Antibióticos naturales y semisintéticos

<p>Impurity Erythromycin EP Impurity F<br>Applications Pseudo Erythromycin A Enol Ether (Erythromycin EP Impurity F) is an Erythromycin impurity.<br>References Lartey, P.A., et al.: Advan. Pharmacol., 28, 307 (1994), Tonini, M., et al.: Pharmacol. Res., 33, 217 (1997),<br></p>

<p>Impurity Azithromycin EP Impurity M<br>Applications Azithromycin (A927000) impurity. A degradation products of Azithromycin.<br>References Anon., et al.: Pharmaeuropa, 13, 750 (2001),<br></p>

<p>Applications (E)-6,6-Dimethylhept-2-en-4-yn-1-ol is an intermediate in the synthesis of N-Desmethyl Terbinafine (D294300), a metabolite of Terbinafine, an orally active, antimycotic allylamine related to naftifine.<br>References Humbert, H., et al.: Pharam. Drug Dispos., 19, 417 (1998); Vickers, A., et al.: Drug Metab. Dispos., 27, 1029 (1999); Iverson, S., et al.: Chem. Res. Toxicol., 14, 175 (2001)<br></p>

<p>Impurity Amoxicillin EP Impurity G ; Amoxicillin USP Related Compound G<br>Applications p-Hydroxy-(D)-phenylglycyl Amoxicillin is a derivative of Amoxicillin (A634235) a semi-synthetic antibiotic related to Penicillin.<br>References Brogden, R.N., et al.: Drugs, 18, 169 (1979), Bird, A.E., et al.: Anal. Profiles Drug Subs. Excip., 23, 1 (1994),<br></p>

<p>Stability Hygroscopic<br>Applications Non-absorbable semisynthetic Rifamycin antibiotic.<br>References Brufani, M., et al.: J. Antibiot., 37, 1611 (1984), Gillis, J.C., et al.: Drugs, 49, 467 (1995), Huang, D.B., et al.: J. Infection, 50, 97 (2005),<br></p>

<p>Applications The more active Zearalenone (Z270500) metabolite.<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 Olsen, M., et al.: Acta Pharmacol. Toxicol., 48, 15 (1981), Chang, W., et al.: Food Chem. Toxicol., 22, 887 (1984), El Golli, E., et al.: Toxicol Lett., 166, 122 (2006), Hassen, W., et al.: Toxicology, 232, 294 (2007), Benzoni, E., et al.: Reprod. Toxicol., 25, 461 (2008),<br></p>

<p>Impurity Cefaclor EP Impurity F/ Ampicillin EP Impurity H<br>Applications 2-Hydroxy-3-phenylpyrazine (Cefaclor EP Impurity F) is a degradation product of Cefaclor (C235250), a second-generation cephalosporin antibiotic.<br>References Baertschi, S.W., et al.: J. Pharma. Sci., 82, 622 (1993); Gray, B.M., et al.: Antimicrob. Agents Chemother., 13, 988 (1978), Lorenz, L.J., et al.: Anal. Profiles Drug Subs., 9, 107 (1980), Hori, R., et al.: J. Pharm. Pharmacol., 40, 646 (1988),<br></p>

<p>Impurity Amoxicillin EP Impurity C ; Amoxicillin USP Related Compound C<br>Applications Amoxicillin Diketopiperazine (Amoxicillin EP Impurity C) is a major metabolite of Amoxicillin (AMO)(A634235).<br>References Dewdney, J., et al.: Food Chem. Toxic, 29, 477 (1991), Connor, S., et al.: J. Pharm. Pharmacol., 46, 128 (1994), Hernandez, E., et al.: Vet. J., 170, 237 (2005),<br></p>

<p>Applications Moxifloxacin intermediate.<br></p>

<p>Applications A Cycloserine dimer as potential impurity of drug Cycloserine (C988800).<br>References Perez-Sala, D., et al.: Biochem. Pharmacol., 38,1037 (1989),<br></p>

