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PD-M6

PD-M6 is an mTOR PROTAC degrader (DC50: 4.8 μM) . PD-M6 promotes the ubiquitination and degradation of mTOR. PD-M6 inhibits the proliferation of HeLa, MCF-7, and HepG2 cancer cell lines (IC50 values of 11.3, 2.58, and 3.23 μM, respectively) and induces autophagy. PD-M6 specifically induces the degradation of LAMTOR1, a key protein in the mTOR signaling pathway. (Pink: target protein mTOR ligand (HY-B0795) ; target protein mTOR ligand activity control (HY-W150930) ; black: linker (HY-W008296) ; blue: E3 ligase CRBN ligand (HY-41547) ; target protein ligand activity control + linker (HY-176167) ) [1].

Product Specifications

CAS Number

[3058330-82-5]

UNSPSC

12352005

Target

MTOR; PROTACs

Related Pathways

PI3K/Akt/mTOR; PROTAC

Applications

Cancer-Kinase/protease

Field of Research

Cancer

Smiles

O=C1N(C2CCC(NC2=O)=O)C(C3=CC=CC(NCCCCCCNC4=NC(N5CCOCC5)=NC(N6CCOCC6)=N4)=C13)=O

Molecular Formula

C30H39N9O6

Molecular Weight

621.69

References & Citations

[1]Zhu L, et al. Reversing an agonist into an inhibitor: Development of mTOR degraders. Eur J Med Chem. 2025 May 17;294:117774.

Shipping Conditions

Room temperature

Product MSDS

http://file.medchemexpress.com/batch_PDF/HY-176166/

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Curated Selection

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