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ChemicalBook--->CAS DataBase List--->265646-85-3

265646-85-3

265646-85-3 Structure

265646-85-3 Structure
IdentificationBack Directory
[Name]

Endovion
[CAS]

265646-85-3
[Synonyms]

NS3728
Endovion
NS3728 >=98% (HPLC)
Urea, N-[3,5-bis(trifluoromethyl)phenyl]-N'-[4-bromo-2-(2H-tetrazol-5-yl)phenyl]-
[Molecular Formula]

C16H9BrF6N6O
[MDL Number]

MFCD28147607
[MOL File]

265646-85-3.mol
[Molecular Weight]

495.18
Chemical PropertiesBack Directory
[density ]

1.791±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble to 100 mM in DMSO and to 50 mM in ethanol
[form ]

Solid
[pka]

3.95±0.10(Predicted)
[color ]

White to off-white
[Water Solubility ]

Water : < 0.1 mg/mL (insoluble)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Spectrum DetailBack Directory
[Spectrum Detail]

Endovion(265646-85-3)1HNMR
Hazard InformationBack Directory
[Biological Activity]

Endovion (NS3728) is an anion channel inhibitor (eg chloride channel) and a specific VRAC/VSOAC blocker.
[in vitro]

Endovion (NS3728, 10-100 μM) reduces TNFα-induced apoptosis and increases p53-protein level as well as downstream signaling, eg, expression of p21 Waf1/Cip1 , Bax, Noxa, MDM2, and activation of Caspase-9/-3 in Cisplatin-sensitive cells.
Endovion (NS3728, 10 μM) inhibits cell proliferation in Capan-1, AsPC-1 and BxPC-3 cell lines.

Western Blot Analysis

< td class="col1"> Result:
Cell Line: Wild -type, resistant, and transiently transfected A2780 cells.
Concentration: 10-100 μM. < /td>
Incubation Time: 18 or 4.5 h.
Reduced the maximal taurine rate constant more than 90% compared with the untreated control cells.
Resulted i n an increased LRRC8A protein expression.
Significantly reduced p53 and p21Waf1/Cip1 protein level in A2780WT cells.

Cell Proliferation Assay

Cell Line: Capan-1, AsPC-1, BxPC-3 and H6c7 cell lines.
Concentration: 10 μM.
Incubation Time: 24 h.
Result: Resulted in the most pronounced inhibition in all cell lines with 77 ± 26 % in Capan-1, 67 ± 9 % in AsPC-1, and 54 ± 8 % in BxPC-3 cells at +67 mV.
[target]

Chloride channel, VRAC/VSOAC.
ANO1.

[storage]

Store at -20°C
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