Alcohols and polyols
- (1)
- (55)
- (343)
- (39)
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- (1)
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- (156)
- (1)
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- (27)
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- (1)
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- (30)
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- (20)
- (10)
- (2)
- (10)
- (4)
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- (395)
- (6)
- (102)
- (21)
- (50)
- (31)
- (62)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (463)
- (9)
- (46)
- (10)
- (46)
- (6)
- (1)
- (6)
- (12)
- (145)
- (116)
- (7)
- (5)
- (1)
- (1)
- (1)
- (1)
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- (1)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
- (6)
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- (1)
- (12)
- (21)
- (5)
- (2)
- (2)
- (2)
- (16)
- (2)
- (30)
- (1)
- (4)
- (1)
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- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (1)
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- (2)
- (2)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (15)
- (4)
- (5)
- (1)
- (2)
- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (15)
- (12)
- (1)
- (2)
- (2)
- (7)
- (12)
- (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)
- (3)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (2)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
- (4)
- (4)
- (1)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (5)
- (4)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
- (5)
- (1)
- (2)
- (2)
- (6)
- (14)
- (2)
- (4)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (1)
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- (2)
- (3)
- (2)
- (4)
- (3)
- (1)
- (4)
- (5)
- (1)
- (4)
- (5)
- (9)
- (1)
- (5)
- (5)
- (2)
- (1)
- (1)
- (2)
- (5)
- (3)
- (5)
- (2)
- (1)
- (2)
- (2)
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- (1)
- (4)
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- (2)
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- (11)
- (9)
- (1)
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- (1)
- (1)
- (10)
- (1)
- (1)
- (1)
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- (4)
- (11)
- (1)
- (2)
- (4)
- (20)
- (21)
- (2)
- (8)
- (2)
- (3)
- (3)
- (1)
- (8)
- (4)
- (2)
- (1)
- (1)
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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)
- (1)
- (1)
- (5)
- (1)
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- (1)
- (1)
- (1)
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- (1)
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- (1)
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- (14)
- (1)
- (1)
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- (1)
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- (5)
- (2)
- (2)
- (1)
- (10)
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- (1)
- (9)
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- (27)
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- (1)
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- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (82)
- (12)
- (4)
- (1)
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- (1)
- (81)
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- (378)
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- (40)
- (21)
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- (1)
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- (279)
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- (278)
- (28)
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- (48)
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- (6)
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- (733)
- (11)
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Filtered Search Results
Medchemexpress LLC Melitracen hydrochloride | 10563-70-9 | MFCD00242905 | 99.8% | 327.89 g/mol | C21H26ClN | 1 ML
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Melitracen hydrochloride is a research-grade small molecule antidepressant and anxiolytic agent supplied for in vitro pharmacology, mechanism-of-action studies, and analytical reference. The material is provided with solubility and stock-solution guidance, and recommended storage conditions for both solid and solution forms.
- High purity of 99.8%.
- CAS number 10563-70-9, formula C21H26ClN, molecular weight 327.89 g/mol.
- Available as solid samples and as a pre-made 10 mM solution (1 mL) in DMSO.
- Soluble in DMSO and water at up to 100 mg/mL; ultrasonic assistance may be required.
- Storage: solid at 4°C; in solution store at -80°C up to 6 months or -20°C up to 1 month.
- Includes stock solution preparation guidance for common concentrations.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Clorgyline hydrochloride | 17780-75-5 | 99.9% | C13H16Cl3NO | 50 MG
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Clorgyline hydrochloride is an irreversible and selective inhibitor of monoamine oxidase A (MAO-A) used in scientific research. It has minimal effect on conjugated dopamine (DA) amounts in superfusates of rat striatum slices. This compound contains an Alkyne group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Irreversible and selective inhibitor of monoamine oxidase A (MAO-A)
- Structurally related to Pargyline
- Contains an Alkyne group for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with Azide groups
- Increases nicotine infusions and motivation to obtain nicotine in rats at 2 mg/kg daily for 28 days
- Pretreatment with 1 mg/kg intravenously for 1 hour has little effect on the efflux of conjugated dopamine (DA) and p-tyramine-evoked release of conjugated DA from slices of rat striatum
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Leelamine hydrochloride | 16496-99-4 | 98.1% | 321.93 | 500 MG
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Leelamine hydrochloride is a tricyclic diterpene molecule extracted from the bark of pine trees. It acts as a cannabinoid receptor type 1 (CB1) agonist and inhibits SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells, independent of androgen receptor status. It also suppresses the transcriptional activity of the androgen receptor, which is known to regulate fatty acid synthesis.
