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 4949 produtos de "Esteroides e Derivados"
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Prednival
CAS:Produto Controlado<p>Applications Prednival was used in the study of inflammation-inhibiting activity of steroids.<br>References Bodor, N., et al.: J. Med. Chem., 26, 318 (1983); Stouch, T., et al.: J. Med. Chem., 29, 2125 (2986);<br></p>Fórmula:C26H36O6Cor e Forma:NeatPeso molecular:444.56Testosterone 17β-Hemisuccinate
CAS:Produto ControladoFórmula:C23H32O5Cor e Forma:NeatPeso molecular:388.4977α-Hydroxy-4-cholesten-3-one
CAS:<p>Applications 7α-Hydroxy-4-cholesten-3-one is a metabolite of Cholesterol (C432501).<br>References Connor, W., et al.: J, Clin. Invest., 48, 1363 (1969), Nestel, P., et al.: Metabolism, 24, 189 (1975), Ellegard, L., et al.: Eur. J. Clin. Nutr., 45, 451 (1991), Pedersen, A., et al.: J. Lipid Res., 41, 1901 (2000),<br></p>Fórmula:C27H44O2Cor e Forma:NeatPeso molecular:400.64Algestone
CAS:Produto Controlado<p>Applications A pregnane steroid, its acetonide is used as anti-inflammatory drug (topical) and combination with enanthate as injectable contraceptive.<br>References Hydorn, A., et al.: Steroids, 3, 493 (1964), Plesner, R., et al.: Acta Endorcinol., 61, 494 (1969),<br></p>Fórmula:C21H30O4Cor e Forma:NeatPeso molecular:346.46Pregnenolone monosulfate
CAS:<p>Pregnenolone monosulfate (3β-Hydroxy-5-pregnen-20-one monosulfate) is a potent nootropic steroid used in the study of neuroticism and depression.</p>Fórmula:C21H32O5SPureza:99.46%Cor e Forma:SolidPeso molecular:396.54Dexamethasone Valerate
CAS:<p>Impurity Betamethasone Valerate EP Impurity C<br>Stability Hygroscopic<br>Applications Dexamethasone Valerate (Betamethasone Valerate EP Impurity C) is an impurity of Dexamethasone (D298800), which is a glucocorticoid that is 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:C27H37FO6Cor e Forma:Off-WhitePeso molecular:476.58Etonogestrel β-D-Glucuronide
Produto Controlado<p>Applications A metabolite of Etonogestrel.<br></p>Fórmula:C28H36O8Cor e Forma:NeatPeso molecular:500.58117β-Estradiol-d4
CAS:Produto 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:C182H4H20O2Cor e Forma:Off-WhitePeso molecular:276.41Lasofoxifene
CAS:<p>Applications A next-generation selective estrogen receptor modulator for treating disorders associated with increased bone turnover and osteopenia.<br>References Baumann, R., et al.: Biochem. Pharmacol., 55, 841 (1998), Ammann, P., et al.: Osteoporos Int., 10, 369 (1999), Alexandersen, P., et al.: J. Clin. Endocrinol. Metab., 86, 755 (2001), Bourrin, S., et al.: Bone, 30, 195 (2002), Buzdar, A., et al.: J. Clin. Oncol., 21, 1007 (2003),<br></p>Fórmula:C28H31NO2Cor e Forma:NeatPeso molecular:413.556β-Hydroxy Betamethasone
CAS:Produto Controlado<p>Applications 6β-Hydroxy Betamethasone can be used as analyte in analytical study for detecting betamethasone metabolites in human urine using liquid chromatography coupled to tandem mass spectrometry.<br>References Matabosch, X., et al.: Drug Testing and Analysis, 7, 663-672 (2015)<br></p>Fórmula:C22H29FO6Cor e Forma:NeatPeso molecular:408.46Ref: 10-F794924
5gA consultar10gA consultar25gA consultar100gA consultar250gA consultar500gA consultar100mgA consultarBetamethasone 11,21-Diacetate
CAS:Produto Controlado<p>Impurity Betamethasone Acetate EP Impurity C<br>Applications Betamethasone 11β,21-Diacetate is an impurity of Betamethasone 21-Acetate (B327025); a glucocorticoid steroid with anti-inflammatory and immunosuppressive properties which can be used in treatment of asthma and itching.<br>References Kerns, E., et al.: J. Pharm. Sci., 90, 1838 (2001); Seidler, J., et al.: J. Med. Chem., 46, 4477 (2003); Alsenz, J., et al.: J. Pharm. Sci., 96, 1748 (2007)<br></p>Fórmula:C26H33FO7Cor e Forma:WhitePeso molecular:476.53Estetrol
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:304.38Estradiol Enanthate
