medchem

name	medchem
description	Medicinal chemistry filters for compound triage. Drug-likeness rules (Lipinski Ro5, Veber, Oprea, CNS, leadlike, REOS, Golden Triangle, Ro3), structural alerts (PAINS, NIBR, Lilly Demerits), chemical group detectors, complexity metrics, and filter composition query language. Built on RDKit/datamol. For hit-to-lead filtering, library design, ADMET pre-screening. For molecular I/O use rdkit-cheminformatics or datamol.
license	Apache-2.0

Medchem

Overview

Medchem is a Python library for molecular filtering and prioritization in drug discovery. It provides hundreds of established medicinal chemistry rules, structural alerts, and chemical group detectors to triage compound libraries at scale. All filters support parallel execution and return structured results.

When to Use

• Applying drug-likeness rules (Lipinski, Veber, Oprea, CNS, REOS) to compound libraries
• Filtering molecules by structural alerts (PAINS, NIBR, Lilly Demerits)
• Detecting specific chemical groups (hinge binders, Michael acceptors, reactive groups)
• Calculating molecular complexity metrics (Bertz, Whitlock, Barone)
• Applying custom property constraints (MW, LogP, TPSA, rotatable bonds)
• Composing complex multi-rule filter queries with Boolean logic
• For SMILES/SDF parsing, descriptors, and fingerprints use rdkit-cheminformatics
• For high-level molecular manipulation use datamol-cheminformatics

Prerequisites

pip install medchem datamol

Medchem depends on RDKit and datamol. All molecule inputs are RDKit Chem.Mol objects; use datamol.to_mol() to convert from SMILES.

Quick Start

import datamol as dm
import medchem as mc

# Convert SMILES to molecules
smiles_list = ["CC(=O)OC1=CC=CC=C1C(=O)O", "c1ccccc1N", "O=C(O)c1ccccc1"]
mols = [dm.to_mol(s) for s in smiles_list]

# Apply Rule of Five + structural alerts in one pass
rule_filter = mc.rules.RuleFilters(rule_list=["rule_of_five"])
alert_filter = mc.structural.CommonAlertsFilters()

rule_results = rule_filter(mols=mols, n_jobs=-1)
alert_results = alert_filter(mols=mols, n_jobs=-1)

print(f"Rule results: {rule_results}")
print(f"Alert results: {[r['has_alerts'] for r in alert_results]}")

Core API

1. Drug-Likeness Rules

Apply established medicinal chemistry rules via mc.rules. Individual rules return bool; RuleFilters applies multiple rules in batch.

import medchem as mc

# Single rule on a SMILES string
passes = mc.rules.basic_rules.rule_of_five("CC(=O)OC1=CC=CC=C1C(=O)O")
print(f"Passes Ro5: {passes}")  # True

# Available individual rules:
# rule_of_five, rule_of_three, rule_of_oprea, rule_of_cns,
# rule_of_leadlike_soft, rule_of_leadlike_strict, rule_of_veber,
# rule_of_reos, rule_of_drug, golden_triangle, pains_filter

import datamol as dm
import medchem as mc

# Batch application with RuleFilters
mols = [dm.to_mol(s) for s in smiles_list]
rfilter = mc.rules.RuleFilters(
    rule_list=["rule_of_five", "rule_of_oprea", "rule_of_cns"]
)
results = rfilter(mols=mols, n_jobs=-1, progress=True)
# Returns list of dicts: [{"rule_of_five": True, "rule_of_oprea": False, ...}, ...]
print(f"First molecule: {results[0]}")

2. Structural Alert Filters

Detect problematic structural patterns via mc.structural. Three filter sets cover different scope and stringency.

import datamol as dm
import medchem as mc

mol = dm.to_mol("c1ccc(N)cc1")
mols = [dm.to_mol(s) for s in smiles_list]

# Common Alerts — general structural alerts from ChEMBL / literature
alert_filter = mc.structural.CommonAlertsFilters()
has_alerts, details = alert_filter.check_mol(mol)  # single molecule
batch_results = alert_filter(mols=mols, n_jobs=-1, progress=True)
# Each result: {"has_alerts": bool, "alert_details": [...], "num_alerts": int}
print(f"Alerts: {batch_results[0]}")

import medchem as mc

# NIBR Filters — Novartis industrial filter set (returns bool list)
nibr_filter = mc.structural.NIBRFilters()
nibr_results = nibr_filter(mols=mols, n_jobs=-1)
print(f"NIBR pass: {nibr_results}")  # [True, False, ...]

# Lilly Demerits — 275 patterns, molecules rejected at >100 demerits
lilly_filter = mc.structural.LillyDemeritsFilters()
lilly_results = lilly_filter(mols=mols, n_jobs=-1)
# Each result: {"demerits": int, "passes": bool, "matched_patterns": [...]}
print(f"Lilly: {lilly_results[0]}")

3. Chemical Groups

Detect specific functional group motifs via mc.groups.ChemicalGroup.

