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Filtered Search Results
MEDCHEMEXPRESS LLC Methyl protodioscin | 54522-52-0 | 1063.23 | 1 ML
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Methyl protodioscin is a multi-target, selective, steroidal diglycoside inhibitor with antitumor activity that induces cell cycle arrest. It exhibits significant antitumor, anti-inflammatory, and anti-restenosis activities, making it suitable for research on various cancers and inflammatory diseases.
- Induces G2/M cell cycle arrest.
- Regulates Bcl-2/Bax apoptotic pathway.
- Inhibits Akt1/c-Myc axis and MAPK/ERK signaling.
- Reduces cholesterol synthesis by downregulating ADAM15 and inducing FOXO1.
- Inhibits JNK/c-Jun pathway to reduce inflammatory factors.
- Shows potent antitumor effects, including inhibiting proliferation, migration, and invasion.
- Demonstrates anti-inflammatory and anti-restenosis properties.
- Useful in lung, prostate, and pancreatic cancer research.
- Applicable in studies of airway inflammation and enteritis.
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MEDCHEMEXPRESS LLC Methyl dihydrojasmonate | 24851-98-7 | 10 MM * 1 ML
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Methyl dihydrojasmonate is a fragrance ingredient known for its jasmine-like odor. It is widely used in various fragrance mixtures, including decorative cosmetics, fine fragrances, shampoos, toilet soaps, and other toiletries. Additionally, it finds application in non-cosmetic products such as household cleaners and detergents.
- Purity of 98.0%
- Liquid appearance with a density of 0.998 g/mL
- Colorless to light yellow
- Molecular weight of 226.31
- Chemical formula C13H22O3
- Structure classification includes ketones, aldehydes, and acids
- Originally sourced from Plants Oleaceae Jasminum grandiflorum
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MEDCHEMEXPRESS LLC Methyl elaidate | 1937-62-8 | 1 ML
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Methyl elaidate is a fatty acid ester derived from elaidic acid, a monounsaturated omega-9 fatty acid found in certain vegetable oils and animal fats. It is commonly used as a reference compound for the analysis of fatty acids and their derivatives by gas chromatography. This product is intended for research use only.
- Derived from elaidic acid
- Monounsaturated omega-9 fatty acid
- Used as a reference compound for fatty acid analysis
- Suitable for gas chromatography
- Purity: 99.22%
- Appearance: Liquid
- Color: Colorless to light yellow
- For research use only
- Store neat at 4°C under nitrogen
- Store in solvent at -80°C for 6 months or -20°C for 1 month under nitrogen
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MEDCHEMEXPRESS LLC (E)-Methyl 4-coumarate (Standard) | 19367-38-5 | 250 MG
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(E)-Methyl 4-coumarate (Standard) is a high-purity chemical compound commonly utilized as a laboratory chemical and in the manufacture of various substances. This solid compound has a molecular formula of C10H10O3 and a molecular weight of 178.19, offering reliable performance for research applications.
- High purity with an assay of 99.21%
- Excellent purity by HPLC at 99.94%
- Stable under recommended storage conditions
- Optimal storage at 4°C, sealed, away from light and moisture
- Molecular formula: C10H10O3
- Molecular weight: 178.19
- Appears as a solid
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MEDCHEMEXPRESS LLC CA/MAO-B-IN-1 | 98.3% | 345.37 | 25 MG
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CA/MAO-B-IN-1 (Compound 78) is a dual inhibitor for human brain carbonic anhydrases (CA) and Monoamine Oxidase-B (MAO-B). It has IC50s of 8.8 and 7.0 nM, respectively, and reveals a human oral absorption of 71.9% through in silico prediction. It is intended for research use only and is not sold to patients.
- Dual inhibitor for human brain carbonic anhydrases (CA)
- Dual inhibitor for Monoamine Oxidase-B (MAO-B)
- IC50s of 8.8 and 7.0 nM for CA and MAO-B, respectively
- Human oral absorption of 71.9% through in silico prediction
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MEDCHEMEXPRESS LLC SRT 2183 | 1001908-89-9 | 98.1% | 468.57 | 5 MG
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SRT 2183 is a selective Sirtuin-1 (SIRT1) activator with an EC1.5 value of 0.36 μM. It induces growth arrest and apoptosis, accompanied by deacetylation of STAT3 and NF-κB, and a reduction in c-Myc protein levels. This product is for research use only and is not sold to patients.
- Selective Sirtuin-1 (SIRT1) activator with an EC1.5 value of 0.36 μM.
- Induces growth arrest and apoptosis.
- Causes deacetylation of STAT3 and NF-κB.
- Reduces c-Myc protein levels.
- Inhibits the growth of Reh and Nalm-6 cells in a time- and dose-dependent manner.
