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Cat. No. Product Name Information
PC-61399

Setafrastat

Setafrastat is a small molecule hair growth stimulator.
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.

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