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 4948 produtos de "Esteroides e Derivados"
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Testosterone-d3 β-D-Glucuronide Monosodium Salt
CAS:Produto Controlado<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>Fórmula:C25H32D3NaO8Cor e Forma:Off-WhitePeso molecular:489.55Betamethasone 17-Propionate-d5
CAS:Produto ControladoFórmula:C25H28D5FO6Cor e Forma:NeatPeso molecular:453.5617-Desacetyl Norgestimate-d6 (Major)
CAS:Produto Controlado<p>Applications A labelled metabolite of Norgestimate.<br>References Phillips, A., et al.: Steroids, 55, 373 (1990)<br></p>Fórmula:C21D6H23NO2Cor e Forma:NeatPeso molecular:333.517-Epiestriol
CAS:Produto Controlado<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>Fórmula:C18H24O3Cor e Forma:White To Light RedPeso molecular:288.38Calcipotriol Monohydrate
CAS:Produto Controlado<p>Applications Calcipotriol Monohydrate is a synthetic derivative of calcitriol, which is a biologically active form of Vitamin D3 (1). Calcipotriol Monohydrate can be used to treat psoriasis (2).<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) Kim, D. H., et al.: Ann Dermatol. 24, 341 (2012) (2) Queille-Roussel, C., et al.: Clin Drug Investig (2016)<br></p>Fórmula:C27H40O3·H2OCor e Forma:NeatPeso molecular:430.62Fulvestrant 9-Sulfone
CAS:Produto Controlado<p>Impurity Fulvestrant EP Impurity B<br>Applications A metabolite of Fulvestrant (F862500).<br>References Rao, P., et al.: J. Steroid Biochem., 25, 417 (1986), Wakeling, A., et al.: J. Steroid Biochem. Mol. Biol., 43, 173 (1992), DeFriend, D., et al.: Cancer Res., 54, 408 (1994),<br></p>Fórmula:C32H47F5O4SCor e Forma:NeatPeso molecular:622.77Ospemifene
CAS:Produto Controlado<p>Applications Ospemifene is used to treat dyspareunia. It is a selective estrogen receptor modulator (SERM) acting similarly to an estrogen.<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 Rutanen, E., et al.: Menopause, 10, 433 (2003);<br></p>Fórmula:C24H23ClO2Cor e Forma:White To Off-WhitePeso molecular:378.895β-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:392.46117-epi-Testosterone
CAS:Produto Controlado<p>Applications Testosterone and epitestosterone 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:C19H28O2Cor e Forma:White To Light YellowPeso molecular:288.42Betamethasone 6α-Bromo 17-Valerate
Produto Controlado<p>Applications Betamethasone 6α-Bromo 17-Valerate is an impurity of Betamethasone (B327000), which is a glucocorticoid used as an anti-inflammatory agent.<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:C27H36BrFO6Cor e Forma:NeatPeso molecular:555.479,11-Anhydrobudesonide(Mixture of Diastereomers)
CAS:Produto Controlado<p>Impurity Budesonide EP Impurity H<br>Applications 9,11-Anhydrobudesonide (Budesonide EP Impurity H) is an impurity of Budesonide (B689460), a non-halogenated glucocorticoid intended for the local treatment of lung disease.<br>References Ryrfeldt, Å., et al.: Eur. J. Respir. Dis., 122, 86 (1981); Vestbo, J., et al.: Lancet, 353, 1819 (1999)<br></p>Fórmula:C25H32O5Cor e Forma:NeatPeso molecular:412.52Triamcinolone 16,21-Diacetate
CAS:Produto Controlado<p>Applications A glucocorticoid that inhibits prolyl hydroxylase activity and used as an antiasthmatic and antiallergic drug.<br>References Kos-Kudla, B. et al.; J. Clin. Pharm. Ther., 28, 103 (2003); Hochhaus, G. et al.; Pharmaceut. Res., 7, 558 (1990); Counts, D. et al.: Mol. Pharmacol., 15, 99 (1979); Cutroneo, K. et al.; Mol. Pharmacol., 11, 632 (1975); Cutroneo, K. et al.: Mol. Pharmacol., 11, 44 (1975)<br></p>Fórmula:C25H31FO8Cor e Forma:NeatPeso molecular:478.5117-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:432.5115-Keto Travoprost
CAS:Produto Controlado<p>Stability Light Sensitive<br>Applications An impurity of the selective FP prostaglandin receptor agonist Travoprost (T715600) used as an ocularly applied intraocular pressure reducing agent.<br></p>Fórmula:C26H33F3O6Cor e Forma:NeatPeso molecular:498.53(22R)-Budesonide
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications Budesonide (B689490) epimer R. Budesonide 22R epimer is more active than 22S epimer. 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:C25H34O6Cor e Forma:NeatPeso molecular:430.53Prednisolone 21-Methanesulfonate
CAS:Produto ControladoFórmula:C22H30O7SCor e Forma:NeatPeso molecular:438.5344-Methoxy Estrone-13C,d3
