General
Preferred name
SODIUM GLUTAMATE
Synonyms
MONOSODIUM GLUTAMATE ()
Glutacyl ()
Glutavene ()
Ajinomoto ()
MSG ()
Monosodium glutamate|MSG ()
Monosodium L-glutamate monohydrate ()
MSG monohydrate ()
L(+)-Monosodium glutamate monohydrate ()
L-Glutamic acid (monosodium salt) ()
L-Glutamic acid (monosodium) (hydrate) ()
Monosodium glutamate, MSG ()
MSG monohydrate, L-Glutamic acid monosodium salt monohydrate, Monosodium L-glutamate monohydrate, Monosodium L-glutamate monohydrate ()
L-Glutamic acid monosodium salt ()
L-Glutamic acid monosodium salt monohydrate ()
E-621 ()
INS NO.621 ()
B1652 ()
Glutamate Sodium ()
RL-50 ()
Chinese seasoning ()
INS-621 ()
P&D ID
PD063922
CAS
16177-21-2
68187-33-7
68187-32-6
68187-34-8
6106-04-3
142-47-2
Tags
available
drug candidate
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure
P&D probe-likeness score
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
PRICE
29
PRICE
29
DESCRIPTION
L-Glutamic acid monosodium salt (MSG) (Monosodium glutamate) is an activator of mGlu1 receptor.
(TargetMol Bioactive Compound Library)
DESCRIPTION
L-Glutamic acid monosodium salt monohydrate (MSG monohydrate) is an important food additive with gastrointestinal protective effects. It plays a critical role in nutrient metabolism, energy demand, immune response, oxidative stress, signal transduction, and synaptic transmission. L-Glutamic acid monosodium salt monohydrate can induce oxidative stress, DNA damage, and apoptosis in mouse liver and brain tissues. It can protect against gastrointestinal damage caused by NSAIDs and Helicobacter pylori through multiple mechanisms.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Compound Sets
5
ChEMBL Drugs
EU-OPENSCREEN Bioactive Compound Library
MedChem Express Bioactive Compound Library
Selleckchem Bioactive Compound Library
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
48
Molecular Weight
169.04
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
2
Rotatable Bonds
4
Ring Count
0
Aromatic Ring Count
0
cLogP
-5.07
TPSA
103.45
Fraction CSP3
0.6
Chiral centers
1.0
Largest ring
0.0
QED
0.41
Structural alerts
0
No structural alerts detected
Related compounds
Custom attributes
(extracted from source data)
Target
Apoptosis
Endogenous Metabolite
Ferroptosis
iGluR
mGluR1
Pathway
Membrane Transporter/Ion Channel
Neuroscience
Metabolic Enzyme/Protease
Neuronal Signaling
MOA
GluR
Source data
