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Merck
CN

C0910

Cibacron Blue 3GA Agarose

Type 100, saline suspension

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About This Item

UNSPSC Code:
23151817
PubChem Substance ID:
329774826
MDL number:
MFCD00043102

Key Documents

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InChI

1S/C29H20ClN7O11S3.3Na/c30-27-35-28(33-13-4-3-5-15(10-13)49(40,41)42)37-29(36-27)34-18-9-8-14(11-20(18)50(43,44)45)32-19-12-21(51(46,47)48)24(31)23-22(19)25(38)16-6-1-2-7-17(16)26(23)39;;;/h1-12,32H,31H2,(H,40,41,42)(H,43,44,45)(H,46,47,48)(H2,33,34,35,36,37);;;/q;3*+1/p-3

SMILES string

[Na+].[Na+].[Na+].Nc1c(cc(Nc2ccc(Nc3nc(Cl)nc(Nc4cccc(c4)S([O-])(=O)=O)n3)c(c2)S([O-])(=O)=O)c5C(=O)c6ccccc6C(=O)c15)S([O-])(=O)=O

InChI key

VZPXDCIISFTYOM-UHFFFAOYSA-K

type

Type 100

form

saline suspension

extent of labeling

0.05-0.2 μmol per mL

matrix

4% beaded agarose

capacity

0.5-3 mg/mL binding capacity (bovine serum albumin)

storage temp.

2-8°C

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Physical form

Suspension in 0.5 M NaCl containing 0.02% thimerosal

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
113H9550

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Younis Baqi et al.
Journal of medicinal chemistry, 53(5), 2076-2086 (2010-02-12)
ecto-5'-Nucleotidase (eN, CD73) plays a major role in controlling extracellular adenosine levels. eN inhibitors have potential as novel drugs, for example, for the treatment of cancer. In the present study, we synthesized and investigated a series of 55 anthraquinone derivatives
Christa E Müller et al.
Bioorganic & medicinal chemistry letters, 16(23), 5943-5947 (2006-09-26)
Polyoxotungstates were identified as potent inhibitors of NTPDases1, 2, and 3. The most potent compound was K(6)H(2)[TiW(11)CoO(40)], exhibiting K(i) values of 0.140 microM (NTPDase1), 0.910 microM (NTPDase2), and 0.563 microM (NTPDase3). One of the compounds, (NH(4))(18)[NaSb(9)W(21)O(86)], was selective for NTPDases2
Andreas Brunschweiger et al.
Journal of medicinal chemistry, 51(15), 4518-4528 (2008-07-18)
Ecto-nucleoside triphosphate diphosphohydrolases (E-NTPDases, subtypes 1, 2, 3, 8 of NTPDases) dephosphorylate nucleoside tri- and diphosphates to the corresponding di- and monophosphates. In the present study we synthesized adenine and uracil nucleotide mimetics, in which the phosphate residues were replaced
Stefanie Weyler et al.
Bioorganic & medicinal chemistry letters, 18(1), 223-227 (2007-11-17)
A library of anilinoanthraquinone derivatives was synthesized by parallel Ullmann coupling reaction of bromaminic acid with aniline derivatives in solution using a compact parallel synthesizer. The products were purified by HPLC and evaluated as antagonists at mouse and human P2Y2
Petra Hillmann et al.
Journal of medicinal chemistry, 52(9), 2762-2775 (2009-05-08)
The P2Y(2) receptor, which is activated by UTP, ATP, and dinucleotides, was studied as a prototypical nucleotide-activated GPCR. A combination of receptor mutagenesis, determination of its effects on potency and efficacy of agonists and antagonists, homology modeling, and chemical experiments
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