chore(validation-output): add gt3 fragment export

Track refreshed validation outputs and add a filtered fragment
library export that retains only side-chain fragments with more
than 3 heavy atoms.

.gitignore

@@ -68,3 +68,4 @@ data/
 output/
 site/
 # docs/ source files should be tracked, only ignore generated site/
+validation_output/

README.md

@@ -62,6 +62,96 @@ pixi run macro-lactone-toolkit fragment \
 
 默认读取 `smiles` 列；若存在 `id` 列则将其作为 `parent_id`，否则自动生成 `row_<index>`。
 
+## MacrolactoneDB 验证模块
+
+用于对 MacrolactoneDB 数据库进行抽样验证、分类、侧链断裂和数据库存储。
+
+### 验证脚本使用
+
+```bash
+# 基本使用（10% 分层抽样）
+pixi run python scripts/validate_macrolactone_db.py \
+  --input data/MacrolactoneDB/ring12_20/temp.csv \
+  --output validation_output \
+  --sample-ratio 0.1
+
+# 处理全量数据
+pixi run python scripts/validate_macrolactone_db.py \
+  --input data/MacrolactoneDB/ring12_20/temp.csv \
+  --output validation_output \
+  --sample-ratio 1.0
+
+# 指定列名（如果 CSV 列名不同）
+pixi run python scripts/validate_macrolactone_db.py \
+  --input data.csv \
+  --output validation_output \
+  --id-col ml_id \
+  --chembl-id-col IDs \
+  --smiles-col smiles
+```
+
+### 输出结构
+
+```
+validation_output/
+├── README.md                    # 目录说明
+├── fragments.db                 # SQLite 数据库
+├── fragment_library.csv         # 最终片段库导出（含 has_dummy_atom / splice_ready）
+├── summary.csv                  # 汇总表（含 ml_id, chembl_id）
+├── summary_statistics.json      # 统计信息
+├── ring_size_12/                # 按环大小组织
+├── ring_size_13/
+...
+└── ring_size_20/
+    ├── standard/
+    │   ├── numbered/            # 带编号的环图（文件名使用 ml_id）
+    │   │   └── {ml_id}_numbered.png
+    │   └── sidechains/          # 片段图
+    │       └── {ml_id}/
+    │           └── {ml_id}_frag_{n}_pos{pos}.png
+    ├── non_standard/original/
+    └── rejected/original/
+```
+
+### 数据库查询示例
+
+```bash
+# 查看表结构
+sqlite3 validation_output/fragments.db ".tables"
+
+# 查询标准大环内酯
+sqlite3 validation_output/fragments.db \
+  "SELECT ml_id, chembl_id, ring_size, num_sidechains \
+   FROM parent_molecules \
+   WHERE classification='standard_macrolactone' LIMIT 5;"
+
+# 查询最终片段库
+sqlite3 validation_output/fragments.db \
+  "SELECT source_type, source_parent_ml_id, cleavage_position, has_dummy_atom, splice_ready \
+   FROM fragment_library_entries LIMIT 10;"
+
+# 查询片段
+sqlite3 validation_output/fragments.db \
+  "SELECT fragment_id, cleavage_position, dummy_isotope, has_dummy_atom, dummy_atom_count \
+   FROM side_chain_fragments LIMIT 10;"
+
+# 按环大小统计
+sqlite3 validation_output/fragments.db \
+  "SELECT ring_size, COUNT(*) FROM parent_molecules GROUP BY ring_size;"
+```
+
+### 关键字段说明
+
+| 字段 | 说明 |
+|------|------|
+| `ml_id` | MacrolactoneDB 唯一 ID（如 ML00000001），用于文件命名 |
+| `chembl_id` | 原始 CHEMBL ID（如 CHEMBL94657），可能为空 |
+| `classification` | standard_macrolactone / non_standard_macrocycle / not_macrolactone |
+| `dummy_isotope` | 裂解位置编号，用于片段重建 |
+| `cleavage_position` | 环上的断裂位置 |
+| `has_dummy_atom` | 该片段是否带 dummy 原子，可用于区分可直接拼接片段 |
+| `splice_ready` | 是否与当前单锚点拼接流程直接兼容 |
+
 ## Legacy Scripts
 
 `scripts/` 目录保留为薄封装或迁移提示，不再承载核心实现。正式接口以 `macro_lactone_toolkit.*` 与 `macro-lactone-toolkit` CLI 为准。

scripts/validate_macrolactone_db.py

@@ -50,8 +50,14 @@ def main():
     parser.add_argument(
         "--id-col",
         type=str,
+        default="ml_id",
+        help="ID column name (default: ml_id)",
+    )
+    parser.add_argument(
+        "--chembl-id-col",
+        type=str,
         default="IDs",
-        help="ID column name",
+        help="CHEMBL ID column name (default: IDs)",
     )
 
     args = parser.parse_args()
@@ -69,6 +75,7 @@ def main():
         sample_ratio=args.sample_ratio,
         smiles_col=args.smiles_col,
         id_col=args.id_col,
+        chembl_id_col=args.chembl_id_col,
     )
 
     results = validator.run(args.input)

