MCB-613

Modify Date: 2024-01-02 20:42:08

MCB-613 Structure
MCB-613 structure
Common Name MCB-613
CAS Number 1162656-22-5 Molecular Weight 304.386
Density 1.159±0.06 g/cm3 Boiling Point 510.4±50.0 °C at 760 mmHg
Molecular Formula C20H20N2O Melting Point N/A
MSDS N/A Flash Point 257.9±36.5 °C

 Use of MCB-613


MCB-613 is a potent, pan steroid receptor coactivator (SRC) stimulator.Target: SRCin vitro: MCB-613 exerts the greatest activation of SRC-1 in the primary screen, is confirmed to be a strong activator of all three SRCs. MCB-613 can super-stimulate SRCs' transcriptional activity. MCB-613 increases SRCs' interactions with other coactivators and markedly induces ER stress coupled to the generation of reactive oxygen species (ROS). MCB-613 selectively and reversibly binds to the RID of SRC-3, and selectively kills cancer cells including MCF-7 (breast), PC-3 (prostate), H1299 (lung), and HepG2 (liver) cells, without toxicity to mouse primary hepatocytes and mouse embryonic fibroblasts (MEFs). MCB-613 also increases SRCs' interactions with other coactivators and markedly induces ER stress coupled to the generation of reactive oxygen species (ROS). [1]in vivo: In an MCF-7 breast cancer mouse xenograft model, MCB-613 (20 mg/kg, i.p.) significantly and dramatically inhibits the growth of the tumor while causing no obvious animal toxicity and body weight less. [1]

 Names

Name 4-ethyl-2,6-bis(pyridin-3-ylmethylene)cyclohexanone
Synonym More Synonyms

 MCB-613 Biological Activity

Description MCB-613 is a potent, pan steroid receptor coactivator (SRC) stimulator.Target: SRCin vitro: MCB-613 exerts the greatest activation of SRC-1 in the primary screen, is confirmed to be a strong activator of all three SRCs. MCB-613 can super-stimulate SRCs' transcriptional activity. MCB-613 increases SRCs' interactions with other coactivators and markedly induces ER stress coupled to the generation of reactive oxygen species (ROS). MCB-613 selectively and reversibly binds to the RID of SRC-3, and selectively kills cancer cells including MCF-7 (breast), PC-3 (prostate), H1299 (lung), and HepG2 (liver) cells, without toxicity to mouse primary hepatocytes and mouse embryonic fibroblasts (MEFs). MCB-613 also increases SRCs' interactions with other coactivators and markedly induces ER stress coupled to the generation of reactive oxygen species (ROS). [1]in vivo: In an MCF-7 breast cancer mouse xenograft model, MCB-613 (20 mg/kg, i.p.) significantly and dramatically inhibits the growth of the tumor while causing no obvious animal toxicity and body weight less. [1]
Related Catalog
References

[1]. Wang L, et al. Characterization of a Steroid Receptor Coactivator Small Molecule Stimulator that Overstimulates Cancer Cells and Leads to Cell Stress and Death. Cancer Cell. 2015 Aug 10;28(2):240-52.

 Chemical & Physical Properties

Density 1.159±0.06 g/cm3
Boiling Point 510.4±50.0 °C at 760 mmHg
Molecular Formula C20H20N2O
Molecular Weight 304.386
Flash Point 257.9±36.5 °C
Exact Mass 304.157562
PSA 42.85000
LogP 4.55
Vapour Pressure 0.0±1.3 mmHg at 25°C
Index of Refraction 1.640
Storage condition -20℃
Water Solubility Practically insoluble (0.061 g/L) (25 ºC)

 Synonyms

(2E,6E)-4-Ethyl-2,6-bis(3-pyridinylmethylene)cyclohexanone
Cyclohexanone, 4-ethyl-2,6-bis(3-pyridinylmethylene)-, (2E,6E)-
MCB-613
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