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915793

Sigma-Aldrich

Methyl-o-nitropiperonyllysine

≥95%

Sinónimos:

N6-((1-(6-Nitrobenzo[d][1,3]dioxol-5-yl)ethoxy)carbonyl)-L-lysine, Light-triggered decaging Lys, Photo-controlled amino acid, Photocaged amino acid, Photocleavable lysine derivative, mNPK

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About This Item

Fórmula empírica (notación de Hill):
C16H21N3O8
Número de CAS:
1221189-11-2
Peso molecular:
383.35
MDL number:
MFCD30474478
UNSPSC Code:
12352209
NACRES:
NA.22

Quality Level

100

assay

≥95%

form

powder

storage temp.

−20°C

SMILES string

[N+](=O)([O-])c1cc2c(cc1C(OC(=O)NCCCC[C@H](N)C(=O)O)C)OCO2

InChI

1S/C16H21N3O8/c1-9(27-16(22)18-5-3-2-4-11(17)15(20)21)10-6-13-14(26-8-25-13)7-12(10)19(23)24/h6-7,9,11H,2-5,8,17H2,1H3,(H,18,22)(H,20,21)/t9?,11-/m0/s1

InChI key

ZXXFKVZFDGUTQW-UMJHXOGRSA-N

Application

Methyl-o-nitropiperonyllysine (mNPK) trifluoroacetic acid is a photo-responsive unnatural amino acid (UAA) for spatiotemporal control of biological molecules or processes as reported by Kneuttinger et al. Irradiation with UV light decages the Lys amino acid, freeing the residue or protein for biological activity. Tools such as mNPK will find wide utility in light regulation of activity, allostery, and enzyme pathways.

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 Photoresponsive Unnatural Amino Acids

Precise Photoremovable Perturbation of a Virus-Host Interaction

Genetic code expansion in the mouse brain

Genetically encoded optical activation of DNA recombination in human cells

Bioorthogonal Chemical Activation of Kinases in Living Systems

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Referencia del producto
Descripción
Precios

907251

H-L-Photo-lysine HCl, ≥98%

907383

Fmoc-L-Photo-Lysine, ≥95%

908576

WinterGreen photocage, ≥95%

914584

Phenylalanine-4′-azobenzene HCl, ≥95%

914339

Fmoc-L-Lys(Nvoc)-OH, ≥98%

913588

O-(2-Nitrobenzyl)-L-tyrosine hydrochloride, ≥95%

914525

o-Nitropiperonyl-O-tyrosine

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Gong Zhang et al.
ACS central science, 2(5), 325-331 (2016-06-10)
Selective manipulation of protein kinases under living conditions is highly desirable yet extremely challenging, particularly in a gain-of-function fashion. Here we employ our recently developed bioorthogonal cleavage reaction as a general strategy for intracellular activation of individual kinases. Site-specific incorporation
Sarah B Erickson et al.
Angewandte Chemie (International ed. in English), 56(15), 4234-4237 (2017-03-16)
Viruses utilize distinct binding interactions with a variety of host factors to gain entry into host cells. A chemical strategy is described to precisely perturb a specific molecular interaction between adeno-associated virus and its host cell, which can be rapidly
Hanna Engelke et al.
ACS synthetic biology, 3(10), 731-736 (2014-06-17)
Controlled manipulation of proteins and their function is important in almost all biological disciplines. Here, we demonstrate control of protein activity with light. We present two different applications-light-triggered transcription and light-triggered protease cleavage-both based on the same concept of protein
Arnaud Gautier et al.
Journal of the American Chemical Society, 133(7), 2124-2127 (2011-01-29)
We report a general strategy for creating protein kinases in mammalian cells that are poised for very rapid activation by light. By photoactivating a caged version of MEK1, we demonstrate the specific, rapid, and receptor independent activation of an artificial
Olivia S Walker et al.
Journal of the American Chemical Society, 138(3), 718-721 (2016-01-14)
Isocitrate dehydrogenase is mutated at a key active site arginine residue (Arg172 in IDH2) in many cancers, leading to the synthesis of the oncometabolite (R)-2-hydroxyglutarate (2HG). To investigate the early events following acquisition of this mutation in mammalian cells we
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