| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC34551 | NSC727371 | FN-439 is a matrix metalloproteinase inhibitor which targets MMP-1 and MMP-9. |
|
| DC34552 | MMP-9 inhibitor I | MMP9-IN-I is a cell-permeable, potent, and reversible MMP-9 inhibitor. |
|
| DC34553 | 360-A | 360A is a stabilizing G-Quadruplex ligand which has potent selectivity toward G-quadruplex structures of the telomeric 3'-overhang. |
|
| DC34554 | 3F-8 | 3F8 is a selective and potent GSK-3? inhibitor. |
|
| DC34555 | Fluvastatin Methyl Ester | Fluvastatin Methyl Ester is a precursor for Fluvastatin, which is a blocker of the liver enzyme HMG-CoA reductase. |
|
| DC34556 | p Tolylmaleimide | p-Tolylmaleimide is a water channel inhibitor which binds to aquaporin Z (AqpZ). |
|
| DC34557 | CI928 | Quinaprilat is an angiotensin converting enzyme inhibitor. |
|
| DC34558 | Tebufenpyrad | Tebufenpyrad is an acaricide and insecticide widely used in greenhouses. It is commonly used to control populations of mites and ticks. |
|
| DC34560 | dt-BHQ | dtBHQ is a non-arylating oxidizable phenol as the source of reactive oxygen species (ROS). |
|
| DC34561 | Bisindolylmaleimide VII | Bisindolylmaleimide VII is a selective inhibitor of protein kinase C. |
|
| DC34562 | NHNB | NHNB is a selective inhibitor of histone deacetylases-8 (HDAC8). NHNB provides the most potent CE4 inhibitor reported to date. |
|
| DC34563 | HC3 | Hemicholinium-3 is a competitive antagonist of CHT-mediated choline transport. |
|
| DC34565 | NSC345308 | WR-1065 Dihydrochloride is a metabolite of Amifostine. |
|
| DC34566 | Galnon | Galnon is a selective, non-peptide agonist at the galanin receptors GALR. |
|
| DC34567 | L48-H37 | L48H37 is a specific myeloid differentiation 2 (MD2) inhibitor. |
|
| DC34568 | LP935509 Featured | LP-935509 is a potent inhibitor of the Adapter protein-2 Associated Kinase 1 (AAK1). |
|
| DC34569 | Carboprost tromethamine | Carboprost tromethamine is a Prostaglandin F2α analog. |
|
| DC34570 | PSEM308 hydrochloride | PSEM308 HCl is an agonist of pharmacologically selective actuator module (PSAM) which activates PSAML141F-GlyR chimeric ion channels. |
|
| DC34571 | TL12186 | TL12-186 is a multikinase degrading PROTAC. |
|
| DC34572 | TL1327 | TL13-27 is a negative control for TL12-186. |
|
| DC34573 | PF913 maleate | Glasdegib Maleate is a potent and orally bioavailable inhibitor of smoothened. |
|
| DC34574 | UK59811 HCl | UK-59811 HCl is a calcium channel blocker which inhibits CaVAb and binds at the outer, lipid-facing surface of the pore at the interface between two CaVAb subunits. |
|
| DC34575 | TFIIH Modulator12 | TFIIH Modulator-12 is a small molecule destabilization inducer of the trichothiodystrophy group A protein (TTD-A or p8) dimerization which modulates TFIIH transcriptional activity. |
|
| DC34576 | TFIIH Modulator19 | TFIIH Modulator-19 is a small molecule destabilization inducer of the trichothiodystrophy group A protein (TTD-A or p8) dimerization which modulates TFIIH transcriptional activity. |
|
| DC34577 | Tuftsin | Tuftsin is a self-immunomodulatory molecule produced by the spleen by enzymatic cleavage of a leukophilic gamma-globulin which stimulates the phagocytic activity of blood polymorphonuclear leukocytes and neutrophils in particular. The peptide is located in the Fd fragment of the gamma-globulin molecule. |
|
| DC34578 | Monosulfuron | Monosulfuron is an herbicide. |
|
| DC34579 | S1-QEL | S1QEL is a suppressor of mitochondrial respiratory complex I site IQ electron leak which suppresses superoxide and/or H2O2 production without altering oxidative phosphorylation. |
|
| DC34580 | Manumycin A | Manumycin A is a Farnesyltransferase inhibitor which suppresses exosome biogenesis and secretion via targeted inhibition of Ras/Raf/ERK1/2 signaling and hnRNP H1 in castration-resistant prostate cancer cells, inhibiting IKKβ activity through covalent cross-linking of IKKβ monomers via C179. |
|
| DC34581 | L4FPG | L-4FPG is an inhibitor of the neutral amino acid transporters ASCT1 and ASCT2. L-4FPG shows good brain penetration and potently reduces amphetamine-induced hyperlocomotion. |
|
| DC34582 | GOY078 | GO-Y078 is an antiangiogenic curcumin analog which inhibits actin stress fiber formation, thereby resulting in mobility inhibition. |
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