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Filtered Search Results
TARGETMOL CHEMICALS INC Teriparatide acetate 5MG
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Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Teriparatide acetate (Forteo) is a PHT agonist, with an IC50 of 2 nM in HEK293 cells.Teriparatide acetate is a recombinant form of parathyroid hormone. It is an effective anabolic (i.e., bone growing) agent used to treat some forms of osteoporosis. Intermittent use of Teriparatide acetate activates osteoblasts more than osteoclasts, which leads to an overall increase in bone. Purity 99.86%
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Medchemexpress LLC RI-AG03 acetate | 98.2% | 2477.93 | 10 MG
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RI-AG03 acetate is an orally active and BBB-penetrable Tau aggregation peptide inhibitor. It inhibits Tau aggregation and improves associated neurodegeneration and behavioral phenotypes in both in vivo and in vitro models. It can be used in the study of tauopathies such as Alzheimer's disease.
- Inhibits Tau aggregation
- Improves associated neurodegeneration and behavioral phenotypes
- Orally active and BBB-penetrable
- Suitable for the study of tauopathies such as Alzheimer's disease
- Molecular weight: 2477.93 (free base)
- Appearance: Solid
- Color: White to off-white
- Formula: C104H189N49O22·xC2H4O2
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TARGETMOL CHEMICALS INC Dichlorisone Acetate 50MG
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Also available in 1 mL, 10 mg and bulk. Please contact Fisher for quotes. Dichlorisone Acetate (Diloderm) is a synthetic glucocorticoid corticosteroid with anti-inflammatory activity. Purity 99.72%
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Medchemexpress LLC TAT-CBD3A6K acetate | 99.8% | 3249.83 (free base) | 1 MG
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TAT-CBD3A6K acetate is a modified TAT-CBD3 peptide that reduces T- and R-type voltage-dependent calcium currents in dorsal root ganglion (DRG) neurons. It shows anti-nociceptive effects in a model of AIDS-induced peripheral neuropathy by preventing CRMP-2-mediated enhancement of T- and R-type calcium channel function.
- Peptides and derivatives
- Inhibitors and substrates
- Neurological applications
- Eye or ear disease research
- Inhibits calcium channels
- Used in AIDS research
- Anti-nociceptive effects
- Peripheral neuropathy studies
- DRG studies
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Medchemexpress LLC Geranyl acetate | 105-87-3 | 100 G
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Geranyl acetate is an acyclic monoterpene ester derived from geraniol. It is widely used in the cosmetics industry due to its pleasant scent and has been shown to induce cell apoptosis. This product appears as a colorless to light yellow liquid.
- Acyclic monoterpene ester
- Derived from geraniol
- Used in cosmetics industry for pleasant scent
- Induces cell apoptosis
- Purity: 99.74%
- Molecular weight: 196.29
- Chemical formula: C12H20O2
- Density: 0.916 g/cm³
- Exhibits significant anti-cancer activity against colo-205 cancer cell line
- Agonist activity at rat TRPA1 (EC50 of 25.8 μM in HEK293 cells)
- Antagonist activity against rat TRPA1 (IC50 of 21.2 μM in HEK293 cells)
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Medchemexpress LLC SPR741 acetate | 99.4% | 1052.18 | 100 MG
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SPR741 acetate is a cationic peptide derived from polymyxin B, functioning as a potentiator molecule. It enhances the permeability of the outer membrane of Gram-negative bacteria, making it useful for treating severe Gram-negative bacterial infections and inhibiting multidrug-resistant Gram-negative bacteria. While it lacks significant antibacterial activity on its own, it increases the accumulation of co-administered antibiotics inside the pathogen and has an improved safety profile compared to polymyxin B.
- Enhances permeability of Gram-negative bacterial outer membrane
- Useful for treating severe Gram-negative bacterial infections
- Inhibits multidrug-resistant Gram-negative bacteria
- Broadens activity spectrum of antibiotics when combined
- Potentiates antibiotics that are substrates of the AcrAB-TolC efflux pump
- Improved safety profile compared to polymyxin B
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Medchemexpress LLC MAIT-203 (acetate) | 10 MG
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MAIT-203 (acetate) | 10 MG
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Medchemexpress LLC Larazotide (acetate) | 881851-50-9 | MFCD31630844 | 99.7% | 785.89 g/mol | C34H59N9O12 | 100 MG
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Larazotide acetate is an eight-amino-acid peptide zonulin antagonist supplied as a research reagent. It is used in studies of celiac disease and intestinal barrier dysfunction and has reported antiviral activity against varicella-zoster virus. For research use only; not for human therapeutic use.
