| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2429 | Guineesine | Acyl-CoA, inhibiting cholesterol acyltransferase |
|
| DCC2430 | Gummadiol | Natural inhibitor of 3C-like protease (3CLpro), targeting SARS-CoV-2 3CLpro, SARS-CoV 3CLpro and MERS-CoV 3CLpro |
|
| DCC2431 | Gv2-20 | Potent inhibitor of cabonic anhydrase 2 (CA2) |
|
| DCC2432 | Gw 791343 Hydrochloride | Negative allosteric modulator of human P2X7 and a positive allosteric modulator of rat P2X7 |
|
| DCC2433 | gw0072 | Potent inhibitor of adipocyte differentiation and weak partial agonist of |
|
| DCC2434 | Gw012x | Novel Selective and Nonpeptidomimetic Proteasome Inhibitor As an Antimalarial, specifically inhibiting the proteasome activity in P. falciparum |
|
| DCC2435 | gw0791 | Novel agonist for retinoid X receptor |
|
| DCC2436 | Gw297361x | Inhibotor of active Vaccinia-Related Kinases (VRK) |
|
| DCC2437 | Gw305178x | Novel inhibitor of CDK |
|
| DCC2438 | Gw3333 | Novel selective and soluble inhibitor of tumor necrosis factor-alpha converting enzyme (TACE) |
|
| DCC2439 | gw409544 | Potent and selective full agonist for peroixisome proliferator-activated receptor-alpha |
|
| DCC2440 | Gw440139a | Novel potent RET kinase inhibitor |
|
| DCC2441 | gw441756 Hydrochloride | Potent TrkA kinase inhibitor |
|
| DCC2442 | Gw493838 | Novel agonist at the adenosine A1 receptor |
|
| DCC2443 | gw5638 | Orally active, nonsteroidal tamoxifen derivative and a ligand for the estrogen receptors (ERs), steroid receptor members of the nuclear receptor superfamily of transcription factors |
|
| DCC2444 | Gw568377a | Inhibitor of Mer Kinase, also inhibiting EGFR |
|
| DCC2445 | Gw612286x | Novel VEGFR inhibitor, also a moderate inhibitor of BET proteins with an IC 50 value of 4.6 μM for BRD4(1) |
|
| DCC2446 | Gw648495 | Potent inhibitor of PfDHODH, showing greater than 4,000-fold selectivity for the malarial enzyme |
|
| DCC2447 | gw693881a | Novel inhibitor of EGFR |
|
| DCC2448 | Gw701427a | Novel inhibitor of firefly luciferase derived from Photinus pyralis (FLuc), the most widely used luciferase |
|
| DCC2449 | Gw780056x | Selective cyclin dependent kinase inhibitor; Inhibitor of Yes1 kinase; Inhibitor of binding or entry into cells for Lassa Virus |
|
| DCC2450 | gw7845 | Selective agonist of peroxisome proliferator-activated receptor-γ (PPARγ) |
|
| DCC2451 | Gw807982x | Potent and selective inhibitor of glycogen synthase kinase 3 (GSK3) |
|
| DCC2452 | Gw809897x | Novel and potent inhibitor of VEGFR2 tyrosine kinase, non-selectivey inhibiting AURKA and AURKB |
|
| DCC2453 | Gw827106x | Potent GSK-3 inhibitor, highly selective over CDK-2 |
|
| DCC2454 | Gw833373x | Novel Inhibitor of GSK3beta |
|
| DCC2455 | Gw837016x | Novel inhibitor of mitosis and cytokinesis in T. brucei which causes human African trypanosomiasis (HAT) |
|
| DCC2456 | Gw844520 | Novel potent and selective inhibitor of the cytochrome bc1 complex of mitochondrial electron transport in P. falciparum |
|
| DCC2457 | gw853606 | Novel polo-like kinase (PLK1) inhibitor |
|
| DCC2458 | Gw856804x | Novel NAD+-competitive Sirt2 inhibitor |
|
