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Farudodstat (ASLAN003) is an orally active and potent inhibitor of DHODH (Human Dihydroorotate Dehydrogenase) with antitumor activity, showing potential as a first-in-class candidate in AML [Acute Myeloid Leukemia].

C15AlkOPP Tetrabutylamine salt is a "clickable" alkyne-modified analogs of the lipid substrates farnesyl diphosphate (FPP).

C15AlkOPP Tetrabutylamine salt (1:2) is an FPP analogue, bearing an alkyne group to allow for post-prenylation protein labeling. C15AlkOPP Tetrabutylamine salt (1:2) can be used for Prenylomic analysis

Copper histidine inhibited Ctr1-mediated cellular uptake of oxaliplatin in vitro without altering oxaliplatin accumulation of platinum or neurotoxicity in DRG tissues in vivo. Copper histidine is administered orally for the treatment of Menkes disease.

Chlorophyllin sodium copper salt (Chlorophyllin coppered trisodium salt) is a semi-synthetic mixture of water-soluble sodium copper salts derived from chlorophyll, primarily used as a food additive and alternative medicine.

Sodium copper chlorophyllin B exerts antiviral activities against Influenza virus and HIV.

Copper(II) gluconate is a non-toxic copper supplement. As a precursor catalyst, it can be used for photoinduced polymerization of acrylates.

EDTA copper(II) disodium salt is a metal chelator with antimicrobial, anti-inflammatory and antioxidant activity, slows down damage caused by metal ions, maintains osmotic pressure during protein purification, and can be used in the study of neurological disorders.

DIETHYLDITHIOCARBAMIC ACID COPPER SALT is a widely used industrial compound. It has been used as a chelating agent in various biochemical and physiological experiments, including experiments involving metals, proteins, and enzymes.

Copper(i)sulfideis a high purity biochemical reagent that can be used in research related to life sciences.

Copper Sulfate Pentahydrate has a variety of antibacterial activities, and has inhibitory activity against Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Candida albicans, etc.

Copper(Ⅱ) Sulfate (Cupric sulfate) has a variety of antibacterial activities and has inhibitory activity against Staphylococcus aureus, Streptococcus pneumoniae, Pseudomonas aeruginosa, Plasmodium falciparum, etc.

Copper(II) acetate is a high-purity copper reagent that can serve as a copper source in inorganic synthesis and also function as an oxidising agent and catalyst in organic synthesis.

4(15)-Oppositene-1,7-diol is a useful organic compound for research related to life sciences and the catalog number is T124496.

TBOPP is a selective DOCK1 inhibitor (IC50 : 8.4 μM), with anti-tumor activity for broader types of tumors.

Poppy acid is a useful organic compound for research related to life sciences and the catalog number is T131392.

Copper(II) ionophore I is a neutral ionophore with high selectivity for Cu2+. It is widely used in ion-selective electrodes (ISE) to accurately measure copper concentrations in biological and environmental samples.

Copper oxychloride is an agent of fungicide.

MCOPPB triHydrochloride (MCOPPB 3HCl) is a nociceptin receptor agonist.

Chlorotris (triphenylphosphine) copper (CuCl(TPP)₃) is a metal complex that targets DNA. Through non-covalent interactions of its copper (I) center, such as groove-binding, it affects DNA function and exhibits inhibitory activity against bacteria, fungi, and tumor cells. Chlorotris (triphenylphosphine) copper holds potential for research as an antimicrobial, antitumor, and antioxidant agent.

Copper(I) chloride is an inorganic compound that can be used to prepare copper(II)-chitosan complexes. Due to its cell compatibility and antibacterial properties, it has potential application prospects as an antibiotic-free antibacterial biomaterial in biomedical devices.

Copper ionophore I is an efficient carrier of copper ions that modulates intracellular copper levels to induce cuproptosis, with effects observed in cells such as 4T1 (IC50= 0.45 μM) and MDA-MB-231 (IC50= 1.21 μM). It elevates ROS, leading to mitochondrial dysfunction, and decreases the expression of proteins FDX1, DLAT, and LIAS. Additionally, it can activate immune-related pathways, enhancing T cell infiltration, making it a valuable compound for cancer research.

MCOPPB is a potent and selective agonist for the nociceptin receptor with a pKi of 10.07, much weaker activity at other opioid receptors. In animal studies, MCOPPB produces potent anxiolytic effects, with no inhibition of motor or memory function, and onl

Poloppin is a protein-protein interactions modulator of the mitotic polo-like kinases that acts by targeting mutant KRAS. It works synergistically with Crizotinib, an inhibitor of the c-MET receptor, against mutant KRAS-expressing cancer cells.