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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Betamethasone-∆17,20 21-Aldehyde(Mixture of Isomers)
CAS:Controlled Product<p>Applications A degradation and metabolic intermediate of Betamethasone (B3270000).<br></p>Formula:C22H27FO4Color and Shape:NeatMolecular weight:374.45Fulvestrant
CAS:Controlled ProductFormula:C32H47F5O3SColor and Shape:White To Off-WhiteMolecular weight:606.771,2-Dihydro Prednicarbate
CAS:<p>Impurity Prednicarbate USP Related Compound A<br>Applications 1,2-Dihydro Prednicarbate is a related compound of Prednicarbate (P703700). Prednicarbate related compound A. Prednicarbate USP Related Compound A.<br>References Conolly, et al.: J. Chem. Soc., 828 (1937),<br></p>Formula:C27H38O8Color and Shape:NeatMolecular weight:490.59Triamcinolone 21-Acetate
CAS:Controlled Product<p>Impurity Triamcinolone EP Impurity B<br>Applications Triamcinolone 21-Acetate is an impurity of Triamcinolone (T767160), a glucocorticoid used as an antiasthmatic.<br>References Florey, K., et al.: Anal. Profiles Drug Subs., 1, 397 (1972), Bernstein, I.L., et al.: Chest, 81, 20 (1982)<br></p>Formula:C23H29FO7Color and Shape:White To Off-WhiteMolecular weight:436.47Pregnenolone-d6
CAS:Controlled Product<p>Applications Pregnenolone-d6 is the labeled analogue of Pregnenolone (P712200), a steroid hormone involved in the steroidogenesis of progesterone, mineralocorticoids, glucocorticoids, androgens, and estrogens. As such it is a prohormone. Pregnenolone is a GABAA antagonist and increases neurogenesis in the hippocampus. It is a modulator of cytochrome P 450-3A.<br>References Bjondahl, K., et al.: Med. Biol., 54, 454 (1976); Geick, A., et al.: J. Biol. Chem., 276, 14581 (2001); Johnson, D., et al.: Toxicol. Sci., 66, 16 (2002); Abe, C., et al.: Lipids, 42, 637 (2007)<br></p>Formula:C21D6H26O2Color and Shape:NeatMolecular weight:322.516β-Muethyl Prednisolone 21-Acetate (>90%)
CAS:Controlled Product<p>Applications 6β-Μethyl Prednisolone 21-Acetate is the 6-methyl isomer of 6α-Methyl Prednisolone 21-Acetate (M326030).<br>References Sugihara, N., et al: Am. J. Cardiol., 69, 1475 (1992), Bracken, M.B., et al.: J. Neurosurg., 89, 699 (1998), Dammers, J.W.H.H., et al.: Brit. Med. J., 319, 884 (1999).<br></p>Formula:C24H32O6Purity:>90%Color and Shape:NeatMolecular weight:416.514-Hydroxy Atorvastatin Hemicalcium Salt
CAS:<p>Applications 4-Hydroxyatorvastatin is a hydroxylated metabolite of Atorvastatin, 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 Smith, S. et al.: Am. J. Cardiol., 80, 10H (1997); Jacobsen, W. et al.: Drug Metab. Dispos., 28, 1369 (2000); Istvan, E. et al.: Science, 292, 1160 (2001); Tabernero, L. et al.: J. Biol. Chem., 278, 19933 (2003); Bratton, L. et al.: Bioorg. Med. Chem., 15, 5576 (2007);<br></p>Formula:C66H68CaF2N4O12Purity:>90%Color and Shape:NeatMolecular weight:1187.34Pregna-4,9(11)-diene-3,20-dione (90%)
CAS:Controlled Product<p>Applications Pregna-4,9(11)-diene-3,20-dione is a Progesterone (P755900) impurity, a steroid hormone produced by the corpus luteum. Induces maturation and secretory activity of the uterine endothelium; suppresses ovulation. Progesterone is implicated in the etiology of breast cancer.<br>References Thomas, P. et al.: Endocrinol., 148, 705 (2007); Anderson, E., et al.: Breast Cancer Res., 4, 197 (2002), Lanari, C., et al.: Breast Cancer Res., 4, 240 (2002), Albrecht, E.D., et al.: Front. Biosci., 8, 416 (2003), Qiu, M., et al.: J. Steroid Biochem. Mol. Biol., 85, 147 (2003),<br></p>Formula:C21H28O2Purity:90%Color and Shape:NeatMolecular weight:312.45Testosterone-d3 β-D-Glucuronide Monosodium Salt
