Alcohols and polyols
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- (462)
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- (1)
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- (1)
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- (1)
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- (1)
- (1)
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- (1)
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- (1)
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- (12)
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- (1)
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- (1)
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Filtered Search Results
Medchemexpress LLC Bms-199264 (hydrochloride) | 186180-83-6 | 99.3% | 567.53 | C26H32Cl2N4O4S | 10 MG
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This hydrochloride salt is a small-molecule inhibitor of mitochondrial F1F0 ATP synthase supplied as a white to off-white solid for laboratory research use. It inhibits ATP hydrolase activity and should be handled and stored according to supplier guidance.
- Potent inhibitor of mitochondrial F1F0 ATP synthase activity.
- High purity (≈99.3%) suitable for research applications.
- Available in small-scale quantities for laboratory testing.
- White to off-white solid; stable when stored sealed at 4°C.
- Solvent stability: -80°C (6 months), -20°C (1 month) for prepared solutions.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC W-7 isomer hydrochloride | 69762-85-2 | 99.7% | 377.33 g·mol⁻¹ | C16H22Cl2N2O2S | 1 ML
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W-7 isomer hydrochloride is the isomeric hydrochloride salt of W-7, a selective calmodulin antagonist used in biochemical and cell-based research. It is supplied as a solid and as prepared solutions for immediate use.
- High purity: 99.65%.
- Available as a 10 mM solution in DMSO (1 mL) and in solid quantities.
- Molecular formula C16H22Cl2N2O2S; molecular weight 377.33 g·mol⁻¹.
- CAS number 69762-85-2 for unambiguous identification.
- Appearance white to off-white solid.
- SDS, COA, and analytical data available for quality confirmation.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Alkali Scientific Ninhydrin Reagent, 100 G
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Ninhydrin Reagent, 100g is a chemical reagent primarily used for the detection of amino acids, peptides, and proteins. When applied, ninhydrin reacts with free amines, turning a purple color, which is commonly used for amino acid quantification in chromatography and electrophoresis. This reagent is widely utilized in laboratory settings for detecting and analyzing amino acids in biological samples, such as urine, blood, and tissue extracts. The 100g pack size is suitable for high-throughput laboratories and research facilities conducting multiple experiments or large-scale studies in proteomics and amino acid analysis. It plays an essential role in protein research and metabolic studies.
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Medchemexpress LLC SB-612111 hydrochloride | 99.6% | 454.86 | 50 MG
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SB-612111 hydrochloride is a novel and potent opiate receptor-like orphan receptor (ORL-1) antagonist with a high affinity for hORL-1 (Ki=0.33 nM). It exhibits selectivity for μ-, κ- and δ-receptors. It effectively antagonizes the pronociceptive action of Nociceptin in an acute pain model.
- Appearance: Solid
- Color: White to off-white
- Shipping: Room temperature in continental US; may vary elsewhere
- Storage: Powder: -20°C for 3 years, 4°C for 2 years. In solvent: -80°C for 6 months, -20°C for 1 month
- Solubility (In Vitro): DMSO: 15.62 mg/mL (34.34 mM; ultrasonic and warming and heat to 60°C; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
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Medchemexpress LLC Zoniporide hydrochloride hydrate | 863406-85-3 | 99.4% | 374.82 g/mol | C17H19ClN6O2 | 25 MG
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Zoniporide hydrochloride hydrate is the hydrochloride hydrate salt of zoniporide, a potent and selective inhibitor of the sodium-hydrogen exchanger isoform 1 (NHE-1) used for research applications. It is provided as a high-purity solid suitable for in vitro and ex vivo studies of NHE-1 function and related cardiovascular and platelet biology.
- Potent and selective NHE-1 inhibition (human IC50 ~14 nM).
- Inhibits ex vivo NHE-1-dependent platelet swelling (IC50 ~59 nM).
- High purity (>99% by HPLC).
- Available as the hydrochloride hydrate salt for improved handling and stability.
- Molecular weight 374.82 g/mol; molecular formula C17H19ClN6O2.
- Supplied in small research quantities, e.g., 25 MG.
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Medchemexpress LLC Antalarmin (hydrochloride) | 220953-69-5 | MFCD05664721 | 99.9% | 415.01 g/mol | C24H35ClN4 | 25 MG
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Antalarmin hydrochloride is a research-grade, non-peptide corticotropin-releasing hormone receptor 1 (CRHR1) antagonist supplied as a solid for preclinical pharmacology and biochemical studies. Intended for laboratory research use only.
- High purity (≈99.9%).
- Molecular weight 415.01 g/mol.
- Molecular formula C24H35ClN4.
- Appearance: solid, white to light yellow.
- Storage: sealed at -20°C; in solution: -80°C for 6 months, -20°C for 1 month.
- Supplied with data sheet, certificate of analysis, and safety data sheet.
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Medchemexpress LLC mAChR-IN-1 hydrochloride | 119391-73-0 | MFCD01725710 | 99.6% | 524.82 g/mol | C23H26ClIN2O2 | 10MG
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mAChR-IN-1 hydrochloride is a research-grade muscarinic acetylcholine receptor antagonist provided as the hydrochloride salt. It exhibits high potency (IC50 = 17 nM) and is characterized by a defined molecular formula and high reported purity, making it suitable for in vitro pharmacology and biochemical assays.
- Potent mAChR antagonist (IC50 = 17 nM).
- Hydrochloride salt form for consistent handling.
- High reported purity (99.6%).
- Molecular weight 524.82 g/mol; formula C23H26ClIN2O2.
