Click Chemistry Probes

The term “click chemistry” was coined to describe a class of efficient and selective reactions that can be used to join molecules together rapidly and in high yield. This class of chemical reactions uses bio-orthogonal or biologically unique moieties to label and join two molecules of interest in a two-step procedure. By labeling a biological moiety with a fluorescent dye, one can track the progress of the biomolecule within a particular environment and also observe interactions with other entities using an array of fluorescent technologies.

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Product Type
Kit 
(4)
Small Molecule 
(297)
Name
1-(2-((1,3-diphenyl-1,3,2-diazaphospholidin-2-yl)oxy)ethyl)-3-phenylthiourea 
(1)
2-butyl-1,3-diphenyl-1,3,2-diazaphospholidine 
(1)
Alkynyl Cholesterol 
(1)
Alkynyl 4-oxo-2-nonenal (aONE) 
(1)
Alkynyl 7-Dehydrocholesterol Epoxide 
(1)
Alkynyl Secosterol A 
(1)
Alkynyl 4-hydroxy-2-nonenal (aHNE) 
(1)
Alkynyl 7-Dehydrocholesterol 
(1)
Alkynyl Arachidonic Acid (aAA) 
(1)
Alkynyl Cholesterol Epoxide 
(1)
Alkynyl hydrazide 
(1)
Alkynyl iodoacetamide 
(1)
Alkynyl Lathosterol 
(1)
Alkynyl Linoleic Acid (aLA) 
(1)
Alkynyl oleic acid 
(1)
Alkynyl palmitic acid 
(1)
Alkynyl Secosterol B 
(1)
Alkynyl stearic acid 
(1)
Biotin-Alkyne 
(1)
Biotin-Azide 
(1)
Cy3 - Alkyne 
(2)
Cy3 - Azide 
(2)
Cy5 - Alkyne 
(2)
Cy5 - Azide 
(2)
Fmoc-Phe(4-N3)-OH 
(1)
ODIBO-EG4-NHS, ODIBO-TEG-NHS 
(1)
Photo-BAPTA, tetramethyl ester 
(1)
Photo-DIBO-EG4-SH, Photo-DIBO-TEG-SH 
(1)
Photo-ODIBO-EG4-NHS; Photo-ODIBO-TEG-NHS 
(1)
Propargyl-Maleimide (1-(Prop-2-yn-1-yl)-1H-pyrrole-2,5-dione ) 
(2)
Pyrene azide 1 
(3)
UV Cleavable Biotin-Alkyne 
(1)
UV Cleavable Biotin-Azide 
(1)
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Quantum Yield
~0.1 
(3)
0.1 
(11)
0.2 
(12)
0.28 
(11)
0.35 
(5)
0.63 
(5)
0.9 
(3)
0.93 
(10)
0.95 
(12)
0.97 
(11)
(11)
Fluorescence quantum yield: 1.0 
(2)
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