t 785

T785 is a TLR7 agonist.

AXC-715 trihydrochloride (T785 trihydrochloride) is a TLR7/TLR8 dual agonist for the synthesis of antibody-adjuvanted immunocouplings. The couplings are mostly programmed death ligand 1 (PD-L1) attached to one or more antibody structures of the adjuvant.

XE991 is a novel and selective Kv7 (KCNQ) channel blocker.XE 991 dihydrochloride inhibits Kv7.1 (KCNQ1), Kv7.2 (KCNQ2), Kv7.2 + Kv7.3 (KCNQ3) channels, and M-current, and can be used for the study of neurological diseases.

KCL-286 is an orally available and potent retinoic acid receptor beta agonist for the amelioration of spinal cord injury (SCI).

GSK-3 Inhibitor XIII, an ATP-competitive GSK-3 inhibitor (Ki: 24 nM), can be used to study diabetes and obesity.

Tropone (Cycloheptatrienone) is a non-benzene aromatic organic compound antiviral and antifungal.Tropolone derivatives inhibit the replication of HBV at the submicromolar level.

Tyramine hydrochloride is a biogenic trace amine that is generated via the decarboxylation of the amino acid tyrosine, exhibiting neuromodulatory properties as well as cardiovascular and immunological effects.

(+)-Sparteine ​​is a quinoline alkaloid extracted from Scotch broom, a sodium channel blocker and a class 1a antiarrhythmic agent. It competitively inhibits the activity of nicotinic acetylcholine receptors in nerve cells and is a ganglionic blocking agent.

Naphthol AS-E (nAS-E) is an the KIX-KID interaction and CREB-mediated gene transcription inhibitor.

RIPK2-IN-3 (FCG806791773) is a receptor-interacting serine/threonine protein kinase 2 (RIPK2) inhibitor with anti-inflammatory and anti-tumor activity. It can be used for research on immune diseases and cancer.

BRD4 Inhibitor-27 is a potent BRD4 inhibitor that inhibits BRD4 BD1 and BRD4 BD2 with IC50s of 9.6 and 11.3 μM, respectively.BRD4 Inhibitor-27 has anticancer activity and can be used for breast cancer research.

Antidepressant agent 5 is a 7-substituted tetrahydroisoquinoline derivative with antidepressant activity.Antidepressant agent 5 acts similarly to magnoflorine in the study of depression and can be used for the prevention and treatment of depressive disorders.

m-Toluoyl chloride is a bioactive chemical.

α-Factor Mating Pheromone (yeast TFA) is a tridecapeptide secreted by Saccharomyces cerevisiae α cells and interacts with the Ste2p receptor [1].

Glucoamylase, an enzyme obtained from various sources such as plants, animals, and microorganisms, is utilized in industrial applications. It is extensively employed in starch saccharification processes and the brewing and distilling industries [1].

4,4-Dimethyl-2-cyclopenten-1-one is a natural product derived from Apocyniveneti Folium that exhibits antitumor activity. 4,4-Dimethyl-2-cyclopenten-1-one selectively kills tumor cells (HSC-2, HL-60). The CC50 (50% cytotoxic concentration) values for 4,4-Dimethyl-2-cyclopenten-1-one are 43.8 μg/mL, 152 μg/mL, 118 μg/mL, and 14.0 μg/mL (HSC-2, HSC-3, HSG, HL-60).

Lavandoside is a compound derived from Helianthemum ruficomum with antioxidant activity.

Ethyl pivaloylacetate is a significant β-ketoester. It is widely employed as a model substrate in biocatalysis to evaluate the catalytic activity and stereoselectivity of ketoreductase (KRED) tool-boxes. Due to the presence of the bulky pivaloyl (tert-butyl) group, it serves as an excellent probe for assessing the substrate pocket size and enantioselectivity of recombinant enzymes. The enzymatic reduction of this compound yields enantiopure β-hydroxyesters, which are essential chiral building blocks for the synthesis of sophisticated pharmaceutical intermediates.

α-Lactose hydrate (α-D-Lactose monohydrate) is the principal carbohydrate found in the milk of most mammals. It is a disaccharide consisting of glucose and galactose linked by a β-1,4-glycosidic bond, existing in two anomeric forms, α and β. α-Lactose hydrate has extensive applications in the food and pharmaceutical industries, serving as a free-flowing or agglomerating agent and a diluent for pigments, flavors, or enzymes. In biological research, it is the fundamental substrate for studying lactose metabolism and the mechanisms of lactose intolerance.

Cefteram (T-2525), an orally active ester of the cephalosporin class, is the free acid form of Cefteram pivoxil. This compound exhibits potent activity against enteropathogenic families Enterobacteriaceae and Vibrionaceae [1].

Delmitide acetate (RDP58) is an orally active d-isomer decapeptide with potent anti-inflammatory properties, suppressing TNF-α, IFN-γ, and interleukin (IL)-12 production, while enhancing heme oxygenase 1 activity. It is utilized in research related to ulcerative colitis [1] [2].

Pyridoxal (Pyridoxaldehyde), a component of vitamin B6, is an aldehyde obtained by oxidizing pyridoxine and is widely found in plants and animals.

Zolimidine, an imidazopyridine derivative, functions as an orally active antiulcer agent. It promotes mucus secretion in intestinal mucosal cells and enhances the intestinal wall's resistance to ulceration. Studies demonstrate its gastroprotective effect in duodenal ulcer research [1] [2].

Oleoyl coenzyme A lithium (Oleoyl-CoA lithium) is an oleic acid and coenzyme A thioester, an efficient h15-LOX-2 allosteric inhibitor that inhibits h12-LOX and h15-LOX-2. It is used in the study of metabolic and cardiovascular diseases.