Predefined groups: hinge_binders, phosphate_binders, michael_acceptors, reactive_groups.

import medchem as mc

# Check for kinase hinge binders and Michael acceptors
group = mc.groups.ChemicalGroup(
    groups=["hinge_binders", "michael_acceptors"]
)

has_matches = group.has_match(mols)        # List[bool]
match_info = group.get_matches(mols[0])    # {group_name: [(atom_indices), ...]}
all_matches = group.get_all_matches(mols)  # List[Dict]
print(f"Has hinge binder: {has_matches}")

# Custom SMARTS patterns
custom = mc.groups.ChemicalGroup(
    groups=["reactive_groups"],
    custom_smarts={"trifluoromethyl_ketone": "[C;H0](=O)C(F)(F)F"}
)

4. Named Catalogs

Access curated chemical structure catalogs via mc.catalogs.

Available catalogs: functional_groups, protecting_groups, reagents, fragments.

import medchem as mc

catalog = mc.catalogs.NamedCatalogs.get("functional_groups")
matches = catalog.get_matches(mol)
print(f"Functional group matches: {matches}")

5. Molecular Complexity

Calculate synthetic accessibility proxies via mc.complexity.

Methods: bertz (topological), whitlock, barone.

import datamol as dm
import medchem as mc

mol = dm.to_mol("CC(=O)OC1=CC=CC=C1C(=O)O")

# Single molecule complexity
score = mc.complexity.calculate_complexity(mol, method="bertz")
print(f"Bertz complexity: {score:.1f}")

# Batch filtering by complexity threshold
cfilter = mc.complexity.ComplexityFilter(max_complexity=500, method="bertz")
results = cfilter(mols=mols, n_jobs=-1)
print(f"Passes complexity: {results}")  # List[bool]

6. Property Constraints

Apply custom property-based constraints via mc.constraints.Constraints.

import medchem as mc

constraints = mc.constraints.Constraints(
    mw_range=(200, 500),
    logp_range=(-2, 5),
    tpsa_max=140,
    rotatable_bonds_max=10,
    hbd_max=5,
    hba_max=10,
    rings_range=(1, 5),
    aromatic_rings_max=3,
)
results = constraints(mols=mols, n_jobs=-1)
# Each result: {"passes": bool, "violations": ["mw_range", ...]}
print(f"Violations: {results[0]}")

7. Query Language

Compose complex filter logic with Boolean expressions via mc.query.

import medchem as mc

# Parse a query combining rules, alerts, and property checks
query = mc.query.parse("rule_of_five AND NOT common_alerts")
results = query.apply(mols=mols, n_jobs=-1)  # List[bool]
print(f"Passing: {sum(results)}/{len(results)}")

# More complex queries
q2 = mc.query.parse("rule_of_cns AND complexity < 400")
q3 = mc.query.parse("(rule_of_five OR rule_of_oprea) AND NOT pains_filter")
q4 = mc.query.parse("mw > 200 AND mw < 500 AND logp < 5")

8. Functional API & Utilities

Shortcut functions in mc.functional and utilities in mc.utils.

import medchem as mc

# Functional API — one-liner filters
nibr_ok = mc.functional.nibr_filter(mols=mols, n_jobs=-1)    # List[bool]
alerts = mc.functional.common_alerts_filter(mols=mols, n_jobs=-1)
lilly = mc.functional.lilly_demerits_filter(mols=mols, n_jobs=-1)

# Utilities
standardized = mc.utils.standardize_mol(mol)  # sanitize, neutralize charges
batch_out = mc.utils.batch_process(
    mols=mols, func=mc.complexity.calculate_complexity,
    n_jobs=-1, progress=True, batch_size=100
)

Key Concepts

Rule Thresholds Quick Reference

Rule	MW	LogP	HBD	HBA	RotBonds	TPSA	Other
Ro5 (Lipinski)	≤500	≤5	≤5	≤10	—	—	—
Veber	—	—	—	—	≤10	≤140	—
Oprea (lead)	200-350	-2 to 4	—	—	≤7	—	Rings ≤4
Leadlike Soft	250-450	-3 to 4	—	—	≤10	—	—
Leadlike Strict	200-350	-2 to 3.5	—	—	≤7	—	Rings 1-3
CNS	≤450	-1 to 5	≤2	—	—	≤90	—
REOS	200-500	-5 to 5	0-5	0-10	—	—	—
Ro3 (fragment)	≤300	≤3	≤3	≤3	≤3	≤60	—
Golden Triangle	200-50*LogP+400	-2 to 5	—	—	—	—	—
Rule of Drug	Ro5 + Veber + no PAINS

