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CGGK acetate is a control peptide of CAQK peptide. It is supplied as a white to off-white solid with a sequence of Cys-Gly-Gly-Lys. This peptide is soluble in DMSO at concentrations of 100 mg/mL or greater.
High purity of 96.78%
Molecular weight of 363.43 (free acid)
Appearance as a solid
Color is white to off-white
Soluble in DMSO (≥ 100 mg/mL)
Storage conditions: -80°C for 2 years or -20°C for 1 year (powder); -80°C for 6 months or -20°C for 1 month (in solvent)
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KLA seq acetate is a cell membrane-penetrating α-helical amphipathic model peptide. It conjugates peptide nucleic acids (PNAs) for delivery to mammalian cells and covalently links targeted mRNA and fluorescein to form a delivery system with low re-export and less resistance to serum effects.
Cell membrane-penetrating α-helical amphipathic model peptide.
Conjugates peptide nucleic acids (PNAs) for delivery to mammalian cells.
Forms a delivery system for targeted mRNA and fluorescein.
Exhibits low re-export and less susceptibility to serum effects.
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Macimorelin (EP-1572) acetate is an orally active GHSR agonist and a GH secretagogue that stimulates GH release. It is utilized in research for adult growth hormone deficiency (AGHD) and Cancer anorexia-cachexia syndrome (CACS).
Orally active GHSR agonist
Stimulates GH release
Used in adult growth hormone deficiency (AGHD) research
Used in cancer anorexia-cachexia syndrome (CACS) research
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Vitamin A Acetate (Retinyl Retinol) is a group of unsaturated nutritional hydrocarbons that includes retinol retinal retinoic acid and several provitamin A carotenoids among which beta-carotene is the most important
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DL-alpha-tocopherol is the synthetic form of vitamin E used as an antioxidant and analytical standard for laboratory research and analytical applications. It has the chemical formula C29H50O2, a molecular weight of 430.71 g/mol, and CAS number 10191-41-0. Supplied in a 100 mg pack for lab-scale use.
Acts as a lipid-soluble antioxidant.
Suitable as an analytical standard for research applications.
Useful in assays that evaluate oxidative stress and lipid protection.
Provided in a small pack size for convenient laboratory handling.
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Flecainide acetate (R-818) is a class 1C antiarrhythmic agent used for the management of supraventricular arrhythmia; it works by blocking the Nav1.5 sodium channel in the heart, causing prolongation of the cardiac action potential.
Class 1C antiarrhythmic agent
Manages supraventricular arrhythmia
Blocks Nav1.5 sodium channels
Prolongs cardiac action potential
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(rel)-β-Tocopherol is a relative configuration of β-Tocopherol. β-Tocopherol is a lipid-soluble form of vitamin E that exhibits antioxidant activity. It is intended for research use only and not for human consumption.
β-Tocopherol (50 μM, 48 hours) has been observed to slightly inhibit the proliferation of A7r5 cells (10% inhibition) and CHO cells (20% inhibition), while showing no inhibitory effect on HeLa cells.
It also inhibits PMA-induced adhesion of human erythroleukemia (HEL) cells (11% inhibition) and the expression of integrins α4 and α5 on the cell surface when applied at 50 μM for 24 hours.
Appearance: Solid-Liquid Mixture
Color: Colorless to off-white
In ethanol: 50 mg/mL (119.99 mM); requires sonication.
In a solution of 10% Ethanol, 40% PEG300, 5% Tween-80, and 45% Saline: ≥ 1.25 mg/mL (3.00 mM) as a clear solution.
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γ-Tocopherol, also known as D-γ-Tocopherol, is a natural form of Vitamin E found in many plant seeds such as corn oil and soybeans. It functions as a potent cyclooxygenase (COX) inhibitor and exhibits anti-inflammatory and anti-cancer properties. This product is supplied as a colorless to light yellow liquid.
Potent cyclooxygenase (COX) inhibitor
Possesses anti-inflammatory properties
Demonstrates anti-cancer activity
Well absorbed and accumulates in some human tissues
Inversely associated with the incidence of cardiovascular disease and prostate cancer
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An acetate form of (±)-α-tocopherol; inhibits heat-stress-induced decreases in blastocyst number in pregnant mice and GSH levels in isolated mouse zygotes in a model of hypothermia-induced pre-implantation embryonic death at 1 g/kg; prevents sidestream cigarette smoke-induced decreases in body weight and lung dynamic compliance and increases in lung resistance in mice at 1,050 IU/kg in the diet; increases IL-1β, IL-4, and IFN-γ levels in BALF in the same model
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(rel)-ML-SI3 is an active ingredient of ML-SI3, targeting three isoforms of TRPML. It functions as an inhibitor of TRPML1 and TRPML3, and a potent activator of TRPML2. This compound is supplied as a 10 mM solution in DMSO, ready for research applications.
Targets three isoforms of TRPML
Inhibitor of TRPML1 (IC50 = 3.1 μM) and TRPML3 (IC50 = 28.5 μM)
Potent activator of TRPML2 (EC50 = 3.3 μM)
Supplied as a 10 mM solution in DMSO
For research use only
Store in solvent at -80°C for 6 months or -20°C for 1 month, protected from light
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Ursolic acid acetate (Acetylursolic acid) is a triterpenoid compound and an inhibitor of *Plasmodium falciparum* heat shock protein 90 (PfHsp90) with a KD of 8.16 μM. It is cytotoxic to KB cells, with an IC50 value of 8.4 μM. Ursolic acid acetate can be used in tumor and antimalarial research.
Triterpenoid compound
Inhibitor of Plasmodium falciparum heat shock protein 90 (PfHsp90) (KD = 8.16 μM)
Cytotoxic to KB cells (IC50 = 8.4 μM)
Potential for use in tumor and antimalarial research
Can reduce the ATPase activity of PfHsp90 in a dose-dependent manner (1-5 mM; 4.5 h)
Has an IC50 of 24.93 μM against the P. falciparum FcB1 strain
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