src/macro_lactone_toolkit/_core.py

@@ -272,6 +272,44 @@ def collect_side_chain_atoms(
     return side_chain_atoms
 
 
+def find_side_chain_ring_connections(
+    mol: Chem.Mol,
+    side_chain_atoms: Iterable[int],
+    ring_atom_indices: Iterable[int],
+) -> list[tuple[int, int]]:
+    ring_atom_set = set(ring_atom_indices)
+    connections: set[tuple[int, int]] = set()
+
+    for atom_idx in side_chain_atoms:
+        atom = mol.GetAtomWithIdx(atom_idx)
+        for neighbor in atom.GetNeighbors():
+            neighbor_idx = neighbor.GetIdx()
+            if neighbor_idx in ring_atom_set:
+                connections.add((atom_idx, neighbor_idx))
+
+    return sorted(connections, key=lambda connection: (connection[1], connection[0]))
+
+
+def collect_fragmentable_side_chain_atoms(
+    mol: Chem.Mol,
+    start_atom_idx: int,
+    ring_atom_indices: Iterable[int],
+    ring_atom_idx: int | None = None,
+) -> list[int] | None:
+    side_chain_atoms = collect_side_chain_atoms(mol, start_atom_idx, ring_atom_indices)
+    if not side_chain_atoms:
+        return None
+
+    ring_connections = find_side_chain_ring_connections(mol, side_chain_atoms, ring_atom_indices)
+    if len(ring_connections) != 1:
+        return None
+
+    if ring_atom_idx is not None and ring_connections[0][1] != ring_atom_idx:
+        return None
+
+    return side_chain_atoms
+
+
 def is_intrinsic_lactone_neighbor(
     mol: Chem.Mol,
     candidate: DetectedMacrolactone,

src/macro_lactone_toolkit/fragmenter.py

@@ -6,7 +6,7 @@ from rdkit.Chem import Descriptors
 from ._core import (
     build_fragment_smiles,
     build_numbering_result,
-    collect_side_chain_atoms,
+    collect_fragmentable_side_chain_atoms,
     ensure_mol,
     find_macrolactone_candidates,
     is_intrinsic_lactone_neighbor,
@@ -44,6 +44,8 @@ class MacrolactoneFragmenter:
         fragments: list[SideChainFragment] = []
 
         for position, ring_atom_idx in numbering.position_to_atom.items():
+            if int(position) <= 2:
+                continue
             ring_atom = mol.GetAtomWithIdx(ring_atom_idx)
             for neighbor in ring_atom.GetNeighbors():
                 neighbor_idx = neighbor.GetIdx()
@@ -52,8 +54,13 @@ class MacrolactoneFragmenter:
                 if is_intrinsic_lactone_neighbor(mol, candidate, ring_atom_idx, neighbor_idx):
                     continue
 
-                side_chain_atoms = collect_side_chain_atoms(mol, neighbor_idx, ring_atom_set)
+                side_chain_atoms = collect_fragmentable_side_chain_atoms(
-                if not side_chain_atoms:
+                    mol=mol,
+                    start_atom_idx=neighbor_idx,
+                    ring_atom_indices=ring_atom_set,
+                    ring_atom_idx=ring_atom_idx,
+                )
+                if side_chain_atoms is None:
                     continue
 
                 try:

src/macro_lactone_toolkit/splicing/scaffold_prep.py

@@ -4,7 +4,7 @@ from typing import Iterable
 
 from rdkit import Chem
 
-from .._core import collect_side_chain_atoms, ensure_mol, find_macrolactone_candidates, is_intrinsic_lactone_neighbor
+from .._core import collect_fragmentable_side_chain_atoms, ensure_mol, find_macrolactone_candidates, is_intrinsic_lactone_neighbor
 from ..fragmenter import MacrolactoneFragmenter
 
 
@@ -26,22 +26,36 @@ def prepare_macrolactone_scaffold(
     for position in positions:
         if position not in numbering.position_to_atom:
             raise ValueError(f"Position {position} not found in ring numbering.")
+        if position <= 2:
+            raise ValueError(f"Position {position} does not contain a single-anchor fragmentable side chain")
         ring_atom_idx = numbering.position_to_atom[position]
         ring_atom = mol.GetAtomWithIdx(ring_atom_idx)
+        position_dummy_specs: list[tuple[int, int, Chem.BondType]] = []
+
         for neighbor in ring_atom.GetNeighbors():
             neighbor_idx = neighbor.GetIdx()
             if neighbor_idx in ring_atom_set:
                 continue
             if is_intrinsic_lactone_neighbor(mol, candidate, ring_atom_idx, neighbor_idx):
                 continue
-            side_chain_atoms = collect_side_chain_atoms(mol, neighbor_idx, ring_atom_set)
+            side_chain_atoms = collect_fragmentable_side_chain_atoms(
+                mol=mol,
+                start_atom_idx=neighbor_idx,
+                ring_atom_indices=ring_atom_set,
+                ring_atom_idx=ring_atom_idx,
+            )
+            if side_chain_atoms is None:
+                continue
             atoms_to_remove.update(side_chain_atoms)
             bond = mol.GetBondBetweenAtoms(ring_atom_idx, neighbor_idx)
             if bond is not None:
-                dummy_specs.append((ring_atom_idx, position, bond.GetBondType()))
+                position_dummy_specs.append((ring_atom_idx, position, bond.GetBondType()))
 
