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mdni caged l glutamate

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    9
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  • Peptide Products
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MDNI-caged-L-glutamate
MDNI-caged-L-glutamate,MDNI-glu
T40973864085-92-7
MDNI-glu is a photosensitive derivative of L-glutamate, a major excitatory amino acid, that is biologically inert. It demonstrates improved utilization of incident light.
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PENB-L-Glutamate
T33911
PENB-L-Glutamate is a caged glutamate.
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L(+)-Monosodium glutamate monohydrate
L(+)-Monosodium glutamate monohydrate,MSG monohydrate,L-Glutamic acid monosodium salt monohydrate,Monosodium L-glutamate monohydrate
T353696106-04-3
L(+)-Monosodium glutamate monohydrate is a useful organic compound for research related to life sciences. The catalog number is T35369 and the CAS number is 6106-04-3.
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7-10 days
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1-Methyl L-Glutamate
T661136384-08-3
1-Methyl L-Glutamate is a useful organic compound for research related to life sciences. The catalog number is T66113 and the CAS number is 6384-08-3.
    7-10 days
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    1,5-Dihexadecyl N-(3-carboxy-1-oxopropyl)-L-glutamate
    T74875125401-63-0
    1,5-Dihexadecyl N-(3-carboxy-1-oxopropyl)-L-glutamate, a lipid, is essential in the synthesis of phospholipid vesicles and improves the encapsulation efficiency of proteins [1].
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    L-Lysine L-glutamate
    T210535408-52-6
    L-Lysine L-glutamate is a bioactive chemical.
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    MNI-caged-L-glutamate
    T23013295325-62-1
    rapidly and efficiently releases glutamate
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    6-8 weeks
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    Dimethyl L-glutamate
    Dimethyl glutamate
    T724606525-53-7
    Dimethyl L-glutamate (Dimethyl glutamate), a membrane-permeable derivative of glutamate, stimulates glucose-induced insulin release, suppresses K_ATP channel activities, inhibits E. gracilis growth, and causes abnormal cell division. This compound is utilized in diabetes research, focusing on glucose transport, phosphorylation, and metabolism.
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    6-8 weeks
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    MNI-caged-L-glutamate TFA
    T843902226362-29-2
    MNI-caged-L-glutamate, a derivative of glutamate conjugated with a 4-methoxy-7-nitroindolinyl (MNI) photoprotective group, remains pharmacologically inactive at neuronal glutamate receptors at concentrations up to mM. Upon light exposure (300 - 380 nm excitation), it rapidly releases L-glutamate by cleaving the MNI group within submicroseconds. This characteristic enables the investigation of fast synaptic glutamate receptor mechanisms in situ.
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    8-10 weeks
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