Esteroides e Derivados
Os esteroides são compostos orgânicos que possuem uma estrutura de quatro anéis fundidos, conhecida como núcleo esteroide. Esse núcleo pode estar ligado a vários grupos funcionais que modificam suas propriedades e funções biológicas. Os esteroides desempenham um papel fundamental na regulação dos processos metabólicos e hormonais. São utilizados na medicina para tratar distúrbios inflamatórios, doenças autoimunes e desequilíbrios hormonais. Além disso, alguns derivados de esteroides possuem potentes propriedades anti-inflamatórias, como os corticosteroides. Em terapias específicas, são utilizados para reduzir a inflamação e controlar a dor em diversas doenças.
Na CymitQuimica, oferecemos uma variedade de esteroides e seus derivados para pesquisa e desenvolvimento farmacêutico.
Foram encontrados 4976 produtos de "Esteroides e Derivados"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
1,2-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>Fórmula:C27H38O8Cor e Forma:NeatPeso molecular:490.59Triamcinolone 21-Acetate
CAS:Produto Controlado<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>Fórmula:C23H29FO7Cor e Forma:White To Off-WhitePeso molecular:436.4717-Epiestriol-d5
CAS:Produto Controlado<p>Applications A labelled metabolite of Estradiol (E888000).<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>Fórmula:C18H19D5O3Cor e Forma:NeatPeso molecular:293.41Digoxigenin 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:Off White SolidPeso molecular:650.8021-Dehydrocorticosterone (mixture of the aldehyde and the hydrated form)
CAS:Fórmula:C21H28O4Cor e Forma:NeatPeso molecular:344.44Protodioscin
CAS:<p>Applications Protodioscin is a steroidal saponin compound found in a number of plant species. It is known to be the active component of the herbal aphrodisiac plant Tribulus terrestris. It has also shown to produce significant increases in the levels of the hormonal levels in animal studies.<br>References Gauthaman, K., et al.: Inter. J. Phytother. Phytopharm., 15, 44 (2008); Ganzera, M., et al.: J. Pharmac. Sci., 90(11), 1752 (2001);<br></p>Fórmula:C51H84O22Cor e Forma:Off-White To Light BeigePeso molecular:1049.20Dexamethasone 21-Phosphate Dimer Sodium Salt
CAS:Produto Controlado<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>Fórmula:C44H56F2NaO12PCor e Forma:White SolidPeso molecular:868.876α-Methyl-9α-fluoro-11β,17α-dihydroxyprogesterone
CAS:Produto Controlado<p>Applications 6α-Methyl-9α-fluoro-11β,17α-dihydroxyprogesterone is an impurity 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:C22H31FO4Cor e Forma:NeatPeso molecular:378.485β-Dihydro Progesterone
CAS:Produto Controlado<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>Fórmula:C21H32O2Cor e Forma:NeatPeso molecular:316.48Estriol Methyl Ether
CAS:<p>Impurity Estriol EP Impurity C<br>Applications Estriol Methyl Ether (Estriol EP Impurity C) is a metabolite (1,2) of Estriol (E888960), which is a produced naturally and also a metabolite of Estradiol (E888000). Estriol is a GPR3 antagonist in estrogen receptor-negative breast cancer cells displaying anti-proliferative effects (3).<br>References 1. Marrian, G. et al.: Biochem. J. 1929;23(5):1090-8.2. Rogerson, B. et al.: Arch. Biochem. Biophys. 1986 Oct;250(1):70-85.3. Lappano, R. et al.: Mol Cell Endocrinol. 2010 May 14;320(1-2):162-70.<br></p>Fórmula:C19H26O3Cor e Forma:NeatPeso molecular:302.414-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:437.4916α-Methyl-11-oxo Prednisolone
