task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H]1C[C@H]1C(=O)N[C@@H]1CCCCC[C@@H]1C(=O)[O-]
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]Cc1cccc(O)c1
Fragment 2: [16*]c1cccc(O)c1
### Response:
C[C@H]1[C@H](Cc2cccc(O)c2)CC[C@@H]1Cl |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCN([5*])CC1
Fragment 2: [14*]c1ncccc1F
### Response:
O=C(c1cc2ccccc2[nH]1)N1CCN(c2ncccc2F)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O(C)c1c(CC(NCC)=O)c2c(cc(Br)cc2)cc1
### Response:
CCNC(=O)Cc1c(OC)ccc2cc(Br)ccc12 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[NH+](Cc1ccccc1NC(=O)N1CCN(Cc2ccncc2)CC1)C1CCCCC1
### Response:
4 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(NC(NCCC)=O)CN1C(=O)[C@](NC1=O)(c1ccccc1)Cc1ccccc1
### Response:
CCCNC(=O)NC(=O)CN1C(=O)N[C@](Cc2ccccc2)(c2ccccc2)C1=O |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(C(N[C@H](c2scc(C)n2)C2CC2)=O)[C@@H](COCC1)C1CC1
### Response:
Cc1csc([C@@H](NC(=O)N2CCOC[C@H]2C2CC2)C2CC2)n1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COCc1nc(C)cc(NCc2cccc(OCC#N)c2)n1
### Response:
0 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccc([C@H]2C[C@H]2C[NH3+])c1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COC(=O)[C@H](C)C[S@](=O)Cc1nc(C)c(C)s1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(c1ccccc1)n1c(n[nH]c1=O)C1CC[NH+](CC1)Cc1cnc(nc1)N
### Response:
Nc1ncc(C[NH+]2CCC(c3n[nH]c(=O)n3Cc3ccccc3)CC2)cn1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(Cc1ccc(OC)cc1)S(=O)(=O)c1sccc1Br
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(N1CCC[C@@H]1c1cccs1)C(C)(C)C
### Response:
CC(C)(C)C(=O)N1CCC[C@@H]1c1cccs1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(-c2nnc(NC(=O)C3CC3)o2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
O=C(CC1CC1)N1CC[C@]2(CCCN(Cc3ccc(F)c(F)c3)C2=O)C1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=c1[nH]c2ccc(-c3csc(NC[C@H]4CCCO4)n3)cc2[nH]1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1cc(C)c(C)cc1S(=O)(=O)NC[C@@](C)(O)CSC
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(/C=N/NC(=O)C(=O)N2CCCCC2)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@H](c1ccccc1)[S@](=O)CC(=O)Nc1cccc(C#N)c1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
O=C1[C@H]([NH+]2CCCC[C@@H]2CN2CCOCC2)CCN1C1CC1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(cc(N2CCN(CC2)C(c2c([nH]c(-c3ccc(C)cc3)c2)C)=O)cc1)Cl
### Response:
Cc1ccc(-c2cc(C(=O)N3CCN(c4cccc(Cl)c4)CC3)c(C)[nH]2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@@H]([8*])C
Fragment 2: [1*]C(=O)C([1*])=O
### Response:
COc1ccc(C)cc1[C@@H](C)NC(=O)C(=O)Nc1ccc(F)c(Cl)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@H]1CCOC1
Fragment 2: [3*]Oc1cc([C@H]([4*])C)ccn1
### Response:
CC[NH2+][C@H](C)c1ccnc(O[C@H]2CCOC2)c1 |
functional_group | ### Instruction:
Does the molecule contain a thiol group?