CAS:<p>Applications Estradiol Enanthate has been used as an injectable contraceptive.<br>References Coutinho, E.M., et. al.: Contraception, 73, 249 (2006)<br></p>Fórmula:C25H36O3Cor e Forma:BeigePeso molecular:384.55Deflazacort
CAS:Produto Controlado<p>Applications A systemic corticosteroid. A derivative of prednisolone. Used for rheumatoid arthritis and lupus.<br>References Nathansohn, G., et al.: J. Med. Chem., 10,799 (1967), Schiatti, P., et al.: Arzneim. Forsch., 30, 1543 (1980), Cavall-Perin, P., et al.: Eur. J. Clin. Pharmacol., 26, 357 (1984), Imbimbo, B., et al.: Adv. Exp. Med. Biol., 171, 241 (1984),<br></p>Fórmula:C25H31NO6Cor e Forma:NeatPeso molecular:441.525(6)-Dehydro-4(5)-dihydro D-(-)-Norgestrel (>90%)
CAS:Produto Controlado<p>Impurity Levonorgestrel EP Impurity P<br>Applications 5(6)-Dehydro-4(5)-dihydro D-(-)-Norgestrel (Levonorgestrel EP Impurity P) is a Norgestrel (N689500) impurity.<br></p>Fórmula:C21H28O2Pureza:>90%Cor e Forma:NeatPeso molecular:312.45Gestrinone
CAS:Produto Controlado<p>Applications Gestrinone is a Steroidal antiestrogen, antiprogestogen, analog of Norgestrienone. Antigonadotropin.Controlled substance.<br>References Azadian-Boulanger, G., et al.: Am. J. Obstet. Gynecol., 125, 1049 (1976), Thomas, E.J., et al.: Br. Med. J., 294, 272 (1987), Coutinho, E.M., et al.: Fertil. Steril., 49, 418 (1988),<br></p>Fórmula:C21H24O2Cor e Forma:NeatPeso molecular:308.40Corticosterone
CAS:Produto Controlado<p>Applications Glucocorticoid; an intermediate in the biosynthesis of aldosterone, isolated from the adrenal cortex.<br>References Schmidt, M., et al.: Endocrinol., 150, 2709 (2009), Bailey, M., et al.: J. Immunol., 182, 7888 (2009), Brunton, P., et al.: J. Neurosci., 29, 6449 (2009), Pruett, S., et al.: Toxicol. Sci., 109, 265 (2009),<br></p>Fórmula:C21H30O4Cor e Forma:NeatPeso molecular:346.4611-Deoxy Prednisolone
CAS:Produto Controlado<p>Impurity Prednisolone EP Impurity J<br>Applications 11-Deoxy Prednisolone (Prednisolone EP Impurity J) is a Prednisolone (P703740) derivative as a corticosteroid.<br>References Kobayashi, Y., et al.: Biol. Pharm. Bull., 16, 1175 (1993), Ogata, M., et al.: J. Pharm. Sci., 87, 91 (1998), Hou, S., et al.: J. Pharm. Biomed. Anal., 24, 371 (2001),<br></p>Fórmula:C21H28O4Cor e Forma:Light BrownPeso molecular:344.4411-Keto Budesonide (Mixture of Diastereomers)
CAS:Produto Controlado<p>Impurity Budesonide EP Impurity L<br>Applications 11-Keto Budesonide (Budesonide EP Impurity L) is an impurity of Budesonide (B689490), an antiinflammatory agent.<br>References Brattsand, R., et al.: J. Steroid Biochem., 16, 779 (1982), Clissold, S., et al.: Drugs, 28, 485 (1984), Edsbacker, S., et al.: Drug Metab. Dispos., 15, 403 (1987), Pozo, O., et al.: Anal. Bioanal. Chem., 398, 1759 (2010),<br></p>Fórmula:C25H32O6Cor e Forma:Off WhitePeso molecular:428.525,6-trans-Vitamin D3
CAS:<p>5,6-trans-Vitamin D3（5,6-trans-Cholecalciferol） is an isoform of Vitamin D3, which is converted from Vitamin D3 on the skin surface after light exposure.</p>Fórmula:C27H44OPureza:98.23%Cor e Forma:SolidPeso molecular:384.64δ7-Stigmasterol
CAS:Produto Controlado<p>Applications Δ7-Stigmasterol 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>Fórmula:C29H46OCor e Forma:White To Light YellowPeso molecular:410.67Ethynyl Estradiol-2,4,16,16-d4
CAS:Produto Controlado<p>Applications Isotope labelled Ethynyl Estradiol (E685100), an oral contraceptive (1), is a synthetic steroid with high oral estrogenic potency. Used in estrogen replacement therapy (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> 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 1. Koetsawang, S. et al.: Contraception. 1982 March:25(3) p231-2412. Cuttler, L. et al.: J. Endocrinol. Metab. 1985 Jun;60(6):1087-92.<br></p>Fórmula:C202H4H20O2Cor e Forma:White To Light YellowPeso molecular:300.434-Hydroxy-17β-estradiol