CAS:Controlled Product<p>Applications Labelled Metabolite of Testosterone (T155000).<br>References Shibata, N., et al.: Biochem. J., 368, 783 (2002), Sonneveld, E., et al.: Toxicol. Sci., 83, 136 (2005), Schulze, J., et al.: J. Clin. Endocrinol. Metab., 93, 2500 (2008), Sten, T., et al.: Drug<br></p>Formula:C25H32D3NaO8Color and Shape:Off-WhiteMolecular weight:489.55Digoxigenin Bisdigitoxoside
CAS:Controlled Product<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>Formula:C35H54O11Color and Shape:NeatMolecular weight:650.80Desonide 21-Acetate
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications Desonide 21-Acetate is a reactant in the synthesis of 7α-halogenocorticosteroids with anti-inflammatory activity.<br>References De, K., et. al.: J. Indian Chem. Soc., 79, 513 (2002)<br></p>Formula:C26H34O7Color and Shape:NeatMolecular weight:458.5421-Dehydrocorticosterone (mixture of the aldehyde and the hydrated form)
CAS:Formula:C21H28O4Color and Shape:NeatMolecular weight:344.44Promestriene
CAS:Controlled Product<p>Applications A synthetic diethyl-ether of Estradiol with no distal hormonal effects, in patients undergoing surgical correction for stress urinary incontinence (SUI).<br>References Kelleher, C., et al.: Br. J. Obstet. Gynaecol., 104, 1374 (1997), Deffieux, X., et al.: J. Gynecol. Obstet. Biol. Reprod., 35, 678 (2006),<br></p>Formula:C22H32O2Color and Shape:NeatMolecular weight:328.495,6-trans Travoprost
CAS:<p>Applications An 5,6-trans isomeric impurity of the selective FP prostaglandin receptor agonist Travoprost (T715600).<br></p>Formula:C26H35F3O6Color and Shape:NeatMolecular weight:500.5517α-Hydroxy Pregnenolone-d3
CAS:Controlled Product<p>Applications A labelled metabolite of Pregnenolone (P712200).<br>References Kramer, R., et al.: J. Steroid Biochemi., 18, 715 (1983), Hiwatashi, A., et al.: J. Biochem., 98, 619 (1985), Eiichi, T., et al.: J. Pharmacol. Sci., 95, 140 (2004),<br></p>Formula:C212H3H29O3Color and Shape:NeatMolecular weight:335.5011b,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:342.43Dexamethasone 21-Phosphate Dimer Sodium Salt
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications Dexamethasone 21-Phosphate Dimer is a derivative of Dexamethasone (D298800), a glucocorticoid used as an anti-inflammatory agent. Dexamethasone regulates T cell survival, growth, and differentiation. Dexamethasone inhibits the induction of nitric oxide synthase.<br>References Wershil, B.K., et al.: Int. Arch. Allergy Immunol., 107, 323 (1995), Riccardi, C., et al.: Cell Death Diff., 6, 1182 (1999), Llanos, S.L. and Roldan, A.: Bio Cell, 23, 29 (1999)<br></p>Formula:C44H56F2NaO12PColor and Shape:White SolidMolecular weight:868.8717-Epiestriol
CAS:Controlled Product<p>Impurity Estriol EP Impurity E<br>Applications 17-Epiestriol (Estriol EP Impurity E) is a metabolite of Estradiol.<br>References Marrian, B., et al.: Biochem. J., 59, 136 (1955), Dietel, M., et al.: Cancer Res., 50, 6100 (1990), Schumacher, G., et al.: Clin. Cancer Res., 5, 493 (1999), Robert, J., et al.: J. Med. Chem., 46, 4805 (2003),<br></p>Formula:C18H24O3Color and Shape:White To Light RedMolecular weight:288.38Andarine
CAS:Controlled Product<p>Applications It is a potent and tissue-selective androgen receptor modulator (SARM) used as antiosteoporotic agent.<br>References Samnegard, E., et al.: Bone, 28, 414 (2001), Hanada, K., et al.: Biol. Pharm. Bull., 26, 1563 (2003), Kearbey, J., et al.: Xenobiotica, 34, 273 (2004), Kearbey, J., et al.: Xenobiotica, 34, 273 (2004), Kearbey, J., et al.: Pharm. Res., 24, 328 (2007),<br></p>Formula:C19H18F3N3O6Color and Shape:Light YellowMolecular weight:441.36