<p>Applications Labelled Clarithromycin (C559750). Clarithromycin is a semi-synthetic macrolide antibiotic. Clarithromycin is a derivative of Erythromycin (E650000).<br>References Benson, C., et al.: Eur. J. Clin. Microbiol., 6, 173 (1987), Boyanova, L., et al.: J. Med. Microb., 61, 85 (2012), Lin, Z., et al.: Toxicol. Sci., 126, 114 (2012),<br></p>

<p>Impurity Tacrolimus Related Compound A USP<br>Applications A potent immunosuppressive agent and could be used as a potential therapeutic agent for autoimmune diseases.<br>References Matuszewski, B., et al.: Anal. Chem., 75, 3019 (2003), Taylor, P., et al.: Clin. Chem., 51, 1890(2005);<br></p>

<p>Applications Thiamphenicol is an antibiotic. Thiamphenicol is the methyl-sulfonyl analogue of chloramphenicol and has a similar spectrum of activity, but is 2.5 to 5 times as potent. Thiamphenicol is used particularly for the treatment of sexually transmitted infections and pelvic inflammatory disease.<br>References Tikhonova, E., et al.: J. Biol. Chem., 279, 32116 (2004), Baucheron, S., et al.: J. Antimicrob. Chemother., 55, 707 (2005), Pages, J., et al.: Trends. Mol. Med., 11, 382 (2005), Lomovskaya, O., et al.: Biochem. Pharmacol., 71, 910 (2006), Samosorn, S., et al.: Bioorg. Med. Chem., 14, 857 (2006),<br></p>

<p>Applications An impurity of Griseofulvin (G787500).<br>References Oda, T., et al.: Chem. Pharma. Bull., 34, 858 (1986),<br></p>

<p>Stability Moisture Sensitive<br>Applications 4-Ethyl-2,3-dioxo-1-piperazinecarbonyl Chloride is used as a reagent in the synthesis of amino(thienyl)benzamide derivatives which are used as histone deacetylase inhibitors and have antitumor activity. 4-Ethyl-2,3-dioxo-1-piperazinecarbonyl Chloride is also a reagent in the synthesis of Cefbuperazone (C242540); a second-generation cephalosporin antibiotic.<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 Hirata, Y., et al.: Bioorg. Med. Chem. Lett., 22, 1926 (2012); Liu, M., et al.: Zhongguo Yiyao Gongye Zazhi, 41, 649 (2010); Izumi, K., et al.: J. Chemother., 7 Suppl 4, 173 (1995)<br></p>

<p>Applications Amoxycilloic Acid Sodium Salt is an impurity of Amoxicillin (A634235), a semi-synthetic antibiotic related to Penicillin. Antibacterial.<br>References Connor, S., et al.: J. Pharm. Pharmacol., 46, 128 (1994); Van G., et al.: J. Vet. Pharmacol. Ther., 26, 139 (2003); Brogden, R.N., et al.: Drugs, 18, 169 (1979); Bird, A.E., et al.: Anal. Profiles Drug Subs. Excip., 23, 1 (1994)<br></p>

<p>Stability Hygroscopic<br>Applications Neamine is normally found as a core structure of aminoglycoside antibiotics. It is used in the synthesis of disaccharide neamine derivatives as antibacterial agents.<br>References Kawaguchi, H., et al.: J. Antibiot., 25, 695 (1972), Fourmy, D., et al.: Science, 274, 1367 (1996), Riguet, E., et al.: J. Med. Chem., 47, 4806 (2004)<br></p>

<p>Applications CP 1282 is the tautomer of the antibiotic Cefotetan (C242970) with similar degradation rates.<br>References Koshiro, A. et al.: Chem. Pharm. Bull., 37, 1864 (1989); Naber, K. et al.: Zeitsch. Antmickrob. Antineoplast. Chemother., 2, 161 (1984);<br></p>

<p>Stability: Hygroscopic<br>Applications: Posaconazole Succinyl Ester is the derivative of Posaconazole (P689600), which is an orally active triazole antifungal.<br>References Cacciapuoti, A., et al.: Antimicrob. Agents Chemother., 44, 2017 (2000), Herbrecht, R., et al.: Int. J. Clin. Pract., 58, 612 (2004), Panackal, A., et al.: J. Clin. Microbiol., 44, 1740 (2006)<br></p>

