Binder profile

ZINC226859898

Virtual-screening candidate from ZINC.

Bound to: PA4235 — bacterioferritin

Via homolog UniProt Q9HY79 C15H12N2O5S
Tanimoto 0.50
Mol. weight 332.34 Da
Permeability Check
PAINS Alert

Identifiers

Database identifiers and provenance.

Ligand ID
ZINC226859898
UniProt (similar protein)
Q9HY79
Tanimoto
0.500
Target protein
PA4235

Structure

2D representation rendered from SMILES.

Physicochemical properties

Computed with RDKit from SMILES.

Molecular weight 332.34 Da
LogP (Crippen) 1.39
H-bond donors 3
H-bond acceptors 5
TPSA 112.57 Ų
Rotatable bonds 3
Aromatic rings 2 / 3
Heavy atoms 23
Fraction sp³ C 0.07
Formula C15H12N2O5S

Drug-likeness

Descriptor-based ADME screening flags from SMILES. These are not experimental toxicity results.

Permeability proxy Check

Estimated from TPSA and LogP only: TPSA ≤ 90 Ų and −1 ≤ LogP ≤ 5 are treated as a favorable small-molecule permeability screen.

Lipinski's Rule of Five Pass 0 violations
  • MW ≤ 500 Da 332.3
  • LogP ≤ 5 1.39
  • H-bond donors ≤ 5 3
  • H-bond acceptors ≤ 10 5
Veber's rules Pass
  • Rotatable bonds ≤ 10 3
  • TPSA ≤ 140 Ų 112.6
PAINS Alert

Matches PAINS filter: sulfonamide_B(41). May be a frequent false positive in HTS — review carefully.

Chemical representations

Canonical representations for cheminformatics workflows.

SMILES 
Cc1cc(O)ccc1NS(=O)(=O)c1ccc2c(c1)C(=O)NC2=O
InChI 
InChI=1S/C15H12N2O5S/c1-8-6-9(18)2-5-13(8)17-23(21,22)10-3-4-11-12(7-10)15(20)16-14(11)19/h2-7,17-18H,1H3,(H,16,19,20)
InChIKey 
TVPNKGADVBOUED-UHFFFAOYSA-N

Provenance

Annotation context from LigQ_2, the internal TPW step that collects PDB, ChEMBL, and ZINC ligand evidence.

Method
LigQ nearest_k
Query
KT7
Homolog
Q9HY79

External resources

Open this ligand in third-party databases and cheminformatics tools.

Other binders for this protein

Quick navigation to other ligands bound to PA4235.

PDB 11

Ligands co-crystallized with this protein (structural evidence).

Ligand PDB entry

ZINC 49

Virtual screening candidates selected by structural similarity to known actives (Tanimoto ≥ 0.5).

Compound Similarity (Tanimoto)