task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1ccc([S@@](C)=O)c(F)c1
Fragment 2: [5*]N1CCC[C@@H](O)C1
### Response:
C[S@@](=O)c1ccc(NC(=O)N2CCC[C@@H](O)C2)cc1F |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1cc(OC)cc([C@@H](N[C@@H](C)c2ccc(F)cn2)c2[nH+]ccn2C)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H](CNC(=O)c1ccc(Cl)c(-n2cnc3cccnc32)c1)c1ccccc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(=O)(c1ccc(NC(=O)C)cc1)N1CCC(Cn2cc[nH+]c2)CC1
### Response:
CC(=O)Nc1ccc(C(=O)N2CCC(Cn3cc[nH+]c3)CC2)cc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1nc(-c2cccc(C(=O)Nc3cnn(C[C@H]4CCCO4)c3)c2)cs1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CCCc1nc([C@H](NC(=O)c2ccsc2)c2ccccc2)no1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(cc(c(cc1)F)F)CN1[C@H](C[NH+](CC1)Cc1c(F)cc(F)cc1)CCO
### Response:
OCC[C@H]1C[NH+](Cc2ccc(F)cc2F)CCN1Cc1ccc(F)c(F)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C1CCCCN1C1CC[NH+](Cc2cc(C(F)(F)F)ccc2Cl)CC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C(CC[NH2+][C@@H]1CC2(CCOCC2)OCC1)C(=O)[O-]
### Response:
O=C([O-])CCC[NH2+][C@H]1CCOC2(CCOCC2)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(cc(cc1C[NH2+]CC(C)C)OC)F
### Response:
COc1cc(F)cc(C[NH2+]CC(C)C)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H]1C[NH2+]CCN1CC(F)(F)F
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [9*]n1cccn1
Fragment 2: [1*]C(=O)C([1*])=O
### Response:
CC(C)[C@H](C)NC(=O)C(=O)Nc1cc(Br)ccc1-n1cccn1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CN1C(=O)CC[C@H](N[C@H]2CCC[C@@H]2[C@@H]2CCC[NH2+]2)C1=O
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)[C@H]1CN(C(=O)c2sc(C)nc2C)C[C@H]1C
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(NC(=O)CCc2cnn(C)c2C)cc1S(C)(=O)=O
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@@H]([8*])C(N)=O
Fragment 2: [5*][NH2+][C@@H]1CCc2cc(F)ccc21
### Response:
NC(=O)[C@@H]([NH2+][C@@H]1CCc2cc(F)ccc21)c1ccccc1 |
functional_group | ### Instruction:
Does the molecule contain a ketone group?
COc1ncccc1CNC(=O)N[C@@H]1C[C@H]2CCCc3cccc1c32
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(=O)N1CCc2cc(S(=O)(=O)Oc3ccccc3Cl)ccc21
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)c1cc(C(=O)N(C)CCOc2ccccc2)on1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCC([15*])CC1
Fragment 2: [4*]Cc1nnc([14*])n1[9*]
### Response:
Cn1nccc1C(=O)N1CCC(c2nnc(C[NH+](C)C)n2C2CC2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cc2c(cc1C[NH+]1C[C@@H]3CC[C@@](O)(c4ncccc4C)[C@@H]3C1)CCCC2
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCN(C(=O)c1ccc(Cl)cc1Cl)[C@@H]1CCS(=O)(=O)C1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CSc1ncccn1)Nc1cccc(Br)c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H](C[NH+]1CCC(Cn2cc(CNC(N)=O)nn2)CC1)c1ccccc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(C)cc(c1CNC(=O)Nc1ccn(n1)C)N(C)C
### Response:
Cc1ccc(CNC(=O)Nc2ccn(C)n2)c(N(C)C)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[C@]1(C[C@@H]2Cc3ccccc32)CCCCC[NH2+]1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Br[C@H]1CCC[C@@H]1C[C@H]1COc2ccccc21
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc2c(c1OC)C(=O)O[C@H]2[C@H]1c2cc3c(cc2CCN1C)OCO3
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(C(=O)Nc1ccc(OC)cc1Cl)NCCCn1ccc2c1cccc2
### Response:
COc1ccc(NC(=O)C(=O)NCCCn2ccc3ccccc32)c(Cl)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cn1ccc2ccccc21)NC[C@@H]1CCS(=O)(=O)C1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
CC(C)[NH2+][C@@](C)(CO)CN(C)C[C@@H]1CCC[NH+]1C
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCC(CC)[NH2+]CC(=O)Nc1ccc(N(C)C)cc1
### Response:
0 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(ccc1OC)-c1onc(n1)Cn1c(=O)cccc1
