Sais e Derivados de API
Os sais dos Ingredientes Farmacêuticos Ativos (API) são compostos formados pela reação de um ácido com uma base, resultando em um equilíbrio iônico. Esses sais frequentemente melhoram a solubilidade e a estabilidade dos APIs, facilitando sua absorção no organismo. Os derivados de API são variantes químicas de um princípio ativo que podem apresentar propriedades aprimoradas ou modificadas para otimizar a eficácia terapêutica. Os sais de APIs são utilizados na formulação de medicamentos orais, injetáveis e tópicos. Além disso, os derivados de API podem melhorar a farmacocinética dos fármacos, permitindo, por exemplo, a liberação controlada de substâncias ativas.
Na CymitQuimica, oferecemos sais e derivados de APIs com a pureza e qualidade necessárias para pesquisa e desenvolvimento de formulações farmacêuticas.
Foram encontrados 79238 produtos de "Sais e Derivados de API"
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Ticagrelor Amine Derivative
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications Ticagrelor Amine Derivative is a metabolite of Ticagrelor (T437700). Ticagrelor is a reversible oral P2Y12 receptor antagonist, provides faster, greater, and more consistent ADP-receptor inhibition than Clopidogrel. Used in the treatment of acute coronary syndromes (ACS).<br>References Matetzky, S., et al.: Circulation, 109, 3171 (2004), Bassand, J., et al.: Eur. Heart J., 28, 1598 (2007), Jakubowski, J., et al.: Cardiovasc. Drug Rev., 25, 357 (2007),<br></p>Fórmula:C23H29F2N7O3SCor e Forma:White To Off-WhitePeso molecular:521.58Mivacurium Chloride (mixture of isomers)
CAS:Produto ControladoFórmula:C58H80N2O14·2ClCor e Forma:NeatPeso molecular:1100.17Dofetilide-d4
CAS:Produto Controlado<p>Applications Potassium channel blocker.<br>References Carmeliet, D., et al.: J. Pharmacol. Exp. Ther., 262, 809 (1992), Norgaard, B.L., et al.: Am. Heart J., 137, 1062 (1999), Torp-Pedersen, C., et al.: N. Engl. J. Med. 341, 857 (1999)<br></p>Fórmula:C19H23D4N3O5S2Cor e Forma:NeatPeso molecular:445.5924,32-Bis-O-(tert-butyldimethylsilyl)-FK-506-13C, D2 (Major)
CAS:Produto Controlado<p>Stability Hygroscopic<br>Applications An intermediate in the preparation of labelled FK-506 (Tacrolimus)<br>References Rokaw, M.D., et al.: Am. J. Physiol., 271, C194 (1996), Knoll, G.A., et al.: Brit. Med. J., 318, 1104 (1999),<br></p>Fórmula:C5513CH95D2NO12Si2Cor e Forma:NeatPeso molecular:1035.544’-Hydroxy Diclofenac-D4
CAS:Produto ControladoFórmula:C142H4H7Cl2NO3Cor e Forma:NeatPeso molecular:316.17(5E)-Bimatoprost
CAS:<p>Applications The trans-isomer used in the improved process for the production and purification of Bimatoprost (B386800).<br></p>Fórmula:C25H37NO4Cor e Forma:NeatPeso molecular:415.56Bispyrazolone
CAS:<p>Applications Bispyrazolone is an impurity of Edaravone (E335000).<br></p>Fórmula:C20H18N4O2Cor e Forma:NeatPeso molecular:346.385,6-trans Travoprost
CAS:<p>Applications An 5,6-trans isomeric impurity of the selective FP prostaglandin receptor agonist Travoprost (T715600).<br></p>Fórmula:C26H35F3O6Cor e Forma:NeatPeso molecular:500.551-(4-Methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-yl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylic Acid
CAS:Fórmula:C25H24N4O5Cor e Forma:Light Orange ColourPeso molecular:460.48Ramiprilat