- Eight-amino-acid peptide sequence: Gly-Gly-Val-Leu-Val-Gln-Pro-Gly.
- Orally active zonulin antagonist that modulates tight junctions.
- Reported in vitro antiviral activity versus varicella-zoster virus.
- Supplied as a powder; recommended sealed, cold storage to preserve stability.
- Well characterized molecular weight and formula for research applications.
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Medchemexpress LLC Histrelin acetate | 220810-26-4 | 99.9% | 1323.50 (free base) | 1 MG
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Histrelin acetate is a GnRH analogue and a GnRH Receptor agonist. It increases serum luteinising hormone (LH), follicle stimulating hormone (FSH), and testosterone levels. It can be used in the research of prostate cancer and endometriosis.
- Stimulates release of vasopressin (VP) from isolated rat hypothalamo-neurohypophysial explants
- Stimulates oxytocin (OT) release from the rat hypothalamo-neurohypophysial system
- Rescues circulating LH concentrations in Csfmop/Csfmop mice
- Reduces the number of endometrial glands and atrophies the stroma in rabbits
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Medchemexpress LLC SOR-C13 acetate | 10MG
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SOR-C13 acetate | 10MG
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Medchemexpress LLC Vapreotide acetate | 849479-74-9 | 98.2% | 1191.42 | 10 MG
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Vapreotide acetate is a neurokinin-1 (NK1) receptor antagonist with an IC50 of 330 nM. It is intended for research use only.
- Attenuates Substance P (SP)-triggered intracellular calcium increases and NF-κB activation.
- Inhibits SP-induced IL-8 and MCP-1 production.
- Inhibits HIV-1 infection of human MDM in vitro.
- Inhibits GH-, PRL, and/or alpha-subunit release by human GH-secreting pituitary adenoma cells.
- Exhibits affinities for SSTR2, -3, and -5.
- Reduces tumor volumes and weights in androgen-independent prostate cancer xenografts.
- Decreases collateral circulation blood flow in cirrhosis and attenuates its development.
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TARGETMOL CHEMICALS INC ABT-510 acetate 5MG
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Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. ABT-510 acetate is an endogenous anti-angiogenic TSP peptide inhibitor, a thrombospondin analog, with anti-inflammatory, anti-cancer and anti-angiogenic activity that induces apoptosis and inhibits ovarian tumor growth in an orthotopic, syngeneic model of epithelial ovarian cancer.ABT-510 acetate reduces angiogenesis and inflammatory responses in a mouse model of inflammatory bowel disease. ABT-510 acetate reduces angiogenesis and inflammation in mouse models of inflammatory bowel disease (IBD) and can be used in cancer research, particularly in epithelial ovarian cancer, as well as in inflammatory bowel disease (IBD). Purity 95.07%
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Medchemexpress LLC Lysipressin acetate | 83968-49-4 | 99.8% | 1116.27 | 2 MG
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Lysipressin (Lysine vasopressin) acetate is an antidiuretic hormone found in pigs and some marsupial families. It induces contraction of the rabbit urinary bladder smooth muscle and activates adenylate-cyclase. This product is suitable for laboratory use and research.
- Induces contraction of rabbit urinary bladder smooth muscle
- Activates adenylate-cyclase
- White to off-white solid appearance
- High purity of 99.8%
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Medchemexpress LLC Aurantiamide acetate | 56121-42-7 | 1 MG
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Aurantiamide acetate is a selective and orally active cathepsin inhibitor isolated from Portulaca oleracea L. It exhibits anti-inflammatory activities and can be used for the study of inflammatory diseases.
- Selective and orally active cathepsin inhibitor
- Isolated from Portulaca oleracea L.
- Exhibits anti-inflammatory activities
- Useful for studying inflammatory diseases
- Inhibits cathepsin L (IC50 of 12 μM)
- Inhibits cathepsin B (IC50 of 49 μM)
- Store powder at -20°C for 3 years or 4°C for 2 years
- Store in solvent at -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC Sifuvirtide acetate | 4727.98 (free base) | 10 MG
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Sifuvirtide (SFT) acetate is a powerful HIV fusion inhibitor that prevents HIV-1 mediated cell fusion in a dose-dependent manner. It demonstrates high potency against both primary and laboratory-adapted HIV-1 isolates across various genotypes, making it suitable for anti-HIV drug research.
- 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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