zinc-database

name	zinc-database
description	Query ZINC15/ZINC22 virtual compound libraries (1.4B compounds, 750M purchasable). Search lead/fragment/drug-like compounds by MW, logP, reactivity, or SMILES similarity; download 3D sets for docking. For bioactivity use chembl-database-bioactivity; for approved drugs use drugbank-database-access.
license	CC-BY-4.0

ZINC Chemical Library Database

Overview

ZINC (ZINC Is Not Commercial) is a free database of commercially available compounds curated for virtual screening. ZINC22 contains over 1.4 billion compounds (ZINC20: 1.4B, including purchasable 3D conformers), organized by molecular property filters (lead-like, fragment-like, drug-like) and reactivity class. The REST API enables SMILES-based searches, property-filtered downloads, and compound subset exports for docking campaigns.

When to Use

• Downloading a purchasable, drug-like or lead-like compound library for virtual screening or docking campaigns
• Filtering compounds by Lipinski/lead-like properties (MW, logP, HBD, HBA) to build focused screening sets
• Searching ZINC for commercially available analogs of a query molecule via SMILES similarity
• Retrieving purchasable fragments (MW < 300, logP < 3) for fragment-based drug discovery
• Building compound diversity libraries for high-throughput screening (HTS) campaigns
• For known drug bioactivity data use chembl-database-bioactivity; for approved drug structures use drugbank-database-access; for RDKit property calculation use rdkit-cheminformatics

Prerequisites

• Python packages: requests, pandas
• Data requirements: SMILES strings, MW/logP ranges, or ZINC subset IDs
• Environment: internet connection; no API key needed for ZINC15; large downloads may take minutes
• Rate limits: reasonable use; avoid crawling all 1.4B records in automated loops

pip install requests pandas

Quick Start

import requests

# Search ZINC15 REST API for drug-like compounds
BASE = "https://zinc15.docking.org"

r = requests.get(f"{BASE}/substances.json",
                 params={"mwt__gte": 250, "mwt__lte": 350,
                         "logp__gte": 0, "logp__lte": 3,
                         "availability": "for-sale", "count": 5})
r.raise_for_status()
compounds = r.json()
print(f"Returned {len(compounds)} compounds")
for c in compounds[:3]:
    print(f"  ZINC: {c['zinc_id']:20s} MW: {c['mwt']:.1f}  logP: {c['logp']:.2f}  SMILES: {c['smiles'][:40]}")

Core API

Query 1: Property-Filtered Compound Search

Search ZINC15 by molecular property ranges (Lipinski, lead-like, fragment-like criteria).

import requests, pandas as pd

BASE = "https://zinc15.docking.org"

def zinc_search(params, max_results=500):
    """Search ZINC15 with property filters. Returns DataFrame."""
    all_results = []
    params = dict(params)
    params["count"] = min(100, max_results)

    r = requests.get(f"{BASE}/substances.json", params=params)
    r.raise_for_status()
    compounds = r.json()
    all_results.extend(compounds)
    return pd.DataFrame(all_results)

# Lead-like set: MW 250-350, logP 1-3, HBD ≤ 3
df_leads = zinc_search({
    "mwt__gte": 250, "mwt__lte": 350,
    "logp__gte": 1, "logp__lte": 3,
    "hbd__lte": 3, "hba__lte": 7,
    "availability": "for-sale",
})
print(f"Lead-like compounds: {len(df_leads)}")
print(df_leads[["zinc_id", "mwt", "logp", "smiles"]].head())

# Fragment-like set: MW < 300, logP < 3 (Rule of Three)
df_frags = zinc_search({
    "mwt__lte": 300,
    "logp__lte": 3,
    "hbd__lte": 3,
    "availability": "for-sale",
})
print(f"\nFragment-like compounds: {len(df_frags)}")
print(df_frags[["zinc_id", "mwt", "logp", "smiles"]].head())

