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Synkit

Skill Kdevos12/ALKYL/skills/synkit

Claude Plugin for CompChem , Drug Discovery & Organic Chemistry reasoning

Install
npx -y skills add Kdevos12/ALKYL --skill synkit

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Use when working with SynKit for graph-based reaction informatics: ITS/MTG graph construction, reaction canonicalization, AAM validation, DPO rule extraction and composition, chemical reaction network (CRN) analysis, subgraph matching, and synthesis planning primitives.

SKILL.md

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SynKit

Graph-based Python toolkit for reaction informatics: ITS graph construction, canonicalization, AAM validation, DPO rule extraction, CRN analysis, and synthesis planning.

Paper: doi:10.1021/acs.jcim.5c02123 | JCIM 2025

When to Use This Skill

  • Converting reaction SMILES → ITS graphs (NetworkX) → DPO rules (GML)
  • Validating or comparing atom-to-atom mappings (AAMValidator)
  • Canonicalizing reaction SMILES (CanonRSMI) or ITS graphs (GraphCanonicaliser)
  • Clustering reactions by structural similarity (WL graph hash)
  • Extracting and composing reaction rules (DPO formalism)
  • Analyzing chemical reaction networks (Feinberg deficiency theory, Petri nets)
  • Detecting autocatalysis, siphons, traps in reaction networks
  • Planning synthetic routes via rule composition (SynReactor)
  • Building reaction databases or curating USPTO/ChEMBL reaction data

Core Concept: ITS Graph

The Imaginary Transition State (ITS) graph merges reactant and product graphs into a single labeled multigraph:

  • Nodes: atoms with attributes (symbol, charge, radical, hybridization, H count)
  • Edges: bonds with attributes (bond type, change flag: formed / broken / unchanged)

ITS ≡ CGR (Condensed Graph of Reaction) — same structure, different naming tradition.

Quick Start

from synkit.IO import load_reaction_smiles
from synkit.Graph import ITSConstruction
from synkit.Chem import CanonRSMI, AAMValidator

# 1. Parse reaction SMILES → ITS graph (NetworkX)
rxn_smiles = "[CH3:1][OH:2].[Na:3][H:4]>>[CH3:1][O:2][Na:3].[H:4][H:5]"
its = ITSConstruction.from_reaction_smiles(rxn_smiles)

# 2. Canonicalize the reaction SMILES
canon = CanonRSMI(rxn_smiles).canonicalize()

# 3. Validate atom-atom mapping
valid = AAMValidator(rxn_smiles).is_valid()

Router — What to Read

TaskReference
Load reactions, format conversion (SMILES ↔ ITS ↔ GML), data I/Oreferences/io-conversion.md
Canonicalization (CanonRSMI), AAM validation, Reaction classreferences/chem-standardization.md
ITS construction, MTG, graph canonicalization, WL hashing, subgraph searchreferences/graph-its.md
DPO rules, GML format, rule composition, SynReactor forward/retroreferences/rule-dpo.md
CRN building, Feinberg deficiency theory, Petri nets, autocatalysisreferences/crn-analysis.md
Synthesis planning, route construction, pathway analysisreferences/synthesis-planning.md

Key Submodules

ModuleRole
synkit.IOReaction SMILES parsing, SMILES ↔ ITS ↔ GML conversion
synkit.ChemCanonRSMI, AAMValidator, Reaction standardization
synkit.GraphITSConstruction, GraphCanonicaliser, WL hash, subgraph search
synkit.RuleDPO rules, GML handling, rule composition
synkit.SynthesisForward/retro prediction, route exploration
synkit.CRNCRN construction, Feinberg theory, Petri-net analysis
synkit.VisReaction and mechanism visualization

Conversion Pipeline

Reaction SMILES (atom-mapped)
    │
    ▼ IO / Graph.ITSConstruction
ITS Graph (NetworkX)         ← cluster, hash, validate
    │
    ▼ Graph.GraphCanonicaliser
Canonical ITS Graph          ← canonical form independent of atom ordering
    │
    ▼ Rule module
DPO Rule (GML format)        ← compose, apply, store

All conversions are lossless for balanced, atom-mapped reactions. Caveats: stereochemistry is omitted; explicit H at reaction centers required for GML → SMILES reversion.

Installation

pip install synkit          # core (RDKit + NetworkX)
pip install synkit[all]     # full (+ transformers for RXNMapper)
# Python ≥ 3.11 required

Related Skills

  • rdkit — molecule preprocessing before SynKit ingestion
  • torchdrug — retrosynthesis with GNNs (complementary ML approach)
  • deepchem — molecular ML when rule-based approach insufficient

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