chembl-database

name	chembl-database
description	Query the ChEMBL database for bioactive molecules, targets, bioactivities, and approved drugs; use this when you need to filter by physicochemical properties (e.g., MW, LogP), chemical structure (SMILES), or retrieve drug mechanism information.
license	MIT
author	AIPOCH

Source: https://github.com/aipoch/medical-research-skills

When to Use

• Find candidate compounds by name or synonym (e.g., searching for “aspirin”) and retrieve their ChEMBL records.
• Filter molecules by physicochemical properties (e.g., molecular weight, LogP) to narrow down drug-like candidates.
• Look up targets (proteins/complexes) and connect them to ligands and known bioactivity measurements.
• Retrieve bioactivity data (e.g., IC50, Ki, EC50) for specific compound–target interactions to support SAR or benchmarking.
• Identify approved drugs and fetch mechanism-of-action information for target validation or competitive landscape analysis.

Key Features

• Molecule search by preferred name and other metadata fields.
• Property-based filtering (e.g., MW, LogP) using ChEMBL API filter syntax.
• Structure-aware querying via SMILES (where supported by the API/client).
• Target lookup and navigation between targets, molecules, and activities.
• Bioactivity retrieval for common endpoints (IC50, Ki, EC50) and related assay context.
• Access to drug-related records, including mechanism information for approved drugs.

Dependencies

• Python 3.9+ (recommended)
• chembl_webresource_client (latest available via pip/uv)

Install:

uv pip install chembl_webresource_client

Additional references (optional, if present in this repository):

• references/api_reference.md (filter syntax and resource list)
• scripts/query_chembl.py (CLI wrapper example)

Example Usage

from chembl_webresource_client.new_client import new_client

def main():
    molecule = new_client.molecule
    target = new_client.target
    activity = new_client.activity
    mechanism = new_client.mechanism

    # 1) Search for molecules by name (case-insensitive substring match)
    mols = list(molecule.filter(pref_name__icontains="aspirin")[:5])
    if not mols:
        raise SystemExit("No molecules found for query.")

    first = mols[0]
    chembl_id = first.get("molecule_chembl_id")
    print("Top molecule hit:", chembl_id, "-", first.get("pref_name"))

    # 2) Filter molecules by a simple property constraint (example: MW <= 500)
    # Note: exact field names and operators depend on ChEMBL API schema.
    druglike = list(molecule.filter(molecule_properties__mw_freebase__lte=500)[:5])
    print("Example drug-like hits (MW<=500):", [m.get("molecule_chembl_id") for m in druglike])

    # 3) Get target information (example: targets containing "COX")
    targets = list(target.filter(pref_name__icontains="cyclooxygenase")[:5])
    print("Example targets:", [(t.get("target_chembl_id"), t.get("pref_name")) for t in targets])

    # 4) Query bioactivity for a molecule (IC50/Ki/EC50 etc. depend on available records)
    
    acts = (activity.(molecule_chembl_id=chembl_id)[:])
     a  acts:
        (
            ,
            a.get(),
            , a.get(),
            , a.get(),
            , a.get(),
            , a.get(),
        )

    
    mechs = (mechanism.(molecule_chembl_id=chembl_id)[:])
     m  mechs:
        (
            ,
            , m.get(),
            , m.get(),
            , m.get(),
        )

 __name__ == :
    main()

Implementation Details

• Client/Resources: Uses chembl_webresource_client.new_client.new_client to access resource endpoints such as molecule, target, activity, and mechanism.
• Filtering Model: Queries are built via .filter(...) with field lookups and operators (e.g., __icontains, __lte). The exact available fields and supported operators are defined by the ChEMBL API schema; consult references/api_reference.md for the authoritative list and examples.
• Pagination/Slicing: Results are iterable and can be sliced (e.g., [:5]) to limit network calls and output size.
• Bioactivity Fields: Common normalized fields include standard_type, standard_value, and standard_units. Not all records contain all fields; code should handle missing keys.
• Mechanism Retrieval: Mechanism-of-action data is accessed via the mechanism resource and is typically most complete for approved/annotated drugs.
• Structure Queries (SMILES): Structure-based search support depends on the API endpoint and client capabilities; when enabled, it is typically performed by passing a SMILES string to the appropriate structure/compound endpoint or filter as documented in references/api_reference.md.