914584
Phenylalanine-4′-azobenzene HCl
≥95%
别名:
(2S)-2-Amino-3-[4-(2-phenyldiazen-1-yl)phenyl]propanoic acid hydrochloride, (E)-2-Amino-3-(4-(phenyldiazenyl)phenyl)propanoic acid HCl, 4-(2-Phenyldiazenyl)-L-phenylalanine hydrochloride, 4-(Phenylazo)-L-phenylalanine, AzoF, Photoswitchable phenylalanine amino acid, Reversible photo-controllable unnatural amino acid
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关于此项目
经验公式（希尔记法）:
C15H16ClN3O2
化学文摘社编号:
分子量:
305.76
UNSPSC Code:
12352209
NACRES:
NA.22
MDL number:
Quality Segment
assay
≥95%
form
powder
storage temp.
2-8°C
SMILES string
Cl.N[C@@H](Cc1ccc(cc1)\N=N\c2ccccc2)C(=O)O
InChI key
LRSKKAMIJGFIDZ-GUFYRWSKSA-N
Application
Phenylalanine-4′-azobenzene HCl (AzoF) is a phenylalanine derivative with an azo bond that isomerizes upon UV irradiation from its E isomer to its Z isomer and reverts back at light above 400 nm. When incorporated into proteins or chemical probes, this reversibility is utilized as a photoswitch with spatial and temporal regulation within biological systems.
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
Product can be used with our line of photoreactors: Including Penn PhD (Z744035) & SynLED 2.0 (Z744080)
Other Notes
Light Regulation of Enzyme Allostery through Photo-responsive Unnatural Amino Acids
Photochemical control of enzymes using photoresponsive compounds on the basis of the interaction mechanism
Photochemical regulation of the activity of an endonuclease BamHI using an azobenzene moiety incorporated site-selectively into the dimer interface
Photochemical control of enzymes using photoresponsive compounds on the basis of the interaction mechanism
Photochemical regulation of the activity of an endonuclease BamHI using an azobenzene moiety incorporated site-selectively into the dimer interface
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable