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| Cat.No. | Product name | Product Description |
| R11886 | CACCINH-A01 | CaCCinh-A01 is an inhibitor of both TMEM16A and calcium-activated |
| R11887 | MELK-T1(JNJ-47117096) | MELK-T1 is a potent and selective inhibitor of protein kinase MELK. MELK-T1 decr |
| R11888 | MELK-T1(JNJ-47117096) HCl | JNJ-47117096 hydrochloride is potent and selective MELK inhibitor, wit |
| R11889 | Delpazolid (LCB01-0371) | Delpazolid is a novel oxazolidinone antibiotic agent which can inhibit the growt |
| R11891 | GSK269962A | GSK269962A is a potent ROCK inhibitor with IC50s of 1.6 and 4 nM for recombinant |
| R11893 | Fuscoside (OPC-21268) | Fuscoside (OPC-21268) is an orally effective, nonpeptide, vasopressin V1&nb |
| R11894 | c646 | C646 is a selective and competitive histone acetyltransferase p300 inh |
| R11895 | de44mt | Dp44mT is an iron chelator with selective anticancer activity. |
| R11897 | cemmec13 | CeMMEC13 is a potent inhibitor of TAF1 (2) bromodomain, with an I |
| R11899 | scriptaid | Scriptaid is a potent histone deacetylase (HDAC) inhibitor, used in cancer resea |
| R11900 | Naphazoline hydrochloride | Naphazoline hydrochloride is an ocular vasoconstrictor and imidazoline derivativ |
| R11901 | PCI 29732 | PCI 29732 is a selective and irreversible Btk inhibitor with IC50 of 8.2 nM in a |
| R11902 | DC10539 | N/A |
| R11903 | azoramide | Azoramide is a small-molecule modulator of the unfolded protein response with an |
| R11904 | 8-oh-dpat | N/A |
| R11905 | 1-(2-Fluoro-5-nitrophenyl)ethan-1-one | N/A |
| R11907 | CB-03-01 | N/A |
| R11908 | LY2835219 Intermediate | N/A |
| R11909 | GLPG1837 | GLPG1837 is a potent and reversible CFTR potentiator, with EC50s |
| R11910 | HDAC8-IN-1 | HDAC8-IN-1 is a HDAC8 inhibitor with an IC50 of 27.2 nM. |
| R11911 | SCH23390 | CAS NO.：87134-87-0 Product Name：SCH23390 Molecular Formula：C17H19Cl2NO Molecular |
| R11912 | CD437 (Synonyms: AHPN) | CD437 is a selective Retinoic Acid Receptor γ (RARγ) agonist. |
| R11913 | PLX51107 | PLX51107 is a potent and selective BET inhibitor, with Kds of 1.6 |
| R11914 | Tropifexor (Synonyms: LJN452) | Tropifexor (LJN452) is a highly potent agonist of FXR with an EC50 of 0.2 nM.&nb |
| R11916 | Lanifibranor (IVA337) | Lanifibranor is a pan peroxisome proliferator-activated receptor (PPAR |
