gates.py

# -*- coding: utf-8 -*-
"""Season 1 admission gates.



Gates decide eligibility, never quality. Anything that reflects how good a molecule is

belongs in the continuous score; a gate only answers "is this a valid Season 1 entry".

Failing a gate does not put a submission at the bottom of the table - it means the entry

is returned, because a covalent warhead in a non-covalent season is not a bad candidate,

it is the wrong kind of candidate.



The one exception is ADMET, and it is deliberate: a candidate that fails a toxicity gate

is still scored in full and still shown, but sorts below every clean entry no matter how

high that score is. A molecule that binds beautifully and is mutagenic is not a lead.



Every threshold here was checked against a panel of approved drugs first. A gate that

rejects an approved drug is a broken gate, and two of the obvious candidates - hERG and

DILI - were thrown out for exactly that reason: our own ADMET model scores ensitrelvir

at hERG 0.978 and DILI 0.995, and caffeine at hERG 0.885. See data/anchors.json.

"""
from rdkit import Chem, RDLogger
from rdkit.Chem import Descriptors
from rdkit.Chem.FilterCatalog import FilterCatalog, FilterCatalogParams

RDLogger.DisableLog("rdApp.*")

_p = FilterCatalogParams()
_p.AddCatalog(FilterCatalogParams.FilterCatalogs.PAINS)
_PAINS = FilterCatalog(_p)

MW_MAX = 550.0          # ensitrelvir is 531.9; a 500 cap would disqualify the reference drug
HEAVY_MAX = 45
AMES_MAX = 0.7          # panel range was 0.024-0.302, so this leaves real headroom
LOGS_MIN = -7.0         # panel low was -5.42

# Electrophiles that form a covalent bond with the catalytic residue. Season 1 excludes
# them: they are a different medicinal-chemistry problem, and a docking-based score
# rewards raw reactivity in ways that are easy to game.
WARHEADS = [
    # A nitrile on its own is not a warhead. Teriflunomide is an approved, non-covalent
    # DHODH inhibitor and a bare [CX2]#[NX1] pattern rejected it - the same mistake as
    # gating on hERG, caught the same way, by running an approved drug through first.
    # What actually reacts with a catalytic cysteine is the peptidyl nitrile: the nitrile
    # carbon sitting on an sp3 centre that carries the amide nitrogen, as in nirmatrelvir.
    ("peptidyl nitrile", "[NX3][CX4][CX2]#[NX1]"),
    # Michael acceptors must be terminal to react. The general C=C-C(=O)N pattern also
    # matches teriflunomide, whose alkene is an enol stabilised by an adjacent nitrile
    # and hydroxyl - an approved drug, and not an electrophile.
    ("acrylamide",      "[CH2X3]=[CHX3][CX3](=O)[NX3]"),
    ("vinyl sulfone",   "[CX3]=[CX3][SX4](=O)(=O)"),
    ("aldehyde",        "[CX3H1](=O)[#6]"),
    ("epoxide",         "[OX2r3]1[#6r3][#6r3]1"),
    ("aziridine",       "[NX3r3]1[#6r3][#6r3]1"),
    ("haloacetamide",   "[NX3][CX3](=O)[CH2][F,Cl,Br,I]"),
    ("boronic acid",    "[BX3]([OX2H1])[OX2H1]"),
    ("alpha-keto amide", "[CX3](=O)[CX3](=O)[NX3]"),
]
_WARHEADS = [(n, Chem.MolFromSmarts(s)) for n, s in WARHEADS]


def canonical(text):
    """Accept SMILES or InChI. A molecular formula cannot be accepted - too many isomers."""
    t = (text or "").strip()
    if not t:
        return None, "빈 입력"
    m = Chem.MolFromInchi(t) if t.upper().startswith("INCHI=") else Chem.MolFromSmiles(t)
    if m is None:
        return None, "구조를 해석할 수 없습니다 (SMILES 또는 InChI로 제출하세요; 분자식은 이성질체가 많아 평가 불가)"
    return m, None


def check(text, ames=None, logs=None, known_inchikeys=(), covalent_rule=True,

          mw_max=None, heavy_max=None, pains_allow=None):
    """Return a verdict dict. `ames`/`logs` come from the ADMET engine; omit them and

    those two gates are simply reported as not evaluated rather than silently passed.



