Esteroides y derivados
Los esteroides son compuestos orgánicos que poseen una estructura de cuatro anillos fusionados, conocida como el núcleo esteroídico. Este núcleo puede unirse a varios grupos funcionales que modifican sus propiedades y funciones biológicas. Los esteroides tienen un papel clave en la regulación de procesos metabólicos y hormonales. Se utilizan en medicina para tratar trastornos inflamatorios, autoinmunes y desequilibrios hormonales. Además, algunos derivados esteroides tienen propiedades antiinflamatorias potentes, como los corticosteroides. En terapias específicas, se usan para reducir la inflamación y controlar el dolor en diversas enfermedades.
En CymitQuimica contamos con una variedad de esteroides y sus derivados para investigación y desarrollo farmacéutico.
Se han encontrado 4964 productos de "Esteroides y derivados"
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4-Hydroxy Testosterone
CAS:Producto controlado<p>Applications 4-Hydroxytestosterone is an anabolic steroid and does not have any therapeutic indication. 4-Hydroxytestosterone is metabolite of the aromatase inhibitor Formestane (F692250). 4-Hydroxytestosterone concentration in the urine can be used as a biomarker for steroid misuse.Controlled Substance.<br>References Kohler, M. et al.: Steroids, 72, 278 (2007); Brodie, A.M. et al.: J. Steroid. Biochem., 14, 693 (1981); Van Renterghem, P. et al.: Steroids, 75, 154 (2010);<br></p>Fórmula:C19H28O3Forma y color:NeatPeso molecular:304.42Fluocinolone Acetonide Acetate
CAS:<p>Applications Glucocorticoid; anti-inflammatory.<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 Sammul, et al.: J. Assoc. Off. Agric. Chem., 47, 952 (1964), Brunmair, B., et al.: J. Pharmacol. Exp. Therap., 311, 109 (2004), Emerson, M.V., et al.: BioDrugs, 21, 245 (2007),<br></p>Fórmula:C26H32F2O7Forma y color:White To Off-WhitePeso molecular:494.52Tibolone
CAS:Producto controlado<p>Applications A synthetic steroid with weak estrogenic, androgenic and progestogenic activity. A pharamceutical used in the treatment of menopausal syndrome.<br>References de Visser, J., et al.: Arzneim.-Forsch., 34, 1010 (1984), Geusens, P., et al.: Maturitas Suppl, 1, 1 (1987)<br></p>Fórmula:C21H28O2Forma y color:WhitePeso molecular:312.45Obeticholic Acid Acyl-β-D-glucuronide
Producto controlado<p>Applications Obeticholic Acid Acyl-β-D-glucuronide is composed of 6-Ethylchenodeoxycholic Acid (E899810) linked with Glucuronic Acid (G596850).<br>References Levene, M., et al.: J. Biol. Chem., 92, 257 (1931); Miyamoto, I., et al.: Anal. Biochem., 115, 308 (1981); Neuschwander-Tetri, B.A., et al.: Lancet., 385, 956 (2015);<br></p>Fórmula:C32H52O10Forma y color:White To Off-WhitePeso molecular:596.75Cyproterone-d4
CAS:Producto controlado<p>Applications Labelled Cyproterone (C989090). An antiandrogen, suppresses Testosterone and its metabolites. Derivatives of Cyproterone are administered to patients suffering from hypersexuality and to help facilitate the sexual transformation of male-to-female transsexuals.<br>References Gracia, T., et al.: Toxicol. App. Pharmacol., 225, 142 (2007), Ahlin, G., et al.: J. Med. Chem., 51, 5932 (2008), Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010), Bovee, T., et al.: J. Steroid Biochem. Mol. Biol., 118, 85 (2010),<br></p>Fórmula:C22H23D4ClO3Forma y color:NeatPeso molecular:378.9317-Iodo-androsta-5,16-diene-3β-ol
