task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[NH+](C)[C@@H](CNC(=O)[C@@H]1CC(=O)N(Cc2ccccn2)C1)c1ccccc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CC(CC[NH+]1C(C)C)N(C(c1ccc(cc1)-n1cccc1)=O)C
### Response:
CC(C)[NH+]1CCC(N(C)C(=O)c2ccc(-n3cccc3)cc2)CC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1OCC[C@H]1C(=O)N1CCN(S(=O)(=O)c2cccc(F)c2)CC1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOCCN(C)C(=O)C1(CC)CCCC1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1CC1
Fragment 2: [4*][C@@H]([8*])CCO
### Response:
OCC[C@@H]([NH2+][C@H]1CCCc2ccc(Cl)cc21)C1CC1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CCc1nnc(N2CCN(C(=O)Cc3cccc(OC)c3)CC2)c2cccn12
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1ccccc1N1CCN(C(=O)c2cccc(S(=O)(=O)N3CCOCC3)c2)CC1
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Clc1nnc(SC2COC2)c2ccccc12
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1F
Fragment 2: [5*][NH2+]CC
### Response:
CC[NH2+]Cc1ncoc1-c1ccc(F)cc1F |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
N#CCC1(CSc2cc3ccccc3[nH]2)CC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
NC1=[NH+]C[C@](c2ccc(C(C)(C)C)cc2)(N1CC1CC1)C
### Response:
CC(C)(C)c1ccc([C@@]2(C)C[NH+]=C(N)N2CC2CC2)cc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@H](C)O[C@@H](CN1C[C@H]1C(=O)O[C@@H]2CC3[C@](C)([C@@H]([C@H]12)O)[C@H](C)CCC=3)C
### Response:
C[C@@H]1CN(C[C@H]2C(=O)O[C@@H]3CC4=CCC[C@@H](C)[C@@]4(C)[C@H](O)[C@@H]32)C[C@H](C)O1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Cc1n(c(nn1)CSCc1nnnn1-c1c(C)cccc1C)C
### Response:
Cc1cccc(C)c1-n1nnnc1CSCc1nnc(C)n1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [3*]OCC
Fragment 2: [5*]Nc1sc2ccccc2c1Cl
### Response:
CCOC(=O)[C@@H](C)CNC(=O)Nc1sc2ccccc2c1Cl |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(Br)cc1F
Fragment 2: [3*]Oc1ccc(Br)cc1F
### Response:
Cc1cc(Oc2ccc(Br)cc2F)c([C@H](C)[NH3+])cc1F |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC[C@H](Cc1ccc(C)cc1)NC(=O)NNC(=O)Nc1ccccc1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(C[NH+]2[C@@H](C)C[C@H](C2)NCc2cn(C)nc2C(C)(C)C)cccc1
### Response:
C[C@H]1C[C@@H](NCc2cn(C)nc2C(C)(C)C)C[NH+]1Cc1ccccc1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C=CCCO[C@H](C)C(=O)N[C@@H]1CC[NH+](C)[C@@H]1c1ccc(Cl)cc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N(C)c1c(C)noc1C
Fragment 2: [16*]c1cc(C)ccc1OC
### Response:
COc1ccc(C)cc1-n1ccc(C(=O)N(C)c2c(C)noc2C)n1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(/C=C/c1ccc(N2CCCC2=O)cc1)NCC(=O)Nc1cccnc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)NC(=O)[C@@]1(Cc2ccccc2-c2cccs2)CCC[NH+](Cc2cnc(N)nc2)C1
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[8*]
Fragment 2: [5*]N[C@H]1CC[C@]2(C)CC[C@H]([15*])[C@H](O)[C@H]2[C@@H]1C
### Response:
CC1CCN(C(=O)[C@@H](C)[C@H]2CC[C@@]3(C)CC[C@H](NC(=O)Cc4ccccc4)[C@@H](C)[C@@H]3[C@H]2O)CC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCO[C@H]([13*])C1
Fragment 2: [4*]Cc1c(C)nc2sccn12
### Response:
Cc1nc2sccn2c1CN1CCO[C@H](c2ccccc2F)C1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
