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Cat. No. Product Name Information
PC-38738

Degradomer D-1

IRAK3 degarder

Degradomer D-1 is a selective proteasomal degrader of IRAK3 with Kd of 100 nM, DC50 of 94 nM, displays no binding affinity against IRAK4 (Ki >10 uM).
PC-38718

CRBN(BRAF)-24

BRAF V600E PROTAC

CRBN(BRAF)-24 is a potent small molecule degrader against oncogenic BRAF V600E protein, potently degrades BRAFV600E in a ubiquitin–proteasome system (UPS)-dependent manner and inhibits the proliferation of BRAFV600E-driven cancer cells.
PC-38566

STING PROTAC SP23

STING PROTAC

SP23 is a STING protein degrader (PROTAC) based on a small-molecule STING inhibitor (C-170) and pomalidomide (a CRBN ligand), shows degradation potency with DC50 of 3.2 uM.
PC-38462

dBRD9 dihydrochloride

BRD9 PROTAC

dBRD9 dihydrochloride is a potent and selective degrader (PROTAC) of BRD9 with IC50 of 56.6 nM in MOLM-13 cells.
PC-73343

YX-2-115

CDK6 inhibitor

YX-2-115 is a palbociclib derivative compound with piperazine-linker tail for PROTAC YX-2-107 synthesis, inhibits CDK6 with IC50 of 4.5 nM.
PC-73342

YX-2-107

CDK6 degrader

YX-2-107 is a CRBN-recruiting and specific CDK6-degrading PROTAC with IC50 of 0.69 and 4.4 nM for CDK4 and CDK6 in vitro, selectively degardes CDK6 in Ph+ BV173 ALL cells with a degradation constant of 4 nM.
PC-73310

CFT-14441

BRD9 BiDAC degrader

CFT-14441 is a potent and selective BRD9 BiDAC degrader with DC50 of 39 nM (2h), high selectivity over BRD4 abd BRD7.
PC-73289

BSJ-04-132

CDK4 degrader

BSJ-04-132 is a selective CDK4 degrader (PROTAC), does not induce IKZF1/3 degradation.
PC-73288

BSJ-03-204

CDK4/6 degrader

BSJ-03-204 is a dual and selective degrader (PROTAC) of CDK 4 and 6, does not induce IKZF1/3 degradation.
PC-73165

ERD-308

Estrogen receptor PROTAC

ERD-308 (ERD308) is a highly potent estrogen receptor (ER) PROTAC degrader with DC50 of 0.17 and 0.43 nM in MCF-7 and T47D ER+ breast cancer cell lines, respectively.
PC-73109

SD-36

STAT3 degrader

SD-36 (STAT3 degrader SD-36) is a potent, selective STAT3 degrader (PROTAC), potently induces the degradation of STAT3 protein in vitro and in vivo.
PC-73098

YKL-06-101

CDK8 degarder

YKL-06-101 is a bivalent small molecule that combines mTOR inhibition (IC50=6 nM) and degradation of CDK8 (CDK8/Cyclin C IC50=31 nM).

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