CC(C)C[C@H](CNC(=O)c1ccc(O)cc1O)C(=O)[O-]
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCC(C[NH+]2C[C@@H](NC(=O)c3cc([nH]n3)C)CC2)C1
### Response:
Cc1cc(C(=O)N[C@H]2CC[NH+](CC3CCCC3)C2)n[nH]1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[NH2+][C@@H](C)CC(C)(C)Cc1nc(C)c(C)s1
### Response:
5 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(c1cc(c(F)cc1)NC(=O)C(N1C[C@@H](C(CC)CC)CC1)=O)N(C)C
### Response:
CCC(CC)[C@H]1CCN(C(=O)C(=O)Nc2cc(C(=O)N(C)C)ccc2F)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1CCC[C@H](C)N1C(=O)CSc1nc2ccccc2n1CC(=O)N1CCCCC1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccc([16*])c1C
Fragment 2: [14*]c1cc2ccccc2o1
### Response:
Cc1c(NC(=O)N[C@H](C)c2cc3ccccc3o2)cccc1C(=O)N1CCOCC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N1(C[C@H]2[C@H](N(CCc3ccccc3)C(=O)CC2)CC1)C(c1n[nH]cc1)=O
### Response:
O=C(c1cc[nH]n1)N1CC[C@@H]2[C@@H](CCC(=O)N2CCc2ccccc2)C1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
C[NH+](C)CCO[C@@H]1C[C@@H]2CC[C@@]1(C)C2(C)C
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
Cc1csc([C@@H](C#N)C(=O)COC(=O)c2cc3c(s2)CC[C@@H](C)C3)n1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(Br)c(O)c(/C=N/NC(=O)CSCc2ccccc2)cc1Br
### Response:
O=C(CSCc1ccccc1)N/N=C/c1cc(Br)cc(Br)c1O |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCOc1ccc2c(c1)O/C(=C\C1=Cc3ccccc3OC1)C2=O
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C)C(=O)c1ccc(C[NH+](C)CCCc2n[nH]c(N)c2C#N)cc1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1ccc(Nc2nnc(C(C)(C)C)c(=O)n2N)cc1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COc1ccc(-n2ncc3c2C[C@@H](c2ccc(F)cc2)CC3=O)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a nitro group?
COCC[NH+]1CCC[C@@H](NC(=O)N(C2CC2)[C@H](C)C2CC2)C1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](CC(=O)N(C)C1CCS(=O)(=O)CC1)c1ccccc1
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CCCOc1cc(N2CCN(C(=O)C(C)C)CC2)nc(C)n1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCCc2c1oc1ccc(OCC(Nc3ccc(cc3)NC(=O)C(C)C)=O)cc21
### Response:
CC(C)C(=O)Nc1ccc(NC(=O)COc2ccc3oc4c(c3c2)CCCC4)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(n1c2c([nH]c(c1=O)=O)cc(C(NCc1nc(C)c(s1)C)=O)cc2)C
### Response:
CCn1c(=O)c(=O)[nH]c2cc(C(=O)NCc3nc(C)c(C)s3)ccc21 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccc(c1)NC(=O)c1ccc(cc1)I)NC(c1cccs1)=O
### Response:
O=C(Nc1ccc(NC(=O)c2cccs2)cc1)c1ccc(I)cc1 |
functional_group | ### Instruction:
Does the molecule contain a carboxyl group?
