Vitamine

Stability Light and Temperature Sensitive
Applications 9-cis-13,14-Dihydroretinoic Acid, is a derivative of Retinal (R240000), corotenoid component of the visual pigments.
References Ball, et al.: Biochem. J., 42, 516 (1948), O’Brien, D.F., et al.: Science, 218, 961 (1982),

Applications MRL-871 is a novel RORγt inhibitor, binding to a previously unidentified allosteric pocket in the RORγt LBD.
References Scheepstra, Marcel., et al.:Nat. Commun., 6, 8833/1 (2015); Fauber, Benjamin P., et al.: Bioorganic Med. Chem. Lett., 25, 2907 (2015);

Applications (24S)-24,25-Epoxycholesterol is a derivative of 4β-Hydroxy Cholesterol (H917980), a metabolite of Cholesterol. It is formed from Cholesterol by the drug-metabolizing enzyme cytochrome P 450 3A4. A potential ligand for the nuclear receptor LXR and also a new endogenous CYP3A marker.
References Breuer, O., et al.: J. Lipid Res., 36, 2275 (1995), Pikuleva, I., et al.: J. Biol. Chem., 273, 18153 (1998), Chawla, A., et al.: Science, 294, 1866 (2001), Bodin, K., et al.: J. Biol. Chem., 276, 38685 (2001),

Stability Light Sensitive
Applications CDDO Imidozolide (CDDO-Im) is a synthetic triterpenoid CDDO-Im inhibits fatty acid synthase expression and has antiproliferative and proapoptotic effects in human liposarcoma cells. Studies show that CDDO-Im is highly active in suppressing cellular proliferation of human leukemia and breast cancer cell lines as well as being an effective therapeutic agent in the treatment of other types of cancers.
References Hughes, D.T. et al.: Cancer Invest., 26, 118 (2008); Place, A.E. et al.: Clin. Cancer Res., 9, 2798 (2003); Samudio, I. et al.: J. Biol. Chem., 280, 36273 (2005);

Applications HX 531 is a novel RXR antagonist used to enhance transactivation of PPARγ and ST 13 preadipocyte differentiation. Helps in the reduction of triglyceride content in white adipose tissue, skeletal muscle and liver.
References Yamauchi, T. et al.: J. Clin. Invest., 108, 1001 (2001);

Applications AC 55649 is a potent and selective RARβ2 receptor agonist (1). RARβ2 receptor agonists are potential drug candidates for developing treatment for type 2 diabetes and hepatic steatosis (2).
References (1) Lund, B. W., et al.: J Med Chem. 48, 7517 (2005) (2) Trasino, S. E., et al.: Diabetes Obes Metab. 18, 142 (2016)

Applications 1-O-Hexadecyl-sn-glycerol restores plasmalogen levels in Chinese hamster ovary (CHO) cells and human pulmonary arterial endothelial cells (PAEC). Plasmalogen may play a role in protecting animal cells against photosensitized killing.
References Zoeller, R., et al.: J. Biol. Chem., 263, 11590 (1988); Zoeller, R., et al.: Am. J. Physiol., 283, H671 (2002)

Stability Light Sensitive, Temperature Sensitive
Applications Used as a treatment for severe acne. Presently being studied in conjuction with the treatment of photoaged skin.
References Lerche, C., et al.: Exp. Dermatol., 17, 972 (2008), Sato, T., et al.: J. Med. Chem., 51, 7705 (2008), Gan, J., et al.: Chem. Res. Toxicol., 22, 690 (2009), Macejova, D., et al.: Toxicol. Lett., 184, 114 (2009), Chen, P., et al.: Toxicol. App. Pharmacol., 234, 143 (2009),

Applications 2-Phospho-L-ascorbic Acid Trisodium Salt is a long-lasting vitamin C derivative used in studies of gene repression. Maximizes the benefical properties of vitamins C for personal care and a main active ingredient in medicated cosmetics for whitening. Also, it is substrate in the chromoamperometric method to detect tungsten in water.
References Fuchihata, M.: Frag. J., 43, 64-68 (2015); Alvarado-Gamez, A. L., et al.: Sens., 15, 2232-2243 (2015);

Applications Α hydroxylated metabolite of Vitamin D2 (V676040); a synthetic analog of Vitamin D.
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 Matsuoka, M. et al.: J. Nutrit. Sci. Vitaminol., 35, 253 (1989); Jones, G. et al.: Arch. Biochem. Biophys., 202, 450 (1980); Goff, J. et al.: J. Nutrit., 112, 1387 (1982);

Stability Temperature and Light Sensitive
Applications 3-Aminopropyl-24,25-dihydroxy Vitamin D3 is a derivative of Vitamin D3 (V676045), an important factor in maintaining bone health, and has also been associated with cardiovascular health in humans.
References Dawson-Hughes, B., et al.: 16, 713 (2005); Lee, J., et al: J. Am. Coll. Cardio., 52, 1949 (2008)