- Intended for in vitro research applications.
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Medchemexpress LLC Aprindine hydrochloride | 33237-74-0 | MFCD01698392 | 99.0% | C22H31ClN2 | 100 MG
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Aprindine hydrochloride is an Ib-class anti-arrhythmic agent primarily used in the study of atrial fibrillation and ventricular arrhythmias. It functions by stabilizing cardiac electrical activity through multiple mechanisms.
- Blocks sodium channels to reduce excitability and conduction velocity of cardiac muscle cells.
- Inhibits delayed potassium currents, prolonging the atrial effective refractory period.
- Inhibits atrial fibrillation.
- Regulates intracellular calcium ion concentration by inhibiting the Na+/Ca2+ exchange current.
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Medchemexpress LLC VU0453379 hydrochloride | 98.0% | 471.03 | 25 MG
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VU0453379 hydrochloride is a highly selective and central nervous system (CNS) penetrant positive allosteric modulator (PAM) of glucagon-like peptide-1R (GLP-1R) with an EC50 of 1.3 μM.
- Highly selective
- CNS penetrant
- Positive allosteric modulator (PAM) of GLP-1R
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Medchemexpress LLC W-7 isomer hydrochloride | 69762-85-2 | 99.7% | 377.33 g·mol⁻1 | C16H22Cl2N2O2S | 1 MG
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W-7 isomer hydrochloride is the positional isomer of W-7 hydrochloride, a selective calmodulin antagonist. Provided for research use, the compound is supplied as a solid in multiple sizes and as a DMSO solution, and is intended for studies probing calcium-dependent signaling where calmodulin inhibition is required.
- High purity (99.65%).
- Molecular weight 377.33 g·mol⁻1.
- Available as solid and 10 mM DMSO solution.
- Offered in multiple pack sizes from milligram quantities to larger amounts.
- Documents available: data sheet, certificate of analysis, and safety data sheet.
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Medchemexpress LLC Almorexant hydrochlo 100mg | 913358-93-7 | 100MG
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Almorexant (ACT 078573) hydrochloride is an orally active potent and competitive dual orexin receptor antagonist with Kd values of 1 3 nM (OX1) and 0 17 nM (OX2) respectively Almorexant hydrochloride reversibly blocks signaling of orexin-A and orexin-B peptides Almorexant hydrochloride totally blocked the intracellular Ca2 signal pathway Almorexant hydrochloride stimulates caspase-3 activity in AsPC-1 cells and induces apoptosis[1 [2 [3 [4
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Medchemexpress LLC CP-640186 hydrochloride | 591778-70-0 | C30H36ClN3O3 | 1 ML
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CP-640186 hydrochloride is an orally active and cell-permeable Acetyl-CoA carboxylase (ACC) inhibitor. It targets ACC1 and ACC2, key enzymes in fatty acid metabolism, and can stimulate muscle fatty acid oxidation.
- Orally active and cell-permeable
- Inhibits Acetyl-CoA carboxylase (ACC)
- Stimulates muscle fatty acid oxidation
- Purity: 99.65%
- Solution in DMSO
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Medchemexpress LLC Cl-amidine (hydrochloride) | 1373232-26-8 | 99.8% | 347.24 | C14H20Cl2N4O2 | 5 MG
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Cl-amidine (hydrochloride) is a high-purity small-molecule inhibitor of peptidylarginine deiminases (PADs), used in biochemical and cellular research to block protein citrullination and probe PAD-mediated pathways.
- Potent inhibition of PAD enzymes, including PAD1, PAD3, and PAD4.
- High chemical purity suitable for biochemical assays.
- Solid form enables flexible preparation of solutions.
- Stable when stored at recommended low temperatures.
- Available in milligram quantities for research use.
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Medchemexpress LLC Buspirone (hydrochloride) | 33386-08-2 | 99.99% | 250 MG
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Buspirone hydrochloride is a 5-HT1A receptor agonist used in anxiety and depression research. It has been shown to have cytotoxic effects in lymphocytes and can induce ROS formation, MMP collapse, lipid peroxidation, lysosomal damage, and elevation of glutathione disulfide (GSSG) in these cells. In mice, it has been observed to reduce anxiety/depression behaviors, restore IS-shifted β-diversity in gut microbiota, and reduce inflammation markers in the hippocampus and colon.
- 5-HT1A receptor agonist
- Used for anxiety and depression research
- Can reduce anxiety/depression behaviors in mice
- Restores IS-shifted β-diversity in the gut microbiota in mice
- Reduces TNF-α expression and NF-κB+/Iba1+ cell population in the hippocampus and myeloperoxidase activity and NF-κB+/CD11c+ cell population in the colon in mice
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Medchemexpress LLC Voreloxin hydrochloride | 175519-16-1 | 99.6% | 437.90 g/mol | C18H20ClN5O4S | 10 MG
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Voreloxin hydrochloride is a research-grade anticancer compound and a first-in-class topoisomerase II inhibitor. It intercalates into DNA and induces site-selective double-strand breaks (DSB), causing G2 cell-cycle arrest and apoptosis. Supplied as a hydrochloride salt for laboratory research use only.
- First-in-class mechanism: topoisomerase II inhibition through DNA intercalation.
- Triggers site-selective DNA double-strand breaks and G2 arrest.
- High purity suitable for biochemical and cell-based assays.
- Well-characterized chemical identity: molecular formula C18H20ClN5O4S, molecular weight 437.90 g/mol.
- Available in accurately weighed small pack sizes for precise dosing in experiments.
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