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Merck

5.06216

Gap Junction Enhancer, PQ7

Synonym(s):

Gap Junction Enhancer, PQ7

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About This Item

Empirical Formula (Hill Notation):
C23H19F3N2O3
CAS Number:
Molecular Weight:
428.40
UNSPSC Code:
12352200

Assay

≥98% (HPLC)

Quality Level

form

powder

potency

100 nM IC50

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
protect from light

color

tan

solubility

DMSO: 100 mg/mL

storage temp.

2-8°C

General description

A cell-permeable quinoline derived compound with low toxicity that enhances gap junctional activity by about 16-fold (at ~500 nM) in T47D breast cancer cells and thereby potentiates the effect of chemotherapeutic agents. Blocks T47D cell colony formation (IC50 = 100 nM) and reduce the growth of T47D xenograft tumors by 100% in Nu/Nu mice. Increases caspase-3, - 8, and -9 expression by 1.6, 2.8, and 3.8-fold, respectively to induce apoptotic cell death. Can work synergistically with cisplatin to reduce or totally eliminate tumor growth. Increases the expression of connexins 26, 32, and 43 to allow more efficient trafficking of cisplatin.

Biochem/physiol Actions

Reversible: yes

Packaging

Packaged under inert gas

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

Shishido, S.N., et al. 2013. PLos One.8, e67174.
Shishido, S.N., et al. 2012. PLos One.7,e444963.
Heiniger, B., et al. 2010. Anticancer Res.30, 3927.
Shi, A., et al. 2008. Bioor. Med. Chem. Lett.18, 3364.

Legal Information

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

Disclaimer

Toxicity: Standard Handling (A)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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