task stringclasses 5
values | input stringlengths 89 339 |
|---|---|
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C(Nc1c(F)ccc(c1)N)CC[NH+](C)Cc1ccccc1O
### Response:
C[NH+](CCC(=O)Nc1cc(N)ccc1F)Cc1ccccc1O |
functional_group | ### Instruction:
Does the molecule contain a phenol group?
CCC(CC)(C(=O)[O-])N1C(=O)[C@@H]2[C@H](C1=O)C2(C)C
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(C[NH+]2C[C@H](COCC)CC2)ncc1
### Response:
CCOC[C@@H]1CC[NH+](Cc2ccccn2)C1 |
functional_group | ### Instruction:
Does the molecule contain a amine group?
CN1O[C@@H](CC(=O)NC2CCCC2)N(c2ccc(Cl)cc2)C1=O
### Response:
No |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ccco1
Fragment 2: [5*][NH+]1CCNC(=O)[C@H]1[13*]
### Response:
CC(C)[C@@H]1C(=O)NCC[NH+]1Cc1ccco1 |
functional_group | ### Instruction:
Does the molecule contain a sulfonyl group?
COc1cc(C(=O)N[C@H]2CCS(=O)(=O)C2)ccc1OC(C)C
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
N([C@H]1C[C@@H]1C)C(=O)Cc1ccc(c(OC)c1)C
### Response:
COc1cc(CC(=O)N[C@H]2C[C@@H]2C)ccc1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [11*]Sc1ccc(Cl)nn1
Fragment 2: [4*][C@@H](C)CC
### Response:
CC[C@H](C)Sc1ccc(Cl)nn1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccc(Cl)cc1C(=O)Nc1ccc(N2CCN(C(=O)C(F)(F)F)CC2)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1occc1[16*]
Fragment 2: [5*]N(C)C
### Response:
CN(C)C(=O)c1cccc(NC(=O)c2occc2-c2ccccc2)c1 |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1cnn([C@@H]2CCCN(C(=O)CCCc3ccccn3)C2)c1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccc(CN[5*])c1
Fragment 2: [5*]N[C@@H](C)CC
### Response:
CC[C@H](C)NC(=O)c1cccc(CNC(=O)c2cncc(Br)c2)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H]1C[C@@H](Nc2ccc([N+](=O)[O-])cn2)CN1c1ccccc1
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC(=S)N[5*]
Fragment 2: [4*]Cc1ccco1
### Response:
S=C(Nc1ccc(Cl)cc1)NC1C[C@H]2CC[C@@H](C1)[NH+]2Cc1ccco1 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
Cc1ccc2nc(COc3ccc(C(=O)N4CCC[C@@H](c5nc6ccccc6[nH]5)C4)cc3)cn2c1
### Response:
No |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cn1ccc2ccc(Cl)cc21)NNC(=O)c1ccccc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1cc(C)ccc1Cl
Fragment 2: [9*]n1ncc(Cl)c(Cl)c1=O
### Response:
Cc1ccc(Cl)c(OS(=O)(=O)c2ccc(-n3ncc(Cl)c(Cl)c3=O)cc2)c1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
Cc1cccc(NC(=O)C(=O)NC[C@@H](c2ccc3c(c2)CCN3C)[NH+]2CCCC2)c1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1csc([C@@H](C)NC(=O)[C@@H]2C[C@@H]2c2ccccc2Cl)n1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NS(=O)(=O)c1cccc2cccnc12
Fragment 2: [4*]C[C@@H]([8*])O
### Response:
O=S(=O)(NC[C@H](O)C1CCCCC1)c1cccc2cccnc12 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
COCCn1nc(C)c(NC(=O)N2CCCCC[C@H]2c2ccc(C)o2)c1C
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cc1onc(-c2ccc(F)cc2F)c1C(=O)Nc1ccccc1Cl
### Response:
Yes |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
n1(CCc2cccs2)c2ncccc2nc1CCl
### Response:
ClCc1nc2cccnc2n1CCc1cccs1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@H](O)[C@H]1CCCC[NH+]1Cc1cn(C)nc1-c1ccncc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CC(C)n1cnnc1CN[C@@H](C)Cc1nc2ccccc2s1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(C(=O)[C@@H]1CC(=O)N(C2CCCC2)C1)C1CCCCC1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COC(=O)C[C@H](C)S[C@H]1CCN(c2c(F)cccc2F)C1=O
### Response:
1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C(c1ccc(F)cc1F)N1CCC(C(=O)N2CCC[C@@H]3CCCC[C@@H]32)CC1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [15*]C1([15*])CC1
Fragment 2: [14*]c1ccc(F)cn1
### Response:
N#C[C@@H](C(=O)C1(c2ccccc2)CC1)c1ccc(F)cn1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C[C@@H]([C@@H](O)c1ccc2ncnn2c1)[N+](=O)[O-]
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COC[C@@H](O)CN(C)C(=O)c1nc(C2CC2)n2ccccc12
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
CC(C)N(Cc1ccccc1)C(=O)c1ccc2nsnc2c1
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cc(OC)cc(OC)c1
Fragment 2: [1*]C(=O)c1c2c(nc3c1cnn3[9*])CCC2
### Response:
COc1cc(NC(=O)c2c3c(nc4c2cnn4C(C)C)CCC3)cc(OC)c1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1cccc(OC[C@H](C)NC(=O)NCc2ncn(C)n2)c1
### Response:
3 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1ccc(Br)c(CC2(c3ccc(C)cc3)C[NH2+]C2)c1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a aldehyde group?