CAS:Produto Controlado<p>Applications Labelled 4-Methoxyestrone (M226135). An endogenous estrogen metabolite, risk-factor for development of breast cancer.<br>References Beral, V., et al.: Lancet, 362, 419 (2003), Nelson, R., et al.: Clin. Chem., 50, 373 (2004), Malekinejad, H., et al.: J. Agric. Food Chem., 54, 9785 (2006),<br></p>Fórmula:CC182H3H21O3Cor e Forma:Off-White To Light YellowPeso molecular:304.40Androstane Spin Label (ASL)
CAS:Produto Controlado<p>Applications Androstane Spin Label (ASL) is a spin labelled Androstane used to mimic Androstane.<br>References Scheidt, H., et al.: J. Biol. Chem., 278, 45563 (2003);<br></p>Fórmula:C23H38NO3Cor e Forma:NeatPeso molecular:376.55(betaS,deltaS)-2-(4-Fluorophenyl)-β,δ-dihydroxy-5- (1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole- 1-heptanoic acid calcium salt (2:1)
CAS:<p>(betaS,deltaS)-2-(4-Fluorophenyl)-beta,delta-dihydroxy-5- (1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole- 1-heptanoic acid calcium salt (2:1) is a fluorinated derivative of the natural metabolite 2-(4-fluorophenyl)-beta,delta-dihydroxy -5-(1 methylethyl)-3 phenyl 4-[(phenylamino)carbonyl]-1H pyrrole 1 heptanoic acid. It is an enantiomer of the racemate with optical purity > 98%. The compound has been used as a pharmacological and supramolecular chemistry probe for assays and chemosensors.</p>Fórmula:C66H68CaF2N4O10Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:1,155.34 g/mol(5α)-17-(3-Pyridinyl)androst-16-en-3-one
CAS:Produto Controlado<p>(5α)-17-(3-Pyridinyl)androst-16-en-3-one is a natural metabolite of testosterone that is produced in the liver. It has been identified as an impurity in API, which can be found in drugs used for the treatment of high blood pressure and prostate cancer. (5α)-17-(3-Pyridinyl)androst-16-en-3-one is not active as a drug itself, but it can be used as a standard to study the metabolism of testosterone and other steroids.</p>Fórmula:C24H31NOPureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:349.51 g/molAtorvastatin lactone
CAS:<p>Atorvastatin lactone is a prodrug for atorvastatin. It is an inhibitor of the enzyme HMG-CoA reductase, which is involved in cholesterol synthesis and reduces LDL cholesterol levels. Atorvastatin lactone is absorbed from the gut into the bloodstream and then converted to atorvastatin, which has a higher potency than atorvastatin lactone. This conversion occurs in the liver by cytochrome P450 enzymes, including cytochrome CYP3A4. The pharmacokinetics of atorvastatin lactone are influenced by drugs that inhibit these enzymes. Atorvastatin and its metabolites are excreted in human serum as glucuronide or sulfate conjugates.</p>Fórmula:C33H33FN2O4Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:540.62 g/molAtorvastatin EP Impurity D
CAS:<p>Soluble in Chloroform & in Methanol Confirmed<br>Insoluble in Water</p>Pureza:95.0% MinCor e Forma:White or Off-White Crystalline Solid, Light SensitivePeso molecular:431,46β-Epoxyabiraterone acetate
CAS:<p>Beta-Epoxyabiraterone acetate is a synthetic and natural metabolite of abiraterone that is used as an API impurity in the synthesis of abiraterone acetate. The drug product is a niche compound with CAS No. 52464-96-6. The Metabolite is an impurity found in the synthesis of beta-epoxyabiraterone acetate. Drug development research and development, analytical methods, and pharmacopoeia are all involved in the production of this compound.</p>Fórmula:C26H33NO3Pureza:Min. 90 Area-%Cor e Forma:White Off-White PowderPeso molecular:407.55 g/molAtorvastatin lactam sodium salt impurity
CAS:<p>Atorvastatin is a drug used for the treatment of hypercholesterolemia and cardiovascular diseases. Atorvastatin lactam, which is an impurity formed during the synthesis of atorvastatin, has been shown to inhibit cholesterol biosynthesis in a rat model. The in vivo metabolism of atorvastatin lactam was studied by HPLC-MS/MS and was found to be identical to that of the parent molecule. This impurity may be useful as a research and development or custom synthesis product, or as an impurity standard for HPLC analysis.</p>Fórmula:C33H34FN2NaO6Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:596.62 g/molDefluoro atorvastatin acetonide tert-butyl ester
CAS:<p>Please enquire for more information about Defluoro atorvastatin acetonide tert-butyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Fórmula:C40H48N2O5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:636.82 g/molDefluoro atorvastatin calcium
