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Polyinosinic-polycytidylic acid sodium (Poly(I:C) sodium) is a synthetic analog of double-stranded RNA and an agonist of toll-like receptor 3 (TLR3) and retinoic acid inducible gene I (RIG-I)-like receptors (RIG-I and MDA5).

Benproperine phosphate (Pirexyl phosphate) is a cough suppressant.

Thioproperazine (RP 7843) is an orally effective antipsychotic also used as a tranquilizer and antiemetic for the treatment of schizophrenia and the manic phase of bipolar disorder, acting as a histamine and adrenergic receptor blocker.

Clenproperol, a β2-adrenergic agonist, is a chemical compound commonly used in veterinary medicine to treat respiratory diseases in animals.

Benproperine is a bioactive molecule with antineoplastic properties.

Properdistatin, a peptide originating from the thrombospondin 1 (TSP-1) domain of properdin, exhibits angiogenesis inhibition and vascular function enhancement capabilities, showing promise for melanoma research [1].

Anti-Properdin Antibody is an inhibitory antibody that can be used in life science related research.

Clenproperol-d7 is a deuterated compound of Clenproperol.

Clenproperol (Standard) is the standard substance of Clenproperol, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Clenproperol is a β2-adrenergic agonist.

L-Proline (proline) is a nonessential amino acid in humans. It is an essential component of collagen and is important for proper functioning of joints and tendons. It also helps maintain and strengthen heart muscles.

1-Methylindazole-3-carboxylic acid is an excellent solvent with a proper boiling point.

7-Keto-27-hydroxycholesterol is a significant bioactive compound known for its ability to activate the smoothened (SMO) protein within the Hedgehog (Hh) signaling pathway, which is crucial for proper cell differentiation in embryonic tissues.

Rhodblock 1a is an inhibitor of the Rho kinase signaling pathway, which disrupts the localization and function of proteins within the Rho pathway. This interference hinders the proper formation of the cleavage furrow during cell division, leading to some cells either failing to form the cleavage furrow or forming a ruptured furrow, resulting in binucleated cells. Rhodblock 1a can be utilized for investigating cell division mechanisms and holds potential for research into cardiovascular diseases and cancer.

DNJ-20 is an α-glucosidase inhibitor with an IC50 of 55.3 μg/mL. It exhibits broad-spectrum activity against SARS-CoV-2. By interfering with the endoplasmic reticulum-associated glycoprotein folding process (ERQC), DNJ-20 hinders the proper processing of viral glycoproteins, thus blocking the formation and infection of viral particles. It is effective against several SARS-CoV-2 variants, as well as HCoV-229E and HCoV-0C43, with IC50 values reaching up to 1.49 μM. DNJ-20 can be utilized for pan-coronavirus research.

Tubulozole is a microtubule inhibitor. It inhibits microtubule dynamics required for proper mitotic function, effectively blocking cell cycle progression and resulting in apoptosis.

BuChE-IN-2 is an excellent inhibitor of butylcholinesterase (BuChE) with IC50 values of 1.28 μM for BuChE and 0.67 μM for NO. It inhibits Aβ aggregation, ROS formation, and Cu2+ chelation, shows proper blood-brain barrier (BBB) penetration, and is suitable for Alzheimer's disease research.

AZD4877 is a synthetic kinesin spindle protein (KSP) inhibitor with potential antineoplastic activity. KSP inhibitor AZD4877 selectively inhibits microtubule motor protein KSP (also called kinesin-5 or Eg5), which may result in the inhibition of mitotic spindle assembly; activation of the spindle assembly checkpoint; induction of cell cycle arrest during the mitotic phase; and cell death in tumor cells that are actively dividing. Because KSP is not involved in postmitotic processes, such as neuronal transport, this agent may be less likely to cause the peripheral neuropathy often associated with the tubulin-targeting agents. Eg5 is essential for the formation of bipolar spindles and the proper segregation of sister chromatids during mitosis.

Sigvotatug Vedotin is an antibody-drug conjugate (ADC) designed to selectively target integrin αvβ6-positive tumor cells through an engineered antibody with high specificity. Sigvotatug Vedotin employs a protease-cleavable linker that delivers the cytotoxic payload monomethyl auristatin E (MMAE), a microtubule inhibitor, directly into tumor cells. Upon internalization, MMAE disrupts microtubule organization, inhibits proper cell division, and ultimately results in tumor cell death, providing a targeted strategy in oncology research.

Proinsulin C-peptide (human) is a 31-amino acid peptide that links the Proinsulin A and B chains, ensuring their proper folding, biological activity, and regulation of cellular functions.

Proinsulin C-peptide human acetate (Proinsulin C-peptide human acetate (33017-11-7 Free base)) is a polypeptide of 31 amino acid residues that links the A and B chains of proinsulin to ensure proper folding, has biological activity and regulates cellular functions.

Polyethylene glycol tert-octylphenyl ether X-405 is a nonionic surfactant widely employed in both industrial and research settings. Belonging to the polyethylene glycol (PEG) ether family, this compound features a hydrophilic head and a lipophilic tail, making it suitable for use in emulsions, detergents, and solubilizers. Notably beneficial in membrane protein studies, it aids in dissolving and stabilizing proteins for structural analysis. Moreover, Polyethylene glycol tert-octylphenyl ether X-405 is utilized in various applications, such as drug delivery systems, nanotechnology, and diagnostic analysis. Due to its emulsifying and solubilizing properties, it is also used in the production of microemulsions, ointments, and lotions. It is important to note that ingestion or inhalation of this compound can be toxic, necessitating proper handling and safety precautions.