| Cat. No. |
Product Name |
Information |
| PC-20779 |
HP661
OXPHOS inhibitor
|
HP661 is a potent, and selective oral complex I OXPHOS inhibitor with 76% inhibition at 1u M in H460 cells using electron flow assays, inhibits high-OXPHOS H460 cell viability with IC50 of 5 nM. |
| PC-20609 |
SN34960
Perforin inhibitor
|
SN34960 is a small molecule Perforin inhibitor, inhibits perforin-induced lysis of Jurkat T-lymphoma cells with IC50 of 6.65 uM, shows suboptimal physicochemical properties and toxicity toward the natural killer (NK) cells that secrete perforin in vivo. |
| PC-20604 |
Auranofin
UBA1 enhancer
|
Auranofin (SKF39162) is a specific inhibitor of thioredoxin reductase (TrxR), also is a potent UBA1 E1 ubiquitin-activating enzyme activity enhancer. |
| PC-20490 |
R805
gp130 modulator
|
R805 is a small molecule modulator of gp130 receptor pro-inflammatory signaling, targets a signaling tyrosine 814 (Y814) within gp130, modulates gp130 Y814 upstream of the SRC and MAPK circuit, elicits a protective effect on tissues after injury. |
| PC-20459 |
Betulin
SREBP inhibitor
|
Betulin (NSC 4644) is a specific small molecule inhibitor of SREBP (Sterol regulatory element-binding protein), specifically inhibits the maturation of SREBP by inducing interaction of SREBP cleavage activating protein (SCAP) and Insig. |
| PC-20457 |
APC655
ATF6 activator
|
APC655 is a potent activator of protein folding and unfolded protein response (UPR) modulator, APC655 activates ATF6 pathway and chaperone expression. |
| PC-20404 |
ASP7967
|
ASP7967 (ASP-7967) is a cell-permeable and low-toxic compound of RNA aptamer AC17-4 with SPR binding Kd of 12 nM, activates gene expression (>10-fold) in aptazyme-based riboswitches with EC50 of 2.3 uM. |
| PC-20337 |
TDRL-551
RPA inhibitor
|
TDRL-551 (TDRL551) is a small molecule Replication Protein A (RPA) inhibitor targeting the Replication Protein A-DNA interaction with IC50 of 18 uM. |
| PC-20306 |
ELOVL6 inhibitor Compound B
ELOVL6 inhibitor
|
ELOVL6 inhibitor Compound B is a potent and selective ELOVL6 inhibitor with IC50 of 85 and 38 nM for human and mouse ELOVL6, respectively. |
| PC-20264 |
Indoluidin E
DHODH inhibitor
|
Indoluidin E is an indoluidin D derivative, and potent selective dihydroorotate dehydrogenase (DHODH) inhibitor, suppresses cancer cell growth. |
| PC-20263 |
Indoluidin D
DHODH inhibitor
|
Indoluidin D is a potent selective dihydroorotate dehydrogenase (DHODH) inhibitor, promotes myeloid differentiation and inhibits the proliferation of acute promyelocytic leukemia HL-60 cells. |
| PC-20258 |
Dichloroallyl lawsone
DHODH inhibitor
|
Dichloroallyl lawsone (Dichlorolapachol, DCL, NSC-126771) is a synthetic analogue of the antimalarial lapachol, inhibits mitochondrial dihydroorotate dehydrogenase (DHODH) with antineoplastic activity. |