CN1CCN(C(=O)Nc2ccc[nH+]c2N2CCCC2)[C@@H](c2ccccc2)C1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CCCCN1C([C@H]2Cc3c([nH]c4c3cccc4)[C@H](N2C(C1)=O)c1cc([N+]([O-])=O)ccc1)=O
### Response:
CCCCN1CC(=O)N2[C@H](c3cccc([N+](=O)[O-])c3)c3[nH]c4ccccc4c3C[C@@H]2C1=O |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COc1n[nH]c(C(=O)Nc2cc(F)ccc2C)c1[N+](=O)[O-]
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1CC1
Fragment 2: [5*]NC1CC[NH+]([5*])CC1
### Response:
CC(=O)NC1CC[NH+](Cc2cnc(C3CC3)s2)CC1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
Cc1cc(C(=O)N2CCC[C@H](CCC(=O)NCc3ccc(F)c(F)c3)C2)nc(C)n1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc2c(c1)[nH]c1c([O-])nc(NC(=O)c3ccccc3)nc12
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@H]([8*])O
Fragment 2: [11*]S[C@@H]1[NH+]=c2ccc(C)cc2=[NH+]1
### Response:
Cc1ccc2c(c1)=[NH+][C@H](SC[C@@H](O)c1ccccc1)[NH+]=2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(cc(N[C@@H]2C(C)(C)CCSC2)c(F)cc1)C(OC)=O
### Response:
COC(=O)c1ccc(F)c(N[C@H]2CSCCC2(C)C)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[NH+](C)CCC(NC(=O)[C@H](N(S(=O)(=O)C)c2cc(cc(C)c2)C)CC)C1
### Response:
CC[C@H](C(=O)NC1CC[NH+](C)CC1)N(c1cc(C)cc(C)c1)S(C)(=O)=O |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1sc2ncn([9*])c(=O)c2c1C
Fragment 2: [5*]Nc1ccccc1
### Response:
Cc1c(C(=O)Nc2ccccc2)sc2ncn(CC(=O)Nc3cccc4ccccc34)c(=O)c12 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CN(C[C@@H]1COc2ccccc2O1)C(=O)c1cccc(S(=O)(=O)NCc2cccs2)c1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@@H]([NH3+])Cc1ccc(OCC2CC2)cn1
### Response:
4 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCSC1(CNC(=O)Nc2cc(-c3ccccc3)on2)CCOCC1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)C[C@H]2C(=O)NCCN2C(=O)C[NH+]2CCN(c3ccccc3F)CC2)cc1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Cc1ccc(C(=O)C2=C([O-])C(=O)N(CCc3ccccc3)[C@@H]2c2ccccc2)cc1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)C(C)(C)C[NH2+][C@@H]1CCCCC[C@H]1C
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]Oc1ccc(N)cc1
Fragment 2: [16*]c1ccc(N)cc1
### Response:
N#CCN(CC#N)C[C@@H](O)COc1ccc(N)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)c1nc(C[NH+]2CCC[C@@H](C(=O)N3CCOCC3)C2)cs1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)[C@H]1CC=CCC1
Fragment 2: [5*]NC[C@H]1N=NC2=C1CCCCC2
### Response:
O=C(NC[C@H]1N=NC2=C1CCCCC2)[C@H]1CC=CCC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC(=O)c1cc(c(OC)cc1)CC(N[C@@H]1[C@H]2[C@@H](C1(C)C)OCC2)=O
### Response:
COc1ccc(C(C)=O)cc1CC(=O)N[C@@H]1[C@@H]2CCO[C@@H]2C1(C)C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [6*]C(=O)NNC(=O)[C@H](C)C[8*]
Fragment 2: [15*]C1CCCC1
### Response:
C[C@H](CC1CCCC1)C(=O)NNC(=O)[C@H]1COc2ccccc2O1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCC([15*])CC1
Fragment 2: [16*]c1ccc(C)nc1
### Response:
Cc1ccc(OC2CCN(C(=O)c3ccc(S(=O)(=O)N4CCCC4)cc3)CC2)cn1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccco1
Fragment 2: [1*]C(=O)CC[8*]
### Response:
Cc1sc2ncn(CCC(=O)N(C)[C@H](C)c3ccco3)c(=O)c2c1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1cnnc1S[11*]
Fragment 2: [5*]Nc1cc(F)ccc1C
### Response:
COCCn1cnnc1S[C@@H](C)C(=O)Nc1cc(F)ccc1C |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc([C@H](C)NC(=O)/C(C#N)=C/[C@H]2C=NN=C2c2ccccc2)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CSc1cccc(NC(=O)CSCc2cccc(Cl)c2)c1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc2c(c1)N(CC=C)C(=O)C(C)(C)CO2
Fragment 2: [1*]C(=O)CCCCl
### Response:
C=CCN1C(=O)C(C)(C)COc2ccc(NC(=O)CCCCl)cc21 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(S(=O)(=O)N2CCCN(C(=O)c3ccc(S(=O)(=O)N4CCCC4)cc3)CC2)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1cccs1
Fragment 2: [4*][C@H]([8*])c1cccs1
### Response:
CC[C@@H](C)[C@@H](O)C[NH2+][C@@H](c1cccs1)C1CC1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1ccc(CCC(=O)N2CCCN(C(=O)C3=Cc4cc(Cl)ccc4OC3)CC2)cc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a halide group?