-        if not any(spec_position == position for _, spec_position, _ in dummy_specs):
+        if not position_dummy_specs:
-            dummy_specs.append((ring_atom_idx, position, Chem.BondType.SINGLE))
+            raise ValueError(f"Position {position} does not contain a single-anchor fragmentable side chain")
+        if len(position_dummy_specs) > 1:
+            raise ValueError(f"Position {position} contains multiple fragmentable side chains")
+        dummy_specs.extend(position_dummy_specs)
 
     rwmol = Chem.RWMol(mol)
     for ring_atom_idx, position, bond_type in dummy_specs:

src/macro_lactone_toolkit/validation/models.py

@@ -1,6 +1,6 @@
 from __future__ import annotations
 
-from datetime import datetime
+from datetime import UTC, datetime
 from typing import List, Optional
 
 from sqlalchemy.orm import Mapped, mapped_column, relationship
@@ -27,7 +27,8 @@ class ParentMolecule(SQLModel, table=True):
     __tablename__ = "parent_molecules"
 
     id: Optional[int] = Field(default=None, primary_key=True)
-    source_id: str = Field(index=True)
+    ml_id: str = Field(index=True)  # MacrolactoneDB unique ID (e.g., ML00000001)
+    chembl_id: Optional[str] = Field(default=None, index=True)  # Original CHEMBL ID
     molecule_name: Optional[str] = None
     smiles: str = Field(index=True)
     classification: str = Field(index=True)
@@ -39,7 +40,7 @@ class ParentMolecule(SQLModel, table=True):
     num_sidechains: Optional[int] = None
     cleavage_positions: Optional[str] = None
     numbered_image_path: Optional[str] = None
-    created_at: datetime = Field(default_factory=datetime.utcnow)
+    created_at: datetime = Field(default_factory=lambda: datetime.now(UTC))
     processed_at: Optional[datetime] = None
 
 
@@ -71,6 +72,8 @@ class SideChainFragment(SQLModel, table=True):
     fragment_smiles_labeled: str
     fragment_smiles_plain: str
     dummy_isotope: int
+    has_dummy_atom: bool = Field(default=True)
+    dummy_atom_count: int = Field(default=1)
     atom_count: int
     heavy_atom_count: int
     molecular_weight: float
@@ -78,6 +81,26 @@ class SideChainFragment(SQLModel, table=True):
     image_path: Optional[str] = None
 
 
+class FragmentLibraryEntry(SQLModel, table=True):
+    """Unified fragment library entries."""
+
+    __tablename__ = "fragment_library_entries"
+
+    id: Optional[int] = Field(default=None, primary_key=True)
+    source_type: str = Field(index=True)
+    source_fragment_id: Optional[str] = Field(default=None, index=True)
+    source_parent_ml_id: Optional[str] = Field(default=None, index=True)
+    source_parent_chembl_id: Optional[str] = Field(default=None, index=True)
+    cleavage_position: Optional[int] = Field(default=None, index=True)
+    fragment_smiles_labeled: Optional[str] = None
+    fragment_smiles_plain: str
+    has_dummy_atom: bool = Field(default=False)
+    dummy_atom_count: int = Field(default=0)
+    splice_ready: bool = Field(default=False, index=True)
+    original_bond_type: Optional[str] = None
+    created_at: datetime = Field(default_factory=lambda: datetime.now(UTC))
+
+
 class ValidationResult(SQLModel, table=True):
     """Manual validation records."""
 

src/macro_lactone_toolkit/validation/validator.py

@@ -1,7 +1,7 @@
 from __future__ import annotations
 
 import json
-from datetime import datetime
+from datetime import UTC, datetime
 from pathlib import Path
 
 import pandas as pd
@@ -12,7 +12,7 @@ from sqlmodel import select
 from macro_lactone_toolkit import MacroLactoneAnalyzer
 from macro_lactone_toolkit._core import (
     build_numbering_result,
-    collect_side_chain_atoms,
+    collect_fragmentable_side_chain_atoms,
     find_macrolactone_candidates,
     is_intrinsic_lactone_neighbor,
 )
@@ -20,6 +20,7 @@ from macro_lactone_toolkit.validation.database import get_engine, get_session, i
 from macro_lactone_toolkit.validation.isotope_utils import build_fragment_with_isotope
 from macro_lactone_toolkit.validation.models import (
     ClassificationType,
+    FragmentLibraryEntry,
     ParentMolecule,
     ProcessingStatus,
     RingNumbering,
@@ -41,12 +42,14 @@ class MacrolactoneValidator:
         output_dir: str | Path,
         sample_ratio: float = 0.1,
         smiles_col: str = "smiles",
-        id_col: str = "IDs",
+        id_col: str = "ml_id",
+        chembl_id_col: str = "IDs",
     ):
         self.output_dir = Path(output_dir)
         self.sample_ratio = sample_ratio
         self.smiles_col = smiles_col
         self.id_col = id_col
+        self.chembl_id_col = chembl_id_col
 
         self.analyzer = MacroLactoneAnalyzer()
 
