| Cat. No. |
Product Name |
Information |
| PC-61393 |
Parimifasor
ATPase modulator
|
Parimifasor (LYC-30937-EC, LYC30937) is an orally bioavailable, enteric-coated ATPase modulator as a gut-directed therapy for the treatment of inflammatory bowel disease (IBD). |
| PC-61376 |
Epeleuton
|
Epeleuton is an orally administered, second-generation ω-3 fatty acid derivative of C20:5 n-3 EPA, protects against cellular stress associated with SCD and supports early initiation of the resolution phase of inflammation. |
| PC-61375 |
Enexasogaol
PPARγ agonist
|
Enexasogaol (6-Shogaol) is a pungent agent isolated from Zingiber officinale Roscoe, has been known to have anti-tumor and anti-inflammatory effects. |
| PC-61361 |
Spindlactone B
TACC3 inhibitor
|
Spindlactone B (SPL-B) is a novel small molecule inhibitor of transforming acidic coiled-coil-containing protein 3 (TACC3) that selectively inhibits the nucleation of centrosome microtubules in ovarian cancer cells. |
| PC-61360 |
Spindlactone A
TACC3 inhibitor
|
Spindlactone A (SPL-A) is a novel small molecule inhibitor of transforming acidic coiled-coil-containing protein 3 (TACC3) that selectively inhibits the nucleation of centrosome microtubules in ovarian cancer cells. |
| PC-61340 |
PF-06928215
cGAS inhibitor
|
PF-06928215 (PF06928215) is a high affinity Cyclic GMP-AMP synthase (cGAS) inhibitor with Kd of 200 nM, IC50 of 4.9 uM. |
| PC-61320 |
RK-33
DDX3 inhibitor
|
RK-33 is a first-in-class small molecule inhibitor of RNA helicase DDX3, binds specifically to DDX3, but not to the closely related proteins DDX5 and DDX17. |
| PC-61316 |
Teglicar
CPT1 inhibitor
|
Teglicar (ST-1326) is a potent, selective and reversible inhibitor of liver carnitine palmitoyl-transferase 1 (L-CPT1) with IC50 of 0.68 uM, Ki of 0.36 uM. |
| PC-61310 |
Me6TREN
ATRP ligand
|
Me6TREN is a small molecule Cu complexing ligand used for atom transfer radical polymerization (ATRP). |
| PC-61262 |
TB-03
Grb2 SH2 inhibitor
|
TB-03 is a small molecule Grb2 SH2 domain binding antagonist that synergistically enhances inhibition of K562 leukemia cell proliferation by imatinib (CI=0.774). |
| PC-61245 |
DC_AC50
|
DC_AC50 (DCAC50) is a small molecule that inhibits the human copper chaperones Atox1 and CCS (Kd=6.8 and 8.2 uM), blocks copper trafficking and significantly attenuates cancer cell proliferation. |
| PC-61244 |
STOML3 inhibitor OB-1
|
STOML3 inhibitor OB-1 is a small-molecule inhibitor of STOML3 oligomerization that reverses pathological mechanical hypersensitivity in vivo. |
