|Description||Foresaconitine is a norditerpenoid alkaloid isolated from the processed tubers of Aconitum carmichaeli.|
ML352 is a potent and non-competitive inhibitor of the presynaptic choline transporter (CHT; Ki value 92 nM).
ARN 272 has been found to be a FLAT inhibitor and could show analgesic activities in CB1-mediated nociceptive and inflammatory pain.
LOC14 is a protein disulfide isomerase modulator with Kd value of 62 nM. It can force protein disulfide isomerase to adopt an oxidized conformation and suppress...
(RS)-4-Carboxy-3-hydroxyphenylglycine has been found to be a broad spectrum EAA ligand.
Isosorbide is a heterocyclic compound that is derived from glucose, used as a diuretic.
NVS-CRF38 is a novel corticotropin-releasing factor receptor 1 (CRF1) antagonist with low water solubility.
Betaine,which is isolated from the roots of Beta vulgaris, improves the amplification of DNA by reducing the formation of secondary structure in GC-rich regions...
Clinafloxacin hydrochloride is a novel fluoroquinolone antimicrobial agent as a potent intraphagocytic bactericidal agent. It displays broad-spectrum antibacter...
HMR 1556 is a potent and selective Iks channel blocker (IC50 = 10.5 and 34 nM in canine and guinea pig ventricular myocytes, respectively). It selectively inhib...
DL-Panthenol is uesd to synthetize organic compound.
W-54011 is a potent, specific high affinity C5a receptor antagonist (Ki = 2.2 nM).
DIM-C-pPhOCH3 is a Nur77 agonist. It was shown to induce apoptosis in cancer cell lines in vitro, enhance long-term potentiation in hippocampal slices and long-...
FK866 is a nicotinamide phosphoribosyltransferase (NMPRTase) inhibitor with potential antineoplastic and antiangiogenic activity. FK866 inhibits the biosynthesi...
Artemotil is a fast acting blood schizonticide. It is a semi-synthetic derivative of artemisinin, which is a natural product of the Chinese plant Artemisia annu...
This active molecular can be applicated as a photosensitizer for PDT (Photodynamic Therapy) of cancer. Redaporfin showed a great efficacy in the treatment of ma...
This active molecular is a cAMP/PKA/CREB pathway activator promoting osteogenic differentiation of human bone marrow derived MSCs in vitro, and it also increase...
tBID specificly inhibits homeodomain–interacting protein kinase 2 (HIPK2) (IC50= 0.33 µM).
(R)-CE3F4 is an Epac inhibitor (IC50 = 4.2 and 44 μM for Epac1 and Epac2(B), respectively), suppressing the activation of Epac by cAMP.
CP-472555 is an effective Glucocorticoid receptor agonist and probably has steroid-like anti-inflammatory properties with anti-GR and anti-obesity activity in a...
BF844 is a CLRN1N48K stabilizer that can attenuate progressive hearing loss and deafness in an Usher syndrome type III (USH3) mouse model.