Alcohols and polyols
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- (50)
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- (13)
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- (1)
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- (1)
- (26)
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- (1)
- (6)
- (1)
- (462)
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- (46)
- (11)
- (45)
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- (1)
- (7)
- (10)
- (145)
- (114)
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- (5)
- (1)
- (1)
- (1)
- (1)
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- (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)
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- (1)
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- (1)
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- (1)
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Filtered Search Results
Medchemexpress LLC Bmt-090605 (hydrochloride) | 2231664-45-0 | 98.8% | 400.90 g·mol⁻¹ | C21H25ClN4O2 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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BMT-090605 hydrochloride is a potent, selective small-molecule inhibitor of adaptor protein-2 associated kinase 1 (AAK1) with additional activity against BIKE and GAK. Supplied as the hydrochloride salt for research use, it is provided as a solid with specified purity and storage recommendations, making it suitable for kinase profiling and target validation studies.
- Potent AAK1 inhibition with low-nanomolar IC50 (0.6 nM).
- Selective activity against related kinases BIKE and GAK.
- High purity (98.8%) suitable for biochemical assays.
- Molecular weight 400.90 g·mol⁻¹.
- Available in small pre-weighed sizes for research, including 5 mg.
- Stable as a powder when stored at recommended temperatures.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC SB-408124 Hydrochloride | 1431697-90-3 | 98.8% | C19H19ClF2N4O | 100 MG
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SB-408124 Hydrochloride is a selective, non-peptide orexin receptor 1 (OX1) antagonist. It demonstrates high potency with Ki values of 57 nM in whole cells and 27 nM in membranes, exhibiting 50-fold selectivity over the OX2 receptor. This compound is for research use only.
- Potent OX1 receptor antagonist (Ki: 57 nM in whole cells, 27 nM in membranes)
- Exhibits 50-fold selectivity over OX2 receptor
- Attenuates orexin A-induced AVP mRNA levels in neuronal cultures
- Reduces anxiety and restores corticoliberin levels in vivo
- Demonstrates an anxiolytic effect
- Reduces mean arterial pressure in salt-sensitive rats
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Taltobulin hydrochloride | 228266-40-8 | 99.3% | 510.11 Da | C27H44ClN3O4 | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Taltobulin hydrochloride is a synthetic analogue of the tripeptide hemiasterlin and a potent antimicrotubule agent. It inhibits tubulin polymerization, disrupts microtubule organization, and induces mitotic arrest, and is supplied as a solid research reagent for in vitro and in vivo studies.
- Potent tubulin inhibitor with low-nanomolar activity in tumor cell lines.
- High purity suitable for research applications.
- Supplied as a solid powder for solution preparation in DMSO or aqueous buffers.
- Recommended solvent and formulation guidance provided for in vitro and in vivo use.
- Store sealed at 4°C; solutions stable at -80°C for long-term storage.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Azasetron hydrochloride (Y-25130 hydrochloride) | 123040-16-4 | 99.8% | C17H21Cl2N3O3 | 50 MG
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Azasetron hydrochloride is a potent and selective 5-HT3 receptor antagonist, a benzamide derivative used in the study of Chemotherapy-induced nausea and vomiting (CINV). This product is for research use only. It has an IC50 for the 5-HT3 Receptor of 0.33 nM and appears as a white to off-white solid with a molecular weight of 386.27.
- Potent and selective 5-HT3 receptor antagonist
- Used in studies for chemotherapy-induced nausea and vomiting (CINV)
- Effectively penetrates skin and enters systemic circulation (demonstrated in in vivo studies)
- Soluble in H2O (20 mg/mL) and DMSO (2.22 mg/mL)
- Clear solution of 50 mg/mL in PBS achievable for in vivo dissolution
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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 Skf-34288 (hydrochloride) | 320386-54-7 | 98.6% | 50 MG
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SKF-34288 hydrochloride is an orally active phosphoenolpyruvate carboxykinase (PEPCK) inhibitor with a Ki of 2-9 μM. It functions as a potent hypoglycemic agent by inhibiting glucose synthesis. Additionally, it inhibits Asn metabolism, leading to an increase in amino acids and amides.
- Inhibits C2C12 cell proliferation
- Induces myogenic differentiation of C2C12 cells
- Reduces mRNA expression of Pck2 and genes associated with serine biosynthesis
- Reduces blood glucose in starved rats
- Neutralizes Salbutamol-mediated hyperglycaemia in rabbits
- Reduces Pyruvate-induced blood glucose level in rats
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Medchemexpress LLC Moexipril (hydrochloride) | 82586-52-5 | 1 ML
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Moexipril hydrochloride is an orally active inhibitor of angiotensin-converting enzyme (ACE) that becomes effective after being hydrolyzed to moexiprila (hydrochloride). It demonstrates antihypertensive and neuroprotective effects and exhibits high potency against both plasma ACE and purified ACE from rabbit lung.
