Steroids and Derivatives
Steroids are organic compounds with a structure of four fused rings, known as the steroid nucleus. This core can be linked to various functional groups that modify their properties and biological functions. Steroids play a key role in regulating metabolic and hormonal processes. They are used in medicine to treat inflammatory disorders, autoimmune diseases, and hormonal imbalances. Additionally, some steroid derivatives have potent anti-inflammatory properties, such as corticosteroids. In specific therapies, they are used to reduce inflammation and manage pain in various diseases.
At CymitQuimica, we offer a variety of steroids and their derivatives for pharmaceutical research and development.
Found 4964 products of "Steroids and Derivatives"
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11b,21-dihydroxypregna-1,4,16-triene-3,20-dione
CAS:<p>Applications 11β,21-dihydroxypregna-1,4,16-triene-3,20-dione is a derivative of Prednisolone (P703740) and an intermediate in the synthesis of isoxazolinopregnadienes which exhibit anti-inflammatory activity.<br>References Khalil, M.A., et al.: Med. Chem. Res., 6, 52 (1996); Kwon, T., et al.: J. Med. Chem., 38, 1048 (1995)<br></p>Formula:C21H26O4Color and Shape:NeatMolecular weight:342.435β-Dihydro Progesterone
CAS:Controlled Product<p>Applications A metabolite of the neuroactive steroid Progesterone (PROG) (P755900).<br>References Wiebe, J., et al.: Cancer Res., 60, 936 (2000), Lacasa, D., et al.: J. Biol. Chem., 276, 11512 (2001), Johansson, I., et al.: Brain Res., 934, 125 (2002), Leonhardt, S., et al.: Steroids, 68, 761 (2003),<br></p>Formula:C21H32O2Color and Shape:NeatMolecular weight:316.48δ-5(6)-Norethindrone Acetate
CAS:Controlled Product<p>Impurity Norethindrone Acetate EP Impurity C<br>Applications Δ-5(6)-Norethindrone Acetate (Norethindrone Acetate EP Impurity C) is an impurity of Norethindrone Acetate (N675990).<br></p>Formula:C22H28O3Color and Shape:NeatMolecular weight:340.46Estrone 3-Acetate
CAS:Controlled ProductFormula:C20H24O3Color and Shape:White To Off-WhiteMolecular weight:312.402-Methyl-N-[3-(trifluoromethyl)phenyl]propanamide
CAS:Controlled ProductFormula:C11H12F3NOColor and Shape:NeatMolecular weight:231.21Pregna-4,14-diene-3,20-dione
CAS:Controlled Product<p>Impurity Progesterone EP Impurity A<br>Applications Pregna-4,14-diene-3,20-dione (Progesterone EP Impurity A) is a Progesterone derivative<br>References Wilks, J., et al.: Steroids, 35, 697 (1980), Templeton, J., et al.: J. Med. Chem., 30, 1502 (1987), Blackmore, P., et al.: Mol. Pharmacol., 49, 727 (1996),<br></p>Formula:C21H28O2Color and Shape:NeatMolecular weight:312.45Testosterone Undecanoate-d3
CAS:Controlled Product<p>Applications A Labelled metabolite of Testosterone (T155000). It is a promising androgen for male hormonal contraception.CONTROLLED SUBSTANCE<br>References Glass, A., et al.: J. Clin. Endocrinol. Metab., 45, 1211 (1977), Behre, H., et al.: Eur. J. Endocrinol., 140, 414 (1999), Nieschlag, E., et al.: Steroids, 68, 965 (2003), Wang, C., et al.: J. Clin. Endocrinol. Metab., 91, 460 (2006),<br></p>Formula:C30H45D3O3Color and Shape:NeatMolecular weight:459.729,11-Didehydrooestriol
CAS:Controlled Product<p>Impurity Estriol EP Impurity A<br>Stability Hygroscopic<br>Applications 9,11-Didehydrooestriol (Estriol EP Impurity A) is an impurity of Estriol (E888960), a metabolite of Estradiol (E888000). An estrogenic metabolite considerably less potent than the hormone Estradiol (E888000).<br>References Marrian, et al.: Biochem. J., 23,1090 (1929), Huffman, et al.: J. Biol. Chem., 169, 167 (1947),<br></p>Formula:C18H22O3Color and Shape:Off-WhiteMolecular weight:286.3719-Hydroxy Cholesterol
CAS:<p>Applications A metabolite of Cholesterol. Cholesterol oxidation product having cytotoxicity effects.<br>References Higley, N., et al.: Food Chem. Toxicol., 22, 983 (1984), Emanuel, H., et al.: J. Food Sci., 56, 843 (1991), Kilsdonk, E., et al.: J. Lipid Res., 36, 505 (1995), Cantwell, H., et al.: Cell Biol. Toxicol., 14, 401 (1998),<br></p>Formula:C27H46O2Color and Shape:NeatMolecular weight:402.6517α-Progesterone
CAS:<p>Applications 17α-Progesterone is a testosterone precursror generated from cholesterol. Also used as a diagnostic agent in the identification and study of ovarian Leydig cell tumor disease.<br>References Vesely, D. et al.: Proc. Natl. Acad. Sci. USA., 76, 3491 (1979); Arhan, E. et al.: J. Pediatric Endocrinol. Metab., 21, 181 (2008);<br></p>Formula:C21H30O2Color and Shape:NeatMolecular weight:314.46δ7-Avenasterol (E/Z mixture)
