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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4668 | Sdz Ser 082 Fumarate |
Selective 5-HT2B/2C receptor antagonist
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| DCC4667 | Sdz Mrl 953 |
Novel immunostimulatory monosaccharidic lipid A analog, down-regulating TNF-alpha and IL-6 production and priming secretion of G-CSF and IL-1 beta
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| DCC4666 | Sdz 90-215 |
Novel inhibitor of the Golgi complex (Vrg4); Antifungal
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| DCC4665 | Sdz 205-557 Hydrochloride |
Selective, surmountable antagonist for 5-HT4 receptors
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| DCC4664 | Sd2590 Hydrochloride |
Potent inhibitor of MMP-2, -3, -9, -8, -13, and -14
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| DCC4663 | S-cw3554 |
Novel irriversible selective PDI inhibitor, selectively labeling protein disulfide isomerase and inhibiting its enzymatic activity, showing unique cytotoxicity in cells derived from multiple myeloma
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| DCC4662 | Scriptene |
NRTI-drug pair of zidovudine (AZT)-didanosine (ddI), being highly cytotoxic and mutagenic
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| DCC4661 | Scr-4026 |
Novel inhibitor of nNOS-PSD-95 interaction, exhibiting neuroprotective activities in NMDA-induced or Oxygen and glucose deprivation (OGD)-induced neuronal damage in primary cortical neurons cultures, and ameliorating focal cerebral ischemic damage in rats
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| DCC4660 | Scr1693 |
Novel dual acetylcholinesterase inhibitor (AChEI) and a calcium channel blocker (CCB)
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| DCC4659 | Scq-14d |
Novel Inhibitor of p53-Murine Double Minute 2 (MDM2) Interaction and Histone Deacetylases (HDACs) with the IC50 values of 140, 910 and 17.5 nmol/L against MDM2, HDAC1, and HDAC6, respectively, showing the tumor growth inhibition (TGI) in the A549 xenograf
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| DCC4658 | scio-469 Hydrochloride |
Selective, ATP-competitive p38
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| DCC4657 | Schembl20148701 |
Novel inhibitor of SARS-CoV-2 main protease (MPro)
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| DCC4656 | Schembl18616095 |
Novel inhibitor of SARS-CoV-2 main protease (MPro)
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| DCC4655 | Schembl18320671 |
Novel glucose transport inhibitor
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| DCC4654 | Schembl15939407 |
Novel Lysine-Specific Demethylase 1 (LSD1) Inhibitor (IC50: 20nM)
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| DCC4653 | Schembl1548848 |
Novel inhibitor of vanilloid receptor subtype 1 (VR1)
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| DCC4652 | Schembl12616233 |
Novel inhibitor of SARS-CoV-2 main protease (MPro)
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| DCC4651 | Sch-900822 |
Novel potent and selective glucagon receptor antagonist
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| DCC4650 | sch-79687 |
Novel histamine H3-receptor antagonist
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| DCC4649 | Sch-53870 |
Inhibitor of p21-hRas nucleotide exchange in vitro
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| DCC4648 | Sch-538415 |
Novel Acyl_carrier_protein_synthase>acyl carrier protein synthase inhibitor; Inhibitor of growth of the bacteria Streptococcus_pneumoniae>Streptococcus pneumoniae and Neisseria_gonorrhoeae>Neisseria gonorrhoeae
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| DCC4647 | Sch-51866 |
Potent and selective PDE1 and PDE5 inhibitor
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| DCC4646 | Sch-43478 |
Non-nucleoside antiviral agent, having potent and selective activity against herpes simplex virus type 2 (HSV-2)
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| DCC4645 | Sch-351591 |
Novel, orally active phosphodiesterase 4 (PDE4) inhibitor
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| DCC4644 | Sch-23985 |
D1 dopamine receptor antagonist
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| DCC4643 | Sch-23982 |
Precursor for radioiosotopically labelled R(+)-SCH-23390
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| DCC4642 | Sch2-1-27 |
Novel Inhibitor of the virus fusion to its cell receptor, targeting SARS-CoV-2 spike protein HR1
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| DCC4641 | Sch2-1-20 |
Novel Inhibitor of the virus fusion to its cell receptor, targeting SARS-CoV-2 spike protein HR1
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| DCC4640 | Sch-202596 |
Natural selective non-peptide antagonist for the receptor GAL-1
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| DCC4639 | Scalaradial |
Natural Potent Inhibitor of Transient Receptor Potential Melastatin 2 (TRPM2) Ion Channels
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