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PubChem PUG REST API Guide

Overview

PubChem is the world's largest free chemistry database, maintained by the National Center for Biotechnology Information (NCBI) at the U.S. National Library of Medicine. It contains information on over 115 million chemical compounds, 300 million substances from hundreds of data sources, and over 1.5 million bioassay experiments. PubChem is a critical resource for researchers in chemistry, pharmacology, drug discovery, toxicology, and related life sciences.

The PUG REST (Power User Gateway RESTful) API provides programmatic access to PubChem's three primary databases: Compound (standardized chemical structures), Substance (depositor-provided records), and BioAssay (biological screening results). The API supports searches by name, molecular formula, structure similarity, substructure, and various identifiers including CID, SID, InChI, and SMILES.

PUG REST is entirely free, requires no authentication, and returns data in JSON, XML, CSV, SDF, and other formats. It is designed for both simple lookups and complex cheminformatics workflows.

Authentication

No authentication is required. PubChem PUG REST is a free public service.

# No API key needed
curl "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/name/aspirin/JSON"

Core Endpoints

Get Compound by Name

GET https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/name/{name}/JSON

curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/name/caffeine/JSON" \
  | python3 -m json.tool

Get Compound Properties

Retrieve specific properties for a compound by CID.

GET https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/cid/{cid}/property/{properties}/JSON

Available properties: MolecularFormula, MolecularWeight, CanonicalSMILES, InChI, InChIKey, IUPACName, XLogP, ExactMass, HBondDonorCount, HBondAcceptorCount, RotatableBondCount, TPSA

curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/name/ibuprofen/property/MolecularFormula,MolecularWeight,CanonicalSMILES,IUPACName,XLogP/JSON" \
  | python3 -m json.tool

Search by Molecular Formula

curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/fastformula/C8H10N4O2/property/IUPACName,MolecularWeight,CanonicalSMILES/JSON" \
  | python3 -m json.tool

Similarity Search

Find compounds structurally similar to a given compound (Tanimoto threshold).

curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/fastsimilarity_2d/cid/2244/property/IUPACName,MolecularWeight,CanonicalSMILES/JSON?Threshold=90" \
  | python3 -m json.tool

Get BioAssay Data

Retrieve biological activity data for a compound.

curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/cid/2244/assaysummary/JSON" \
  | python3 -m json.tool

Python Example: Drug-Likeness Screening

import requests
import time

PUG_REST = "https://pubchem.ncbi.nlm.nih.gov/rest/pug"

def get_compound_properties(name):
    """Fetch key drug-likeness properties for a named compound."""
    props = "MolecularWeight,XLogP,HBondDonorCount,HBondAcceptorCount,TPSA,RotatableBondCount,IUPACName"
    url = f"{PUG_REST}/compound/name/{name}/property/{props}/JSON"
    resp = requests.get(url)
    resp.raise_for_status()
    data = resp.json()
    return data.get("PropertyTable", {}).get("Properties", [{}])[0]

def check_lipinski(props):
    """Check Lipinski's Rule of Five for oral drug-likeness."""
    violations = 0
    mw = props.get("MolecularWeight", 0)
    logp = props.get("XLogP", 0)
    hbd = props.get("HBondDonorCount", 0)
    hba = props.get("HBondAcceptorCount", 0)

    if mw > 500: violations += 1
    if logp > 5: violations += 1
    if hbd > 5: violations += 1
    if hba > 10: violations += 1
    return violations

drug_candidates = ["metformin", "atorvastatin", "lisinopril", "omeprazole"]
print(f"{'Compound':<20} {'MW':>8} {'LogP':>6} {'HBD':>4} {'HBA':>4} {'Violations':>10}")
print("-" * 60)

for drug in drug_candidates:
    props = get_compound_properties(drug)
    violations = check_lipinski(props)
    print(f"{drug:<20} {props.get('MolecularWeight', 0):>8.1f} "
          f"{props.get('XLogP', 0):>6.1f} "
          f"{props.get('HBondDonorCount', 0):>4} "
          f"{props.get('HBondAcceptorCount', 0):>4} "
          f"{violations:>10}")
    time.sleep(0.3)

Python Example: Compound Comparison

import requests

def compare_compounds(cid_list):
    """Compare properties of multiple compounds by CID."""
    cids = ",".join(str(c) for c in cid_list)
    props = "IUPACName,MolecularFormula,MolecularWeight,CanonicalSMILES,XLogP"
    url = f"{PUG_REST}/compound/cid/{cids}/property/{props}/JSON"
    resp = requests.get(url)
    resp.raise_for_status()
    return resp.json().get("PropertyTable", {}).get("Properties", [])

# Compare aspirin (2244), ibuprofen (3672), acetaminophen (1983)
results = compare_compounds([2244, 3672, 1983])
for compound in results:
    print(f"\n{compound.get('IUPACName', 'Unknown')}")
    print(f"  Formula: {compound.get('MolecularFormula')}")
    print(f"  MW: {compound.get('MolecularWeight')}")
    print(f"  SMILES: {compound.get('CanonicalSMILES')}")
    print(f"  LogP: {compound.get('XLogP')}")

Common Research Patterns

Structure-Activity Relationship (SAR) Analysis: Use similarity searches to find structural analogs of lead compounds, then retrieve bioassay data to compare biological activity across the series.

Virtual Screening: Screen large compound libraries against drug-likeness filters (Lipinski's rules, Veber's rules) using property endpoints to prioritize candidates for experimental testing.

Chemical Identifier Resolution: Translate between compound names, CIDs, InChI, InChIKey, and SMILES notations. Essential for data integration across heterogeneous chemistry databases.

Toxicology Research: Access bioassay results and safety data for compounds to support toxicity profiling and risk assessment in environmental health research.

Rate Limits and Best Practices

Rate limit: Maximum 5 requests per second; add 200ms delays between requests
No more than 400 requests per minute from a single IP
Batch requests: Use comma-separated CIDs (up to 200) in a single request to minimize API calls
Async operations: For large similarity/substructure searches, use the async workflow with list keys
Response formats: Use JSON for programmatic access, SDF for structure files, CSV for tabular data
Caching: Compound data is relatively static; cache property lookups aggressively
Error handling: HTTP 404 means compound not found; 503 means server busy (retry with backoff)

References

PubChem PUG REST Documentation: https://pubchem.ncbi.nlm.nih.gov/docs/pug-rest
PubChem PUG REST Tutorial: https://pubchem.ncbi.nlm.nih.gov/docs/pug-rest-tutorial
PubChem Compound Database: https://pubchem.ncbi.nlm.nih.gov/
PubChem Power User Gateway: https://pubchem.ncbi.nlm.nih.gov/docs/power-user-gateway

pubchem-api-guide

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