CAS:Produto Controlado<p>Applications A metabolite of Estradiol.<br>References Bucala, R., et al.: J. Clin. Endocrinol. Metab., 60, 841 (1985), Telang, N., et al.: Anticancer Res., et al.: 11, 1021 (1991), Seeger, H., et al.: Med. Sci. Res., 26, 481 (1998), Bolton, J., et al.: Chem. Res. Toxicol., 13, 135 (2000),<br></p>Fórmula:C18H24O3Cor e Forma:FluidPeso molecular:288.383α-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:314.46D-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:286.41Estrone sulfate sodium
CAS:<p>Estrone sulfate sodium, an inactive estrogen ester, transforms into estrone via steroid sulfatase. It's studied for targeting polypeptide transporters.</p>Fórmula:C18H21NaO5SPureza:98% - 99.83%Cor e Forma:SolidPeso molecular:372.41trans-Latanoprost Acid
CAS:Produto Controlado<p>Applications The trans metabolite of Latanoprost (L177280), Prostaglandin analog.<br>References Botchkareva, N., et al.: FASEB J., 115, 645 (2001),<br></p>Fórmula:C23H34O5Cor e Forma:NeatPeso molecular:390.5139α-Bromodesonide ~90%
CAS:Produto Controlado<p>Applications 9α-Bromodesonide is a bromo derivative of Desonide (D296940); an anti-inflammatory agent.<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:C24H31BrO6Pureza:~90%Cor e Forma:YellowPeso molecular:495.403320α-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:314.462Dienestrol
CAS:<p>Applications Dienestrol is a metabolite of Diethylstilbestrol, a non-steroidal synthetic estrogen derivative.<br>References Liehr, J.G., et al.: Steroids, 40, 713 (1982); Yearley, E. et al.: J. Mol. Struct., 890, 240 (2008);<br></p>Fórmula:C18H18O2Cor e Forma:NeatPeso molecular:266.335α-Pregnane-3β,20(S)-diol
CAS:Produto Controlado<p>Applications 5α-Pregnane-3β,20(S)-diol, is a metabolite of Progesterone (P755900).<br>References Beall, et al.: Biochem. J., 31, 35 (1937), Okuda, A., et al.: J. Biol. Chem., 259, 7519 (1984), Russell, D., et al.: Biochemistry, 31, 4737 (1992), Kondo, K., et al.: Eur. J. Biochem., 219, 357 (1994), Westerbacka, J., et al.: J. Clin. Endocrinol. Metab., 88, 4924 (2003),<br></p>Fórmula:C21H36O2Cor e Forma:NeatPeso molecular:320.511,2-Dihydrobudesonide (Mixture of diastereomers)
CAS:Produto Controlado<p>Impurity Budesonide EP Impurity G<br>Applications 1,2-Dehydrobudesonide (Budesonide EP Impurity G) is an impurity in the synthesis of Budesonide (B689490), a non-halogenated glucocorticoid related to triamcinolone hexacetonide. Used as an antiinflammatory agent.<br>References Ryrfeldt., A., et a.: J. Steroid Biochem., 10, 317 (1979), Roth, G., et al.: J. Pharm. Sci., 69, 766 (1980), Clissold, S.P., et al.: Drugs, 28, 485 (1984),<br></p>Fórmula:C25H36O6Cor e Forma:NeatPeso molecular:432.55Budesonide-d6
CAS:Produto Controlado<p>Applications Labelled Budesonide, a non-halogenated glucocorticoid related to triamcinolone hexacetonide. Used as an antiinflammatory agent.<br>References Ryrfeldt., A., et a.: J. Steroid Biochem., 10, 317 (1979), Roth, G., et al.: J. Pharm. Sci., 69, 766 (1980), Clissold, S.P., et al.: Drugs, 28, 485 (1984),<br></p>Fórmula:C25H28D6O6Cor e Forma:NeatPeso molecular:436.5722α-Hydroxy Cholesterol
CAS:Produto Controlado<p>Applications The 22R-metabolite of Cholesterol (C432501). 22-Hydroxycholesterol inhibits chemokine receptor activity.<br>References Samson, M., et al.: J. Biol. Chem., 272, 24934 (1997), Mackay, C., et al.: Nature Immunol., 2, 95 (2001), Navenot, J., et al.: J. Mol. Biol., 313, 1181 (2001),<br></p>Fórmula:C27H46O2Cor e Forma:NeatPeso molecular:402.65Norgestrel
CAS:Produto Controlado<p>Applications Norgestrel 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:C21H28O2Cor e Forma:White To Off-WhitePeso molecular:312.45Testosterone 17-O-Acetate