CAS:Produto Controlado<p>Applications A 16α-substituted Prednisolone as potent topical antiinflammatory agent.<br>References Lutsky, B.N., et al.: Arzneim.-Forsch., 29, 1662 (1979),<br></p>Fórmula:C22H28O5Cor e Forma:White SolidPeso molecular:372.453-O-Methyl Estradiol
CAS:Produto Controlado<p>Applications Estradiol derivative which shows antioxidant activity.<br>References Fotsis, T., et al.: J. Steroid. Biochem., 28, 215 (1987), Sack, M., et al.: Lancet, 343, 269 (1994), Brunelli, R., et al.: Biochemistry, 39, 13897 (2000), Li, A., et al.: Nat. Med., 8, 1235 (2002),<br></p>Fórmula:C19H26O2Cor e Forma:White To Light YellowPeso molecular:286.415β-Dihydro Progesterone-d8
CAS:Produto Controlado<p>Applications 5β-Dihydro Progesterone-d8 is labelled which is labelled 5β-Dihydro Progesterone (D449280), 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>Fórmula:C21H24D8O2Cor e Forma:NeatPeso molecular:324.53Dexamethasone Sodium Phosphate Impurity C
<p>Applications Dexamethasone Sodium Phosphate Impurity C is a derivative of Dexamethasone Sodium Phospahte, which is an impurity compound of Dexamethasone (D298800). Dexamethasone regulates T cell survival, growth, and differentiation. it also 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>Fórmula:C22H29FO5Cor e Forma:NeatPeso molecular:392.461Estrone 3-Acetate
CAS:Produto ControladoFórmula:C20H24O3Cor e Forma:White To Off-WhitePeso molecular:312.40Mifepristone
CAS:Produto Controlado<p>Applications Mifepristone is a progesterone receptor antagonist with partial agonist activity. Abortifacient.<br>References Healy, D.L., et al.: J. Clin. Endocrinol. Metab., 57, 863 (1983), Rauch, M., et al.: Eur. J. Biochem., 148, 213 (1985), Baulieu, E.E., et al.: Science, 245, 1351 (1989), Brogden, R.N., et al.: Drugs, 45, 384 (1993)<br></p>Fórmula:C29H35NO2Cor e Forma:White To Light YellowPeso molecular:429.59Chlormadinone
CAS:Produto Controlado<p>Applications It has been used in combinations as an oral contraceptive.<br>References Brennan, D.M., et al.: Acta Endocrinol., 44, 367 (1963), Honma., s., et al.: Chem Pharm. Bull., 25 2019 (1977), Usui, T., et al.: Acta Urol. Jpn., 27, 327 (1981),<br></p>Fórmula:C21H27ClO3Cor e Forma:NeatPeso molecular:362.89Bexarotene
CAS:Produto Controlado<p>Applications Bexarotene is a selective retinoid X receptor (RXR) agonist and an antineoplastic agent (1,2,3).<br>References (1) Boehm, M.F., et al.: J. Med. Che., 37,2930 (1994) (2) Gottardis, M.M., et al.: Cancer Res., 56, 5566 (1996) (3) Mukherjee, R., et al.: Nature, 386, 407 (1997)<br></p>Fórmula:C24H28O2Cor e Forma:NeatPeso molecular:348.48Estetrol
CAS:Produto Controlado<p>Applications A metabolite of Estradiol. It is an estrogenic steroid synthesized exclusively by the fetal liver during human pregnancy and reaching the maternal circulation through the placenta.<br>References Gurpide, E., et al.: J. Clin. Endocrinol., 26, 1355 (1966), Hagen, A., et al.: J. Clin. Endocrinol., 30, 763 (1970), Schollberg, K., et al.: Exp. Clin. Endocrinol., 85, 204 (1985), Coelingh Bennink, H., et al.: Contraception, 77, 186 (2008),<br></p>Fórmula:C18H24O4Cor e Forma:Off White SolidPeso molecular:304.385-Oxo Atorvastatin