- Tricyclic diterpene molecule
- Extracted from the bark of pine trees
- Cannabinoid receptor type 1 (CB1) agonist
- Inhibits SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells
- Suppresses transcriptional activity of androgen receptor
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Medchemexpress LLC AMXI-5001 hydrochloride | 98.1% | C25H21ClFN5O3 | 100 MG
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AMXI-5001 hydrochloride is a potent, orally active, and dual PARP1/2 and microtubule polymerization inhibitor. It exhibits selective antitumor cytotoxicity across a wide variety of human cancer cells with much lower IC50s than existing clinical PARP1/2 inhibitors. This compound induces complete regression of established tumors, even very large ones. It is intended for research use only and not sold to patients.
- Potent and orally active
- Functions as a dual PARP1/2 and microtubule polymerization inhibitor
- Demonstrates selective antitumor cytotoxicity against various human cancer cells
- Has significantly lower IC50s compared to existing clinical PARP1/2 inhibitors
- Induces complete regression of established tumors
- For research use only
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Medchemexpress LLC Bevantolol hydrochloride | 42864-78-8 | 10 MG
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Bevantolol hydrochloride is a beta-1 and alpha-1 adrenergic receptor antagonist supplied as an analytical standard for laboratory research in adrenergic pharmacology.
- Selective β1 and α1 adrenergic receptor antagonist.
- Supplied as an analytical standard for research use.
- CAS number 42864-78-8.
- Molecular formula C20H28ClNO4; molecular weight 381.89 g/mol.
- Available in small milligram pack sizes, including 10 MG for analytical applications.
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Medchemexpress LLC Imidapril hydrochloride | 89396-94-1 | 99.91% | 5 MG
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Imidapril hydrochloride (TA-6366) is an orally active angiotensin-converting enzyme (ACE) and MMP-9 inhibitor. It suppresses the conversion of angiotensin I to angiotensin II, which reduces total peripheral resistance and systemic blood pressure. It can be used for research on hypertension, type 1 diabetic nephropathy, and chronic heart failure.
- Orally active ACE and MMP-9 inhibitor
- Suppresses the conversion of angiotensin I to angiotensin II
- Reduces total peripheral resistance and systemic blood pressure
- Applicable for research in hypertension, type 1 diabetic nephropathy, and chronic heart failure
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Medchemexpress LLC Pirlimycin hydrochloride | 78822-40-9 | MFCD27952783 | 99.1% | 447.42 g·mol⁻¹ | C17H32Cl2N2O5S | 1 MG
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Pirlimycin hydrochloride is a lincosamide-class antibiotic supplied as the hydrochloride salt for research use. It inhibits bacterial protein synthesis by binding the 50S ribosomal subunit and is primarily active against Gram-positive organisms. The material is provided as a solid at high purity for analytical and laboratory applications.
- Lincosamide antibiotic.
- Inhibits bacterial protein synthesis via 50S ribosomal binding.
- Primarily active against Gram-positive bacteria.
- High purity (99.1%).
- Supplied as a solid suitable for analytical use.
- Available in small-scale quantities for research.
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Medchemexpress LLC Sri-37330 hydrochloride | 2322245-49-6 | 99.72% | C16H20ClF3N4O2S | 1 G
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SRI-37330 hydrochloride is an orally bioavailable thioredoxin-interacting protein (TXNIP) inhibitor. It inhibits glucagon secretion and function, reduces hepatic glucose production, and reverses hepatic steatosis. This compound can be used for type 2 diabetes research.
- Inhibits human TXNIP promoter activity in INS-1 cells.
