Ligand profile

CHEMBL205091

Bioactivity hit from ChEMBL on a similar protein.

Bound to: VK055_2379 — 1-deoxy-D-xylulose 5-phosphate reductoisomerase

Via homolog UniProt P45568 Formula C₅H₁₀NO₅P
pchembl 6.50 ~316.2 nM
Mol. weight 195.11 Da
Permeability Check
PAINS Clean

Identifiers

Database identifiers and provenance.

Ligand ID
CHEMBL205091
UniProt (similar protein)
P45568
pchembl
6.500 (~316.2 nM)
Target protein
VK055_2379

Structure

2D representation rendered from SMILES.

Physicochemical properties

Computed with RDKit from SMILES.

Molecular weight 195.11 Da
LogP (Crippen) -0.60
H-bond donors 3
H-bond acceptors 3
TPSA 98.07 Ų
Rotatable bonds 4
Aromatic rings 0 / 1
Heavy atoms 12
Fraction sp³ C 0.80
Formula C₅H₁₀NO₅P

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 98.1
  • −1 ≤ LogP ≤ 5 -0.60
Lipinski's Rule of Five Pass 0 violations
  • MW ≤ 500 Da 195.1
  • LogP ≤ 5 -0.60
  • H-bond donors ≤ 5 3
  • H-bond acceptors ≤ 10 3
Veber's rules Pass
  • Rotatable bonds ≤ 10 4
  • TPSA ≤ 140 Ų 98.1
PAINS Clean

No PAINS structural alerts detected.

Chemical representations

Canonical representations for cheminformatics workflows.

SMILES 
O=CN(O)C[C@@H]1C[C@H]1P(=O)(O)O
InChI 
InChI=1S/C5H10NO5P/c7-3-6(8)2-4-1-5(4)12(9,10)11/h3-5,8H,1-2H2,(H2,9,10,11)/t4-,5+/m0/s1
InChIKey 
UQUOLLQTLQTTFU-CRCLSJGQSA-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
Curation
pdb_similarity_tanimoto
Binding sites
PF02670' 'PF08436' 'PF13288

External resources

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

Other ligands for this protein

Quick navigation to other ligands bound to VK055_2379.

PDB 7

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

Ligand PDB entry

ChEMBL 41

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)