CAS:<p>Applications Atorvastatin Derivative<br></p>Fórmula:C33H33FN2O5Cor e Forma:NeatPeso molecular:556.62D-Ethyl Gonendione
CAS:Produto Controlado<p>Impurity Levonorgestrel EP Impurity L<br>Applications D-Ethyl Gonendione (Levonorgestrel EP Impurity L) is a Norgestrel intermediate.<br>References Hiraga, K., et al.: Chem. Pharm. Bull., 13, 1289 (1965), Bergink, F.W., et al.: J. Steroid Biochem., 14, 175 (1981), Phillips, A., et al.: Contraception, 36, 181 (1987), Corson, S.L., et al.: Am. J. Obstet. Gynecol., 168, 1017 (1993),<br></p>Fórmula:C19H26O2Cor e Forma:NeatPeso molecular:286.41Digitoxin
CAS:<p>Stability Hygroscopic<br>Applications Cardiotonic.<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 Foerster, et al.: Arch. Int. Pharmacodyn. Ther., 159, 1 (1966), Jakovljevic, I.M., Anal. Profiles Drug Subs., 3, 149 (1974)<br></p>Fórmula:C41H64O13Cor e Forma:White To Off-WhitePeso molecular:764.94(11α,16α)-9,11-Epoxy-17,21-dihydroxy-16-methylpregna-1,4-diene-3,20-dione
CAS:<p>Applications (11α,16α)-9,11-Epoxy-17,21-dihydroxy-16-methylpregna-1,4-diene-3,20-dione, can be used for the synthesis of Calicoferol E, a vitamin D3 analogues.<br>References Vir Singh, T., et al.: ARKAT USA, INc., (2002);<br></p>Fórmula:C22H28O5Cor e Forma:White To Light RedPeso molecular:372.45Hydroxy Flutamide-d6
CAS:Produto ControladoFórmula:C11H5D6F3N2O4Cor e Forma:Light Yellow SolidPeso molecular:298.254-Hydroxy Atorvastatin-d5 Hemicalcium Salt
CAS:Produto Controlado<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>Fórmula:C66H58D10CaF2N4O12Cor e Forma:Beige SolidPeso molecular:1197.4Finasteride Carboxylic Acid Methyl Ester
CAS:Produto Controlado<p>Applications Finasteride Carboxylic Acid Methyl Ester is an metabolite of Finasteride (F342000), an inhibitor of 5α-reductase, the enzyme which converts testosterone to the more potent androgen, 5α-dihydrotestosterone.<br>References Koronkowski, M.J., et al.: Pharmacotherapy, 13, 309 (1993), Tenover, J.L., et al.: Clin. Ther., 19, 243 (1997), McConnell, J.D., et al.: N. Engl. J. Med., 338, 557 (1998),<br></p>Fórmula:C24H36N2O4Cor e Forma:NeatPeso molecular:416.554Progesterone
CAS:Produto Controlado<p>Applications 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.This compound is a contaminant of emerging concern (CECs).<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:C21H30O2Cor e Forma:WhitePeso molecular:314.4620α-Dihydrodydrogesterone
CAS:<p>Applications 20α-Dihydrodydrogesterone is the major active metabolite of dydrogesterone (D826000).<br>References Olbrich, M., et al.: Xenobiotica, 46, 868-874 (2016)<br></p>Fórmula:C21H30O2Cor e Forma:NeatPeso molecular:314.462δ4-Androstene-3β,17β-diol
CAS:Produto Controlado<p>Applications A metabolite of Testosterone (T155000).<br>References Janer, G., et al.: Aquat. Toxicol., 75, 32 ( 2005), Lavado, R., et al.: Steroids, 71, 489 (2006),<br></p>Fórmula:C19H30O2Cor e Forma:NeatPeso molecular:290.44(17β)-N-(1,1-Dimethylethyl)-3-oxoandrost-4-ene-17-carboxamide
CAS:Produto ControladoFórmula:C24H37NO2Cor e Forma:Off-WhitePeso molecular:371.56Prednisolone Tebutate
