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Cat. No. Product Name Target Signaling Pathways
T6189 Mirdametinib

PD325901,PD0325901

Apoptosis; MEK; Autophagy Apoptosis; Autophagy; MAPK
Mirdametinib (PD325901) 是一种 MEK 抑制剂 (IC50=0.33 nM),具有选择性、非 ATP 竞争性和口服活性。Mirdametinib 具有抗肿瘤活性,可以抑制 p-ERK1/2 的表达并诱导细胞凋亡。
T40217 PD0325901-O-C2-dioxolane

PD0325901-O-C2-dioxolane

PD0325901-O-C2-dioxolane is a chemical compound primarily composed of the MEK inhibitor PD0325901. It can be utilized, in conjunction with either a VHL or CRBN E3 ligase ligand, for the synthesis of MEK1/2 degrader.
T13782 MS432

MEK MAPK
MS432 is a highly selective PD0325901-based VHL-recruiting PROTAC degrader for MEK1 and MEK2.
T18668 (S,R,S)-AHPC-Me-C10-Br

Others Others
(S,R,S)-AHPC-Me-C10-Br is a chemically synthesized conjugate that functions as a ligand-linker for E3 ligases. This compound incorporates a VHL E3 ligase linker and MS432, derived from the MEK1/2 inhibitor PD0325901[1].

化合物

Mirdametinib
Cat.No: T6189
Synonym: PD325901,PD0325901
Target: Apoptosis, MEK, Autophagy
PD0325901-O-C2-dioxolane
Cat.No: T40217
Synonym: PD0325901-O-C2-dioxolane
Target:
MS432
Cat.No: T13782
Synonym:
Target: MEK
(S,R,S)-AHPC-Me-C10-Br
Cat.No: T18668
Synonym:
Target: Others
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