- Decreases TXNIP mRNA and protein levels in INS-1 cells.
- Blocks polymerase II binding to the E-box motif of the TXNIP promoter.
- Reduces glucagon secretion in TC1-6 cells.
- Inhibits glucagon-induced glucose output from primary hepatocytes.
- Decreases glucagon secretion and action, and blocks hepatic glucose output in vivo.
- Well tolerated in male C57BL/6J mice.
- Reverses obesity- and STZ-induced diabetes and hepatic steatosis in mice.
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Medchemexpress LLC Alosetron hydrochloride | 122852-69-1 | MFCD03453647 | 99.6% | 10 MG
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Alosetron hydrochloride is a potent, selective 5-HT3 receptor antagonist provided for research use in studies of irritable bowel syndrome and visceral nociception. It is supplied as a high-purity solid and is also available as ready-to-use 10 mM solutions for laboratory assays.
- Potent and selective 5-HT3 receptor antagonist.
- Used in research on diarrhea-predominant irritable bowel syndrome and visceral nociception.
- High purity suitable for analytical and in vitro applications.
- Available as a solid and as pre-made 10 mM solutions for convenience.
- Characterization includes CAS 122852-69-1 and molecular weight 330.81 g/mol.
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Medchemexpress LLC 2(1H)-Isoquinolineacetamide, 3,4-dihydro-6,7-dimethoxy-N-methyl-a-phenyl-1-[2-[4-(trifluoromethy | 913358-93-7 | MFCD22419385 | 100.0% | 549.02 g/mol | C29H32ClF3N2O3 | 25 MG
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Almorexant hydrochloride is the hydrochloride salt of a potent, orally active dual orexin (OX1/OX2) receptor antagonist used in neuroscience research of sleep and arousal mechanisms. It is supplied as a high-purity solid and as a DMSO solution, with batch COA documentation for research use.
- Potent dual orexin receptor antagonist suitable for receptor pharmacology studies
- High purity suitable for in vitro and in vivo experiments
- Available in multiple solid pack sizes and as a DMSO solution
- Certificate of analysis provided for batch-specific quality assurance
- Hydrochloride salt form for improved handling and formulation stability
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Medchemexpress LLC Amprolium (hydrochloride) | 137-88-2 | 98.8% | 1 ML
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Amprolium hydrochloride is provided as a 10 mM solution in 1 mL, with a purity of 98.8%. This product is intended for research use only and should be handled by qualified personnel in appropriately equipped facilities.
- 10 mM solution in 1 mL
- Purity: 98.8% (HPLC)
- Recommended storage: 4°C for sealed solutions, away from moisture
- For longer-term storage in solvent: -80°C for 6 months or -20°C for 1 month
- Can be shipped at room temperature if shipment duration is less than 2 weeks
- Intended for research applications
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Medchemexpress LLC Fendiline (hydrochloride) | 13636-18-5 | 99.8% | 1 ML
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Fendiline hydrochloride is a diphenylalkylamine type of antianginal agent that acts as an L-type calcium channel blocker with an IC50 of 17 μM. It is also identified as a selective K-Ras inhibitor, showing no effect on H-Ras and N-Ras. It inhibits K-Ras plasma membrane localization (IC50 of 9.64 μM) and K-Ras signal output. Additionally, Fendiline hydrochloride is a STING agonist and has demonstrated the ability to inhibit the growth of multiple refractory cold tumors. This product is provided as a 10 mM solution in 1 mL of DMSO with a purity of 99.78%.
- Acts as an L-type calcium channel blocker
- Functions as a selective K-Ras inhibitor
- Inhibits K-Ras plasma membrane localization
- Suppresses K-Ras signal output
- Prevents proliferation of various cancer cell lines
- Serves as a STING agonist
- Inhibits growth of refractory cold tumors
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380988 AMSACRINE HYDROCHLO 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000382915 PDK4-IN-1 HYDROCHLO 1G
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Sigma Aldrich Fine Chemicals Biosciences Hexyl alcohol FCC FG170KG
Hexyl alcohol FCC FG170KG
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