Alcohols and polyols
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- (1)
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- (1)
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- (1)
- (36)
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- (1)
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- (1)
- (1)
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- (3)
- (1)
- (15)
- (12)
- (1)
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- (7)
- (12)
- (1)
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- (24)
- (1)
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- (1)
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- (1)
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- (1)
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- (24)
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- (1)
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- (1)
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- (1)
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Filtered Search Results
Medchemexpress LLC Caroverine hydrochloride | 55750-05-5 | MFCD01684929 | 98.9% | 401.93 g/mol | C22H28ClN3O2 | 5 MG
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Caroverine hydrochloride is a research reagent that acts as a potent, competitive, and reversible antagonist of NMDA and AMPA glutamate receptors. It also exhibits antioxidant and calcium-blocking activity with vasorelaxant effects, and is used in studies such as inner-ear tinnitus research. The compound is supplied as a white to off-white solid with high purity.
- Antagonist of NMDA and AMPA glutamate receptors.
- Exhibits antioxidant and calcium-blocking activity.
- Displays vasorelaxant effects useful in vascular studies.
- Suitable for research into inner-ear tinnitus mechanisms.
- High purity for research applications (98.9%).
- White to off-white solid, stable when stored sealed and protected from moisture.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Claramine (hydrochloride) | 99.6% | 625.45 | 5 MG
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Claramine hydrochloride is a steroid polyamine with blood-brain barrier permeability. It can regulate the properties of lipid membranes and protect cells from various biological toxins, including misfolded protein oligomers and biological protein-based toxins.
- Steroid polyamine
- Blood-brain barrier permeability
- Regulates properties of lipid membranes
- Protects cells from various biological toxins, including misfolded protein oligomers and biological protein-based toxins
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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![Medchemexpress LLC Benzamide, N-(3-aminopropyl)-N-[(1R)-1-[7-chloro-4-oxo-3-(phenylmethyl)-4H-1-benzopyran-2-yl]-2-methylpropyl]-4-methyl-, hydrochloride | 940929-33-9 | 99.8% | 553.52 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000438369-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC Benzamide, N-(3-aminopropyl)-N-[(1R)-1-[7-chloro-4-oxo-3-(phenylmethyl)-4H-1-benzopyran-2-yl]-2-methylpropyl]-4-methyl-, hydrochloride | 940929-33-9 | 99.8% | 553.52 | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Benzamide, N-(3-aminopropyl)-N-[(1R)-1-[7-chloro-4-oxo-3-(phenylmethyl)-4H-1-benzopyran-2-yl]-2-methylpropyl]-4-methyl-, hydrochloride | 940929-33-9 | 99.8% | 553.52 | 25 MG
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Agn 192403 hydrochloride | 175521-95-6 | >95.0% | 189.73 | C10H19N·HCl | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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AGN 192403 hydrochloride is a small-molecule I1 (imidazoline-1) receptor ligand used in cardiovascular and neurological research. It has been reported to show neuroprotective effects, and in cellular studies to bind the TMED9 cargo receptor, affecting MUC1-fs trafficking. The compound is used as a research tool to probe imidazoline receptor pharmacology and related mitochondrial pathways.
- Selective I1 receptor activity suitable for receptor pharmacology studies.
- Reported neuroprotective effects for neurological research applications.
- Demonstrated interaction with TMED9, useful in cellular trafficking studies.
- Applicable to in vitro assays and exploratory in vivo models.
- Available from multiple research suppliers with supporting COA/technical data.
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Medchemexpress LLC SRI-011381 hydrochloride | 2070014-88-7 | 99.6% | 365.94 g/mol | C20H32ClN3O | 10 MG
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SRI-011381 hydrochloride is an orally active TGF-β signaling agonist used in research. It promotes fibroblast proliferation and increases TGF-β1, NALP3, collagen-1, and α-SMA expression in vitro, and reduces neuronal loss and inflammatory infiltration in animal models.
- Orally active TGF-β signaling agonist for in vivo and in vitro studies.
- Promotes fibroblast proliferation and extracellular matrix marker expression.
- Demonstrated neuroprotective effects in animal disease models.
- High purity suitable for research applications.
- Soluble in DMSO, water, and PBS with ultrasonic assistance.
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Medchemexpress LLC VU6036720 hydrochloride | 3026597-12-3 | 99.7% | 473.39 | 1 ML
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VU6036720 hydrochloride is a potent and specific in vitro inhibitor of Kir4.1/5.1 channels, demonstrating an IC50 value of 0.24 μM. This compound is suitable for various research applications, particularly those related to brain and kidney studies.
- Potent and specific in vitro Kir4.1/5.1 inhibitor
- Inhibits Kir4.1/5.1 channels with an IC50 of 0.24 μM
- Suitable for brain and kidney research
- High purity of 99.65%
- Supplied as 10 mM solution in 1 mL DMSO
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Medchemexpress LLC VU6036720 (hydrochloride) | 99.65% | 473.39 | 25 MG
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VU6036720 hydrochloride is a potent and specific in vitro inhibitor of Kir4.1/5.1, effectively inhibiting these channels with an IC50 value of 0.24 μM. This compound is utilized in research focusing on brain and kidney functions.
