| Cat. No. |
Product Name |
Information |
| PC-25660 |
B32B3
VprBP inhibitor
|
B32B3 is a specific, small‐molecule inhibitor of DCAF1 (Vpr-binding protein, VprBP) with IC50 of 0.6 uM, selectively inhibits H2AT120p with IC50 of 0.5 uM. |
| PC-25656 |
EPIC-1042
PTRF-CAV1 inhibitor
|
EPIC-1042 is a potent, small molecule PTRF/Cavin1-caveolin-1 interaction inhibitor with IC50 of 38 uM, inhibits the binding of PTRF to Caveolin-1 (CAV1), resulting in decreased secretion of small extracellular vesicles (sEVs). |
| PC-25644 |
ISR activator A8
RIG-I binder, ISR activator
|
ISR activator A8 is a specific small molecule activator of integrated stress response (ISR) through the binding of the cytosolic pattern recognition receptor RIG-I, subsequently activates the heme-regulated inhibitor (HRI) ISR kinase independent of an interferon response. |
| PC-25634 |
ZDHHC2 inhibitor TTZ1
zDHHC2 inhibitor
|
zDHHC2 inhibitor TTZ1 (Tetrazole-1, TTZ-1) is a specific enzymatic inhibitor of palmitoyltransferase ZDHHC2, inhibits human zDHHC2-mediated substrate (SNAP25) S-acylation in vitro with IC50 of 4.7 uM. |
| PC-25627 |
Vav1 inhibitor AB19
Vav1 inhibitor
|
Vav1 inhibitor AB19 is a small molecule inhibitor of guanine nucleotide exchange factor Vav1 atypical C1 domain (Vav1C1), effectly inhibits proliferation of Vav1-expressing cells, inhibits growth of patient-derived organoids models of pancreatic cancer. |
| PC-25612 |
W478
SHMT2 inhibitor
|
W478 is a potent novel serine hydroxymethyltransferase 2 (SHMT2) inhibitor with IC50 of 1.21 uM, binds to SHMT2 with ITC KD of 10.6 uM. |
| PC-25596 |
T2M-010
TREM2 agonist
|
T2M-010 is a potent small molecule binder of Triggering receptor expressed on myeloid cells 2 (TREM2) with MST KD of 0.83 uM, functions as an activator of TREM2 signaling. |
| PC-25586 |
RAGE406R
RAGE inhibitor
|
RAGE406R is a small molecule antagonist of RAGE-DIAPH1 interaction, prevents the formation of the RAGE-DIAPH1, binds to cytosolic tail of RAGE (ctRAGE) with Kd of 0.3 nM. |
| PC-25580 |
CIA1 free base
COUP-TFII inhibitor
|
CIA1 free base (COUP-TFII inhibitor A1) is a potent and specific inhibitor of COUP-TFII activity, inhibits COUP-TFII–driven NGFIA reporter expression with IC50 of 3.2 uM, disturbs COUP-TFII binding to FOXA1 to regulate target gene expression. |
| PC-25556 |
α-difluoromethylornithine
Ornithine decarboxylase inhibitor
|
α-difluoromethylornithine (DFMO, Eflornithine, MDL71782) is a specific, irreversible inhibitor of polyamine biosynthesis enzyme Ornithine decarboxylase (ODC) with biochemicals IC50 of 252 uM, binding competitively with ornithine. |
| PC-25526 |
MSC778
FEN1 inhibitor
|
MSC778 (MSC-778) is a potent, selective, and orally bioavailable inhibitor of Flap endonuclease 1 (FEN1) with IC50 of 3.0 nM and SPR KD of 2.9 nM, >65-fold selective over closely related RAD2 family members EXO1, GEN1 and XPG. |
| PC-25516 |
iOXCT1
OXCT1 inhibitor
|
iOXCT1 (D574-0246) is a specific small molecule 3-Oxoacid CoA-transferase 1 (OXCT1) inhibitor, inhibits the dual enzymatic ketolytic and succinyltransferase activities of OXCT1 specifically. |