CAS:Producto controlado<p>Impurity Abiraterone Impurity 5<br>Applications 17-Iodo-androsta-5,16-diene-3β-ol is an analog of Abiraterone (A108490) and is used as a reagent in the synthesis of C-17-heteroaryl steroidal CYP17 inhibitors/antiandrogens which exhibit antitumor activity. Abiraterone Impurity 5<br>References Handratta, V.D., et al.: J. Med. Chem., 48, 2972 (2005)<br></p>Fórmula:C19H27IOForma y color:White To Off-WhitePeso molecular:398.32Testosterone Undecylenate
CAS:Producto controlado<p>Applications Testosterone Undecylenate is an ester metabolite of Testosterone (T155000), which is the main hormone of the testes, produced by the interstitial cells. It is a major circulating androgen; converted by 5α-reductase in androgen-dependent target tissues to 5α-dehydrotestosterone that is required for normal male sexual differentiation. Also converted by aromatization to Estradiol.<br>References McFarland, K., et al.: Science, 245, 494 (1989); Heckert, L., et al.: Mol. Endocrinol., 12, 1499 (1998); Themmen, A., et al.: Endocr. Rev. 21, 551 (2000); Kumar, R., et al.: Biol. Reprod., 65, 710 (2001);<br></p>Fórmula:C30H46O3Forma y color:NeatPeso molecular:454.684Finasteride Carboxylic Acid
CAS:Producto controladoFórmula:C23H34N2O4Forma y color:Light Yellow SolidPeso molecular:402.53di(2-Hydroxy Atorvastatin-d5) Calcium Salt
CAS:Producto controlado<p>Applications di(2-Hydroxy Atorvastatin-d5) Calcium Salt is the labeled analogue of di(2-Hydroxy Atorvastatin) Calcium Salt (H828930), a 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>Fórmula:C66H58D10CaF2N4O12Forma y color:NeatPeso molecular:1197.423-epi-Pregnenolone
CAS:Producto controlado<p>Applications An epimer of Pregnenolone (P712200), a GABAA antagonist and increases neurogenesis in the hippocampus.<br>References Li, W. et al.: J, Pharmacol. Exp. Therap., 323, 236 (2007); Sunol, C. et al.: J. Med. Chem., 49, 3225 (2006);<br></p>Fórmula:C21H32O2Forma y color:NeatPeso molecular:316.48Equilenin
CAS:<p>Applications Equilenin is a naturally occuring estrogenic steroidal hormone (1,2) isolated from urine of pregnant mares (3). Not found in human urine. Component of conjugated estrogenic hormones. Estrogen. This compound is a contaminant of emerging concern (CECs). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<br>References 1. Corbellini, A. et L.: Farmaco Sci. 1964 Nov;19:913-22.2. Stein, R. et al.: Tetrahedron 1970 Apr;26(8):1917-33.3. Nett, T. et al.: J. Reprod. Fertil. Suppl. 1975 Oct;(23):457-62.<br></p>Fórmula:C18H18O2Forma y color:Light Beige To Light YellowPeso molecular:266.334-[(5,6,7,8-Tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)carbonyl]benzoic Acid
CAS:Producto controlado<p>Applications 4-[(5,6,7,8-Tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)carbonyl]benzoic Acid is used in the preparation of pentamethylnaphthylmethylbenzoates as a selective retinoid X receptor ligands that induce apoptosis in leukemia cells.<br>References Boehm, M.F., et al.: J. Med. Chem., 38, 3146-55 (1995); Furmie, J.K., et al.: ChemMedChem, 7, 1551-66 (2012)<br></p>Fórmula:C23H26O3Forma y color:NeatPeso molecular:350.45Pregnenolone-d4