- Potent and specific in vitro inhibitor of Kir4.1/5.1 channels
- Inhibits Kir4.1/5.1 channels with an IC50 value of 0.24 μM
- Useful for research related to the brain and kidney
- Storage conditions: 4°C, sealed storage, away from moisture and light. In solvent: -80°C for 6 months; -20°C for 1 month (sealed storage, away from moisture and light).
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Medchemexpress LLC Befiradol hydrochloride | 2436760-81-3 | 99.9% | 430.32 | 50 MG
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Befiradol hydrochloride (NLX-112 hydrochloride) is a selective 5-HT1A receptor agonist. It is intended for research use only.
- Selective 5-HT1A receptor agonist
- Intended for research use only
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Medchemexpress LLC BMS-199264 hydrochloride | 186180-83-6 | 99.3% | 567.53 g/mol | C26H32Cl2N4O4S | 25 MG
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BMS-199264 hydrochloride is a research-grade small-molecule inhibitor of the F1F0 ATP hydrolase provided as a high-purity solid for biochemical and cardiac ischemia/reperfusion studies in vitro and in vivo.
- High purity (99.28%).
- Molecular weight 567.53 g/mol.
- Chemical formula C26H32Cl2N4O4S.
- Supplied as a 25 MG package.
- Appearance: solid; storage: 4°C; in solution store at -80°C (6 months) or -20°C (1 month).
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Medchemexpress LLC Tipiracil hydrochloride | 183204-72-0 | 99.9% | C9H12Cl2N4O2 | 50 MG
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Tipiracil hydrochloride is a thymidine phosphorylase inhibitor (TPI) used for cancer research. It exhibits antiangiogenic effects and inhibits the proliferation of endothelial cells. This compound is also a potent inhibitor of thymidine phosphorylase, the enzyme responsible for degrading FTD.
- Thymidine phosphorylase inhibitor
- Used in cancer research
- Exhibits antiangiogenic effect
- Inhibits proliferation of endothelial cells
- Potent inhibitor of thymidine phosphorylase
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Medchemexpress LLC Tipiracil hydrochloride | 183204-72-0 | 99.9% | C9H12Cl2N4O2 | 200 MG
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Tipiracil hydrochloride is a thymidine phosphorylase inhibitor (TPI) that is used for cancer research. It exhibits an antiangiogenic effect and inhibits the proliferation of endothelial cells. Tipiracil is a potent inhibitor of thymidine phosphorylase, the enzyme that degrades FTD.
- Thymidine phosphorylase inhibitor (TPI)
- Antiangiogenic effect
- Inhibits proliferation of endothelial cells
- Potent inhibitor of thymidine phosphorylase
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Medchemexpress LLC Donepezil Hydrochloride | 120011-70-3 | 99.8% | C24H30ClNO3 | 1 G
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Donepezil Hydrochloride (E2020) is a reversible, selective Acetylcholinesterase (AChE) inhibitor. It demonstrates high selectivity for AChE over Butyrylcholinesterase (BuChE) and exhibits neuroprotective effects against Aβ42 neurotoxicity. Its IC50 for AChE activity is 6.7 nM.
- Reversible, selective AChE inhibitor
- High selectivity for AChE over BuChE
- Exhibits neuroprotective effects against Aβ42 neurotoxicity
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Medchemexpress LLC Verapamil hydrochloride (Standard) | 152-11-4 | 99.8% | C27H39ClN2O4 | 50 MG
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Verapamil hydrochloride (Standard) is the analytical standard of Verapamil hydrochloride, intended for research and analytical applications. It is a calcium channel blocker and a potent, orally active first-generation P-glycoprotein (P-gp) inhibitor, also inhibiting CYP3A4. It has potential for high blood pressure, heart arrhythmias, and angina research.
- Used as an analytical standard and reference standard in assays
- Commonly employed in qualitative, quantitative, and methodological research experiments
- Suitable for techniques such as HPLC, GC, and MS
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Medchemexpress LLC VTP-27999 Hydrochloride | 1264191-73-2 | 98.2% | C26H42Cl2N4O5 | 10MM/1ML
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VTP-27999 Hcl is an alkyl amine Renin inhibitor that is useful for Hypertension and End-Organ Diseases. Its IC50 value targets Renin.
- Molecular weight: 561.54
- Appearance: Solid
- Color: White to yellow
- Solubility in water: ≥ 100 mg/mL (178.08 mM)
- Storage as solid: 4°C, sealed, away from moisture
- Storage in solvent: -80°C for 6 months; -20°C for 1 month (sealed, away from moisture)
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Medchemexpress LLC Tipiracil hydrochloride | 183204-72-0 | 99.9% | C9H12Cl2N4O2 | 10 MM 1 ML
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Tipiracil hydrochloride is a thymidine phosphorylase inhibitor (TPI) used for cancer research.
- Thymidine phosphorylase inhibitor
- Suitable for cancer research
- White to off-white solid appearance
- Molecular weight: 279.12
- Requires sealed storage at 4°C, away from moisture
- In solvent, store at -80°C for 6 months or -20°C for 1 month
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