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MYF-01-37 is a small-molecule covalent inhibitor of TEAD that targets cysteine 380 and produces reversible inhibition of the YAP-TEAD protein-protein interaction. It is characterized for research use with defined molecular properties and high analytical purity.
Targets cysteine 380 on TEAD, enabling covalent engagement.
Inhibits YAP-TEAD interaction relevant to Hippo/Wnt signaling pathways.
High purity for reproducible experimental results.
Available as solid and as DMSO solution for flexible assay setup.
Intended for research use only; not for clinical or diagnostic use.
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2'-TOM MeC(Ac) amidite is a Amidite reagent (Subcategory: 2'-OH Series) sold by WuXi TIDES. Offered in 5 g. Store at -20 °C. Ships on dry ice. SDS available for reference.
Specifications - CAS: 872548-65-7 - MDL: No data - InChIKey: OBHVHGNMPRNNPM-RNGKMJNNSA-N - Molecular Weight: 988.247761998 - Molecular Formula: C52H74N5O10PSi - Purity: ≥95% - Container Type: 250 mL Glass (28-400) - Pack Size: 5 g - Net Weight: 5 g - Gross Weight: 174.7 g - Commodity Code: 29349990 - Country Of Origin: China - IUPAC: (2R,3R,4R,5R)-5-(4-acetamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-(((triisopropylsilyl)oxy)methoxy)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite - SMILES: CC(N(P(O[C@@H]1[C@H](O[C@@H](N2C=C(C(NC(C)=O)=NC2=O)C)[C@@H]1OCO[Si](C(C)C)(C(C)C)C(C)C)COC(C3=CC=C(C=C3)OC)(C4=CC=C(C=C4)OC)C5=CC=CC=C5)OCCC#N)C(C)C)C
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Deslanoside is a cardiac glycoside (desacetyllanatoside C) used as a research reagent for studies of cardiac function, ion transport, and Na+/K+-ATPase inhibition. It is supplied as a high-purity solid and is also available as a DMSO solution for biochemical assays.
Cardiac glycoside for research use.
High purity (99.79%).
Molecular weight 943.08 g/mol.
Chemical formula C47H74O19.
CAS number 17598-65-1.
Available as 10 MG solid and 10 mM in DMSO solution.
Suitable for biochemical and pharmacological studies of arrhythmia mechanisms and ion transport.
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MT 63-78 is a small-molecule research compound that functions as a direct activator of AMP-activated protein kinase (AMPK) and inhibits mTORC1 signaling. It induces mitotic arrest and apoptosis, and has reported antitumor effects, including blocking prostate cancer growth via suppression of lipogenesis and mTORC1 pathways.
Direct AMPK activator with reported EC50 25 μM
Induces mitotic arrest and apoptosis in cellular assays
Reported antitumor activity, including inhibition of prostate cancer growth
Molecular weight 326.35 g/mol; formula C21H14N2O2
Purity 98.0%
Available in 1 mg, 5 mg, 10 mg, 50 mg, 100 mg packs; store protected from light at 4°C (in solvent: -80°C for 6 months, -20°C for 1 month)
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More