CAS:<p>Defluoro atorvastatin calcium is a bulk drug that has been approved to be used as an adjunct to diet to reduce elevated cholesterol levels in adults. Defluoro atorvastatin calcium is the desfluoro-enantiomer of atorvastatin, which is a statin that inhibits the enzyme HMG-CoA reductase. This enzyme catalyzes the conversion of HMG-CoA to mevalonic acid, which is an early step in the synthesis of cholesterol. The fluoro group on defluoro atorvastatin calcium is not expected to have any significant effect on its potency or metabolic pathways and any impurities are not expected to have any therapeutic effect.</p>Fórmula:C66H70CaN4O10Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:1,119.36 g/mol3-Oxo-4-aza-5a-androst-1-ene-17b-carboxylic acid
CAS:<p>3-Oxo-4-aza-5a-androst-1-ene-17b-carboxylic acid is a covalently bonded prodrug that is metabolized to its active form, finasteride, in the body. It has been shown to have physiological activities such as skin permeation and cell growth. 3-Oxo-4-aza-5a-androst-1-ene 17b carboxylic acid also has immunotherapy properties and can be conjugated with other compounds for use in cancer treatment.</p>Fórmula:C19H27NO3Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:317.42 g/molAtorvastatin epoxydione impurity
CAS:<p>Atorvastatin epoxydione impurity (EPI) is a heptanoic, hydrate, diastereoisomer, racemic mixture, enantiomer and impurity of Atorvastatin. The EPI has been minimized in the formulation process by using a novel synthesis route that employs a chiral pyrrole derivative as an intermediate. This minimization has allowed for the elimination of the tautomer and other impurities present in the original compound.</p>Fórmula:C26H22FNO4Pureza:Min. 95 Area-%Cor e Forma:White PowderPeso molecular:431.46 g/molCalcipotriol EP Impurity G
<p>Calcipotriol EP Impurity G is an impurity in calcipotriol, which is a drug product. Calcipotriol EP Impurity G has a CAS number of 126825-26-3 and is a natural metabolite of calcipotriol. It is also known as calcipotriol EP Impurity G or calcipotriol EPIG. It has been shown to be an analytical impurity in calcipotriol, and it has been detected by HPLC analysis. Calcipotriol EP Impurity G can be used for research and development, as well as for the production of pharmacopoeia standards.</p>Fórmula:C54H78O5Pureza:Min. 95 Area-%Cor e Forma:White PowderPeso molecular:807.19 g/molDutasteride impurity F
CAS:<p>Dutasteride impurity D is a natural impurity found in dutasteride and has been reported to be an analytical marker for dutasteride. It is also used as an impurity standard, HPLC standard, and custom synthesis for drug development. Metabolism studies have shown that the major route of elimination for Dutasteride impurity D is through glucuronidation with minor amounts being excreted in urine unchanged.</p>Fórmula:C27H31ClF6N2O2Pureza:Min. 95 Area-%Peso molecular:564.99 g/molCalcipotriol EP impurity E
<p>Calcipotriol EP Impurity E is a synthetic impurity that is found in the calcipotriol EP API. Calcipotriol EP Impurity E is an impurity standard for HPLC and can be used in drug development, research and development, and pharmacopoeia. It has been shown to have no significant effect on the pharmacological activity of calcipotriol EP.</p>Fórmula:C27H42O3Pureza:Min. 95 Area-%Cor e Forma:PowderPeso molecular:414.62 g/molFluticasone propionate EP Impurity F
CAS:<p>Fluticasone Propionate EP Impurity F is an impurity of Fluticasone Propionate. Fluticasone Propionate is a synthetic glucocorticoid used in the treatment of asthma and other allergic disorders. Impurity F is a metabolite of Fluticasone Propionate and has been detected in human plasma at low levels (5% of total fluticasone propionate). The metabolism of Fluticasone Propionate to Impurity F has been studied in rat, mouse, dog and man.<br>br>br><br>The following table summarizes the metabolic pathways that have been identified for this impurity:<br>br>br><br>Metabolism studies indicate that Impurity F is mainly metabolized by CYP3A4 to form conjugates with glucuronic acid or sulfates. It may also be hydrolyzed to form 5α-flurostan-3β,17β-d</p>Fórmula:C25H29F3O5SPureza:Min. 95%Cor e Forma:PowderPeso molecular:498.56 g/molCalcipotriol EP Impurity B
<p>Calcipotriol EP Impurity B is a drug product that is an impurity in Calcipotriol EP. It is produced during the synthesis of calcipotriol and may be present in the natural product. It has been shown to have anti-inflammatory properties, and can be used as a research tool to study calcipotriol metabolism.</p>Fórmula:C27H40O3Pureza:Min. 95%Peso molecular:412.6 g/molDifluoro atorvastatin