@@ -78,12 +81,14 @@ class MacrolactoneValidator:
         # Generate outputs
         self._generate_readme()
         self._generate_summary()
+        self._generate_fragment_library()
 
         return results
 
     def _process_molecule(self, row: pd.Series) -> str:
         """Process a single molecule. Returns status."""
-        source_id = str(row[self.id_col])
+        ml_id = str(row[self.id_col])
+        chembl_id = str(row[self.chembl_id_col]) if self.chembl_id_col in row and pd.notna(row[self.chembl_id_col]) else None
         smiles = row[self.smiles_col]
         name = row.get("molecule_pref_name", None)
 
@@ -105,7 +110,8 @@ class MacrolactoneValidator:
 
         # Create parent record
         parent = ParentMolecule(
-            source_id=source_id,
+            ml_id=ml_id,
+            chembl_id=chembl_id,
             molecule_name=name,
             smiles=smiles,
             classification=classification,
@@ -124,7 +130,7 @@ class MacrolactoneValidator:
                 parent.processing_status = ProcessingStatus.SKIPPED
                 session.add(parent)
                 session.commit()
-                self._save_original_image(smiles, source_id, ring_size, classification)
+                self._save_original_image(smiles, ml_id, ring_size, classification)
                 return "skipped"
 
             # Process standard macrolactone
@@ -134,7 +140,7 @@ class MacrolactoneValidator:
             except Exception as e:
                 parent.processing_status = ProcessingStatus.FAILED
                 parent.error_message = str(e)
-                parent.processed_at = datetime.utcnow()
+                parent.processed_at = datetime.now(UTC)
                 session.add(parent)
                 session.commit()
                 return "failed"
@@ -172,7 +178,7 @@ class MacrolactoneValidator:
 
         # Save numbered image
         paths = get_output_paths(
-            self.output_dir, parent.source_id, parent.ring_size, "standard_macrolactone"
+            self.output_dir, parent.ml_id, parent.ring_size, "standard_macrolactone"
         )
         image_path = save_numbered_molecule(smiles, paths["numbered_image"], parent.ring_size)
         if image_path:
@@ -184,6 +190,8 @@ class MacrolactoneValidator:
         fragment_idx = 0
 
         for position, ring_atom_idx in numbering.position_to_atom.items():
+            if int(position) <= 2:
+                continue
             ring_atom = mol.GetAtomWithIdx(ring_atom_idx)
 
             for neighbor in ring_atom.GetNeighbors():
@@ -196,8 +204,13 @@ class MacrolactoneValidator:
                     continue
 
                 # Collect side chain atoms
-                side_chain_atoms = collect_side_chain_atoms(mol, neighbor_idx, ring_atom_set)
+                side_chain_atoms = collect_fragmentable_side_chain_atoms(
-                if not side_chain_atoms:
+                    mol=mol,
+                    start_atom_idx=neighbor_idx,
+                    ring_atom_indices=ring_atom_set,
+                    ring_atom_idx=ring_atom_idx,
+                )
+                if side_chain_atoms is None:
                     continue
 
                 # Build fragment with isotope tagging
@@ -217,13 +230,15 @@ class MacrolactoneValidator:
                 # Create fragment record
                 fragment = SideChainFragment(
                     parent_id=parent.id,
-                    fragment_id=f"{parent.source_id}_frag_{fragment_idx}",
+                    fragment_id=f"{parent.ml_id}_frag_{fragment_idx}",
                     cleavage_position=int(position),
                     attachment_atom_idx=ring_atom_idx,
                     attachment_atom_symbol=ring_atom.GetSymbol(),
                     fragment_smiles_labeled=labeled_smiles,
                     fragment_smiles_plain=plain_smiles,
                     dummy_isotope=int(position),
+                    has_dummy_atom=True,
+                    dummy_atom_count=1,
                     atom_count=atom_count,
                     heavy_atom_count=heavy_atom_count,
                     molecular_weight=round(mw, 4),
@@ -231,11 +246,26 @@ class MacrolactoneValidator:
                 )
                 session.add(fragment)
                 fragments.append(fragment)
+                session.add(
+                    FragmentLibraryEntry(
+                        source_type="validation_extract",
+                        source_fragment_id=fragment.fragment_id,
+                        source_parent_ml_id=parent.ml_id,
+                        source_parent_chembl_id=parent.chembl_id,
+                        cleavage_position=int(position),
+                        fragment_smiles_labeled=labeled_smiles,
+                        fragment_smiles_plain=plain_smiles,
+                        has_dummy_atom=True,
+                        dummy_atom_count=1,
+                        splice_ready=True,
+                        original_bond_type=bond_type,
+                    )
+                )
                 fragment_idx += 1
 