CAS:Produto Controlado<p>Applications An Androgen.Controlled substance.<br>References Alikhan, A., et al.: J. App. Toxicol., 29, 590 (2009), Christy H., et al.: J. Steroid Biochem. Mol. Biol., 116, 171 (2009), Li, C., et al.: Steroids, 75, 859 (2010),<br></p>Fórmula:C21H30O3Cor e Forma:NeatPeso molecular:330.46Testosterone-d3 (100 ug/mL in Acetonitrile)
CAS:Produto ControladoFórmula:C192H3H25O2Cor e Forma:Single SolutionPeso molecular:291.4417α-Hydroxy Progesterone-d8
CAS:Produto Controlado<p>Applications Labelled 17α-Hydroxyprogesterone (H952330). 17α-Hydroxy Progesterone is a metabolite of Progesterone. It was isolated from adrenal glands.<br>References Pfiffner, N., et al.: J. Biol. Chem., 132, 459 (1940), Florey, K., et al.: Anal. Profiles Drug Subs.,4, 209 (1975),<br></p>Fórmula:C212H8H22O3Cor e Forma:Off-WhitePeso molecular:338.5116α-Homo 2-(Hydroxymethyl)betamethasone
CAS:Produto ControladoFórmula:C22H29FO5Cor e Forma:NeatPeso molecular:392.4615β-Dihydrocortisone Acetate 21-Acetate
CAS:Produto Controlado<p>Applications Cortisone (C696500) derivative.<br></p>Fórmula:C23H32O6Cor e Forma:NeatPeso molecular:404.5Pregnenolone-d6
CAS:Produto Controlado<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>Fórmula:C21D6H26O2Cor e Forma:NeatPeso molecular:322.51Estradiol Benzoate
CAS:<p>Applications Estradiol is the major estrogen secreted by the premenopausal ovary. Estradiol benzoate is an estradiol analog which contains a benzyl ester at the C-3 position. Estradiol benzoate is useful in the treatment of lesions produced by diminution of bodily production of estrogens.<br>References MacLusky, N., et al.: Endocrinology, 106, 192 (1980), Apostolakis, E., et al.: J. Neurosci., 16, 4823 (1996), Guarraci, F., et al.: Brain Res., 999, 40 (2004), Petralia, S., et al.: J. Neuroendocrinol., 18, 902 (2006),<br></p>Fórmula:C25H28O3Cor e Forma:WhitePeso molecular:376.49Betamethasone 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:560.65Estriol Trisulfate Trisodium Salt
CAS:<p>Applications Estriol Trisulfate Trisodium Salt (cas# 100940-55-4) is a compound useful in organic synthesis.<br></p>Fórmula:C18H21Na3O12S3Cor e Forma:NeatPeso molecular:594.52Digoxin
CAS:Produto Controlado<p>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 Aronson, J.K., et al.: Clin. Pharmacokinet, 5,137 (1980), Foss, P.R.B., Anal. Profiles Drug Subs., 9, 207 (1980),<br></p>Fórmula:C41H64O14Cor e Forma:WhitePeso molecular:780.942-Hydroxymethylene Ethisterone
CAS:Produto Controlado<p>Applications A derivative of Danazol (D145000).<br>References Manson, A.J., et al.: J. Med. Chem., 6, 1 (1963), Jordan, V.C., et al.: Endocrinology, 124, 1717 (1989),<br></p>Fórmula:C22H28O3Cor e Forma:NeatPeso molecular:340.46Estrone b-D-Glucuronide Sodium Salt (>97% by HPLC)
CAS:Produto Controlado<p>Applications A metabolite of 17β -Estradiol (E888000).<br>References Cekan, S., et al.: J. Steroid Biochem., 27, 95 (1989), Martin, R., et al.: Clin. Chem., 46, 100 (2000), Blackwell, L., et al.: Steroids, 68, 465 (2003)<br></p>Fórmula:C24H29O8·NaPureza:>97% by HPLCCor e Forma:White To Light BrownPeso molecular:468.475β-Pregnan-3α-ol-20-one
CAS:Produto Controlado<p>Applications A hyponotic-anaesthetic agent.<br>References Gyermek, et al.: J. Med. Chem., 11, 117 (1968)<br></p>Fórmula:C21H34O2Cor e Forma:NeatPeso molecular:318.50Hexestrol-d4
CAS:Produto Controlado<p>Applications Estrogen; antineoplastic (hormonal).<br>References Aboul-Enein, H.Y., et al.: Anal. Profiles Drug Subs., 11, 347 (1982),<br></p>Fórmula:C182H4H18O2Cor e Forma:White To Off-WhitePeso molecular:274.395a-Dihydrolevonorgestrel
CAS:Produto Controlado<p>Applications 5α-Dihydrolevonorgestrel is the reduced analogue of levonorgestrel (N689510), a safe, tolerated and effective emergency contraceptive for women.<br>References Cabeza, M., et al.: Steroids., 60, 630 (1995); Lemus, A.E., et al.: J. Steroid. Biochem. Molec. Biol., 41,881 (1992); Bergink. E.W., et al.: J. Steroids. Biochem., 14, 175 (1981);<br></p>Fórmula:C21H30O2Cor e Forma:NeatPeso molecular:314.4621-Deacetoxy Deflazacort
