M_Products

5-Methoxy-DL-tryptophan is an derivative of tryptophan.

5-Methoxy-L-tryptophan is a tryptophan derivative.

5-Methoxyindole Ultra Pure is used to synthesize and analyze interactions between indole species. It displays dual agonist and inverse agonist activity at the 5-HT_3B receptor and partial agonism at the 5-HT_3A receptor.

5-Methoxyindole-3-acetic acid is an indole. 5-Methoxyindole-3-acetic acid itself has antibacterial properties, and can be used to enhance lipid peroxidation and can also function like an antioxidant. It has been used to synthesize Gli1 antitumor agents, inhibitors of NO production and selective COX-2 inhibitors.

5-Methyl-DL-tryptophan is an analog of tryptophan. It is an inhibitor of anthranilate compound synthesis. Additionally, 5-methyl-DL-tryptophan is used to select for genetic mutants of Methanococcus voltae. It is a repressor of the Trp operon and a tryptophanase substrate as well.

5-Methylindole-3-acetic acid is a reagent used in chemical synthesis. It has been used to prepare PKC inhibitors, VEGF-R inhibitors, antiangiogenic agents and protein kinase inhibitors.

5-Methylindole-3-carboxaldehyde is a reagent used in chemical synthesis. It has been used in the synthesis of carboline derivatives for the treatment of cancer, pyrimidines inhibiting h. pylori infections 5-ht2c agonists, and flexible tripodal ligands useful with metal complexes.

6-Methoxyindole reactant used in the synthesis of tryptophan dioxygenase inhibitors, antitumor agents, T cell kinase inhibitors, VEGFR-2 inhibitors, and HIV-1 inhibitors. Additionally, it is used to study protonated, excited-state forms of serotonin and inhibits myeloperoxidase.

6-Methyl-DL-tryptophan is an analog of tryptophan.

7-Methoxycoumarin, commonly referred to as Herniarin, is a methoxy derivative of coumarin and substrate for dealkylase. It has been used in the synthesis of anti-first-pass effect compounds and detergents. 7-Methoxycoumarin has been used in hepatic studies and antioxidant studies and when bound to bromomethyl at the 4 position it can be used as a fluorescent label for fatty acids.

7-Methoxyindole is a reagent used in the preparation of tryptophan dioxygenase inhibitors, indolylindazoles and indolylpyrazolopyridines, HIV-1 inhibitors, and histone deacetylase inhibitors. Additionally, it is used to study how methoxy and amino substitutions affect indole rings and has been shown to inhibit the growth of tobacco cells.

7-Methyl-DL-tryptophan is a tryptophan analog.

7-Methylindole is a reagent used in chemical synthesis. It has been used in the synthesis of HIV-1 inhibitors, plant growth inhibitors and antifungal agents.

7-Methylindole-2-carboxylic acid is a reagent used in chemical synthesis. It has been used to synthesize CCK1 receptor antagonists and Xa inhbiitors.

7-Methylindole-3-acetic acid is a reagent used in chemical synthesis. It can be used to synthesize alpha-amino-indole-3-acetic acids that are used as anti-diabetic, anti-obesity and anti-atherosclerotic agents.

8-Methoxypyrene-1,3,6-trisulfonic acid is used as a fluorescent marker or as a fluorescent probe for studying cationic surfactants.

FGF1 is a member of the Fibroblast Growth Factor family of proteins. Also called FGF-acidic or aFGF, FGF1 lacks signal peptides and is believed to be secreted by a nonclassical mechanism. It has been detected in large amounts in the brain and is expressed in hepatocyte cells, vascular smooth muscle cells, CNS neurons, skeletal muscle cells, fibroblasts, keratinocytes, endothelial cells, intestinal columnar epithelial cells and pituitary basophils and acidophils. FGF1 exhibits considerable species cross-reactivity and stimulates the proliferation of cells of mesodermal origin as well as many cells of neuroectodermal, ectodermal, and endodermal origin. It is most closely associated with FGF2 (bFGF) (see additional information).

FGF2 is a member of the Fibroblast Growth Factor family of proteins. It is often called FGF-basic or bFGF. FGF2 is a single-chain polypeptide growth factor that plays a significant role in wound healing, it is a potent inducer of angiogenesis and it is essential for the growth of many stem and progenitor cells. FGF2 shares a 55% amino acid residue identity with FGF1 and interacts with heparin sulfate with nanomolar affinity. It is a potent inducer of DNA synthesis in a variety of cell types. FGF2 activates mesenchymal splice variants of FGF receptors (c splice variants) and also activates FGF Receptor 1b, but has little activity against FGFR2b or FGFR3b. It is most closely associated with FGF1 (aFGF) (see additional information).

beta-D-Maltose octaacetate is a reagent used for chemical synthesis. It has been used in a binary mixture of beta-D-Maltose octaacetate and CO2 to create carbon dioxide-soluble polymers for petroleum engineering applications.