ChemicalBook--->CAS DataBase List--->2320561-35-9

2320561-35-9

2320561-35-9 Structure

2320561-35-9 Structure
IdentificationBack Directory
[Name]

ERD-308
[CAS]

2320561-35-9
[Synonyms]

ERD-308
[Molecular Formula]

C55H65N5O9S2
[MDL Number]

MFCD32067979
[Molecular Weight]

1004.26
Chemical PropertiesBack Directory
[Boiling point ]

1173.0±65.0 °C(Predicted)
[density ]

1.271±0.06 g/cm3(Predicted)
[storage temp. ]

4°C, protect from light
[solubility ]

DMSO:50.0(Max Conc. mg/mL);49.79(Max Conc. mM)
[form ]

Solid
[pka]

8.83±0.15(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Description]

ERD-308 is a Highly Potent Proteolysis Targeting Chimera (PROTAC) Degrader of Estrogen Receptor (ER) ERD-308 achieves DC50_x000D_ (concentration causing 50% of protein degradation) values of 0.17 and 0.43 nM in MCF-7 and T47D ER+ breast cancer cell lines, respectively, and induces >95% of ER degradation at concentrations as low as 5 nM in both cell lines. Significantly, ERD-308 induces more complete ER degradation than fulvestrant, the only approved selective ER degrader (SERD), and is more effective in inhibition of cell proliferation than fulvestrant in MCF-7 cells.
[in vitro]

ERD-308 achieves DC50 (concentration causing 50% of protein degradation) values of 0.17 and 0.43 nM in MCF-7 and T47D ER+ breast cancer cell lines, respectively, and induces >95% of ER degradation at concentrations as low as 5 nM in both cell lines. Significantly, ERD-308 induces more complete ER degradation than fulvestrant, the only approved selective ER degrader (SERD), and is more effective in inhibition of cell proliferation than fulvestrant in MCF-7 cells._x000D_ _x000D_ Reference: J Med Chem. 2019 Feb 14;62(3):1420-1442. https://pubmed.ncbi.nlm.nih.gov/30990042/
[target]

ERD-308 is a highly potent PROTAC degrader of estrogen receptor (ER) for ER positive breast cancer treatment.
[storage]

4°C, protect from light
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