CAS:Produto Controlado<p>Applications An intermediate of Deflazacort (D228975), a systematic corticosteroid.<br>References Nathansohn, G. et al.: Steroids, 13, 365 (1969); Nathansohn, G., et al.: J. Med. Chem., 10,799 (1967), Schiatti, P., et al.: Arzneim. Forsch., 30, 1543 (1980),<br></p>Fórmula:C23H29NO4Cor e Forma:NeatPeso molecular:383.48Fluocinolone Acetonide-21-aldehyde
CAS:<p>Impurity Fluocinolone Acetonide EP Impurity D<br>Stability Hygroscopic<br>Applications Fluocinolone acetonide-21-aldehyde, is a derivative of Fluocinolone Acetonide (F455800), which is a Corticosteroid, used in dermatology to reduce skin inflammation and relieve itching.<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:C24H28F2O6Cor e Forma:White To Light YellowPeso molecular:450.47(17a)-3-Ethynyl-19-norpregna-3,5-dien-20-yn-17-ol
CAS:<p>Impurity Norethindrone EP Impurity E<br>Applications (17α)-3-Ethynyl-19-norpregna-3,5-dien-20-yn-17-ol (Norethindrone EP Impurity E) is an impurity of Norethindrone (N676000).<br></p>Fórmula:C22H26OCor e Forma:NeatPeso molecular:306.44Fluvastatin
CAS:<p>Fluvastatin (XU-62320) is an HMG-CoA reductase inhibitor used to lower plasma cholesterol levels and prevent cardiovascular disease.</p>Fórmula:C24H26FNO4Pureza:98.94%Cor e Forma:SolidPeso molecular:411.477b-Fulvestrant
CAS:Produto Controlado<p>Impurity Fulvestrant EP Impurity A<br>Applications Fulvestrant (F862500) impurity A. The S-isomer of Fulvestrant.<br>References Sharman, G.J., et al.: Mag. Resonance Chem., 39, 549 (2001),<br></p>Fórmula:C32H47F5O3SCor e Forma:Light Brown SolidPeso molecular:606.776-β-Hydroxy Eplerenone
CAS:<p>Applications A metabolite of Eplerenone, which is used alone or in combination with other medications to treat high blood pressure. Eplerenone is in a class of medications called mineralocorticoid receptor antagonists. It works by blocking the action of aldosterone, a natural substance in the body that raises blood pressure.<br></p>Fórmula:C24H30O7Cor e Forma:White To Off-WhitePeso molecular:430.49Dydrogesterone
CAS:Produto Controlado<p>Applications A synthetic progestin largely used in hormone therapy, on the central nervous system by studying two markers of the neuroendocrine function: the neurosteroid allopregnanolone and the opioid .beta.-endorphin. Progestogen.<br>References Bernardi, F., et al.: Eur. J. Endocrinol., 138, 316 (1998), Rupprecht, R., et al.: Steroids, 64, 83 (1999), Uzunova, V., et al.: Brain Res., 976, 1 (2003), Pluchino, N., et al.: J. Steroid Biochem. Mol. Biol., 102, 205 (2006),<br></p>Fórmula:C21H28O2Cor e Forma:NeatPeso molecular:312.45Spironolactone
CAS:Produto Controlado<p>Applications It is a synthetic 17-lactone steroid which is a renal competitive aldosterone antagonist in a class of pharmaceuticals called potassium-sparing diuretics, used primarily to treat ascites in patients with liver disease, low-renin hypertension, hypokalemia, and Conn’s syndrome.<br>References Sutter, J.L., et al.: Anal. Profiles Drug Subs., 4, 431 (1975),<br></p>Fórmula:C24H32O4SCor e Forma:Off-WhitePeso molecular:416.57Testosterone Undecylenate
CAS:Produto 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:C30H46O3Cor e Forma:NeatPeso molecular:454.684Eplerenone 7-Carboxylic Acid
CAS:<p>Applications Eplerenone 7-Carboxylic Acid is an impurity of Eplerenone (E588775). Eplerenone is a selective aldosterone receptor antagonist (SARA), structurally similar to Spiranolactone. Eplerenone is used alone or in combination with other medications to treat high blood pressure. Eplerenone is in a class of medications called mineralocorticoid receptor antagonists. It works by blocking the action of aldosterone, a natural substance in the body that raises blood pressure.<br>References de Gasparo, M., et al.: J. Pharmacol. Exp. Ther., 240, 650 (1987), Delyani, J.A., et al.: Cardiovasc. Drug Rev., 19, 185 (2001), Burgess, E., et al.: Expert. Opin. Pharmacother., 5, 2573 (2004), Ravis, W.R., et al.: J. Clin. Pharmacol., 45, 810 (2005),<br></p>Fórmula:C23H28O6Cor e Forma:Off-White To Light YellowPeso molecular:400.462-Hydroxy Atorvastatin-d5 Sodium Salt
