Dataset Viewer
Auto-converted to Parquet Duplicate
image_id
stringlengths
1
32
image
imagewidth (px)
61
3.28k
SMILES
stringlengths
4
251
1
O=C(N1S[R'])CCC1=O
2
COC(C=C1)=CC=C1C#CC(C=CC=C2)=C2C3=C(C=O)N4C=CC=CC4=C3C(OCC)=O
3
O=C(N[R])CCC(N[R])=O
4
ClC(CCC(Cl)=O)=O
5
CC1=CC([R2])=C([R2])[P-]1
6
[R]C(NC1=NC2=CC=CC=C2S1)=O
7
[R]C(NC1=C(SC)C=CC=C1)=O
8
O=C(C(C=CC=C1)=C1C2=O)[C-]2C3=CC4=CC=CC=C4N=C3.[Na+]
9
[Ar]C(O)C
10
[Ar]C(NC1=C2C(C=CC=N2)=CC=C1)=O
11
BrC1=CC=C(C)C=C1
12
O=[N+](/C=C/C1=CC=CC=C1)[O-]
13
CC(C=C1)=CC=C1S(C([N+]([O-])=O)C2=CC(Cl)=CC=C2)(=O)=O
14
COC1CCCC2=C1C=C(C3=CC=CC=C3)O2
15
C1(SSC2=CC=CC=C2)=CC=CC=C1
16
O=C(C[C@@]1([H])[C@@]2(C)CC[C@]3([H])[C@]1(C)CCCC3(C)C)C4=C2C=C(OC)C(OC)=C4N
17
ClC1=CC=CC=C1[N+]([O-])=O
18
O=C/C=C/C1=CC=CC=C1
19
ClC1=NC=CC=C1
20
BrC1=C(C)C=CC=C1
21
ClC1=CC=C(C#N)C=C1
22
CC1=CC(F)=CC(C)=C1
23
CN1C2=C(C=C(B3OC(C)(C)C(C)(C)O3)C=C2)C4=CC=CC=C41
24
CN(C1=C2C3=C4C1C(C=CC=C5)=C5CCC4=CC=C3)C(N(C)C2=O)=O
25
CN(C(C1=C(C=CC=C2)C2=CC3=C1C=CC=C3)C4)C(N(C)C4=O)=O
26
CC(C=C)=O
27
ClC(C=C1)=CC=C1C2CC(O)OC(C)O2
28
CC(C1=CC=C(Cl)C=C1)=C
29
O=C(C1=CC=CC=C1)C2=C(C3=CC=C(C)C=C3)C(C)=C4N2C=CC=C4
30
O=S(C1=CC=CC=C1)(C(F)(F)F)=NS(=O)(C(F)(F)F)=O
31
COC1=C(OC)C=C(C(NC2=NC(C(OC)=O)=CS2)=O)C(O)=C1
32
COC1=C(OC)C=C(C(Cl)=O)C(OC)=C1
33
[H]C(C1CCCO1)=O
34
OC1=CC=C(C[C]=O)C=C1
35
C=C[C@@H]1C2=CC(O)=C(C)C=C2OC(C)(C)[C@@H](O)C1
36
[R]C1=C(C=CC=C2)C2=C(C3=CC=CC=C3)C4=C1OC5=C4C=CC=C5
37
O=CC(C=CC=C1)=C1/C(C2=CC=CC=C2)=C3COC4=C/3C=CC=C4
38
C1CCCO1
39
C1(C=CC2=CC(C=CC=C3)=C3C=C2)CCCO1
40
O=CC1=CC=CC=C1
41
SC1=CC=CC=C1S
42
O=C(/C(C)=C1OC(C2=C/1C=CC=C2)=O)C3=CC=C(Br)C=C3
43
O=C(/C(C)=C1OC(C2=C\1C=CC=C2)=O)C3=CC=C(Br)C=C3
44
O=C(C1=C([H])C=CC=C1)NC2=CC=CC=C2N3C=CC=N3
45
O=C(C1=C(NS(C)(=O)=O)C=CC=C1)NC2=CC=CC=C2N3C=CC=N3
46
O=C(C1=C([H])C=CC=C1)NC2=CC=CC=C2N3C=CC=N3
47
CN1N=NC(C2=CC=CC([N+]([O-])=O)=C2)=N1
48
C1(/C=C2CC\2)=CC=CC=C1
49
BrC1=C(C(C2=CC=CC=C2)=C(C(F)(F)F)CC3)C3=CC(OC)=C1OC
50
FC(C1=CC2=CC=CC(OCC3=CC=CC=C3)=C2CC1)(F)F
51
CC1=C(C2=CC=CC=C2)C=CC=C1
52
O=C(C1=CC=CC=C1)C2=CC=C(Br)C=C2
53
O=C(C1=CC=CC=C1)C2=CC=C(Cl)C=C2
54
O=C(C1=CC=CC=C1)C2=CC=CC=C2OC
55
O=C(C1=CC=CC=C1)C2=CC=CC=C2
56
O=C(C1=CC=CC=C1)C2=CC=CC=C2C
57
O=C1C2=C(C3=CC=CC=C3)C=CC=C2CCC1
58
C=C1C2=CC=CC=C2CCC1
59
[H]C(C1=CC=CC=C1O)=O
60
O=C1[C@H](C2=CC=CC=C2)[C@@H](C)OC3=CC=CC=C31
61
[R]C1=NC=NC(C)=C1C
62
CC(C1=CC=CC=C1)=C
63
NC(C1=CC=CC=C1)=C
64
CCOC(=O)C1C(c2ccccc2)=C2C(c3ccccc31)c1ccccc1N2Cc1ccccc1
65
c1ccc2oc(N3CCN(c4cc5ccccc5o4)CC3)cc2c1
66
FC1=C(N2CCCCC2)N=C(Cl)C=C1
67
BrC1=CSC([C@H]2[C@H]3[C@@](CCCC3)(OCC4)[C@@H]4CO2)=C1
68
CC1=CC=CC=C1
69
C1COCCN1
70
CC1=C(C2=CC=C([N+]([O-])=O)C=C2)C(C3=CC=CC=C3)=NO1
71
IC1=CC=C([N+]([O-])=O)C=C1
72
CC(C1=CC(C)(C)CC1OC)=C
73
COCC#CC1=CC=CC=C1
74
CC1=CC=C(C(C2C(CCCC2=O)=O)=O)C([N+]([O-])=O)=C1
75
NC1=CC(C)=CC=C1
76
CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OCC(C)=C
77
C[C@@H](C1=CC=CC=C1)N(CC2=CC=CC=C2)[C@H]([C@H](OCC3=CC=CC=C3)CC(C#CC#CC#C[CH])=O)CC4=CC=CC=C4
78
O=C(C([R2])C)N1CCC2=C1N=CC=C2
79
ClC(C=C1)=CC=C1C2=C(C(C3=CC=CC=C3)=O)N=NN2CSC
80
ClC(C=C1)=CC=C1C2=C(C(C3=CC=CC=C3)=O)N=NN2CSC
81
COC1=CC=C(/C=C/C=C/C(C)=O)C=C1
82
ClC1=CC=C(S)C=C1
83
OC(C)(C1=CC=CC=C1)C#C
84
O=CC1=C(O)C(O)=CC2=C1OC3=C2[C@]4(C)[C@](CC[C@H]3C)([H])C(C)(C)CCC4
85
O=C/C=C/C1=CC=CC=C1
86
OC(C#C)C1=CC=CC=C1
87
OC1(C#C)CCCCC1
88
O=C(C(CCO)C(OCC)=O)C1=CC=CC=C1
89
O=C(CC(OCC)=O)C1=CC=CC=C1
90
NC(CC(C1=CC=CC=C1)C2=CC=CC=C2)=O
91
CC1=CC=C(N=C(C)C(C2=CC=CC=C2)=C3C4=CC=CC=C4)C3=C1
92
CC1=NC2=CC=C(C(F)(F)F)C=C2C(C3=CC=CC=C3)=C1C4=CC=CC=C4
93
O=C1C(C(N2CCCC2)=O)=CN(C(CCC=C)=O)CC1
94
CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1
95
C1CCCN1
96
CC1=CC2(CC3=C1C=CC=C3)C4=C(C=CC=C4)C5=CC=CC=C52
97
CC(C1)(C2=CC=C(OC)C=C2)C3=C(C=CC=C3)CC41C5=C(C=CC=C5)C6=CC=CC=C64
98
O=C(C1=CC=CC=C1)C2=C(C3=CC=CC=C3)C(C(C)=O)=C(C)N2
99
O=C1C=COC2=C1C=CC=C2
100
NS(=O)(C1=CC=CC=C1)=O
End of preview. Expand in Data Studio