         # Save fragment images
         if fragments and paths["sidechains_dir"]:
-            image_paths = save_fragment_images(fragments, paths["sidechains_dir"], parent.source_id)
+            image_paths = save_fragment_images(fragments, paths["sidechains_dir"], parent.ml_id)
             for frag, img_path in zip(fragments, image_paths):
                 frag.image_path = img_path
                 session.add(frag)
@@ -244,13 +274,13 @@ class MacrolactoneValidator:
         parent.processing_status = ProcessingStatus.SUCCESS
         parent.num_sidechains = len(fragments)
         parent.cleavage_positions = json.dumps([f.cleavage_position for f in fragments])
-        parent.processed_at = datetime.utcnow()
+        parent.processed_at = datetime.now(UTC)
         session.add(parent)
         session.commit()
 
-    def _save_original_image(self, smiles: str, source_id: str, ring_size: int, classification: str):
+    def _save_original_image(self, smiles: str, ml_id: str, ring_size: int, classification: str):
         """Save original image for non-standard molecules."""
-        paths = get_output_paths(self.output_dir, source_id, ring_size, classification)
+        paths = get_output_paths(self.output_dir, ml_id, ring_size, classification)
         try:
             from rdkit.Chem import Draw
 
@@ -272,6 +302,7 @@ This directory contains validation results for MacrolactoneDB 12-20 membered rin
 validation_output/
 ├── README.md                    # This file
 ├── fragments.db                 # SQLite database with all data
+├── fragment_library.csv         # Unified fragment library export
 ├── summary.csv                  # Summary of all processed molecules
 ├── summary_statistics.json      # Statistical summary
 │
@@ -301,6 +332,7 @@ validation_output/
 - **parent_molecules**: Original molecule information
 - **ring_numberings**: Ring atom numbering details
 - **side_chain_fragments**: Fragmentation results with isotope tags
+- **fragment_library_entries**: Unified fragment library rows for downstream design
 - **validation_results**: Manual validation records
 
 ### Key Fields
@@ -308,6 +340,8 @@ validation_output/
 - `classification`: standard_macrolactone | non_standard_macrocycle | not_macrolactone
 - `dummy_isotope`: Cleavage position stored as isotope value for reconstruction
 - `cleavage_position`: Position on ring where side chain was attached
+- `has_dummy_atom`: Whether the fragment contains a dummy atom for splicing
+- `dummy_atom_count`: Number of dummy atoms in the fragment
 
 ## Ring Numbering Convention
 
@@ -325,13 +359,21 @@ Fragments use isotope values to mark cleavage position:
 
 ### summary.csv
 
-- `source_id`: Original molecule ID from MacrolactoneDB
+- `ml_id`: MacrolactoneDB unique ID (e.g., ML00000001)
+- `chembl_id`: Original CHEMBL ID (if available)
 - `classification`: Classification result
 - `ring_size`: Detected ring size (12-20)
 - `num_sidechains`: Number of side chains detected
 - `cleavage_positions`: JSON array of cleavage positions
 - `processing_status`: pending | success | failed | skipped
 
