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Ligand · 0SD

0SD · 2-(1-{[2-(2H-indazol-4-yl)-4-(morpholin-4-yl)pyrido[3,2-d]pyrimidin-6-yl]methyl}piperidin-4-yl)propan-2-ol

0SD, 2-(1-{[2-(2H-indazol-4-yl)-4-(morpholin-4-yl)pyrido[3,2-d]pyrimidin-6-yl]methyl}piperidin-4-yl)propan-2-ol (C27 H33 N7 O2, 487.6 g/mol), in the MolNFT structures on GenesisL1: bound in 2 records (1 PDB entry). Every binding site with…

Component
0SD
Formula
C27 H33 N7 O2
Class
ligand
Structures
2
PDB entries
1

Binding sites

0SD in 2 structures; the first of them:

  • 4EZK · Potent and Selective Inhibitors of PI3K-delta: Obtaining Isoform Selectivity from the… · 0SD A4000 · binds THR802, MET804, ALA805, TRP812, ILE831, LYS833, ASP841, TYR867 and 11 more
  • 4EZK · Potent and selective inhibitors of PI3K-delta: obtaining isoform selectivity from the… · 0SD A4000 · binds THR802, MET804, ALA805, TRP812, ILE831, LYS833, ASP841, TYR867 and 11 more

Residues it binds most

ILE 2, ALA 2, ASP 2, LYS 2, MET 2, THR 2, GLU 2, PHE 2, TRP 2, TYR 2 (residue and the binding sites it lines).

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