CAS:Produto Controlado<p>Impurity Ramipril EP Impurity E<br>Stability Hygroscopic<br>Applications Ramiprilat (Ramipril EP Impurity E) is a metabolite of Ramipril (R111000), and acts as an ACE inhibitor (1). Reduces the need for dialysis among patients previously on angiotensin-converting-enzyme inhibitors (2). Ramipril is used in stroke prevention. (3)<br>References 1. Teetz, V. et al.: Arzneimittelforschung. 1984;34(10B):1399-401.2. Ruggenenti, P. et al.: Lancet. 1998 Oct 17;352(9136):1252-6.3. Badrinath, P. et al.; BMJ. 2002 Aug 24; 325(7361): 439.<br></p>Fórmula:C21H28N2O5Cor e Forma:Light YellowPeso molecular:388.464’-Hydroxy Diclofenac
CAS:Produto Controlado<p>Stability Light Sensitive<br>Applications A metabolite of Diclofenac, a nonsteroidal inflammatory compound and cyclooxygenase (COX) inhibitor.<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 Kretz-Rommel, A., et al.: Toxicol. Appl. Pharmacol., 120, 155 (1993), Petronilli, V., et al.: J. Biol. Chem., 269, 16638 (1994), Bort, R., et al.: J. Pharmacol. Exp. Ther., 288, 65 (1998), Poon, G., et al.: Drug Metab. Dispos., 29, 1608 (2001),<br></p>Fórmula:C14H11Cl2NO3Cor e Forma:White To Light PurplePeso molecular:312.15Desbutyl Dronedarone Hydrochloride
CAS:<p>Impurity Dronedarone USP Related Compound A<br>Applications A metabolite of Dronedarone (D679445). Dronedarone impurity D. Dronedarone USP Related Compound A.<br>References Bolderman, R.W. et al.: J Chrom. B:Anal. Tech. Biomed. Life Sci., 887, 1727 (2009); Singh, B., et al.: J. Cardiovas. Pharmacol., 52, 300 (2008); Hoy, S., et al.: Drugs, 69, 1647 (2009);<br></p>Fórmula:C27H36N2O5S·ClHCor e Forma:NeatPeso molecular:537.11Raloxifene
CAS:<p>Raloxifene (LY139481) is an estrogen receptor modulator exhibiting estrogen agonist and antagonist activity at different sites, with antiviral activity.</p>Fórmula:C28H27NO4SPureza:99.39%Cor e Forma:Light-Yellow SolidPeso molecular:473.58N-Nitro-1,2,3,4-tetradehydro Argatroban Ethyl Ester
CAS:<p>Applications N-Nitro-1,2,3,4-tetradehydro Argatroban Ethyl Ester is an intermediate in the preparation of Argatroban (A769000).<br></p>Fórmula:C25H35N7O7SCor e Forma:Off White SolidPeso molecular:577.65rel-(1R,3S,5S)-8-Methyl-8-azabicyclo[3,2,1]oct-6-en-yl-2-hydroxy-2,2-dithiophen-2-yl acetate
CAS:Produto Controlado<p>Impurity Tiotropium EP impurity D<br>Applications (1R,3S,5S)-8-Methyl-8-azabicyclo[3,2,1]oct-6-en-yl-2-hydroxy-2,2-dithiophen-2-ylacetate is an impurity in the synthesis of Tiotropium Bromide (T444850), a muscarinic receptor antagonist. Bronchodilator.<br>References Haddad, E.-B., et al.: Mol. Pharmacol., 45, 899 (1994); Donohue, J. F., et al.: Chest, 122, 47 (2002); Profita, M., et al.: Allergy, 60, 1361 (2005); Dusser, D., et al.: Eur. Respir. J., 27, 547 (2006);<br></p>Fórmula:C18H19NO3S2Cor e Forma:NeatPeso molecular:361.483-(Formylamino)-1H-pyrazole-4-carboxamide
CAS:Produto Controlado<p>Impurity Allopurinol EP Impurity B / Allopurinol USP Related Compound B<br>Stability Hygroscopic<br>Applications 3-(Formylamino)-1H-pyrazole-4-carboxamide (Allopurinol EP Impurity B) is an impurity of Allopurinol (A547300) with inhibitory effects on human hypoxanthine phosphoribosyltransferase.<br>References Krenitzky, T.A. et al.: J. Biol. Chem., 244, 1263 (1969);<br></p>Fórmula:C5H6N4O2Cor e Forma:White To Off-WhitePeso molecular:154.1274-Ethoxycarbonyl-3-ethoxyphenylacetic Acid
