Getting it into your agent
One page per mod, every tool's command on it. A separate URL per tool would split the same page into five that compete with each other.
npx agentmods add skills/synthetic-sciences/openscience/deepchemnpx skills add synthetic-sciences/openscience --skill deepchemgit clone --depth 1 https://github.com/synthetic-sciences/openscienceWhat it costs to keep this loaded
Counted locally with the o200k_base tokenizer, which is exact for GPT models; Claude uses its own tokenizer and its counts differ. Treat this as one consistent yardstick across the catalogue rather than a bill. Prices are per million input tokens.
| Model | Per session | Once invoked |
|---|---|---|
| Fable 5 | $0.00078 | $0.04430 |
| Opus 5 | $0.00039 | $0.02215 |
| Sonnet 5 | $0.00016 | $0.00886 |
| Haiku 4.5 | $0.00008 | $0.00443 |
Grade A, and why
deepchem scanned grade A with 0 findings against 26 rules in 11 categories — prompt injection, anti-refusal, data exfiltration, privilege escalation, supply chain, agent snooping, system-prompt leakage, SSRF and excessive agency — measured 2d ago.
A static scan of the body, not an audit. Every finding is printed with the line that produced it so you can judge whether it matters here. A mod is markdown that instructs an agent; that is exactly why what it instructs is worth reading.
Nothing flagged
None of the 26 patterns this scan looks for appear in this file: no shell pipes, no recursive deletes, no credential paths, no hidden text, no instruction-override or anti-refusal phrasing, no agent-config snooping. That is not a guarantee, it is the absence of the things that are checkable.
Copies of this mod
8 near-identical copies found in the catalogue:
- deepchem — 95% identical, 7 lines differ
- deepchem — 95% identical, 7 lines differ
- deepchem — 95% identical, 7 lines differ
- deepchem — 91% identical, 11 lines differ
- deepchem — 89% identical, 10 lines differ
- deepchem — 86% identical, 50 lines differ
- deepchem — 86% identical, 50 lines differ
- deepchem — 86% identical, 50 lines differ
How it starts
The opening of the file, as written. The whole thing — 601 lines — stays where its author put it; the contents beside it link to each section on GitHub.
DeepChem
Overview
DeepChem is a comprehensive Python library for applying machine learning to chemistry, materials science, and biology. Enable molecular property prediction, drug discovery, materials design, and biomolecule analysis through specialized neural networks, molecular featurization methods, and pretrained models.
When to Use This Skill
This skill should be used when:
- Loading and processing molecular data (SMILES strings, SDF files, protein sequences)
- Predicting molecular properties (solubility, toxicity, binding affinity, ADMET properties)
- Training models on chemical/biological datasets
- Using MoleculeNet benchmark datasets (Tox21, BBBP, Delaney, etc.)
- Converting molecules to ML-ready features (fingerprints, graph representations, descriptors)
- Implementing graph neural networks for molecules (GCN, GAT, MPNN, AttentiveFP)
- Applying transfer learning with pretrained models (ChemBERTa, GROVER, MolFormer)
- Predicting crystal/materials properties (bandgap, formation energy)
- Analyzing protein or DNA sequences
Core Capabilities
1. Molecular Data Loading and Processing
DeepChem provides specialized loaders for various chemical data formats:
import deepchem as dc
# Load CSV with SMILES
featurizer = dc.feat.CircularFingerprint(radius=2, size=2048)
loader = dc.data.CSVLoader(
tasks=['solubility', 'toxicity'],
feature_field='smiles',
featurizer=featurizer
)
dataset = loader.create_dataset('molecules.csv')
# Load SDF files
loader = dc.data.SDFLoader(tasks=['activity'], featurizer=featurizer)
dataset = loader.create_dataset('compounds.sdf')
# Load protein sequences
loader = dc.data.FASTALoader()
dataset = loader.create_dataset('proteins.fasta')
Key Loaders:
CSVLoader: Tabular data with molecular identifiersSDFLoader: Molecular structure filesFASTALoader: Protein/DNA sequencesImageLoader: Molecular imagesJsonLoader: JSON-formatted datasets
2. Molecular Featurization
Convert molecules into numerical representations for ML models.
What ships with it
5 files beside SKILL.md in the same directory: the scripts, references and assets a skill reads on demand. Not counted in the per-session cost; read them before you install if any of them is executable.
What this file has done since we first saw it
Hashed on every crawl. A supply-chain change to an agent config is a question of when, not whether, so the history is kept rather than the latest state alone.
- 2d ago First seen · 601 lines · 78 tokens per session scan A 558717712682
deepchem is a skill published in the GitHub repository synthetic-sciences/openscience (3,385 stars, last pushed today), licensed Apache-2.0. It adds 78 tokens to every session and 4,430 once invoked, about $0.0004 per session on Opus 5. A static security scan graded it A with 0 findings. No closer match exists in the catalogue, so it is treated as the original; first seen 2026-08-30.
Other skills, from other repositories
admet_genetic
ADMET-guided genetic molecule optimization workflow from seed SMILES; use when the agent needs to build or run an RDKit/SA-Score/ADMET-AI GA pipeline for molecule optimization, enforce molecule lineage logs, render optimization-history HTML dashboards, and write candidate triage reports.
target-based-lead-design
Generate diverse lead compounds for a specific protein target using structure-based drug design with MolCraft. Use this skill when: (1) Designing drug candidates for a known protein target (PDB ID or disease name), (2) Generating structurally diverse molecules with optimized binding affinity, (3) Filtering candidates…
admet-prediction
Predict comprehensive ADMET (Absorption, Distribution, Metabolism, Excretion, Toxicity) properties for drug candidate molecules using GraphMVP ensemble models. Use this skill when: (1) Predicting blood-brain barrier penetration, (2) Assessing side effect profiles, (3) Estimating Caco-2 permeability, half-life, or LD50…
drug-lead-analysis
Analyze drug candidate molecules for drug-likeness, ADMET properties, and safety profiles. Use this skill when: (1) Evaluating a molecule's potential as a drug candidate, (2) Checking drug-likeness scores (QED, Lipinski), (3) Predicting blood-brain barrier penetration, (4) Assessing side effects and ADMET properties…
chem-spectrum-matcher
Match an experimental spectrum (1H NMR, 13C NMR, IR) against predicted or database reference spectra for candidate ranking and structure confirmation. Supports local catalog lookup, public database fallback, and pluggable similarity metrics.
chem-msms-predict
Predict LC-MS/MS (MS2, tandem mass spectra) from SMILES via ICEBERG, a two-stage deep neural network. Outputs predicted m/z vs intensity spectrum, fragment ion SMILES, and a spectrum plot.