tetrahydrochloride

FGI-106 tetrahydrochloride demonstrates potent inhibitory activity across a broad spectrum of viruses, including those causing hemorrhagic fevers such as Ebola, Rift Valley, and Dengue Fever, with half-maximal effective concentrations (EC50s) of 100 nM, 800 nM, and 400-900 nM, respectively. Additionally, it effectively inhibits non-hemorrhagic fever viruses, notably HCV and HIV-1, with EC50s of 200 nM and 150 nM, respectively, indicating its broad-spectrum antiviral potential.

Muvalaplin tetrahydrochloride (LY3473329) is an orally active lipoprotein (a)Lp(a) agent currently under investigation. Research on the oral formulation of Muvalaplin tetrahydrochloride is ongoing.

Conteltinibtetrahydrochloride (CT-707 tetrahydrochloride) is the tetrahydrochloride form of Conteltinib. It acts as an inhibitor for FAK (IC50=1.6 nM), ALK, and Pyk2. When used in combination with Cabozantinib, Conteltinib tetrahydrochloride exhibits a synergistic antitumor effect.

Triethylenetetramine (Trientine) tetrahydrochloride is an orally active, potent, and selective copper chelator. It aids in the excretion of divalent copper ions from the body, reduces intestinal copper absorption, and minimizes copper accumulation. Additionally, Triethylenetetramine tetrahydrochloride exhibits potential anticancer properties through mechanisms such as telomerase inhibition, anti-angiogenesis, and promoting cancer cell apoptosis (apoptosis). This compound shows promise in the study of Wilson's disease, cancer, and diabetic complications.

Methoctramine tetrahydrochloride is a potent and cardioselective antagonist of the M2 muscarinic receptor, capable of inhibiting muscarine-induced bradycardia in vivo.

Brilacidin tetrahydrochloride (PMX 30063 tetrahydrochloride) is a defensin mimetic antibiotic exhibiting potent antimicrobial activity against various bacteria, with MIC90 values of 1 μg/mL for Streptococcus pneumoniae, 8 μg/mL for Streptococcus viridans and Haemophilus influenzae, and 4 μg/mL for Pseudomonas aeruginosa.

RG7800 hydrochloride is an orally active SMN2 splicing modulator with EC50 values of 23 nM for splicing and 87 nM for SMN protein production, holding promise as a therapeutic agent for [spinal muscular atrophy].

PG-11047 (CGC-11047) is a polyamine analogue that competitively inhibits the function of the natural polyamine spermine. It exhibits broad-spectrum anticancer activities [1] [2].

Spermine-D8 tetrahydrochloride is the deuterated form of Spermine tetrahydrochloride (TMSM-2110), which is an endogenous metabolite.

Spermine-D8 Tetrahydrochloride (Standard) is a reference standard of Spermine-D8 Tetrahydrochloride intended for quantitative analysis, quality control, and related biochemical research applications. Spermine-d8 (tetrahydrochloride) is the deuterated form of spermine tetrahydrochloride, which is an endogenous metabolite.

CB-TE2A (tetrahydrochloride) is a bifunctional chelator (Bifunctional Chelator; BFC) and a derivative of the macrocyclic ligand TETA, featuring a fourteen-membered chain. It is utilized for the conjugation of peptides and radionuclides.

Spermine tetrahydrochloride (Musculamine tetrahydrochloride) is a polyamine involved in cellular metabolism found in all eukaryotic cells. It is a major natural intracellular compound capable of protecting DNA from free radical attack.

Semapimod tetrahydrochloride (CPSI-2364 tetrahydrochloride) is a synthetic ornithine mitogen-activated protein kinase blocker and pro-inflammatory cytokine production inhibitor that interferes with macrophage and microglia function. Sematimod tetrahydrochloride inhibits TLR4 signaling, TNF-α, IL-1β, and IL-6, and is used in the study of Crohn's disease and other inflammatory conditions.

