| Cat. No. |
Product Name |
Information |
| PC-24310 |
NFS1 inhibitor Compound 53
NFS1 inhibitor
|
NFS1 inhibitor Compound 53 is the first potent, selective inhibitor of human cysteine desulfurase (NFS1) with IC50 of 40.5 uM and Ki of 6.4 uM. |
| PC-24282 |
BKT300
PRC1 inhibitor
|
BKT300 is a small molecule inhibitor of leukemic cell migration and survival by targeting the PRC1 pathways, efficiently and specifically binds protein regulator of cytokinesis 1 (PRC1) with SPR Kd of 28.3 nM. |
| PC-24261 |
SARM1 inhibitor NB-7
SARM1 inhibitor
|
SARM1 inhibitor NB-7 is a potent, selective and uncompetitive inhibitor of the nicotinamide adenine dinucleotide (NAD) hydrolase SARM1 with biochemical IC50 of 0.025 uM, and IC50 of 0.008 uM in SARM-induced cell-death rescue assays. |
| PC-24260 |
SARM1 inhibitor 7
SARM1 inhibitor
|
SARM1 inhibitor 7 is a potent, selective sterile alpha and TIR Motif Containing 1 (SARM1) inhibitor with biochemical IC50 of 0.3 uM (hSARM1). |
| PC-24247 |
ACUPA TFA
PSMA inhibitor
|
ACUPA TFA is a potent prostate-specific membrane antigen (PSMA, GCPII) antagonist with Ki of 44.3 nM. |
| PC-24246 |
ACUPA
PSMA inhibitor
|
ACUPA is a potent prostate-specific membrane antigen (PSMA, GCPII) antagonist with Ki of 44.3 nM. |
| PC-24245 |
Vitamin B5 calcium
GOLPH3L inhibitor
|
Vitamin B5 calcium (VB5) is a small molecule inhibitor of Golgi phosphoprotein 3 like (GOLPH3L) with Kd of 1.15 uM in ITC assays, effectively blocks the binding of GOLPH3L and STING, subsequently promoting STING-NLRP3-mediated pyroptosis after radiotherapy (RT). |
| PC-24238 |
hCES2A inhibitor 14n
hCES2A inhibitor
|
hCES2A inhibitor 14n is a potent, selective and covalent human carboxylesterase 2A (hCES2A) inhibitor with IC50 of 0.04 nM. |
| PC-24230 |
NSC167409
HMGB1 inhibitor, EV-A71 inhibitor
|
Glycyrrhizin (NSC167409, Glycyrrhizic acid) is a direct HMGB1(high mobility group box 1) inhibitor, also is a specific inhibitor of EV-A71, blocks EV-A71 replication both in vivo and in vitro. |
| PC-24216 |
5-Ph-IAA
AID2 ligand
|
5-Ph-IAA is a derivative of IAA that could establishes the auxin-inducible degron 2 (AID2) system together with an OsTIR1 (F74G) mutant, induces rapid and efficient depletion of mAID-fused proteins to study protein function in living cells, causing tumor suppression. |
| PC-24192 |
Tapencarium
Fat-reducing agent
|
Tapencarium (Utenpanium chloride, RZL-012) is a fat-reducing and small molecule thermogenic regulator, destroys adipocytes by directly disrupting cell membrane integrity. |
| PC-24179 |
Riztunitide
CAS 2963586-07-2
|
Riztunitide is an anti-inflammatory pepetide ameliorating neurodegenerative disorders, decreases inflammation and rescues cells with dysregulated energy metabolism. |