C=CC[NH2+]CC(=O)Nc1ccccc1-n1cccn1
### Response:
No |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1ccc(O[C@@H](C)C(=O)NNC(=O)COc2ccccc2Cl)cc1C
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O[C@H](CN(Cc1cnc2cnccn12)C1CC1)c1ccc(F)cc1
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
N#Cc1ccccc1N1CCCN(Cc2cccn2Cc2cccs2)CC1
### Response:
1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
C=CCn1c(-c2ccc3ccccc3n2)nn(C)c1=S
### Response:
1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c12c(c(C(CSc3nc(cc([nH]3)=O)C)=O)c(C)[nH]2)cccc1
### Response:
Cc1cc(=O)[nH]c(SCC(=O)c2c(C)[nH]c3ccccc23)n1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCc1ccc(N2C[C@H](c3nnc(NC(=O)c4cccs4)s3)CC2=O)cc1
### Response:
No |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@@H]2C[C@H](C1)C(C)(C)/C2=C/C(=O)OC
### Response:
COC(=O)/C=C1\[C@@H]2CC[C@@H](C2)C1(C)C |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCN(C1CCN(Cc2c[nH]c[nH+]2)CC1)S(C)(=O)=O
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)c1cccc([16*])c1
Fragment 2: [5*]NCCOC
### Response:
COCCNC(=O)c1cccc(C(=O)OC)c1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]C(F)(F)F
Fragment 2: [6*]C(=O)N1N=C(c2ccc(Cl)cc2)C[C@]1([13*])O
### Response:
Cc1ccc(C(=O)N2N=C(c3ccc(Cl)cc3)C[C@@]2(O)C(F)(F)F)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [13*][C@@H]1CCCCC[NH2+]1
Fragment 2: [4*][C@@H](C)C[8*]
### Response:
CC(C)[NH+]1CC[C@@H](C[NH2+][C@@H](C)C[C@@H]2CCCCC[NH2+]2)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1ccccc1NC(=S)NCc1ccc(S(N)(=O)=O)cc1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]NC[C@@H]1CCCS1
Fragment 2: [1*]C(=O)c1cn(C)nc1CC
### Response:
CCc1nn(C)cc1C(=O)NC[C@@H]1CCCS1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N([5*])c1ccncc1
Fragment 2: [1*]C(=O)c1cc2c(F)cccc2[nH]1
### Response:
O=C(c1cc2c(F)cccc2[nH]1)N(C[C@@H]1CCCO1)c1ccncc1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
O=C1c2c3c(sc2N[C@@H](c2oc(cc2)-c2cc(Cl)c(Cl)cc2)N1)C[NH+](CC3)C
### Response:
C[NH+]1CCc2c(sc3c2C(=O)N[C@H](c2ccc(-c4ccc(Cl)c(Cl)c4)o2)N3)C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
C[C@@H]1CN(S(=O)(=O)N[C@H](C(=O)[O-])[C@@H](C)O)C[C@@H](C)O1
### Response:
4 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [11*]S[C@H]1CCCc2ccccc21
Fragment 2: [14*]c1nnc([14*])o1
### Response:
COc1cc(OC)cc(-c2nnc(S[C@H]3CCCc4ccccc43)o2)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cc(C(=O)N/N=C/c2ccc(OC(=O)/C=C\c3ccco3)cc2)[nH]n1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [8*]Cc1ccc([14*])nc1
Fragment 2: [5*]N1CCC[C@@H]([15*])C1
### Response:
COc1cccc(CC(=O)N2CCC[C@@H](c3ccc(Cc4ccccc4)cn3)C2)c1 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCS(=O)(=O)c1ccc(NC(=O)NC2(C)Cc3ccccc3C2)cc1
### Response:
1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CSc1nnc(CN2C(=O)NC3(CCC(C(C)C)CC3)C2=O)s1
### Response:
3 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1cccc(NC(=O)O[C@@H](C)c2sc3ncnn3c2C)c1
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*][NH2+]CC[8*]
