To enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2474 | Ha Protein Inhibitor 1 |
Novel hemagglutinin (HA) protein inhibitor, inhibiting entry and replication of diverse influenza viruses via the HA protein, showing potent antiviral activity against diverse H1N1, H5N1, and H3N2 influenza viruses encoding HA proteins from both groups 1
More description
|
|
| DCC2473 | H77-77 |
Inhibitor of monoamine oxidase (MAO)
More description
|
|
| DCC2472 | H-4073 |
Novel inhibitor of STAT3 activation, inhibiting head and neck cancer cell proliferation in a dose dependent manner
More description
|
|
| DCC2471 | h2lassbio-1064 |
Inhibitor of acetic acid-induced writhing response
More description
|
|
| DCC2470 | H2a-4t |
Novel water-soluble and biocompatible small-molecule near-infrared II (NIR-II) fluorescent dye
More description
|
|
| DCC2469 | H2-005 |
Novel class of selective diacylglycerol acyltransferase 2 (DGAT2) inhibitor
More description
|
|
| DCC2468 | H2-003 |
Novel class of selective diacylglycerol acyltransferase 2 (DGAT2) inhibitor
More description
|
|
| DCC2467 | h1-agonist-39 |
Novel full H1 agonist
More description
|
|
| DCC2466 | H-0106 Dihydrochloride |
Novel Rho-associated coiled coil-formed protein kinase (ROCK) inhibitor, exerting strong intraocular pressure (IOP)-lowering effects into the eyes of monkeys
More description
|
|
| DCC2465 | H-0104 Dihydrochloride |
Novel Rho-associated coiled coil-formed protein kinase (ROCK) inhibitor, exerting strong intraocular pressure (IOP)-lowering effects into the eyes of monkeys
More description
|
|
| DCC2464 | Gyramide A |
Novel bacterial DNA gyrase inhibitor, exhibiting antimicrobial activity and inhibiting bacterial cell division
More description
|
|
| DCC2463 | Gyki-53655 |
AMPA antagonist
More description
|
|
| DCC2462 | Gx-629 |
GX-936 analog, antagonist of voltage-gated sodium 1.7 (Nav1.7) channels
More description
|
|
| DCC2461 | Gx-585 |
Novel potent inhibitor of NaV1.7 and highly selective against NaV1.5, having limited selectivity against NaV1.1 and NaV1.2
More description
|
|
| DCC2460 | Gx-395 |
Novel inhibitor of Nav1.7
More description
|
|
| DCC2458 | Gw856804x |
Novel NAD+-competitive Sirt2 inhibitor
More description
|
|
| DCC2457 | gw853606 |
Novel polo-like kinase (PLK1) inhibitor
More description
|
|
| DCC2456 | Gw844520 |
Novel potent and selective inhibitor of the cytochrome bc1 complex of mitochondrial electron transport in P. falciparum
More description
|
|
| DCC2455 | Gw837016x |
Novel inhibitor of mitosis and cytokinesis in T. brucei which causes human African trypanosomiasis (HAT)
More description
|
|
| DCC2454 | Gw833373x |
Novel Inhibitor of GSK3beta
More description
|
|
| DCC2453 | Gw827106x |
Potent GSK-3 inhibitor, highly selective over CDK-2
More description
|
|
| DCC2452 | Gw809897x |
Novel and potent inhibitor of VEGFR2 tyrosine kinase, non-selectivey inhibiting AURKA and AURKB
More description
|
|
| DCC2451 | Gw807982x |
Potent and selective inhibitor of glycogen synthase kinase 3 (GSK3)
More description
|
|
| DCC2450 | gw7845 |
Selective agonist of peroxisome proliferator-activated receptor-γ (PPARγ)
More description
|
|
| DCC2449 | Gw780056x |
Selective cyclin dependent kinase inhibitor; Inhibitor of Yes1 kinase; Inhibitor of binding or entry into cells for Lassa Virus
More description
|
|
| DCC2448 | Gw701427a |
Novel inhibitor of firefly luciferase derived from Photinus pyralis (FLuc), the most widely used luciferase
More description
|
|
| DCC2447 | gw693881a |
Novel inhibitor of EGFR
More description
|
|
| DCC2446 | Gw648495 |
Potent inhibitor of PfDHODH, showing greater than 4,000-fold selectivity for the malarial enzyme
More description
|
|
| DCC2445 | Gw612286x |
Novel VEGFR inhibitor, also a moderate inhibitor of BET proteins with an IC 50 value of 4.6 μM for BRD4(1)
More description
|
|
| DCC2444 | Gw568377a |
Inhibitor of Mer Kinase, also inhibiting EGFR
More description
|
|