
Esteróides
Os esteroides são uma classe de compostos orgânicos com uma estrutura molecular característica composta por quatro anéis fusionados. Eles desempenham um papel vital em vários processos biológicos, atuando como hormônios que regulam o metabolismo, a função imunológica e a reprodução. Os esteroides são amplamente utilizados na medicina por suas propriedades anti-inflamatórias, imunossupressoras e anabólicas. Na pesquisa, eles são estudados por seu potencial terapêutico no tratamento de condições como artrite, asma e desequilíbrios hormonais. Na CymitQuimica, você encontrará uma ampla seleção de esteroides, essenciais para pesquisa em farmacologia, bioquímica e desenvolvimento de terapias à base de esteroides.
Subcategorias de "Esteróides"
Foram encontrados 1702 produtos de "Esteróides"
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Digoxigenin Bisdigitoxoside
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications A metabolite of Digoxin (Dx) (D446575).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Fujii, Y., et al.: Clin. Chem., 37, 476 (1991), Salphati, L., et al.: Xenobiotica, 29, 171 (1999), Song, S., et al.: Drug Metab. Dispos., 27, 689 (1999),<br></p>Fórmula:C35H54O11Cor e Forma:NeatPeso molecular:650.806α-Hydroxy Norethindrone Acetate
CAS:Produto Controlado<p>Applications An oxidative product of the drug Norethindrone (N676000). Norethindrone impurity.<br>References Reif, V., et al.: Pharmaceutical Res., 4, 54 (1987), Rao, P., et al.: Steroids, 59, 621 (1994),<br></p>Fórmula:C22H28O4Cor e Forma:Off-WhitePeso molecular:356.46Betamethasone 21-Acetate 17-Propionate
CAS:<p>Impurity Betamethasone Dipropionate EP Impurity D<br>Applications Betamethasone 21-acetate-17-propionate (Betamethasone Dipropionate EP Impurity D) is a related compound of Betamethasone dipropionate (B327005).<br>References Grootveld, M., et al.: Biochem. Pharmacol., 37, 271 (1988), Chen, B., et al.: Steriods, 74, 30 (2009), Mikami, E., et al.: J. Pharm. Biomed. Anal., 28, 261 (2002),<br></p>Fórmula:C27H35FO7Cor e Forma:NeatPeso molecular:490.5616β-Hydroxy Progesterone (Contains up to 20% 17α-Hydroxy Progesterone)
CAS:Fórmula:C21H30O3Pureza:>80%Cor e Forma:NeatPeso molecular:330.46Finasteride Carboxylic Acid
CAS:Produto ControladoFórmula:C23H34N2O4Cor e Forma:Light Yellow SolidPeso molecular:402.536β-Hydroxy-21-desacetyl Deflazacort
CAS:<p>Applications The major metabolite of Deflazacort.<br>References Bernareggi, A., et al.: J. Pharma. Biomed. Anal., 5, 177-81 (1987), Assandri, A., et al.: Xenobiotica, 13(3), 185 (1983), Martinelli, E., et al.: Drug Metab. Dispos., 7, 335 (1979),<br></p>Fórmula:C23H29NO6Cor e Forma:NeatPeso molecular:415.48Daidzein 7-β-D-Glucuronide 4’-Sulfate Disodium Salt
CAS:<p>Stability Very Hygroscopic<br>Applications Mixed conjugate of dietary phytoestrogen.<br>References Adlercreutz, H;., et al.: J. Steroid Mol. Biol., 52, 97 (1995), Kinjo, J., et al.: Biol. Pharm. Bull., 27, 185 (2004),<br></p>Fórmula:C21H16Na2O13SCor e Forma:NeatPeso molecular:554.39Digoxigenin Monodigitoxoside
CAS:Produto Controlado<p>Applications A metabolite of Digoxin (Dx) (D446575).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Fujii, Y., et al.: Clin. Chem., 37, 476 (1991), Salphati, L., et al.: Xenobiotica, 29, 171 (1999), Song, S., et al.: Drug Metab. Dispos., 27, 689 (1999),<br></p>Fórmula:C29H44O8Cor e Forma:BeigePeso molecular:520.654a-Methyl-cholesterol
CAS:<p>Applications 4α-Methyl-cholest-5-en-3β-ol is a derivative of Cholesterol (C432501), a major component of all biological membranes; ~25% of total brain lipid is Cholesterol. Cholesterol is the principal sterol of the higher animals. Cholesterol was found in all body tissues, especial in the brain, spinal cord, and in animal fats or oils. Cholesterol is the main constituent of gallstones.<br>References Rosin, Z., et al.: Physiol. Chem., 124, 282 (1923), Schoenheimer, et al.: J. Biol. Chem., 105, 355 (1934), Gemant, et al.: Life Sci., 1, 233 (1962), Johnson, K., et al.: 4, 457 (1964),<br></p>Fórmula:C28H48OCor e Forma:White To Off-WhitePeso molecular:400.6817-Desacetyl Rocuronium Bromide
