ChemicalBook--->CAS DataBase List--->1428-67-7

1428-67-7

1428-67-7 Structure

1428-67-7 Structure
IdentificationBack Directory
[Name]

2,3-BIS(4-HYDROXYPHENYL)-PROPIONITRILE
[CAS]

1428-67-7
[Synonyms]

DPN
SC-4473
Diarylpropionitrile
2,3-bis(p-hydroxyphenyl)propionitrile
2,3-BIS(4-HYDROXYPHENYL)-PROPIONITRILE
propionitrile,2,3-bis(p-hydroxyphenyl)
2,3-Bis(4-hydroxyphenyl)propanenitrile
2,3-Bis(4-hydroxyphenyl)propiononitrile
2,3-Bis(4-hydroxyphenyl)propionitrile >
Benzenepropanenitrile, 4-hydroxy-α-(4-hydroxyphenyl)-
4-Hydroxy-alpha-(4-hydroxyphenyl)benzenepropanenitrile
[Molecular Formula]

C15H13NO2
[MDL Number]

MFCD01695412
[MOL File]

1428-67-7.mol
[Molecular Weight]

239.27
Chemical PropertiesBack Directory
[Melting point ]

200.0 to 204.0 °C
[RTECS ]

UG0900000
[storage temp. ]

Desiccate at -20°C
[solubility ]

DMSO: soluble10mg/mL, clear
[form ]

powder
[color ]

white to beige
[Water Solubility ]

Soluble in 1eq. NaOH (30 mM), ethanol (100 mM), DMSO (100 mM), DMF (~30 mg/ml), and water (0.5 mg/ml at 25°C).
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
Safety DataBack Directory
[Hazard Codes ]

Xi,N
[Risk Statements ]

36-50
[Safety Statements ]

26-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
[HS Code ]

2926.90.4801
[HazardClass ]

9
Hazard InformationBack Directory
[Description]

DPN (1428-67-7) is a potent estrogen ERβ receptor agonist. Displays a 70-fold selectivity over ERα, EC50 = 0.85 and 66 nM, respectively.1 Regulates expression of GluR1, 2 and 3 in rat hippocampus.2 Ameliorates portal hypertension in a carbon tetrachloride-induced liver cirrhosis rat model.3 Stimulates proliferation of androgen-independent prostate cancer cell line PC-3 via a novel pathway involving ERβ-mediated activation of β-catenin.4 A useful tool for elucidating the biological function of ERβ.5
[Uses]

2,3-Bis(4-hydroxyphenyl)propionitrile is an estrogen receptor β and α specific with pro- and anti-nociceptive actions in mice.
[Definition]

ChEBI: A nitrile that is acetonitrile in which one of the hydrogens is replaced by a 4-hydroxyphenyl group while a second hydrogen is replaced by a 4-hydroxybenzyl group. It is a specific agonist for estrogen receptor beta (ERbeta).
[Biological Activity]

Highly potent estrogen ER β receptor agonist with a 70-fold selectivity over ER α (EC 50 values are 0.85 and 66 nM respectively). Relaxes mesenteric arteries in vitro .
[Biochem/physiol Actions]

2,3-Bis(4-hydroxyphenyl)-propionitrile (Diarylprepionitrile, DPN) is an ERβ-selective agonist; IC50 = 15nM. DPN protects WT and ARKO mice and significantly decreases IL-1β following LPS treatment in young adult-derived microglia. PPT (Cat. No.H6036, ERa agonist) enhances cell proliferation, while DPN inhibits it. PPT increases Bcl-2 expression, while DPN decreases it. DPN also elevates Bax expression. DPN induces a dose-dependent increase on vitellogenin synthesis. PPT and DPN are effective in dynamically, but differentially regulating intracellular calcium signaling in hippocampal neurons. DPN is more efficacious than PPT in potentiating a physiological concentration of glutamate-induced intracellular Ca2+ rise in these neurons. DPN prevents the development of prostatic hyperplasia and inflammation in testosterone-treated LuRKO mice.
[storage]

Desiccate at -20°C
[References]

1) Meyers et al. (2001), Estrogen receptor-beta potency-selective ligands: structure-activity relationship studies of diarylpropionitriles and their acetylene and polar analogues; J. Med. Chem., 44 4230 2) Waters et al. (2009), Estrogen receptor alpha and beta specific agonists regulate expression of synaptic proteins in rat hippocampus; Brain Res., 1290 1 3) Zhang et al. (2016), Role of estrogen receptor beta selective agonist in ameliorating portal hypertension in rats with CC14-induced liver cirrhosis; World J. Gastroenterol., 22 4484 4) Lombardi et al. (2016), Estrogen receptor beta (ERβ) mediates expression of β-catenin and proliferation in prostate cancer cell line PC-3; Mol. Cell. Endocrin. 430 12 5) Harrington et al. (2003), Activities of estrogen receptor alpha- and beta-selective ligands at diverse estrogen responsive gene sites mediating transactivation and transrepression; Mol. Cell. Endocrinol., 206 13
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