ClC1(Cl)[C@@H](c2ccccc2)[C@@H]1c1ccccc1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]CC(C)C
Fragment 2: [14*]c1c(Cl)c(C)nn1C
### Response:
Cc1nn(C)c(C[C@@H](O)c2ccc(CC(C)C)cc2)c1Cl |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cccc(C(=O)Nc2ccc(NC=C3C(=O)OC(C)(C)OC3=O)cc2)c1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1ccc(C(=O)Nc2ccc(-n3ncn(C)c3=O)cc2)c(C)n1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](CCN1CCOCC1)[NH2+][C@H]1CCc2cc(Br)ccc2C1
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Fc1cc(C[NH2+]CCCn2cc[nH+]c2)cc(F)c1F
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(S(=O)(N2CC[NH2+][C@H](C)C2)=O)nccc(C#N)c1
### Response:
C[C@@H]1CN(S(=O)(=O)c2cc(C#N)ccn2)CC[NH2+]1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
NC(=S)COc1ccc(cc1)NC(c1ccc(cc1)F)=O
### Response:
NC(=S)COc1ccc(NC(=O)c2ccc(F)cc2)cc1 |
functional_group | ### Instruction:
Does the molecule contain a nitrile group?
CN(C(=O)N[C@H]1CC[C@@H]([NH+](C)C)C1)[C@@H]1CCN(c2ccccc2F)C1=O
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
N#Cc1ccc(OC2CCC(NC(=O)c3ccc[nH]3)CC2)nc1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(c(CNc2cc(OC)c(cc2)OC)cc1)Br
### Response:
COc1ccc(NCc2ccccc2Br)cc1OC |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccc(Cl)cn1
Fragment 2: [8*]C[C@H]([8*])[NH3+]
### Response:
COc1cccc(C[C@@H]([NH3+])c2ccc(Cl)cn2)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N([5*])S(=O)(=O)c1ccccc1Br
Fragment 2: [4*]CC1CC1
### Response:
CC(C)N(CC1CC1)S(=O)(=O)c1ccccc1Br |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC(CC)(CC)CC
Fragment 2: [5*]N[C@@H](C)CSC
### Response:
CCC(CC)(CC)NC(=O)N[C@@H](C)CSC |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1Br
Fragment 2: [3*]Oc1ccc([N+](=O)[O-])c(N)n1
### Response:
Nc1nc(Oc2ccc(F)cc2Br)ccc1[N+](=O)[O-] |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(/C=C/c1ccc(Cl)cc1)OCC1CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)c(F)c1
Fragment 2: [4*][C@@H](C)c1ccc(F)c(F)c1
### Response:
C[C@@H](c1ccc(F)c(F)c1)[NH+](C)Cc1cn2cc(Cl)ccc2n1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cscc1[C@H]([NH3+])c1cc(F)cc(F)c1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1(c(C)cc(cc1C)Br)NC(N[C@H](CCO)CSC)=O
### Response:
CSC[C@@H](CCO)NC(=O)Nc1c(C)cc(Br)cc1C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1cc(C)c2occ(C(C)=O)c2c1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
Clc1ccc(C[C@H](C)[NH2+]Cc2ccc(NC(=O)N)cc2)cc1
### Response:
C[C@@H](Cc1ccc(Cl)cc1)[NH2+]Cc1ccc(NC(N)=O)cc1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
COC(=O)c1cccc(-c2ccc(/C=C3/NC(=O)N(Cc4ccccc4F)C3=O)o2)c1C
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(CNC(=O)[C@H](C)Oc2ccc(C#N)cc2)cc1OC
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(CC)C(=O)Cc1cn(Cc2ccc(Cl)cc2)c2ccccc12
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CN(CC1CC[NH+](C)CC1)C(=O)c1cccc(-c2noc(C3CC3)n2)c1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N[C@H]([8*])CC
Fragment 2: [4*]CC=C(C)C
### Response:
CC[C@H](NC(=O)c1ccccc1SCC=C(C)C)c1nccs1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CN(C[C@@H](O)c2ccccc2Cl)CCN1S(=O)(C)=O
