| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC9130 | Azelastine HCl | Azelastine HCl is a potent, second-generation, selective, histamine antagonist. |
|
| DC8338 | Azeliragon（PF-04494700,TTP488） Featured | Azeliragon is an oral, small-molecule inhibitor of RAGE. |
|
| DCAPI1590 | Azelnidipine | Azelnidipine is an L-type calcium channel protein inhibitor |
|
| DC20156 | Azetidine-2-carboxylic acid Featured | Azetidine-2-carboxylic acid is a non proteinogenic amino acid homologue of proline. Found in common beets. Azetidine-2-carboxylic acid can be misincorporated into proteins in place of proline in many species, including humans. Toxic and teratogenic agent. |
|
| DC4210 | Azilsartan kamedoxomil Featured | Azilsartan medoxomil is an angiotensin II receptor antagonist indicated for the treatment of mild to moderate essential hypertension. |
|
| DCAPI1469 | azilsartan Featured | Azilsartan(TAK-536) is a specific and potent angiotensin II type 1 receptor antagonist with IC50 of 2.6 nM. |
|
| DC9596 | Azimilide (Dihydrochloride) | Azimilide 2Hcl(NE-10064 2Hcl) is a class III antiarrhythmic compound, inhibits I(Ks) and I(Kr) in guinea-pig cardiac myocytes and I(Ks) (minK) channels expressed in Xenopus oocytes. |
|
| DCAPI1362 | Azithromycin (Zithromax) | Azithromycin (Zithromax) |
|
| DC4141 | Azocosterol 2HCL | Azocosterol is a potential avian reproductive inhibitor. |
|
| DCAPI1225 | Azomycin (2-Nitroimidazole) | Azomycin (2-Nitroimidazole) |
|
| DC9818 | Azoramide Featured | Azoramide is a small-molecule modulator of the unfolded protein response with antidiabetic activity. |
|
| DC10992 | Azosemide | Azosemide (Azosemidum) is a potent Na-K-Cl Cotransporter NKCC1 with IC50 of 0.246 and 0.197 uM for hNKCC1A and NKCC1B, being about 4-times more potent than bumetanide. |
|
| DC12497 | (Z)-Azoxystrobin Featured | Azoxystrobin is a systemic, broad-spectrum fungicide belonging to the class of methoxyacrylates,which are derived from the naturally-occurring strobilurins. |
|
| DC22953 | AZSMO-23 | AZSMO-23 (AZSMO 23, AZSMO23) is a potent hERG potassium channel (Kv11.1) activator that activates WT hERG pre-pulse and tail current with EC50 of 28.6 and 11.2 μM respectively. |
|
| DCAPI1341 | Aztreonam (Azactam, Cayston) | Aztreonam (Azactam, Cayston) |
|
| DC21570 | Azvudine Featured | Azvudine (RO 0622) is a potent HCV NS5B RNA polymerase inhibitor, inhibits HCV replication in the replicon system with IC50 of 24 nM; inhibits RNA synthesis by HCV polymerases from either HCV genotypes 1a and 1b or containing S96T or S282T point mutations (IC50=10-100 nM). |
|
| DC23756 | Aβ polymerization stimulator O4 | Aβ polymerization stimulator O4 is an orcein-related small molecule can drive polymerization of amyloid-β (Aβ). |
|
| DC12114 | B I09 | B I09 is an IRE-1 RNase inhibitor, with an IC50 of 1230 nM. |
|
| DC10026 | B02 Featured | B02 is a cell-permeable pyridinylvinyl-quinazolinone compound that is shown to specifically inhibit human RAD51 (IC50 = 27.4 µM). |
|
| DC22010 | B591 | B591 (B-591) is a potent, specific pan-PI3K inhibitor with IC50 of 1.3/0.36/1.1/1.58 uM for PI3Kα/β/γ/δ, respectively. |
|
| DC12033 | (S)-B-973B Featured | B-973 (B973) is a potent, selective α7 nAChR ago-PAM, denonstrates analgesic effect with attenuating pain behavior and decreasing paw edema in vivo. |
|
| DC22011 | BAA473 | BAA473 (BAA-473) is a bile acid analogue that functions as the first small molecule activator of the Pyrin inflammasome, induces secretion of IL18 in LPS-primed PBMCs. |
|
| DC10859 | Baccatin III Featured | Baccatin III is the precursor to paclitaxel/ taxol. Antileukaemic and antitumor agent isolated from the bark of the Pacific yew tree (Taxus breviofolia). |
|
| DC20063 | BACE1-IN-2 | BACE1-IN-2 is a 1,4-Oxazine β-Secretase 1 (BACE1) inhibitor with an IC50 of 22 nM. |
|
| DCAPI1066 | Bacitracin zinc | Bacitracin zinc |
|
| DC8971 | Baclofen | Baclofen is a gamma-amino-butyric acid (GABA) derivative used as a skeletal muscle relaxant. |
|
| DC2013 | Bafetinib (INNO-406) Featured | Bafetinib (INNO-406) is a potent and selective dual Bcr-Abl/Lyn inhibitor with IC50 of 5.8 nM and 19 nM, respectively. |
|
| DC8858 | Bafilomycin A1(Baf-A1) Featured | Bafilomycin A1 is a vacuolar H+-ATPase inhibitor with IC50 of 0.44 nM. |
|
| DC20740 | BAL30072 | BAL30072 is a monocyclic beta-lactam antibiotic that shows potent activity against MDR Pseudomonas aeruginosa and Acinetobacter sp. Isolates with MIC90 of 8 and 4 ug/ml. |
|
| DC10994 | Balamapimod | Balamapimod (MKI-833) is an orally active, reversible Ras/Raf/MEK inhibitor developed for antineoplastic potential.. |
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