CAS:Producto controlado<p>Applications Pregnenolone-d4, is the labeled analogue of the Pregnenolone (P712200), which is a steroid hormone involved in the steroidogenesis of progesterone, mineralocorticoids, glucocorticoids, androgens, and estrogens.<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>Fórmula:C212H4H28O2Forma y color:Off-WhitePeso molecular:320.50Etonogestrel Sulfate Sodium Salt
Producto controlado<p>Applications A metabolite of Etonogestrel.<br></p>Fórmula:C22H27NaO5SForma y color:NeatPeso molecular:426.50220b-Dihydroprogesterone
CAS:Producto controlado<p>Impurity Progesterone EP Impurity C<br>Applications 20β-Dihydroprogesterone (Progesterone EP Impurity C) is an impurity of Progesterone (P755900), a steroid hormone secreted by the corpus luteum. Progesterone have various significant physiological roles, such as inducing the maturation and secretory activities of the uterine endothelium and the suppression of ovulation. Progesterone is also implicated in the etiology of breast cancer.<br>References 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>Fórmula:C21H32O2Forma y color:White To Off-WhitePeso molecular:316.48Testosterone 17β-Hemisuccinate
CAS:Producto controladoFórmula:C23H32O5Forma y color:NeatPeso molecular:388.4979,11-Dehydro Ethynyl Estradiol
CAS:<p>Impurity Ethinylestradiol EP Impurity B<br>Applications 9,11-Dehydro Ethynyl Estradiol (Ethinylestradiol EP Impurity B) is a degradation product of Ethynyl Estradiol (EE); an impurity of Ethynyl Estradiol (E685100).<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 Pang, C., et al.: Steroids, 23, 203 (1974), Leese, M., et al.: J. Med. Chem., 49, 7683 (2006), Krstic, N., et al.: Steroids, 72, 406 (2007),<br></p>Fórmula:C20H22O2Forma y color:NeatPeso molecular:294.396β-Hydroxy Dutasteride
<p>Applications 6β-Hydroxy Dutasteride is a hydroxylated derivative of Dutasteride (D735000).<br></p>Fórmula:C27H30F6N2O3Forma y color:NeatPeso molecular:544.43Dutasteride
CAS:Producto controlado<p>Applications Dutasteride is a dual inhibitor of 5α-reductase isoenzymes type 1 and 2; structurally related to Finasteride (F342000). Dutasteride is used in the treatment of benign prostatic hyperplasia.<br>References Bakshi, R.K., et al.: J. Med. Chem., 38, 3189 (1995), Gisleskog, P.O., et al.: Brit. J. Clin. Pharmacol., 47, 53 (1999), Djavan, B., et al.: Expert Opin. Pharmacother., 6, 311 (2005),<br></p>Fórmula:C27H30F6N2O2Forma y color:NeatPeso molecular:528.533-O-Methyl Estrone
CAS:Producto controladoFórmula:C19H24O2Forma y color:White To Dark BrownPeso molecular:284.3917-epi-Norethindrone
CAS:Producto controlado<p>Impurity Norethindrone EP Impurity G<br>Applications Norethindrone (N676000) epimer. Norethindrone and acetate is used in combination with estrogen as contraceptive (oral). Norethindrone EP Impurity G.<br>References Angel, P., et al.: Biochim. Biophys. Acta., 1072, 129 (1991), Chenu, C., et al.: J. Cell Biol., 127, 1149 (1994), Schmidt, M., et al.: J. Endocrinol., 158, 401 (1998),<br></p>Fórmula:C20H26O2Forma y color:Off White SolidPeso molecular:298.4214,15-Dehydro Budesonide
CAS:Producto controlado<p>Impurity Budesonide EP Impurity E<br>Applications 14,15-Dehydro Budesonide (Budesonide EP Impurity E) is a Budesonide (B689490) impurity.<br>References Aherne, G., et al.: J. Steroid Biochem., 17, 559 (1982), Assi, K., et al.: J. Pharm. Biomed. Anal., 41, 325 (2006),<br></p>Fórmula:C25H32O6Forma y color:WhitePeso molecular:428.518Desonide-13C3
