Alcohols and polyols
- (1)
- (55)
- (343)
- (39)
- (4)
- (8)
- (7)
- (55)
- (3)
- (7)
- (18)
- (1)
- (4)
- (156)
- (1)
- (64)
- (27)
- (14)
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- (1)
- (1)
- (10)
- (3)
- (2)
- (2)
- (1)
- (1)
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- (1)
- (1)
- (1)
- (6)
- (3)
- (30)
- (4)
- (20)
- (10)
- (2)
- (10)
- (4)
- (5)
- (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)
- (2)
- (1)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
- (6)
- (5)
- (1)
- (12)
- (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)
- (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)
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- (1)
- (1)
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- (3)
- (2)
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- (3)
- (1)
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- (1)
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- (9)
- (1)
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- (5)
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- (1)
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- (1)
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- (20)
- (21)
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- (1)
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- (1)
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- (1)
- (1)
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- (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)
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- (1)
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- (1)
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- (1)
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- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (82)
- (12)
- (4)
- (1)
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- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
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- (40)
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- (1)
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- (1)
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- (1)
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- (1)
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- (279)
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- (1)
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- (278)
- (28)
- (2)
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- (1)
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- (1)
- (8)
- (2)
- (733)
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- (1)
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Filtered Search Results
Medchemexpress LLC Alfuzosin (hydrochloride) | 81403-68-1 | 99.7% | 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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Alfuzosin hydrochloride is an orally active, selective, and competitive α1-adrenoceptor antagonist. It relaxes the muscles of the prostate and bladder neck, aiding in urination. This compound is used in the study of benign prostatic hyperplasia (BPH).
- Orally active compound
- Selective and competitive α1-adrenoceptor antagonist
- Relaxes prostate and bladder neck muscles
- Aids in urination
- Used for benign prostatic hyperplasia (BPH) studies
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Alectinib hydrochloride | 1256589-74-8 | 99.9% | 25 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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Alectinib hydrochloride is a potent, selective, and orally available ALK inhibitor. It demonstrates effective central nervous system (CNS) penetration.
- Potent and selective ALK inhibitor
- Orally available
- Inhibits ALK F1174L and ALK R1275Q
- Effective central nervous system (CNS) penetration
- Reduces cell activity in a dose-dependent manner
- Leads to dose-dependent tumor growth inhibition and regression
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC AR-R17779 hydrochloride | 178419-42-6 | MFCD20926337 | 99.0% | 218.68 | C9H15ClN2O2 | 5 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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AR-R17779 hydrochloride is a selective agonist of α7 nicotinic acetylcholine receptors supplied as the hydrochloride salt for laboratory research. It has been reported to influence learning and memory, show anxiolytic activity, and modulate anti-inflammatory cholinergic pathways. Purity is typically 99.0%.
- Selective α7 nicotinic receptor agonist.
- Provided as the hydrochloride salt.
- Used in neuroscience and pharmacology research.
- Reported effects on learning, memory, anxiety, and inflammation pathways.
- High purity (99.0%).
- Molecular weight 218.68; formula C9H15ClN2O2.
- Available in small pack sizes for laboratory use.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Iptacopan (hydrochloride) | 1646321-63-2 | 99.83% | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Iptacopan (LNP023) hydrochloride is an effective, orally-active, and highly selective factor B inhibitor. With an IC50 of 10 nM and a KD of 7.9 nM, it exerts a proximal effect in the complement cascade reaction, preventing the destruction of red blood cells in PNH and damage to renal cells in IgAN and C3G. It is used for studying complement-mediated diseases, including paroxysmal nocturnal hemoglobinuria (PNH), primary immunoglobulin A nephropathy (IgAN), and complement 3 glomerulopathy (C3G).
- Highly selective factor B inhibitor.
- Orally active.
- Potent inhibition of alternative complement pathway (AP)-induced membrane attack complex (MAC) formation.
- Excellent selectivity over other proteases.
