Ligand profile

CHEMBL5170454

Bioactivity hit from ChEMBL on a similar protein.

Bound to: KP13_02722 — Agmatinase

Via homolog UniProt P78540 Formula C₁₅H₃₀BN₃O₅S
pchembl 6.70 ~199.5 nM
Mol. weight 375.30 Da
Permeability Check
PAINS Clean

Identifiers

Database identifiers and provenance.

Ligand ID
CHEMBL5170454
UniProt (similar protein)
P78540
pchembl
6.700 (~199.5 nM)
Target protein
KP13_02722

Structure

2D representation rendered from SMILES.

Physicochemical properties

Computed with RDKit from SMILES.

Molecular weight 375.30 Da
LogP (Crippen) -0.76
H-bond donors 6
H-bond acceptors 7
TPSA 158.90 Ų
Rotatable bonds 10
Aromatic rings 0 / 1
Heavy atoms 25
Fraction sp³ C 0.87
Formula C₁₅H₃₀BN₃O₅S

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.

  • TPSA ≤ 90 Ų 158.9
  • −1 ≤ LogP ≤ 5 -0.76
Lipinski's Rule of Five Pass 1 violation
  • MW ≤ 500 Da 375.3
  • LogP ≤ 5 -0.76
  • H-bond donors ≤ 5 6
  • H-bond acceptors ≤ 10 7
Veber's rules Fail
  • Rotatable bonds ≤ 10 10
  • TPSA ≤ 140 Ų 158.9
PAINS Clean

No PAINS structural alerts detected.

Chemical representations

Canonical representations for cheminformatics workflows.

SMILES 
CSCC[C@H](N)C(=O)NC[C@@H]1CC[C@@H](CCB(O)O)C[C@]1(N)C(=O)O
InChI 
InChI=1S/C15H30BN3O5S/c1-25-7-5-12(17)13(20)19-9-11-3-2-10(4-6-16(23)24)8-15(11,18)14(21)22/h10-12,23-24H,2-9,17-18H2,1H3,(H,19,20)(H,21,22)/t10-,11-,12-,15+/m0/s1
InChIKey 
FAAXPLPGKGINLR-JUFZMCDQSA-N

Provenance

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

Method
LigQ nearest_k
Source
ChEMBL
Binding sites
PF00491

External resources

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

Other ligands for this protein

Quick navigation to other ligands bound to KP13_02722.

PDB 12

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

Ligand PDB entry

ChEMBL 99

Compounds with measured inhibitory activity on this target (higher pchembl = more potent).

Compound Potency (pchembl)

ZINC 50

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

Compound Similarity (Tanimoto)