CAS:Produto Controlado<p>Applications A deuterated 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>Fórmula:C332H5H28FN2O6·2NaCor e Forma:NeatPeso molecular:623.637α-Thiomethyl Spironolactone-d7 (Major)
CAS:Produto Controlado<p>Applications A labelled metabolite of Spironolactone.<br>References Gochman, N., et al.: J. Pharmacol. Exp. Ther., 135, 312 (1962), Tori, K., et al.: Steroids, 4, 713 (1964), Solymoss, B., et al.: Toxicol. Appli. Pharmacol., 18, 586 (1971),<br></p>Fórmula:C23H25D7O3SCor e Forma:NeatPeso molecular:395.617α-Hydroxy Cholesterol
CAS:Produto Controlado<p>Applications Secondary metabolite of Cholesterol.<br>References Notaro, G., et al.: J. Nat. Prod., 55, 1588 (1992), Aydogmus, Z., et al.: Nat. Prod. Res., 18, 43 (2004), Mao, S., et al.: J. Nat. Prod ., 69, 1209 (2006), Shoji, T., et al.: J. Agric. Food Chem., 54, 884 (2006),<br></p>Fórmula:C27H46O2Cor e Forma:Off-WhitePeso molecular:402.65Dexamethasone-∆17,20 21-Aldehyde
CAS:<p>Applications A degradation and metabolic intermediate of Dexamethasone (D298800). A Dexamethasone enol aldehyde as inflammation inhibitor.<br>References Weiss, G., et al.: J. Clin. Endocrinol. Metab., 43, 696 (1976), Hirschmann R., et al.: Steroids, 57, 579 (1992),<br></p>Fórmula:C22H27FO4Cor e Forma:White To Off-WhitePeso molecular:374.457-Ketoabiraterone Acetate
CAS:Produto Controlado<p>Applications 7-Ketoabiraterone Acetate is an impurity of Abiraterone (A108490), a steroidal cytochrome P 450 17α-hydroxylase-17,20-lyase inhibitor (CYP17), is currently undergoing phase II clinical trials as a potential drug for the treatment of androgen-dependent prostate cancer.<br>References Denis, L., et al.: Cancer, 72, 3888 (1993); Potter, G.A., et al.: J. Med. Chem., 38, 2463 (1995); Denmeade, S., et al.: Nat. Rev., 2, 389(2002); Scher, H., et al.: J. Clin. Oncol., 23, 8253 (2005)<br></p>Fórmula:C26H31NO3Cor e Forma:NeatPeso molecular:405.53o-Flutamide
CAS:Produto Controlado<p>Impurity Flumazenil EP Impurity F<br>Applications o-Flutamide is an isomer of Flutamide (F598850), a nonsteroidal antiandrogen drug; antineoplastic (hormonal).<br>References Neri, et al.: Endocrinology, 91, 427 (1972), Sogani, P.C., et al.: J. Urol., 122, 640 (1979), Greenway, B.A., et al.: Br. Med. J., 316, 1935 (1998),<br></p>Fórmula:C11H11F3N2O3Cor e Forma:NeatPeso molecular:276.21Norethindrone β-D-Glucuronide
CAS:<p>Applications A metabolite of Norethindrone (N676000).<br>References Layne, D.S., et al.: Biochem. Pharmacol., 12, 905 (1963),<br></p>Fórmula:C26H34O8Cor e Forma:NeatPeso molecular:474.54Isovitamin D3 (90%)
CAS:Produto Controlado<p>Stability Light Sensitive<br>Applications Isovitamin D3 is a metabolite of Vitamin D. Studies show that Isovitamin D3 is biologically active in normal rats but inactive in anephric rats.<br>References Holick, M.F. et al.: Science, 180, 964 (1973); Wilczek, H. et al.: Prak. Lek., 59, 794 (1979);<br></p>Fórmula:C27H44OPureza:90%Cor e Forma:NeatPeso molecular:384.644-Hydroxy-17β-estradiol-16,16,17-d5
CAS:Produto Controlado<p>Applications A labelled metabolite of Estradiol.<br>References Bucala, R., et al.: J. Clin. Endocrinol. Metab., 60, 841 (1985), Telang, N., et al.: Anticancer Res., et al.: 11, 1021 (1991), Seeger, H., et al.: Med. Sci. Res., 26, 481 (1998), Bolton, J., et al.: Chem. Res. Toxicol., 13, 135 (2000),<br></p>Fórmula:C182H5H19O3Cor e Forma:NeatPeso molecular:293.41Isoflupredone
CAS:Produto Controlado<p>Applications Anti-inflammatory.<br>References Buchwald, P., et al.: Steroids, 73, 193 (2008), Holbeck, S., et al.: Mol. Endocrinol., 24, 1287 (2010),<br></p>Fórmula:C21H27FO5Cor e Forma:NeatPeso molecular:378.43Testosterone-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:291.4421-Chloro-9-fluoro-11b,17-dihydroxy-16a-methylpregna-1,4-diene-3,20-dione 17-Propionate (>90%)