Neamine tetrahydrochloride is a broad-spectrum aminoglycoside antibiotic with antibacterial, antitumor and neuroprotective activities, inhibits the growth of pancreatic cancer cells, and inhibits the proliferation of oral cancer cells. Neamine tetrahydrochloride inhibits xenogeneic human tumor growth and angiogenesis in athymic mice and can be used to study oral and pancreatic cancer.

LDN-193189 Tetrahydrochloride (DM-3189 Tetrahydrochloride) is a selective inhibitor of BMP type I receptors, inhibiting ALK2 and ALK3 (IC₅₀ = 5/30 nM), with weaker activity against ALK4, ALK5, and ALK7, and can be used for research into progressive osseous fibrodysplasia.

Spermine tetrahydrochloride (Standard) is the standard substance of Spermine tetrahydrochloride, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Spermine tetrahydrochloride (Musculamine tetrahydrochloride) is a polyamine involved in cellular metabolism found in all eukaryotic cells. It is a major natural intracellular compound capable of protecting DNA from free radical attack.

DAB (tetrahydrochloride hydrate) is commonly utilized as a chromogenic substrate in immunohistochemistry and enzyme histochemistry to reveal specific antigens or enzymes. Upon oxidation by hydrogen peroxide, DAB (tetrahydrochloride hydrate) forms a brown precipitate at the location of the antigen or enzyme, facilitating microscopic detection and observation. Additionally, DAB (tetrahydrochloride hydrate) holds potential applications in various research fields, such as the development of biosensors and the study of cellular oxidative stress.

(Rac)-AMXT-1501 4HCl is a polyamine transport inhibitor that inhibits polyamine transport and acts synergistically with cisplatin in HNSCC. (Rac)-AMXT-1501 4HCl has potential antimicrobial activity and inhibits neuroblastoma cell proliferation and pneumococcal pod biosynthesis by targeting ornithine decarboxylase and polyamine transport.

GC813 is a potent and permeable inhibitor of MERS coronavirus 3CL protease. GC813 is analogue of GC376.

(2S,2'S)-1,1'-Bis(pyridin-2-ylmethyl)-2,2'-bipyrrolidine hydrochloride ((2S,2'S)-[N,N'-Bis(2-pyridylmethyl)]-2,2'-bipyrrolidine tetrahydrochloride) is a metal-organic framework.

Chitotetraose tetrahydrochloride is a short-chain chitin oligomer derived from arbuscular mycorrhizal (AM) fungi. This compound effectively activates the conserved symbiosis signaling pathway (CSSP) in actinorhizal plant species.

Diethylnorspermine HCl (N1,N11-Diethylnorspermine tetrahydrochloride) potently induces SSAT (spermidine/spermine N1-acetyltransferase) mRNA and effectively stabilizes SSAT enzyme activity.

Me6TREN 4HCl is a potent and efficacious mobilizing agent of hematopoietic stem and progenitor cells (HSPCs) that can act by activating MMP-9 expression and disrupting the SDF-1α/CXCR4 axis, exhibiting more significant mobilizing effects than G-CSF or AMD

Spermine-15N2 (NSC 268508-15N2) is the 15N-labeled version of Spermine. This compound acts as a natural antioxidant and anti-inflammatory agent. Spermine is effective in inhibiting certain bacterial cultures, particularly strains of Staphylococcus aureus, and induces dose-dependent neurotoxicity in the striatum. It can reversibly inhibit DNA synthesis reactions, mixed lymphocyte reactions, and cytotoxic lymphocyte responses in primary cultures of mouse splenocytes. As a polyamine nitric oxide donor, Spermine tetrahydrochloride supplies nitric oxide to platelets and inhibits platelet activation in a concentration-dependent manner. This compound is present in mammalian tissues, plants, bacteria, ribosomes, and bacteriophages, and it can inhibit primary human embryonic lung fibroblast cells in vitro.