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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
Purity99.98% (May vary between batches)
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
Quality Guarantee

Quality Guarantee

Explore bioreagents carefree to elevate your research. All our products are rigorously tested for performance. If a product does not perform as described on its datasheet, our scientific support team will provide expert troubleshooting, a prompt replacement, or a refund. For full details, please see our Terms & Conditions and Buying Guide. Contact us at [email protected].

Key Properties

No computed properties available.

Protocol Information

Available Sizes

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1 mg
$ 90.00
5 mg
$ 140.00
10 mg
$ 180.00
25 mg
$ 280.00
DispatchUsually dispatched within 5-10 working days
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