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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC9209 | Carbazeran |
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| DC9221 | Cefatrizine |
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| DC9228 | Quinfamide |
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| DC9203 | Gadopentetate dimeglumine |
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| DC9210 | Ormetoprim |
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| DC9204 | Pteroic acid |
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| DC9222 | A967079 |
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| DC9178 | Ketanserin Tartrate |
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| DC9113 | Ketanserin |
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| DC20286 | β-catenin-IN-37 |
β-catenin-IN-37 is a novel potent, and selective small-molecule inhibitor for the β-catenin/Tcf4 protein-protein interaction with Ki of 17 uM.
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| DC20285 | β-catenin-IN-11a |
β-catenin-IN-11a is a β-catenin/CD44/Nanog axis inhibitor, docks into the β-catenin allosteric site and interferes β-catenin/TCF-4 complex.
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| DC12123 | α-Cyclodextrin |
α-Cyclodextrin is a multifunctional, soluble dietary fiber marketed for use as a fiber ingredient.
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| DC23115 | alpha-Amanitin |
α-Amanitin, an 8-Aa cyclic peptide, is an selective inhibitor of RNA polymerase II and III.
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| DC7642 | Α5ia (α5IA) |
α5IA is a selective inverse agonist for Α5 subtype of GABAA receptor with a higher intrinsic activity at the A5 subtype than other drugs.
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| DC20284 | α2β1 integrin-IN-15 |
α2β1 integrin-IN-15 highly potent, selective, allosteric small-molecule inhibitor of integrin α2β1 with IC50 of 12 nM.
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| DC21860 | ZYZ-488 |
ZYZ-488 is a novel inhibitor of apoptotic protease activating factor-1 (Apaf-1), inhibits the activation of binding protein procaspase-9 and procaspase-3.
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| DC11139 | ZYTP1 |
ZYTP1 is a novel, oral PARP inhibitor that inhibits PARP1, PARP2, Tankyrase-1 and Tankyrase-2 with IC50 of 5.4, 0.7, 133.3 and 289.8 nM, respectively.
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| DC21976 | ZXH-3-26 |
ZXH-3-26 is a novel BRD4 heterobifunctional small-molecule ligand (PROTAC), shows activity exclusively on the BRD4 BD1 (DC50/5h=5 nM) and spares degradation of BRD2 or BRD3 in cellular degradation assays.
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| DC21639 | ZTM000990 |
ZTM000990 is a small-molecule antagonist of the oncogenic Tcf4/β-catenin protein complex with IC50 of 0.64 uM.
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| DC22120 | ZT55 |
ZT55 (JAK inhibitor ZT55) is a novel potent, highly-selective tyrosine kinase JAK2 inhibitor with IC50 of 31 nM.
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| DC22275 | ZST316 |
ZST316 (ZST-316) is a small molecule DDAH1 (Dimethylarginine dimethylaminohydrolase 1) inhibitor with IC50 of 3 uM, Ki of 1 uM.
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| DC22274 | ZST152 |
ZST152 (ZST-152) is a small molecule DDAH1 (Dimethylarginine dimethylaminohydrolase 1) inhibitor.
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| DC23323 | ZPCK |
ZPCK (NSC 251810.
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| DCAPI1517 | Zotepine |
Zotepine is a SR-2A and D2DR inhibitor (Ki values are 0.69 and 2.3 nM respectively). Zotepine is also a potent histamine H1 receptor antagonist (IC50 = 8.0 nM).
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| DCAPI1538 | Zopiclone |
Zopiclone
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| DCAPI1302 | Zonisamide |
Zonisamide
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| DC21841 | Zonampanel |
Zonampanel (YM 872) is a selective, potent and highly water-soluble, competitive AMPA receptor (AMPAR) antagonist with Ki of 96 nM.
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| DCAPI1454 | Zolmitriptan |
Zolmitriptan is a Serotonin 5HTID-receptor agonist.
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| DC9328 | Zofenopril (calcium) |
Zofenopril Calcium(SQ26991) is an antioxidant that acts as an angiotensin-converting enzyme inhibitor.
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| DC1083 | ZM323881 hydrochloride |
ZM323881 a receptor tyrosine kinase inhibitor of VEGFR-2 (Flk-1), PDGFR-beta, EGFR, and FGFR1
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