
Vitaminas
Foram encontrados 1115 produtos de "Vitaminas"
2-Chloro-5-nitro-N-4-phenylbenzamide
CAS:Produto ControladoApplications A cell-permeable, selective and irreversible PPARγ antagonist (IC50 = 3.3 nM, 32 nM, and 2 µM for PPARγ, PPARα, and PPARδ, respectively). Reported to covalently modify a cysteine residue in the binding site of PPAR. At a concentration of 10 µM, also acts as an agonist of human pregnane X receptor (PXR) and farnesoid X receptor (FXR). Does not activate liver X receptor-a (LXRa), retinoic acid receptor (RAR), retinoid X receptor-a (RXRa) and thyroid receptors a and b (TRa and TRb
References Huang, J.T., et al.: Nature, 400, 378 (1999), Wilson, T.M., et al.: J. Med. Chem., 43, 527 (2000), Leesnitzer, L.M., et al.: Biochemistry, 41, 6640 (2002)Fórmula:C13H9ClN2O3Cor e Forma:NeatPeso molecular:276.68Auraptene
CAS:Produto ControladoApplications Auraptene is a natural bioactive monoterpene coumarin ether. Auraptene has shown a remarkable effect in the prevention of degenerative diseases.
References Brunhofer, G., et al.: Bioorg. Med. Chem., 20, 669 (2012); Furukawa, Y., et al.: Int. J. Mole. Sci., 13, 5338 (2012);Fórmula:C19H22O3Cor e Forma:NeatPeso molecular:298.382-(Methyl-d3)-1,4-naphthalenedione (Vitamin K3-d3)
CAS:Produto ControladoApplications Isotope labelled d3; 1,4-Dihydro-1,4-dioxo-2-methylnaphthalene-d3; (Vitamin K3), precursor to various types of Vitamin K. Used as a micronutrient for livestock and pet foods.
References Sakamoto, S., et al.: Anal. Bioanal. Chem., 396, 2955 (2010), Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010), Hu, W., et al.: Anal. Biochem., 398, 245 (2010),Fórmula:C11H5D3O2Cor e Forma:NeatPeso molecular:175.2Menaquinone 4-d7 (Mixture of cis-trans isomers) (100ug/mL in Acetonitrile)
CAS:Produto ControladoFórmula:C31H33D7O2Cor e Forma:Yellow To Light YellowPeso molecular:451.69(20S)-Protopanaxatriol (~91% HPLC)
CAS:Produto ControladoApplications (20S)-Protopanaxatriol acts as an inhibitor in the production of corticosteroids in fasciculata cells. Used in the clinical treatment of heart diseases.
References Hasegawa, E. et al.: Life Sci., 92, 687 (2013); Wang, X. et al.: Pathobiol., 79, 285 (2012);Fórmula:C30H52O4Cor e Forma:NeatPeso molecular:476.732O1-(ABM-14 ether), O4-(Methylcarboxamide with AHPC) Butanediol
CAS:Produto ControladoFórmula:C53H56F3N7O7S2Cor e Forma:NeatPeso molecular:1024.18SR9243
CAS:Produto ControladoApplications SR9243 is used in new compounds targeting warburg effcts, killing cancer cells and inhibiting lipid production.
References Anon.: Cancer Discovery, 5, 898 (2015)Fórmula:C31H32BrNO4S2Cor e Forma:NeatPeso molecular:626.62Vitamin D3-d7 (Major)
CAS:Produto ControladoStability Light Sensitive, Temperature Sensitive
Applications The vitamin that mediates intestinal calcium absorbtion, bone calcium metabolism and probably, muscle activity. Occurs in and is isolated from fish liver oils. Vitamin D acts through a receptor that is a member of the ligand-dependent transcription factor superfamily. Modulates the proliferation and differentiation of both normal and cancer cells. Has antiproliferative and antimetastatic effects on breast, colon, and prostate cancer cells. Activated vitamin D receptors in intestine and bone maintain calcium absorbance and homeostasis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Haussler, R., et al.: J. Biol. Chem., 247, 2328 (1972), Holick, M.F., Rec. Res. Canc. Res., 164, 3 (2003), Palmer, H.G., et al.: Cancer Res., 63, 7799 (2003), Welsh, J., et al.: J. Nutr., 133, 2425S (2003),Fórmula:C27D7H37OCor e Forma:ColourlessPeso molecular:391.68S-(1-Pentyl-5-biotinylamido)glutathione
Produto ControladoFórmula:C25H42N6O8S2Cor e Forma:NeatPeso molecular:618.77Vitamin D3 Sulfate Sodium Salt
CAS:Produto ControladoApplications The main metabolite of Vitamin D3. It has potent biological activity. Vitamin D3-sulfate had <5% of the activity of vitamin D3 to mobilize Ca from bone and .apprx.1% of the ability of Vitamin D3 to stimulate Ca transport, elevate serum P, or support bone calcification.
References Bell, P.A., et al.: Biochem. J., et al.: 115, 663 (1969), Kumar, R.S., et al.: J. Clin. Invest., 65, 277 (1980), Reeve, L.E. , et al.: J. Biol. Chem., 256, 823 (1981), Armas, L., et al.: J. Clin. Endocrinol. Metab., 89, 5387 (2004),Fórmula:C27H43O4S·NaCor e Forma:NeatPeso molecular:486.68