Query 2: Retrieve Compound by ZINC ID

Fetch full compound data for a known ZINC identifier.

import requests

BASE = "https://zinc15.docking.org"

zinc_id = "ZINC000000029632"

r = requests.get(f"{BASE}/substances/{zinc_id}.json")
r.raise_for_status()
c = r.json()

print(f"ZINC ID  : {c['zinc_id']}")
print(f"SMILES   : {c['smiles']}")
print(f"MW       : {c['mwt']:.2f}")
print(f"logP     : {c['logp']:.2f}")
print(f"HBD      : {c['hbd']}")
print(f"HBA      : {c['hba']}")
print(f"TPSA     : {c.get('tpsa', 'n/a')}")
print(f"Rotatable: {c.get('rotatable_bonds', 'n/a')}")
print(f"Suppliers: {len(c.get('suppliers', []))}")

Query 3: Download Compound Subsets (Tranches)

ZINC organizes compounds into "tranches" by MW and logP. Download pre-built SDF/SMILES files.

import requests

# ZINC15 tranche download (MW 200-250, logP 1-2 range)
# Tranche naming: letters encode MW range (A-K) and logP range (A-J)
# See http://zinc15.docking.org/tranches/home

def download_zinc_tranche(tranche_name, dest_file, fmt="smi"):
    """Download a ZINC tranche SMILES file."""
    url = f"https://zinc15.docking.org/tranches/{tranche_name}.{fmt}"
    r = requests.get(url, stream=True)
    r.raise_for_status()
    with open(dest_file, "wb") as f:
        for chunk in r.iter_content(chunk_size=8192):
            f.write(chunk)
    print(f"Downloaded {dest_file}")

# Download one tranche as SMILES
download_zinc_tranche("AABA", "zinc_AABA.smi", fmt="smi")

Query 4: SMILES Similarity Search

Find ZINC compounds similar to a query molecule.

import requests, pandas as pd

BASE = "https://zinc15.docking.org"

query_smiles = "c1ccc(NC(=O)c2ccccc2)cc1"  # benzanilide analog

r = requests.get(f"{BASE}/substances.json",
                 params={
                     "smiles": query_smiles,
                     "similarity": 0.6,       # Tanimoto similarity threshold
                     "count": 20,
                     "availability": "for-sale"
                 })
r.raise_for_status()
results = r.json()
print(f"Similar compounds found: {len(results)}")
df = pd.DataFrame(results)[["zinc_id", "smiles", "mwt", "logp"]]
print(df.head())

Query 5: Catalog and Supplier Information

Retrieve purchasability and supplier catalog data for compounds.

import requests

BASE = "https://zinc15.docking.org"

# Check purchasability and catalog info
zinc_id = "ZINC000000029632"
r = requests.get(f"{BASE}/substances/{zinc_id}/suppliers.json")
r.raise_for_status()
suppliers = r.json()

print(f"Suppliers for {zinc_id}: {len(suppliers)}")
for sup in suppliers[:5]:
    print(f"  {sup.get('name', 'n/a'):30s} | Catalog: {sup.get('catalognum', 'n/a')}")

Query 6: Bulk Download via ZINC Slices

For large-scale virtual screening, download entire ZINC subsets as compressed SMILES.

import requests, gzip, io, pandas as pd

# ZINC15 drug-like purchasable slice (public URL pattern)
# Full drug-like: https://zinc15.docking.org/substances/subsets/drug-like.smi.gz

def download_zinc_subset(subset_name, max_lines=1000):
    """Download a ZINC subset SMILES file and return a DataFrame sample."""
    url = f"https://zinc15.docking.org/substances/subsets/{subset_name}.smi.gz"
    r = requests.get(url, stream=True)
    r.raise_for_status()

    lines = []
    with gzip.open(r.raw, "rt") as f:
        for i, line in enumerate(f):
            if i >= max_lines:
                break
            lines.append(line.strip().split())

    df = pd.DataFrame(lines, columns=["smiles", "zinc_id"] + [f"col{i}" for i in range(max(0, len(lines[0])-2))])
    return df[["smiles", "zinc_id"]]

