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Dibucaine (Cinchocaine), a local anesthetic of the amide type, is now usually used for surface anesthesia.

Dibucaine hydrochloride (Cinchocaine hydrochloride), a long-acting local amide anestheticsis, is usually used for surface anesthesia.

Scheffursoside C is a useful organic compound for research related to life sciences. The catalog number is T125696 and the CAS number is 160669-29-4.

Crotaleschenine is a useful organic compound for research related to life sciences and the catalog number is T126243.

Isofischeric acid is a useful organic compound for research related to life sciences and the catalog number is T131493.

CBP bromodomain inhibitor

Lipopolysaccharides from Escherichia coli O111:B4 are key components of the outer membrane of Gram-negative bacteria. As a smooth-type LPS, they consist of lipid A, an R3-type core oligosaccharide, and an O-specific polysaccharide. These LPS molecules exhibit high immunogenicity, can trigger strong immune responses and gastric disorders by activating the TLR-4 receptor on immune cells, and help maintain the structural integrity of the bacterial outer membrane while protecting against bile salts and lipid-based antibiotics. They are widely used to establish inflammation-related disease models, such as chronic obstructive pulmonary disease (COPD) and acute respiratory distress syndrome (ARDS).

SCHEMBL12616233 is a novel inhibitor of SARS-CoV-2 main protease (MPro).

Hexokinase (ScHEX1), a glycolytic enzyme, is inhibited by n-acetylglucosamine, which causes it to detach from the mitochondrial outer membrane. This detachment activates the NLRP3 inflammasome [1].

SCHEMBL19801452-D3 is a deuterated compound of SCHEMBL19801452.SCHEMBL19801452 has a CAS number of 2173409-13-5.

Fischeria A is a natural product of Euphorbia, Euphorbiaceae. The catalog number is TN4059 and the CAS number is 221456-63-9. Fischeria A can be used as a reference standard.

Scheffoleoside A is a natural product.

Phosphatase, Escherichia coli (EC 3.1.3.-), is an enzyme that removes phosphate groups from substrates, generating phosphate ions and molecules with free hydroxyl groups through the hydrolysis of phosphate monoesters.

Trehalose-6-phosphate hydrolase, Escherichia coli (EC 3.2.1.93), is a member of the hydrolase family, functioning as a glycosidase that hydrolyzes O- and S-glycosyl compounds. This enzyme plays a role in the metabolism of starch and sucrose, with substrates α,α-trehalose-6-phosphate and water, producing D-glucose and D-glucose-6-phosphate.

Sugar-phosphatase, Escherichia coli (EC 3.1.3.23) is a member of the hydrolase enzyme family, specifically targeting the hydrolysis of phosphomonoester bonds. Its substrates include sugar phosphates and water, with its reaction products being sugar and phosphate.

α-Galactosidase, positionally specific, Escherichia coli (EC 3.2.1.22), is a glycoside hydrolase enzyme that catalyzes the hydrolysis of α-galactosyl residues from the termini of glycolipids and glycoproteins. It exists in two recombinant forms known as α-galactosidase (INN) and β-galactosidase (INN).

α-Glucosidase, Escherichia coli (EC 3.2.1.20), is a glucosidase found in the brush border of the small intestine that acts on 1,4-α-glycosidic bonds, breaking down starches and disaccharides into glucose.

α-Amylase, Escherichia coli (EC 3.2.1.1) is a protein enzyme that hydrolyzes the α-glycosidic bonds of large α-linked polysaccharides, such as starch and glycogen, producing glucose and maltose.

Dermaseptin acetate, a peptide isolated from frog skin, exhibits potent antimicrobial activity against bacteria, fungi, and protozoa at micromolar concentration[1].

Colivelin is a neuroprotective peptide and activator of STAT3. Colivelin is a hybrid peptide synthesized to enhance the neuroprotective effects of humanin (HN).

CB2 modulator 1 is a potent CB2 modulator. It can be used for the research for immune disorders, osteoporosis, inflammation, renal ischemia.

Ancriviroc (SCH-351125) is an oxime-piperidine compound with strong antiretroviral activity and an orally bioavailable small molecule chemokine receptor CCR5 antagonist (Kd value 9.27nM) that enters HIV-1 through the CCR5 co-receptor and is used to study HIV-1.

Vedaprofen (PM 150) inhibits COX-1 and reduces prostaglandin H2 synthesis with anti-inflammatory activities. Vedaprofen is an inhibitor of Escherichia coli sliding clamp with the IC50 of 222 μM and Ki of 131 μM.

Nicorandil (SG-75)(Ikorel) acts by relaxing the smooth muscle of the blood vessels, especially those of the venous system. It undertakes this through two methods. Firstly, by activating potassium channels, and secondly by donating nitric oxide to activate the enzyme guanylate cyclase. Guanylate cyclase causes activation of cGMP leading to both arterial and venous vasodilatation by de-phosphorylation of the myosin light chain.