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CCC(C)(C)C1CCC2(CC1)NC(=O)N(CC(=O)NCCCc1ccccc1)C2=O
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413.562
3.6524
78.51
0.625
O=C(NC(=S)N1CCCCC1c1cccnc1)c1ccc(Br)cc1
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404.333
4.086
45.23
0.277778
COC(c1ccccc1)c1c(-c2ccccc2)nn(C)c1Cl
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312.8
4.4763
27.05
0.166667
O=C(NC(Cc1ccc(I)cc1)C(=O)O)c1ccc(Br)cc1
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474.092
3.4794
66.4
0.125
COc1ccc(NC(=O)c2ccc(S(=O)(=O)NCc3cccnc3)cc2)cc1
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397.456
2.821
97.39
0.1
Cc1ccc2c(c1)C(=O)C(=O)N2CC(=O)Nc1ccc(N2CCOCC2)cc1
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379.416
1.99962
78.95
0.285714
COc1ccc(-c2[nH]c3c(C#N)cnn3c2NC2CCCC2)cc1
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321.384
3.56418
78.14
0.333333
CCCCN1C(=O)C(CC(=O)NCCCN(C)C)CC(C(=O)N2CCOCC2)=C1C
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422.57
1.2258
82.19
0.772727
CCOC(=O)c1cnc2c(N=Nc3ccccc3)c(N)nn2c1N
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325.332
2.4858
133.25
0.133333
COC(=O)C1(NC(=O)NC23CC4CC(CC(C4)C2)C3)CCCCC1
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334.46
3.1303
67.43
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O=C1C=C(NCc2ccc(Cl)cc2)CC(c2ccco2)C1
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COCCCN(C(C)=O)c1nc(-c2ccc(OC)cc2)cs1
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Cl.O=S(=O)(NCCN1CCOCC1)c1cccs1
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O=C(c1ccc(-c2ccccc2)cc1)C1CCCN(C(=O)c2cncs2)C1
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Cc1cccc(N2CCN(C(=O)c3ccccc3OCc3c(C)noc3C)CC2)c1C
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COC(=O)Nc1ccc2ccc3c(NC(=O)OC)ccc4ccc1c2c43
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CCOCCCNC(=O)CN1CCN(Cc2ccccc2C)C1=O
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Cc1ccc(S(=O)(=O)N2CCN(C(=O)COC(=O)c3cnc(C)cn3)CC2)c(C)c1
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Cc1ccc(CNS(=O)(=O)c2cc3[nH]c(=O)c(=O)[nH]c3cc2C)cc1
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O=C(NNC(=O)c1ccc2c(c1)C(=O)N(C1CCCCC1)C2=O)c1cccnc1
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0.285714
COc1ccc(C(C(=O)NC2CCCC2)N(C(=O)c2snc(-c3ccc(F)cc3)c2N)c2ccccc2)cc1
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97.55
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Cc1ccc(S(=O)(=O)c2cc3c(=O)n4cccc(C)c4nc3n(CC3CCCO3)c2=N)cc1C
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478.574
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O=C(Cn1c(-c2ccccc2)c[n+]2ccsc12)c1ccccc1.[Br-]
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COc1ccc(C(=O)Nc2ccc3nc(SCC(=O)N4CCCC4)sc3c2)cc1
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427.551
4.2717
71.53
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COc1cc(NC(=O)CSc2nnc(Cn3nnc4ccccc43)n2C)cc(OC)c1
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439.501
2.3561
108.98
0.25
C=CCn1c(SCC(=O)NC2CCS(=O)(=O)C2)nc2scc(C3CC3)c2c1=O
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439.584
1.9168
98.13
0.5
CS(=O)(=O)Nc1ccc2c(c1)oc(=O)c1ccccc12
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CCn1cc(C(=O)NNC(=O)c2ccc(Cl)cc2)c(=O)c2ccc(C)nc21
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C=C(C)C(=O)OCC(O)CO
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COc1ccc(OC)c(CNC(=O)C2CCC(=O)N2C(C)C)c1
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CCC(=O)N1Cc2cc(C(=O)NCC(F)(F)F)nc(-c3cccc(-c4cncnc4)c3)c2[C@@H]1CCO
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CN(C(=O)COC(=O)/C=C/c1ccc2ccccc2n1)C1CCS(=O)(=O)C1
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CC[C@@H](CCCC[C@H]1CC[C@@H]2CC(=O)C[C@H]12)OC
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252.398
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Cl.N=C(N)SCc1cccc([N+](=O)[O-])c1
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CC1CC2(CC(C)(C(=O)CSc3nc4ccccc4s3)OC2=O)C(=O)O1
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CCCC(=O)OCCNC(=O)c1cc2ccccc2oc1=O
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NC(=O)C1CCN(C(=O)/C(=C/c2ccco2)NC(=O)c2ccccc2)CC1
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O=S(=O)(Cc1ccccc1)NCC1CCCN(Cc2ccc3nonc3c2)C1
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2.5544
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CCO/C(O)=C(\C(C)=O)C(=Nc1ccccc1)Nc1ccccc1
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324.38
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COc1ccccc1NC(=O)NC1CCCCCCC1
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276.38
3.9296
50.36
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Cc1cc2c([nH]c3ccccc32)c2c1OC(C)(C)C1C3CC(C)(C)Oc4c(C)cc5c6ccccc6n(c5c43)C21
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526.68
9.08074
39.18
0.333333
CC(=O)N1CCc2cc(S(=O)(=O)CCC(=O)Nc3ccc4c(c3)OCCO4)ccc21
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430.482
2.1693
102.01
0.333333
CC(C)c1cc(N=NC(N)=O)cc(C(C)C)c1O
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Cc1cccc(NC(=O)Nc2ccc(Cl)c(Cl)c2)n1
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CCOC(=O)C(=O)Nc1c(F)cc(F)cc1Br
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O=C1CN(C(=O)COC(=O)c2cccc(Br)c2)c2ccccc2N1
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CCOc1ccc(OCc2ccc(C(=O)N3CCCC(C)C3)cc2)cc1
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O=C(NCCCN1CCCC1=O)c1ccccc1OCc1ccc(Cl)cc1Cl
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CC(C)(Oc1ccc(Cl)cc1)C(=O)OCC(=O)N1CCCC1
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325.792
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COc1ccc(-n2c(SCC(=O)c3ccc(Cl)cc3)nc3c([nH]c4ccccc43)c2=O)cc1
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COc1ccc(C2=Nc3ccccc3SC(C)C2)cc1
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283.396
4.7003
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CCOC(=O)COc1ccc(S(=O)(=O)N2CCN(c3ccccc3F)CC2)cc1
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422.478
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CC1=NN(C(=O)Cc2ccccc2)C(=O)/C1=C\C=C\c1ccccc1
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330.387
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CC(=O)Cc1nsc(NC(=O)c2ccc(Br)o2)n1
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330.163
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85.09
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O=C(O)CC(c1ccc2c(c1)OCO2)N1CCS(=O)(=O)CC1
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327.358
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Cn1cc2ccccc2c1-c1nc(N)nc(F)n1
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243.245
1.7516
69.62
0.083333
COc1ccc(C(C)(C)C)cc1NC(=O)COC(=O)CSCc1c(C)noc1C
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FC(F)(F)c1ccccc1N1CCN(c2nc(-c3cccs3)nc3ccc(Br)cc23)CC1
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519.39
6.4662
32.26
0.217391
N#Cc1cccc(NC(=O)C2CCCN(C(=O)c3ccc(Cl)cc3)C2)c1
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367.836
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O=C(Nc1cccc(F)c1)N1CCCCCC1
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236.29
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0.461538

