Lipids and Lipid Derivatives
Medchemexpress LLC Aurantiamide acetate | 56121-42-7 | MFCD17214814 | 99.9% | 444.52 g·mol⁻¹ | C27H28N2O4 | 10 MG
Aurantiamide acetate is a small-molecule cathepsin inhibitor used as a research reagent with reported anti-inflammatory activity. It inhibits cathepsin L (IC50 12 μM) and cathepsin B (IC50 49 μM), is supplied as a white to off-white solid, and is reported at ~99.9% purity (CAS 56121-42-7).
- Selective cathepsin L and B inhibitor (IC50 12 μM and 49 μM).
- Demonstrated anti-inflammatory activity for disease research.
- High purity suitable for analytical and preclinical use.
- Soluble in DMSO (50 mg/mL) and formulatable for in vivo dosing.
- Stable when stored under recommended conditions for powder and solutions.
Sigma Aldrich Fine Chemicals Biosciences Citronellyl acetate >=95%, FCC, FG | 150-84-5 | MFCD00015039 | 1KG
Citronellyl acetate >=95%, FCC, FG | Purity: >=95% | Mol Wt: 198.3 | 150-84-5 | MFCD00015039 | 1KG
Medchemexpress LLC Roxatidine Acetate Hydrochloride | 93793-83-0 | 99.6% | 1 ML
Roxatidine Acetate Hydrochloride is a potent, selective, competitive, and orally active histamine H2-receptor antagonist. It has antisecretory potency against gastric acid secretion and can suppress inflammatory responses. This product can be used for gastric and duodenal ulcers research and exhibits antitumor activity.
- Potent, selective, competitive, and orally active histamine H2-receptor antagonist
- Exhibits antisecretory potency against gastric acid secretion
- Can suppress inflammatory responses
- Suitable for gastric and duodenal ulcers research
- Shows antitumor activity
Selleck Chemical LLC TL13-112-E1846-25MG
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
Medchemexpress LLC Phenyl acetate | 122-79-2 | 99.7% | 1 ML
Phenyl acetate is an endogenous metabolite and a metabolite of 2-phenylethylamine, found in urine. It plays a role in regulating glutamine metabolism and has been investigated as a potential detection index for certain diseases, including depression. This product is supplied as a high-purity liquid.
- Endogenous metabolite
- Metabolite of 2-phenylethylamine
- Regulates glutamine metabolism
- Potential detection index for diseases like depression
- Can block glutaminolysis in lung cancer cell lines in vitro
- Colorless to light yellow liquid appearance
- High purity of 99.7%
Medchemexpress LLC L-796778 acetate | 2922280-21-3 | 1MG
L-796778 acetate is a selective agonist of the sst3 receptor In CHO-K1 cells expressing the hsst3 receptor L-796778 acetate is a partial agonist that inhibits Forskolin (HY-15371)-stimulated cAMP production with an IC50 value of 18 nM L-796778 acetate has anticonvulsant effect[1]
Medchemexpress LLC Larixyl acetate | 4608-49-5 | 99.5% | 348.52 g·mol⁻¹ | C22H36O3 | 1 ML
Larixyl acetate is a diterpenoid research reagent that acts as a potent, selective TRPC6 inhibitor. Supplied as a 10 mM solution in DMSO, it is intended for laboratory pharmacology and biochemical studies targeting TRPC channels and related pathways.
- Potent, selective TRPC6 inhibition demonstrated in cellular assays.
- Provided as a ready-to-use 10 mM solution for convenient dosing.
- High purity suitable for analytical and research applications.
- Well-characterized molecular weight (348.52 g·mol⁻¹) for dosing calculations.
- Storage recommendations available for both powder and solution to preserve stability.
Selleck Chemical LLC TL13-112-E1846-100MG
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
Apexbio Technology LLC Bazedoxifene acetate 198481-33-3 10mg
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
Medchemexpress LLC Citronellyl acetate | 150-84-5 | MFCD00015039 | 1 G
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
Apexbio Technology LLC Pasireotide Acetate 396091-76-2 10mg
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
Medchemexpress LLC KY-02327 acetate | 2989396-34-9 | 99.2% | 433.50 g/mol | C22H31N3O6 | 10MM 1ML
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.
Medchemexpress LLC ATIC-IN-1 acetate | 3067165-96-9 | C23H37N7O7 | 50 MG
ATIC-IN-1 acetate is an inhibitor that targets Aminoimidazole carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase (ATIC) dimerization with a Ki value of 685 nM. ATIC catalyzes de novo purine biosynthesis, and its dimerization is crucial for AICAR transformylase activity. This inhibitor demonstrates anti-tumor activity by reducing cell numbers and cell division rates and inhibits the proliferation of MCF-7 cells.
- Targets ATIC dimerization with a Ki value of 685 nM
- Inhibits proliferation of MCF-7 cells
- Reduces cell numbers and cell division rates
- Suitable for studying respiratory diseases, cancer, pulmonary disease, and lung fibrosis
Medchemexpress LLC Flecainide (acetate) | 54143-56-5 | 99.4% | 474.39 | 50 MG
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