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Retinyl acetate is a synthetic acetate ester derived from retinol, demonstrating potential antineoplastic and chemopreventive activities. It has been shown to inhibit the proliferation of tumor cells and is suitable for various in vitro and in vivo studies.
Inhibits proliferation of tumor cells, such as melanoma cell lines B16 and S91
Inhibits DMBA-induced mammary carcinogenesis in Sprague-Dawley rats
Appears as a solid, off-white to light yellow in color
Soluble in DMSO and corn oil for experimental applications
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Anecortave acetate is a steroidal angiostatic agent used in research on ocular neovascularization and age-related macular degeneration. It is supplied as a high-purity research reagent with supporting analytical documentation and handling guidance.
High reported purity, suitable for research use.
Molecular weight 386.5 g/mol and formula C23H30O5.
Available in a 10 mg research package.
Analytical documentation available, including COA, HNMR, and LCMS.
Used in studies of angiogenesis and retinal neovascular disorders.
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Flecainide acetate (R-818) is a class 1C antiarrhythmic agent primarily used for managing supraventricular arrhythmia. It functions by blocking the Nav1.5 sodium channel in the heart, which results in the prolongation of the cardiac action potential. This product is for research use only.
It is a class 1C antiarrhythmic agent.
It is especially used for the management of supraventricular arrhythmia.
It works by blocking the Nav1.5 sodium channel in the heart.
It causes prolongation of the cardiac action potential.
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PRT062607 acetate is a solid chemical identified for laboratory use and substance manufacturing. It is recommended to store this product at 4°C, sealed and away from moisture. When in solvent, store at -80°C for up to 6 months or -20°C for 1 month, also sealed and away from moisture. Shipping at room temperature is acceptable for periods less than 2 weeks.
Identified for laboratory chemicals and manufacture of substances
Stable under recommended storage conditions
Recommended storage at 4°C, sealed, away from moisture
Storage in solvent at -80°C for 6 months or -20°C for 1 month, sealed, away from moisture
Appearance: Solid
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Lefamulin acetate is an orally active antibiotic that inhibits protein synthesis by binding to the peptidyl transferase center of the 50S bacterial ribosome. It also demonstrates anti-inflammatory activity and is utilized in research pertaining to bacterial infections, such as bacterial pneumonia.
Inhibits protein synthesis by binding to 50S bacterial ribosome.
Exhibits anti-inflammatory activity.
Effective against C. trachomatis, N. gonorrhoeae, and M. genitalium.
Potent activity against M. pneumoniae strains.
Shows antibacterial effect in S. pneumoniae or S. aureus challenged lung infection mice.
Reduces BALF neutrophil cell counts and levels of pro-inflammatory cytokines and chemokines in LPS-induced lung neutrophilia mouse model.
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Sifuvirtide acetate is a potent HIV fusion inhibitor. It inhibits HIV-1 mediated cell fusion in a dose-dependent manner and is highly potent against infection by primary and laboratory-adapted HIV-1 isolates of multiple genotypes. Sifuvirtide acetate can be used in the research of anti-HIV drugs.
Potent HIV fusion inhibitor
Inhibits HIV-1 mediated cell fusion in a dose-dependent manner
Highly potent against infection by primary and laboratory-adapted HIV-1 isolates of multiple genotypes
Can be used in the research of anti-HIV drugs
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NN1213 acetate is a long-acting human amylin peptide analog and a selective amylin receptor agonist. It has EC50 values of 0.177 nM for hAMY3R and 0.262 nM for rAMY3R. This compound significantly reduces food intake and fat mass, leading to body weight reduction in diet-induced obese rats, making it suitable for obesity research.
Selective amylin receptor agonist
EC50 values of 0.177 nM for hAMY3R and 0.262 nM for rAMY3R
Produces dose-dependent body weight loss in diet-induced obese rats
Reduces food intake in rats and beagle dogs
Decreases body weight and food intake in diet-induced obese rats
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CGGK acetate is a control peptide for CAQK peptide. This peptide is provided as a solid, white to off-white appearance with a purity of 96.78%. It is suitable for various research applications.
