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Filtered Search Results
eMolecules BISNEOPENTYLGLYCOLATO D 100G
5000192053 BISNEOPENTYLGLYCOLATO D 100G
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Aobchem AOBCHEM
5000973287 4-BROMO-2 5-DIFLUORO-N N-DIMET
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Sigma Aldrich Fine Chemicals Biosciences SKI II >=98% (HPLC), solid | 312636-16-1 | MFCD00733553 | 10MG
SKI II >=98% (HPLC), solid | Purity: >=98% (HPLC) | Mol Wt: 302.78 | 312636-16-1 | MFCD00733553 | 10MG
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Sigma Aldrich Fine Chemicals Biosciences SKI II >=98% (HPLC), solid | 312636-16-1 | MFCD00733553 | 50MG
SKI II >=98% (HPLC), solid | Purity: >=98% (HPLC) | Mol Wt: 302.78 | 312636-16-1 | MFCD00733553 | 50MG
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Medchemexpress LLC HY-112149 10mg Medchemexpress, ZL0420 CAS:2230496-80-5 Purity:>98%
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Medchemexpress, HY-112149 10mg ZL0420 CAS:2230496-80-5 ZL0420 is a potent and selective bromodomain-containing protein 4 (BRD4) inhibitor with IC50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Ethylenediaminetetraacetic acid sodium hydrate | 85715-60-2 | MFCD00013305 | 97.0% | 376.20 g/mol | C10H13N2Na3O8 · xH2O | 50 G
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EDTA hydrate sodium is the trisodium salt hydrate form of ethylenediaminetetraacetic acid used as a chelating agent and biochemical reagent in life-science research. Supplied as a white to off-white solid with ~97.0% purity and a molecular weight of 376.20 g/mol, it is commonly used to sequester metal ions, stabilize formulations, and buffer solutions in laboratory applications.
- Chelates divalent and trivalent metal ions to prevent metal-catalyzed reactions.
- Stabilizes enzyme preparations and biochemical assays by binding trace metals.
- Acts as a buffer component in solution preparation and pH control.
- High-purity solid, easy to weigh and dissolve for reproducible results.
- Available in common laboratory pack sizes for convenient use.
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Medchemexpress LLC Scopine hydrochloride | 85700-55-6 | 99.7% | 100 MG
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Scopine hydrochloride is a metabolite of Scopolamine and a brain-targeting compound. It significantly increases the brain exposure of Chlorambucil and enhances its anti-glioma activity. This compound can be used in targeted therapy research for brain gliomas.
- Metabolite of scopolamine
- Brain-targeting compound
- Increases brain exposure of chlorambucil
- Enhances anti-glioma activity
- Suitable for targeted therapy research for brain gliomas
- Molecular weight: 191.66
- Formula: C8H14ClNO2
- Appearance: solid, white to off-white
- For research use only
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Chemscene ChemScene | 2,3-Diaminophenol | 10G | CS-W005863 | 0.97 | 59649-56-8| MFCD00075199 | 124.14
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ChemScene | 2,3-Diaminophenol | 10G | CS-W005863 | 0.97 | 59649-56-8| MFCD00075199 | 124.14
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Medchemexpress LLC MK-8033 hydrochloride | 1283000-43-0 | MFCD18633221 | ≥98.0% | C24H22Cl2N6O | 10MG
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MK-8033 hydrochloride is a small-molecule, ATP-competitive dual inhibitor of c-Met and Ron kinases supplied as the hydrochloride salt for research use. It has been used in oncology research and was evaluated in early clinical trials; supplier listings report high purity and analytical characterization for laboratory applications.
- Potent dual c-Met and Ron kinase inhibitor
- Hydrochloride salt form
- Purity ≥98.0%
- Characterized by molecular formula and molecular weight
- Intended for research use in oncology studies
- Documented in early-phase clinical investigations
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000760649 MYRISTAMIDOPROPYL DI 10MM/1ML
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000758215 DECANEDIOIC ACID DI 25G
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Medchemexpress LLC HY-117288A 5mg Medchemexpress, S55746 (hydrochloride) CAS:1448525-91-4 Purity:>98%
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Medchemexpress, HY-117288A 5mg S55746 (hydrochloride) CAS:1448525-91-4 S55746 hydrochloride (BCL201 hydrochloride) is a potent, orally active and selective BCL-2 inhibitor, with a Ki of 1.3 nM and a Kd of 3.9 nM. S55746 hydrochloride (BCL201 hydrochloride) has antitumor activity with low toxicity. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC UNC9994 hydrochloride | 2108826-33-9 | 99.5% | 457.84 | 10 MG
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UNC9994 hydrochloride is a functionally selective, β-arrestin-biased dopamine D2 receptor (D2R) agonist. It selectively activates β-arrestin recruitment and signaling, demonstrating antipsychotic-like activity. It also acts as an antagonist of Gi-regulated cAMP production and a partial agonist for D2R/β-arrestin-2 interactions.
- Selectively activates β-arrestin recruitment and signaling.
- Antagonist of Gi-regulated cAMP production.
- Partial agonist for D2R/β-arrestin-2 interactions.
- Shows antipsychotic-like activity.
- Induces D2-mediated β-arrestin-2 translocation with EC50s of 6.1 nM and 448 nM.
- Acts as an antagonist at 5HT2A and 5HT2B receptors.
- Acts as an agonist at 5HT2C and 5HT1A receptors.
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Medchemexpress LLC Sotalol hydrochloride | 959-24-0 | 99.9% | 500 MG
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Sotalol hydrochloride is an orally active, non-selective β-adrenergic receptor blocker. It is a potent antiarrhythmic agent used for the research of pediatric arrhythmias. This compound blocks β-receptors and potassium KCNH2 channels, and acts as an antiepileptic agent.
- Orally active
- Non-selective β-adrenergic receptor blocker
- Potent antiarrhythmic agent
- Used for the research of pediatric arrhythmias
- Blocks β-receptors
- Blocks potassium KCNH2 channels
- Acts as an antiepileptic agent
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Apexbio Technology LLC Clemizole hydrochloride 1163-36-6 10mM (in 1mL DMSO)
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Clemizole hydrochloride is a histamine H1 receptor antagonist reported to inhibit hepatitis C virus (HCV) replication by targeting the viral NS4B protein a component essential for viral RNA replication Clemizole demonstrates antiviral activity in vitro against HCV genotype 2a subgenomic replicons exhibiting an IC50 value around 8 mM When combined with HCV protease inhibitors (such as VX950 or SCH503034) clemizole displays synergistic antiviral effects In contrast additive antiviral effects occur in combination with interferon ribavirin or polymerase inhibitors Clemizole is utilized in research contexts aimed at evaluating its efficacy potential antiviral combinations metabolism pathways and pharmacokinetics relevant to its consideration as a therapeutic candidate for HCV infection
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