    `covalent_rule` is target-scoped on purpose. Excluding covalent binders makes sense

    for Mpro, where warheads react with a catalytic cysteine and a docking score can be

    gamed by raw reactivity. PfDHODH is not inhibited that way, so for Season 1 the rule

    buys nothing and only creates false rejections - two approved drugs were wrongly

    turned away here before the patterns were tightened.



    `mw_max`, `heavy_max` and `pains_allow` are per-season and default to the module

    constants, which are Season 1's. They are arguments rather than module state because

    the Space is one process serving every season at once: reading them from the

    environment would give Season 3's limits to Season 1's entries. seasons.py carries

    each season's values and app.py passes them through."""
    m, err = canonical(text)
    if m is None:
        return {"admitted": False,
                "reject": [{"code": "parse", "text": err}], "relegate": []}

    smi = Chem.MolToSmiles(m)
    key = Chem.MolToInchiKey(m)
    mw = Descriptors.MolWt(m)
    heavy = m.GetNumHeavyAtoms()

    reject, relegate, notes = [], [], []

    # Each reason carries a code as well as a sentence. The sentence is a fallback; the
    # code is what lets the page say it in the reader's language.
    for name, patt in (_WARHEADS if covalent_rule else []):
        if patt is not None and m.HasSubstructMatch(patt):
            reject.append({"code": "covalent", "arg": name,
                           "text": "공유결합 warhead 검출 (%s) — Season 1은 비공유 트랙입니다" % name})
            break

    mw_cap = MW_MAX if mw_max is None else float(mw_max)
    heavy_cap = HEAVY_MAX if heavy_max is None else int(heavy_max)
    # no module-level default here on purpose: in the Space every season's limits arrive as
    # arguments, and a module constant is exactly the thing that would leak across seasons
    allow = tuple(pains_allow or ())

    if mw > mw_cap:
        reject.append({"code": "mw", "arg": "%.1f" % mw, "limit": mw_cap,
                       "text": "분자량 %.1f > %.0f" % (mw, mw_cap)})
    if heavy > heavy_cap:
        reject.append({"code": "heavy", "arg": heavy, "limit": heavy_cap,
                       "text": "무거운 원자 %d > %d" % (heavy, heavy_cap)})

    hits = [h for h in _PAINS.GetMatches(m)
            if not any(h.GetDescription().startswith(a) for a in allow)]
    if hits:
        d = ", ".join(h.GetDescription() for h in hits)[:80]
        reject.append({"code": "pains", "arg": d, "text": "PAINS 구조 (%s)" % d})

    if key in set(known_inchikeys):
        reject.append({"code": "duplicate",
                       "text": "기존 제출 또는 기준물질과 동일한 구조입니다"})

    # ADMET does not reject. It relegates: full score, shown, but below every clean entry.
    if ames is None:
        notes.append("Ames 미평가")
    elif ames > AMES_MAX:
        relegate.append({"code": "ames", "arg": "%.3f" % ames, "limit": AMES_MAX,
                         "text": "변이원성(Ames) %.3f > %.2f" % (ames, AMES_MAX)})
    if logs is None:
        notes.append("용해도 미평가")
    elif logs < LOGS_MIN:
        relegate.append({"code": "solubility", "arg": "%.2f" % logs, "limit": LOGS_MIN,
                         "text": "극단적 불용성 (logS %.2f < %.1f)" % (logs, LOGS_MIN)})

    return {"admitted": not reject, "reject": reject, "relegate": relegate,
            "notes": notes, "smiles": smi, "inchikey": key,
            "mw": round(mw, 2), "heavy_atoms": heavy}


if __name__ == "__main__":
    import json, os, sys
    # the Windows console defaults to cp949 here and dies on the em-dash in a reject reason
    try:
        sys.stdout.reconfigure(encoding="utf-8")
    except Exception:
        pass
    A = json.load(open(os.path.join("data", "anchors.json"), encoding="utf-8"))
    print("%-30s %-9s %-7s %-6s %s" % ("compound", "admitted", "MW", "heavy", "reason"))
    print("-" * 100)
    for a in A["anchors"]:
        ad = a.get("measured_admet", {})
        v = check(a["smiles"], ames=ad.get("ames"), logs=ad.get("solubility-aqsoldb"))
        why = "; ".join(v["reject"] + ["[강등] " + r for r in v["relegate"]]) or "-"
        print("%-30s %-9s %-7s %-6s %s"
              % (a["label"][:29], "PASS" if v["admitted"] else "REJECT",
                 v.get("mw"), v.get("heavy_atoms"), why[:60]))