CAS:<p>Impurity Rocuronium EP Impurity C<br>Applications 17-Desacetyl Rocuronium Bromide (Rocuronium EP Impurity C) is a metabolite of Rocuronium (R639500), in human plasma.<br>References Kleef, U., et al.: J. Chromatogr., 621, 65 (1993), Proost, J., et al.: Br. J. Anaesth., 85, 717 (2000),<br></p>Fórmula:C30H51N2O3·BrCor e Forma:NeatPeso molecular:567.64Glycochenodeoxycholic Acid 3-Sulfate Disodium Salt
CAS:<p>Stability Hygroscopic<br>Applications A bile salt formed in the liver from chenodeoxycholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic.<br>References Parmentier, G. , et al.: Steroids, 30, 583 (1977), Tserng, K.Y., et al.: Lipids, 13, 479 (1978),<br></p>Fórmula:C26H41NNa2O8SCor e Forma:White To Off-WhitePeso molecular:573.65Ethynyl Estradiol 3-Sulfate Sodium Salt (>85%)
CAS:Fórmula:C20H23NaO5SPureza:>85%Cor e Forma:White To Light OrangePeso molecular:398.4516α-Hydroxy Estrone
CAS:<p>Impurity Estriol EP Impurity H<br>Applications 16α-Hydroxy Estrone (Estriol EP Impurity H) is a major metabolite of Estradiol.<br>References Fishman, H.G, et al.: Biochemistry, 8, 4304 (1969), Ryan, Sugar, J., et al.: J. Clin. Endocrinol. Metab., 50, 137 (1980), Numazawa, M., et al.: Steroids, 38, 149 (1981), Travis, R., et al.: Breast Cancer Res., 5, 239 (2003),<br></p>Fórmula:C18H22O3Cor e Forma:White To BeigePeso molecular:286.376α-Hydroxy Progesterone (>80%)
CAS:Produto ControladoFórmula:C21H30O3Pureza:>80%Cor e Forma:NeatPeso molecular:330.46(17β)-17-Hydroxyandrost-5-en-3-one
CAS:Produto Controlado<p>Applications (17β)-17-Hydroxyandrost-5-en-3-one is a reagent in the synthesis of new hedgehog signaling inhibitors which may be used in cancer treatments.<br>References Xu, C. et al.: J. Am. Chem. Soc., 141, 5381 (2019)<br></p>Fórmula:C19H28O2Cor e Forma:NeatPeso molecular:288.424Nor Cholic Acid
CAS:Produto Controlado<p>Applications A novel bile acid, an analogue of Cholic acid (C432600).<br>References Yamaga, N., et al.: J. Biochem., 116, 1123 (1994),<br></p>Fórmula:C23H38O5Cor e Forma:NeatPeso molecular:394.543-Sulfoglycolithocholic Acid Disodium Salt
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications 3-Sulfoglycolithocholic Acid Disodium Salt is a derivative of Lithocholic acid (L469180). Lithocholic acid (LCA) is a putative tumor promoter,that is shown to be able to inhibit mammalian DNA polymerase β.<br>References Ogawa, A., et al.: Jap. J. Canc. Res., 89, 1154 (1998)<br></p>Fórmula:C26H41NO7S·2NaCor e Forma:NeatPeso molecular:557.65Trestolone Acetate
CAS:Produto Controlado<p>Applications Trestolone acetate is a derivative of Trestolone (T719600), a synthetic androgen used as a potential hormonal male contraceptive method that induces a state of temporary infertility.<br>References Garcia-Becerra, R., et al.: Reproduction., 143, 211 (2012); Attardi, B.J., et al.: J. Steroid. Biochem. Molec. Biol., 122, 212 (2010)<br></p>Fórmula:C21H30O3Cor e Forma:NeatPeso molecular:330.466β-Hydroxy Norethindrone Acetate
CAS:Produto Controlado<p>Impurity Norethindrone Acetate EP Impurity F<br>Applications 6β-Hydroxy Norethindrone Acetate (Norethindrone Acetate EP Impurity F) is an oxidative product of the drug Norethindrone (N676000). Norethindrone impurity.<br>References Reif, V., et al.: Pharmaceutical Res., 4, 54 (1987), Rao, P., et al.: Steroids, 59, 621 (1994),<br></p>Fórmula:C22H28O4Cor e Forma:Off-WhitePeso molecular:356.464-Hydroxy Estradiol 1-N7-Guanine
CAS:Produto Controlado<p>Applications 4-Hydroxy Estradiol 1-N7-Guanine is an estrogen metabolite formed with DNA which can lead to the mutations that initiate breast, prostate, and other types of cancer. Estrogen-DNA depurinating adducts as biomarkers of cancer risk and their use in cancer detection and prevention.<br>References Chakravarti, D., et al.: Mutat. Res., 456, 17 (2000), Liehr, J., et al.: Endocr. Rev., 21, 4054 (2000), Chakravarti, D., et al.: Oncogene, 20, 7945 (2001), Cavalieri, E., et al.: Chem. Res. Toxicol., 14, 1041 (2002),<br></p>Fórmula:C23H27N5O4Cor e Forma:NeatPeso molecular:437.49