CAS:Producto controlado<p>Applications Anti-inflammatory.<br>References Phillips, et al.: Toxicol. Appl. Pharmacol., 20, 522 (1971), Sanen, F.J., et al.: Int. J. Clin. Pharmacol. Biopharm., 12, 174 (1975), Tarayre, J.P., et al.: Pharmacol., 19, 323 (1979).<br></p>Fórmula:C2113C3H32O6Forma y color:NeatPeso molecular:419.49Ethyl 3-Oxo-4-aza-5α-androst-1-ene-17β-carboxylate
CAS:Producto controlado<p>Impurity Dutateride EP Impurity C<br>Applications Ethyl 3-Oxo-4-aza-5α-androst-1-ene-17β-carboxylate (Dutateride EP Impurity C) is a compound synthesized in the production of azasteroids. Used in the inhibition of 5α-reductase and of androgen receptor binding, both major effecters in the male hormonal system.<br>References Ramusson, G. et al.: J. Med. Chem., 29, 2298 (1986);<br></p>Fórmula:C21H31NO3Forma y color:White To Off-WhitePeso molecular:345.483α,5β-Tetrahydro Norgestrel
CAS:Producto controlado<p>Applications The major metabolite of the progestational agent Norgestrel (N689500).<br>References DeJongh, D.C. et al.: Steroids, 11, 649 (1968); Uniyal, J.P. et al.: Acta Endocrinol., 84, 155 (1977); Sisenwine, S.F. et al.: Drug Metab. Disp., 7, 1 (1979);<br></p>Fórmula:C21H32O2Forma y color:NeatPeso molecular:316.48Norgestimate
CAS:Producto controlado<p>Applications Progestogen. In combination with estrogen as oral contraceptive.<br>References Hahn, D.W., et al.: Contraception, 16, 541 (1977), Weintraub, H.S., et al.: J. Pharm. Sci., 67, 1406 (1978),<br></p>Fórmula:C23H31NO3Forma y color:White SolidPeso molecular:369.5017β-Estradiol 17β-D-Glucuronide
CAS:Producto controlado<p>Stability Hygroscopic<br>Applications A metabolite of Estradiol (E888000).<br>References Agasan, A., et al.: J. Immunol. Methods., 177, 251 (1994), Stone, R., et al.: Science, 265, 308 (1994), Tacey, R., et al.: J. Pharm. Biomed. Anal., 2, 1303 (1994),<br></p>Fórmula:C24H32O8Forma y color:Off White SolidPeso molecular:448.51Pregnenolone Carbonitrile
CAS:Producto controlado<p>Applications Pregnenolone Carbonitrile is a glucocorticoid receptor antagonist that induces the expression of the CYP3A family of steroid hydroxylases and modulates sterol and bile acid biosynthesis in vivo. Pregnenolone Carbonitrile is an an activator of rat pregnane X receptor (PXR).<br>References Kliewer, S.A., et. al.: Cell, 92, 73 (1998); Savas, U., et. al.: Drug Metab. Dispos., 28, 529 (2000)<br></p>Fórmula:C22H31NO2Forma y color:NeatPeso molecular:341.49Hexestrol
CAS:Producto controlado<p>Applications Estrogen; antineoplastic (hormonal).<br>References Aboul-Enein, H.Y., et al.: Anal. Profiles Drug Subs., 11, 347 (1982),<br></p>Fórmula:C18H22O2Forma y color:Off-WhitePeso molecular:270.37Betamethasone-d5
CAS:Producto controlado<p>Stability Hygroscopic<br>Applications Glucocorticoid.<br>References Ferrante, M.G., et al.: Anal. Profiles Drug Subs., 6, 43 (1977), Li, A., et al.: Chem. Biol. Interact., 142, 7 (2002), Cruz-Monteagudo, M., et al.: Eur. J. Med. Chem., 40, 1030 (2005), Rothfuss, A., et al.: Chem. Res. Toxicol., 19, 1313 (2006),<br></p>Fórmula:C22H24D5FO5Forma y color:Off-White To Light YellowPeso molecular:397.49(-)-Estra-4,9-diene-3,17-dione
CAS:Producto controlado<p>Applications A potential metabolite of STS 557 (Dienogest)(D441870). A steroid with antiglucocorticoid activity.<br>References Kloosterboer, H., et al.: J. Steroid Biochem., 31, 567 (1988),<br></p>Fórmula:C18H22O2Forma y color:NeatPeso molecular:270.37Norgestrel-d6 (Major)