+### fragment_library.csv
+
+- `source_type`: validation_extract | supplemental (reserved)
+- `has_dummy_atom`: Whether the fragment contains a dummy atom
+- `dummy_atom_count`: Number of dummy atoms
+- `splice_ready`: Whether the fragment is directly compatible with single-anchor splicing
+
 ## Querying the Database
 
 ```bash
@@ -363,7 +405,8 @@ sqlite3 fragments.db "SELECT ring_size, COUNT(*) FROM parent_molecules GROUP BY
             for p in parents:
                 data.append({
                     "id": p.id,
-                    "source_id": p.source_id,
+                    "ml_id": p.ml_id,
+                    "chembl_id": p.chembl_id,
                     "molecule_name": p.molecule_name,
                     "smiles": p.smiles,
                     "classification": p.classification,
@@ -395,6 +438,47 @@ sqlite3 fragments.db "SELECT ring_size, COUNT(*) FROM parent_molecules GROUP BY
             print(f"\nSummary saved to {self.output_dir / 'summary.csv'}")
             print(f"Statistics: {stats}")
 
+    def _generate_fragment_library(self):
+        """Generate unified fragment library CSV."""
+        columns = [
+            "id",
+            "source_type",
+            "source_fragment_id",
+            "source_parent_ml_id",
+            "source_parent_chembl_id",
+            "cleavage_position",
+            "fragment_smiles_labeled",
+            "fragment_smiles_plain",
+            "has_dummy_atom",
+            "dummy_atom_count",
+            "splice_ready",
+            "original_bond_type",
+            "created_at",
+        ]
+
+        with get_session(self.engine) as session:
+            entries = session.exec(select(FragmentLibraryEntry)).all()
+            data = [
+                {
+                    "id": entry.id,
+                    "source_type": entry.source_type,
+                    "source_fragment_id": entry.source_fragment_id,
+                    "source_parent_ml_id": entry.source_parent_ml_id,
+                    "source_parent_chembl_id": entry.source_parent_chembl_id,
+                    "cleavage_position": entry.cleavage_position,
+                    "fragment_smiles_labeled": entry.fragment_smiles_labeled,
+                    "fragment_smiles_plain": entry.fragment_smiles_plain,
+                    "has_dummy_atom": entry.has_dummy_atom,
+                    "dummy_atom_count": entry.dummy_atom_count,
+                    "splice_ready": entry.splice_ready,
+                    "original_bond_type": entry.original_bond_type,
+                    "created_at": entry.created_at,
+                }
+                for entry in entries
+            ]
+
+        pd.DataFrame(data, columns=columns).to_csv(self.output_dir / "fragment_library.csv", index=False)
+
 
 class MacrolactoneDetectionError(Exception):
     """Raised when macrolactone detection fails."""

tests/helpers.py

@@ -78,6 +78,108 @@ def build_non_standard_ring_atom_macrolactone(
     )
 
 
+def build_macrolactone_with_fused_side_ring(
+    ring_size: int = 16,
+    fused_positions: tuple[int, int] = (5, 6),
+    side_chains: Mapping[int, str] | None = None,
+) -> BuiltMacrolactone:
+    base = build_macrolactone(ring_size=ring_size, side_chains=side_chains)
+    position_a, position_b = fused_positions
+    rwmol = Chem.RWMol(Chem.Mol(base.mol))
+
+    atom_x = rwmol.AddAtom(Chem.Atom("C"))
+    atom_y = rwmol.AddAtom(Chem.Atom("C"))
+    rwmol.AddBond(base.position_to_atom[position_a], atom_x, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_x, atom_y, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_y, base.position_to_atom[position_b], Chem.BondType.SINGLE)
+
+    mol = rwmol.GetMol()
+    Chem.SanitizeMol(mol)
+    return BuiltMacrolactone(
+        mol=mol,
+        smiles=Chem.MolToSmiles(mol, isomericSmiles=True),
+        position_to_atom=base.position_to_atom,
+    )
+
+
+def build_macrolactone_with_bridge_side_chain(
+    ring_size: int = 16,
+    bridge_positions: tuple[int, int] = (5, 8),
+    side_chains: Mapping[int, str] | None = None,
+) -> BuiltMacrolactone:
+    base = build_macrolactone(ring_size=ring_size, side_chains=side_chains)
+    position_a, position_b = bridge_positions
+    rwmol = Chem.RWMol(Chem.Mol(base.mol))
+
+    atom_x = rwmol.AddAtom(Chem.Atom("C"))
+    atom_y = rwmol.AddAtom(Chem.Atom("C"))
+    rwmol.AddBond(base.position_to_atom[position_a], atom_x, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_x, atom_y, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_y, base.position_to_atom[position_b], Chem.BondType.SINGLE)
+
+    mol = rwmol.GetMol()
+    Chem.SanitizeMol(mol)
+    return BuiltMacrolactone(
+        mol=mol,
+        smiles=Chem.MolToSmiles(mol, isomericSmiles=True),
+        position_to_atom=base.position_to_atom,
+    )
+
+
+def build_macrolactone_with_shared_atom_side_ring(
+    ring_size: int = 16,
+    position: int = 5,
+    side_chains: Mapping[int, str] | None = None,
+) -> BuiltMacrolactone:
+    base = build_macrolactone(ring_size=ring_size, side_chains=side_chains)
+    rwmol = Chem.RWMol(Chem.Mol(base.mol))
+
+    atom_x = rwmol.AddAtom(Chem.Atom("C"))
+    atom_y = rwmol.AddAtom(Chem.Atom("C"))
+    atom_z = rwmol.AddAtom(Chem.Atom("C"))
+    ring_atom_idx = base.position_to_atom[position]
+
