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Filtered Search Results
Medchemexpress LLC 4-(aminomethyl)-2-methoxyphenol hydrochloride | 7149-10-2 | MFCD00012864 | 99.8% | 189.64 g/mol | C8H12ClNO2 | 25 G
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Vanillylamine (hydrochloride) is the hydrochloride salt of vanillylamine supplied for research use as a biochemical reagent. It is a crystalline, high-purity intermediate used in organic synthesis and biochemical studies, including the synthesis of capsaicinoids and related vanillyl derivatives.
- High purity suitable for analytical and synthetic applications (reported ~99.8%).
- Molecular formula C8H12ClNO2 and molecular weight 189.64 g/mol.
- Available in multiple small-scale and bulk pack sizes for laboratory use.
- Useful as a building block for synthesis of capsaicinoids and other vanillyl compounds.
- Intended for research use only; not for clinical or patient use.
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Medchemexpress LLC 7-MAD-MDCPT hydrochloride | 2740593-09-1 | 457.86 g/mol | C22H20ClN3O6 | 5 MG
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7-MAD-MDCPT hydrochloride is a camptothecin analog used as a cytotoxic payload in antibody-drug conjugates for research applications. Supplied as the hydrochloride salt in small laboratory quantities, it requires low-temperature, moisture-free storage. Soluble in DMSO; consult safety and handling documentation before use.
- Camptothecin analog suitable as an ADC toxin payload.
- Hydrochloride salt form for improved handling.
- Molecular formula C22H20ClN3O6; molecular weight 457.86 g/mol.
- CAS number 2740593-09-1 for unambiguous identification.
- DMSO solubility approximately 6.67 mg/mL (14.57 mM).
- Store at -20°C under inert gas; in solution store at -80°C for long-term.
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Medchemexpress LLC N-[(3-(Anilinomethylene)-2-chloro-1-cyclohexen-1-yl)methylene]aniline hydrochloride | 63857-00-1 | 96.5% | 359.29 g·mol-1 | C20H20Cl2N2 | 10 G
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N-[(3-(Anilinomethylene)-2-chloro-1-cyclohexen-1-yl)methylene]aniline hydrochloride is an aniline-derived chemical building block provided as the hydrochloride salt for research and synthetic applications. It is used primarily to synthesize cyanine-containing and related conjugated dyes and is supplied as a solid with a reported purity of 96.5%.
- Aniline-derived building block for dye synthesis.
- Useful for synthesis of cyanine-containing and conjugated dyes.
- Supplied as the hydrochloride salt, improving handling and stability.
- Solid form, dark purple to black appearance.
- High purity (96.5%), suitable for research and synthesis.
- Molecular weight 359.29 g·mol-1; formula C20H20Cl2N2.
- Available in multiple pack sizes to support small-scale and larger-scale work.
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Medchemexpress LLC Pf-07038124 hydrochloride | 2415317-57-4 | 99.3% | 363.64 g/mol | C18H23BClNO4 | 5 MG
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PF-07038124 hydrochloride is the hydrochloride salt of a selective phosphodiesterase 4 (PDE4) inhibitor supplied for laboratory research into inflammatory skin diseases and immune signaling pathways. Intended for research use only; not for human or clinical use.
- High purity suitable for biochemical and cellular assays.
- Potent inhibition of PDE4B2 (IC50 ≈ 0.5 nM).
- Demonstrated cytokine inhibition of IL-13, IL-4, and IFN-γ in reported assays.
- Available in small milligram quantities for early-stage studies.
- Hydrochloride salt form improves solubility for aqueous assays.
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Medchemexpress LLC Ar-m 1000390 (hydrochloride) | 209808-47-9 | MFCD20926357 | 98.2% | 384.94 g/mol | C23H29ClN2O | 10 MG
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AR-M 1000390 hydrochloride is a selective and potent δ-opioid receptor agonist supplied as the hydrochloride salt for research use. It exhibits an EC50 of 7.2 ± 0.9 nM for δ agonist potency, a reported purity of 98.2%, and a molecular weight of 384.94 g/mol. The compound is provided as a white to off-white solid intended for in vitro and in vivo pharmacology studies.
- Selective δ-opioid receptor agonist for receptor pharmacology studies.
- Potent activity with EC50 7.2 ± 0.9 nM for δ agonist potency.
- High reported purity (98.2%), suitable for research assays.
- Solid form, white to off-white, convenient for handling and formulation.
- Recommended storage: 4°C sealed; in solvent -80°C (6 months) or -20°C (1 month).
- Available in small research pack sizes, including 10 mg.
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Medchemexpress LLC Valnivudine hydrochloride | 956483-03-7 | 99.0% | 534.04 | 25 MG
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Valnivudine hydrochloride (FV-100) is a potent, selective, and orally active anti-varicella zoster virus agent. It is a proagent of CF-1743 and exhibits very low toxicity in vivo. It is intensely fluorescent when illuminated by wavelengths of 340-380 nm and produces a different distribution in HeLa cells within 1 hour. In rats, Valnivudine hydrochloride (50-500 mg/kg; p.o.) does not induce biologically relevant respiratory changes or any apparent neuropharmacological effects.