CAS:Produto Controlado<p>Applications Prednisolone Tebutate is an anaesthetic corticosteroid.<br>References Lewis, A. et al.: Agents and Actions, 10, 258 (1980); Myers, S. et al.: Arthris. Rheum., 28, 1275 (1985);<br></p>Fórmula:C27H38O6Cor e Forma:NeatPeso molecular:458.59Bisnorcholenaldehyde
CAS:Produto Controlado<p>Applications Bisnorcholenaldehyde can be used to prepare 27-Nor-Δ4-dafachronic acid as a synthetic ligand of Caenorhabditis elegans DAF-12 receptor. It is also used to synthesize 3β,6α-dihydroxy-5α-cholan-23-one.<br>References Samaja, G., et al.: Bioorg. Med. Chem. Lett., 23, 2893 (2013); Nahar, L., et al.: Tetrahedron, 59, 8623 (2003)<br></p>Fórmula:C22H32O2Cor e Forma:NeatPeso molecular:328.49Digitoxigenin
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications Digitoxigenin has been used in a study to assess its stereochemical effects in cancer cytotoxicity. It has also been used in a study to investigate the advantage of gold(I)-catalyzed glycosidation of glycosyl o-alkyl benzoates to assemble digitoxin.<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 Hinds, J., et al.: Chemmedchem, 8, 63 (2013); Ma, Y., et al.: J. Org. Chem., 76, 9748 (2011)<br></p>Fórmula:C23H34O4Cor e Forma:NeatPeso molecular:374.51Lathosterol
CAS:<p>Applications A Cholesterol (C432501) metabolite. Lathosterol (indicating cholesterol synthesis) and Sitosterol (indicating cholesterol absorption) also decreased with deteriorating health. Low Lathosterol, Sitosterol (S497050), and Cholesterol (C432501) predicted mortality additively and independently of each other.<br>References Chyou, P., et al.: Age Ageing, 29, 69 (2000), Schatz, I., et al.: Lancet, 358, 351 (2001), Bjorkman, M., et al.: Eur. J. Endocrinol., 158, 749 (2008),<br></p>Fórmula:C27H46OCor e Forma:White To Off-WhitePeso molecular:386.65Betamethasone Tripropionate
CAS:<p>Impurity Betamethasone Dipropionate EP Impurity G<br>Applications Betamethasone Tripropionate (Betamethasone Dipropionate EP Impurity G) is a Betamethasone (B327000) related compound.<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:C31H41FO8Cor e Forma:NeatPeso molecular:560.652,3-Dichloro-5,6-dicyanobenzoquinone
CAS:<p>Applications An oxidizing agent, especially in steroid synthesis.<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></p>Fórmula:C8Cl2N2O2Cor e Forma:NeatPeso molecular:227.011-Deoxy Corticosterone-d7
CAS:Produto Controlado<p>Applications Labelled Deoxycorticosterone. A mineralocorticoid that occurs in adrenal cortex. It acts as a precursor to Aldosterone (A514700).<br>References Bohl, C., et al.: J. Med.Chem., 47, 3765 (2004), Smith, J., et al.: Steroids, 73, 1160 (2008),<br></p>Fórmula:C21H23D7O3Cor e Forma:White To Off-WhitePeso molecular:337.53β-Hydroxy Tibolone
CAS:Produto Controlado<p>Applications A metabolite of Tibolone. A synthetic steroid with weak estrogenic, androgenic and progestogenic activity. A pharamceutical used in the treatment of menopausal syndrome.<br>References Belman, S., et al.: Cancer Res., 32, 450 (1972), Shirahashi, H., et al.: Chem. Pharm. Bull., 41, 1664 (1993), Hoyte, R., et al.: Steroids, 58, 13 (1993), Sandker, G., et al.: Xenobiotica, 24, 143 (1994), Colombo, D., et al.: Eur. J. Med. Chem., 40, 69 (2005),<br></p>Fórmula:C21H30O2Cor e Forma:White To Off-WhitePeso molecular:314.46Betamethasone 17-Butyrate
