Alcohols and polyols
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- (41)
- (4)
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- (7)
- (55)
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- (1)
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- (155)
- (1)
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- (29)
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- (1)
- (1)
- (10)
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- (2)
- (2)
- (1)
- (1)
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- (1)
- (1)
- (1)
- (6)
- (3)
- (30)
- (4)
- (20)
- (10)
- (2)
- (10)
- (4)
- (5)
- (399)
- (6)
- (102)
- (22)
- (50)
- (31)
- (62)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (463)
- (9)
- (46)
- (10)
- (46)
- (6)
- (1)
- (6)
- (13)
- (148)
- (114)
- (9)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
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- (1)
- (1)
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- (2)
- (1)
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- (16)
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- (1)
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- (1)
- (2)
- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
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- (6)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
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- (4)
- (2)
- (5)
- (4)
- (17)
- (14)
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- (1)
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- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (9)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (14)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (22)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (6)
- (4)
- (1)
- (3)
- (6)
- (11)
- (5)
- (4)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (3)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
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- (4)
- (1)
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- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (1)
- (1)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (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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- (1)
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- (1)
- (1)
- (15)
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- (1)
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- (16)
- (1)
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- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (81)
- (12)
- (4)
- (1)
- (3)
- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
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- (40)
- (21)
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- (1)
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- (1)
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- (2)
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- (1)
- (67)
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- (72)
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- (281)
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- (1)
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- (279)
- (28)
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- (25)
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- (48)
- (3)
- (418)
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- (3)
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- (5)
- (47)
- (6)
- (3)
- (1)
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- (21)
- (16)
- (2)
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- (11)
- (1)
- (8)
- (2)
- (731)
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Filtered Search Results
Ambeed AMBEED
5000894421 1-BENZOFURAN-6-AMINE 250MG
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Medchemexpress LLC Riviciclib hydrochloride | 920113-03-7 | 99.08% | 438.30 | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Riviciclib hydrochloride is a potent cyclin-dependent kinase (CDK) inhibitor. It inhibits CDK9-cyclinT1, CDK4-cyclin D1, and CDK1-cyclinB with IC50s of 20 nM, 63 nM, and 79 nM, respectively. This compound shows antitumor activity on cisplatin-resistant cells.
- IC50 & Target information available
- In vitro studies show activity in various cancer cell lines
- In vivo studies demonstrate significant inhibition of tumor growth
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC AR-C102222 hydrochloride | 1781934-50-6 | 99.8% | 50 MG
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AR-C102222 hydrochloride is a selective inducible nitric oxide synthase (iNOS) inhibitor (IC50 = 37 nM) provided as the hydrochloride salt for research use. It exhibits reported antinociceptive and anti-inflammatory activity and is supplied as a high-purity solid suitable for in vitro and in vivo studies.
- Purity 99.83%.
- Molecular weight 418.83 g/mol.
- Chemical formula C19H17ClF2N6O.
- Soluble in DMSO (100 mg/mL); formulatable for in vivo dosing (≥5 mg/mL in recommended vehicles).
- Storage: 4°C sealed; in solvent store at -80°C (6 months) or -20°C (1 month).
- Available as solid in multiple sizes, including 50 mg.
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Medchemexpress LLC Ro 41-1049 hydrochloride | 127917-66-2 | MFCD00900596 | 100.0% | 301.77 g·mol⁻¹ | C12H13ClFN3OS | 1 ML
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Ro 41-1049 hydrochloride is a reversible, selective monoamine oxidase A (MAO-A) inhibitor supplied for research use. It is available as a solid and as a pre-made 10 mM solution in DMSO (1 mL), and is provided with a high reported purity to support reproducible in vitro experiments.
- Reversible, selective MAO-A inhibition suitable for biochemical assays.
- Supplied as solid or pre-made 10 mM solution in DMSO (1 mL) for convenience.
- High reported purity to reduce confounding impurities.
- Characterized by CAS number 127917-66-2 and known molecular weight for accurate dosing.
- Intended for research use only; not for human or clinical use.
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Medchemexpress LLC BMS-199264 hydrochloride | 186180-83-6 | 99.3% | 567.53 g·mol⁻¹ | C26H32Cl2N4O4S | 100 MG
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BMS-199264 hydrochloride is a research compound that selectively inhibits the F1F0 ATP hydrolase (reported IC50 = 0.5 μM), preventing ATP decline during ischemia and reducing cardiac necrosis while improving contractile recovery after reperfusion.
- Inhibits F1F0 ATP hydrolase with reported IC50 of 0.5 μM.
- Reduces ATP decline during ischemic conditions.
- Helps limit cardiac necrosis and supports functional recovery.
- Supplied as a hydrochloride salt with high reported purity.
- Available in multiple pack sizes to suit experimental needs.
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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 SGK1-IN-3 hydrochloride | 96.7% | C23H21Cl3N6O3S | 25 MG
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SGK1-IN-3 hydrochloride is a potent SGK1 inhibitor with an IC50 of less than 1 μM. It has the potential for the research of osteoarthritis.
- Potent SGK1 inhibitor with an IC50 of <1 μM
- Potential for osteoarthritis research
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Medchemexpress LLC Oxyfedrine hydrochloride | 16777-42-7 | 99.9% | 349.85 | C19H24ClNO3 | 25 MG
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Oxyfedrine hydrochloride is the hydrochloride salt of oxyfedrine, an orally active beta-adrenoreceptor agonist and vasodilator used in pharmacological research. Supplied as a solid research-grade powder, it includes batch analytical data to support experimental use and handling.