Filter Selection by Discovery Stage

Stage	Recommended Filters	Rationale
Initial screening	Ro5, PAINS, Common Alerts	Broad triage, remove obvious liabilities
Hit-to-lead	Oprea or Leadlike Soft, NIBR, Lilly	Lead-like space, industrial filters
Lead optimization	Rule of Drug, Leadlike Strict, Complexity	Strict drug-likeness + synthetic feasibility
CNS targets	Rule of CNS, TPSA ≤90, HBD ≤2	BBB permeability requirements
Fragment-based	Ro3, low complexity (≤250)	Fragments have "room to grow"

Rules Are Guidelines, Not Absolutes

~10% of marketed drugs violate Ro5. Exceptions are common for natural products, antibiotics, PROTACs, and prodrugs. Always combine rule-based filtering with domain expertise and target-class knowledge. Different modalities (oral, IV, topical) and target classes (kinases, GPCRs, ion channels) have distinct optimal property spaces.

Common Workflows

Workflow 1: Compound Library Triage

Full pipeline from raw SMILES to filtered drug-like candidates.

import pandas as pd
import datamol as dm
import medchem as mc

# Load compound library
df = pd.read_csv("compounds.csv")
mols = [dm.to_mol(s) for s in df["smiles"]]
print(f"Input: {len(mols)} molecules")

# Step 1: Drug-likeness rules
rfilter = mc.rules.RuleFilters(rule_list=["rule_of_five", "rule_of_veber"])
rule_results = rfilter(mols=mols, n_jobs=-1, progress=True)

# Step 2: Structural alerts
alert_filter = mc.structural.CommonAlertsFilters()
alert_results = alert_filter(mols=mols, n_jobs=-1, progress=True)

# Step 3: Combine results
df["passes_rules"] = [all(r.values()) for r in rule_results]
df["has_alerts"] = [r["has_alerts"] for r in alert_results]
df["drug_like"] = df["passes_rules"] & ~df["has_alerts"]

filtered = df[df["drug_like"]]
print(f"Output: {len(filtered)} drug-like molecules ({len(filtered)/len(df)*100:.1f}%)")
filtered.to_csv("filtered_compounds.csv", index=False)

Workflow 2: Lead Optimization Filter Cascade

Apply progressively stricter filters with detailed reporting.

import datamol as dm
import medchem as mc
import pandas as pd

mols = [dm.to_mol(s) for s in smiles_list]

# Cascade: rules → structural alerts → complexity → Lilly demerits
filters = [
    ("Leadlike Strict", mc.rules.RuleFilters(rule_list=["rule_of_leadlike_strict"])),
    ("NIBR Alerts", mc.structural.NIBRFilters()),
    ("Complexity ≤400", mc.complexity.ComplexityFilter(max_complexity=400)),
    ("Lilly Demerits", mc.structural.LillyDemeritsFilters()),
]

surviving = list(range(len(mols)))
for name, filt in filters:
    results = filt(mols=[mols[i] for i in surviving], n_jobs=-1)
    # Handle different result formats
    if isinstance(results[0], dict):
        passed = [i for i, r in zip(surviving, results)
                  if r.get("passes", not r.get("has_alerts", True))]
    else:
        passed = [i for i, r in zip(surviving, results) if r]
    print(f"{name}: {len(surviving)} → {len(passed)}")
    surviving = passed

()

Key Parameters

Parameter	Module	Default	Range	Effect
rule_list	RuleFilters	—	See rules table	Which drug-likeness rules to apply
n_jobs	All filters	1	-1 to N	Parallel workers (-1 = all cores)
progress	All filters	False	bool	Show progress bar
max_complexity	ComplexityFilter	—	0-1000+	Bertz complexity threshold
method	calculate_complexity	"bertz"	bertz/whitlock/barone	Complexity metric
mw_range	Constraints	None	tuple(float, float)	Molecular weight range (Da)
logp_range	Constraints	None	tuple(float, float)	LogP range
tpsa_max	Constraints	None	0-200+	Max topological polar surface area
groups	ChemicalGroup	—	list of names	Predefined chemical groups to detect
custom_smarts	ChemicalGroup	None	dict	Custom SMARTS patterns {name: SMARTS}

Best Practices

1. Start broad, then narrow: Apply permissive filters first (Ro5, PAINS), then progressively tighten (NIBR, Lilly, complexity) as the pipeline narrows the candidate set.

2. Always use parallelization: For libraries >1000 molecules, set n_jobs=-1 to use all CPU cores.

3. Combine rules with structural alerts: Rules check physicochemical properties; alerts check substructure patterns. Both are needed for robust triage.