+    rwmol.AddBond(ring_atom_idx, atom_x, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_x, atom_y, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_y, atom_z, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_z, ring_atom_idx, Chem.BondType.SINGLE)
+
+    mol = rwmol.GetMol()
+    Chem.SanitizeMol(mol)
+    return BuiltMacrolactone(
+        mol=mol,
+        smiles=Chem.MolToSmiles(mol, isomericSmiles=True),
+        position_to_atom=base.position_to_atom,
+    )
+
+
+def build_macrolactone_with_single_anchor_side_ring(
+    ring_size: int = 16,
+    position: int = 5,
+    side_chains: Mapping[int, str] | None = None,
+) -> BuiltMacrolactone:
+    base = build_macrolactone(ring_size=ring_size, side_chains=side_chains)
+    rwmol = Chem.RWMol(Chem.Mol(base.mol))
+
+    atom_x = rwmol.AddAtom(Chem.Atom("C"))
+    atom_y = rwmol.AddAtom(Chem.Atom("C"))
+    atom_z = rwmol.AddAtom(Chem.Atom("C"))
+    ring_atom_idx = base.position_to_atom[position]
+
+    rwmol.AddBond(ring_atom_idx, atom_x, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_x, atom_y, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_y, atom_z, Chem.BondType.SINGLE)
+    rwmol.AddBond(atom_z, atom_x, Chem.BondType.SINGLE)
+
+    mol = rwmol.GetMol()
+    Chem.SanitizeMol(mol)
+    return BuiltMacrolactone(
+        mol=mol,
+        smiles=Chem.MolToSmiles(mol, isomericSmiles=True),
+        position_to_atom=base.position_to_atom,
+    )
+
+
 def build_overlapping_candidate_macrolactone() -> BuiltMacrolactone:
     rwmol = Chem.RWMol()
 

tests/test_fragmentation.py

@@ -2,7 +2,12 @@ from rdkit import Chem
 
 from macro_lactone_toolkit import MacrolactoneFragmenter
 
-from .helpers import build_macrolactone
+from .helpers import (
+    build_macrolactone,
+    build_macrolactone_with_fused_side_ring,
+    build_macrolactone_with_shared_atom_side_ring,
+    build_macrolactone_with_single_anchor_side_ring,
+)
 
 
 def test_fragmentation_returns_empty_list_without_sidechains():
@@ -51,3 +56,24 @@ def test_fragmentation_preserves_attachment_bond_type():
         neighbor = dummy_atom.GetNeighbors()[0]
         bond = mol.GetBondBetweenAtoms(dummy_atom.GetIdx(), neighbor.GetIdx())
         assert bond.GetBondType() == Chem.BondType.DOUBLE
+
+
+def test_fragmentation_skips_fused_side_ring_but_keeps_single_anchor_sidechains():
+    built = build_macrolactone_with_fused_side_ring(side_chains={10: "methyl"})
+    result = MacrolactoneFragmenter().fragment_molecule(built.smiles, parent_id="fused")
+
+    assert {fragment.cleavage_position for fragment in result.fragments} == {10}
+
+
+def test_fragmentation_skips_shared_atom_multi_anchor_component():
+    built = build_macrolactone_with_shared_atom_side_ring(side_chains={11: "ethyl"})
+    result = MacrolactoneFragmenter().fragment_molecule(built.smiles, parent_id="shared_atom")
+
+    assert {fragment.cleavage_position for fragment in result.fragments} == {11}
+
+
+def test_fragmentation_allows_single_anchor_side_ring():
+    built = build_macrolactone_with_single_anchor_side_ring()
+    result = MacrolactoneFragmenter().fragment_molecule(built.smiles, parent_id="single_anchor_ring")
+
+    assert {fragment.cleavage_position for fragment in result.fragments} == {5}

tests/test_splicing_engine.py

@@ -5,7 +5,7 @@ from macro_lactone_toolkit import MacrolactoneFragmenter
 from macro_lactone_toolkit.splicing.engine import splice_molecule
 from macro_lactone_toolkit.splicing.scaffold_prep import prepare_macrolactone_scaffold
 
-from .helpers import build_macrolactone, canonicalize
+from .helpers import build_macrolactone, build_macrolactone_with_fused_side_ring, canonicalize
 
 
 def test_splice_benzene_methyl():
@@ -49,3 +49,14 @@ def test_prepare_scaffold_and_reassemble_fragment():
     product = splice_molecule(scaffold, Chem.MolFromSmiles(fragment.fragment_smiles_labeled), position=5)
 
     assert canonicalize(product) == canonicalize(built.mol)
+
+
+def test_prepare_scaffold_rejects_position_without_single_anchor_fragment():
+    built = build_macrolactone_with_fused_side_ring(side_chains={10: "methyl"})
+
+    with pytest.raises(ValueError, match="Position 5 does not contain a single-anchor fragmentable side chain"):
+        prepare_macrolactone_scaffold(
+            built.smiles,
+            positions=[5],
+            ring_size=16,
+        )

tests/validation/test_validator.py

@@ -0,0 +1,57 @@
+from __future__ import annotations
+
+import json
+import sqlite3
+
+import pandas as pd
+
+from macro_lactone_toolkit.validation.validator import MacrolactoneValidator
+
+from ..helpers import build_macrolactone_with_fused_side_ring
+
+
+def test_validator_exports_only_single_anchor_fragments_and_fragment_library(tmp_path):
+    built = build_macrolactone_with_fused_side_ring(side_chains={10: "methyl"})
+    input_path = tmp_path / "input.csv"
+    output_dir = tmp_path / "validation_output"
+
+    pd.DataFrame(
+        [
+            {
+                "ml_id": "ML00000001",
+                "IDs": "CHEMBL0001",
+                "smiles": built.smiles,
+            }
+        ]
+    ).to_csv(input_path, index=False)
+
+    validator = MacrolactoneValidator(output_dir=output_dir, sample_ratio=1.0)
+    results = validator.run(input_path)
+
+    assert results == {"total": 1, "success": 1, "failed": 0, "skipped": 0}
+
