task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@](O)(CNC(=O)COc1ccccc1Cl)c1ccc(F)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc2c(c1)[C@@](O)(CC(=O)c1ccc(Cl)cc1Cl)C(=O)N2
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)c1ccccc1C(=O)NCc1cc(-c2cccc(OC)c2)on1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
COC([C@H](c1ccccc1)Oc1ccc(C=O)cc1)=O
### Response:
COC(=O)[C@@H](Oc1ccc(C=O)cc1)c1ccccc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(C1C[C@@]2(NN=1)C(N(c1cc(C)ccc1C)C(=O)C2)=O)(OCc1ccccc1)=O
### Response:
Cc1ccc(C)c(N2C(=O)C[C@@]3(CC(C(=O)OCc4ccccc4)=NN3)C2=O)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Cn1c2ccc(Cl)cc2nc1[C@H]([NH2+][C@H](C)c1c(cccc1)C)C
### Response:
Cc1ccccc1[C@@H](C)[NH2+][C@H](C)c1nc2cc(Cl)ccc2n1C |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(N(C(/C=C/c1ccc(N2CCOCC2)cc1)=O)C[C@H]1CCCCO1)(C)C
### Response:
CC(C)N(C[C@H]1CCCCO1)C(=O)/C=C/c1ccc(N2CCOCC2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
Cc1ccc(-n2ncc3c2ncn2nc(CCc4ccccc4)nc32)cc1Cl
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCCOc1cccc(/C=C(/C#N)C(=O)NC)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(Nc2nc(N)nc(C[NH+]3CCCC3)n2)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*][C@@H]1CCCC1(C)C
Fragment 2: [1*]C(=O)N[5*]
### Response:
C[C@@H]1CCN(C(=O)N[C@@H]2CCCC2(C)C)C[C@@H]1O |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [10*]N1C(=O)CCC1=O
Fragment 2: [4*][C@@H]([8*])c1ccc(F)cc1
### Response:
O=C(NCCN1C(=O)CCC1=O)N[C@H](c1ccc(F)cc1)C1CCCC1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCN(CC)S(=O)(=O)c1ccc(N2CCOCC2)c(NC(=O)c2cc3ccccc3oc2=O)c1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCOC(=O)C1CCN([C@H]2/C(=N/O)[C@H]3CC[C@@H]2C3)CC1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC1(C)[C@H]2CC[C@]1(C)[C@H](OC(=O)CSc1nc3ccccc3o1)C2
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1nc(sc1)CC(c1c(c(ccc1)C(F)(F)F)F)=O
### Response:
O=C(Cc1nccs1)c1cccc(C(F)(F)F)c1F |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC1(C(=S)C(c2cc(C)ccc2N1)=C1SC(=C(C(OC)=O)S1)C(=O)OC)C
### Response:
COC(=O)C1=C(C(=O)OC)SC(=C2C(=S)C(C)(C)Nc3ccc(C)cc32)S1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12ccccc1oc(C(N(c1ncccc1)[C@@H](c1occc1)C)=O)c2
### Response:
C[C@H](c1ccco1)N(C(=O)c1cc2ccccc2o1)c1ccccn1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cn1c(CNC(=O)[C@H](Oc2ccc(F)c(F)c2)c2ccccc2)n[nH]c1=S
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(Cl)cc(c(NC(=O)C=C(C)C)cc1)-c1nc(CCOC)no1
### Response:
COCCc1noc(-c2cc(Cl)ccc2NC(=O)C=C(C)C)n1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C1CCN([5*])CC1
Fragment 2: [5*]N1CCC[C@@H]([15*])C1
### Response:
O=C(/C=C/c1ccccc1)N1CCC(C(=O)N2CCC[C@@H](c3nc(-c4cccc(F)c4)no3)C2)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(c1ccc(Oc2ccccc2)cc1)N1CCC(CC1)Cn1c([nH+]cc1)CC
### Response:
CCc1[nH+]ccn1CC1CCN(C(=O)c2ccc(Oc3ccccc3)cc2)CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(=O)c1cccc(OC[C@@H](O)Cn2cnc([N+](=O)[O-])c2)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1Cc2cc(C(=O)C3=C([O-])C(=O)N(CCN4CCOCC4)[C@H]3c3ccco3)ccc2O1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1nnc(NCCC(=O)N2C[C@H](C)O[C@@H](C)C2)c(C#N)c1C
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[nH]1/c(n(nc1C(C)C)C)=N\S(=O)(=O)c1ccc(cc1)OCCC(C)C
### Response:
CC(C)CCOc1ccc(S(=O)(=O)/N=c2\[nH]c(C(C)C)nn2C)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccnc(-n2nc(-c3ccccc3)nc2C2(C(N)=O)CC2)c1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccc(I)c1)NC(=O)[C@]12C(C)([C@@](C)(CC2)/C(C1)=N/O)C
### Response:
CC1(C)[C@]2(C(=O)Nc3ccc(I)cc3)CC[C@@]1(C)/C(=N/O)C2 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CN(C)c1nc(Nc2ccc(Cl)cc2Cl)nc(N(C)C)n1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
O=C(NCCc1cccc(O)c1)NC[C@]1(O)CCCc2ccccc21
