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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2476 | Halobetasol |
Topical corticosteroid with anti-inflammatory, antipruritic, and vasoconstrictor activities, inducing phospholipase A2 inhibitory proteins, activating gene expression of anti-inflammatory proteins mediated via the corticosteroid receptor response element
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| DCC2475 | Halauxifen |
Herbicide, being used for the control of broad-leaved weeds in cereals and oilseed rape
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| 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
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| DCC2473 | H77-77 |
Inhibitor of monoamine oxidase (MAO)
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| DCC2472 | H-4073 |
Novel inhibitor of STAT3 activation, inhibiting head and neck cancer cell proliferation in a dose dependent manner
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| DCC2471 | h2lassbio-1064 |
Inhibitor of acetic acid-induced writhing response
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| DCC2470 | H2a-4t |
Novel water-soluble and biocompatible small-molecule near-infrared II (NIR-II) fluorescent dye
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| DCC2469 | H2-005 |
Novel class of selective diacylglycerol acyltransferase 2 (DGAT2) inhibitor
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| DCC2468 | H2-003 |
Novel class of selective diacylglycerol acyltransferase 2 (DGAT2) inhibitor
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| DCC2467 | h1-agonist-39 |
Novel full H1 agonist
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| 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
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| 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
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| DCC2464 | Gyramide A |
Novel bacterial DNA gyrase inhibitor, exhibiting antimicrobial activity and inhibiting bacterial cell division
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| DCC2463 | Gyki-53655 |
AMPA antagonist
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| DCC2462 | Gx-629 |
GX-936 analog, antagonist of voltage-gated sodium 1.7 (Nav1.7) channels
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| DCC2461 | Gx-585 |
Novel potent inhibitor of NaV1.7 and highly selective against NaV1.5, having limited selectivity against NaV1.1 and NaV1.2
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| DCC2460 | Gx-395 |
Novel inhibitor of Nav1.7
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| DCC2459 | Gwl-78 |
Novel modulator of NF-Y transcription, inhibiting the binding of NF-Y to DNA, blocking cellular proliferation and cell cycle progression, interacting with a variety of CCAAT-containing promoters leading to p53-independent cell cycle arrest
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| DCC2458 | Gw856804x |
Novel NAD+-competitive Sirt2 inhibitor
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| DCC2457 | gw853606 |
Novel polo-like kinase (PLK1) inhibitor
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| DCC2456 | Gw844520 |
Novel potent and selective inhibitor of the cytochrome bc1 complex of mitochondrial electron transport in P. falciparum
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| DCC2455 | Gw837016x |
Novel inhibitor of mitosis and cytokinesis in T. brucei which causes human African trypanosomiasis (HAT)
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| DCC2454 | Gw833373x |
Novel Inhibitor of GSK3beta
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| DCC2453 | Gw827106x |
Potent GSK-3 inhibitor, highly selective over CDK-2
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| DCC2452 | Gw809897x |
Novel and potent inhibitor of VEGFR2 tyrosine kinase, non-selectivey inhibiting AURKA and AURKB
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| DCC2451 | Gw807982x |
Potent and selective inhibitor of glycogen synthase kinase 3 (GSK3)
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| DCC2450 | gw7845 |
Selective agonist of peroxisome proliferator-activated receptor-γ (PPARγ)
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| DCC2449 | Gw780056x |
Selective cyclin dependent kinase inhibitor; Inhibitor of Yes1 kinase; Inhibitor of binding or entry into cells for Lassa Virus
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| DCC2448 | Gw701427a |
Novel inhibitor of firefly luciferase derived from Photinus pyralis (FLuc), the most widely used luciferase
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| DCC2447 | gw693881a |
Novel inhibitor of EGFR
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