<p>Stability Light Sensitive<br>Applications A labelled metabolite of Rifampicin.<br>References Blumenfeld,O.O., et al.: J. Biol. Chem., 236, 2472 (1961), Cowxan, R.A., et al.: Biochem. Biophys. Res. Commun, 23, 799 (1966)<br></p>

<p>Applications (2S,3S)-3-Amino-2-[[(2Z)-2-(2-amino-4-thiazolyl)-2-[(1-carboxy-1-methylethoxy)imino]acetyl]amino]butanoic Acid is an impurity of Aztreonam (A965200), the first totally synthetic monocyclic β-lactam antibiotic.<br>References Murugan, R., Narayanan, S.S.: Anal. Chem. Indian J., 8, 36 (2009); Sykes, R.B., et al.: Antimicrob. Agents Chemother., 21, 85 (1982); Florey, K., et al.: Anal. Profiles Drug Subs., 17, 1 (1988)<br></p>

<p>Applications Labelled semi-synthetic antibiotic related to Penicillin. Antibacterial.<br>References Brogden, R.N., et al.: Drugs, 18, 169 (1979), Bird, A.E., et al.: Anal. Profiles Drug Subs. Excip., 23, 1 (1994),<br></p>

<p>Impurity Enrofloxacin USP Related Compound Mixture<br>Applications Fluorinated quinolone antibacterial. Enrofloxacin USP Related Compound Mixture.<br>References Altreuther, P., et al.: Vet. Med. Rev., 2, 87 (1987),<br></p>

<p>Impurity Clavulanate Potassium EP Impurity C<br>Applications 3-Ethyl-2,5-pyrazinediethanol (Clavulanate Potassium EP Impurity C) is an impurity of Clavulanic acid (C563750). High concentrations of Clavulanic acid but not of its degradation products decrease glycerol consumption and oxygen uptake rates in cultures of Streptomyces clavuligerus.<br>References Zupke, C., et al.: Biotechnol. Prog., 10, 489 (1994), Finlay, J., et al.: J .Antimicrob. Chemother., 52, 18 (2003), Alper, H., et al.: Science, 314, 1565 (2006), Brethauer, S., et al.: Biotechnol. Bioeng., 98, 356 (2007),<br></p>

<p>Applications The S,S-stereoisomer of Chloramphenicol (C325030). Broad spectrum antibiotic obtained from cultures of the soil bacterium Streptomyces venezuelae. It has a broad spectrum of activity against Gram-positive and gram-negative bacteria. Antibacterial; antirickettsial.<br>References Bartz, et al.: J. Biol. Chem., et al.: 172, 445 (1948), Gottlieb, et al.: J. Bacteriol., 55, 409 (1948), Szulczewski, D., et al.: Anal. Profiles Drug Subs., 4, 47 (1975), Price, A., et al.: J. Antibiot., 43, 118 (1981), Shalit, I., et al.: Drugs, 28, 281 (1984),<br></p>

<p>Stability Hygroscopic<br>Applications 6-Hydroxy-6-defluoro Ciprofloxacin Hydrochloride (Ciprofloxacin EP Impurity F) is a the salt form of 6-Hydroxy-6-defluoro Ciprofloxacin (H825210), hydroxy analog of Ciprofloxacin (C482500).<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 Ge, L., et al.: Environ. Sci. Technol., 44, 2400 (2010),<br></p>

<p>Impurity Clarithromycin EP Impurity I<br>Applications De(cladinosyl) Clarithromycin (Clarithromycin EP Impurity I) is an impurity of Clarithromycin (C559750). De(cladinosyl) Clarithromycin showed significantly potent antibacterial activity against community acquired respiratory pathogens.<br>References Morimoto, S., et al.: J. Antibiot., 37, 187 (1984), Buxbaum, A., et al.: J. Antimicrob. Chemother., 52, 371 (2003), Westphal, J., et al.: Br. J. Clin. Pharmacol., 50, 285 (2000), Ma, Z., et al.: J. Med. Chem., 44, 4137 (2001),<br></p>

