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Filtered Search Results
Medchemexpress LLC HY-12037A 5mg Medchemexpress, Rigosertib CAS:592542-59-1 Purity:>98%
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Medchemexpress, HY-12037A 5mg Rigosertib CAS:592542-59-1 Rigosertib (ON-01910) is a multi-kinase inhibitor and a selective anti-cancer agent, which induces apoptosis by inhibition the PI3 kinase/Akt pathway, promots the phosphorylation of histone H2AX and induces G2/M arrest in cell cycle[2]. Rigosertib is a selective and non-ATP-competitive inhibitor of PLK1 with an IC50 of 9 nM[3]. 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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Anatrace D310-CH210 - 10:1 DDM/CHS Pre-Made Solution, 1ml
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Dodecyl Maltoside (D310) and Cholesteryl Hemisuccinate (CH210) Solution • DDM/CHS Solution • Dodecyl-β-D-Maltoside (100 mg/ml):CHS-TRIS (10 mg/ml) Solution
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Apexbio Technology LLC Diethylmaleate 141-05-9 100mg
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Diethylmaleate (141-05-9) is a small-molecule compound that depletes intracellular glutathione (GSH) modulating cellular redox-sensitive pathways Diethylmaleate exerts its biological activity primarily through induction of oxidative stress and ROS generation leading to modulation of cell cycle apoptosis gene expression and activation of MAPK signaling pathways In vitro studies demonstrate that Diethylmaleate-mediated GSH depletion triggers cell cycle arrest and apoptosis Animal research shows effects on reproductive systems including altered testicular antioxidant status and sperm parameters Based on these pharmacological properties Diethylmaleate holds research potential in studies of oxidative stress redox regulation and toxicology
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Medchemexpress LLC 4-Phenoxybenzylamine | 107622-80-0 | 98.45% | 199.25 | 50 MG
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4-Phenoxybenzylamine inhibits the function of the NS3 protein by stabilizing an inactive conformation. This action targets a highly conserved novel binding site located at the interface between the protease and helicase domains of the Hepatitis C Virus (HCV) NS3 protein, representing a new class of direct acting antiviral agents.
- Inhibits NS3 protein function
- Stabilizes inactive conformation of NS3 protein
- Targets highly conserved novel binding site
- Acts as a direct acting antiviral agent
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eMolecules Medchem Express / HLY78 / 5mg / 482204238 / HY-122816 / / 854847-61-3 / MFCD26961120 / 267.328 / C17H17NO2
Medchem Express / HLY78 / 5mg / 482204238 / HY-122816 / / 854847-61-3 / MFCD26961120 / 267.328 / C17H17NO2
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000380327 R -VERAPAMIL HYDRO 50MG
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eMolecules AstaTech / 4-TERT-BUTOXYANILINE / 0.25g / 721956548 / AB10504 / 95.000 / 57120-36-2 / MFCD11196184 / 165.236 / C10H15NO
AstaTech / 4-TERT-BUTOXYANILINE / 0.25g / 721956548 / AB10504 / 95.000 / 57120-36-2 / MFCD11196184 / 165.236 / C10H15NO
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Medchemexpress LLC RVX-297 25mg | 1044871-04-6 | 25 MG
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RVX-297 is a BD2-selective BET bromodomain inhibitor supplied for laboratory research. It is a small-molecule compound characterized for activity against BET family bromodomains and is used in preclinical studies of inflammation and autoimmune disease.
- Selective BD2 bromodomain inhibition for research applications.
- Chemical formula C24H29N3O4 and molecular weight 423.50 g/mol.
- Supplied as a dry powder with ≥95% purity.
- Available in small-scale vials suitable for laboratory experiments.
- Recommended cold storage to preserve stability (powder and solution guidelines).
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MEDCHEMEXPRESS LLC AZD9567 5MG
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501872563 AZD9567 5MG
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MEDCHEMEXPRESS LLC AUT1 5MG
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501872552 AUT1 5MG
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MEDCHEMEXPRESS LLC ZK824859 HYDROCHLORIDE 5MG
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501872518 ZK824859 HYDROCHLORIDE 5MG
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Apexbio Technology LLC 9-AC 723-62-6 100mg
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9-AC (CAS 723-62-6) also known as anthracene-9-carboxylic acid is an anthracene derivative commonly utilized as an inhibitor of Ca -activated Cl channels (CaCCs) It selectively blocks Ca -dependent chloride conductance in various cell types including smooth muscle epithelial and salivary gland cells By modulating ion channel activity 9-AC serves as a valuable tool for investigating cellular electrophysiological processes signal transduction pathways and ion channel pharmacology Its inhibitory action on CaCCs enables studies of cell excitability regulation and chloride transport in both physiological and pathological contexts
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![eMolecules Medchem Express / TFMB-(S)-2-HG / 5mg / 719836548 / HY-129079A / / 1445703-64-9 / [null] / 288.222 / C13H11F3O4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502452903.PNG-250.jpg)
eMolecules Medchem Express / TFMB-(S)-2-HG / 5mg / 719836548 / HY-129079A / / 1445703-64-9 / [null] / 288.222 / C13H11F3O4
Medchem Express / TFMB-(S)-2-HG / 5mg / 719836548 / HY-129079A / / 1445703-64-9 / [null] / 288.222 / C13H11F3O4
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eMolecules Medchem Express / AM-92016 (hydrochloride) / 5mg / 482203787 / HY-101253 / / 133229-11-5 / MFCD00673947 / 483.830 / C19H25Cl3N2O4S
Medchem Express / AM-92016 (hydrochloride) / 5mg / 482203787 / HY-101253 / / 133229-11-5 / MFCD00673947 / 483.830 / C19H25Cl3N2O4S
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Medchemexpress LLC HY-101203A 5mg Medchemexpress, GJ103 (sodium salt) CAS:1459687-96-7 Purity:>98%
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Medchemexpress, HY-101203A 5mg GJ103 (sodium salt) CAS:1459687-96-7 GJ103 sodium salt is an active analog of the read-through compound GJ072. 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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