Ligand · 0T2
0T2 · 2-chloro-3-[(2-cyanopropan-2-yl)oxy]-N-{5-[{2-[(cyclopropylcarbonyl)amino][1,3]thiazolo[5,4-b]pyridin-5-yl}(methyl)amino]-2-fluorophenyl}benzamide
0T2, 2-chloro-3-[(2-cyanopropan-2-yl)oxy]-N-{5-[{2-[(cyclopropylcarbonyl)amino][1,3]thiazolo[5,4-b]pyridin-5-yl}(methyl)amino]-2-fluorophenyl}benzamide (C28 H24 Cl F N6 O3 S, 579.0 g/mol), in the MolNFT structures on GenesisL1: bound in 2…
- Component
- 0T2
- Formula
- C28 H24 Cl F N6 O3 S
- Class
- ligand
- Structures
- 2
- PDB entries
- 1
Binding sites
0T2 in 2 structures; the first of them:
- 4FC0 · Crystal Structure of Human Kinase Domain of B-raf with a DFG-out Inhibitor · 0T2 A901 · binds ILE462, VAL470, ALA480, LYS482, GLU500, VAL503, LEU504, LEU513 and 15 more
- 4FC0 · Crystal structure of human kinase domain of B-RAF with a dfg-out inhibitor · 0T2 A901 · binds ILE462, VAL470, ALA480, LYS482, GLU500, VAL503, LEU504, LEU513 and 15 more
Residues it binds most
ILE 4, LEU 4, GLU 4, GLY 4, PHE 4, VAL 4, ALA 4, THR 4, ASP 4, CYS 4 (residue and the binding sites it lines).
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