ChemicalBook--->CAS DataBase List--->3053716-98-3

3053716-98-3

3053716-98-3 Structure

3053716-98-3 Structure
IdentificationBack Directory
[Name]

yj1206
[CAS]

3053716-98-3
[Synonyms]

yj1206
[Molecular Formula]

C49H52FN11O5
[MOL File]

3053716-98-3.mol
[Molecular Weight]

894.01
Chemical PropertiesBack Directory
[density ]

1.404±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
[form ]

Solid
[pka]

10.587±0.40(predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

YJ1206 is an orally active, selective CDK12/CDK13 PROTAC degrader with an IC50 of 12.55 nM for in VCaP cells. YJ1206 increases DNA damage, induces apoptosis, and promotes tumor regression in orthotopic WA74 patient-derived xenograft (PDX) mice models of resistant prostate cancer. YJ1206 suppresses tumor growth in vivo in conjunction with AKT pathway inhibitors. YJ1206 is composed of the CDK12/CDK13 degradation agent (HY-168658), a linker (HY-W004328), and a VHL E3 ubiquitin ligase (HY-W453548). (Pink: Navitoclax; Blue: VHL ligand; Black: linker)[1].
[IC 50]

CDK12; CDK13
[References]

[1] Yu Chang, et al. Development of an orally bioavailable CDK12/13 degrader and induction of synthetic lethality with AKT pathway inhibition. Cell Rep Med. 2024 Oct 15;5(10):101752. DOI:10.1016/j.xcrm.2024.101752
Spectrum DetailBack Directory
[Spectrum Detail]

yj1206(3053716-98-3)1HNMR
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