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Merck
CN

SML3099

Glyght

≥95% (HPLC)

别名:

(E)-5-Phenyl-7-(pyridin-2-yldiazenyl)-1,3-dihydro-2H-benzo[e][1,4]diazepin-2-one

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关于此项目

经验公式(希尔记法):
C20H15N5O
化学文摘社编号:
分子量:
341.37
UNSPSC Code:
12352200
NACRES:
NA.77
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InChI

1S/C20H15N5O/c26-19-13-22-20(14-6-2-1-3-7-14)16-12-15(9-10-17(16)23-19)24-25-18-8-4-5-11-21-18/h1-12H,13H2,(H,23,26)/b25-24+

InChI key

MQMSSOZUTXPEIC-OCOZRVBESA-N

SMILES string

O=C1NC(C=CC(/N=N/C2=NC=CC=C2)=C3)=C3C(C4=CC=CC=C4)=NC1

assay

≥95% (HPLC)

form

powder

storage condition

protect from light at room temperature

color

yellow to orange

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

Quality Level

General description

Glyght is a benzodiazepine-containing azobenzene compound that acts as a light-controlled negative allosteric modulator that is selective to glycine receptors. It is a powerful and effective compound that can operate in vivo. Glyght attaches to an allosteric site within the interface between the extracellular and transmembrane domains. It is an effective tool for researchers since it has broad activity in both homo- and heteromeric GlyRs across several species of fish and mammals. Moreover, Glyght is photo-switchable at 365 nm for trans-cis isomerization and 455 to 530 nm for cis-trans isomerization.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

Lot/Batch Number

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Photomodulation of Inhibitory Neurotransmission. Insights from Molecular Modeling
Nin-Hill
Biophysical Journal, 118 (2020)
Alexandre M J Gomila et al.
Cell chemical biology, 27(11), 1425-1433 (2020-08-28)
Glycine receptors (GlyRs) are indispensable for maintaining excitatory/inhibitory balance in neuronal circuits that control reflexes and rhythmic motor behaviors. Here we have developed Glyght, a GlyR ligand controlled with light. It is selective over other Cys-loop receptors, is active in vivo

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