Alcohols and polyols
- (1)
- (55)
- (343)
- (39)
- (4)
- (8)
- (7)
- (55)
- (3)
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- (1)
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- (156)
- (1)
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- (1)
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- (30)
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- (20)
- (10)
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- (395)
- (6)
- (102)
- (21)
- (50)
- (31)
- (62)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (464)
- (9)
- (46)
- (11)
- (46)
- (6)
- (1)
- (7)
- (12)
- (145)
- (116)
- (7)
- (5)
- (1)
- (1)
- (1)
- (1)
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- (1)
- (1)
- (4)
- (7)
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- (2)
- (1)
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- (1)
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- (21)
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- (2)
- (2)
- (2)
- (16)
- (2)
- (30)
- (1)
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- (1)
- (2)
- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (1)
- (2)
- (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)
- (7)
- (4)
- (1)
- (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)
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- (9)
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- (2)
- (12)
- (4)
- (1)
- (1)
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- (1)
- (1)
- (1)
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- (1)
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- (1)
- (1)
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- (1)
- (1)
- (30)
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- (733)
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Filtered Search Results
Medchemexpress LLC SB-277011 hydrochloride | 215804-67-4 | 99.59% | 475.02 | 50 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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SB-277011 hydrochloride is a potent and selective dopamine D3 receptor (D3R) antagonist, demonstrating high oral bioavailability and brain penetrance. It exhibits significant selectivity over other dopamine receptors and possesses an excellent pharmacokinetic profile in rats. This compound has been shown to effectively reverse the effects of quinelorane and reduce cocaine self-administration in preclinical studies.
- Potent and selective D3 receptor antagonist
- High oral bioavailability and brain penetrance
- 80- to 100-fold selectivity over other dopamine receptors
- Excellent pharmacokinetic profile
- Reverses quinelorane effects in nucleus accumbens
- Reduces intravenous cocaine self-administration
- Inhibits basal and cocaine-enhanced locomotion
- Appearance: solid, off-white to light yellow
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Nordoxepin hydrochloride | 2887-91-4 | 99.9% | 301.81 g/mol | C18H20ClNO | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Nordoxepin hydrochloride is the primary metabolite of the tricyclic antidepressant doxepin and is provided as a solid research reagent for analytical, pharmacological, and metabolic studies. It is supplied with characterized purity and storage recommendations and is intended for research use only (not for human or veterinary use).
- Chemical identity: CAS 2887-91-4; formula C18H20ClNO; MW 301.81 g/mol.
- High purity (99.94%).
- Appearance: solid; store sealed and away from moisture.
- Storage in solvent: -80°C up to 6 months; -20°C up to 1 month.
- Intended applications: analytical and pharmacokinetic research.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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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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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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 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 SRI-37330 hydrochloride | 2322245-49-6 | 99.7% | C16H20ClF3N4O2S | 25 MG
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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 activity of human TXNIP promoter in INS-1 cells.
- Decreases mRNA and protein levels of TXNIP in INS-1 cells.
- Inhibits polymerase II (Pol II) binding to the E-box motif region of the TXNIP promoter.
- Lowers glucagon secretion in TC1-6 cells.
- Inhibits glucagon-induced glucose output from primary hepatocytes.
- Decreases glucagon secretion and action in mice.
- Blocks hepatic glucose output in mice.
- Reverses obesity- and streptozotocin-induced diabetes and hepatic steatosis in mice.
- Well tolerated in male C57BL/6J mice.
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Medchemexpress LLC DC-BPi-11 hydrochloride | 00-00-0 | 97.0% | 433.95 g·mol⁻¹ | C20H24ClN5O2S | 5 MG
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DC-BPi-11 hydrochloride is a small-molecule BPTF inhibitor supplied as a hydrochloride salt in powder form for research use. It has demonstrated inhibition of leukemia cell proliferation and a reported IC50 of approximately 698 nM, with handling and storage guidance provided for both solid and solution states.
- Inhibitor of bromodomain PHD finger transcription factor (BPTF).
- Reported IC50 ≈ 698 nM.
- Powder hydrochloride salt form.
- Molecular formula C20H24ClN5O2S.
- Molecular weight 433.95 g·mol⁻¹.
- Purity 97.0%.
- Storage: powder -20°C; in solvent -80°C (6 months) or -20°C (1 month).
- Available as a 5 mg sample pack.
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Medchemexpress LLC Leelamine hydrochloride | 16496-99-4 | 98.1% | 321.93 | 25 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 an inhibitor of SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells. Its activity is not affected by androgen receptor status, and it suppresses the transcriptional activity of the androgen receptor.