- Induces expression of DNA-damage response genes associated with accumulation of phospho-H2A.X levels.
- Inhibits RANKL-induced osteoclast differentiation, fusion, and resorptive capacity without affecting osteoclast survival.
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MEDCHEMEXPRESS LLC 2-Amino-1,3-bis(carboxylethoxy)propane hydrochloride | 2421153-68-4 | ≥97.0% | 271.70 | 100 MG
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2-Amino-1,3-bis(carboxylethoxy)propane hydrochloride is a non-protein amino acid, sulfamic acid. It contains one amino group and two terminal carboxylic acids. This compound has a variety of physiological functions and is for research use only.
- Non-protein amino acid
- Sulfamic acid
- Contains one amino group and two terminal carboxylic acids
- Maintains stability of cell membranes
- Regulates cholesterol metabolism
- Supports normal function of the nervous system
- Participates in collagen synthesis
- Anti-oxidation
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MEDCHEMEXPRESS LLC Pyridine, 2,6-dichloro-4-iodo- | 98027-84-0 | 99.6% | 273.89 | 10 G
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2,6-Dichloro-4-iodopyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
- Used as a biochemical reagent.
- Functions as a biological material.
- Acts as an organic compound.
- Suitable for life science related research.
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MEDCHEMEXPRESS LLC 2,6-Dichloro-4-iodopyridine | 98027-84-0 | MFCD07368400 | 99.6% | 273.89 | 5 G
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2,6-Dichloro-4-iodopyridine is a biochemical reagent intended for life science research. It functions as a biological material or organic compound, particularly useful in biochemical assays.
- Suitable for biochemical assay applications
- Store at 4°C, protected from light
- Unstable in solutions, fresh preparation recommended
- Soluble in DMSO for in vitro studies
- Soluble in corn oil for in vivo studies
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MEDCHEMEXPRESS LLC HDHODH-IN-1 100 mg
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HDHODH-IN-1 100MG
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MEDCHEMEXPRESS LLC 2 6-DICHLORO-2 3 5 10MM 1ML
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2 6-DICHLORO-2 3 5 10MM 1ML
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MEDCHEMEXPRESS LLC Famciclovir | 104227-87-4 | ≥98% | 321.33 | 500 MG
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Famciclovir (BRL 42810) is an orally active nucleoside analogue and an antiviral agent with potent activities against HBV, HSV and VZV. It can be used for the research of herpesvirus infection. It effectively cures necrotic hepatitis in mice.
- Orally active nucleoside analogue
- Antiviral agent with potent activities against HBV, HSV and VZV
- Used for the research of herpesvirus infection
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MEDCHEMEXPRESS LLC Olmesartan | 144689-24-7 | 99.9% | 446.50 | 50 MG
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Olmesartan, also known as RNH-6270, is an angiotensin II receptor (AT1R) antagonist that is utilized in the treatment of high blood pressure. It is intended for research use only.
- It is an angiotensin II receptor (AT1R) antagonist.
- It is used to treat high blood pressure.
- It inhibits the growth of HeLa cells in a concentration- and time-dependent manner.
- Repeated dosing decreases mean arterial blood pressure without significantly influencing body weight or food intake.
- Treatment inhibits cardiac hypertrophy.
- Treatment reverses decreased gene expressions of ACE2 and Mas receptor, and inhibits enhanced NADPH oxidase (Nox)4 expression and reactive oxygen species.
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MEDCHEMEXPRESS LLC Clofenapate methyl ester; MCP | 21340-68-1 | 99.0% | 304.77 | 1 ML
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Methyl clofenapate (Clofenapate methyl ester; MCP) is a peroxisome proliferator that can induce hypolipidemia, peroxisome proliferation, and hepatocarcinogenesis. This compound appears as a white to off-white solid. It has been tested and complies with given specifications.
- Appearance: White to off-white solid
- Storage conditions for powder: -20°C for 3 years, 4°C for 2 years
- Storage conditions in solvent: -80°C for 6 months, -20°C for 1 month
- 1H NMR spectrum consistent with structure
- LCMS consistent with structure
- For research use only
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MEDCHEMEXPRESS LLC CA/MAO-B-IN-1 | 98.3% | 345.37 | 50 MG
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CA/MAO-B-IN-1 is a dual inhibitor targeting human brain carbonic anhydrases (CA) and Monoamine Oxidase-B (MAO-B). It demonstrates high potency with IC50s of 8.8 nM and 7.0 nM, respectively, and shows a predicted human oral absorption of 71.9%. This compound is for research use only.
- Dual inhibitor for human brain carbonic anhydrases and Monoamine Oxidase-B
- Reverts the formation of reactive oxygen species (ROS)
- Exhibits neuro- and mitochondrial protective effects
- Improves cell viability in SH-SY5Y cells damaged by Aβ1-42
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