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SR10067, REV-ERB Agonist

SR10067, REV-ERB Agonist

$129.00
A potent and specific synthetic REV-ERB agonist.
Catalog No. Unit Price Qty
M60240-2s 2 mg solid $129.00

Details

Product Information
Molecular Weight: 465.58
Formula: C31H31NO3
Purity: ≥98%
CAS#: n/a
Solubility: DMSO up to 50 mM
Chemical Name: (3-((4-(tert-butoxy)phenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)(naphthalen-1-yl)methanone
Storage: Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year.

Biological Activity:

SR10067 is a potent and specific synthetic REV-ERB agonist that binds to REV-ERB-α with an EC50 ~170 nM and REV-ERB-β with EC50 ~160 nM. Potency of SR10067 was also considerably better in a cotransfection assay using full-length REV-ERBa along with the BMAL1 promoter luciferase reporter (EC50 ~140 nM). It also has good in vivo plasma/brain exposure. Comparing to SR9011 and SR9009, SR10067 has 4-5 folds improvement in potency both in vitro and in vivo. IP administration of SR10067 regulates sleep architecture and emotional behaviour in mice. It induces wakefulness and reduces REM and slow-wave sleep. It can also reduce anxiety-like behaviour. These results indicate that pharmacological targeting of REV-ERB may lead to the development of novel therapeutics to treat sleep disorders and anxiety.

How to Use:


In vitro: SR10067 was used at 5-10 µM concentration in vitro and in cellular assays.
In vivo: IP administration of SR10067 was used at 30 mg/kg to mice.

Reference:

  • 1. Banerjee S, et al. Pharmacological targeting of the mammalian clock regulates sleep architecture and emotional behaviour. (2014) Nat Commun. 5:5759.

SR10067_spec.pdf   
SR10067_MSDS.pdf   

Products are for research use only. Not for human use. 

Description

Details

Product Information
Molecular Weight: 465.58
Formula: C31H31NO3
Purity: ≥98%
CAS#: n/a
Solubility: DMSO up to 50 mM
Chemical Name: (3-((4-(tert-butoxy)phenoxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)(naphthalen-1-yl)methanone
Storage: Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year.

Biological Activity:

SR10067 is a potent and specific synthetic REV-ERB agonist that binds to REV-ERB-α with an EC50 ~170 nM and REV-ERB-β with EC50 ~160 nM. Potency of SR10067 was also considerably better in a cotransfection assay using full-length REV-ERBa along with the BMAL1 promoter luciferase reporter (EC50 ~140 nM). It also has good in vivo plasma/brain exposure. Comparing to SR9011 and SR9009, SR10067 has 4-5 folds improvement in potency both in vitro and in vivo. IP administration of SR10067 regulates sleep architecture and emotional behaviour in mice. It induces wakefulness and reduces REM and slow-wave sleep. It can also reduce anxiety-like behaviour. These results indicate that pharmacological targeting of REV-ERB may lead to the development of novel therapeutics to treat sleep disorders and anxiety.

How to Use:


In vitro: SR10067 was used at 5-10 µM concentration in vitro and in cellular assays.
In vivo: IP administration of SR10067 was used at 30 mg/kg to mice.

Reference:

  • 1. Banerjee S, et al. Pharmacological targeting of the mammalian clock regulates sleep architecture and emotional behaviour. (2014) Nat Commun. 5:5759.

SR10067_spec.pdf   
SR10067_MSDS.pdf   

Products are for research use only. Not for human use. 

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