### Response:
CS(=O)(=O)N1CCN(C[C@@H](O)c2ccccc2Cl)CC1 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
O=Cc1ccc(N2CCC[C@@H](c3nc4ccccc4[nH]3)C2)c([N+](=O)[O-])c1
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(NC(Cn2cc([nH+]c2)-c2nc(C3CC3)on2)=O)ccc(c1Cl)OC
### Response:
COc1ccc(NC(=O)Cn2c[nH+]c(-c3noc(C4CC4)n3)c2)cc1Cl |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
O=S(=O)(c1ccc(Br)cc1Cl)N1CCN(Cc2cc(-c3ccccc3)no2)CC1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC(C)(Nc1ccc(Cl)cc1)C(=O)[O-]
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C#CCNC(=O)N[C@H](C)c1cc(OC)c(OC)c(OC)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCC(C)(C)NC(=O)[C@@H](C)N1CCN(c2ccc(OC)c(F)c2)CC1
### Response:
0 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N([5*])C(C)C
Fragment 2: [16*]c1cccc(Cl)c1
### Response:
Cc1c(C(=O)N(CC(N)=O)C(C)C)nnn1-c1cccc(Cl)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCn1cnnc1S[C@H]1C[C@@H](C)OC1=O
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cc1cccnc1C[C@H]([NH3+])[C@H]1C[C@@H]1C
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C1CN(C(=O)c2cnn3cccnc23)C[C@H](OCc2cccnc2)CN1CC1CCOCC1
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
FC(F)(c1ccc(-c2ocnc2C[NH2+]C)cc1)F
### Response:
C[NH2+]Cc1ncoc1-c1ccc(C(F)(F)F)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH+]1CCC[C@H]1CO
Fragment 2: [15*][C@@H]1CCOC2(CCSCC2)C1
### Response:
OC[C@@H]1CCC[NH+]1[C@@H]1CCOC2(CCSCC2)C1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]CC([6*])=O
Fragment 2: [3*]Oc1ccc(F)cc1Br
### Response:
O=C(COc1ccc(F)cc1Br)c1cccc(Br)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CCS[C@H]1C[C@H](CCC1)NC(=O)N[C@@H](C)c1c(noc1C)C
### Response:
CCS[C@@H]1CCC[C@H](NC(=O)N[C@@H](C)c2c(C)noc2C)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCSC1(CNC(=O)Nc2cc(-c3ccccc3)on2)CCOCC1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1CN(C(=O)C2(C#N)CCCC2)CCC1n1c2c(cccc2)[nH]c1=O
### Response:
N#CC1(C(=O)N2CCC(n3c(=O)[nH]c4ccccc43)CC2)CCCC1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(C1CCN(S(=O)(=O)c2cccs2)CC1)N1CCN(Cc2cccc3ccccc23)CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1nc([14*])c([N+](=O)[O-])c(C)n1
Fragment 2: [16*]c1ccccc1O
### Response:
Cc1nc(Nc2ccccc2O)nc(N(C)c2ccccc2)c1[N+](=O)[O-] |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@H](Cc1cccs1)C(=O)NCCN1C(=O)CCCC1=O
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC(=O)[C@](O)(c1cc(C)c(O)c(Cl)c1)C(F)(F)F
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O[C@@H]1C2(CCN(CC2)C(=O)CCc2cccnc2)c2ccccc2[C@H]1[NH+](C)C
### Response:
C[NH+](C)[C@@H]1c2ccccc2C2(CCN(C(=O)CCc3cccnc3)CC2)[C@H]1O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)[C@@H](NC(=O)c1cnc(-c2ccoc2)s1)C(=O)N1CCOCC1
### Response:
4 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(CS(=O)(=O)[C@@H](c1ccccc1)c1ccc(Cl)cc1)N1CCOCC1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O[C@H]1CC[NH+](CCCOc2cccc(Cl)c2)Cc2ccccc21
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(/C=N/NC(=O)c2ccccc2)cc1
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a ester group?
