Cat. No. |
Product Name |
Information |
PC-63109 |
ESI-05
EPAC2 inhibitor
|
ESI-05 is a potent EAPC2-specific antagonist that inhibits cAMP-mediated EPAC2 GEF activity with apparent IC50 of 0.43 uM. |
PC-63108 |
HJC0197
EPAC inhibitor
|
HJC0197 is a potent Exchange proteins directly activated by cAMP (EPAC) inhibitor with IC50 of 4.0 uM. |
PC-63107 |
NSC 45576
EPAC inhibitor
|
NSC 45576 is a potent Exchange proteins directly activated by cAMP (EPAC) inhibitor with IC50 of 1.7 uM. |
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. |