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Filtered Search Results
Medchemexpress LLC Pevonedistat hydrochloride | 1160295-21-5 | 98.6% | 479.98 | 10 MG
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Pevonedistat hydrochloride | 1160295-21-5 | 98.6% | 479.98 | 10 MG
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Cayman Chemical 8piperazin1ylIsoquinoline hy
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A synthetic intermediate useful for pharmaceutical synthesis.
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Medchemexpress LLC Guretolimod hydrochloride | 00-00-0 | 98.7% | 550.01 | C24H35ClF3N5O4 | 5 MG
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Guretolimod hydrochloride is a synthetic small-molecule Toll-like receptor 7 (TLR7) agonist supplied for research use. It is used in preclinical studies to stimulate innate immune signaling and evaluate immunostimulatory and antitumor responses in vitro and in vivo models.
- Potent TLR7 agonist for immune activation studies.
- Suitable for in vitro and in vivo preclinical research.
- High purity (approximately 98.7%) for consistent results.
- Hydrochloride salt form to improve solubility and handling.
- Characterized chemical identity with molecular formula C24H35ClF3N5O4 and molecular weight 550.01.
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Medchemexpress LLC Miransertib hydrochloride (ARQ-092 hydrochloride) | 1313883-00-9 | 99.7% | 468.98 | 100 MG
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Miransertib hydrochloride (ARQ-092 hydrochloride) is a potent, orally active, selective, and allosteric Akt inhibitor. It exhibits specific IC50s for Akt1, Akt2, and Akt3, and is a potent inhibitor of the AKT1-E17K mutant protein. This compound is considered for research into PI3K/AKT-driven tumors, Proteus syndrome, and is effective against Leishmania.
- Potent, orally active, selective, and allosteric Akt inhibitor.
- Exhibits specific IC50s for Akt1, Akt2, and Akt3.
- Inhibits the AKT1-E17K mutant protein.
- Suitable for research in PI3K/AKT-driven tumors and Proteus syndrome.
- Effective against Leishmania.
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Medchemexpress LLC Valnivudine hydrochloride | 956483-03-7 | 98.99% | 534.04 | 50 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 intended for research use only.
- 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 (In Vitro).
- Does not induce biologically relevant respiratory changes or apparent neuropharmacological effects in rats at 50-500 mg/kg; p.o. (In Vivo).
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Medchemexpress LLC Seltorexant (hydrochloride) | 1293284-49-7 | 99.9% | 443.91 | 5 MG
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Seltorexant hydrochloride is an orally active, high-affinity, and selective OX2R antagonist. It has pKi values of 8.0 and 8.1 for human and rat OX2R, respectively. This compound crosses the blood-brain barrier and quickly occupies OX2R binding sites in the rat brain. It is intended for research use only.
- Orally active, high-affinity, and selective OX2R antagonist
- pKi values of 8.0 for human OX2R and 8.1 for rat OX2R
- Crosses the blood-brain barrier
- Quickly occupies OX2R binding sites in the rat brain
- For research use only
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Medchemexpress LLC Ifebemtinib hydroch 10mg | 10MG
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Ifebemtinib hydroch 10mg | 10MG
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Medchemexpress LLC Norverapamil hydrochloride | 67812-42-4 | MFCD00078605 | 99.8% | 477.04 g/mol | C26H37ClN2O4 | 100 MG
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Norverapamil hydrochloride is the N-demethylated metabolite of verapamil. It functions as an L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor and is supplied for research use in solid form or as a DMSO solution.
- High purity: 99.8% for reliable experimental results.
- White to off-white solid for easy handling.
- Soluble in water (≥50 mg/mL) and DMSO (≥31 mg/mL) for formulation flexibility.
- Stable when stored sealed at 4°C; in solvent store -80°C (6 months) or -20°C (1 month).
- Suitable as a research reagent for studies of calcium channel modulation and P-gp function.
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Medchemexpress LLC Galidesivir hydrochloride | 222631-44-9 | 99.9% | 301.73 | 25 MG
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Galidesivir hydrochloride is an adenosine analog and a direct-acting antiviral agent that disrupts viral RNA-dependent RNA polymerase (RdRp) activity. It is active in vitro against many RNA viral pathogens, including filoviruses and emerging infectious agents like MERS-CoV, SARS-CoV, and SARS-CoV-2. It inhibits some negative-sense RNA viruses with EC50s ranging from ~3 to ~68 μM.
- Adenosine analog
- Direct-acting antiviral agent
- Disrupts viral RNA-dependent RNA polymerase (RdRp) activity
- Active against many RNA viral pathogens
- Inhibits negative-sense RNA viruses
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Medchemexpress LLC Dalbavancin hydrochloride | 2227366-51-8 | 99.7% | 1853.15 | 50 MG
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Dalbavancin hydrochloride | 2227366-51-8 | 99.7% | 1853.15 | 50 MG
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Medchemexpress LLC Martinostat hydrochloride | 1629052-58-9 | 99.0% | 390.95 | C22H31ClN2O2 | 10 MG
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Martinostat hydrochloride is a histone deacetylase (HDAC) inhibitor that can be labeled with radionuclides for quantitative in vivo imaging of HDACs in the central nervous system and major peripheral organs.
- Histone deacetylase inhibitor suitable for imaging applications.
- Can be labeled with radionuclides for quantitative in vivo imaging.
- High purity (99.01%).
- Available as solid (5-500 mg; larger sizes by quote) and as 10 mM solution in DMSO.
- Storage: 4°C sealed; in solvent store at -80°C (6 months) or -20°C (1 month).
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Medchemexpress LLC Dl-3-phenylserine hydrate | 313222-82-1 | 100.0% | 199.20 | C9H13NO4 | 10 G
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DL-3-Phenylserine hydrate is the hydrated form of DL-3-phenylserine, a serine derivative supplied for laboratory research use. It is an off-white to light yellow solid with properties suitable for biochemical and synthetic chemistry applications; it is intended for research purposes only and not for human or animal use. Typical identifiers include CAS 313222-82-1, molecular formula C9H13NO4, and molecular weight 199.20 g/mol.
- High chemical purity suitable for research applications.
- Hydrated solid form compatible with aqueous experiments.
- Characterized by CAS number and molecular formula for unambiguous identification.
- Available in laboratory-scale pack sizes such as 5 G, 10 G, and 25 G.
- Stable at room temperature when stored as recommended.
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Medchemexpress LLC Regorafenib hydrochloride | 835621-07-3 | MFCD22417053 | C21H16Cl2F4N4O3 | 10MG
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Regorafenib hydrochloride is the hydrochloride salt of regorafenib, a potent multi-target kinase inhibitor. Supplied as an analytical standard for research use, it inhibits VEGFR1/2/3, PDGFRβ, Kit, RET, and Raf-1 with low-nanomolar potency, and is intended for in vitro and analytical applications such as HPLC, GC, and MS.
- Multi-target kinase inhibitor active against VEGFR1/2/3, PDGFRβ, Kit, RET, and Raf-1.
- Low-nanomolar potency reported for key kinase targets.
- High purity analytical standard (99.6%).
- Intended for research and analytical applications, including HPLC, GC, and MS.
- Suitable for method development and quantitative assays.
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Medchemexpress LLC Tolperisone hydrochloride | 3644-61-9 | 99.8% | 5 MG
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Tolperisone hydrochloride | 3644-61-9 | 99.8% | 5 MG
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Medchemexpress LLC 3-CHLOROIMINODIBENZY 50G | 50G
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3-CHLOROIMINODIBENZY 50G | 50G
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