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Filtered Search Results
eMolecules Ambeed / 2-Phenoxyethyl isobutyrate / 25g / 490489950 / A104169 / / 103-60-6 / MFCD00027363 / 208.257 / C12H16O3
Ambeed / 2-Phenoxyethyl isobutyrate / 25g / 490489950 / A104169 / / 103-60-6 / MFCD00027363 / 208.257 / C12H16O3
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Medchemexpress LLC HY-15313B 5mg Medchemexpress, CBB1007 (hydrochloride) CAS: Purity:>98%
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Medchemexpress, HY-15313B 5mg CBB1007 (hydrochloride) CAS: Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC U-99194 maleate (U-99194A) | 234757-41-6 | 99.2% | 50 MG
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U-99194 (PNU-99194) maleate is a selective and potent dopamine D3 receptor antagonist. It inhibits the activation of D3 receptors mediated by endogenously released dopamine or exogenous D3 agonists. This compound can be used for the study of dopamine D3 receptor-mediated motor disorders, particularly kinetic tremors.
- Selective, potent dopamine D3 receptor antagonist (Ki = 160 nM).
- Inhibits D3 receptor activation.
- Abrogates IPSC-suppressive effect of D3 agonist PD 128907 in rat hippocampal slices.
- Significantly suppresses nicotine-induced tremor in mice.
- Useful for studying dopamine D3 receptor-mediated motor disorders, especially kinetic tremors.
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eMolecules 2-chloro-N-(2-methylpropyl)-3-nitroquinolin-4-amine | 133860-75-0 | MFCD09030724 | 250mg
WuXi ChemSupply | 2-chloro-N-(2-methylpropyl)-3-nitroquinolin-4-amine | 250mg | 599170462 | LN03249080 | 95.000 | 133860-75-0 | MFCD09030724 | 279.720 | C13H14ClN3O2
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Cayman Chemical FluoresceIn dIacetate 5g
A cell-permeable fluorogenic cell viability probe; cleaved by intracellular esterases to produce fluorescein which displays excitation/emission maxima of 490/520 nm, respectively
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Medchemexpress LLC Perhexiline maleate | 6724-53-4 | MFCD00057329 | 98.0% | 393.56 | C23H39NO4 | 10 MG
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Perhexiline maleate is the maleate salt of perhexiline, a small-molecule inhibitor of carnitine palmitoyltransferase 1 and 2 (CPT1/CPT2) used in preclinical research to probe mitochondrial fatty-acid metabolism, cancer biology, and cardiovascular disease models. It is provided as a solid salt intended for biochemical and cell-based assays.
- Inhibits CPT1 and CPT2, reducing fatty-acid oxidation
- Maleate salt form improves aqueous handling for assays
- Available in research-scale quantities, including 10 mg
- High reported purity suitable for in vitro and preclinical studies
- Documented chemical identifiers include CAS 6724-53-4 and molecular weight 393.56
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Medchemexpress LLC Enalapril (maleate) | 76095-16-4 | 99.99% | 5 G
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Enalapril (MK-421) maleate is an angiotensin-converting enzyme (ACE) inhibitor and the active metabolite of enalapril. This prodrug is rapidly metabolized in the liver to enalaprilat after oral administration. It is a potent, competitive inhibitor of ACE, an enzyme crucial for converting angiotensin I to angiotensin II, which regulates blood pressure and is a key component of the renin-angiotensin-aldosterone system (RAAS).
- Treats essential or renovascular hypertension
- Treats symptomatic congestive heart failure
- Functions as a potent, competitive ACE inhibitor
- Metabolized to enalaprilat in the liver
- For research use only
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Apexbio Technology LLC Rosiglitazone maleate(Synonyms: Avandia, BRL 49653, BRL49653C, Rosiglitazone maleate salt, BRL49653, RGZ, Rosiglizole maleate), 200mg, CAS: 155141-29-0.
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Rosiglitazone maleate (CAS 155141-29-0) is the maleate salt formulation of rosiglitazone a thiazolidinedione compound targeting the nuclear receptor peroxisome proliferator-activated receptor gamma (PPAR ) By selective activation of PPAR rosiglitazone increases insulin sensitivity of peripheral tissues facilitating glucose uptake and reduction of blood glucose levels Due to its insulin-sensitizing activity rosiglitazone maleate serves as an important research tool in diabetes and metabolic syndrome investigations However recent clinical studies also report associations with adverse cardiovascular events fluid retention and anemia underscoring considerations for risk-benefit evaluation in ongoing research
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Matrix Scientific 2,2,2-TRIFLUOROETHYL METH-100G
2, 2,2-Trifluoroethyl methacrylate, 99%; 100g,C6H7F3O2, MFCD00013576, mw 168.12, [352-87-4]
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Sigma Aldrich Fine Chemicals Biosciences 3-Acetyldeoxynivalenol from Fusarium roseum | 50722-38-8 | MFCD00135964 | 5MG
3-Acetyldeoxynivalenol from Fusarium roseum | Mol Wt: 338.35 | 50722-38-8 | MFCD00135964 | 5MG
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eMolecules Ambeed / (E)-(3-Chloroprop-1-en-1-yl)benzene / 5g / 532081312 / A1149049 / / 21087-29-6 / MFCD00000986 / 152.620 / C9H9Cl
Ambeed / (E)-(3-Chloroprop-1-en-1-yl)benzene / 5g / 532081312 / A1149049 / / 21087-29-6 / MFCD00000986 / 152.620 / C9H9Cl
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Medchemexpress LLC ER-27319 maleate | 1204480-26-1 | 99.4% | 396.44 | 100 MG
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ER-27319 maleate is an acridone derivative, a potent and selective SYK inhibitor that inhibits the tyrosine phosphorylation of SYK and its activity. It inhibits the release of antigen-induced allergic mediators from human and rat mast cells with an IC50 of 10 μM, making it suitable for the study of allergic diseases.
- Inhibits antigen-induced generation of inositol phosphates
- Inhibits release of arachidonic acid
- Inhibits secretion of histamine and tumor necrosis factor α
- Selectively inhibits the tyrosine phosphorylation of SYK
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Chemscene CHEMSCENE
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5000579945 DIETHYL MALEATE 25G
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Medchemexpress LLC Ciproxifan (maleate) | 184025-19-2 | MFCD06411563 | 99.7% | 386.40 g/mol | C20H22N2O6 | 10 MG
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Ciproxifan maleate is a potent, selective, orally bioavailable competitive antagonist of the histamine H3 receptor supplied as a white to off-white powder for research use. It is used as an analytical standard and research reagent in neuroscience and aging-disease studies, with reported nanomolar potency.
- Potent H3 receptor antagonist (IC50 ≈ 9.2 nM)
- High purity (≈ 99.7%)
- Provided as a powdered maleate salt for stability and handling
- Suitable for neuroscience and Alzheimer's disease research
- Available in small pack sizes for analytical and screening use
- Includes CAS number 184025-19-2 and molecular weight 386.40 g/mol
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Medchemexpress LLC AZD9496 maleate | 1639042-28-6 | 99.4% | 50 MG
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AZD9496 maleate is a potent and selective estrogen receptor (ERα) antagonist with an IC50 of 0.28 nM. It functions as an orally bioavailable selective estrogen receptor degrader (SERD), identified as a laboratory chemical.
- Potent and selective estrogen receptor (ERα) antagonist
- Orally bioavailable selective estrogen receptor degrader (SERD)
- Suitable for scientific research
- Used in signaling pathways
- For research use only
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