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Filtered Search Results
Medchemexpress LLC Hypidone hydrochloride | 1339058-04-6 | 99.7% | 334.84 g/mol | C18H23ClN2O2 | 10 MG
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Hypidone hydrochloride is the hydrochloride salt of a research compound reported to modulate 5-HT receptors and inhibit serotonin uptake in preclinical studies. It is supplied as a high-purity solid for laboratory use, typically in milligram-scale vials for in vitro and in vivo research.
- High reported purity (>99%).
- Molecular weight 334.84 g/mol.
- Solid hydrochloride salt, white to off-white powder.
- Reported activity as a 5-HT receptor modulator and uptake inhibitor in preclinical models.
- Packaged in small, milligram-scale quantities suitable for research.
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eMolecules DICHLOROBIS DI-TERT-BUTYL4 5G
5000163530 DICHLOROBIS DI-TERT-BUTYL4 5G
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Medchemexpress LLC His-Pro hydrochloride | 2415727-78-3 | 99.8% | 288.73 | 100 MG
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His-Pro (Histidyl-proline) hydrochloride is a dipeptide consisting of histidyl and proline. It is for research use only and not sold to patients.
- Appearance: Solid
- Color: White to off-white
- Shipping: Room temperature in continental US
- Storage: Sealed storage, away from moisture and light. Powder: -80°C for 2 years, -20°C for 1 year. In solvent: -80°C for 6 months, -20°C for 1 month.
- Solubility (In Vitro): DMSO: 125 mg/mL (432.93 mM)
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Medchemexpress LLC Rs 67333 hydrochloride | 168986-60-5 | 99.7% | 389.36 | C19H30Cl2N2O2 | 100 MG
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RS 67333 hydrochloride is a research-grade 5-HT4 (serotonin 4) receptor partial agonist supplied as the hydrochloride salt for use in neuroscience and pharmacology studies. It is commonly used to probe 5-HT4 receptor function in vitro and in vivo, with reported neuroprotective and pro-cognitive activity.
- Partial agonist at 5-HT4 receptors, useful for receptor pharmacology studies.
- Hydrochloride salt form for improved solubility in aqueous media.
- High purity (99.68%) suitable for research applications.
- Characterized by CAS 168986-60-5 and defined molecular properties for formulation.
- Available in small research quantities (e.g., 100 MG) for in vitro and in vivo use.
- Relevant for studies of cognition, neuroprotection, and serotonergic signaling.
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Medchemexpress LLC RS 67333 (hydrochloride) | 168986-60-5 | MFCD00938576 | 99.7% | 389.36 | C19H30Cl2N2O2 | 25 MG
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RS 67333 hydrochloride is a research-grade, selective 5-HT4 receptor partial agonist used in preclinical and in vitro neuroscience studies to investigate serotonergic signaling and neuroprotective mechanisms.
- Potent, selective 5-HT4 receptor partial agonist for neuroscience research.
- High purity, 99.7% (as listed by manufacturer).
- Molecular weight 389.36 g/mol; formula C19H30Cl2N2O2.
- Solid, light yellow to yellow appearance supplied as a dry powder.
- Storage: 4°C, sealed and away from moisture; in solvent store at -80°C for long-term.
- Available as a 25 MG vial for laboratory use.
- CAS number 168986-60-5.
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Medchemexpress LLC SKI-I | 5MG
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SKI-I is a potent and selective inhibitor of human sphingosine kinase (SK) with an IC50 of 1 2 M for ST-hSK SKI-I also inhibits hERK2 (IC50 11 M) SKI-I induces apoptosis in tumor cell lines[1][2]
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Medchemexpress LLC Levacetylleucine (N-Acetyl-L-leucine) | 1188-21-2 | 98.0% | C8H15NO3 | 1000 G
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Levacetylleucine is an orally bioavailable and brain-penetrant acetylated derivative of amino acid Leucine. It is the active form of N-acetyl-leucine (NAL), shown to attenuate neuronal death and neuroinflammation, and potentially ameliorate lysosomal and metabolic dysfunction. This compound improves compensation of postural symptoms and is promising for research into neurological manifestations of Niemann-Pick disease type C, traumatic brain injury, and neurodegeneration prevention.