CAS:Produto Controlado<p>Applications Betamethasone 17-Butyrate is an impurity of Clobetasone 17-Butyrate (C583550), an glucocorticoid used for anti-inflammatory purposes.<br></p>Fórmula:C26H35FO6Cor e Forma:NeatPeso molecular:462.55Lithocolic acid
CAS:Pureza:98.0%Cor e Forma:Solid, White to very pale yellow powderPeso molecular:376.58099365234375Tetrahydrocortisol
CAS:Produto Controlado<p>Applications Tetrahydrocortisol is excreted in large amounts in premenopausal patients with early breast cancer. Tetrahydrocortisol has been found to be produced by lymphocytes in both normal and cancer bearing patients however, the concentration of Tetrahydrocortisol has increased in patients with cancer.<br>References Kodama, M., et. al.: J. Natl. Cancer I., 54, 1275 (1975); Klein, A., et. al.: Metabolism, 27, 731 (1978)<br></p>Fórmula:C21H34O5Cor e Forma:Off-WhitePeso molecular:366.49(6a,11b,16a)-21-(Acetyloxy)-6,9-difluoro-11,16,17-trihydroxypregna-1,4-diene-3,20-dione
CAS:Produto Controlado<p>Applications (6α,11β,16α)-21-(Acetyloxy)-6,9-difluoro-11,16,17-trihydroxypregna-1,4-diene-3,20-dione is an impurity of Fluocinolone Acetonide, Glucocorticoid; anti-inflammatory.<br>References Sammul, et al.: J. Assoc. Off. Agric. Chem., 47, 952 (1964), Emerson, M.V., et al.: BioDrugs, 21, 245 (2007),<br></p>Fórmula:C23H28F2O7Cor e Forma:NeatPeso molecular:454.466-Ethylchenodeoxycholic-d5 Acid
CAS:Produto Controlado<p>Applications 6-Ethylchenodeoxycholic-d5 Acid is an isotope labelled compound of 6-Ethylchenodeoxycholic Acid (E899810), which is used in the investigative treatment of primary biliary cholangitis. Primary biliary cholangitis is an autoimmune disease of the liver that slowly progresses to cirrhosis.<br>References Ali, A. H, et al.: Expert Opin. Orphan Drugs, 4, 1011 (2016)<br></p>Fórmula:C26H39D5O4Cor e Forma:NeatPeso molecular:425.66Testosterone-16,16,17-d3
CAS:Produto Controlado<p>Applications Labelled Testosterone (T155000). Principal hormone of the testes, produced by the interstitial cells. Major circulating androgen; converted by 5α-reductase in androgen-dependent target tissues to 5α-dehydrotestosterone which is required for normal male sexual differentiation. Also converted by aromatization to Estradiol.Controlled substance (anabolic steroid). Androgen.<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 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:C192H3H25O2Cor e Forma:NeatPeso molecular:291.44Desmosterol
CAS:<p>Applications A metabolite of Cholesterol (C432501).<br>References Marx, J., et al.: Science, 294, 508 (2001), Plosch, T., et al.: J. Biol. Chem., 277, 33870 (2002), Lund, E., et al.: J .Biol. Chem., 278, 22980 (2003),<br></p>Fórmula:C27H44OCor e Forma:White To Off-WhitePeso molecular:384.6417-Deoxy Cortienic Acid
CAS:<p>Applications 17-Deoxy Cortienic Acid was used in the synthetic preparation of macrolactonolides, a class of potential antiinflammatory drugs.<br>References Tomaskovic, L., et al.: Bioorg. Med. Chem., 21, 321 (2013); Little, R.J., et al.: Pharma. Res., 16, 961 (1999); Manz. B., et al.: J. Steroid. Biochem., 17, 335 (1982);<br></p>Fórmula:C20H28O4Cor e Forma:NeatPeso molecular:332.43