OCSR Benchmarks

A collection of ten benchmark datasets for Optical Chemical Structure Recognition (OCSR) — the task of converting chemical structure diagram images into machine-readable SMILES strings.

These benchmarks were used to evaluate the COMO model (Closed-Loop Optical Molecule Recognition).

Subsets

Config Split Size Domain
CLEF test 992 Real
JPO test 449 Real
UOB test 5,740 Real
USPTO test 5719 Real
USPTO-10K test 9,999 Real
Staker test 50,000 Real
ACS test 331 Real
WildMol-10K test 9,889 Real
Indigo test 5,719 Synthetic
ChemDraw test 5,719 Synthetic

Schema

Each sample has three fields:

Field Type Description
image_id string Original identifier for the sample
image Image PNG image of the chemical structure diagram
SMILES string Ground-truth SMILES string

Usage

from datasets import load_dataset

# Load a single benchmark
ds = load_dataset("Keylab/OCSR-Benchmarks", name="USPTO", split="test")
sample = ds[0]
sample["image"].show()   # PIL Image
print(sample["SMILES"])

# Iterate over all benchmarks
for config in ["CLEF", "JPO", "UOB", "USPTO", "USPTO-10K",
               "Staker", "ACS", "WildMol-10K", "Indigo", "ChemDraw"]:
    ds = load_dataset("Keylab/OCSR-Benchmarks", name=config, split="test")
    print(f"{config}: {len(ds)} samples")

Bulk Download

Pre-packaged .tar.gz archives (images + CSV) are also available in the COMO model repository for direct download without the datasets library.

License

These benchmarks are collected from existing public OCSR datasets. Please refer to the original sources for attribution and applicable terms:

Dataset Source
USPTO, CLEF, JPO, UOB, Staker Rajan et al., 2020, Xiong et al., 2023
Indigo, ChemDraw, ACS, Staker Qian et al., 2023
USPTO-10K Morin et al., 2023
WildMol-10K Fang et al., 2025

Citation

If you use these benchmarks, please cite the COMO paper and the original benchmark sources:

@article{lyu2026closed,
  title={COMO: Closed-Loop Optical Molecule Recognition with Minimum Risk Training},
  author={Lyu, Zhuoqi and Ke, Qing},
  journal={arXiv preprint arXiv:2604.23546},
  year={2026}
}
Downloads last month
32

Paper for Keylab/OCSR-Benchmarks