| Cat. No. |
Product Name |
Information |
| PC-72381 |
HKB99
PGAM1 inhibitor
|
HKB99 (PGAM1 allosteric inhibitor HKB99) is a novel potent, cellularly active PGAM1 (Phosphoglycerate mutase 1) allosteric inhibitor, HKB99 is noncompetitive with the substrate 3-PG with IC50 of 0.85 uM in in vitro enzyme assays. |
| PC-72380 |
SUCNR1 inhibitor 20
SUCNR1 (GPR91) antagonist
|
SUCNR1 inhibitor 20 is a potent, selective inhibitor (antagonist) of GPCR SUCNR1 (succinate receptor 1/GPR91) with IC50 of 88 nM. |
| PC-72374 |
NF-56-EJ40
SUCNR1 (GPR91) antagonist
|
NF-56-EJ40 is a highly potent, human-selective antagonist of SUCNR1 (GPR91) with IC50 of 25 nM and Ki of 33 nM. |
| PC-72370 |
Ophiobolin A
Calmodulin inhibitor
|
Ophiobolin A (OphA) is a potent, covalent CaM inhibitor, with broad toxicity against plants, microbes, and cancer cells, OphA also is a K-Ras4B but not an H-Ras selective inhibitor. |
| PC-72352 |
Calmirasone1
Calmodulin inhibitor
|
Calmirasone1 (Calmirasone 1) is a novel and potent covalent calmodulin (CaM) inhibitor with Kd of 0.87 uM. |
| PC-72347 |
JNJ-54302833
FASN inhibitor
|
JNJ-54302833 (JNJ 54302833) is a potent, selective fatty acid synthase (FASN) inhibitor with IC50 of 28 nM. |
| PC-72338 |
AGI-25696
MAT2A inhibitor
|
AGI-25696 (AGI 25696) is a potent and selective inhibitor of methionine adenosyltransferase MAT2A, blocks the growth of MTAP-deleted tumors in vivo. |
| PC-72337 |
MAT2A inhibitor 28
MAT2A inhibitor
|
MAT2A inhibitor 28 (AZ-28) is a potent and selective inhibitor of methionine adenosyltransferase MAT2A with IC50 of 22 nM. |
| PC-72301 |
SW2_110A
CBX8 inhibitor
|
SW2_110A (SW2-110A) is a selective, cell-permeable inhibitor of chromobox homolog protein CBX8, binds CBX8 N-terminal chromodomain (ChD) with Kd of 800 nM. |
| PC-72298 |
CBX6 inhibitor 5
CBX6 inhibitor
|
CBX6 inhibitor 5 is a selective inhibitor of methyllysine reader protein CBX6 with Kd of 0.9 uM, 90×, 20×, 18×, 6×, and 7× selective for CBX6 over CBX1/2/4/7/8, respectively. |
| PC-72270 |
SHR170008
CD73 inhibitor
|
SHR170008 is a highly potent, small molecule CD73 inhibitor with IC50 of 0.05 nM against human CD73 soluble enzyme. |
| PC-72269 |
OP-5244
CD73 inhibitor
|
OP-5244 is a highly potent, orally bioavailable CD73 inhibitor with biochemical IC50 of 0.25 nM. |