For research use only
Ships at room temperature in continental US
Store sealed, away from moisture
Soluble in DMSO (≥ 100 mg/mL)
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α-Amyrin acetate is a pentacyclic triterpenoid compound with oral activity. It inhibits cancer cell proliferation, induces apoptosis, and reduces blood glucose levels. This compound is used for research in cancer and metabolic diseases, such as breast cancer and diabetes.
Inhibits proliferation and colony formation in MDA-MB-231 cells.
Induces apoptosis and increases caspase-3 activity in MDA-MB-231 cells.
Promotes cleavage of Poly polymerase, increases E-cadherin, and inhibits vimentin and phosphorylated extracellular signal-regulated activation in MDA-MB-231 cells.
Reduces blood glucose levels in diabetic rats.
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JMV 449 acetate is a potent neurotensin receptor agonist. It exhibits an IC50 of 0.15 nM for inhibiting 125I-neurotensin binding to neonatal mouse brain and an EC50 of 1.9 nM in contracting the guinea-pig ileum. This product also demonstrates highly potent and long-lasting hypothermic and analgesic effects in mice.
Potent neurotensin receptor agonist
IC50 of 0.15 nM for inhibition of 125I-neurotensin binding
EC50 of 1.9 nM in contracting guinea-pig ileum
Highly potent and long-lasting hypothermic effects
Highly potent and long-lasting analgesic effects in mice
White to off-white solid appearance
Soluble in H2O at 100 mg/mL (requires ultrasonic)
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LSD acetate is a peptide utilized in targeted therapy and diagnosis research for tumor lymphatics. It specifically recognizes the lymphatics of C8161 melanoma, without binding to normal tissue lymphatics or tumor blood vessels. When conjugated with a proapoptotic peptide, it can effectively reduce the number of tumor lymphatics.
Recognizes C8161 melanoma lymphatics
Does not bind to normal tissue lymphatics or tumor blood vessels
Reduces tumor lymphatics when conjugated with proapoptotic peptides
Suitable for targeted therapy research
Suitable for diagnosis of tumor lymphatics
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DALDA acetate is a potent and highly selective μ-opioid receptor agonist with a Kᵢ of 1.69 nM. It exhibits antinociceptive and respiratory effects. This compound carries a net positive charge (3+) at physiological pH, making it hydrophilic and more polar than morphine.
Potent and highly selective μ-opioid receptor agonist
Kᵢ of 1.69 nM
Exhibits antinociceptive effects
Exhibits respiratory effects
Carries a net positive charge (3+) at physiological pH
More polar than morphine
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BIMAX1 acetate is a tool peptide used to investigate the interaction of RBBP4 with importin β1 and its effects on the nuclear import pathway. It can be employed to study RBBP4's role in regulating nuclear import efficiency and cellular senescence.
Utilized for investigating RBBP4 and importin β1 interactions
Helps study nuclear import efficiency
Can be used to research cellular senescence
Appears as a white to off-white solid
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sGnRH-A acetate is a salmon gonadotropin-releasing hormone (GnRH) analogue. It stimulates growth hormone secretion and can be used as an inducer of ovulation by artificial insemination.
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Tris Acetate Ultra Pure is a high-purity buffering agent used in laboratory applications where a stable pH is required. The 100g size is suitable for preparing buffer solutions in a variety of molecular biology and biochemistry experiments. Tris Acetate is particularly useful in gel electrophoresis for nucleic acids, where it provides an optimal buffering capacity to stabilize the pH during the separation process. The high purity of this reagent ensures that it does not interfere with the analysis of proteins or nucleic acids, making it ideal for high-precision experiments. This buffering agent is widely used in research and diagnostics where reliable pH control is essential for reproducible results.
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