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Filtered Search Results
Takara Bio BspQ I HQ
BspQ I HQ
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![Medchemexpress LLC 8-Quinolinol, 7-[(3-ethoxy-4-methoxyphenyl)[(4-methyl-2-pyridinyl)amino]methyl]- | 430462-93-4 | 98.05% | 415.48 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000388123-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 8-Quinolinol, 7-[(3-ethoxy-4-methoxyphenyl)[(4-methyl-2-pyridinyl)amino]methyl]- | 430462-93-4 | 98.05% | 415.48 | 100 MG
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HQ-415 is a biologically active metal chelator related to Clioquinol, with an EC50 of 15 μM.
- Purity: 98.05%
- Molecular weight: 415.48
- Formula: C25H25N3O3
- CAS No.: 430462-93-4
- Appearance: Solid
- Color: White to off-white
- Shipping: Room temperature in continental US
- Storage: Powder -20°C for 3 years, 4°C for 2 years; In solvent -80°C for 2 years, -20°C for 1 year
- Solubility (In Vitro): DMSO : 5.6 mg/mL (13.48 mM; requires ultrasonic and warming; hygroscopic DMSO has a significant impact on solubility, use newly opened DMSO)
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Eagle Biosciences Inc Tau-383 0N4R Wild-Type Monomer, 100 ug
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Tau-383 (0N4R) Wild-Type Monomers
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eMolecules Isopropenyl p-nitrophenyl carbonate | 96916-42-6 | MFCD27935132 | 1g
Synthonix - Stock | Isopropenyl p-nitrophenyl carbonate | 1g | 495881470 | P64600 | | 96916-42-6 | MFCD27935132 | 223.184 | C10H9NO5
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eMolecules Building Block Tool
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eMolecules AstaTech / 2-(TRIFLUOROMETHYL)-3-FUROIC ACID / 0.25g / 402180709 / 71457 / 95.000 / 536718-30-6 / MFCD03662621 / 180.082 / C6H3F3O3
AstaTech / 2-(TRIFLUOROMETHYL)-3-FUROIC ACID / 0.25g / 402180709 / 71457 / 95.000 / 536718-30-6 / MFCD03662621 / 180.082 / C6H3F3O3
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Sigma Aldrich Fine Chemicals Biosciences 4-Acetoxy-2,5-dimethyl-3(2H)furanone >=95%, FG | 4166-20-5 | MFCD00799462 | 5KG
4-Acetoxy-2,5-dimethyl-3(2H)furanone >=95%, FG | Purity: >=95% | Mol Wt: 170.16 | 4166-20-5 | MFCD00799462 | 5KG
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Eagle Biosciences Inc Tau-412 1N4R Wild-Type Monomer, 100 ug
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Tau-412 (1N4R) Wild-Type Monomers
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Medchemexpress LLC Zaldaride maleate | 109826-27-9 | MFCD04113002 | 99.7% | 544.60 | C30H32N4O6 | 1 MG
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Zaldaride maleate is a potent, orally active, and selective calmodulin inhibitor used in biochemical and cellular research. It inhibits calmodulin-stimulated cAMP phosphodiesterase activity (IC50 ≈ 3.3 nM), modulates ion-channel currents, and is supplied for laboratory research use only.
- Potent calmodulin inhibitor.
- Orally active in pharmacological studies.
- Low nanomolar IC50 for cAMP phosphodiesterase inhibition.
- Reversibly blocks voltage-activated Na+, Ca2+, and K+ currents.
- High purity suitable for research applications.
- Provided as a small solid quantity for laboratory use.
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Selleck Chemical LLC Prochlorperazine dimaleate salt S4631-500mg
Prochlorperazine dimaleate salt is a dopamine (D2) receptor antagonist
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Medchemexpress LLC Zamifenacin fumarate | 127308-98-9 | 99.0% | 531.60 g/mol | C31H33NO7 | 5 MG
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Zamifenacin fumarate is the fumarate salt of zamifenacin (UK-76654), a gut-selective muscarinic M3 receptor antagonist used in research to study gastrointestinal motility. It is provided as a high-purity solid for use in in vitro and in vivo pharmacology studies targeting colonic motility.
- Potent gut-selective muscarinic M3 receptor antagonist that reduces colonic motility.
- High purity suitable for research applications (99.0%).
- Solid, white to off-white form for convenient handling and dosing.
- Molecular weight 531.60 g/mol, molecular formula C31H33NO7.
- Recommended storage at 4°C; in solution, -80°C for long-term stability.
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Apexbio Technology LLC Paroxetine maleate 64006-44-6 50mg
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Paroxetine maleate (CAS 64006-44-6) is a selective serotonin reuptake inhibitor (SSRI) that blocks the reabsorption of serotonin into presynaptic neurons resulting in elevated synaptic serotonin levels and modulation of neurotransmission This compound is widely utilized in the investigation of serotonergic signaling related to anxiety disorders including generalized anxiety disorder post-traumatic stress disorder and premenstrual dysphoric disorder Additionally paroxetine maleate serves as a research tool in studies probing the neuropharmacological mechanisms of chronic headache and its prospective therapeutic interventions
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Medchemexpress LLC SU14813 maleate | 849643-15-8 | MFCD24682713 | 99.0% | 558.56 g/mol | C27H31FN4O8 | 50 MG
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SU14813 maleate is the maleate salt of SU14813, a small-molecule multi-targeted receptor tyrosine kinase inhibitor with nanomolar potency against VEGFR1, VEGFR2, PDGFRβ, and KIT. It is supplied for research use and characterized by a defined chemical formula and high purity suitable for biochemical and cellular studies.
- Potent inhibition of VEGFR1 (IC50 2 nM), VEGFR2 (IC50 50 nM), PDGFRβ (IC50 4 nM), and KIT (IC50 15 nM).
- Maleate salt form to aid solubility and handling in aqueous systems.
- High purity suitable for research-grade experiments.
- Applicable to biochemical kinase assays and cellular target validation studies.
- Provided in small, laboratory-scale quantities for research applications.
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Sigma Aldrich Fine Chemicals Biosciences Methyl 4-bromocrotonate 85%, technical grade | Purity: 85% | Mol Wt: 179.01 | 1117-71-1 | MFCD00000246 | 25G
Methyl 4-bromocrotonate 85%, technical grade | Purity: 85% | Mol Wt: 179.01 | 1117-71-1 | MFCD00000246 | 25G
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TARGETMOL CHEMICALS INC Ro 25-6981 Maleate 25MG
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Also available in 1 mL, 1 mg, 5 mg, 10 mg and bulk. Please contact Fisher for quotes. Ro 25-6981 Maleate is a potent and selective activity-dependent NMDA receptor blocker, specifically targeting the NR2B subunit (IC50 values are 0.009 uM for NR1C/NR2B and 52 uM for NR1C/NR2A receptor subunit combinations). Purity 99.42%
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Medchemexpress LLC Dizocilpine maleate | 77086-22-7 | C20H19NO4 | 25 MG
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Dizocilpine maleate (MK-801 maleate) is a potent, selective, and non-competitive NMDA receptor antagonist. It effectively blocks N-Me-D-Asp-induced current and inhibits microglial activation, reducing TNF-α output. This compound is also utilized for inducing schizophrenia models in rats.
- Potent, selective, and non-competitive NMDA receptor antagonist
- Blocks current induced by N-Me-D-Asp
- Inhibits activation of microglia induced by LPS
- Reduces microglial TNF-α output
- Used to induce schizophrenia models in rats
- Cited in over 40 publications
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