### Response:
COc1ccc(-c2nc(Cn3ccccc3=O)no2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH2+][C@H](C)CCCO
Fragment 2: [4*]Cc1csc([14*])n1
### Response:
C[C@H](CCCO)[NH2+]Cc1csc(-c2ccc(F)cc2)n1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C=C[C@@]1(C)CC(=O)[C@]2(O)[C@@]3(C)CCCC(C)(C)[C@@H]3[C@H](O)[C@H](O)[C@@]2(C)O1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC[C@H](C)[C@@H](NC(=O)c1ccc(=O)[nH]c1)c1nc2ccccc2[nH]1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O[C@H]1CN(Cc2ccc(Cl)s2)Cc2ccccc21
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1nnnn1[9*]
Fragment 2: [16*]c1ccccc1
### Response:
C[NH+]1CCN(C(=O)CCCn2nnnc2C[NH+]2CCOCC2)C[C@H]1c1ccccc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C(C)(C)C
Fragment 2: [15*]C1CCC([15*])(C#N)CC1
### Response:
CC(C)(C)C1CCC(C#N)(C(C)(C)O)CC1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(NCCC)CSc1nnc(n1C)-c1ccc(C(C)(C)C)cc1
### Response:
CCCNC(=O)CSc1nnc(-c2ccc(C(C)(C)C)cc2)n1C |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CCn1c(=O)c(=O)[nH]c2cc(C(=O)Nc3ccc(C(C)C)cc3)ccc21
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCCC[C@H]1[13*]
Fragment 2: [14*]c1noc([14*])n1
### Response:
CCC(=O)N1CCCC[C@H]1c1nc(-c2ccncc2)no1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C([O-])COc1ccc(/C=C2\C(=O)N(c3ccc(Cl)cc3Cl)C(=O)N=C2[O-])cc1Cl
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCO[C@H]([13*])C1
Fragment 2: [4*]CCS(C)(=O)=O
### Response:
CS(=O)(=O)CCN1CCO[C@H](c2ccc(Cl)s2)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cnccc1C
Fragment 2: [5*]Nc1ccc(C)cc1
### Response:
Cc1ccc(NS(=O)(=O)c2ccc(C(=O)Nc3cnccc3C)cc2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
COCCCN(C)C(=O)C(=O)Nc1nnc(C23CC4CC(CC(C4)C2)C3)s1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[nH]1c(c(C(=O)N[C@@H](C)C(OCCCC)=O)cc2CCCCc12)=O
### Response:
CCCCOC(=O)[C@H](C)NC(=O)c1cc2c([nH]c1=O)CCCC2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCCOCC(=O)N1CCO[C@]2(C[NH2+]CCOC2)C1
### Response:
4 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)[NH+]1CCN(Cc2cc3n(n2)CCN(C(=O)c2ncn[n-]2)C3)C[C@H]1C
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CCO[C@@H]1CNC(=O)c1cc2cc(ccc2o/c1=[NH+]\c1ccccc1C)Cl
### Response:
Cc1ccccc1/[NH+]=c1\oc2ccc(Cl)cc2cc1C(=O)NC[C@@H]1CCCO1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC(=O)C1=C(C)C(C(=O)CSc2nc3ccccc3o2)=N[C@H]1C
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1Cc2n(ncc2[C@@H]([NH2+]C[C@@]2(CCc3ccccc32)O)C1)C
### Response:
Cn1ncc2c1CCC[C@@H]2[NH2+]C[C@]1(O)CCc2ccccc21 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](OC(=O)c1nc(C2CC2)n2ccccc12)c1cnc2ccccc2c1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cn1cncc1C(=O)N1CCc2[nH]nc(-c3ccc(-c4ccccc4)cc3)c2C1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(ccc(S(=O)(=O)N2C[C@H](CCC2)C(OCC(F)(F)F)=O)s1)C
### Response:
Cc1ccc(S(=O)(=O)N2CCC[C@H](C(=O)OCC(F)(F)F)C2)s1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COCCCN1C(=O)c2ccc(C(=O)Nc3c(C)cc(C)cc3Cl)cc2C1=O
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(S[C@H]1CS(=O)(=O)C[C@@H]1Cl)c1ccc([N+](=O)[O-])cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cnc2ccccc2n1
Fragment 2: [14*]c1nc2ccccc2[nH]1
### Response:
c1ccc2nc(NCCCc3nc4ccccc4[nH]3)cnc2c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H](c1ccccn1)N(C)C(=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1(CCCCC1)NC(=O)N1CCC(CC1)N1CCN(C(=O)C1=O)Cc1ccc(cc1)C
### Response:
Cc1ccc(CN2CCN(C3CCN(C(=O)NC4CCCCC4)CC3)C(=O)C2=O)cc1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCOc1nnnn1-c1ccccc1
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a halide group?