CAS:<p>Impurity Clobetasol Propionate EP Impurity C<br>Applications 21-Chloro-9-fluoro-11β,17-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione 17-Propionate (Clobetasol Propionate EP Impurity C) is an impurity of Clobetasol 17-Propionate (C583500), an topical corticosteroid with anti-inflammatory properties.<br>References Sugai, S., et al.: Chem. Pharma. Bull., 31, 12 (1983);<br></p>Fórmula:C25H32ClFO5Cor e Forma:NeatPeso molecular:466.974-Hydroxy Estrone 1-N7-Guanine
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications 4-Hydroxy Estrone 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:C23H25N5O4Cor e Forma:NeatPeso molecular:435.48Eplerenone
CAS:<p>Applications Selective aldosterone receptor antagonist (SARA), structurally similar to Spiranolactone. Eplerenone is used alone or in combination with other medications to treat high blood pressure. Eplerenone is in a class of medications called mineralocorticoid receptor antagonists. It works by blocking the action of aldosterone, a natural substance in the body that raises blood pressure.<br>References de Gasparo, M., et al.: J. Pharmacol. Exp. Ther., 240, 650 (1987), Delyani, J.A., et al.: Cardiovasc. Drug Rev., 19, 185 (2001), Burgess, E., et al.: Expert. Opin. Pharmacother., 5, 2573 (2004), Ravis, W.R., et al.: J. Clin. Pharmacol., 45, 810 (2005),<br></p>Fórmula:C24H30O6Cor e Forma:NeatPeso molecular:414.494-Hydroxy Atorvastatin-d5 Disodium Salt
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications A deuterated 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>Fórmula:C33H28D5FN2Na2O6Cor e Forma:NeatPeso molecular:623.63O,O-Dimethyl Methylphosphonate
CAS:Produto Controlado<p>Applications O,O-Dimethyl Methylphosphonate is a commercially used preignition additive for gasoline, anti-foaming agent, plasticizer, stabilizer and antistatic agents.<br>References Jang, S.H., et al.: J. Korean. Phy. Soc., 55, 294 (2009); Schneider, B.B., et al.: Int. J. Mass. Spectro., 298, 45 (2010);<br></p>Fórmula:C3H9O3PCor e Forma:NeatPeso molecular:124.07621-O-Acetyl Dexamethasone-d5
CAS:Produto Controlado<p>Applications Isotope labelled intermediate in the synthesis of Dexamethasone (D298800), a glucocorticoid anti-inflammatory agent.<br>References Liu, Y., et al.: Anal. Bioanal. Chem., 395, 591 (2009), Rodgers, A., et al.: Chem. Res. Toxicol., 23, 724 (2010), Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010),<br></p>Fórmula:C24D5H26FO6Cor e Forma:NeatPeso molecular:439.53Cholesterol-d7
CAS:Produto Controlado<p>Applications Labelled Cholesterol (C432501). 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:C272H7H39OCor e Forma:NeatPeso molecular:393.70Cortisol-9,12,12-d3
CAS:Produto Controlado<p>Applications Isotope labelled Cortisol (H714615) a topical corticosteroid, more specifically a glucocorticoid, produced by the zona fasciculata of the adrenal gland . Cortisol is released in response to stress and a low level of blood glucocorticoids. Its primary functions are to increase blood sugar through gluconeogenesis; suppress the immune system; and aid in fat, protein and carbohydrate metabolism.<br>References Vigore, L., et al.: Cancer Biol Ther.. 15. :699 (2014); Puurunen, J. et al.: J. Clin. Endocrinol. Metab., 94, 1973 (2009);<br></p>Fórmula:C21D3H27O5Cor e Forma:NeatPeso molecular:365.48Lithocolic acid
CAS:Pureza:98.0%Cor e Forma:Solid, White to very pale yellow powderPeso molecular:376.58099365234375Testosterone β-D-Glucuronide Monosodium Salt
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications 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 Metab. Disposition, 37, 417 (2009),<br></p>Fórmula:C25H35O8·NaCor e Forma:White To Off-WhitePeso molecular:486.53Cyproterone-d4
