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Selepressin (FE 202158) acetate is a selective vasopressin V1A receptor agonist Selepressin acetate is a potent vasopressin Selepressin acetate can be used in the study of septic shock
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CIGB-300 acetate (P15-Tat acetate) is an anti-casein kinase 2 (CK2) peptide that exhibits anticancer properties by interfering with the phosphorylation of protein kinase CK2. CIGB-300 acetate induces apoptosis in multiple tumor cell lines and can be used in cancer research.
Exhibits anticancer properties
Interferes with phosphorylation of protein kinase CK2
Induces apoptosis in multiple tumor cell lines
Useful in cancer research
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TL13-112 is a degrader of anaplastic lymphoma kinase (ALK) with an IC50 of 0 60 nM It demonstrates anti-proliferative activity in non-small-cell lung cancer (NSCLC) and anaplastic large cell lymphoma (ALCL) cell lines
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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. It also covalently links targeted mRNA and fluorescein to form a delivery system. This system demonstrates low re-export and is less resistant to serum effects.
Storage: Sealed storage, away from moisture. Powder stored at -80°C for 2 years or -20°C for 1 year. In solvent, stored at -80°C for 6 months or -20°C for 1 month.
Solubility (in vitro): ≥ 100 mg/mL in H2O.
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R5 peptide (acetate) is a synthetic peptide used as a laboratory chemical for research purposes. It appears as a white to off-white solid with a molecular weight of 2013.26 (free base) and a high purity of 98.99%. This peptide is stable under recommended storage conditions.
Suitable for laboratory research
Stable under recommended storage conditions
White to off-white solid
High purity
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DOTATATE (acetate) is a DOTA-conjugated peptide used in research for positron emission tomography (PET) imaging and peptide receptor radionuclide therapy. It functions as a precursor for radiolabeling with diagnostic and therapeutic radionuclides and for synthesis of radionuclide-drug conjugates, supplied as an acetate salt for laboratory use.
High purity (>98%).
Suitable for radiolabeling with diagnostic and therapeutic radionuclides.
Provided with supporting documents (datasheet, SDS, COA).
Available in multiple package sizes including 100 MG.
Peptide format designed for chelation and stable conjugation.
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Decyl methyl ether is a fatty ether reagent supplied for research use. It is described by the manufacturer as a strong fatty ether that is non-genotoxic and phototoxic/photosensitizing. Use and storage instructions are provided in the product certificate of analysis.
Fatty ether reagent for biochemical assays.
Non-genotoxic according to manufacturer data.
Phototoxic/photosensitizing properties reported.
Certificate of analysis provides recommended storage and handling.
Suitable as a reagent or solvent in laboratory research.
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Bazedoxifene acetate (CAS 198481-33-3) is a selective estrogen receptor modulator (SERM) targeting estrogen receptors (ER) It is designed to modulate ER activity thereby regulating estrogen-dependent cellular pathways Bazedoxifene acetate exerts its biological activity primarily through tissue-specific agonism and antagonism of ER In in vitro studies Bazedoxifene acetate demonstrates receptor modulation with reported affinities (Ki) of 26 nM for ER and 99 nM for ER Based on these pharmacological properties Bazedoxifene acetate holds research potential in osteoporosis and bone metabolism studies as well as in investigations of hormone-responsive cellular mechanisms and pancreatic cancer
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Citronellyl acetate is a monoterpene product derived from the secondary metabolism of plants. It functions as an orally active antinociceptive agent, modulating various receptors and kinases involved in nociception, and is suitable for acute pain research.
Derived from secondary metabolism of plants
Functions as an orally active antinociceptive agent
Modulates TRPV1, TRPM8, ASIC, glutamate receptors, PKC, and PKA-mediated nociception
Suitable for acute pain research
Purity of 98.0%
Appearance as a colorless to light yellow liquid
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Pasireotide Acetate (CAS 396091-76-2) is a cyclohexapeptide somatostatin analog that acts as a multi-receptor ligand selectively activating several somatostatin receptor subtypes (sst1/2/3/5 with pKi values of 8 2 9 0 9 1 and 9 9 respectively) By modulating these receptors Pasireotide Acetate regulates the secretion of growth hormone insulin-like growth factor I (IGF-I) and adrenocorticotropic hormone (ACTH) at the cellular level Preclinical investigations indicate its capacity to alter endocrine hormone release with implications for studies in acromegaly and Cushing s disease Its demonstrated effects on secretion inhibition proliferation control and induction of apoptosis make it a valuable tool in studies of related biological pathways
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KY-02327 acetate is a small-molecule inhibitor of the Dishevelled (Dvl)-CXXC5 interaction that activates the Wnt/β-catenin signaling pathway. It is supplied as a solution in DMSO for cell biology and biochemical assays and is commonly used to study osteoblast differentiation and pathway modulation. The compound has formula C22H31N3O6, molecular weight 433.50 g/mol, and reported purity ~99.2%.
Provided as a ready-to-use solution for rapid experimental setup.
Reported high purity to minimize impurity-related effects.
Suitable for Wnt pathway and osteoblast differentiation studies.
Available in solid form for custom formulation or storage.
Compact packaging reduces storage footprint and waste.
Stable under recommended storage conditions for reliable results.
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nor-NOHA (acetate) (CAS 1140844-63-8) is a potent reversible inhibitor of rat liver arginase (Ki 0 5 M) By competitively inhibiting arginase nor-NOHA modulates the cellular balance between the L-arginine-dependent pathways of nitric oxide synthase (NOS) and arginase affecting nitric oxide production and urea cycle metabolism In vitro studies have shown that nor-NOHA suppresses proliferation migration and invasion of HepG2 hepatocellular carcinoma cells induces apoptosis and alters expression of Arg1 MMP-2 P53 and ECD In vivo nor-NOHA improves endothelial function in rat models of inflammation by enhancing NOS activity increasing EDHF and reducing superoxide anion production This compound is widely used to investigate arginase-related mechanisms in cellular and vascular biology
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Flecainide acetate (R-818) is a class 1C antiarrhythmic agent primarily used for the management of supraventricular arrhythmia. It functions by blocking the Nav1.5 sodium channel in the heart, leading to the prolongation of the cardiac action potential.
Class 1C antiarrhythmic agent
Blocks the Nav1.5 sodium channel
Causes prolongation of the cardiac action potential
For research use only
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Cetrorelix Acetate, also known as SB-75 acetate, is a potent gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM. It is intended for research use only.
Inhibits the growth of ES-2 cell line at 1000 ng/mL
Shows comparable antiproliferative effects to GnRH-I agonists
Utilized in research for conditions such as Polycystic Ovarian Syndrome and Infertility
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RVG-Cys (RVG29-Cys) acetate is a peptide derived from rabies virus glycoprotein (RVG29) with Cys attached to facilitate subsequent conjugation. It enhances the specific targeted delivery of proteins in brain tissue and neurons.
Peptide derived from rabies virus glycoprotein (RVG29)
Includes Cys for subsequent conjugation
Enhances specific targeted delivery of proteins
Delivers to brain tissue and neurons
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