Lipids and Lipid Derivatives
Medchemexpress LLC Aurantiamide acetate | 56121-42-7 | 1 MG
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
Medchemexpress LLC Sifuvirtide acetate | 4727.98 (free base) | 10 MG
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.
Medchemexpress LLC Eugenol acetate | 93-28-7 | MFCD00026191 | 99.8% | 206.24 g/mol | C12H14O3 | 50 MG
Eugenol acetate (acetyleugenol) is an analytical standard and research reagent used in biochemical and analytical applications. It exhibits antibacterial, anti-inflammatory, antioxidant, and anticancer activity in vitro, and has been reported to inhibit NF-κB signaling while modulating p53 and p21 expression.
- Analytical standard for research and quality control.
- Reported antibacterial and antioxidant activity.
- Inhibits NF-κB signaling in vitro.
- Modulates p53 and p21 (WAF1) expression.
- High purity listed at 99.83%.
- Molecular formula C12H14O3; molecular weight 206.24 g/mol.
Aobchem Carvacryl acetate | ≥97% | CAS 6380-28-5 | C12H16O2 | 10g
Carvacryl acetate | ≥97% | CAS 6380-28-5 | C12H16O2 | 10g
TARGETMOL CHEMICALS INC Alarelin Acetate 25MG
Also available in 1 mL, 5 mg, 10 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Alarelin Acetate is a synthetic GnRH agonist which can directly inhibit proliferation and DNA synthesis of rat GSMC through GnRH receptors.
TARGETMOL CHEMICALS INC Enfuvirtide acetate 25MG
Also available in 2 mg, 5 mg, 10 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus. Purity 99.34%
Medchemexpress LLC RI-AG03 acetate | 98.2% | 2477.93 | 10 MG
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
Medchemexpress LLC KLA seq acetate | 98.1% | 1876.47 (free base) | 1 MG
KLA seq acetate is a cell membrane-penetrating α-helical amphipathic model peptide. It conjugates peptide nucleic acids (PNAs) for delivery to mammalian cells, forming a delivery system that covalently links targeted mRNA and fluorescein. This system exhibits low re-export and is less resistant to serum effects.
- Cell membrane-penetrating alpha-helical amphipathic model peptide
- Conjugates peptide nucleic acids (PNAs) for mammalian cell delivery
- Covalently links targeted mRNA and fluorescein
- Low re-export and reduced serum effects
- Purity: 98.1%
- Molecular weight: 1876.47 (free base)
- Appearance: Solid, white to off-white
- Solubility: ≥ 100 mg/mL in H2O
Medchemexpress LLC Incensole Acetate | 34701-53-6 | 1 MG
Incensole Acetate, a main constituent of Boswellia carterii resin, demonstrates neuroprotective effects against neuronal damage from traumatic and ischemic head injury. It has been shown to reduce Aβ25-35-triggered apoptosis in hOBNSCs and, in in vitro studies, significantly ameliorates Aβ25-35-induced cell death.
- Demonstrates neuroprotective effects against neuronal damage
- Reduces Aβ25-35-triggered apoptosis in hOBNSCs
- Ameliorates Aβ25-35-induced cell death in in vitro studies
- High purity of 99.08%
- Soluble in DMSO
Medchemexpress LLC MK2-IN-5 acetate (Hsp25 kinase inhibitor acetate) | 99.64% | 1396.68 | 10 MG
MK2-IN-5 acetate (Hsp25 kinase inhibitor acetate) is a Mk2 pseudosubstrate with a Ki of 8 μM. It targets the protein interaction domain in the MAPK pathway and inhibits HSP25 and HSP27 phosphorylation. In vitro, MK2-IN-5 acetate (5-10 μM, 2 hours) inhibits TGF-β1 induced connective tissue growth factor (CTGF) and collagen type I in primary human keloid fibroblasts. In vivo, a single intraperitoneal injection of 2 mg/kg of MK2-IN-5 acetate decreased HSP25 phosphorylation in a ventilator-associated lung injury model.
Medchemexpress LLC Protirelin Acetate | 120876-23-5 | 99.9% | 452.46 | 100 MG
Protirelin Acetate is a highly conserved neuropeptide that exerts hormonal control of thyroid-stimulating hormone (TSH) levels and has neuromodulatory functions. This product is for research use only.
- Exerts hormonal control of thyroid-stimulating hormone (TSH) levels
- Has neuromodulatory functions
- Targeted to the thyroid hormone receptor
- Involved in the vitamin D related/nuclear receptor pathway
- Appears as a white to off-white solid
- Sequence: {pGlu}-His-Pro-NH2
- Sequence shortening: {pGlu}-HP-NH2
Medchemexpress LLC Protirelin acetate | 120876-23-5 | CB8947811 | 99.9% | 452.46 | 50 MG
Protirelin acetate is a highly conserved neuropeptide that exerts hormonal control of thyroid-stimulating hormone (TSH) levels and also has neuromodulatory functions.
- Exerts hormonal control of thyroid-stimulating hormone (TSH) levels
- Functions as a neuromodulator
- Targets the thyroid hormone receptor
- Stable as powder for 2 years at -80°C or 1 year at -20°C
- Stable in solvent for 6 months at -80°C or 1 month at -20°C
Medchemexpress LLC 1-O-n-Octyl-B-D-gluc 1mg | 129522-81-2 | 309.47 g·mol^-1 | C14H11D17O6 | 1 MG
Deuterated n-octyl β-D-glucopyranoside (d17) is a deuterium-labeled non-ionic detergent used to solubilize membrane proteins and as an analytical standard in quantitative methods. It is supplied in small, research-scale quantities for biochemical and analytical workflows.
- Deuterium-labeled non-ionic detergent for membrane protein solubilization.
- Serves as a tracer and internal standard for quantitative NMR, GC-MS, and LC-MS.
- Supplied in small, research-grade quantities suitable for analytical use.
- Deuteration provides a mass shift for clear distinction from unlabeled analogs in mass spectrometry.
- Batch-specific certificate of analysis available for purity and isotopic enrichment verification.
Medchemexpress LLC PNC-27 acetate | 99.98% | 4031.73 (free base) | 10 MG
PNC-27 acetate is a chimeric p53-penetratin peptide that binds to HDM-2 in a p53 peptide-like structure, inducing selective membrane-pore formation and leading to cancer cell lysis. It is an anticancer peptide that can be used in acute myeloid leukemia research.
- Binds to HDM-2 in a p53 peptide-like structure.
- Induces selective membrane-pore formation.
- Leads to cancer cell lysis.
- Anticancer peptide.
- Can be used in acute myeloid leukemia research.
- Induces cancer cell death (e.g., 100% cell death in MIA-PaCa-2 cells in 90 minutes at 50 μg/mL).
- Shows anti-leukemia activity in mice (e.g., reduced AML engraftment and prolonged survival at 40 mg/kg intraperitoneal injection once daily for 2-3 weeks).
Medchemexpress LLC PNC-27 acetate | 99.98% | 4031.73 (free base) | 100 MG
PNC-27 acetate is a chimeric p53-penetratin peptide that binds to HDM-2 in a p53 peptide-like structure.
- Induces selective membrane-pore formation, leading to cancer cell lysis.
- Utilized in acute myeloid leukemia research.