COc1ccc(-c2noc(CN(C(=O)c3ccc(C)c([N+](=O)[O-])c3)C3CCCCC3)n2)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(C1OCCCC=1)NCCC(=O)Nc1c(C)ccc(Br)c1
### Response:
Cc1ccc(Br)cc1NC(=O)CCNC(=O)C1=CCCCO1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[C@@H]([NH2+][C@@H]1CSCC(C)(C)C1)C(=O)[O-]
### Response:
4 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCN(CC(=O)N(C)C)C(=O)[C@@H]1CC[C@@H]2CCCC[C@@H]2[NH2+]1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(N=[P@@](c2ccncc2)(N2CCCC2)C(C)(C)C)c(C)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H]1CC=CC[C@@H]1COC(=O)C1CCN(C(=O)c2ccc(F)cc2)CC1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC(=O)Oc1cccc([N+](=O)[O-])c1C
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cn1cc[nH+]c1CN[C@@H]1CCC[C@@H]1[C@@H]1CCC[NH2+]1
### Response:
0 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CC(=O)N1CCc2cc(C(=O)N[C@@H](CC(C)C)c3nc4ccccc4[nH]3)ccc21
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(-c2cc(-c3ccccc3)cc(-c3ccc(I)cc3)[o+]2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
COC(=O)N1CCC[C@@H]1C(=O)N[C@H](C)c1cn(C)nc1C
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(C(=O)Nc1cc(C)ccc1C)Sc1cc(-c2ccccn2)nc(C)n1
### Response:
Cc1ccc(C)c(NC(=O)CSc2cc(-c3ccccn3)nc(C)n2)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
s1c(c(N)c2c1nccc2)C(=O)N1CCC(C)CC1
### Response:
CC1CCN(C(=O)c2sc3ncccc3c2N)CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cn1c([C@H]2CCCN(S(C)(=O)=O)C2)nn(CC(=O)Nc2ccccc2)c1=O
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1c2ccc(OC)cc2C=C[C@H]1C#N
Fragment 2: [1*]C(=O)c1ccccc1
### Response:
COc1ccc2c(c1)C=C[C@@H](C#N)N2C(=O)c1ccccc1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
COc1ccc(CNC(=O)COc2c(C)cc(Cl)cc2C=O)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCCC(n2c(nnc2SCCOC(C)C)-c2occc2)C1
### Response:
CC(C)OCCSc1nnc(-c2ccco2)n1C1CCCCC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Nc1ccc(OC(=O)Nc2ccc(O)cc2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
O=C(CN1CCN(C(=O)[C@H]2CCCO2)CC1)Nc1ccc(F)c(Cl)c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a halide group?
C[C@]12CCC(=O)N1c1ccccc1C(=O)N2CCC(=O)NCc1ccc(O)cc1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
N#Cc1ccc(NC(=O)C(=O)N2C[C@H]3CC=CC[C@@H]3C2)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(C(=O)[C@H]1CCCCN1C(=O)c1nc2c(cc1)cccc2)C
### Response:
CNC(=O)[C@H]1CCCCN1C(=O)c1ccc2ccccc2n1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)c1ccco1)c1ccc2ccccc2c1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1C[NH+](CCn2c(=O)oc3cccnc32)CCN1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](Cc1cccs1)N(C)C(=O)N1CC[C@@H](CC(=O)[O-])C1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C#CCNCC(=O)Nc1ccc(S(C)(=O)=O)nc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(C(=O)N[C@H](C)Cn2nc(C)cc2C)c2cccc(C)c2n1
### Response:
3 |
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