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MS-8709

SKU: orb2815252

Description

MS-8709 is a potent and selective PROTAC degrader of G9a/GLP (EHMT2/EHMT1) with DC50 values of 274 nM and 260 nM, respectively. It induces target degradation via the UPS and demonstrates superior anti-proliferative activity in prostate cancer, leukemia, and lung cancer cell models compared to inhibitor UNC0642, supported by favorable murine PK for in vivo studies.

Research Area

Epigenetics & Chromatin, Pharmacology & Drug Discovery

Images & Validation

Key Properties

CAS Number3060730-06-2
MW1200.57
FormulaC64H95F2N11O7S
SMILESN(C=1C2=C(N=C(N1)N3CCC(F)(F)CC3)C=C(OCCCN4CCCC4)C(OC)=C2)C5CCN(CCCC(NCCCCCCCCCCCC(N[C@H](C(=O)N6[C@H](C(NCC7=CC=C(C=C7)C8=C(C)N=CS8)=O)C[C@@H](O)C6)[C@@](C)(C)C)=O)=O)CC5
TargetPROTACs,Histone Methyltransferase

Storage & Handling

Storage-20°C
Expiration Date12 months from date of receipt.
DisclaimerFor research use only
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Key Properties

No computed properties available.

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Protocol Information

MS-8709 (orb2815252)

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