- Prevents destruction of red blood cells in PNH.
- Prevents damage to renal cells in IgAN and C3G.
- Used for studying complement-mediated diseases.
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Medchemexpress LLC SCH-23390 hydrochloride | 125941-87-9 | 99.8% | 324.24 | 1 ML
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SCH-23390 hydrochloride is a potent and selective dopamine D1-like receptor antagonist with Kis of 0.2 nM and 0.3 nM for the D1 and D5 receptor, respectively. It is also a potent and high efficacy human 5-HT2C receptor agonist with a Ki of 9.3 nM, and binds with high affinity to 5-HT2 and 5-HT1C receptors. It inhibits G protein-coupled inwardly rectifying potassium (GIRK) channels with an IC50 of 268 nM. For research use only.
- Potent and selective dopamine D1-like receptor antagonist.
- Potent and high efficacy human 5-HT2C receptor agonist.
- Binds with high affinity to 5-HT2 and 5-HT1C receptors.
- Inhibits G protein-coupled inwardly rectifying potassium (GIRK) channels.
- Used in studies of neurological disorders like psychosis and Parkinson's disease.
- Used in topographical determination of brain D1 receptors.
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Medchemexpress LLC Golotimod (hydrochloride) | 1029401-59-9 | 99.79% | 369.80 | 1 ML
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Golotimod hydrochloride (SCV 07 hydrochloride) is an immunomodulating peptide with antimicrobial activity. It significantly increases the efficacy of antituberculosis therapy, stimulates thymic and splenic cell proliferation, and improves macrophage function. It also inhibits STAT3 signaling and modulates the duration and severity of oral mucositis, showing potential as a therapeutic for recurrent genital herpes simplex virus type 2 (HSV-2).
- Immunomodulating peptide with antimicrobial activity
- Enhances antituberculosis therapy efficacy
- Stimulates thymic and splenic cell proliferation
- Improves macrophage function
- Inhibits STAT3 signaling
- Modulates duration and severity of oral mucositis
- Potential therapeutic for recurrent genital herpes simplex virus type 2 (HSV-2)
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Medchemexpress LLC Dopexamine hydrochloride | 86484-91-5 | 429.42 | 100 MG
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Dopexamine hydrochloride is a β2 adrenergic receptor agonist, intended for research use only. This dopamine analogue exhibits agonist activity at β2 and dopaminergic receptors, making it suitable for studies on inflammatory response and organ protection.
- Attenuates systemic inflammatory response
- Reduces tissue leukocyte infiltration
- Protects against organ injury
- Reduces systemic inflammatory response to endotoxin, including cytokine release, endothelial adhesion molecules, and oxidative stress
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Medchemexpress LLC Tocainide hydrochloride | 71395-14-7 | 99.49% | 50 MG
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Tocainide hydrochloride is a sodium channel blocker that blocks sodium channels in the pain-producing foci in nerve membranes. It is a primary amine analog of lidocaine and can be used for the treatment of tinnitus. It is for research use only and not sold to patients.
- Blocks sodium channels in pain-producing foci in nerve membranes
- Can be used for the treatment of tinnitus
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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.
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Medchemexpress LLC Cp-640186 hydrochloride | 591778-70-0 | MFCD28167776 | 99.7% | 522.08 g/mol | C30H36ClN3O3 | 10 MG
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CP-640186 hydrochloride is the hydrochloride salt of a research-grade acetyl-CoA carboxylase (ACC) inhibitor used in metabolic studies. It is orally active and cell-permeable, with reported low-nanomolar potency against ACC isoforms, and can stimulate muscle fatty acid oxidation. Intended for laboratory research use only.
- Inhibits acetyl-CoA carboxylase with reported IC50s of 53 nM (ACC1) and 61 nM (ACC2).
- Orally active and cell-permeable research compound.
- High purity suitable for biochemical assays and cellular studies.
- Solid, light yellow to pink appearance.