CAS:Produto 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:C22H23D4ClO3Cor e Forma:NeatPeso molecular:378.936b-Hydroxy Norethindrone
CAS:Produto Controlado<p>Impurity Norethindrone EP Impurity H<br>Applications 6β-Hydroxynorethindrone (Norethindrone EP Impurity H) is the 6β-hydroxy analogue of Norethindrone (N676000). 6β-Hydroxynorethindrone is also a metabolite of the progestagen hormone, Lynestrenol.<br>References Choudhary, M.I. et al.: Nat. Prod. Res., 24, 1 (2010); Bagocsi, B. et al.: J. Plan. Chrom. Mod. TLC, 16, 359 (2003);<br></p>Fórmula:C20H26O3Cor e Forma:NeatPeso molecular:314.4217-β-Hydroxy Exemestane
CAS:Produto Controlado<p>Applications A metabolite of Exemestane; exerts biological effects as an androgen.<br>References Howell, A., et al.: Lancet, 365, 60 (2005), Goss, P., et al.: Clin. Cancer Res., 10, 5717 (2004), Buzdar, A., et al.: Lancet Oncol., 7, 633 (2006), Coates, A., et al.: J. Clin. Oncol., 25, 486 (2007), Jordan, V., et al.: Steroids, 72, 7 (2007),<br></p>Fórmula:C20H26O2Cor e Forma:White To Light YellowPeso molecular:298.42Prednisolone 17-Ethyl Carbonate
CAS:<p>Applications A metabolite of Prednicarbate (P703700).<br>References Kumar, R., et al.: Steroids, 64, 310 (1999), Kauppi, B., et al.: Biol. Chem., 278, 22748 (2003), Buchwald, P., et al.: J. Med. Chem., 49, 883 (2006),<br></p>Fórmula:C24H32O7Cor e Forma:White To Off-WhitePeso molecular:432.513,3-Dimethoxyestra-5(10),9(11)-dien-17-one
CAS:<p>Applications 3,3-Dimethoxyestra-5(10),9(11)-dien-17-one, can be used for the synthesis of Trenbolone Acetate (T719080).<br>References Zhang, H., et al.: Fudan Xuebao, Yixueban, 29 (3), 211 (2002);<br></p>Fórmula:C20H28O3Cor e Forma:NeatPeso molecular:316.4317β-Estradiol 3-β-D-Glucuronide
CAS:Produto Controlado<p>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:C24H32O8Cor e Forma:White To Off-WhitePeso molecular:448.51(20S)-21-Hydroxy-20-methylpregn-4-en-3-one
CAS:Produto Controlado<p>Applications (20S)-21-Hydroxy-20-methylpregn-4-en-3-one is a side chain degradation product of natural sterols. It is also an intermediate in the preparation of follicular fluid-meiosis activating sterol.<br>References Andor, A. et al.: Appl. Environ. Microbiol., 72, 6554 (2006); Blume, T. et al.: Org, Lett., 5, 1837 (2003);<br></p>Fórmula:C22H34O2Cor e Forma:Off-WhitePeso molecular:330.56α-Methyl Hydrocortisone 21-Hemisuccinate
CAS:<p>Applications An impurity of Methylhydrocortisone.<br>References Wang, C., et al.: Steroids, 66, 811 (2001),<br></p>Fórmula:C26H36O8Cor e Forma:NeatPeso molecular:476.5620b-Dihydroprogesterone
CAS:Produto 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:C21H32O2Cor e Forma:White To Off-WhitePeso molecular:316.4821-Dehydro Betamethasone (mixture of the aldehyde and the hydrated form)
CAS:Produto Controlado<p>Applications 21-Dehydro Betamethasone is an impurity of Betamethasone (B327000), a corticosteroid used as an anti-inflammatory agent.<br>References Chen, B., et al.: Steroids, 74, 30 (2009); Li, M., et al.: J. Pharm. Sci., 98, 894 (2009); Xiong, Y., et al.: J. Pharm. Biomed. Anal., 49, 646 (2009);<br></p>Fórmula:C22H27FO5Cor e Forma:NeatPeso molecular:390.45Testosterone 17-Valerate
CAS:Produto Controlado<p>Applications Testosterone ester. Testosterone 17-Valerate has been a useful compound in the development of immunochemical techniques for detection of anabolic androgenic steroids in food supplements.<br>References Ruelle, P., et al.: Int. J. Pharm., 157, 219 (1997), de la Torre, X., et al.: J. Pharm. Biomed. Anal., 24, 645 (2001), Adat, S., et al.: Lett. Drug Des. Discov., 1, 334 (2004), Holubova, B., et al.: Eur. Food Res. Technol., 245, 1011 (2019)<br></p>Fórmula:C24H36O3Cor e Forma:NeatPeso molecular:372.5416β-Hydroxy Budesonide
CAS:Produto ControladoFórmula:C25H34O7Cor e Forma:White To Light YellowPeso molecular:446.53