Fragment 2: [16*]c1ccccc1F
### Response:
Cc1c(C[NH2+]CCc2ccccc2F)cnn1C |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
Cc1nn(C)c(Cl)c1[C@@H](O)[C@@H]1CCO[C@]2(CCSC2)C1
### Response:
2 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
NC(=O)[C@@H]1CCC[C@H]1NC(=O)NCCc1cccs1
### Response:
No |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CCc1nc(-c2csc(S(=O)(=O)N3CCC[C@H](C(=O)Nc4ccc(F)c(Cl)c4)C3)c2)no1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
CCOC(=O)C(C(=O)OCC)[C@@]1(O)CCCC1(C)C
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]Cc1ncn([9*])n1
Fragment 2: [16*]c1ccccc1
### Response:
CCn1c(SCc2ncn(-c3ccccc3)n2)nc2ccccc2c1=O |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [16*]c1ccc(F)cc1
Fragment 2: [5*]N1CCN([5*])CC1
### Response:
COc1cc(CN2CCN(c3ccc(F)cc3)CC2)cc(OC)c1O |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCc1cnc([C@@H](C)NC(=O)c2ccc(-c3cscn3)cc2)s1
### Response:
2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1C[NH+](CCN1C(=O)c1ccc(C#N)cc1)CCNC(=O)c1cc2OCOc2cc1
### Response:
N#Cc1ccc(C(=O)N2CC[NH+](CCNC(=O)c3ccc4c(c3)OCO4)CC2)cc1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]Nc1cccc(CC)c1
Fragment 2: [1*]C(=O)c1cncc(Br)c1
### Response:
CCc1cccc(NC(=O)c2cncc(Br)c2)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cccc(c1O[C@H]1CCC[C@@H]([NH3+])C1)C(F)(F)F
### Response:
[NH3+][C@@H]1CCC[C@H](Oc2ccccc2C(F)(F)F)C1 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCn1cc(C[NH+]2CCC(CN3C[C@@H](C)O[C@@H](C)C3)CC2)cn1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCCOc1nc(Oc2cccc(Cl)c2Cl)ccc1N
### Response:
3 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [10*]N1C(=O)N2CCC3=c4ccccc4=[NH+][C@H]3[C@@]2(C)C1=O
Fragment 2: [5*]Nc1ccc([16*])cc1
### Response:
CCOc1ccc(NC(=O)c2ccc(N3C(=O)N4CCC5=c6ccccc6=[NH+][C@H]5[C@@]4(C)C3=O)cc2)cc1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(C[NH+]1CCC(O)CC1)Nc1ccccc1[N+](=O)[O-]
### Response:
2 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
Cc1ccc([C@@H](CNC(=O)c2cccnc2NC(C)C)[NH+]2CCCC2)cc1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
CC([C@@]1(CC(N(C1=O)[C@H](C)c1ccc(cc1)N)=O)C)C
### Response:
CC(C)[C@]1(C)CC(=O)N([C@H](C)c2ccc(N)cc2)C1=O |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
COc1cc(OC)c2cc(C(=O)N[C@H](C)C(=O)N=c3[nH]c4ccccc4[nH]3)n(C)c2c1
### Response:
2 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
O=C1/C(=C\c2cc3ccccc3o2)SC(=S)N1c1ccc(F)cc1
### Response:
2 |
ring_counting | ### Instruction:
Count the five-membered rings in the following molecule.
COc1ccccc1/C=C1\C(=O)N(CN2CC[NH+](C)CC2)c2cc(Cl)ccc21
### Response:
1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [6*]C(N)=O
Fragment 2: [1*]C(=O)c1ccc2[nH]c3c(c2c1)C[C@@H](C)CC3
### Response:
C[C@H]1CCc2[nH]c3ccc(C(=O)N4CCC(C(N)=O)CC4)cc3c2C1 |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CCOC(=O)C1(C)CCN(C(=O)[C@H]2CCCC[NH+]2C(C)C)CC1
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a ether group?