- High purity powder (~99.9%).
- Acts as a beta-adrenoreceptor agonist and vasodilator for pharmacology studies.
- Solid form with defined molecular weight and formula for dosing calculations.
- Stable when stored sealed, protected from moisture and light.
- Provided with batch-specific analytical documents (COA, HNMR, LCMS).
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Medchemexpress LLC SB-612111 hydrochloride | 99.6% | 454.86 | 1 ML
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SB-612111 hydrochloride is a novel and potent opiate receptor-like orphan receptor (ORL-1) antagonist with high affinity for hORL-1 (Ki = 0.33 nM). It demonstrates selectivity for μ-, κ-, and δ-receptors. This compound effectively antagonizes the pronociceptive action of Nociceptin in an acute pain model.
- Potent ORL-1 antagonist with high affinity.
- Exhibits selectivity for μ-, κ-, and δ-receptors.
- Effectively antagonizes pronociceptive action of Nociceptin.
- Demonstrates antihyperalgesic effects in animal models.
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Medchemexpress LLC m-PEG-NH2 hydrochloride (MW 2000) | 99.1% | 2000 (Average) | 250 MG
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m-PEG-NH2 hydrochloride (MW 2000) is a methoxy-terminated polyethylene glycol bearing a terminal primary amine, supplied as the hydrochloride salt. It is used as a reactive PEG building block for PEGylation, bioconjugation, hydrogel synthesis, and formulation of adsorption/size-exclusion gels for biological separations.
- Average molecular weight 2000 (average).
- Terminal primary amine as hydrochloride salt.
- High purity (~99.1%).
- Suitable for PEGylation and bioconjugation reactions.
- Compatible with hydrogel and AdSEC gel formulation.
- Available in research sizes such as 250 MG.
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Medchemexpress LLC Fadrozole hydrochloride | 102676-31-3 | 99.9% | C14H14ClN3 | 25 MG
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Fadrozole hydrochloride (CGS 16949A) is a potent, selective, and nonsteroidal inhibitor of aromatase with an IC50 of 6.4 nM. It inhibits estrogen production in hamster ovarian slices and has various in vivo effects, including the prevention of certain tumors and reduction of parasite burden.
- Potent, selective, and nonsteroidal inhibitor of aromatase with an IC50 of 6.4 nM.
- Inhibits estrogen production with an IC50 of 0.03 μM.
- Inhibits progesterone production with an IC50 of 120 μM.
- Inhibits aromatase-mediated uterine hypertrophy in immature female rats with an oral ED50 of 0.03 mg/kg.
- Prevents development of benign and malignant spontaneous mammary neoplasms.
- Slows spontaneous development of pituitary pars distalis adenomas.
- Reduces incidence of spontaneous hepatocellular tumors.
- Reduces parasite burden in male and female mice by 70%.
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Medchemexpress LLC Vu6036720 hydrochloride | 3026597-12-3 | 99.7% | 473.39 | C20H23Cl2FN4O2S | 10 MG
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VU6036720 hydrochloride is the hydrochloride salt of a potent, selective in vitro inhibitor of heteromeric Kir4.1/5.1 inward-rectifier potassium channels, used for research into neural and renal channel function. The compound is supplied as a high-purity solid suitable for biochemical and electrophysiological assays.
- Potent Kir4.1/5.1 inhibition with IC50 0.24 μM.
- High purity suitable for research applications.
- Available in small solid quantities for assay workflows.
- Stable solid with recommended sealed storage at 4°C.
- Compatible with DMSO stock preparations for in vitro testing.
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Medchemexpress LLC Gyki 53655 (hydrochloride) | 143692-48-2 | 98.4% | 388.85 g·mol⁻¹ | C19H21ClN4O3 | 100 MG
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GYKI 53655 hydrochloride is a research-grade small molecule that acts as a non-competitive antagonist of AMPA and kainate receptors. It is supplied as a light yellow to yellow solid with reported purity of ~98.4% and molecular formula C19H21ClN4O3. Intended for in vitro research use only.
- Non-competitive AMPA and kainate receptor antagonist.
- High purity (~98.4%) for consistent experimental results.
- Light yellow to yellow solid, soluble in DMSO and water with recommended handling precautions.
- Recommended storage: solid at 4°C; prepared solutions at -80°C (up to 6 months) or -20°C (short term).
- Available in multiple solid sizes, including 100 mg, for lab-scale studies.
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Medchemexpress LLC Imeglimin (hydrochloride) | 775351-61-6 | 99.98% | 191.66 | 100 MG
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Imeglimin hydrochloride (EMD 387008) is an oral glucose-lowering agent. Imeglimin also reduces reactive oxygen species (ROS) production, increases mitochondrial DNA, and improves mitochondrial function.
- Oral glucose-lowering agent
- Reduces reactive oxygen species (ROS) production
- Increases mitochondrial DNA
- Improves mitochondrial function
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Medchemexpress LLC ARG1-IN-1 hydrochloride | 00-00-0 | 90.0% | C11H22BClN2O4 | 10MG
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ARG1-IN-1 hydrochloride is a research compound that selectively inhibits human arginase 1, with a reported IC50 of 29 nM. Supplied as the hydrochloride salt, the material is typically offered at 90.0% purity and is intended for biochemical and pharmacological research applications only.
- Potent arginase 1 inhibition (IC50 = 29 nM).
- Supplied as a hydrochloride salt for chemical stability.
- Typical purity 90.0% suitable for research use.
- Appropriate for in vitro biochemical and cell-based assays.
- Provided in milligram-scale quantities for laboratory studies.
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