CAS:Produto Controlado<p>Applications Repaglinide intermediate.<br>References Wolfenbuttel, B., et al.: Eur. J. Clin. Pharmacol., 45, 113 (1993), Grell, W., et al.: J. Med. Chem., 41, 5219 (1998), Anon., et al.: Drugs Future, 24, 815 (1999),<br></p>Fórmula:C13H16O5Cor e Forma:NeatPeso molecular:252.26Ivermectin B1 Aglycon
CAS:<p>Stability Hygroscopic, Temperature Sensitive<br>Applications Ivermectin B1 Aglycon is an impurity of Ivermectin (I940800), an antiparasitic drug that is active against a wide variety of nematode and arthropod parasites and is used to treat scabies and lice in humans. An invitro inhibitor of SARS-CoV-2/ Covid-19.<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 Campbell, W., et al.: Science, 221, 823 (1983); Glaziou, P., et al.: Trop. Med. Parasitol., 45, 253 (1994); Meinking, T., et al.: New Engl. J. Med., 333, 26 (1995); Caly, L., et al.: Antivir. Res., 178<br></p>Fórmula:C34H50O8Cor e Forma:Off White PowderPeso molecular:586.76N-(2,6-Dichlorophenyl)aniline
CAS:Produto Controlado<p>Applications N-(2,6-Dichlorophenyl)aniline is an analog of Diclofenac (D436450), a nonsteroidal anti-inflammatory compound an decycloxygenase (COX) inhibitor.<br>References Moser, P. et al.: J. Med. Chem., 33, 2358 (1990); Encinas, S. et al.: Photochem. Photobiol., 68,640 (1998); Kenny, J. R., et al.: J. Med. Chem., 47, 2816 (2004), Sasaki, A., et al.: J. Pharmacol. Sci., 108, 266 (2008), Dalvie, D., et al.: Chem. Res. Toxicol., 22, 357 (2009),<br></p>Fórmula:C12H9Cl2NCor e Forma:WhitePeso molecular:238.114-Chlorobenzal Chloride
CAS:<p>Applications 4-Chlorobenzal Chloride is an impurity that is formed in the synthesis of Benoxaprofen (B165300); a non-steroidal anti-inflammatory ophthalmic agent.<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 Cockerill, A.F., et al.: J. Chromatogr., 129, 339 (1976); Mathur, K., et al.: Bioorg. Med. Chem., 11, 1915 (2003); Zhao, M., et al.: Bioorg. Med. Chem., 15, 2815 (2007); Roy, K., et al.: Eur. J. Med. Chem., 44, 2913 (2009)<br></p>Fórmula:C7H5Cl3Cor e Forma:NeatPeso molecular:195.47Diclofenac Alcohol (Diclofenac Impurity)
CAS:<p>Impurity Diclofenac EP Impurity C<br>Applications Diclofenac Alcohol (Diclofenac EP Impurity C) is a Diclofenac impurity. Anti-inflammatory.<br>References Brogden, R., et al.: Drugs, 20, 24 (1980), Orienti, I., et al.: Eur. J. Pharm. Biopharm., 37, 110 (1991), Sagara, K., et al.: Chem. Pharm. Bull., 40, 3303 (1992), Connors, K., et al.: J. Pharm. Sci., 84, 843 (1995),<br></p>Fórmula:C13H11Cl2NOCor e Forma:WhitePeso molecular:268.141,2-Bismethylphenidate (Mixture of Diastereomers)
Produto Controlado<p>Applications 1,2-Bismethylphenidate is an impurity of methylphenidate (M325880), an CNS stimulant.<br>References Greenblatt, E.N., et al.: J. Pharmacol. Exp. Ther., 131, 115 (1961), Padmanabhan, G.R., Anal. Profiles Drug Subs., 10, 473 (1981), Srinivas, N.R., et al.: Pharm. Res., 10, 14 (1993),<br></p>Fórmula:C23H27NO4Cor e Forma:NeatPeso molecular:381.46N-Carbamoyl Oxcarbazepine
Produto Controlado<p>Applications N-Carbamoyl Oxcarbazepine is an impurity of Oxcarbazepine (O869250), a metabolite of Eslicarbazepine acetate, (BIA 2-093), a novel central nervous system drug. A keto derivative of Carbamazepine. Used as an anticonvulsant.<br>References Dam., M., et al.: Epilepsy Res., 3, 70 (1989), Beydoun, A., et al.: Expert Opin. Pharmacother., 3, 59 (2001),<br></p>Fórmula:C16H13N3O3Cor e Forma:NeatPeso molecular:295.291-Chloroethyl Cyclohexyl Carbonate