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)N[C@@H](C)c2ccc(F)c(F)c2)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CN(C(=O)c1ccc(NC(=O)CC2(O)CCCC2)cc1)C1CCCCC1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCNC(=O)CO[C@@H]1CC[C@@H]([NH3+])C1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cc(N[C@H](CN2CC[NH+](C)CC2)c2ccccc2)ncc1[N+](=O)[O-]
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(NC(=O)N2CCC[C@H]2C(=O)NCCc2ccccc2)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@H]([8*])CO
Fragment 2: [16*]c1ccc(F)cc1
### Response:
CCc1ccc([C@H](CO)NC(=O)[C@H]2C[C@@H]2c2ccc(F)cc2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
Nc1cc(N)nc(SCc2cc(=O)n3ccccc3n2)n1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COC(=O)[C@H](c1ccccc1)N1CC[NH+](C2CCCC2)CC1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCN(CC)C(=O)CC1(C(=O)[O-])CCCCCCCCCCC1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(NC(=S)NCc1ccccc1)C(c1c(nn(c1)C)CC)=O
### Response:
CCc1nn(C)cc1C(=O)NNC(=S)NCc1ccccc1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
COc1ccc(N[C@H](C)C(=O)NC(N)=O)c(OC)c1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
COc1cc(OC)ccc1NC(CSc1nc(-c2ccccc2)c(N)s1)=O
### Response:
COc1ccc(NC(=O)CSc2nc(-c3ccccc3)c(N)s2)c(OC)c1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CCO[C@@H]1C[C@@H]([O-])C12CCN(C(=O)c1cccs1)CC2
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1COC[C@H](C1)C[NH2+][C@@H]1C(C)(CCCC1)C
### Response:
CC1(C)CCCC[C@@H]1[NH2+]C[C@H]1CCCOC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](NC(=O)NCc1ccc(CN2CCOCC2)cc1)c1ccccc1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CN(C)c1nc2ccccc2cc1C[NH+]1CCc2c([nH]c(N3CCOCC3)nc2=O)C1
### Response:
5 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C/C(=N\Nc1ncnc2sc(C)c(C)c12)c1cccc(OC(F)F)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
N#Cc1csc(C(=O)N2CCC(C(=O)c3cccs3)CC2)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H](NC(=O)c1ccccc1F)c1cccc(-n2cccn2)c1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccccn1
Fragment 2: [9*]n1c([14*])nnc1[S-]
### Response:
COc1ccc(-n2c([S-])nnc2-c2ccccn2)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1cn(C(=O)O[C@H](C)C=C)cc1
### Response:
C=C[C@@H](C)OC(=O)n1ccnc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1noc(NC(=O)CSc2nc3ccccc3[nH]2)n1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
COc1ccc(-n2ccnc2C[NH+]2Cc3[nH]cnc3C[C@@H]2C(=O)[O-])cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]Oc1cccc(C)c1
Fragment 2: [16*]c1ccccc1
### Response:
Cc1cccc(OCC(=O)N[C@@H](c2ccccc2)c2cccnc2)c1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cc1ccccc1NC(=O)Cn1c(=O)oc2cc(S(=O)(=O)N3C[C@H](C)C[C@@H](C)C3)ccc21
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(c1cncc(Br)c1)N1CCN(S(=O)(=O)/C=C/c2ccccc2)CC1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1CCCC1
Fragment 2: [5*]Nc1ccc2c(c1)OCO2
### Response:
O=C(Nc1ccc2c(c1)OCO2)C1CCN(C(=O)CCC2CCCC2)CC1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCn1cc(S(=O)(=O)N[C@@H]2C[C@H]2c2cccc(Cl)c2)cn1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCc2cc(C)ccc21
Fragment 2: [4*]Cc1nc2c(oc3ccccc32)c(=O)[nH]1
### Response:
Cc1ccc2c(c1)CCN2Cc1nc2c(oc3ccccc32)c(=O)[nH]1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1nn(C)cc1NC(=O)N[C@H](CO)C1CC1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
COc1ccc([C@H](O)[C@H](C)NC(=O)c2ccc(C)s2)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ccsc1
Fragment 2: [6*]C(C)=O
### Response:
CC(=O)c1ccc(S(=O)(=O)NCc2ccsc2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
O=C(NCC[C@H]1CCCCN1S(=O)(=O)c1cccs1)c1cc(Cl)ccc1Cl
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
[NH3+][C@H]1CCC[C@@H]1NC(=O)N1CCCC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1c(noc1CC[C@@H](C)[NH2+]C)[C@@]1(OCCC1)C
### Response:
C[NH2+][C@H](C)CCc1nc([C@@]2(C)CCCO2)no1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(=O)(c1ccccc1)Nc1cc(c(C)cc1)NC(=O)c1cc2c(ccc(c2)F)[nH]1
### Response:
Cc1ccc(NC(=O)c2ccccc2)cc1NC(=O)c1cc2cc(F)ccc2[nH]1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)N1CCC[C@@H]1[13*]
Fragment 2: [5*][NH+]1CCCCC1
