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Filtered Search Results
Medchemexpress LLC Bromophenol blue sodium salt | 34725-61-6 | MFCD00013793 | 691.94 g/mol | C19H9Br4NaO5S | 5 G
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Bromophenol blue sodium salt is a water-soluble pH indicator and tracking dye used as a biochemical assay reagent. It is supplied as a brown to dark brown solid and is commonly used as a tracking dye in nucleic acid and protein electrophoresis, and as a pH indicator in buffer systems.
- cas number: 34725-61-6
- chemical formula: C19H9Br4NaO5S
- molecular weight: 691.94 g/mol
- appearance: solid, brown to dark brown
- solubility: soluble in DMSO (100 mg/mL with ultrasonic warming)
- applications: biochemical assay reagent, electrophoresis tracking dye
- package sizes: includes 5 g, 10 g, 25 g, 50 g, 100 g
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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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BOC SCIENCES CARBADOX 5G
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NC3802626 CARBADOX 5G
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Medchemexpress LLC Maprotiline (hydrochloride) | 10347-81-6 | 99.99% | 100 MG
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Maprotiline (hydrochloride) (Standard) is the analytical standard of Maprotiline (hydrochloride). It is a highly selective noradrenergic reuptake inhibitor with strong antidepressant, antitumor, and neuropathic pain-relieving effects. It induces cancer cell apoptosis by targeting the ERK signaling pathway and CRABP1. This compound is an analytical standard used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS.
- Analytical standard
- Highly selective noradrenergic reuptake inhibitor
- Strong antidepressant effects
- Antitumor effects
- Neuropathic pain-relieving effects
- Induces cancer cell apoptosis by targeting the ERK signaling pathway and CRABP1
- Used in qualitative research experiments
- Used in quantitative research experiments
- Used in methodological research experiments
- Suitable for HPLC, GC, and MS applications
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Ambeed Methyl 7bromo1Hindole5carboxyl
Methyl 7-bromo-1H-indole-5-carboxylate, 885523-35-3, 96%
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Chemscene CHEMSCENE
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5000575436 ISONICOTINAMIDE 1KG
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Chemscene CHEMSCENE
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5000575417 FDPP 100G
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eMolecules Combi-Blocks Bis(pinacolato)diboron 1kg 205381782 BB-2214 98 000 73183-34-3 MFCD00799570 253 940 C12H24B2O4
Combi-Blocks Bis(pinacolato)diboron 1kg 205381782 BB-2214 98 000 73183-34-3 MFCD00799570 253 940 C12H24B2O4
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Medchemexpress LLC Pyrazoloadenine | 2380-63-4 | 100.0% | 135.13 | 25 G
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Pyrazoloadenine is a potent inhibitor of the RET (REarranged during Transfection) lung cancer oncoprotein, demonstrating anticancer activity. It is intended for research use only and not for sale to patients.
- Potent RET lung cancer oncoprotein inhibitor.
- Shows anticancer activity.
- Inhibits a wide range of protein kinases, including BTK, CDK1/2, Src kinase, and RIPK1.
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Medchemexpress LLC Pitavastatin impurity 12 | 185105-98-0 | 366.39 | 25 G
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Pitavastatin impurity 12 is an impurity of Pitavastatin. It is a solid, intended for research use only and not for patient administration.
- For research use only.
- Solid appearance.
- Store at room temperature for 3 years.
- Store in solvent at -80°C for 2 years or -20°C for 1 year.
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Medchemexpress LLC AR antagonist 1 | 1818885-54-9 | 99.0% | 1 ML
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AR antagonist 1 is a potent androgen receptor (AR) antagonist. This compound serves as a ligand for the target E3 ligase complex, demonstrating micromolar binding affinity. It is suitable for the design of highly potent and efficient PROTAC degraders, which utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Potent androgen receptor (AR) antagonist.
- Functions as a ligand for the E3 ligase complex.
- Exhibits micromolar binding affinity.
- Used in the synthesis of PROTACs.
- Enables the design of highly potent and efficient PROTAC degraders.
- Utilizes the ubiquitin-proteasome system for selective protein degradation.
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Medchemexpress LLC AZD-8835 | 1620576-64-8 | 98.6% | 100 MG
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AZD-8835 is a potent and selective inhibitor of PI3Kα and PI3Kδ, with IC50s of 6.2 nM and 5.7 nM, respectively. It also potently inhibits commonly occurring PI3Kα mutants. This compound is intended for research use only and not sold to patients.
- Potent mixed inhibitor of PI3Kα and PI3Kδ
- Selective against PI3Kβ and PI3Kγ
- Inhibits commonly occurring PI3Kα mutants
- Exhibits good solubility and permeability
- Low in vivo clearance and high bioavailability in rats and dogs
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Medchemexpress LLC Raxatrigine (hydrochloride) | 934240-31-0 | 99.1% | 100 MG
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Raxatrigine hydrochloride, also known as Vixotrigine hydrochloride or GSK-1014802 hydrochloride, is a novel small molecule state-dependent sodium channel blocker and a Nav1.7 sodium channel inhibitor. It is intended for research use only and received orphan-drug designation from the US Food and Drug Administration in July 2013.
- Novel small molecule state-dependent sodium channel blocker
- Nav1.7 sodium channel inhibitor
- Received orphan-drug designation from US FDA
- Potential in the treatment of cognitive symptoms of schizophrenia
- Not sold to patients; for research use only
- Purity of 99.1%
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Medchemexpress LLC Maprotiline (hydrochloride) | 10347-81-6 | 99.9% | 500 MG
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Maprotiline hydrochloride is a highly selective noradrenergic reuptake inhibitor with strong antidepressant, antitumor, and neuropathic pain-relieving effects, exhibiting oral activity. This compound induces cancer cell apoptosis by targeting the ERK signaling pathway and CRABP1.
- Induces cell apoptosis and inhibits cell viability in a dose- and time-dependent manner.
- Inhibits metastasis and restrains migration of liver cancer cells.
- Affects the ERK pathway and inhibits SREBP2 phosphorylation.
- Targets CRABP1 and regulates cholesterol biosynthesis.
- Effectively reduces neuropathic pain in mice.
- Inhibits liver cancer tumor growth in vivo.
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Medchemexpress LLC Oxacillin sodium monohydrate | 7240-38-2 | 99.6% | 1 ML
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Oxacillin sodium monohydrate is an antibiotic used in the study of resistant staphylococci infections, similar to Flucloxacillin.
- Purity of 99.62%
- Molecular weight of 441.43
- Chemical formula C19H20N3NaO6S
- Appearance as a white to off-white solid
- Soluble in H2O (≥ 100 mg/mL) and DMSO (50 mg/mL)
- Storage at 4°C for solid, and -80°C (6 months) or -20°C (1 month) in solvent under sealed, moisture-free conditions
- Can be prepared using various in vivo dissolution protocols
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