Basic information Safety Supplier Related

BODIPY 630/650-X NHS Ester (Succinimidyl Ester)

Basic information Safety Supplier Related

BODIPY 630/650-X NHS Ester (Succinimidyl Ester) Basic information

Product Name:
BODIPY 630/650-X NHS Ester (Succinimidyl Ester)
Synonyms:
  • BODIPY 630/650-X NHS Ester (Succinimidyl Ester)
  • BDY 630-X, SE
  • (T-4)-[2,5-Dioxo-1-pyrrolidinyl 6-[[2-[4-[2-[5-[[5-(2-thienyl)-2H-pyrrol-2-ylidene-κN]methyl]-1H-pyrrol-2-yl-κN]ethenyl]phenoxy]acetyl]amino]hexanoato]difluoroboron
  • BODIPY?630/650-XNHSEster(SuccinimidylEster), >97%
  • BDP 630/650 NHS ester
  • BODIPY 630/650X succinimide ester
  • BODIPY 630-X SE
CAS:
380367-48-6
MF:
C33H31BF2N4O6S
MW:
660.5
Mol File:
380367-48-6.mol
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BODIPY 630/650-X NHS Ester (Succinimidyl Ester) Chemical Properties

solubility 
Soluble in DMF, DMSO
form 
A solid
color 
Dark purple to black
Appearance
Solid Powder
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BODIPY 630/650-X NHS Ester (Succinimidyl Ester) Usage And Synthesis

Description

BODIPY 630/650X succinimide ester (SE) is an amine-reactive fluorescent probe that contains an integrated aminohexanoyl linker (X). It displays excitation/emission maxima of 630/650 nm, respectively. BODIPY 630/650X SE has been used, linked to adenosine A1 receptor ligands, as a fluorescent probe to quantify ligand-receptor binding using fluorescence correlation spectroscopy.

Uses

BDY 630-X, SE, can be used as Fluorescent reagent for the labeling of amines.

Definition

ChEBI: BODIPY 630/650-X is a pyrrolidinone and a BODIPY dye. It has a role as a fluorochrome. It is functionally related to a 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene.

References

[1] S J BRIDDON. Quantitative analysis of the formation and diffusion of A1-adenosine receptor-antagonist complexes in single living cells.[J]. Proceedings of the National Academy of Sciences of the United States of America, 2004, 101 13: 4673-4678. DOI: 10.1073/pnas.0400420101
[2] CLARE L. DALE B K S Hill. New potent, short-linker BODIPY-630/650? labelled fluorescent adenosine receptor agonists[J]. MedChemComm, 2012, 3 1: 333-338. DOI: 10.1039/c2md00247g

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