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ChemicalBook--->CAS DataBase List--->15982-84-0

15982-84-0

15982-84-0 Structure

15982-84-0 Structure
IdentificationBack Directory
[Name]

Dual Specificity Protein Phosphatase 1/6 Inhibitor
[CAS]

15982-84-0
[Synonyms]

NSC 150117
(E/Z)-BCI (NSC150117)
(E/Z)-BCI(DUSP6 inhibitor)
Dual Specificity Protein Phosphatase 1/6 Inhibitor
1H-Inden-1-one, 3-(cyclohexylamino)-2,3-dihydro-2-(phenylmethylene)-
[Molecular Formula]

C22H23NO
[MDL Number]

MFCD20232928
[MOL File]

15982-84-0.mol
[Molecular Weight]

317.42
Chemical PropertiesBack Directory
[Boiling point ]

484.6±45.0 °C(Predicted)
[density ]

1.15±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[solubility ]

DMSO: 63 mg/mL (198.48 mM);Ethanol: 20 mg/mL (63.01 mM)
[form ]

solid
[pka]

7.74±0.20(Predicted)
[color ]

yellow
[Water Solubility ]

Water: Insoluble
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H412
[Precautionary statements ]

P273-P305+P351+P338
[HS Code ]

2922390090
Hazard InformationBack Directory
[Uses]

(E/Z)-BCI (NSC 150117) is a dual-specificity phosphatase 6 (DUSP6) inhibitor with anti-inflammatory activities. (E/Z)-BCI attenuates LPS-induced inflammatory mediators and ROS production in macrophage cells via activating the Nrf2 signaling axis and inhibiting the NF-κB pathway[1].
[in vivo]

(E/Z)-BCI hydrochloride (35 mg/kg; intraperitoneal injection; every 7 days; for four weeks; female BALB/c nude mice) treatment enhances cisplatin efficacy in PDX models[2].

Animal Model:Patient-derived xenograft (PDX) models (4-5-week-old female BALB/c nude mice)[2]
Dosage:35 mg/kg
Administration:Intraperitoneal injection; every 7 days; for four weeks
Result:Tumor weights in the PDX models treated plus CDDP were significantly suppressed compared with tumors from PDX model mice treated with either agent alone.
[storage]

Store at -20°C
[References]

[1] Zhang F, et al. DUSP6 Inhibitor (E/Z)-BCI Hydrochloride Attenuates Lipopolysaccharide-Induced Inflammatory Responses in Murine Macrophage Cells via Activating the Nrf2 Signaling Axis and Inhibiting the NF-κB Pathway. Inflammation. 2019 Apr;42(2):672-681. DOI:10.1007/s10753-018-0924-2
[2] Wu QN,et al. Pharmacological inhibition of DUSP6 suppresses gastric cancer growth and metastasis and overcomes cisplatin resistance. Cancer Lett. 2018 Jan 1;412:243-255. DOI:10.1016/j.canlet.2017.10.007
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