General
Preferred name
ULK-101
Synonyms
ULK101 ()
P&D ID
PD117586
CAS
2443816-45-1
Tags
available
probe
Probe info
Probe type
experimental probe
Probe targets
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
COMMENT ULK-101 looks to be an appropriate tool for in vitro/in cellulo studies. Kinase selectivity data is included within the supplementary data. Further confidence in use as probe would come from availability of wider selectivity data (i.e. targets other than kinases) and ideally a negative chemical probe. The molecule may be suitable for in vivo use but no data are available. Additionally these data at present come from a single publication. Jul 11 2020 - 3:31pm; ULK-101 is a potentially valuable probe for studying ULK1 biology in cells, as it is potent against ULK-1 (8.3 nM) and quite selective against the kinome, with only 2 off-target kinases inhibited at similar potency levels (it was determined that the IC50 for DRAK1 is 14 nM and that of MNK2 to be 22 nM). Moreover, ULK-101 inhibits ULK2 at 30 nM, suggesting that at least at doses above 1 uM in cell tissue studies it has good coverage for this possibly redundant target as well. These features suggest that ULK-101 is a “best in class” probe against ULK1. It is slightly less potent than the structurally related analog ULK-100, but it is significantly more selective. There is no data disclosed against targets outside the kinase class, but the scaffold appears to have no features suggesting it should potently modify other protein classes (e.g ion channels, GPCRs). There is no disclosed in vivo efficacy or pharmacokinetic data, so use in the context of in vivo experiments should proceed with care until pharmacokinetic data or pharmacodynamic data is determined. Aug 28 2020 - 7:55am
DESCRIPTION ULK-101 is a potent and selective ULK1 inhibitor, with IC50 values of 1.6 nM and 30 nM for ULK1 and ULK2, respectively. ULK-101 suppresses autophagy and sensitizes cancer cells to nutrient stress[1].
PRICE 428
MOA Inhibitor (Chemical Probes.org)
DESCRIPTION ULK-101 is a potent and selective ULK1 inhibitor with IC50 values of 8.3 nM and 30 nM for ULK1 and ULK2, respectively. It suppresses autophagy and sensitizes cancer cells to nutrient stress. (BOC Sciences Bioactive Compounds)
DESCRIPTION ULK-101 is a potent and selective inhibitor of ULK1 (IC50s: 8.3/30 nM for ULK1/ULK2). It can suppress autophagy. (TargetMol Bioactive Compound Library)
Cell lines
5
Organisms
0
Compound Sets
9
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
Chemical Probes.org
CZ-OPENSCREEN Bioactive Library
EUbOPEN Chemogenomics Library
High-quality chemical probes
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
External IDs
6
Properties
(calculated by RDKit )
Molecular Weight
460.1
Hydrogen Bond Acceptors
5
Hydrogen Bond Donors
1
Rotatable Bonds
5
Ring Count
5
Aromatic Ring Count
4
cLogP
5.33
TPSA
59.29
Fraction CSP3
0.23
Chiral centers
1.0
Largest ring
6.0
QED
0.41
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
ULK
Autophagy,ULK
ULK1, ULK2
ULK1
Pathway
Autophagy
Target subclass
Autophagy Activating Kinases
Autophagy Activating Kinases, Autophagy Activating Kinases
Target class
Protein kinase
Kinase, Kinase
Recommended Cell Concentration
None
Source data