| Cat. No. |
Product Name |
Information |
| PC-63106 |
NY0173
EPAC1 inhibitor
|
NY0173 is a potent Exchange proteins directly activated by cAMP (EPAC) inhibitor with IC50 of 4.0 uM for EPAC1. |
| PC-63105 |
HJC0726
EPAC2 inhibitor
|
HJC0726 (HJC-0726) is a potent Exchange proteins directly activated by cAMP (EPAC) inhibitor, inhibits cAMP-mediated EPAC2 GEF activity with IC50 of 1.0 uM. |
| PC-63104 |
NY0123
EPAC inhibitor
|
NY0123 is a novel potent Exchange proteins directly activated by cAMP (EPAC) antagonist with IC50 of 0.9 and 2.4 uM for EPAC1 and EPAC2, respectively. |
| PC-62968 |
Imazapic
Herbicide
|
Imazapic is a herbicide that controls many broad leaf weeds and controls or suppresses some grasses in pasture.. |
| PC-62967 |
Imazaquin
Herbicide
|
Imazaquin is an imidazolinone herbicide that effectively controls a broad spectrum of weed species, by inhibiting acetohydroxy acid synthase (AHAS).. |
| PC-62954 |
K-604
ACAT-1 inhibitor
|
K-604 is a potent, selective and competitive ACAT-1 inhibitor with IC50 of 0.45 uM for human ACAT-1, displays 229-fold selectivity over ACAT-2. |
| PC-62928 |
Buthionine Sulfoximine
GCS inhibitor
|
Buthionine Sulfoximine (BSO) is a glutathione (GSH)-depleting reagent that inhibits gamma-glutamylcysteine synthetase, the enzyme required in the first step of glutathione synthesis. |
| PC-62918 |
PSB-12431
CD73 inhibitor
|
PSB-12431 is an α,β-Methylene-ADP (AOPCP) derivative, potent, selective ecto-5′-Nucleotidase (eN, CD73) inhibitor with Ki of 9.2 nM for rat recombinant eN. |
| PC-62917 |
PSB-12553
CD73 inhibitor
|
PSB-12553 is an α,β-Methylene-ADP (AOPCP) derivative, potent, selective ecto-5′-Nucleotidase (eN, CD73) inhibitor with Ki of 9.5 nM for rat recombinant eN. |
| PC-62916 |
PSB-12379
CD73 inhibitor
|
PSB-12379 is an α,β-Methylene-ADP (AOPCP) derivative, potent, selective ecto-5′-Nucleotidase (eN, CD73) inhibitor with Ki of 9.03/2.21 nM for rat/human recombinant eN. |
| PC-62880 |
DDD85646
NMT1/NMT2 inhibitor
|
DDD 85646 is a potent, specific, dual N-Myristoyltransferase NMT1/NMT2 inhibitor with IC50 of 17 nM/22 nM respectively. |
| PC-62875 |
STK16-IN-1
|
STK16-IN-1 is a potent, highly selective ATP competitive STK16 inhibitor with IC50 of 0.295 uM, displays excellent selectivity across the kinome. |
