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 4967 productos de "Esteroides y derivados"
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rac-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%Forma y color:PowderPeso molecular:578.61 g/mol(5α)-17-(3-Pyridinyl)androst-16-en-3-one
CAS:Producto 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-%Forma y color:White PowderPeso molecular:349.51 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/molVitamin A EP Impurity C
CAS:<p>Soluble in Chloroform & in Methanol Confirmed<br>Insoluble in Wate</p>Pureza:90% minForma y color: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-%Forma y color:PowderPeso molecular:807.19 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%Forma y color:PowderPeso molecular:580.62 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-%Forma y color:White 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/molLevonorgestrel EP Impurity P
CAS:<p>Soluble in Chloroform & in Methanol Confirmed<br>Insoluble in Wate</p>Pureza:90% minForma y color:Off White or Beige SolidPeso molecular:312.45Levonorgestrel EP Impurity O
CAS:<p>Soluble in Chloroform & in Methanol Confirmed<br>Insoluble in Water</p>Pureza:95.0% MinForma y color:Off White or Beige SolidPeso molecular:344.49Dutasteride 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/mol1b-(4-Fluorophenyl)hexahydro-β,7-dihydroxy-7-(1-methylethyl)-1a-phenyl-7a-[(phenylamino)carbonyl]-3H-oxireno[3,4]pyrrolo[2,1-b][1,3] oxazine-3-butanoic acid sodium
CAS:<p>Fluoxetine is a selective serotonin reuptake inhibitor that is used to treat major depressive disorder, obsessive-compulsive disorder (OCD), bulimia nervosa, panic disorder, premenstrual dysphoric disorder (PMDD), and social anxiety disorder. It is also used as an appetite suppressant in some countries. Fluoxetine inhibits the neuronal uptake of serotonin by blocking the presynaptic transporter protein. The most common adverse effects are nausea, diarrhea, drowsiness, dry mouth, blurred vision and sexual dysfunction.</p>Fórmula:C33H35FN2O7•NaPureza:Min. 95%Forma y color:PowderPeso molecular:613.63 g/molAtorvastatin EP Impurity D
CAS:<p>Soluble in Chloroform & in Methanol Confirmed<br>Insoluble in Water</p>Pureza:95.0% MinForma y color:White or Off-White Crystalline Solid, Light SensitivePeso molecular:431,46Atorvastatin 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-%Forma y color:White PowderPeso molecular:431.46 g/molβ-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-%Forma y color:White Off-White PowderPeso molecular:407.55 g/molDesfluoro atorvastatin
CAS:<p>Desfluoro atorvastatin is a crystalline polymorph of atorvastatin that has been shown to have improved flowrate and dissolution profile compared with the conventional form. Desfluoro atorvastatin is synthesized by adding a fluorine atom to a specific position in the molecule. The synthesis procedure includes chromatographic purification and analysis of impurities, which are then eliminated by diode laser irradiation. Impurities may also be eliminated through hydrogenation or recrystallization.</p>Fórmula:C33H36N2O5Pureza:Min. 95%Forma y color:PowderPeso molecular:540.65 g/mol
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