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 |
|---|---|---|---|
| DCC1010 | Bisthianostat |
Novel Orally Efficacious Pan-HDAC Inhibitor
More description
|
|
| DCC1009 | Bis-salicyl Fumarate |
Potent activator of the Neh2-luc reporter
More description
|
|
| DCC1008 | Bisoctrizole |
UV stabilizer
More description
|
|
| DCC1007 | bis-n-norgliovictin |
Novel inhibitor of LPS-induced inflammation in macrophages, improving survival in sepsis
More description
|
|
| DCC1006 | Bisleuconothine A |
Novel and selective Wnt signaling inhibitor
More description
|
|
| DCC1005 | Bisindole-pbd |
Novel inhibitor of angiogenesis by regulating STAT3 and VEGF in breast cancer cells
More description
|
|
| DCC1004 | Bisdionin F |
Selective hAMCase Inhibitor
More description
|
|
| DCC1003 | Bis-cyclosal-d4tmp |
Novel anti-HIV active dimeric prodrug of 2‘,3‘-dideoxy-2‘,3‘-didehydrothymidine monophosphate (d4TMP)
More description
|
|
| DCC1002 | Bisaramil |
Class I antiarrhythmic agent with chronotropic, inotropic, dromotropic and coronary vasodilator effects, potently blocking sodium channel
More description
|
|
| DCC1001 | Bis-5-methyl-cyclosal-d4tmp |
Novel anti-HIV active dimeric prodrug of 2‘,3‘-dideoxy-2‘,3‘-didehydrothymidine monophosphate (d4TMP)
More description
|
|
| DCC1000 | Bis-2-ai Adjuvant-2 |
Novel adjuvant to repurpose azithromycin for use against Pseudomonas aeruginosa, exhibiting a 1024-fold reduction in the minimum inhibitory concentration of azithromycin in vitro and displays activity in a Galleria mellonella model of infection
More description
|
|
| DCC0999 | Biphalin |
Potent peptide opioid receptor agonist, alleviating LPS-Induced activation in rat primary microglial cultures in opioid receptor-dependent and receptor-independent manners
More description
|
|
| DCC0998 | Biph(2,3',4,5',6)p5 |
Potent inhibitor of SHIP-2 catalytic activity; Novel inositol polyphosphate surrogate modulating Ca responses in rat hepatocytes
More description
|
|
| DCC0997 | Bipbipu |
Novel heparanase inhibitor
More description
|
|
| DCC0996 | Bio-0554019 |
Novel selective RORgamma inhibitor, selectively inhibiting Th17 differentiation and RORgamma signature gene expression
More description
|
|
| DCC0995 | Bin-01-07-07 |
Novel USP28 inhibitor
More description
|
|
| DCC0994 | bim5078 |
Potent HNF4α antagonist
More description
|
|
| DCC0993 | Biliatresone |
Natural Biliary Toxin, causing extrahepatic biliary atresia
More description
|
|
| DCC0992 | Biii-890cl |
Novel potent blocker of Nav1.2 sodium channels, protecting of brain tissue from ischemia
More description
|
|
| DCC0991 | Biii-277cl |
Novel potent blocker of the NMDA receptor ion channel
More description
|
|
| DCC0990 | Biib068 Hemi-adipate |
Novel, Selective, Potent, Reversible Bruton's Tyrosine Kinase (BTK) Inhibitor as an Orally Efficacious Agent for Autoimmune Diseases
More description
|
|
| DCC0989 | Biib-057 |
Selective Syk inhibitor
More description
|
|
| DCC0988 | Biib028 |
Novel selective heat shock protein 90 inhibitor, prodrug of CF2772
More description
|
|
| DCC0987 | Bifeprunox Mesylate |
Partial agonist at dopamine D2 and serotonin 1A receptors
More description
|
|
| DCC0986 | Biemamide A |
Novel inhibitor of the TGF-β pathway, blocking the epithelial to mesenchymal transition
More description
|
|
| DCC0985 | bicuculline Methobromide |
GABAA receptor antagonist
More description
|
|
| DCC0984 | Biclofibrate |
Antilipidemic agent
More description
|
|
| DCC0983 | Bicifadine |
Triple reuptake inhibitor (TRI)
More description
|
|
| DCC0982 | Bibx-1382 Dihydrochloride |
Potent, selective inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase
More description
|
|
| DCC0981 | Bi-btk-1 |
Novel, highly selective and potent irreversible BTK inhibitor
More description
|
|