- Molecular weight 522.08 g/mol; formula C30H36ClN3O3.
- Available in multiple small vial sizes for dose-ranging experiments.
- For research use only; not for human or clinical applications.
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Medchemexpress LLC Ansofaxine hydrochloride | 916918-84-8 | 417.97 | 10 MG
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Ansofaxine hydrochloride is a triple reuptake inhibitor that inhibits serotonin, dopamine, and norepinephrine reuptake. It is for research use only and not sold to patients. This compound rapidly penetrates the rat striatum, converts into desvenlafaxine, and shows greater total exposure compared to desvenlafaxine administration.
- Inhibits serotonin reuptake with IC50 value of 723 nM.
- Inhibits dopamine reuptake with IC50 value of 491 nM.
- Inhibits norepinephrine reuptake with IC50 value of 763 nM.
- Acute and chronic oral administration increases 5-HT, dopamine, and norepinephrine levels more than desvenlafaxine.
- Reduces immobility time more effectively than desvenlafaxine.
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Medchemexpress LLC Amiloride hydrochloride | 2016-88-8 | 99.8% | 1 ML
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Amiloride hydrochloride is an inhibitor of both epithelial sodium channel (ENaC) and urokinase-type plasminogen activator receptor (uTPA). It also acts as a blocker of the polycystin-2 (PC2; TRPP2) channel. This compound is suitable for research applications targeting these pathways.
- Inhibitor of epithelial sodium channel (ENaC)
- Inhibitor of urokinase-type plasminogen activator receptor (uTPA)
- Blocker of polycystin-2 (PC2; TRPP2) channel
- Relatively selective ENaC inhibitor with IC50 ranging from 0.1 to 0.5 μM
- Demonstrated to reverse initial increases in collagen deposition in DOCA-salt hypertensive rats
- Delays the onset of proteinuria in stroke-prone spontaneously hypertensive rats (SHRSP)
- Antagonizes or prevents aldosterone actions in animal models of salt-dependent hypertension
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Medchemexpress LLC 1-benzyl-3-cyclohexyl-1-(piperidin-4-ylmethyl)urea; hydrochloride | 2070014-88-7 | 99.6% | 365.94 g/mol | C20H32ClN3O | 500 MG
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SRI-011381 hydrochloride is a small-molecule TGF-β/Smad signaling agonist (C381) that targets lysosomes and shows neuroprotective effects in preclinical models. Supplied as the hydrochloride salt for research use, it has been used to study lysosomal function and neurodegeneration mechanisms.
- Orally active TGF-β/Smad signaling agonist.
- Targets lysosomes to promote acidification and proteolysis.
- Demonstrated neuroprotective effects in preclinical studies.
- Hydrochloride salt form for improved solubility and handling.
- Available in multiple solid sizes and as DMSO solutions for assay-ready use.
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Medchemexpress LLC Proadifen hydrochloride | 62-68-0 | 100.0% | 500 MG
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Proadifen hydrochloride | 62-68-0 | 100.0% | 500 MG
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Medchemexpress LLC Kanosamine hydrochloride | 57649-10-2 | MFCD01725274 | ≥98.0% | 215.63 g/mol | C6H14ClNO5 | 5 MG
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Kanosamine hydrochloride is the hydrochloride salt of kanosamine, an aminoglycoside sugar antibiotic used in biochemical and microbiological research. It inhibits certain plant-pathogenic oomycetes, select fungi, and some bacteria and is employed as a reference compound to study cell wall biosynthesis and pathogen growth.
- Hydrochloride salt form of kanosamine.
- CAS 57649-10-2.
- Molecular formula C6H14ClNO5; molecular weight 215.63 g/mol.
- Reported activity: inhibits Phytophthora medicaginis and Aphanomyces euteiches (MICs 25 and 60 μg/mL).
- Available in small research quantities (for example, 5 mg).
- Purity commonly ≥98% depending on supplier and lot.
- Used as a reference standard in microbiology and biochemical studies.
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