---

name: compound-profile description: | Generate comprehensive compound profiles including structure, properties, bioactivity, and development status. Use for drug analysis, SAR studies, and competitive profiling.

Keywords: compound, drug, molecule, structure, SMILES, bioactivity, IC50 category: Compound Analysis tags: [compound, drug, structure, bioactivity, chembl] version: 1.0.0 author: Drug Discovery Team dependencies:

• chembl-database
• pubchem-database
• drugbank-database

---

Compound Profile Skill

Comprehensive compound analysis for drug discovery and medicinal chemistry.

Quick Start

Copy/compound erlotinib
/compound-profile CC1=CC=C(C=C1)CNC(=O)C1=NC=C(C=C1)N
Analyze osimertinib properties and bioactivity
Compare gefitinib, erlotinib, afatinib profiles

What's Included

Output Structure

Copy# Compound Profile: Erlotinib

## Executive Summary
Erlotinib is a first-generation EGFR TKI approved for NSCLC (2004).
Key characteristics: Oral bioavailability, good brain penetration,
resistance mutations limit long-term efficacy.

## Basic Information
| Field | Value |
|-------|-------|
| Name | Erlotinib |
| Brand Names | Tarceva |
| ChEMBL ID | CHEMBL880 |
| Type | Small molecule |
| Class | Kinase inhibitor |
| Status | Approved |
| Approval Year | 2004 |
| Company | Astellas (OSI) |
| Indications | NSCLC, pancreatic cancer |

## Structure & Properties
**SMILES:** `COc1cc2nc(Nc3ccc(Oc4ccc(O)cc4)cc3)nc2cc1OC`

| Property | Value | Rule of 5 Check |
|----------|-------|----------------|
| MW | 393.4 Da | ✓ (<500) |
| LogP | 3.1 | ✓ (<5) |
| HBD | 1 | ✓ (≤5) |
| HBA | 7 | ✓ (≤10) |
| TPSA | 76.3 Ų | ✓ (<140) |
| Rotatable Bonds | 6 | |

## Bioactivity

| Target | Type | Affinity | Units |
|--------|------|----------|-------|
| EGFR | IC50 | 0.5 | nM |
| ERBB2 | IC50 | 1200 | nM |
| LCK | IC50 | 5 | nM |

## Development History
| Year | Milestone |
|------|-----------|
| 2004 | FDA Approval (NSCLC) |
| 2005 | EMEA Approval |
| 2010 | Pancreatic cancer approval |
| 2011 | Generic launch (US) |

## Similar Compounds
| Compound | Similarity | Difference |
|----------|------------|------------|
| Gefitinib | 85% | Different core scaffold |
| Afatinib | 72% | Irreversible binder |
| Osimertinib | 68% | 3rd-gen, mutant-selective |
| Icotinib | 82% | China-approved analog |

## Safety Profile
**Common AEs:** Rash, diarrhea, fatigue, anorexia
**Boxed Warning:** Interstitial lung disease
**Contraindications:** Hypersensitivity to erlotinib

## Patent Status
| Patent | Number | Expiry |
|--------|---------|--------|
| Base patent | US5747498 | 2019 (expired) |
| Formulation | US6943129 | 2020 |
| Method of use | US6900221 | 2021 |

Examples

By Name

Copy/compound erlotinib
/compound-profile sotorasib

By Structure

Copy/compound "CC1=CC=C(C=C1)CNC(=O)C1=NC=C(C=C1)N"
/compound-profile SMILES

Comparison

CopyCompare compounds erlotinib, gefitinib, afatinib
Analyze bioactivity across EGFR inhibitors

Property Analysis

Copy/compound erlotinib --focus properties
Analyze drug-likeness of this compound
Check Lipinski rule of 5 violations

Running Scripts

Copy# Fetch compound by name
python scripts/fetch_compound_data.py erlotinib --output compound.json

# Fetch by SMILES
python scripts/fetch_compound_data.py --smiles "CC1=CC=C..." -o data.json

# Similarity search
python scripts/fetch_compound_data.py --similar CHEMBL880 --threshold 0.7

# Bioactivity summary
python scripts/fetch_compound_data.py erlotinib --bioactivity -o activity.json

# Structure search
python scripts/fetch_compound_data.py --scaffold quinazoline --limit 20

Requirements

Copypip install requests pandas rdkit

Additional Resources

• ChEMBL API Reference
• PubChem API
• Property Calculation

Best Practices

1. Use standard names: Generic names preferred over brand
2. Verify ChEMBL ID: Most reliable identifier
3. Check bioactivity: Cross-reference multiple sources
4. Analog analysis: Use similarity searches for SAR
5. Validate SMILES: Check structure validity

Common Pitfalls