Applications 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)

Applications SR 1078 is a selective agonist of RORα and RORγ that stimulates ROR transcriptional activity in HEK293 cell reporter assays.
References Wang, Y., et al.: ACS Chem. Biol., 5, 1029 (2010); Wang, Y., et al.: PLoS One, 7, 1 (2012)

Applications SC-58236 is a highly selective and potent cyclooxygenase-2 inhibitor which has been shown to induce apoptosis in gastric cells via down-regulation of Akt and then release of cytochrome c. Its anti-inflammatory effects allows for potential use in therapy for inflammatory allergic diseases.
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 Fan, X.M. et al.: Digestion, 2, 75 (2006); Kim, S. et al.: Life Sci., 81, 863 (2007); Kim, S. et al.: J. Pharmacol. Exp. Therap., 313, 27 (2005);

Applications 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),

Stability Light Sensitive, Temperature Sensitive
Applications The epimer metabolite of Calcifediol or 25-hydroxyvitamin D3 (C125700).
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 Sakaki, T., et al.: Eur. J. Biochem., 267, 6158 (2000), Kamao, M., et al.: J. Biol. Chem., 278, 1463 (2003),

Applications 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);

Applications Antagonizes Wnt/β-catenin/Tcf-mediated transcription as well as PPARγ and δ activity. Able to inhibit the recruitment of the co-activators β-catenin and GRIP1, both of which are activators for both pathways.
References Handeli, S., et al.: Mol. Cancer Ther., 7, 521 (2008),

Applications Vitamin D3 (V676045) analog.
References Roy, A., et al.: Steroids, 60, 530 (1995);

Applications 17beta-Estradiol-16,16-d2 (CAS# 3188-46-3) is a useful isotopically labeled research compound.

Applications GW3965 Hydrochloride, is a potent, selective liver X receptor (LXR) agonist for hLXRα and hLXR. GW3965 has shown potent anti-inflammatory activity in both irritant and allergic contact models of dermatitis, requiring the participation of both LXRα and LXRβ.
References Fowler, A.J., et. al.: J. Invest. Dermatol., 120, 246 (2003)

Stability Hygroscopic! Store Under Inert Atmosphere.
Applications An active Biotinylation reagent.
References Giubellino, A., et al.: J. Med. Chem., 51, 7459 (2008), Wang, Z., et al.: Nat. Chem. Biol., 4, 557 (2008),

Applications (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);

Applications The active labelled metabolite of Vitamin D2 (V676040).
References Lam, H., et al.: Science, 186, 1038 (1974), Dilworth, F., et al.: J. Biol. Chem., 270, 16766 (1995), Horst, R., et al.: Biochem. Pharmacol. 60, 701 (2000), Horst, R., et al.: J. Cell Biochem., 88, 282 (2003),

Applications SR 8278 is a synthetic antagonist of the nuclear heme receptor REV-ERB.
References Kojetin, D., et al.: ACS. Chem. Biol., 6, 131 (2011);

alpha-Tocotrienol is a chemical compound known as a vitamin E isoform, which is derived primarily from certain plant oils, such as palm oil, rice bran oil, and annatto. This compound exhibits a unique unsaturated side chain, distinguishing it from tocopherols and enabling it to integrate into cellular membranes with greater efficiency.

Riboflavin-2,4,4α,10α-13C4-1,3-15N2 is a stable isotope-labeled form of riboflavin, which is a type of vitamin B2 molecule. This compound is synthesized with carbon-13 and nitrogen-15 isotopes, providing a distinct mass that enables precise tracking in metabolic studies. The source of this compound is derived from isotopically enriched materials, employing advanced chemical synthesis processes to incorporate stable isotopes into the riboflavin structure without altering its fundamental biochemical properties.

Beta-Tocotrienol is a biochemical compound that belongs to the vitamin E family. It is derived from sources such as palm oil, rice bran, and certain cereal grains. This compound exhibits its mode of action through the modulation of oxidative stress pathways and inhibition of certain enzymes involved in cell proliferation and cholesterol synthesis, which differentiates it from other tocopherols.

Vitamin D3 is a fat-soluble vitamin that can be obtained from some fish, mushrooms, and dairy products. The most common form of the vitamin is cholecalciferol (vitamin D3) which can be converted in the liver to calcidiol (25-hydroxycholecalciferol) and in the kidneys to calcitriol (1,25-dihydroxycholecalciferol). Vitamin D3 has been shown to have a positive effect on calcium absorption and bone mineralization. It also has important physiological functions such as regulation of cell growth and differentiation. The solubility of vitamin D3 is dependent on the presence of a hydroxy group at position 3' or 25'. This liquid chromatography method uses an experimental solubility data set for the determination of solubility data for compounds with a hydroxy group at position 3'.