CAS:<p>Difluoro atorvastatin is a filtrate of atorvastatin, which is a cholesterol-lowering drug. It is synthesized by reacting butyric acid with atorvastatin in an organic solvent. The reaction solution was filtered to remove impurities and then purified by liquid chromatography. The product was characterized by diffraction and LC-MS analysis. Difluoro atorvastatin has a high purity and is suitable for further use in the preparation of pharmaceuticals.</p>Fórmula:C33H34F2N2O5Pureza:Min. 95%Peso molecular:576.63 g/molrac-3-Oxo atorvastatin sodium salt
CAS:<p>Racemic 3-Oxo atorvastatin sodium salt (3OAS) is a drug product that has been tested in the laboratory and found to be suitable for further development. It is a natural substance that has not been chemically synthesized. Racemic 3-Oxo atorvastatin sodium salt is an impurity standard that can be used to establish the purity of API drugs. It can also be used as a metabolite in metabolism studies. Racemic 3-Oxo atorvastatin sodium salt is high purity and can be used for niche applications such as pharmacopoeia production.</p>Fórmula:C33H32FN2NaO5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:578.61 g/molVitamin A EP Impurity C
CAS:<p>Soluble in Chloroform & in Methanol Confirmed<br>Insoluble in Wate</p>Pureza:90% minCor e Forma:Off White or Beige SolidPeso molecular:312.45Calcipotriol EP Impurity H
<p>Calcipotriol EP Impurity H is an impurity found in calcipotriol EP. It is a metabolite of calcipotriol EP, which is the active ingredient in Dovonex. Calcipotriol EP Impurity H can be detected by HPLC with a retention time of 11.5 minutes and its purity can be determined by UV spectroscopy at 254 nm with a purity of >98%. Calcipotriol EP Impurity H can also be synthesized from natural or synthetic sources.</p>Fórmula:C54H78O5Pureza:Min. 95 Area-%Cor e Forma:PowderPeso molecular:807.19 g/molAtorvastatin epoxy pyrrolooxazin tricyclic impurity
<p>Atorvastatin is a drug product that is metabolized to atorvastatin epoxy pyrrolooxazin tricyclic impurity. Due to the presence of this impurity, the purity of the drug product is not 100%. Atorvastatin epoxy pyrrolooxazin tricyclic impurity is a natural metabolite with CAS number 516-80-1. It has been shown to have effects on metabolism and may be involved in the development of atherosclerosis. Metabolism studies have been conducted on animals, but not humans.</p>Fórmula:C33H32FN2NaO6Pureza:Min. 95%Peso molecular:594.61 g/molAtorvastatin epoxy tetrahydrofuran impurity
CAS:<p>Atorvastatin epoxy tetrahydrofuran impurity is a byproduct of the synthesis process. It is a white crystalline powder that is soluble in organic solvents and sparingly soluble in water. Atorvastatin epoxy tetrahydrofuran impurity has been shown to be an impurity of atorvastatin. It is not known to have any biological activity, but it may pose a health risk if present in large quantities.</p>Fórmula:C26H24FNO5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:449.47 g/molO-Methyl atorvastatin calcium
CAS:<p>O-Methyl atorvastatin calcium is a drug product that is an HPLC standard. It is a natural metabolite of atorvastatin, which is synthesized by cytochrome P450 3A4 in the liver. O-Methyl atorvastatin calcium has been shown to be an impurity in some batches of atorvastatin calcium. It has been observed to have pharmacological effects similar to those of atorvastatin. O-Methyl atorvastatin calcium has been used as a research and development (R&D) tool for studies on the metabolism of drugs, including its own synthesis and the study of the effect on other drugs such as amiodarone.</p>Fórmula:CaC68H71F2N4O10Pureza:Min. 95%Cor e Forma:PowderPeso molecular:1,182.39 g/mol(3S,5S)-Atorvastatin sodium salt
CAS:<p>Atorvastatin is a statin drug that inhibits the enzyme HMG-CoA reductase, which is responsible for cholesterol synthesis. Atorvastatin is used to lower LDL cholesterol and total cholesterol levels in the blood. It also lowers triglyceride levels and raises HDL cholesterol levels. Atorvastatin has been shown to inhibit fibrinogen production, reduce TNF-α production, and improve body mass index (BMI) in obese patients. This drug has been shown to be effective in reducing the size of atherosclerotic lesions by decreasing the amount of cholesteryl esters transferred from high-density lipoprotein (HDL) to low-density lipoprotein (LDL). It has also been shown to inhibit collagen production and stimulate muscle cell proliferation.</p>Fórmula:C33H34FN2NaO5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:580.62 g/mol
