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Organic compounds with acidic properties, organic acids are generally weak acids incapable of complete dissociation in water. Available in a range of chemical compositions and acid strengths, they can be used for various industrial and everyday applications.
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Thymotrinan TFA is a biologically active fragment of the thymus hormone thymopoietin, provided as the trifluoroacetate (TFA) salt for research use. It modulates immune responses, affecting both humoral and cellular immunity, and is supplied as a purified synthetic peptide for laboratory studies.
Immunomodulating peptide that affects humoral and cellular responses.
Supplied as the trifluoroacetate salt for improved stability and handling.
High purity suitable for in vitro and preclinical research.
Available in small-scale quantities for peptide research workflows.
Molecular weight 531.48 g·mol⁻¹; formula C18H32F3N7O8.
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TP-5801 TFA is an orally active TNK1 (non-receptor tyrosine kinase) inhibitor with an IC50 of 1.40 nM. This compound demonstrates anti-tumor activity and is suitable for various research applications.
Inhibits TNK1-driven, BCR-ABL-driven, and IL-3-driven Ba/F3 cell growth.
Inhibits TNK1-dependent L540 cell growth at low nM levels.
Shows efficacy in mouse survival models, significantly prolonging lifespan.
Inhibits localized tumor growth in mouse xenograft models.
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Glycyl-Exatecan TFA is a derivative of Exatecan and functions as an anticancer agent. It exhibits significant antitumor activity and can be utilized for research concerning cancers like solid tumors.
Derivative of Exatecan
Functions as an anticancer agent
Exhibits significant antitumor activity
Utilized in research concerning cancers like solid tumors
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Mazdutide TFA is a long-acting synthetic oxyntomodulin analog. It acts as a co-agonist of glucagon-like peptide (GLP-1R) and glucagon receptor (GCGR). It stimulates insulin secretion from mouse islets and is utilized in studies for obesity and type 2 diabetes (T2D).
Acts as a co-agonist of GLP-1R and GCGR
Stimulates insulin secretion from mouse islets
Used in studies of obesity and type 2 diabetes
Reduces body weight and physical intake in diabetic mice with diet-induced obesity
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Ac-DEVD-CMK TFA is a selective and irreversible caspase-3 inhibitor. It significantly inhibits apoptosis induced by high levels of glucose or 3,20-dibenzoate, and can be used in various experimental approaches to inhibit apoptosis.
Selective and irreversible caspase-3 inhibitor.
Significantly inhibits apoptosis induced by high levels of glucose or 3,20-dibenzoate.
Suitable for various experimental approaches to inhibit apoptosis.
Inhibits IDB-induced apoptosis.
Attenuates acetaminophen-induced liver injury.
Mitigates liver damage by inhibiting GSK‐3β or caspase‐3 activity.
Effective in inhibiting citrate-induced p21 cleavage and G2/M accumulation in human pharyngeal squamous carcinoma cell lines.
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Pyrophosphatase Inorganic (E coli) purified from recombinant E coli strain carrying the E coli inorganic pyrophosphatase gene Inorganic pyrophosphatase (PPase) is a ubiquitous enzyme that catalyzes the hydrolysis of inorganic pyrophosphate into orthophosphate
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