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Cat. No. Product Name Information
PC-24675

Linker-free PROTAC Pro-DA

BCR-ABL degrader

Linker-free PROTAC Pro-DA is a linker-free PROTAC degarder of BCR-ABL protein with DC50 of 8 nM in K562 cells, achieving a 93% reduction at 20 nM, shows cell growth IC50 of 0.9 nM.
PC-24674

Linker-free PROTAC Pro-BA

EML4-ALK degrader

Linker-free PROTAC Pro-BA is a linker-free PROTAC degarder of EML4-ALK protein with DC50 of 74 nM and achieves an 82% reduction at 500 nM in H3122 cells, shows cell growth IC50 of 34 nM.
PC-24668

BMS-986458

BCL6 degrader

BMS-986458 is a potent, highly selective, orally bioavailable CRL4 CRBN E3 ubiquitin ligase-dependent BCL6 ligand directed degrader.
PC-24667

PRT3789

SMARCA2 degrader

PRT3789 is a first-in-class potent and selective SMARCA2 (BRM) degrader with DC50 of 0.72 nM in Hela cells, effectively catalyze the polyubiquitination of specific lysine residues of SMARCA2, resulting in SMARCA2 selective degradation over SMARCA4.
PC-24664

BMS-986449

IKZF2/4 degrader

BMS-986449 is a highly potent and selective, orally bioavailable degrader of the transcription factors Helios (IKZF2) and Eos (IKZF4).
PC-24663

GDC-2992

AR PROTAC

GDC-2992 (Compound 28A) is a potent, selective and orally active androgen receptor (AR) PROTAC degrader with DC50 of 2.7 nM, inhibits proliferation with IC50 of 9.7 nM in VCaP cells.
PC-24640

HDAC7 PROTAC B14

HDAC7 degrader

HDAC7 PROTAC B14 is a potent, exceedingly selective HDAC7 PROTAC degrader with DC50 of 25.1 nM in NB4 cells.
PC-24632

MS9117

LSD1 PROTAC

MS9117 is a potent, selective CRBN-based LSD1 PROTAC degrader, effectively degrades LSD1 and demonstrates superior antiproliferative effects in AML cells.
PC-24575

RP03707

KRAS G12D PROTAC

RP03707 is a CRBN-involving, highly potent, and selective KRAS G12D PROTAC degrader with DC50 of 0.7 nM in PK-59 cells (Dmax=96%).
PC-24558

MNK1 PROTAC P11-2

MNK1 PROTAC

MNK1 PROTAC P11-2 is a first-in-class, selective MNK1-targeting PROTAC degrader with DC50 of 11.92 nM (MV4-11 cells), Dmax>96%, shows remarkable selectivity for MNK1 over MNK2.
PC-24557

ERD-1233

ERα degrader

ERD-1233 is a potent and orally efficacious PROTAC degrader of estrogen receptor α (ERα) with DC50 of 0.9 nM in MCF-7 cell line, Dmax=100%.
PC-24555

PLX-4545

IKZF2 degrader

PLX-4545 (PLX4545) is a potent and selective, orally bioavailable IKZF2 degrader, that depletes IKZF2 and converts suppressive Tregs into effector-like T-cells leading to antitumor immunity.

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