Chem Nmr Predict

1H NMR Spectrum Prediction

When to Use This Skill

The agent should use this skill when:

• A SMILES string is known and the agent needs a predicted 1H NMR spectrum (ppm vs intensity) for that compound.
• The agent needs a signal list (chemical shifts, multiplicities, coupling constants, proton counts) for a compound.
• Reference spectra are needed for mixture deconvolution (called by the chem-nmr-analysis skill).
• The user wants to compare a predicted spectrum against an experimental one for structure confirmation.

When NOT to Use This Skill

• The user already has an experimental or digitized spectrum file — no prediction is needed; the agent should use the existing file directly.
• The user has a compound name but not a SMILES — the agent should first resolve the name to SMILES using the drug-db-pubchem skill, then call this skill.
• 13C NMR prediction — this skill predicts 1H NMR only. The NMRdb.org SPINUS endpoint does not support 13C.
• Polymers, organometallics, or molecules with >50 heavy atoms — the SPINUS neural network may not produce reliable predictions, and nmrsim QM simulation is limited to ~11 coupled spins per spin system.
• The user asks about reaction products or mixture composition — the agent should use chem-nmr-analysis instead, which calls this skill internally.

Workflow: SMILES → Predicted 1H NMR

Step 1 — Ensure SMILES Are Available

If the user provides compound names instead of SMILES, the agent should first resolve them:

${CLAUDE_SKILL_DIR}/../../venv/run cpu python ${CLAUDE_SKILL_DIR}/../drug-db-pubchem/scripts/query_pubchem.py \
  --name "camphor" --outdir <research_dir>/pubchem/

The agent should extract CanonicalSMILES from the JSON output.

If PubChem returns no results, the agent should try alternate names or ask the user to provide the SMILES directly.

Step 2 — Predict NMR Spectra

${CLAUDE_SKILL_DIR}/../../venv/run cpu python ${CLAUDE_SKILL_DIR}/scripts/predict_nmr.py \
  --smiles "<smiles_1>" "<smiles_2>" \
  --names "compound1" "compound2" \
  --field_mhz 400 \
  --output_dir <research_dir>/nmr_predictions/

Arguments:

• --smiles (required): one or more SMILES strings.
• --names: human-readable labels for filenames. If omitted, defaults to comp0, comp1, etc. The agent should always provide meaningful names.
• --field_mhz: spectrometer frequency in MHz (default: 400). The agent should match the field strength of the user's experimental spectrum if known.
• --linewidth: Lorentzian FWHM in Hz (default: 1.0). The agent should increase this (e.g., 2.0–5.0) if the user's experimental spectrum has broad lines.
• --n_points: spectrum resolution (default: 8192). The agent should not change this unless the user requests higher resolution.
• --output_dir: where to save results.

Outputs per compound:

• <name>.xy — two-column tab-separated file (ppm, intensity), descending ppm. Compatible with all NMR processing tools and the chem-nmr-analysis deconvolution scripts.
• <name>_signals.csv — signal table with columns: shift_ppm, multiplicity, J_Hz, nH.
• predictions.json — manifest listing all found/failed compounds and parameters.

Step 3 — Verify Predictions

After prediction, the agent must:

1. Check the manifest (predictions.json) for any failed compounds.
2. Read the signal table (_signals.csv) and verify it is chemically reasonable:
   • The total number of protons across all signals should match the molecular formula.
   • Chemical shifts should be in expected ranges (e.g., alkyl 0–2 ppm, aromatic 6–8 ppm, aldehyde 9–10 ppm).
3. If the user has an experimental spectrum, the agent should overlay them using chem-nmr-analysis's plot.py for visual comparison.

If SPINUS returns no atoms for a SMILES → the SMILES may be invalid, the molecule may lack hydrogen atoms (e.g., CCl4), or the molecule may be too complex. The agent should:

1. Verify the SMILES is valid (try parsing with RDKit).
2. Check if the molecule actually has hydrogen atoms.
3. If valid but SPINUS fails, inform the user that prediction is unavailable for this compound.

If nmrsim simulation fails → the script falls back to a stick spectrum (chemical shifts only, no multiplet structure). The agent should note this in its response — the predicted spectrum will lack splitting patterns but chemical shifts will still be approximate.