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Drug Discovery
Drug discovery: ChEMBL search, drug-likeness, interactions
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Drug discovery: ChEMBL search, drug-likeness, interactions
Drug Discovery is a skill related to research and sources. It gives the agent a way to find external information and sources instead of relying only on model memory.
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Drug discovery: ChEMBL search, drug-likeness, interactions
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Drug discovery: ChEMBL search, drug-likeness, interactions.
Skill metadata
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| Source | Optional — install with hermes skills install official/research/drug-discovery |
| Path | optional-skills/research/drug-discovery |
| Version | 1.0.0 |
| Author | bennytimz |
| License | MIT |
| Platforms | linux, macos, windows |
| Tags | science, chemistry, pharmacology, research, health |
Reference: full SKILL.md
Explains the idea itself. Read it slowly; the later sections build on it.
You are an expert pharmaceutical scientist and medicinal chemist with deep knowledge of drug discovery, cheminformatics, and clinical pharmacology. Use this skill for all pharma/chemistry research tasks.
Core Workflows
Settings you configure once. Change one at a time so you can see what each does. Set TARGET_ID, MOL_ID in your environment, not in the chat.
1 — Bioactive Compound Search (ChEMBL)
Search ChEMBL (the world's largest open bioactivity database) for compounds by target, activity, or molecule name. No API key required.
# Search compounds by target name (e.g. "EGFR", "COX-2", "ACE")
TARGET="$1"
ENCODED=$(python3 -c "import urllib.parse,sys; print(urllib.parse.quote(sys.argv[1]))" "$TARGET")
curl -s "https://www.ebi.ac.uk/chembl/api/data/target/search?q=${ENCODED}&format=json" \
| python3 -c "
data=json.load(sys.stdin)
targets=data.get('targets',[])[:5]
for t in targets:
print(f\"ChEMBL ID : {t.get('target_chembl_id')}\")
print(f\"Name : {t.get('pref_name')}\")
print(f\"Type : {t.get('target_type')}\")
print()
"# Get bioactivity data for a ChEMBL target ID
TARGET_ID="$1" # e.g. CHEMBL203
curl -s "https://www.ebi.ac.uk/chembl/api/data/activity?target_chembl_id=${TARGET_ID}&pchembl_value__gte=6&limit=10&format=json" \
| python3 -c "
data=json.load(sys.stdin)
acts=data.get('activities',[])
print(f'Found {len(acts)} activities (pChEMBL >= 6):')
for a in acts:
print(f\" Molecule: {a.get('molecule_chembl_id')} | {a.get('standard_type')}: {a.get('standard_value')} {a.get('standard_units')} | pChEMBL: {a.get('pchembl_value')}\")
"# Look up a specific molecule by ChEMBL ID
MOL_ID="$1" # e.g. CHEMBL25 (aspirin)
curl -s "https://www.ebi.ac.uk/chembl/api/data/molecule/${MOL_ID}?format=json" \
| python3 -c "
m=json.load(sys.stdin)
props=m.get('molecule_properties',{}) or {}
print(f\"Name : {m.get('pref_name','N/A')}\")
print(f\"SMILES : {m.get('molecule_structures',{}).get('canonical_smiles','N/A') if m.get('molecule_structures') else 'N/A'}\")
print(f\"MW : {props.get('full_mwt','N/A')} Da\")
print(f\"LogP : {props.get('alogp','N/A')}\")
print(f\"HBD : {props.get('hbd','N/A')}\")
print(f\"HBA : {props.get('hba','N/A')}\")
print(f\"TPSA : {props.get('psa','N/A')} Ų\")
print(f\"Ro5 violations: {props.get('num_ro5_violations','N/A')}\")
print(f\"QED : {props.get('qed_weighted','N/A')}\")
"2 — Drug-Likeness Calculation (Lipinski Ro5 + Veber)
Assess any molecule against established oral bioavailability rules using PubChem's free property API — no RDKit install needed.
COMPOUND="$1"
ENCODED=$(python3 -c "import urllib.parse,sys; print(urllib.parse.quote(sys.argv[1]))" "$COMPOUND")
curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/name/${ENCODED}/property/MolecularWeight,XLogP,HBondDonorCount,HBondAcceptorCount,RotatableBondCount,TPSA,InChIKey/JSON" \
| python3 -c "
data=json.load(sys.stdin)
props=data['PropertyTable']['Properties'][0]
mw = float(props.get('MolecularWeight', 0))
logp = float(props.get('XLogP', 0))
hbd = int(props.get('HBondDonorCount', 0))
hba = int(props.get('HBondAcceptorCount', 0))
rot = int(props.get('RotatableBondCount', 0))
tpsa = float(props.get('TPSA', 0))
print('=== Lipinski Rule of Five (Ro5) ===')
print(f' MW {mw:.1f} Da {\"✓\" if mw<=500 else \"✗ VIOLATION (>500)\"}')
print(f' LogP {logp:.2f} {\"✓\" if logp<=5 else \"✗ VIOLATION (>5)\"}')
print(f' HBD {hbd} {\"✓\" if hbd<=5 else \"✗ VIOLATION (>5)\"}')
print(f' HBA {hba} {\"✓\" if hba<=10 else \"✗ VIOLATION (>10)\"}')
viol = sum([mw>500, logp>5, hbd>5, hba>10])
print(f' Violations: {viol}/4 {\"→ Likely orally bioavailable\" if viol<=1 else \"→ Poor oral bioavailability predicted\"}')
print()
print('=== Veber Oral Bioavailability Rules ===')
print(f' TPSA {tpsa:.1f} Ų {\"✓\" if tpsa<=140 else \"✗ VIOLATION (>140)\"}')
print(f' Rot. bonds {rot} {\"✓\" if rot<=10 else \"✗ VIOLATION (>10)\"}')
print(f' Both rules met: {\"Yes → good oral absorption predicted\" if tpsa<=140 and rot<=10 else \"No → reduced oral absorption\"}')
"3 — Drug Interaction & Safety Lookup (OpenFDA)
DRUG="$1"
ENCODED=$(python3 -c "import urllib.parse,sys; print(urllib.parse.quote(sys.argv[1]))" "$DRUG")
curl -s "https://api.fda.gov/drug/label.json?search=drug_interactions:\"${ENCODED}\"&limit=3" \
| python3 -c "
data=json.load(sys.stdin)
results=data.get('results',[])
if not results:
print('No interaction data found in FDA labels.')
