--- license: cc-by-4.0 pretty_name: SynthonBench tags: - chemistry - cheminformatics - drug-discovery - virtual-screening - combinatorial-chemical-space - synthon - benchmark - docking size_categories: - 100M Search methods over synthon spaces never enumerate the full product library; > they propose **reaction-component tuples** `(reaction_id, synthon_ids)` and pay > a fixed oracle-call budget. SynthonBench scores such methods *fairly and > reproducibly* against frozen score tables and the **top-k DCRF** efficiency > metric (random search ≈ 1.0). Companion code: [`synthonbench`](https://github.com/mireklzicar/synthonbench) (`pip install synthonbench`). The package downloads this dataset for you: ```bash pip install "synthonbench[hf]" synthonbench download --scale 1M # spaces + glide_1M + surrogate_1M + seeds synthonbench download --scale all # everything, including the 100M table (~5 GB) ``` ## Targets & scales Three Glide docking targets — **KIF11**, **PYRD**, **TGFR1** — over the same 42 canonical reactions, at three scales of the synthon product space: | scale | products | unique synthons | |-------|----------|-----------------| | 1M | 990,610 | 6,270 | | 10M | 10,022,100 | 13,880 | | 100M | 99,851,700 | 31,993 | ## Files ``` spaces/ synthon_space_{1M,10M,100M}.synthons.tsv # smiles synthon_id position reaction_id synthon_space_{1M,10M,100M}.properties.csv # synthon_id + synthetic per-synthon attributes reactions.tsv # 42 canonical reactions (SMIRKS) + reagent patterns scores/ glide_1M.parquet # REAL Glide @1M, headline docking oracle (LE/medchem-filtered), all 3 targets glide_1M.parquet.sidx/ # mmap product_id -> score index (bounded-memory oracle lookup) glide_1M.parquet.topk/ # top-100k product cache per score column (exact top-k for DCRF) surrogate_1M.parquet # LightGBM docking surrogate, all 3 targets surrogate_1M.parquet.sidx/ surrogate_1M.parquet.topk/ surrogate_10M.parquet (+ .sidx/ .topk/) surrogate_100M.parquet # ~4.6 GB (+ .sidx/ ~3.8 GB, .topk/) seeds/ seeds__s{0,1,2}.parquet # 3 shared 100k warm-start pools per target (one per protocol seed) ``` ### Sidecars (`*.parquet.sidx`, `*.parquet.topk`) Large score tables are **not** loaded into a Python `{product_id: score}` dict. Each table ships two bounded-memory sidecars that `synthonbench` reads directly: - **`.sidx`** — a memory-mapped `product_id → score` index. `synthonbench.load_oracle` returns an `IndexedScoreTableOracle` backed by it, so oracle lookups never materialise the table. - **`.topk`** — the best 100k products per `(score column, direction)`, so top-k recall / DCRF and the reported docking-score means need no full-table sort. `synthonbench download` fetches these alongside each parquet automatically. If you stage a parquet by hand, rebuild them with `synthonbench build-score-index` and `synthonbench build-topk-cache` (the glide table needs `_glide_le`@maximize + `_glide_raw`@minimize; the surrogate tables need `_predicted_dock_score`@minimize, for each of the three targets). ### `scores/glide_1M.parquet` (headline real-Glide oracle) One row per product (990,610). Keyed by `product_id` (md5 of the assembled product) which also keys every surrogate table. | column | meaning | |--------|---------| | `product_id`, `reaction_id` | product id and its reaction | | `smiles`, `canonical_smiles` | assembled product | | `_glide_raw` | raw Glide docking score | | `_glide_le` | **benchmark score**: medchem-filtered, lipophilicity-penalized (−Glide−cLogP) ligand-efficiency score; `0.0` if the product fails the medchem filter or docking | | `_le_ratio`, `_valid` | ligand efficiency and validity flag | | `passes_exp27_exact_filter`, `exp27_filter_reason` | medchem filter outcome | | `mol_wt`, `mol_logp`, `hba`, `hbd`, `rotatable_bonds`, `fraction_csp3`, `tpsa`, `aromatic_rings`, `fluorine_count`, `amide_count` | RDKit physchem descriptors | `` ∈ {`kif11`, `pyrd`, `tgfr1`}. ### `scores/surrogate_{1M,10M,100M}.parquet` | column | meaning | |--------|---------| | `product_id`, `reaction_id`, `smiles` | product identity | | `synthon1_id`, `synthon2_id`, `synthon3_id` | the synthon tuple (`synthon3` null for 2-component reactions) | | `kif11_predicted_dock_score`, `pyrd_predicted_dock_score`, `tgfr1_predicted_dock_score` | LightGBM surrogate scores | ### `seeds/seeds__s{0,1,2}.parquet` (shared warm-start pools) Three independent uniform-random 100k samples of the 1M product space per target — one per protocol seed `0,1,2`. Every method may **initialize from the same pool** so warm-start does not confound the comparison. Columns: `target`, `seed`, `product_id`, `reaction_id`, `synthon1_id`, `synthon2_id`, `synthon3_id`, `smiles`, `surrogate_score`, `glide_le_score`. (The maximum benchmark budget is 100k oracle calls, so a full seed pool is itself within budget.) ## Quick load ```python from datasets import load_dataset glide = load_dataset("mireklzicar/synthonbench", "glide_1M", split="train") seeds = load_dataset("mireklzicar/synthonbench", "seeds", split="train") ``` or directly with pandas / pyarrow: ```python import pandas as pd df = pd.read_parquet("hf://datasets/mireklzicar/synthonbench/scores/glide_1M.parquet") ``` ## Provenance & licensing Synthon spaces are derived from publicly described make-on-demand reaction schemes; real-Glide scores were produced with Schrödinger Glide and the LightGBM surrogate was trained on them. The **scores and synthon tables** released here are redistributable under CC-BY-4.0. Docking/space construction *software* (Glide, BiosolveIT FTrees/CoLibri, SpaceHASTEN) is **not** included and requires the respective vendor licenses; see the code repository for how external methods are wired in optionally. ## Citation See [`CITATION.cff`](https://github.com/mireklzicar/synthonbench/blob/main/CITATION.cff).