- Orally bioavailable and brain-penetrant
- Attenuates neuronal death and neuroinflammation
- Potentially ameliorates lysosomal and metabolic dysfunction
- Improves compensation of postural symptoms
- Suitable for research into neurological diseases and neurodegeneration prevention
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eMolecules Medchem Express / SKI-178 / 5mg / 599150633 / HY-12892 / / 1259484-97-3 / MFCD01913555 / 394.431 / C21H22N4O4
Medchem Express / SKI-178 / 5mg / 599150633 / HY-12892 / / 1259484-97-3 / MFCD01913555 / 394.431 / C21H22N4O4
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Medchemexpress LLC LY294002 (hydrochloride) | 934389-88-5 | 99.9% | 369.8 g/mol | C19H17NO3·HCl | 5 MG
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LY294002 hydrochloride is the hydrochloride salt of LY294002, a cell-permeable small-molecule inhibitor of phosphoinositide 3-kinase (PI3K) and casein kinase 2 (CK2) used in in vitro studies of cell signaling, apoptosis, and autophagy. Supplied for research use with supporting documentation.
- Inhibits PI3K and CK2 signaling pathways.
- Suitable for in vitro cell signaling and apoptosis research.
- High purity (99.9%).
- Chemical formula C19H17NO3·HCl; molecular weight 369.8 g/mol.
- Supplied in small research quantities (e.g., 5 mg).
- Comes with SDS and certificate of analysis.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000378000 FTI-277 HYDROCHLORI 1MG
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Medchemexpress LLC BN82002 hydrochloride | 1049740-43-3 | 99.4% | 395.88 | 50 MG
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BN82002 hydrochloride is a potent, selective, and irreversible inhibitor of the CDC25 phosphatase family. It inhibits CDC25A, CDC25B2, CDC25B3, CDC25C, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 μM, respectively. The compound demonstrates approximately 20-fold greater selectivity over CD45 tyrosine phosphatase and inhibits cell proliferation in several human tumor cell lines in a concentration-dependent manner in the low micromolar range. Treatment with 50 μM BN82002 modestly affects cell cycle distribution, suggesting cell cycle arrest at various stages.
- Potent, selective, and irreversible inhibitor of CDC25 phosphatase family.
- Displays approximately 20-fold greater selectivity over CD45 tyrosine phosphatase.
- Inhibits cell proliferation in various human tumor cell lines.
- For research use only.
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eMolecules ACETAMINOPHEN 100G
5000163833 ACETAMINOPHEN 100G
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Medchemexpress LLC ZK824190 hydrochloride | 2629177-12-2 | 99.2% | 450.86 g/mol | C22H21ClF2N2O4 | 10MM 1ML
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ZK824190 hydrochloride is the hydrochloride salt of a selective, orally available urokinase plasminogen activator (uPA) inhibitor used in research into uPA biology and potential therapies for multiple sclerosis. It is supplied as a high-purity solid and as a pre-made 10 mM solution in DMSO for in vitro and preclinical studies; not for human use.
- Selective urokinase plasminogen activator (uPA) inhibitor.
- Supplied as 10 mM solution in DMSO and as solid quantities.
- High purity suitable for research applications.
- Molecular formula: C22H21ClF2N2O4.
- Molecular weight: 450.86 g/mol.
- CAS: 2629177-12-2 for substance identification.
- Provided as the hydrochloride salt for stability and handling.
- Intended for in vitro and preclinical research only, not for human use.
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Medchemexpress LLC Metixene hydrochloride hydrate | 7081-40-5 | 99.9% | 50 MG
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Metixene hydrochloride hydrate is an anticholinergic and antiparkinsonian research chemical supplied as a white to off-white solid for laboratory research. It is offered in multiple lab-scale pack sizes and in ready-to-use DMSO solution formats.
- White to off-white solid appearance.
- High reported purity of 99.9%.
- Available in multiple pack sizes including 50 MG.
- Chemical formula C20H26ClNOS; molecular weight 363.94.
- Offered in DMSO solution formats for ready use.
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eMolecules 3-(3,5-Dibromo-4-hydroxyphenyl)propanoic acid | 13811-12-6 | MFCD00816760 | 1g
Apollo Scientific | 3-(3,5-Dibromo-4-hydroxyphenyl)propanoic acid | 1g | 562430610 | OR29368 | | 13811-12-6 | MFCD00816760 | 323.968 | C9H8Br2O3
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