General
Preferred name
VU0119498
Synonyms
1-(4-Bromobenzyl)indole-2,3-dione ()
P&D ID
PD049347
CAS
79183-37-2
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
VU0119498 is a pan Gq mAChR M1, M3, M5 positive allosteric modulator (PAM), with EC50s of 6.04, 6.38, and 4.08 ¦ÌM, respectively. VU0119498 has antidiabetic activity[1][2][3].
PRICE
29
DESCRIPTION
VU0119498 is a M1 muscarinic receptor agonist (EC50 = 3.1 ??M) and pan mAChR M3, M5 positive allosteric modulator (PAM),and is a neuroprotective agent.
DESCRIPTION
1-(4-Bromobenzyl)indole-2,3-dione is a pan Gq mAChR (muscarinic acetylcholine receptor) M1, M3, M5 positive allosteric modulator, with EC50s of 6, 6.4, and 4.1 µM, respectively.
(Enamine Bioactive Compounds)
DESCRIPTION
VU0119498 is an M1 muscarinic receptor agonist (EC50 = 3.1 μM) and pan-mAChR M3, M5 positive allosteric modulator (PAM), and a neuroprotective agent. It has anti-diabetic activity.
(BOC Sciences Bioactive Compounds)
DESCRIPTION
VU0119498 is a M1 muscarinic receptor agonist (EC50 = 3.1 μM) and pan mAChR M3, M5 positive allosteric modulator (PAM),and is a neuroprotective agent.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
9
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
DrugMAP
Enamine Bioactive Compounds
Enamine BioReference Compounds
Guide to Pharmacology
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
16
Molecular Weight
314.99
Hydrogen Bond Acceptors
2
Hydrogen Bond Donors
0
Rotatable Bonds
2
Ring Count
3
Aromatic Ring Count
2
cLogP
3.18
TPSA
37.38
Fraction CSP3
0.07
Chiral centers
0.0
Largest ring
6.0
QED
0.8
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target
mAChR
AChR
Pathway
Neuroscience
GPCR/G protein
Neuronal Signaling
Source data

