Hydrocarbons
Cayman Chemical 3-oxo StearIc AcId 1mg
An intermediate in the dissociated (or type II) fatty acid biosynthesis that occurs in bacteria; generated following the reaction of hexadecenoyl-ACP with malonyl-ACP by the enzyme β-ketoacyl-ACP synthase II, which produces 3-oxo octadecenoyl-ACP
Sigma Aldrich Fine Chemicals Biosciences Beta-Caryophyllene | 87-44-5 | MFCD00075925 | 1 kg
Beta-Caryophyllene | Purity: ≥80% | Mol Wt: 204.35 | 87-44-5 | MFCD00075925 | 1 kg
Medchemexpress LLC MF-766 10mM 1mL | 1050656-06-8 | 478.46 | C27H21F3N2O3 | 1 ML
MF-766 is a potent, selective EP4 antagonist provided for preclinical research. It is supplied as a ready-to-use 10 mM solution in DMSO (1 mL) and as solid quantities for assay and in vivo studies.
- Supplied as 10 mM solution in DMSO, 1 mL.
- Also available as solids (5 mg-500 mg) for custom preparations.
- High purity suitable for research (99.83%).
- Molecular weight 478.46, formula C27H21F3N2O3.
- Recommended solvent for stocks: DMSO; in vivo vehicle example: 10% DMSO in corn oil.
Medchemexpress LLC Ovalbumin (154-159) | 1370698-94-4 | 99.9% | 672.77 | 1 MG
Ovalbumin (154-159) | 1370698-94-4 | 99.9% | 672.77 | 1 MG
Medchemexpress LLC ETC-159 | 1638250-96-0 | 99.1% | 391.38 | 1 ML
ETC-159 is a potent, orally available PORCN inhibitor that inhibits β-catenin reporter activity with an IC50 of 2.9 nM. It is intended for research use only.
- Inhibits β-catenin reporter activity
- Potent and orally available PORCN inhibitor
- Active in multiple cancer models with high Wnt signaling
- Efficacious in colorectal cancers with R-spondin translocations
- Good oral pharmacokinetics in mice with 100% oral bioavailability
![Aobchem 2-(4-Methoxy-3-tricyclo[3 3 1 13 7]dec-1-ylphenyl)-4 4 5 5-tetramethyl-1 3 2- | ≥95% | CAS 1036766-56-9 | C23H33BO3 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000925844.png-250.jpg)
Aobchem 2-(4-Methoxy-3-tricyclo[3 3 1 13 7]dec-1-ylphenyl)-4 4 5 5-tetramethyl-1 3 2- | ≥95% | CAS 1036766-56-9 | C23H33BO3 | 1g
2-(4-Methoxy-3-tricyclo[3 3 1 13 7]dec-1-ylphenyl)-4 4 5 5-tetramethyl-1 3 2- | ≥95% | CAS 1036766-56-9 | C23H33BO3 | 1g
Aobchem 1-(4-Methoxy-3-tricyclo[3 3 1 13 7]dec-1-ylphenyl)ethanone | 95% | CAS 142651-49-8 | C19H24O2 | 500mg
1-(4-Methoxy-3-tricyclo[3 3 1 13 7]dec-1-ylphenyl)ethanone | 95% | CAS 142651-49-8 | C19H24O2 | 500mg
Medchemexpress LLC N,N,N′,N′-Tetracyclohexyl-3-oxapentanediamide (Calcium ionophore II) | 74267-27-9 | 99.4% | 460.69 | 25 MG
N,N,N′,N′-Tetracyclohexyl-3-oxapentanediamide (Calcium ionophore II) is a lipophilic ionophore that can be used in preparing calcium ion-selective electrodes. Calcium ion-selective electrodes can be used to measure intracellular free calcium.
- Lipophilic ionophore
- Used in preparing calcium ion-selective electrodes
- Enables measurement of intracellular free calcium
- For research use only
Sigma Aldrich Fine Chemicals Biosciences Lycopene 98 HPLC from toma10MG
Lycopene is a carotenoid found in many red fruits and vegetables such as watermelon pink guava and tomato. Lycopene is a potent antioxidant. It is suggested that lycopene is used by the plant to protect against reactive oxygen species (ROS).
Medchemexpress LLC Bay 65-1942 hydrochloride | 600734-06-3 | 99.4% | C22H26ClN3O4 | 100 MG
Bay 65-1942 hydrochloride is an ATP-competitive and selective IKKβ inhibitor. This compound is intended for research use only. In vitro studies show that delivery of Bay 65-1942 prior to ischemia significantly decreases left ventricular infarct size. In vivo, it demonstrates synergistic inhibition of cell viability and induces caspase 3/7 activation when combined with AZD6244 in MYL-R cells.
- Acts as an ATP-competitive and selective IKKβ inhibitor
- Decreases left ventricular infarct size in vitro
- Attenuates CK-MB levels in vivo
- Demonstrates synergistic inhibition of cell viability with AZD6244
- Induces caspase 3/7 activation with AZD6244
- Suitable for research applications
Medchemexpress LLC Butyne-DOTA-tris(t-butyl ester) | 2125661-54-1 | 98.5% | 623.82 g·mol⁻¹ | C32H57N5O7 | 100 MG
Butyne-DOTA-tris(t-butyl ester) is a DOTA-derived bifunctional chelator featuring an alkyne functional group and tert-butyl protected carboxylates. It is intended for conjugation to peptides and radionuclides in radiopharmaceutical and imaging probe synthesis; the protected ester form simplifies handling and allows controlled deprotection to the metal-chelating DOTA core.
- Bifunctional chelator for peptide and radionuclide conjugation.
- Alkyne handle enables click chemistry.
- Tert-butyl protected carboxylates allow controlled deprotection.
- High HPLC purity (98.5%).
- Available in research-scale quantities for probe synthesis.