CAS:<p>Applications 1-Chloroethyl Cyclohexyl Carbonate is a genotoxic impurity used in the synthesis of Candesartan Cilexetil. an angiotensin II receptor antagonist.<br>References Kakasaheb, N. et al.: Int. J. Pharm. Sci., 6, 370 (2014); Mao, Y. et al.: Heterocycles, 81, 1503 (2010);<br></p>Fórmula:C9H15ClO3Cor e Forma:NeatPeso molecular:206.67N-[[(5S)-2-Oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-acetamide
CAS:Produto Controlado<p>Applications N-[[(5S)-2-Oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-acetamide is an impurity of Rivaroxaban (R538000), which is a novel antithrombotic agent. A highly potent and selective, direct FXa inhibitor.<br>References Ansell, J., et al.: Drugs, 64, 1 (2004), Eriksson, B., et al.: J. Thromb. Haemost., 3, 103 (2005), Kubitza, D., et al.: Clin. Pharmacol. Ther., 78, 412 (2005),<br></p>Fórmula:C16H19N3O5Cor e Forma:NeatPeso molecular:333.34Diclofenac Amide-13C6 (~5% unlabelled)
CAS:Produto Controlado<p>Applications Diclofenac Amide-13C6 is a labelled analogue of Diclofenac Amide (D436440), which is a potential prodrug of Diclofenac and possible impurity during its commercial synthesis. Diclofenac Amide-13C6 is also an intermediate in synthesizing Diclofenac-13C6 Sodium Salt (D436453), which is a labelled analogue of Diclofenac Sodium Salt (D436450).<br>References Gaudiano, M.C., et al.: J. Pharm. Biomed. Anal., 32, 151 (2003); De Castro, W.V., et al.: Drug Develop. Ind. Pharm., 32, 1103 (2006); Kenny, J. R., et al.: J. Med. Chem., 47, 2816 (2004), Sasaki, A., et al.: J. Pharmacol. Sci., 108, 266 (2008); Dalvie, D., et al.: Chem. Res. Toxicol., 22, 357 (2009)<br></p>Fórmula:C813C6H9Cl2NOCor e Forma:White To Light YellowPeso molecular:284.092-Chloroethylamine Hydrochloride
CAS:Produto Controlado<p>Applications 2-Chloroethylamine Hydrochloride is used as a reagent in the synthesis of 6-desfluoroquinolones as potential anti-HIV drugs. Also used as a reagent in the synthesis of ellipticine derivatives as anticancer agents.<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 Sancineto, L., et al.: Bioorg. Med. Chem., 22, 4658 (2014); Mori, R., et al.: Eur. J. Med. Chem., 82, 16 (2014)<br></p>Fórmula:C2H6ClN·ClHCor e Forma:NeatPeso molecular:115.99Ivermectin B1 Monosaccharide
CAS:Produto Controlado<p>Applications Ivermectin B1 Mono-sugar Derivative is an impurity of Ivermectin (I940800), an antiparasitic drug that is active against a wide variety of nematode and arthropod parasites and is used to treat scabies and lice in humans. An invitro inhibitor of SARS-CoV-2/ Covid-19.<br>References Campbell, W., et al.: Science, 221, 823 (1983); Glaziou, P., et al.: Trop. Med. Parasitol., 45, 253 (1994); Meinking, T., et al.: New Engl. J. Med., 333, 26 (1995); Caly, L., et al.: Antivir. Res., 178<br></p>Fórmula:C41H62O11Cor e Forma:NeatPeso molecular:730.92Oxindole (2-Indolone)
CAS:Produto Controlado<p>Applications Indole analogue; shows pharmacological activity.<br>References Mohammadi, M., et al.: Science, 276, 955 (1997), Bramson, H., et al.: J. Med. Chem., 44, 4339 (2001), Lane, M., et al.: Cancer Res., 61, 6170 (2001), Yu, B., et al.: Biochem. Pharmacol., 64, 1091 (2002),<br></p>Fórmula:C8H7NOCor e Forma:Light RedPeso molecular:133.152-[3-Carboxy-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic Acid
CAS:Produto Controlado<p>Applications 2-[3-Carboxy-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic Acid is an impurity of Febuxostat (F229000), an xanthine oxidase/ xanthine dehydrogenase inhibitor used for the treatment of hyperuricemia and chronic gout.<br>References Kadivar, M.H.,e t al.: J. Pharm. Biomed. Anal., 56, 749 (2011);<br></p>Fórmula:C16H17NO5SCor e Forma:White SolidPeso molecular:335.37Desisobutyl Febuxostat