CCC[C@@H](NC(=O)C1C[C@@H](C)O[C@H](C)C1)C(=O)OC
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
O=C(NCCCO)N[C@H](Cc1ccc(F)cc1)c1ccccc1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
CC(C)c1[nH+]ccn1[C@H](C)C(=O)Nc1ncc(Cc2ccccc2)s1
### Response:
3 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
[C@@]1(O)(N(C(=S)N[C@@H](c2c(cccc2F)F)[C@@H]1C(=O)OC)c1cc2c(OCCO2)cc1)C(C)C
### Response:
COC(=O)[C@H]1[C@H](c2c(F)cccc2F)NC(=S)N(c2ccc3c(c2)OCCO3)[C@@]1(O)C(C)C |
functional_group | ### Instruction:
Does the molecule contain a amide group?
COCC[C@@H](C)C(=O)Nc1ccc(Oc2ccc(C)cn2)cc1
### Response:
Yes |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
CC[NH2+][C@H](Cc1ccccc1Cl)[C@H]1C[NH+](C)CCN1C
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N1CCOCC1
Fragment 2: [15*][C@@]12CC[C@@H](CC1=O)C2(C)C
### Response:
CC1(C)[C@H]2CC[C@]1(CS(=O)(=O)NCc1ccccc1N1CCOCC1)C(=O)C2 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1c(c(nc(NC[C@@H](c2ccccn2)N2CCOCC2)n1)-c1n(ncn1)C)C
### Response:
Cc1cnc(NC[C@@H](c2ccccn2)N2CCOCC2)nc1-c1ncnn1C |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [5*]N([5*])CC
Fragment 2: [16*]c1ccccc1
### Response:
CCN(c1ccccc1)c1[nH+]cnc(Nc2nc3ccccc3s2)c1N |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
COc1ccccc1/C=C(/C#N)C(=O)NCc1ccc2c(c1)OCO2
### Response:
3 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
COc1ccc([C@H](C)NS(=O)(=O)c2ccc3c(c2)CCO3)cc1F
### Response:
Yes |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [1*]C(=O)C[4*]
Fragment 2: [5*]NC1=NS(=O)(=O)c2ccccc21
### Response:
CN(C(=O)CNC1=NS(=O)(=O)c2ccccc21)c1cccc(C#N)c1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
C1[C@](C)(CCN1Cc1n2c(nc1C)sc(c2)C)C(OC)=O
### Response:
COC(=O)[C@@]1(C)CCN(Cc2c(C)nc3sc(C)cn23)C1 |
canonicalization | ### Instruction:
Canonicalize the following SMILES string.
c1cc(ccc1Cl)-n1c2c(C3N(CCC[NH+]=3)C(=N2)SCC(=O)N2CCCCC2)cn1
### Response:
O=C(CSC1=Nc2c(cnn2-c2ccc(Cl)cc2)C2=[NH+]CCCN12)N1CCCCC1 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [14*]c1ccco1
Fragment 2: [3*]OCC
### Response:
CCOC(=O)[C@@H]1C(=O)N=C(N2CCCCC2)N[C@H]1c1ccco1 |
functional_group | ### Instruction:
Does the molecule contain a aromatic_ring group?
Cc1ccc(Cl)cc1/N=C1/S[C@@H](CC(=O)Nc2cc(Cl)ccc2C)C(=O)N1C
### Response:
Yes |
functional_group | ### Instruction:
Does the molecule contain a amide group?
Cc1ccc(-c2ccncc2)cc1NC(=O)C(=O)N[C@H]1CC[C@@H]([NH+](C)C)C1
### Response:
Yes |
chain_length | ### Instruction:
What is the length of the longest acyclic carbon chain in the molecule?
O=C(Cc1ccc(F)cc1)NCCn1ncc2c(N3CCN(c4ccccc4)CC3)ncnc21
### Response:
2 |
fragment_assembly | ### Instruction:
Assemble these two molecular fragments into a single molecule.
Fragment 1: [4*]C[C@@H](C)N([5*])C
Fragment 2: [11*]SCC
### Response:
CCSC[C@@H](C)N(C)C(=O)c1ccc(-c2cscn2)cc1 |
ring_counting | ### Instruction:
Count the six-membered rings in the following molecule.
N#Cc1ccc(NC(=O)CN2C(=O)[C@@H]3CCCC[C@H]3C2=O)cc1
### Response:
2 |
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