# Load first 1000 from lead-like subset
df_sample = download_zinc_subset("lead-like", max_lines=1000)
print(f"Loaded {len(df_sample)} compounds from lead-like subset")
print(df_sample.head())

Key Concepts

ZINC Tranches

Compounds are organized into a 2D grid of "tranches" based on MW (rows A–K: <200 to >600 Da) and logP (columns A–J: <-1 to >5). Each tranche can be downloaded as a SMILES or SDF file. This tranching enables targeted downloads of specific property spaces for docking.

Availability Classes

• for-sale: Purchasable from ≥1 supplier
• in-stock: Available for immediate purchase
• wait-ok: Longer lead time acceptable
• on-demand: Custom synthesis required

Common Workflows

Workflow 1: Build a Focused Docking Library

Goal: Curate a purchasable, lead-like compound library within specific property ranges, deduplicate, and export for docking.

import requests, pandas as pd

BASE = "https://zinc15.docking.org"

# Fetch lead-like purchasable compounds with Lipinski compliance
params = {
    "mwt__gte": 200, "mwt__lte": 500,
    "logp__gte": -1, "logp__lte": 5,
    "hbd__lte": 5, "hba__lte": 10,
    "rotatable_bonds__lte": 10,
    "availability": "for-sale",
    "count": 200,
}
r = requests.get(f"{BASE}/substances.json", params=params)
r.raise_for_status()
compounds = r.json()

df = pd.DataFrame(compounds)[["zinc_id", "smiles", "mwt", "logp", "hbd", "hba"]]
df = df.drop_duplicates(subset=["smiles"])
print(f"Curated library: {len(df)} unique compounds")

# Export as SMILES for docking input
df[["smiles", "zinc_id"]].to_csv("docking_library.smi", sep=" ", index=False, header=False)
print("Saved: docking_library.smi")
print(df.head())

Workflow 2: Fragment Library for FBDD

Goal: Download fragment-like (Rule of Three) compounds for fragment-based drug discovery.

import requests, pandas as pd

BASE = "https://zinc15.docking.org"

# Rule of Three: MW ≤ 300, logP ≤ 3, HBD ≤ 3, HBA ≤ 3, RotB ≤ 3
params = {
    "mwt__lte": 300,
    "logp__lte": 3,
    "hbd__lte": 3,
    "hba__lte": 3,
    "rotatable_bonds__lte": 3,
    "availability": "for-sale",
    "count": 200,
}
r = requests.get(f"{BASE}/substances.json", params=params)
fragments = r.json()
df = pd.DataFrame(fragments)[["zinc_id", "smiles", "mwt", "logp"]]

print(f"Fragment library: {len(df)} compounds (Rule of Three)")
df.to_csv("fragment_library.smi", sep=" ", index=False, header=False)
print("Saved: fragment_library.smi")
df.describe()

Key Parameters

Parameter	Module	Default	Range / Options	Effect
mwt__gte / mwt__lte	Search	—	numeric (Da)	Molecular weight lower/upper bound
logp__gte / logp__lte	Search	—	numeric	logP (lipophilicity) range
hbd__lte	Search	—	integer	Max hydrogen bond donors
hba__lte	Search	—	integer	Max hydrogen bond acceptors
rotatable_bonds__lte	Search	—	integer	Max rotatable bonds
availability	Search	all	"for-sale", "in-stock", "on-demand"	Purchasability filter
count	Search	10	1–1000	Max compounds returned per request
similarity	Similarity	—	0.0–1.0	Tanimoto similarity threshold

Best Practices

1. Use tranches for large docking campaigns: Downloading entire MW/logP tranches as pre-built SDF files is faster than paginating the API. Use the ZINC tranches page to identify the subset of property space you need.