CAS:Produto ControladoFórmula:C12H8N2O3SCor e Forma:Light Yellow SolidPeso molecular:260.27Apixaban Dimer
CAS:Produto Controlado<p>Applications Apixaban Dimer is an impurity compound of Apixaban (A726700). Apixaban is a potent, direct, selective, and orally active inhibitor of coagulation factor Xa. It is a potential new oral coagulant that may be useful in the prevention of venous thromboembolism in total hip, knee replacement orthopedic surgery and stroke in treatment of patient with venous thromboembolic disorder or with atrial fibrillation.<br>References Luettgen, J. M. et al.: J. Enz. Inhib. Med. Chem., 26, 514 (2011); Glanis, T. et al.: J. Thromb. Thrombol., 31, 310 (2011); barrett, Y.C. et al.: Thromb. Haemos., 105, 181 (2011);<br></p>Fórmula:C40H34N10O6Cor e Forma:NeatPeso molecular:750.783-Descyano-3-((hydroxyimino)methyl) Febuxostat
CAS:Produto ControladoFórmula:C16H18N2O4SCor e Forma:NeatPeso molecular:334.39Diclofenac Dodecyl Ester
<p>Applications Diclofenac Dodecyl Ester is a Diclofenac impurity. Diclofenac is a nonsteroidal inflammatory compound and cyclooxygenase (COX) inhibitor.<br>References Kretz-Rommel, A., et al.: Toxicol. Appl. Pharmacol., 120, 155 (1993), Petronilli, V., et al.: J. Biol. Chem., 269, 16638 (1994), Bort, R., et al.: J. Pharmacol. Exp. Ther., 288, 65 (1998), Poon, G., et al.: Drug Metab. Dispos., 29, 1608 (2001),<br></p>Fórmula:C26H35Cl2NO2Cor e Forma:NeatPeso molecular:464.474-(Trifluoromethyl)aniline
CAS:Produto Controlado<p>Impurity Leflunomide EP Impurity A; Leflunomide USP Related Compound A<br>Applications 4-(Trifluoromethyl)aniline (Leflunomide EP Impurity A; Leflunomide USP Related Compound A) is a 4-Substituted aniline derivatives exert special hematotoxicity on the red blood cells and induce leukocytosis.<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 Weber, W., et al.: Pharmacol. Rev., 37, 25 (1985), Hein, D., et al.: Carcinogenesis, 14, 1633 (1993), Payton, M., et al.: Microbiology, 147, 1137 (2001), Mushtaq, A., et al.: J. Biol. Chem., 277, 12175 (2002),<br></p>Fórmula:C7H6F3NCor e Forma:NeatPeso molecular:161.12Cyclosporin C
CAS:Produto Controlado<p>Applications A group of nonpolar cyclic oligopeptides with immunosupppressant activity.<br>References van Wartburg, A., et al.: Prog. Med. Chem., 25, 1 (1988), Jorgensen, K.A., et al.: Scand. J. Imunol., 57, 93 (2003), Vollenbroeker, et al.: Transplant. Proc., 37, 1741 (2005),<br></p>Fórmula:C62H111N11O13Pureza:>80%Cor e Forma:NeatPeso molecular:1218.61
![1-(4-Methoxyphenyl)-7-oxo-6-[4-(2-oxopiperidin-1-yl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]p…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FM266420.webp&w=3840&q=75)
![rel-(1R,3S,5S)-8-Methyl-8-azabicyclo[3,2,1]oct-6-en-yl-2-hydroxy-2,2-dithiophen-2-yl acetate](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FM288620.webp&w=3840&q=75)
![N-[[(5S)-2-Oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-5-oxazolidinyl]methyl]-acetamide](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FO870195.webp&w=3840&q=75)
![2-[3-Carboxy-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic Acid](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FTR%2Fthumb-webp%2FC180600.webp&w=3840&q=75)
