Glycosyl compounds
Sigma Aldrich Fine Chemicals Biosciences Amygdalin from apricot kernels, >=99% | 29883-15-6 | MFCD00006598 | 1G
Amygdalin from apricot kernels, >=99% | Purity: >=99% | Mol Wt: 457.43 | 29883-15-6 | MFCD00006598 | 1G
Sigma Aldrich Fine Chemicals Biosciences Sucrose anhydrous, free-flowing, Redi-Dri(TM), ACS reagent | 57-50-1 | MFCD00006626 | 500G
Sucrose anhydrous, free-flowing, Redi-Dri(TM), ACS reagent | Mol Wt: 342.3 | 57-50-1 | MFCD00006626 | 500G
Sigma Aldrich Fine Chemicals Biosciences Sucrose octaacetate >=97%, FG | 126-14-7 | MFCD00006623 | 25KG
Sucrose octaacetate >=97%, FG | Purity: >=97% | Mol Wt: 678.59 | 126-14-7 | MFCD00006623 | 25KG
Medchemexpress LLC (2R)-2-hydroxy-2-methyl-4-(2,4,5-trimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)butanamide | 1147883-03-1 | MFCD00824427 | 99.3% | 265.30 g/mol | C14H19NO4 | 100MG
EPI-589 is a redox-active, quinone-derived neuroprotective small molecule (CAS 1147883-03-1) used in preclinical research to study neurodegenerative disorders. It functions as an oxidoreductase inhibitor and free-radical scavenger, demonstrates blood-brain barrier penetration and oral activity, and is supplied as a high-purity research reagent.
- High purity suitable for research (99.34%).
- Molecular formula C14H19NO4.
- Molecular weight 265.30 g/mol.
- Soluble in DMSO.
- Available in small research quantities, including 100 mg.
- Used in neuroprotection and motor neuron disease models.
Sigma Aldrich Fine Chemicals Biosciences Amyloid beta Protein fragm1MG
Amyloid Protein fragment 1-40 (A40) is derived from the amyloid- protein (A) which is mapped to human chromosome 21q21.3. A40 is predominantly present in the vascular amyloid deposits. A40 comprises of C-terminal membrane insertion domain. It shows structural transition from random coil to a helical structure in a water-micelle medium.
Cell Signaling Technology Estrogen Receptor beta (E2K7F) Rabbit mAb 20 ul
Estrogen Receptor beta (E2K7F) Rabbit mAb 20 ul
Medchemexpress LLC Norbinaltorphimine dihydrochloride | 113158-34-2 | MFCD00069374 | >98.0% | 734.71 g/mol | C40H45Cl2N3O6 | 1 ML
Norbinaltorphimine dihydrochloride is a selective κ-opioid receptor antagonist used in pharmacology research to probe kappa opioid receptor function. The dihydrochloride salt has CAS 113158-34-2 and a molecular weight of 734.71 g/mol; it is typically supplied at high purity for in vitro studies and is available as a ready-to-use 10 mM solution in DMSO.
- Selective kappa-opioid receptor antagonist for receptor pharmacology studies.
- Supplied as a dihydrochloride salt for improved solubility.
- High purity suitable for in vitro assays.
- Available as ready-to-use solution (10 mM) to simplify dosing.
- Store sealed, protect from moisture, and keep solution aliquots frozen.
Medchemexpress LLC 2-(5-Phenyl-4-(pyridin-4-yl)-1H-1,2,3-triazol-1-yl)-N-(5-phenylpyridin-2-yl)acetamide | 2074607-48-8 | 99.8% | 432.48 g·mol⁻1 | C26H20N6O | 25 MG
A potent small-molecule Porcn inhibitor for research use that blocks Wnt protein secretion and downstream signaling. It exhibits an EC50 of 80 pM in L-Wnt-STF cells and suppresses phosphorylation of Dvl2/3 and LRP6 in cell-based assays. Supplied as a high-purity solid or as a 10 mM solution in DMSO for experimental convenience.
- Potent Porcn inhibition with an EC50 of 80 pM in L-Wnt-STF cells.
- Blocks secretion of Wnt proteins and downstream signaling pathways.
- Suppresses phosphorylation of Dvl2/3 and LRP6 in cell-based assays.
- High purity (≈99.8%) suitable for biochemical and cellular studies.
- Available as solid quantities (including 25 mg) and as a 10 mM solution in DMSO.
- Recommended storage: solid at 4°C; in solvent at -80°C for long-term stability.
![Research Products International Corp [ONPG] 2-Nitrophenyl-B-D-Galactopyranoside, 5 Grams](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00006095-N81000-5.0.JPG-250.jpg)
Research Products International Corp [ONPG] 2-Nitrophenyl-B-D-Galactopyranoside, 5 Grams
Colorimetric and spectrophotometric substrate for detection of β-D-Galactosidase.
![Research Products International Corp X-GAL [5-Bromo-4-chloro-3-indolyl-B-D-galactoside], 10 Grams](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00006095-B71800-10.0.JPG-250.jpg)
Research Products International Corp X-GAL [5-Bromo-4-chloro-3-indolyl-B-D-galactoside], 10 Grams
Chromogenic substrate of β-Galactosidase used in combination with IPTG for detection of β-Galactosidase activity in bacterial colonies. X-GAL is cleaved at the B1-4 bond between galactose and the 5-Bromo-4-chloro-3-indolyl portion of X-GAL by β-Galactosidase via hydrolysis. The cleavage of X-GAL results in the production of a water insoluble blue dichloro-dibromo-indigo precipitate. In cloning strategies with vectors such as Lambda-11, M13mp18 and 19, pUC18 and 19, pUR222 the E. coli lacZ gene is transformed to lac+ cells. After transformation the cells show β-Galactosidase activity in the presence of media containing X-GAL and IPTG. The insertion of a DNA fragment into the cloning sites of the lacZ gene results in the disruption of β-Galactosidase activity leading to the appearance of white colonies. Non-recombinant cells produce a blue indigo dye.
Water Content: 0.05% (K. Fisher)
Protect from light and moisture
Medchemexpress LLC D-NMAPPD | 35922-06-6 | MFCD08062172 | 99.7% | 422.56 g/mol | C23H38N2O5 | 10MM 1ML
D-NMAPPD ((1R,2R)-B13) is a research-grade small molecule that inhibits acid ceramidase and modulates NMDA receptor function by increasing endogenous ceramide levels. It is supplied for in vitro pharmacological and cell biology studies, including apoptosis and anticancer research. Available as solution and solid formats for assay development.
- Acts as an acid ceramidase inhibitor.
- Modulates NMDA receptor properties by enhancing ceramide production.
- Available as 10 mM solution in DMSO and multiple solid sizes for flexible dosing.
- High purity (99.74% by HPLC).
- Molecular weight 422.56 g/mol; formula C23H38N2O5.
- Intended for in vitro research use only.
Cayman Chemical Derythro Lysosphingomyelin d
A bioactive sphingolipid; agonist of S1P1, S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors); agonist of ORG1 that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM); levels are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A