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New maleimide spirobenzopyran derivatives as photochromic labels for macromolecules with sulfhydryl groups

Alexey Vladimirovich Laptev 1
Alexey Vladimirovich Laptev
Alexei Yur'evich Lukin 1
Alexei Yur'evich Lukin
Nikolay Evgen'evich Belikov 1
Nikolay Evgen'evich Belikov
Olga Viktorovna Demina 2
Olga Viktorovna Demina
Andrey Aleksandrovich Khodonov 1
Andrey Aleksandrovich Khodonov
Vitalii Ivanovich Shvets 1
Vitalii Ivanovich Shvets
Published 2014-06-25
CommunicationVolume 24, Issue 4, 245-246
6
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Laptev A. V. et al. New maleimide spirobenzopyran derivatives as photochromic labels for macromolecules with sulfhydryl groups // Mendeleev Communications. 2014. Vol. 24. No. 4. pp. 245-246.
GOST all authors (up to 50) Copy
Laptev A. V., Lukin A. Y., Belikov N. E., Demina O. V., Khodonov A. A., Shvets V. I. New maleimide spirobenzopyran derivatives as photochromic labels for macromolecules with sulfhydryl groups // Mendeleev Communications. 2014. Vol. 24. No. 4. pp. 245-246.
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TY - JOUR
DO - 10.1016/j.mencom.2014.06.020
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2014.06.020
TI - New maleimide spirobenzopyran derivatives as photochromic labels for macromolecules with sulfhydryl groups
T2 - Mendeleev Communications
AU - Laptev, Alexey Vladimirovich
AU - Lukin, Alexei Yur'evich
AU - Belikov, Nikolay Evgen'evich
AU - Demina, Olga Viktorovna
AU - Khodonov, Andrey Aleksandrovich
AU - Shvets, Vitalii Ivanovich
PY - 2014
DA - 2014/06/25
PB - Mendeleev Communications
SP - 245-246
IS - 4
VL - 24
ER -
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@article{2014_Laptev,
author = {Alexey Vladimirovich Laptev and Alexei Yur'evich Lukin and Nikolay Evgen'evich Belikov and Olga Viktorovna Demina and Andrey Aleksandrovich Khodonov and Vitalii Ivanovich Shvets},
title = {New maleimide spirobenzopyran derivatives as photochromic labels for macromolecules with sulfhydryl groups},
journal = {Mendeleev Communications},
year = {2014},
volume = {24},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2014.06.020},
number = {4},
pages = {245--246},
doi = {10.1016/j.mencom.2014.06.020}
}
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Laptev, Alexey Vladimirovich, et al. “New maleimide spirobenzopyran derivatives as photochromic labels for macromolecules with sulfhydryl groups.” Mendeleev Communications, vol. 24, no. 4, Jun. 2014, pp. 245-246. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2014.06.020.

Abstract

Two new photochromic labels of spiro[chromene-2,2’-indole] series supplied with 5-positioned maleimide moieties suitable for labelling macromolecules with sulfhydryl groups were synthesized.

References

1.
The Stability of N-Ethylmaleimide and its Reaction with Sulfhydryl Groups
Gregory J.D.
Journal of the American Chemical Society, 1955
2.
Reactions of N-ethylmaleimide with peptides and amino acids
Smyth D., Blumenfeld O., Konigsberg W.
Biochemical Journal, 1964
3.
Characterization of the receptor binding residues of kisspeptins by positional scanning using peptide photoaffinity probes
Misu R., Oishi S., Setsuda S., Noguchi T., Kaneda M., Ohno H., Evans B., Navenot J., Peiper S.C., Fujii N.
Bioorganic and Medicinal Chemistry Letters, 2013
4.
αvβ3-Integrin-targeting lanthanide complex: Synthesis and evaluation as a tumor-homing luminescent probe
Ito T., Inoue M., Akamatsu K., Kusaka E., Tanabe K., Nishimoto S.
Bioorganic and Medicinal Chemistry Letters, 2011
5.
DOTA derivatives for site-specific biomolecule-modification via click chemistry: Synthesis and comparison of reaction characteristics
Wängler C., Schäfer M., Schirrmacher R., Bartenstein P., Wängler B.
Bioorganic and Medicinal Chemistry, 2011
6.
Multivalent, High-Relaxivity MRI Contrast Agents Using Rigid Cysteine-Reactive Gadolinium Complexes
Garimella P.D., Datta A., Romanini D.W., Raymond K.N., Francis M.B.
Journal of the American Chemical Society, 2011
7.
10.1016/j.mencom.2014.06.020_sbref0010e
Liu
Bioconjugate Chem., 2012
8.
Evaluation of a Maleimido Derivative of NOTA for Site-Specific Labeling of Affibody Molecules
Tolmachev V., Altai M., Sandström M., Perols A., Karlström A.E., Boschetti F., Orlova A.
Bioconjugate Chemistry, 2011
10.
Displacement Assay for the Detection of Stabilizers of Inactive Kinase Conformations
Klüter S., Grütter C., Naqvi T., Rabiller M., Simard J.R., Pawar V., Getlik M., Rauh D.
Journal of Medicinal Chemistry, 2009
12.
10.1016/j.mencom.2014.06.020_sbref0025a
Sakata
J. Org. Chem., 2005, 2009
13.
10.1016/j.mencom.2014.06.020_sbref0025b
Marriott
US Patent 0195309, 2007
14.
Laptev A.V., Lukin A.Y., Belikov N.E., Barachevskii V.A., Demin O.V., Khodonov A.A., Varfolomeev S.D., Shvets V.I.
Mendeleev Communications, 2013
16.
10.1016/j.mencom.2014.06.020_sbref0040a
Photochromism: Molecules and Systems, 2003
17.
Synthesis and properties of spiropyrans that are capable of reversible opening of the pyran ring (review)
Zakhs �.R., Martynova V.M., �fros L.S.
Chemistry of Heterocyclic Compounds, 1979
18.
Synthesis and photochromic reaction kinetics of unsaturated spiropyran derivatives
Demina O.V., Levin P.P., Belikov N.E., Laptev A.V., Lukin A.Y., Barachevsky V.A., Shvets V.I., Varfolomeev S.D., Khodonov A.A.
Journal of Photochemistry and Photobiology A: Chemistry, 2013
19.
Synthesis and study of the photochromic behavior of 3-[6′-nitro-1,3,3-trimethylspiro(indolino-2,2′-[2H]-chromen-5-yl)]propenoic acid and its ethyl ester
Laptev A.V., Lukin A.Y., Belikov N.E., Zemtsov R.V., Shvets V.I., Demina O.V., Varfolomeev S.D., Barachevskii V.A., Khodonov A.A.
High Energy Chemistry, 2010