Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy-

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Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy- Basic information
Product Name:Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy-
Synonyms:Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy-;ZT-1a, 10 mM in DMSO;ZT-1a
CAS:212135-62-1
MF:C22H15Cl3N2O2
MW:445.73
EINECS:
Product Categories:
Mol File:212135-62-1.mol
Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy- Structure
Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy- Chemical Properties
Boiling point 538.7±50.0 °C(Predicted)
density 1.442±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: 125 mg/mL (280.44 mM)
form Solid
pka7+-.0.43(Predicted)
color White to off-white
Safety Information
MSDS Information
Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy- Usage And Synthesis
UsesZT-1a is a potent, non-ATP-competitive and selective SPAK inhibitor. ZT-1a inhibits SPAK activity with IC50s of 44.3, 35.0, 46.7 μM at ATP concentrations of 0.01, 0.1 and 1 mM, respectively[1].
in vivo

ZT-1a (10-100 mg/kg) inhibits SPAK-dependent cation-Cl cotransporters (CCC) phosphorylation in vivo[1].

Animal Model:Naive mice[1]
Dosage:10, 30, 50, and 100mg/kg
Administration:Intraperitoneal (i.p.) administration
Result:Inhibited SPAK-dependent cation-Cl- cotransporters (CCC) phosphorylation in vivo.
References[1] Jinwei Zhang, et al. Modulation of Brain cation-Cl- Cotransport via the SPAK Kinase Inhibitor ZT-1a. Nat Commun. 2020 Jan 7;11(1):78. DOI:10.1038/s41467-019-13851-6
Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy- Preparation Products And Raw materials
Tag:Benzamide, 5-chloro-N-[5-chloro-4-[(4-chlorophenyl)cyanomethyl]-2-methylphenyl]-2-hydroxy-(212135-62-1) Related Product Information
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