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251650

Damnacanthal

A cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase.

Synonim(y):

Damnacanthal, 3-Hydroxy-1-methoxyanthraquinone-2-aldehyde

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Rozmiar/SKUDostępnośćCena netto
1 mg
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1020,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C16H10O5
Numer CAS:
Masa cząsteczkowa:
282.25
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥95% (HPLC)
Form:
solid
Storage condition:
OK to freeze, protect from light

1020,00 zł


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Quality Segment

assay

≥95% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

orange-yellow

solubility

DMSO: 5 mg/mL

shipped in

ambient

storage temp.

−20°C

SMILES string

O(C)c1c2c(cc(c1C=O)O)C(=O)c3c(cccc3)C2=O

InChI

1S/C16H10O5/c1-21-16-11(7-17)12(18)6-10-13(16)15(20)9-5-3-2-4-8(9)14(10)19/h2-7,18H,1H3

InChI key

IPDMWUNUULAXLU-UHFFFAOYSA-N

General description

A cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase. Inhibits p56lck autophosphorylation (IC50 = 17 nM) and phosphorylation of an exogenous peptide by p56lck (IC50 = 620 nM). Exhibits over 100-fold greater selectivity for p56lck over PKA and PKC, 40-fold greater selectivity for p56lck over EGF receptor kinase, c-ErbB2, insulin receptor kinase, and PDGF receptor kinase, and 7 - 20-fold greater selectivity for p56lck over p60src and p59fyn. Inhibition of p56lck is not significantly affected by the presence of sulfhydryl reagents. Also known to have antimalarial properties and to reverse the phenotype of ras-transformed cells.

Biochem/physiol Actions

Cell permeable: yes
Primary Target
p56lck autophosphorylation
Product does not compete with ATP.
Reversible: yes
Target IC50: 17 nM against p56lck autophosphorylation

Packaging

Packaged under inert gas

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.

Other Notes

Faltynek, C.R., et al. 1995. Biochemistry34, 12404.
Hiramatsu, T., et al. 1993. Cancer Lett.73, 161.
Koumaglo, K., et al. 1992. Planta Med.58, 533.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)
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Ta pozycja
390602218710553014
description

A cell-permeable, potent, reversible, and selective inhibitor of p56lck tyrosine kinase.

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A cell-permeable, hydroxylated metabolite of HA 1077 that displays anti-anginal properties.

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description

The Raf Kinase Inhibitor IV, also referenced under CAS 303727-31-3, controls the biological activity of Raf Kinase. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

assay

≥95% (HPLC)

assay

≥98% (HPLC)

assay

≥95% (HPLC)

assay

≥97% (HPLC)

form

solid

form

liquid

form

solid

form

solid

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

manufacturer/tradename

Calbiochem®

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

storage condition

OK to freeze, protect from light

storage condition

OK to freeze, protect from light

storage condition

protect from light, OK to freeze

storage condition

protect from light, OK to freeze


Klasa składowania

11 - Combustible Solids

wgk

WGK 1



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