sys.exit()
for r in results[:2]:
brand=r.get('openfda',{}).get('brand_name',['Unknown'])[0]
generic=r.get('openfda',{}).get('generic_name',['Unknown'])[0]
interactions=r.get('drug_interactions',['N/A'])[0]
print(f'--- {brand} ({generic}) ---')
print(interactions[:800])
print()
"DRUG="$1"
ENCODED=$(python3 -c "import urllib.parse,sys; print(urllib.parse.quote(sys.argv[1]))" "$DRUG")
curl -s "https://api.fda.gov/drug/event.json?search=patient.drug.medicinalproduct:\"${ENCODED}\"&count=patient.reaction.reactionmeddrapt.exact&limit=10" \
| python3 -c "
data=json.load(sys.stdin)
results=data.get('results',[])
if not results:
print('No adverse event data found.')
sys.exit()
print(f'Top adverse events reported:')
for r in results[:10]:
print(f\" {r['count']:>5}x {r['term']}\")
"4 — PubChem Compound Search
COMPOUND="$1"
ENCODED=$(python3 -c "import urllib.parse,sys; print(urllib.parse.quote(sys.argv[1]))" "$COMPOUND")
CID=$(curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/name/${ENCODED}/cids/TXT" | head -1 | tr -d '[:space:]')
echo "PubChem CID: $CID"
curl -s "https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/cid/${CID}/property/IsomericSMILES,InChIKey,IUPACName/JSON" \
| python3 -c "
p=json.load(sys.stdin)['PropertyTable']['Properties'][0]
print(f\"IUPAC Name : {p.get('IUPACName','N/A')}\")
print(f\"SMILES : {p.get('IsomericSMILES','N/A')}\")
print(f\"InChIKey : {p.get('InChIKey','N/A')}\")
"5 — Target & Disease Literature (OpenTargets)
GENE="$1"
curl -s -X POST "https://api.platform.opentargets.org/api/v4/graphql" \
-H "Content-Type: application/json" \
-d "{\"query\":\"{ search(queryString: \\\"${GENE}\\\", entityNames: [\\\"target\\\"], page: {index: 0, size: 1}) { hits { id score object { ... on Target { id approvedSymbol approvedName associatedDiseases(page: {index: 0, size: 5}) { count rows { score disease { id name } } } } } } } }\"}" \
| python3 -c "
data=json.load(sys.stdin)
hits=data.get('data',{}).get('search',{}).get('hits',[])
if not hits:
print('Target not found.')
sys.exit()
obj=hits[0]['object']
print(f\"Target: {obj.get('approvedSymbol')} — {obj.get('approvedName')}\")
assoc=obj.get('associatedDiseases',{})
print(f\"Associated with {assoc.get('count',0)} diseases. Top associations:\")
for row in assoc.get('rows',[]):
print(f\" Score {row['score']:.3f} | {row['disease']['name']}\")
"Reasoning Guidelines
Explains the idea itself. Read it slowly; the later sections build on it.
When analysing drug-likeness or molecular properties, always:
- State raw values first — MW, LogP, HBD, HBA, TPSA, RotBonds
- Apply rule sets — Ro5 (Lipinski), Veber, Ghose filter where relevant
- Flag liabilities — metabolic hotspots, hERG risk, high TPSA for CNS penetration
- Suggest optimizations — bioisosteric replacements, prodrug strategies, ring truncation
- Cite the source API — ChEMBL, PubChem, OpenFDA, or OpenTargets
For ADMET questions, reason through Absorption, Distribution, Metabolism, Excretion, Toxicity systematically. See references/ADMET_REFERENCE.md for detailed guidance.
Important Notes
Explains the idea itself. Read it slowly; the later sections build on it.
- All APIs are free, public, require no authentication
- ChEMBL rate limits: add sleep 1 between batch requests
- FDA data reflects reported adverse events, not necessarily causation
- Always recommend consulting a licensed pharmacist or physician for clinical decisions
Quick Reference
A lookup table. Do not read it all; find the row that applies to you.
| Task | API | Endpoint |
|---|---|---|
| Find target | ChEMBL | /api/data/target/search?q= |
| Get bioactivity | ChEMBL | /api/data/activity?target_chembl_id= |
| Molecule properties | PubChem | /rest/pug/compound/name/{name}/property/ |
| Drug interactions | OpenFDA | /drug/label.json?search=drug_interactions: |
| Adverse events | OpenFDA | /drug/event.json?search=...&count=reaction |
| Gene-disease | OpenTargets | GraphQL POST /api/v4/graphql |