+    with sqlite3.connect(output_dir / "fragments.db") as connection:
+        fragments = connection.execute(
+            "SELECT cleavage_position, has_dummy_atom, dummy_atom_count FROM side_chain_fragments"
+        ).fetchall()
+        library_entries = connection.execute(
+            """
+            SELECT source_type, source_parent_ml_id, source_parent_chembl_id,
+                   cleavage_position, has_dummy_atom, dummy_atom_count, splice_ready
+            FROM fragment_library_entries
+            """
+        ).fetchall()
+
+    assert fragments == [(10, 1, 1)]
+    assert library_entries == [("validation_extract", "ML00000001", "CHEMBL0001", 10, 1, 1, 1)]
+
+    summary = pd.read_csv(output_dir / "summary.csv")
+    assert summary.loc[0, "num_sidechains"] == 1
+    assert json.loads(summary.loc[0, "cleavage_positions"]) == [10]
+
+    fragment_library = pd.read_csv(output_dir / "fragment_library.csv")
+    assert fragment_library.loc[0, "source_type"] == "validation_extract"
+    assert int(fragment_library.loc[0, "cleavage_position"]) == 10
+    assert bool(fragment_library.loc[0, "has_dummy_atom"]) is True
+    assert int(fragment_library.loc[0, "dummy_atom_count"]) == 1
+    assert bool(fragment_library.loc[0, "splice_ready"]) is True

validation_output/README.md

@@ -0,0 +1,97 @@
+# MacrolactoneDB Validation Output
+
+This directory contains validation results for MacrolactoneDB 12-20 membered rings.
+
+## Directory Structure
+
+```
+validation_output/
+├── README.md                    # This file
+├── fragments.db                 # SQLite database with all data
+├── fragment_library.csv         # Unified fragment library export
+├── summary.csv                  # Summary of all processed molecules
+├── summary_statistics.json      # Statistical summary
+│
+├── ring_size_12/                # 12-membered rings
+├── ring_size_13/                # 13-membered rings
+...
+└── ring_size_20/                # 20-membered rings
+    ├── molecules.csv            # Molecules in this ring size
+    ├── standard/                # Standard macrolactones
+    │   ├── numbered/            # Numbered ring images
+    │   │   └── {id}_numbered.png
+    │   └── sidechains/          # Fragment images
+    │       └── {id}/
+    │           └── {id}_frag_{n}_pos{pos}.png
+    ├── non_standard/            # Non-standard macrocycles
+    │   └── original/
+    │       └── {id}_original.png
+    └── rejected/                # Not macrolactones
+        └── original/
+            └── {id}_original.png
+```
+
+## Database Schema
+
+### Tables
+
+- **parent_molecules**: Original molecule information
+- **ring_numberings**: Ring atom numbering details
+- **side_chain_fragments**: Fragmentation results with isotope tags
+- **fragment_library_entries**: Unified fragment library rows for downstream design
+- **validation_results**: Manual validation records
+
+### Key Fields
+
+- `classification`: standard_macrolactone | non_standard_macrocycle | not_macrolactone
+- `dummy_isotope`: Cleavage position stored as isotope value for reconstruction
+- `cleavage_position`: Position on ring where side chain was attached
+- `has_dummy_atom`: Whether the fragment contains a dummy atom for splicing
+- `dummy_atom_count`: Number of dummy atoms in the fragment
+
+## Ring Numbering Convention
+
+1. Position 1 = Lactone carbonyl carbon (C=O)
+2. Position 2 = Ester oxygen (-O-)
+3. Positions 3-N = Sequential around ring
+
+## Isotope Tagging
+
+Fragments use isotope values to mark cleavage position:
+- `[5*]CCO` = Fragment from position 5, dummy atom has isotope=5
+- This enables precise reconstruction during reassembly
+
+## CSV Columns
+
+### summary.csv
+
+- `ml_id`: MacrolactoneDB unique ID (e.g., ML00000001)
+- `chembl_id`: Original CHEMBL ID (if available)
+- `classification`: Classification result
+- `ring_size`: Detected ring size (12-20)
+- `num_sidechains`: Number of side chains detected
+- `cleavage_positions`: JSON array of cleavage positions
+- `processing_status`: pending | success | failed | skipped
+
+### fragment_library.csv
+
+- `source_type`: validation_extract | supplemental (reserved)
+- `has_dummy_atom`: Whether the fragment contains a dummy atom
+- `dummy_atom_count`: Number of dummy atoms
+- `splice_ready`: Whether the fragment is directly compatible with single-anchor splicing
+
+## Querying the Database
+
+```bash
+# List tables
+sqlite3 fragments.db ".tables"
+
+# Get standard macrolactones with fragments
+sqlite3 fragments.db "SELECT * FROM parent_molecules WHERE classification='standard_macrolactone' LIMIT 5;"
+
+# Get fragments for a specific molecule
+sqlite3 fragments.db "SELECT * FROM side_chain_fragments WHERE parent_id=1;"
+
+# Count by ring size
+sqlite3 fragments.db "SELECT ring_size, COUNT(*) FROM parent_molecules GROUP BY ring_size;"
+```

validation_output/summary_statistics.json

@@ -0,0 +1,23 @@
+{
+  "total_molecules": 11036,
+  "by_classification": {
+    "non_standard_macrocycle": 6336,
+    "standard_macrolactone": 4482,
+    "not_macrolactone": 218
+  },
+  "by_ring_size": {
+    "14.0": 3017,
+    "16.0": 1879,
+    "15.0": 1613,
+    "12.0": 1419,
+    "19.0": 855,
+    "18.0": 809,
+    "13.0": 679,
+    "20.0": 243,
+    "17.0": 196
+  },
+  "by_status": {
+    "skipped": 6554,
+    "success": 4482
+  }
+}