General
Preferred name
ILK-IN-2
Synonyms
OSU-T315 ()
ILK-IN-1 ()
PMID21823616C22 ()
OSU-T315 analog ()
compound 22 [PMID: 21823616] ()
P&D ID
PD050009
CAS
1333146-24-9
Tags
available
drug candidate
Drug indication
Discovery agent
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
ILK-IN-2 (OSU-T315 analog) is an oral PDK2 inhibitor and also an ILK inhibitor, with an IC50 of 0.6 ¦ÌM. ILK-IN-2 induces cell autophagy and apoptosis, showing anti-tumor activity. ILK-IN-2 directly abolishes AKT activation by preventing AKT from translocating to lipid rafts, triggering Caspase-dependent apoptosis in chronic lymphocytic leukemia (CLL) and extending the lifespan in TCL1 mouse models[1][2].
PRICE
131
DESCRIPTION
ILK-IN-2 (OSU-T315) is a novel potent, orally active ILK (integrin-linked kinase) inhibitor with IC50 of 0.6 ??M.
DESCRIPTION
Compound 22 was a lead reported as the result of a compound screen for inhibitors of the protein kinase integrin-linked kinase (ILK) .
(GtoPdb)
DESCRIPTION
ILK-IN-2 (OSU-T315) is a novel potent, orally active ILK (integrin-linked kinase) inhibitor with IC50 of 0.6 μM.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
6
Organisms
0
Compound Sets
7
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
13
Molecular Weight
533.24
Hydrogen Bond Acceptors
5
Hydrogen Bond Donors
2
Rotatable Bonds
7
Ring Count
5
Aromatic Ring Count
4
cLogP
5.31
TPSA
62.19
Fraction CSP3
0.27
Chiral centers
0.0
Largest ring
6.0
QED
0.34
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
ILK
Integrin
Ser/Thr Kinase
Caspase
PDHK
Member status
member
Pathway
Metabolic Enzyme/Protease
Cytoskeletal Signaling
Apoptosis
Autophagy
cytoskeleton
Source data