CAS:Producto controlado<p>Applications Labelled Norgestrel. It is an excellent progestational and ovulation inhibiting steroid. The bioactive enantiomer is levorotatory. Progestogen; oral contraceptive.<br>References Sopirak, A.M., et al.: Anal. Profiles Drug Subs., 4, 294 (1975), Dunson, T.R., et al.: Contraception, 48, 109 (1993),<br></p>Fórmula:C21H22D6O2Forma y color:White To Light YellowPeso molecular:318.49Estrone
CAS:Producto controlado<p>Impurity Estradiol EP Impurity A/ Ethinylestradiol EP Impurity C<br>Applications Estrone is a metabolite of 17β-Estradiol (E888000). During the metabolism, it is in rapid equilibrium with Estriol (E888960) and 17β-Estradiol (E888000) (1). Causes the feminization of male fish at human and animal waste sites (2).This compound is a contaminant of emerging concern (CECs). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<br>References 1. Both, D. et al.: Anal. Prof. Drug Subst. 1983 12 pp135-1892. Goodman-Gruen, D. et al.: J. Clin. Endocrinol. Metab. 1996 Aug;81(8):2999-3003.<br></p>Fórmula:C18H22O2Forma y color:White To Off-WhitePeso molecular:270.37(3α)-Allopregnanolone-d5
CAS:Producto controlado<p>Applications Labelled (3α)-Allopregnanolone. (3α)-Allopregnanolone acts as a GABAA receptor positive allosteric modulator. (3α)-Allopregnanolone is a metabolite of Progesterone (P755900). (3α)-Allopregnanolone is a neuroactive steroid present in the blood and also the brain.<br>References Puja, G. et al.: Neuron, 4, 759 (1990); Belelli, D. et ael. Neurosteroid, 6, 565 (2006); Viapiano, M. et al.: Neurochem. Res., 23, 155 (1998);<br></p>Fórmula:C21H29D5O2Forma y color:NeatPeso molecular:323.5217β-Estradiol-16,16,17-d3
CAS:Producto controlado<p>Applications Isotope labelled 17β-Estradiol (E888000), which is the major estrogen (1) secreted by the premenopausal ovary (2).Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<br>References 1. Salole, E. et al.: Anal. Profiles Drug Subs. 1986 15, 23 283-3182. Lievertz, R. et al.: Am. J. Obstet. Gynecol. 1987 May;156(5):1289-93.<br></p>Fórmula:C182H3H21O2Forma y color:NeatPeso molecular:275.40Deltamedrane
CAS:<p>Stability Hygroscopic<br>Applications Deltamedrane is an impurity in the synthesis of Fluorometholone (F593145), a glucocorticoid; anti-inflammatory.<br>References Kupferman, A., et al.: Arch. Ophthlmol., 640, 100 (1982); Tokunaga H., et al.: Chem. Pharm. Bull., 32, 4012 (1984);<br></p>Fórmula:C22H30O4Forma y color:BeigePeso molecular:358.47Triamcinolone Hexacetonide
CAS:Producto controlado<p>Applications Triamcinolone Hexacetonide is the Intra-articular glucocorticoid treatment for rheumatoid arthritis.<br>References Abd-El-Barr, M.M., et al.: J. Ocul. Pharmacol. Ther., 24, 197 (2007); Eberhard, B.A., et al.: J. Rheumatol., 31, 2507 (2004);<br></p>Fórmula:C30H41FO7Forma y color:WhitePeso molecular:532.64S-deacetyl spironolactone
CAS:<p>Applications A metabolite of Spironolactone.<br>References Morris, R., et al.: Eur. J. Clin. Pharmacol., 34, 233 (1988), Dasgupta, A., et al.: Am. J. Clin. Pathol., 111, 406 (1999)<br></p>Fórmula:C22H30O3SForma y color:NeatPeso molecular:374.54Latanoprost Acid-d4(>85%)
