC[C@@H](C[C@@H](C)O)C)-c1cocc1
### Response:
C[C@@H](CNC(=O)c1cccc(-c2ccoc2)c1)C[C@@H](C)O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(C)nc(nc1C)NNC(=O)[C@H]1CN(c2c(ccc(Cl)c2)OC)C(=O)C1
### Response:
COc1ccc(Cl)cc1N1C[C@H](C(=O)NNc2nc(C)cc(C)n2)CC1=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1cccc1[C@@H]1CCC[NH+]1CC(=O)Nc1sc2c(c1C(N)=O)CCC2
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CCn1c(C)c(C)n2c3c(=O)n(C)c(=O)n(C)c3nc12
Fragment 2: [5*]Nc1cc(OC)ccc1OC
### Response:
COc1ccc(OC)c(NCCn2c(C)c(C)n3c4c(=O)n(C)c(=O)n(C)c4nc23)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1ncc2c(NNC(=O)c3cccc([N+](=O)[O-])c3)ncnc21
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C1C[C@@H](NC2=NS(=O)(=O)c3ccccc32)CN1CC(F)(F)F
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=S(=O)(c1cc(NC(c2c(ccc(Br)c2)F)=O)ccc1)NC1CC1
### Response:
O=C(Nc1cccc(S(=O)(=O)NC2CC2)c1)c1cc(Br)ccc1F |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COCCCC(=O)N[C@@H](C)c1sc(-c2ccccc2F)nc1C
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)c1ccc([C@@H]2Nc3ccc([N+](=O)[O-])cc3[C@@H]3C=CC[C@H]32)cc1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
CCN(C(=O)[C@H]1C=C2C(=O)[NH+]=c3ccc(C)cc3=C2S1)c1cccc(C)c1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(C)c(-n2nnnc2SCC(=O)N2c3c(cccc3)OC[C@H]2c2ccccc2)ccc1
### Response:
Cc1ccccc1-n1nnnc1SCC(=O)N1c2ccccc2OC[C@H]1c1ccccc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [7*]C1S/C(=N/c2ccc(OC)cc2)NC1=O
Fragment 2: [7*]Cc1cc([16*])c(O)c([N+](=O)[O-])c1
### Response:
CCOc1cc(/C=C2\S/C(=N/c3ccc(OC)cc3)NC2=O)cc([N+](=O)[O-])c1O |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
CC(=O)Nc1ccc(NC(=O)c2ccc(C)c(-n3cccc3)c2)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CC[C@H]([8*])C
Fragment 2: [16*]c1ccc(OC)cc1
### Response:
CCn1ccnc(NCC[C@@H](C)c2ccc(OC)cc2)c1=O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1ccccc1-n1c(C)ncc1C[NH2+][C@@H]1CCC[C@@H](C1)S(=O)(C)=O
### Response:
Cc1ncc(C[NH2+][C@@H]2CCC[C@H](S(C)(=O)=O)C2)n1-c1ccccc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(C(=O)NCCc2nc3ccc(F)cc3[nH]2)ccc1F
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
c1ccc(CN2CCCC3(C[NH2+]C3)C2)cc1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCN(Cc1ccccc1)C(=O)[C@H](C)Sc1nnc2c(Cl)cc(C(F)(F)F)cn12
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC[C@H](NC(=O)Cc1coc(-c2ccc(Cl)cc2)n1)C(N)=O
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cn1c(=O)oc2cc([N-]S(=O)(=O)c3ccc(Br)s3)ccc21
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H]1CCCN(C(=O)CSc2nnc(-c3ccc([N+](=O)[O-])cc3)o2)C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=c1oc2ccccc2cc1C1=NN[C@@H](c2ccccc2Cl)C1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@H]1CCC[NH2+]1
Fragment 2: [5*]Nc1nc2c(C)cccn2n1
### Response:
Cc1cccn2nc(NC[C@H]3CCC[NH2+]3)nc12 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cnc(C(C)(C)NC(=O)N[C@H]2C[C@H]2C2CCCCC2)s1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(-c2nnc(CN3CC[NH+](CC4CCCCC4)CC3)o2)c(C)o1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CCc1c[nH]c2ccc(F)cc12
Fragment 2: [5*]Nc1cc(C)cc(C)c1
### Response:
Cc1cc(C)cc(NC(=O)[C@H]2CC(=O)N(CCc3c[nH]c4ccc(F)cc34)C2)c1 |
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