ChEMBL Drug-Target Activity Dataset

This dataset was extracted from ChEMBL34 database. It is designed for multitask classification of drug-target activities. It links compound structures with activity data for multiple assays, enabling multitask learning experiments in drug discovery. Key features of the dataset include:

Multitask Format

  • Each assay ID is treated as a separate binary classification task.
  • Binary labels (0 for inactive, 1 for active) and masks (indicating valid labels) are provided for each task.

ChEMBL Assay IDs

This dataset includes 281 ChEMBL assays, corresponding to 281 binary-classification tasks. You can find the full list of assay_ids (same sequence as in labels and mask) in the assay_ids.json file.

Detail of the assays can be found from ChEMBL Assays.

Column Descriptions

Column Name Description
smiles Simplified Molecular Input Line Entry System (SMILES) representation of chemical compounds.
labels A list of length = number of tasks. Could be 0 for inactive, 1 for active, and -1 for missing labels
mask A list of length = number of tasks. Could be 0 for non-present and 1 for present and valid label
chembl_id Unique identifier for the compound in the ChEMBL database.
MW Molecular weight of the compound, representing the sum of atomic masses in Daltons (g/mol).
LogP Partition coefficient (LogP) of the compound, indicating its lipophilicity or hydrophobicity.
TPSA Topological polar surface area of the compound, reflecting the molecule's polarity and transportability.
Complexity Molecular complexity, measured as the fraction of sp³ hybridized carbons in the molecule (0–1 range).
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