CAS:Producto controlado<p>Applications Latanoprost Acid-d4 is the labeled analogue of Latanoprost Acid (L177310), a metabolite of Latanoprost. Latanoprost Acid (L177310) is a potent, selective FP prostanoid receptor agonist, a F-series Prostaglandin analog and is 200 times as potent as isopropyl ester form.<br>References Sjoquist, B., et al.: Drug Metab. Dispos., 26, 745 (1998), Watson, P., et al.: Drugs Today, 35, 449 (1999), Kashiwagi, K., et al.: Exp. Eye Res., 74, 41 (2002),<br></p>Fórmula:C23H30D4O5Pureza:>85%Forma y color:ColourlessPeso molecular:394.542-Nitrobenzotrifluoride
CAS:Producto controlado<p>Applications 2-Nitrobenzotrifluoride can be used for self-repairing polyimide based on dynamic imine bond.<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 Lei, X., et.al., Faming Zhuanli Shenqing, 15, (2019);<br></p>Fórmula:C7H4F3NO2Forma y color:NeatPeso molecular:191.107Dexamethasone Phenylpropionate
CAS:Producto controladoFórmula:C31H37FO6Forma y color:NeatPeso molecular:524.622-Methoxy-17α-ethynyl Estradiol
CAS:Producto controlado<p>Applications 2-Methoxy-17α-ethynyl Estradiol is a metabolite of the potent synthetic estrogen 17α-Ethynylestradiol (E685100).<br>References Maggs, J.L. et al.: Xenobiotica, 13, 421 (1983); Maggs, J.L. et al.: Biochem. Pharmacol., 32, 2793 (1983); Abdel-Aziz, M.T. et al.: Steroids, 15, 695 (1970);<br></p>Fórmula:C21H26O3Forma y color:NeatPeso molecular:326.43Pregnenolone Acetate
CAS:Producto controlado<p>Applications Pregnenolone (P712200) derivative, a steroid hormone involved in the steroidogenesis of progesterone, mineralocorticoids, glucocorticoids, androgens, and estrogens<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>Fórmula:C23H34O3Forma y color:NeatPeso molecular:358.5125-Hydroxy Vitamin D2
CAS:Producto controlado<p>Stability Light Sensitive, Temperature Sensitive<br>Applications A metabolite of Vitamin D2 (V676040).<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 Barnes, P., et al.: J. Clin. Invest., 83, 1527 (1989), Holick, M., et al.: J. Cell Biochem., 88(2), 296 (2003), Maunsell, Z., et al.: Clin. Chem., 51, 1683 (2005),<br></p>Fórmula:C28H44O2Forma y color:White To Light YellowPeso molecular:412.6516-Keto 17β-Estradiol-d5 (Major)
CAS:Producto controlado<p>Applications A labelled metabolite of Estradiol (E888000).<br>References Ball, P., et al.: Steroids, 33, 563 (1979), Wong, T., et al.: Clin. Chem., 38, 1830 (1992), Xu, X., et al.: J. Clin. Endocrinol. Metab., 84, 3914 (1999), Todorovic, R., et al.: Carcinogenesis, 22, 905 (2001), Travis, R., et al.: Breast Cancer Res., 5, 239 (2003),<br></p>Fórmula:C18H17D5O3Forma y color:NeatPeso molecular:291.417-epi-Testosterone-d3
CAS:Producto controlado<p>Applications 17-epi-Testosterone-d3 is the labelled analog of 17-epi-Testosterone.Testosterone (T155000) and epitestosterone (T155005) are endogenous steroids that differ in the configuration of the hydroxyl-bearing carbon at C-17. Testosterone is the predominant male sex hormone, whereas the role of epitestosterone is largely unclear. In humans, both androgens are excreted mainly as glucuronide conjugates.<br>References Wudy, S., et al.: Steroids, 66, 759 (2001), Kootstra, P., et al.: Anal. Chim. Acta., 586, 82 (2007), Sten, T., et al.: Drug Metab. Dispos., 37, 417 (2009),<br></p>Fórmula:C192H3H25O2Forma y color:NeatPeso molecular:291.4417-Oxo Dexamethasone
CAS:Producto controladoFórmula:C20H25FO3Forma y color:WhitePeso molecular:332.41
![4-[(5,6,7,8-Tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)carbonyl]benzoic Acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FT294945.webp&w=3840&q=75)