- Potent, selective, and orally active anti-varicella zoster virus agent
- Proagent of CF-1743
- Exhibits very low toxicity in vivo
- Intensely fluorescent when illuminated by wavelengths of 340-380 nm
- Produces a different distribution in HeLa cells within 1 hour
- Does not induce biologically relevant respiratory changes or apparent neuropharmacological effects in rats
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Medchemexpress LLC (R)-viloxazine hydrochloride | 56287-63-9 | MFCD18379655 | 99.1% | 273.76 | C13H20ClNO3 | 5MG
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(R)-Viloxazine hydrochloride is the R-enantiomer of viloxazine hydrochloride supplied as a high-purity research chemical for laboratory pharmacology and biochemical studies. It is described as a less active enantiomer of viloxazine and is characterized by a defined molecular composition, physical form, and recommended storage conditions.
- R-enantiomer of viloxazine hydrochloride.
- Cas 56287-63-9.
- Purity 99.1%.
- Molecular formula C13H20ClNO3.
- Molecular weight 273.76.
- Appearance solid powder.
- Recommended storage: powder at -20°C (3 years) or 4°C (2 years); in solvent at -80°C (6 months) or -20°C (1 month).
- For research use only; not intended for human consumption.
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Medchemexpress LLC Diphenylpyraline hydrochloride | 132-18-3 | 99.9% | 1 ML
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Diphenylpyraline hydrochloride is a potent histamine H1 receptor antagonist, functioning as an orally active antihistamine agent with antimuscarinic and antiallergic effects.
- Relieves allergic conditions such as rhinitis and hay fever.
- Addresses pruritic skin disorders in vivo.
- Inhibits dopamine uptake in mouse nucleus accumbens slices.
- Elevates extracellular dopamine levels in mouse nucleus accumbens.
- Induces locomotor activation in mice.
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Medchemexpress LLC Pyridine, 3-ethynyl- | 2510-23-8 | 100.0% | 103.12 | 10 G
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3-Ethynylpyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. It is a click chemistry reagent, containing an alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing azide groups. It is for research use only and not sold to patients.
- Biochemical reagent for life science research.
- Click chemistry reagent with an alkyne group.
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide groups.
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Medchemexpress LLC Rimantadine (hydrochloride) | 1501-84-4 | 98.0% | 1 ML
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Rimantadine hydrochloride (Flumadine hydrochloride) is an orally active inhibitor for M2 protein, which blocks hydrogen ion channel activity, prevents virus entry and replication, and exhibits broad-spectrum antiviral activity. It is intended for research use only.
- Orally active M2 protein inhibitor.
- Blocks hydrogen ion channel activity.
- Prevents virus entry and replication.
- Exhibits broad-spectrum antiviral activity.
- Inhibits RNA levels of hepatitis A virus (HAV).
- Promotes autophagy in HAV-infected Huh7 cells.
- Exhibits anti-infectious activity with Oseltamivir in H3N2-infected mouse models.
- Solubility in DMSO: 50 mg/mL (231.74 mM).
- Solubility in H2O: 33.33 mg/mL (154.48 mM).
- Store at room temperature, keep dry and cool.
- Store in solvent at -80°C for 1 year or -20°C for 6 months.
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Medchemexpress LLC Maprotiline (hydrochloride) | 10347-81-6 | MFCD00078833 | >99.9% | 50 MG
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Maprotiline hydrochloride is an analytical standard and a highly selective noradrenergic reuptake inhibitor. It exhibits strong antidepressant, antitumor, and neuropathic pain-relieving effects. This compound induces cancer cell apoptosis by targeting the ERK signaling pathway and CRABP1, making it a valuable subject for research in various therapeutic areas.
- Inhibits the growth of Huh7 and HepG2 cells and induces cell apoptosis.
- Inhibits the metastasis of liver cancer cells.
- Targets CRABP1 and regulates cholesterol biosynthesis in HCC cells.
- Restrains HCC cell migration with inhibition of epithelial-mesenchymal transition.
- Inhibits liver cancer tumor growth in mice.
- Effectively reduces neuropathic pain in mice.
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Aobchem 2-Bromo-3-chlorophenol | ≥97% | CAS 855836-62-3 | C6H4BrClO | 25g
2-Bromo-3-chlorophenol | ≥97% | CAS 855836-62-3 | C6H4BrClO | 25g
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Aobchem 2-Bromo-6-chlorophenol | 97% | CAS 2040-88-2 | C6H4BrClO | 500g
2-Bromo-6-chlorophenol | 97% | CAS 2040-88-2 | C6H4BrClO | 500g
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Aobchem 4-Bromo-3-chlorophenol | 97% | CAS 13631-21-5 | C6H4BrClO | 100g
4-Bromo-3-chlorophenol | 97% | CAS 13631-21-5 | C6H4BrClO | 100g
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Aobchem 4-Bromo-3-chlorophenol | 97% | CAS 13631-21-5 | C6H4BrClO | 1kg
4-Bromo-3-chlorophenol | 97% | CAS 13631-21-5 | C6H4BrClO | 1kg
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