CCC[NH2+][C@@H]1c2c(C)ccc(C)c2S(=O)(=O)[C@H](C)[C@@H]1C
### Response:
No |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cc2ncn(-c3ccc(N)c(N)n3)c2cc1C
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C(Nc1nnc([C@H]2CCCO2)o1)C1CCN(S(=O)(=O)c2ccc(Cl)s2)CC1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*][C@H]([8*])c1ccccc1
Fragment 2: [5*]N[C@H]([8*])c1ccccc1
### Response:
O=C(N[C@@H](c1ccccc1)C1CC1)N1CCN(S(=O)(=O)c2cccc(Cl)c2)CC1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COc1cccc(CNC(=O)c2n[nH]c3ccc([N+](=O)[O-])cc23)c1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1cc(=O)n2cc(C)ccc2n1
Fragment 2: [14*]c1cccs1
### Response:
CCn1c(SCc2cc(=O)n3cc(C)ccc3n2)nnc1-c1cccs1 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
C[C@H]1CN(Cc2ccc(Cl)cc2Cl)C[C@H](C)O1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1nn2c(C)c(C(=O)/C=C/c3ccccc3)nnc2c1-c1ccccc1
### Response:
3 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[C@@H](CS)COc1cccc2cccnc12
### Response:
4 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
COc1ccc(NC(=O)[C@H]2CC(=O)N/C(=N\N=C(\C)c3ccccc3)S2)cc1
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC(C)(C)C
Fragment 2: [1*]C(=O)N[5*]
### Response:
CC(C)(C)NC(=O)N1CC[C@@]2(C1)C(=O)Nc1ccccc12 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(SCC[C@H]2C[NH2+]CCC2)ccnc1
### Response:
c1cc(SCC[C@@H]2CCC[NH2+]C2)ccn1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CN(C(=O)c1cnn(-c2ccccc2)c1)c1ccc(Br)cn1
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC1(C)CS(=O)(=O)N(c2cc(C(=O)N3CCc4ccccc43)ccc2Cl)C1=O
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a halide group?
Cc1c(C)c(O)c(C(=O)Cl)c(C)c1O
### Response:
Yes |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
O=C(NCCCSc1ccccc1)c1cc(Br)ccc1Cl
### Response:
0 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC[NH2+][C@@H](CCC(F)(F)F)[C@H]1CCOC2(CCC2)C1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@H]1OC[C@@H](N[5*])[C@@H]1O
Fragment 2: [4*]Cc1c[nH]c[nH+]1
### Response:
Cc1ccc(S(=O)(=O)NC[C@H]2OC[C@@H](NCc3c[nH]c[nH+]3)[C@@H]2O)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1ccc(C)o1
Fragment 2: [12*]S(=O)(=O)c1ccc(C#N)cc1
### Response:
Cc1ccc(C(=O)NC2CCN(S(=O)(=O)c3ccc(C#N)cc3)CC2)o1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc(-n2c(SCC(N)=O)nc3c(sc4ccccc43)c2=O)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Clc1ccccc1Cn1ccnc1
### Response:
1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCCSCc1noc([C@H]2CC[C@@H]3CCCC[C@@H]3[NH2+]2)n1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccncc1
Fragment 2: [16*]c1ccc([16*])cc1
### Response:
C[C@@H](NC(=O)[C@@H]1COc2ccccc21)c1ccc(-c2ccncc2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CSC[C@H](NCc1cccc(C(N)=O)c1)c1ccccc1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
C[C@@H]1CN(C(=O)c2nn(-c3ccc(F)cc3)c3c2CCC3)CCO1
### Response:
2 |
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