CAS:<p>Applications Δ7-Avenasterol is an analog of Stigmasterol (S686750); a plant sterol that is used as a precursor in the synthesis of progesterone.<br>References Han, P., et al.: Biotechnol. App. Biochem., 54, 105 (2009); Matsunaga, I., et al.: Anal. Biochem., 393, 222 (2009); Huang, C., et al.: Plant Physiol., 150, 1192 (2009)<br></p>Formula:C29H48OColor and Shape:White To Off-WhiteMolecular weight:412.6924(R/S)-Hydroxycholesterol-d7
CAS:Controlled Product<p>Applications 24(R/S)-Hydroxycholesterol-d7 is used in the study of biochemical methods for quantitative detection of steroids containing quantitative charge tags and oxidizing agents and using mass spectroscopy for detection.<br>References Groffoths, Williams., US 20150233953, (2015)<br></p>Formula:C272H7H39O2Color and Shape:NeatMolecular weight:409.70Testosterone 17-Decanoate
CAS:Controlled Product<p>Applications Testosterone 17-Decanoate, is an ester of Testosterone (T155000). Testosterone 17-Decanoate, can be used as a potential long-acting male contraceptive, with the combination of subcutaneous etonogestrel implants .<br>References Brady, B. M., et al.: Human Reproduction, 21 (1), 285 (2006); Themmen, A., et al.: Endocr. Rev. 21, 551 (2000);<br></p>Formula:C29H46O3Color and Shape:NeatMolecular weight:442.67Exemestane-19-d3
CAS:Controlled Product<p>Stability Light Sensitive<br>Applications An antineoplastic (hormonal).<br>References Giudici, D., et al.: J. Steroid Biochem., 30, 391 (1988), Evans, T.R.J., et al.: Cancer Res., 52, 5933 (1992), Zilembo, N., et al.: Brit. J. Cancer, 72, 1007 (1995)<br></p>Formula:C20H21D3O2Color and Shape:NeatMolecular weight:299.42Betamethasone 17-Propionate
CAS:Controlled Product<p>Impurity Clobetasol Propionate EP Impurity A / Betamethasone Dipropionate EP Impurity B<br>Applications Betamethasone 17-Propionate (Clobetasol Propionate EP Impurity A) is a degradation product of Betamethasone. Glucocorticoid.<br>References Andersson, P., et al.: J. Pharm. Pharmacol., 36, 763 (1984), Wurthwein, G., et al.: Biopharm. Drug Dispos., 11, 381 (1990), Samtani, M., et al.: J. Pharm. Sci., 93, 726 (2004), Samtani, M., et al.: Drug Metab. Dispos., 33, 1124 (2005),<br></p>Formula:C25H33FO6Color and Shape:Off-WhiteMolecular weight:448.52Hydroxy Flutamide-d6
CAS:Controlled ProductFormula:C11H5D6F3N2O4Color and Shape:Light Yellow SolidMolecular weight:298.254-Hydroxy Atorvastatin-d5 Hemicalcium Salt
CAS:Controlled Product<p>Applications di(4-Hydroxy Atorvastatin-d5) Calcium Salt is a labeled metabolite of Atorvastatin Calcium Salt (A791750), a selective, competitive HMG-CoA reductase inhibitor. Atorvastatin is the only drug in its class specfically indicated for lowering both elevated LDL-cholesterol and triglycerides in patients with hypercholesterolemia.<br>References Kearney, A.S., et al.: Pharm. Res., 10, 1461 (1993); Heinonen, T.M., et al.: Clin. Ther., 18, 853 (1996); Whitfield, L.R., et al.: Eur. J. Drug Metab. Pharmacokinet., 25, 97 (2000)<br></p>Formula:C66H58D10CaF2N4O12Color and Shape:Beige SolidMolecular weight:1197.411a-Hydroxy Canrenone
CAS:Controlled Product<p>Applications 11α-Hydroxy Canrenone is the key intermediate in the synthesis of Eplerenone, a cardiovascular drug. Canrenone was biotransformed into 11α-Hydroxycanrenone by Aspergillus ochraceus SIT34205.<br>References Luetscher, J., et al.: J. Clin. Invest., 29, 1576 (1950), Gaunt, R., et al.: J. Clin. Endocrinol. Metab., 15, 621 (1955), McMahon, E., et al.: Curr. Opin. Pharm., 1, 190 (2001), McMahon, E., et al.: Curr. Pharm. Des., 9, 1065 (2003),<br></p>Formula:C22H28O4Color and Shape:NeatMolecular weight:356.46Aldosterone
CAS:<p>Applications Aldosterone is an adrenocortical steroid which exerts regulatory influence on metabolism of electrolytes and water. Biologically active aldosterone isomer; a mineralocorticoid produced by the adrenal cortex that induces urinary excretion of K+ and renal reabsorptioon of Na+. Exists as an equilibrium mixture of the aldehyde and the hemiacetal.<br>References Simpson, et al.: Experienta, 9, 333 (1953), Morel, A., et al.: Nature, 356, 523 (1992), Arima, S., et al.: Clin. Exp. Nephrol., 7, 172 (2003), Hirasawa, A., et al.: Eur. J. Pharmacol., 267, 71 (1994), Hiroyama, M., et al.: Mol. Endocrinol., 21, 247 (2007),<br></p>Formula:C21H28O5Color and Shape:White To Off-WhiteMolecular weight:360.44
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