4. Anti-pattern — blind filtering: Do not blindly reject everything that fails Ro5. Consider the target class and modality before filtering.

5. Anti-pattern — ignoring prodrugs: Prodrugs intentionally violate standard rules. Flag them as exceptions rather than filtering them out.

6. Document filtering decisions: Track which molecules were removed and why for reproducibility and regulatory compliance.

7. Validate with known actives: Run your filter cascade on known active compounds for your target to estimate false-positive rate.

Common Recipes

Recipe: DataFrame Integration

import pandas as pd
import datamol as dm
import medchem as mc

df = pd.read_csv("molecules.csv")
df["mol"] = df["smiles"].apply(dm.to_mol)

rfilter = mc.rules.RuleFilters(rule_list=["rule_of_five", "rule_of_cns"])
results = rfilter(mols=df["mol"].tolist(), n_jobs=-1)

df["passes_ro5"] = [r["rule_of_five"] for r in results]
df["passes_cns"] = [r["rule_of_cns"] for r in results]
filtered = df[df["passes_ro5"] & df["passes_cns"]]
print(f"CNS drug-like: {len(filtered)}")

Recipe: Combining with ML Scoring

import medchem as mc

# Rule-based pre-filter
rule_results = mc.rules.RuleFilters(rule_list=["rule_of_five"])(mols, n_jobs=-1)
filtered_mols = [mol for mol, r in zip(mols, rule_results) if r["rule_of_five"]]

# ML model scoring on filtered set (reduces compute cost)
ml_scores = ml_model.predict(filtered_mols)
candidates = [mol for mol, score in zip(filtered_mols, ml_scores) if score > 0.8]
print(f"ML-scored candidates: {len(candidates)}")

Recipe: Custom SMARTS Group Screening

import medchem as mc

# Define project-specific warheads for covalent inhibitor screening
custom_warheads = {
    "acrylamide": "[C;H1](=O)[CH]=[CH2]",
    "vinyl_sulfonamide": "[NH]S(=O)(=O)[CH]=[CH2]",
    "chloroacetamide": "ClCC(=O)N",
}

group = mc.groups.ChemicalGroup(groups=[], custom_smarts=custom_warheads)
has_warhead = group.has_match(mols)
warhead_mols = [mol for mol, match in zip(mols, has_warhead) if match]
print(f"Covalent warhead candidates: {len(warhead_mols)}")

Troubleshooting

Problem	Cause	Solution
None in molecule list	Invalid SMILES in input	Pre-filter: mols = [m for m in mols if m is not None]
All molecules fail Ro5	Library is fragment-like or PPI space	Use rule_of_three or rule_of_leadlike_soft instead
No PAINS alerts found	Molecules are simple/fragment-like	Expected — PAINS patterns target screening-hit-size molecules
Lilly demerits all >100	Highly functionalized molecules	Check individual patterns; consider raising threshold or using NIBR instead
Slow processing	Large library without parallelization	Set n_jobs=-1 for parallel execution
ImportError: medchem	Missing dependency	pip install medchem datamol (requires RDKit)
Query parse error	Invalid query syntax	Check operators: AND, OR, NOT, comparisons: <, >, ==
Inconsistent result formats	Different filter classes return different types	Check docs: RuleFilters → dict, NIBRFilters → bool, LillyDemeritsFilters → dict

Bundled Resources

references/rules_catalog.md

Complete catalog of all medicinal chemistry rules and structural alert filters with literature references, threshold criteria, chemical group patterns, custom SMARTS examples, and stage-specific filter selection guidelines. API function signatures were consolidated into Core API code blocks above.

Related Skills

• rdkit-cheminformatics — Low-level cheminformatics: SMILES/SDF parsing, descriptors, fingerprints, substructure search
• datamol-cheminformatics — High-level molecular manipulation: standardization, scaffolds, fragmentation, 3D conformers
• pubchem-compound-search — Database queries: retrieve compound properties and bioactivity data for validation

References

• Lipinski CA et al. Adv Drug Deliv Rev (1997) 23:3-25 — Rule of Five
• Veber DF et al. J Med Chem (2002) 45:2615-2623 — Veber rules
• Oprea TI et al. J Chem Inf Comput Sci (2001) 41:1308-1315 — Lead-likeness
• Baell JB & Holloway GA. J Med Chem (2010) 53:2719-2740 — PAINS filters
• Congreve M et al. Drug Discov Today (2003) 8:876-877 — Rule of Three
• Johnson TW et al. J Med Chem (2009) 52:5487-5500 — Golden Triangle
• Walters WP & Murcko MA. Adv Drug Deliv Rev (2002) 54:255-271 — REOS
• Official docs: https://medchem-docs.datamol.io/
• GitHub: https://github.com/datamol-io/medchem