2. Apply reactivity filters: ZINC marks reactive compounds with "reactivity" flags. Exclude compounds with reactive groups (reactivity: "clean" filter) for cell-based assays.

3. Deduplicate by SMILES: API results may contain duplicates across supplier catalog entries. Canonical SMILES deduplication with RDKit (Chem.MolToSmiles(Chem.MolFromSmiles(smi))) before docking.

4. Combine with RDKit filtering: After downloading, apply additional filters (PAINS, Brenk alerts) using rdkit-cheminformatics or medchem before investing compute in docking.

5. Cache SMILES downloads: ZINC data is updated periodically. Cache downloads with a date-stamped filename and avoid re-downloading within a project.

Common Recipes

Recipe: Lookup ZINC ID from SMILES

When to use: Find the ZINC ID for a known compound to check purchasability.

import requests

BASE = "https://zinc15.docking.org"
smiles = "CC(=O)Nc1ccc(O)cc1"  # paracetamol / acetaminophen

r = requests.get(f"{BASE}/substances.json",
                 params={"smiles": smiles, "count": 3})
for c in r.json():
    print(f"ZINC: {c['zinc_id']} | MW: {c['mwt']:.1f} | In stock: {c.get('availability')}")

Recipe: Export SDF for Docking

When to use: Download 3D SDF conformers for a list of ZINC IDs for use in docking software.

import requests

BASE = "https://zinc15.docking.org"
zinc_ids = ["ZINC000000029632", "ZINC000001532592"]

for zid in zinc_ids:
    r = requests.get(f"{BASE}/substances/{zid}.sdf")
    if r.ok:
        with open(f"{zid}.sdf", "w") as f:
            f.write(r.text)
        print(f"Downloaded {zid}.sdf")
    else:
        print(f"Not available: {zid}")

Recipe: Property Distribution of a Library

When to use: Quickly assess the property coverage of a downloaded compound set.

import pandas as pd

df = pd.read_csv("docking_library.smi", sep=" ", names=["smiles", "zinc_id"])
print(f"Library size: {len(df)}")

# If you have the full ZINC metadata:
# df = pd.DataFrame(compounds)[["mwt", "logp", "hbd", "hba"]]
# print(df.describe())
# import matplotlib.pyplot as plt
# df[["mwt", "logp"]].hist(bins=30, figsize=(10, 4)); plt.show()

Troubleshooting

Problem	Cause	Solution
HTTP 404 for compound ID	ZINC ID format incorrect	Use full 12-digit ZINC ID (e.g., ZINC000000029632)
Empty results for property search	Filters too restrictive	Relax ranges; check mwt__gte < mwt__lte is not inverted
Similarity search returns nothing	SMILES invalid or unusual scaffold	Validate SMILES with RDKit first; try lower similarity threshold
Tranche file download fails	Tranche code wrong	Verify tranche naming at zinc15.docking.org/tranches/home
API returns HTML error page	Server maintenance	Retry after a few minutes; check ZINC status
Slow large downloads	Large compound sets	Download tranche files via FTP/HTTP bulk download instead of API pagination

Related Skills

• rdkit-cheminformatics — Compute additional properties and apply PAINS filters on downloaded ZINC compounds
• autodock-vina-docking — Use downloaded ZINC SMILES/SDF files for molecular docking campaigns
• chembl-database-bioactivity — Bioactivity data for compounds identified in ZINC virtual screens
• medchem — Apply medicinal chemistry filters (Lipinski, PAINS, NIBR) on ZINC libraries

References

• ZINC15 website — Main ZINC15 database and API
• ZINC15 REST API reference — Query parameters and endpoint documentation
• ZINC22 update paper — Irwin et al., J. Chem. Inf. Model. 2022
• ZINC tranches download page — Bulk compound subset downloads by MW/logP