C[C@@H]([NH2+][C@@H]1CCSc2ccc(F)cc21)c1ccc(-n2ccnn2)cc1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCOC(=O)NCCCn1c(C)cc2ccccc21
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[NH2+]Cc1ccc(CN(C)c2ccccc2F)nc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[NH+]([5*])C
Fragment 2: [1*]C(=O)C[4*]
### Response:
C[NH+](CC(=O)NCC1CCC1)Cc1ccc(C(F)(F)F)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O[C@H](C[NH+](Cc1ccccc1)C1CC1)c1ccc(F)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CSc1nc(-c2ccc(C)cc2)c(C#N)c(=O)[nH]1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)CC[8*]
Fragment 2: [3*]OCC
### Response:
CCOC(=O)CC[C@H]1CCC[NH+](Cc2ccc(C#N)o2)C1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(OC)c2[nH]c(=O)c(CCNC(=O)c3ccccc3F)cc12
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
COc1ccc2ccc(OC(=O)c3cccnc3N3CCCCC3)cc2c1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O(c1ccc(C2(CCOCC2)C[NH2+]Cc2c[nH]cc2)cc1)CC
### Response:
CCOc1ccc(C2(C[NH2+]Cc3cc[nH]c3)CCOCC2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cccc([C@@H]2[NH2+][C@@](CCSC)(C(=O)[O-])[C@@H]3C(=O)N(C(C)C)C(=O)[C@@H]32)c1O
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c([C@@H](N(C(=O)Nc2c(cc(F)cc2F)F)C2CC2)C)occ1
### Response:
C[C@@H](c1ccco1)N(C(=O)Nc1c(F)cc(F)cc1F)C1CC1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
CCC(=O)N(Cc1ccco1)Cc1cc2ccc(C)cc2[nH]c1=O
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(C2=C[C@@H](C(=O)N/N=C/c3ccc(C)cc3)N=N2)cc1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H](NC(=O)N[C@@H]1C[C@@H]1c1ccccc1F)[C@@H](O)c1ccc(Cl)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC1(C)C[NH+]=C(N2CCN(C(=O)c3cccc(-n4cccn4)c3)CC2)S1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C(COCC(=O)N([C@H]2CCCC[C@@H]2S(C)(=O)=O)C)C1
### Response:
CN(C(=O)COCC1CC1)[C@H]1CCCC[C@@H]1S(C)(=O)=O |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H]1COC[C@@H](C)N1C(=O)CSc1nnnn1C
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC[C@H](NC(=O)N[C@H](C)CCCO)c1cccs1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C([C@H]2N(C(=O)NCC3(Cc4ccccc4)CC3)CCOC2)C1
### Response:
O=C(NCC1(Cc2ccccc2)CC1)N1CCOC[C@H]1C1CC1 |
functional_group | ### Instruction:
Does the molecule contain a hydroxyl group?
COc1cc(F)cc(CNC(=O)Cc2nc(-c3ccsc3)oc2C)c1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COc1ccccc1/N=N\c1c(O)n[nH]c1C
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](NC(=O)NCc1ccc([N+](=O)[O-])cc1)[C@@H](C)CO
### Response:
4 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(NCCc1cc(Cl)c2c(c1)OCCO2)C1CCN(C(=O)c2cccs2)CC1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
C[C@H](NC(=O)N[C@H](C)c1ccncc1)c1ccc(N2CCCC2=O)cc1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cccc(N2CC[C@@H](CNC(=O)c3c(C)oc(C)c3C)C2)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@H]1[C@@H]([C@H]([NH3+])[C@@H](C)c2ccccn2)[C@@H](C)O[C@H]1C
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
N#CCC(=O)Nc1ccc(-c2nc3ccccc3o2)cc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(C(=O)N2[C@@H]3CCCC[C@@H]3CCC2)ccc1NC(=O)CSc1n(C)nnn1
### Response:
Cn1nnnc1SCC(=O)Nc1ccc(C(=O)N2CCC[C@H]3CCCC[C@H]32)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(ccc(C[C@H](N(C(c2ccc(cc2)-c2nnc(o2)C)=O)C)C)c1)Cl
### Response:
Cc1nnc(-c2ccc(C(=O)N(C)[C@H](C)Cc3ccc(Cl)cc3)cc2)o1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(NCC(NCCc2ccccc2)=O)ccc(c(c1)C)-n1nnnc1
### Response:
Cc1cc(NCC(=O)NCCc2ccccc2)ccc1-n1cnnn1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1
Fragment 2: [5*]N/C=C1\C(=O)NC(=S)N([10*])C1=O
### Response:
CCN(CC)c1ccc(N/C=C2\C(=O)NC(=S)N(c3ccc(F)cc3)C2=O)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]Oc1cccc(Cl)c1
Fragment 2: [3*]O[C@@H]1CCN([5*])C1
### Response:
Clc1cccc(O[C@@H]2CCN(Cc3cnc(N4CCOCC4)nc3)C2)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N(S(c1ccc(CC#N)cc1)(=O)=O)[C@H](C(=O)[O-])C(C)(C)C
### Response:
CC(C)(C)[C@H](NS(=O)(=O)c1ccc(CC#N)cc1)C(=O)[O-] |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
Cc1ccc(C(=O)NCc2cnc(C)s2)c(NN)c1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOc1ccc(C(=O)CN2C(=O)N[C@@]3(CCCC[C@@H]3C)C2=O)cc1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[NH2+]1C[C@H]([C@H](C1)C(N(CC(=O)[O-])CC#C)=O)C
### Response:
C#CCN(CC(=O)[O-])C(=O)[C@H]1C[NH2+]C[C@H]1C |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C=C1CCC[C@]2(C)C[C@H]3OC(=O)[C@H](CN(C)CC4OCCO4)[C@H]3C[C@@H]12
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cc1csc(-c2ccoc2)n1)N[C@H](c1ccccc1)C1CCC1
### Response:
2 |
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