- Tricyclic diterpene molecule
- Extracted from the bark of pine trees
- Cannabinoid receptor type 1 (CB1) agonist
- Inhibitor of SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells
- Suppresses transcriptional activity of androgen receptor
- Appearance: solid
- Color: white to off-white
- For research use only
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Medchemexpress LLC NNMT-IN-6 hydrochloride | 3031756-18-7 | 98.2% | C25H30ClN7O5 | 10MG
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NNMT-IN-6 hydrochloride is the hydrochloride salt of a small-molecule inhibitor of nicotinamide N-methyltransferase (NNMT) intended for research use. It exhibits in vitro inhibitory activity (IC50 = 1.41 μM; Kd = 5.6 μM) and is supplied as a high-purity solid with documented solubility and storage recommendations for biochemical and cellular assays.
- High purity (98.2%).
- Confirmed NNMT inhibitory activity (IC50 = 1.41 μM; Kd = 5.6 μM).
- Hydrochloride salt form for improved solubility.
- Validated solubility in DMSO and water (250 mg/mL with sonication).
- Suitable for biochemical and cellular assays targeting NNMT.
- Recommended sealed storage away from moisture, with solvent stability guidelines.
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Medchemexpress LLC Abeprazan hydrochloride | 1902954-87-3 | 99.9% | 446.87 | 50 MG
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Abeprazan hydrochloride (DWP14012 hydrochloride) is a potassium-competitive acid blocker that inhibits H+, K+- ATPase through reversible potassium-competitive ionic binding without requiring acid activation. It is being developed as a potential alternative to proton pump inhibitors for treating acid-related diseases.
- Potassium-competitive acid blocker.
- Inhibits H+, K+- ATPase by reversible potassium-competitive ionic binding.
- Does not require acid activation for its inhibitory mechanism.
- Developed as a potential alternative for proton pump inhibitors.
- Inhibits acid secretion in a dose-dependent manner in in vivo studies.
- Efficacy is equal to or greater than that of vonoprazan in various in vivo studies.
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Medchemexpress LLC Sultopride hydrochloride | 23694-17-9 | MFCD01319147 | 99.9% | 390.93 | C17H27ClN2O4S | 10 MG
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Sultopride hydrochloride (LIN-1418 hydrochloride) is a selective dopamine D2 receptor antagonist supplied as a white to off-white solid for laboratory research applications. It is provided at high reported purity and in small pack sizes for bench-top experiments.
- Selective dopamine D2 receptor antagonist.
- High purity (≈99.9%).
- White to off-white solid physical form.
- CAS number 23694-17-9.
- Molecular weight 390.93 g/mol.
- Available in small pack sizes, including 10 MG.
- Intended for research use only; not for human or clinical use.
- Storage: 4°C, sealed and away from moisture; in solvent: -80°C for 6 months, -20°C for 1 month.
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Medchemexpress LLC 1-Piperazinebutanol, α-(4-fluorophenyl)-4-(5-fluoro-2-pyrimidinyl)-, hydrochloride (1:1) | 105565-55-7 | 98.0% | 384.85 | 50 MG
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BMY-14802 hydrochloride is a potent agonist of 5-HT1A and adrenergic α1 receptors, known for its antipsychotic effects.
- Appearance: white to off-white solid.
- Storage: -20°C, sealed storage, away from moisture. In solvent: -80°C, 6 months; -20°C, 1 month.
- ¹H NMR spectrum consistent with structure.
- MS consistent with structure.
- Product tested and complies with given specifications.
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Medchemexpress LLC Imidapril (hydrochloride) | 89396-94-1 | 99.9% | 50 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, reducing total peripheral resistance and systemic blood pressure. It is used for research related to hypertension, type 1 diabetic nephropathy, and chronic heart failure.
- Orally active ACE inhibitor
- MMP-9 inhibitor
- Suppresses angiotensin I to angiotensin II conversion
- Reduces total peripheral resistance
- Reduces systemic blood pressure
- Used for hypertension research
- Used for type 1 diabetic nephropathy research
- Used for chronic heart failure research
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Medchemexpress LLC Pociredir hydrochloride | 2490676-19-0 | 99.9% | 439.87 | 10 MM/1 ML
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Pociredir hydrochloride, also known as FTX-6058, is a potent and orally active inhibitor of Embryonic Ectoderm Development (EED). It is utilized in research for select hemoglobinopathies like sickle cell disease and β-thalassemia by inducing HbF protein expression in cell and murine models.
- Potent and orally active inhibitor of EED
- Induces HbF protein expression in cell and murine models
- Used in research for select hemoglobinopathies, including sickle cell disease and β-thalassemia
- Inhibits PRC2 via binding to EED
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Medchemexpress LLC Amelparib hydrochloride | 98.4% | 379.88 | C19H26ClN3O3 | 5 MG
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Amelparib hydrochloride is the hydrochloride salt form of a PARP-1 inhibitor used as a research reagent to investigate DNA damage response and PARP-related pathways. It is supplied as a high-purity solid suitable for biochemical and cellular assays.
- Potent PARP-1 inhibitor activity
- Hydrochloride salt for improved water solubility
- High purity (98.4%)
- Molecular weight 379.88 g/mol
- Suitable for biochemical and cellular research applications
- Supplied as a 5 mg solid package
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