### Response:
O=C(NCCC[NH+]1CCCCC1)N1CCC[C@@H]1c1ccc2c(c1)OCO2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccc(-c2nnc(C[NH+]3CCCC[C@@H]3CNC(=O)OC(C)(C)C)o2)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [13*][C@H]1C[NH+]2CCN1CC2
Fragment 2: [16*]c1cc(OC)ccc1OC
### Response:
COc1ccc(OC)c([C@@H](N)[C@H]2C[NH+]3CCN2CC3)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(NCCc1cscn1)[C@H]1CSCN1C(=O)c1cccc(F)c1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
O=C(Nc1ccc(F)cc1)N[C@H](c1ccccc1)c1ccccn1
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cccn2c(=O)c(C(=O)NC[C@H]3CCO[C@@H]3C(C)C)cnc12
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1(C)c2c(cc(S(N3C[C@@H](CCC3)C(Nc3ccc(cc3)C(=O)C)=O)(=O)=O)cc2)oc1=O
### Response:
CC(=O)c1ccc(NC(=O)[C@@H]2CCCN(S(=O)(=O)c3ccc4c(c3)oc(=O)n4C)C2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Nc1cccc(N2CCCC2=O)c1)C(=O)N[C@H]1CCC[C@@H](C2CC2)C1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CC(C)C[C@H](CNC(=O)c1ccn(-c2ccccc2)n1)[NH+](C)C
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C#CCOC(=O)c1cccc(OCC(F)F)n1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
CCOC(=O)c1ccc(NCc2ccc(N3CC[NH+](C)CC3)nc2)nc1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOC(=O)c1cc2n(n1)C[C@@](C)(C(=O)NC1CCC(C)CC1)N(c1cccc(Cl)c1C)C2=O
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC[C@]1(C)C[NH2+][C@@H](C(C)(C)C)CN1Cc1cccc(O)c1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C[C@@H]1N(CCN(c2c(nccn2)C#N)C1)CN1CCCCC1=O
### Response:
C[C@H]1CN(c2nccnc2C#N)CCN1CN1CCCCC1=O |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C#CCN1CCN([C@@H](C)C(=O)Nc2cc(F)ccc2C)CC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc2cn[nH+]c(c21)N1CCC(CC1)OC([C@@H]1C[C@@H]1OCC)=O
### Response:
CCO[C@H]1C[C@H]1C(=O)OC1CCN(c2[nH+]ncc3ccccc23)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccc([16*])c1
Fragment 2: [5*]NCCC1=CCCCC1
### Response:
O=C(NCCC1=CCCCC1)c1cccc(NC2=N[C@@H]3CS(=O)(=O)C[C@H]3S2)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
SC[C@@H](C[NH+]1CCCSCC1)c1ccccc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12nc(C3CC3)n(C)c2ccc(NC(c2ccc(n(n2)CCC)=O)=O)c1
### Response:
CCCn1nc(C(=O)Nc2ccc3c(c2)nc(C2CC2)n3C)ccc1=O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(C(=O)c2ccc(SC)cc2)cc1Cl
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cc(C[S@](=O)Cc2csc(C3CCCCC3)n2)no1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@]1(NC(=O)CNc2cc(F)cc(F)c2)CCS(=O)(=O)C1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C([C@H](c2ccc(cc2)OC)[NH2+]CCc2c(C)noc2C)C1
### Response:
COc1ccc([C@H]([NH2+]CCc2c(C)noc2C)C2CC2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC(C)(O)CNC(=O)[C@@H]1C[C@@H]1c1cccc(F)c1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC[C@]([8*])(C)O
Fragment 2: [4*][C@H](C)c1ccc(OC)c(F)c1
### Response:
COc1ccc([C@@H](C)NC[C@](C)(O)c2ccc(C)o2)cc1F |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCOc1ccccc1NC(=O)[C@@H]1C=C(c2ccccn2)N=N1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ocnc1CNC(=O)N[C@@H]1CCCN(c2ccccc2F)C1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cn1cc([C@@](C)(O)CN[C@@H](c2cccs2)C2CCCC2)cn1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C1=C(C)Nc2nnnn2[C@H]1c1ccc([16*])cc1
Fragment 2: [1*]C(=O)C1=C(C)Nc2nnnn2[C@H]1c1ccc(O[3*])cc1
### Response:
CC1=C(C(=O)Nc2ccccc2)[C@H](c2ccc(OCc3ccccc3)cc2)n2nnnc2N1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC[C@H]2N1C[C@@H](OC2)C[NH2+]CC#CC
### Response:
CC#CC[NH2+]C[C@H]1CN2CCC[C@@H]2CO1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccsc1CN(C)C(=O)Nc1cccc(CC[NH+]2CCCC2)c1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCn1c(N2CCOCC2)nn(CN(C)Cc2ccc(C#N)cc2)c1=S
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cc(C(=O)NCCn2ccc3ccc(F)cc32)c2c(C)nn(C)c2n1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCC[C@H]([NH2+]C)c1ccn(Cc2cc(C)nn2CC)c1
### Response:
4 |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.