Phycocyanobilin

Catalog#: P14137

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Phycocyanobilin (Microbial Source)

MDL: MFCD22684686

Phycocyanobilin SDS

Phycocyanobilin TDS

Molecular weight: 586.68 g/mol

Molecular Formula: C33H38N4O6                               

CAS Number:  20298-86-6

Storage:  Store at -20 °C, protect from light

Synonyms:          

phycocyanobilin, CTK6D0370, 20298-86-6, NCI60_011911, FT-0673886, 3-[2-[[3-(2-carboxyethyl)-5-[(4-ethyl-3-methyl-5-oxo-pyrrol-2-yl)methylene]-4-methyl-pyrrol-2-ylidene]methyl]-5-[(3-ethylidene-4-methyl-5-oxo-pyrrolidin-2-ylidene)methyl]-4-methyl-1h-pyrrol-3-yl]propanoic acid

Field of Interest: Natural Products From Algae, Light Harvesting Proteins, Photochromes and Photosynthesis sensing

Background: Phycocyanobilin  is a linear pyrrole blue phycobilin based natural product found in Spirulina species that acts a photosensor in light harvesting arrays in photosynthesis 1,2   It also is a potent peroxyl radical scavenger and is indicative of specific algae species as fluorometric markers of  different photosynthetic antenna pigments .3,4

** Please Note: This material is sold with a specification of 65% purity.  This compound is known to be susceptible to isomerization under specific conditions.  Unfortunately, during the purity determination for this product, the material is put under the conditions where isomerization may occur. As a result, we have low confidence in the actual purity of this material and the specification is based on our current best methods for analysis.**

References:

1.) Levskaya, Anselm; Weiner, Orion D.; Lim, Wendell A.; Voigt, Christopher A., Spatiotemporal control of cell signalling using a light-switchable protein interaction Nature (London, United Kingdom) (2009), 461(7266), 997-1001. DOI:10.1038/nature08446.

2.)  Hughes, Jon; Lamparter, Tilman; Mittmann, Franz; Hartmann, Elmar; Wilde, Annegret; Borner, Thomas A prokaryotic phytochrome , Nature (London) (1997), 386(6626), 663, DOI:10.1038/386663a0.

3.)  Bhat, Vadiraja B.; Madyastha, K. M., C-phycocyanin: a potent peroxyl radical scavenger in vivo and in vitro, Biochemical and Biophysical Research Communications (2000), 275(1), 20-25. DOI:10.1006/bbrc.2000.3270.

4.)  Beutler, M.; Wiltshire, K. H.; Meyer, B.; Moldaenke, C.; Luering, C.; Meyerhoefer, M.; Hansen, U.-P.; Dau, H., A fluorometric method for the differentiation of algal populations in vivo and in situ, Photosynthesis Research (2002), 72(1), 39-53.

Categories

Porphyrins

Scaffold/Subcategory

Natural Porphyrins & Derivatives

CAS #

[20298-86-6]

Purity %

65% – Please see product note

Smiles

CCC1=C(C)/C(NC1=O)=CC1=NC(=CC2=C(CCC(O)=O)C(C)=C(N2)C=C2NC(=O)C(C)C2=C/C)C(CCC(O)=O)=C1C

Molecular Weight

586.678

Molecular Formula

C33H38N4O6

Functional Groups

Alkene, Alkyl, Amide, Carboxy, Carboxylic Acid

Porphyrin Family

Bilirubin Derivatives, Linear Tetra-Pyrroles

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