- Functions as an orally active ACE inhibitor
- Becomes effective after hydrolysis to moexiprila
- Demonstrates antihypertensive and neuroprotective effects
- High potency against plasma ACE and purified ACE from rabbit lung
- Reduces damaged neurons in a dose-dependent manner
- Attenuates Fe2+/3+-induced neurotoxicity
- Exhibits dose-dependent antihypertensive effects in various hypertensive rat and dog models
- Significantly reduces infarct area and cortical infarct volume in mouse and rat models of ischemic brain injury
- Supplied as a 10 mM solution in DMSO
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Medchemexpress LLC Eperisone hydrochloride | 56839-43-1 | MFCD00941459 | 100.0% | 500 MG
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Eperisone Hydrochloride ((±)-Eperisone hydrochloride) is an orally active antispastic agent with a vasodilator effect, used for the research of muscle stiffness and pain. It is a potent and selectively P2X7 receptor antagonist, and also shows antagonism for human P2X3. Eperisone Hydrochloride works by relaxing both skeletal muscles and vascular smooth muscles, demonstrating a variety of effects such as reduction of myotonia, improvement of circulation and suppression of the pain reflex.
- Orally active antispastic agent
- Vasodilator effect
- Used for research of muscle stiffness and pain
- Potent and selective P2X7 receptor antagonist
- Shows antagonism for human P2X3
- Relaxes both skeletal muscles and vascular smooth muscles
- Reduces myotonia
- Improves circulation
- Suppresses the pain reflex
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Medchemexpress LLC Enerisant hydrochloride | 1152749-07-9 | 98.7% | 434.96 | 5 MG
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Enerisant hydrochloride | 1152749-07-9 | 98.7% | 434.96 | 5 MG
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Medchemexpress LLC Bobcat339 hydrochloride | 2436747-44-1 | 99.6% | 334.20 | 50 MG
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Bobcat339 hydrochloride is a potent and selective cytosine-based inhibitor of the TET enzyme, with IC50s of 33 μM and 73 μM for TET1 and TET2, respectively. It is useful in epigenetics and serves as a starting point for new therapeutics targeting DNA methylation and gene transcription.
- Potent and selective cytosine-based inhibitor of TET enzyme.
- Useful in epigenetics.
- Serves as a starting point for new therapeutics that target DNA methylation and gene transcription.
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Medchemexpress LLC Preclamol hydrochloride | 88768-67-6 | MFCD00069366 | 98.0% | 255.78 g/mol | C14H22ClNO | 5 MG
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Preclamol hydrochloride is a research compound that functions as a selective dopamine autoreceptor agonist. It is used in preclinical pharmacology to probe dopamine receptor activity and has been investigated for applications related to schizophrenia research. The substance is provided in solid form and as a ready-to-use DMSO solution for laboratory assays.
- Selective dopamine autoreceptor agonist.
- Used for preclinical studies of dopamine receptor function.
- Investigated in schizophrenia-related research.
- Supplied as a solid and as a 10 mM solution in DMSO.
- High purity: 98.0%.
- Molecular formula C14H22ClNO; molecular weight 255.78 g/mol.
- White to light yellow solid appearance.
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Medchemexpress LLC Pirlimycin hydrochloride | 78822-40-9 | MFCD27952783 | 99.1% | 447.42 | C17H32Cl2N2O5S | 5 MG
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Pirlimycin hydrochloride is the hydrochloride salt of pirlimycin, a lincosamide-class antibiotic provided as a research-grade reagent. It is primarily active against Gram-positive bacteria and is supplied as a purified, stable salt for laboratory applications.
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Medchemexpress LLC Etifoxine (hydrochloride) | 56776-32-0 | 99.8% | 337.24 | 50 MG
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Etifoxine hydrochloride is a non-benzodiazepine GABAergic compound that acts as a positive allosteric modulator of α1β2γ2 and α1β3γ2 subunit-containing GABAA receptors, demonstrating anxiolytic and anticonvulsant properties.
- Non-benzodiazepine GABAergic compound
- Acts as a positive allosteric modulator of α1β2γ2 and α1β3γ2 subunit-containing GABAA receptors
- Demonstrates anxiolytic and anticonvulsant properties
- Increases [3H]muscimol binding
- Competitively inhibits [35S]TBPS binding
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U.S. Pharmacopeia BUDESONIDE 200 MG USP
Budesonide (200 mg) USP
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5000744169 AZIDO-PEG9-ALCOHOL 250MG
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