<p>Impurity Erythromycin EP Impurity E<br>Applications Erythromycin A Enol Ether (Erythromycin EP Impurity E) is an impurity of Erythromycin.<br>References McGuire, J.M., et al.: Antibiot. Chemother., 6, 281 (1952), Steffansen, B., et al.: Int. J. Pharm., 56, 159 (1989), Goldman, R.C., et al.: Antimicrob. Agents Chemother., 34, 1973 (1990),<br></p>

<p>Stability Hygroscopic<br>Applications Vancomycin Hydrochloride is an antibiotic used against gram-positive bacterial strains.<br>References Yao, N., et al.: Biopolymers, 90, 421 (2008); Lai, H., et al.: ACS Appl. Mater. Interfaces, 7, 2046 (2015);<br></p>

<p>Applications Intermediate in the production of biosynthetic antibiotics<br>References Horton, D., et al.: Anal. Biochem., 59, 452 (1974), Kamenik, Z., et al.: Anal. Bioanal. Chem., 393, 1779 (2009),<br></p>

<p>Impurity Clindamycin Phosphate EP Impurity L<br>Applications 7-Epiclindamycin 2-Phosphate (Clindamycin Phosphate EP Impurity L) is an impurity of Clindamycin (C580000), a semi-synthetic antibiotic prepared from Lincomycin. Antibacterial.<br>References Birkenmeyer, R.D., et al.: J. Med. Chem., 13, 616 (1970); Oesterling, et al.: J. Pharm. Sci., 59, 63 (1970); Gray, J.E., et al.: Toxicol. Appl. Pharmacol., 21, 516 (1972); Brown, L.W., et al.: Anal. Profiles Drug Subs., 10, 75 (1981)<br></p>

<p>Ledipasvir (GS-5885) is a Hepatitis C Virus NS5A Inhibitor.</p>

<p>Applications Epothilones are polyketide natural products that inhibit cancer cells by a mechanism similar to paclitaxel, and also are effective against paclitaxel-resistant tumours. Epothilone D is in phase I clinical testing of in patients with advanced solid tumours. Epothilone D is a cytotoxic macrolide that stabilises malignant cells' microtubules and arrests mitosis, a characteristic it shares with other epothilones. They bind to the same hepatic sites as does paclitaxel (Taxol) in a 1:1 stoichiometric ratio of a, b-tubulin heterodimers.<br>References Bollag, D.M., et al.: Cancer. Res., 55, 2325 (1995), Hardt, I.H., et al.: J. Nat. Prod., 64, 847 (2001), Gerth, K., et al.: J. Antibiot., 55, 41, 45 (2002)<br></p>

<p>Applications Semi-synthetic macrolide antibiotic. Antibacterial.<br>References Malmborg, A.-S., et al.: J. Antimicrob. Chemother., 5, 591 (1979),<br></p>

<p>Applications A metabolite of the fluorinated quinolone antibacterial Ciprofloxacin (C482500).<br>References Hoffken, G., et al.: Antimicrob. Ag. Chemother., 27, 375 (1985), Scully, B.E., et al.: Lancet, 1, 819 (1986)<br></p>

<p>Applications Sisomicin is an Antibacterial. Gentamicin-like aminoglycoside antibiotic; has broad spectrum antibiotic activity.<br>References Weinstein, M.J., et al.: J. Antibiot., 23, 551 (1970), Sculier, J.P., et al.: J. Antimicrob. Chemother., 9, 63 (1982), Noone, P., et al.: Drugs, 27, 548 (1984),<br></p>

<p>Applications An antibacterial.<br>References Bauernfeind, A.: J. Antimicro. Chemother., 40, 639 (1997), Fukuda, H., et al.: Antimicrob. Ag. Chemother., 42, 1917 (1998),<br></p>

<p>Applications Amoxicillin Closed-loop Dimer is a dimer of Amoxicillin(A634528) which is an antibiotic used in the treatment of various bacterial infections.<br></p>

<p>Applications A mixture of semi-synthetic Avermectins; containing 90% or more of component B1a and 10% or less of component B1b. Antiparasitic.<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 Jones, T.K., et al.: J. Agric. Food Chem., 42, 1786 (1994), Arena, J.P., et al.: J. Parasitol., 81, 286 (1995),<br></p>

<p>Applications Third generation, orally active cephalosporin antibiotic. Antibacterial.<br>References Wise, R., et al.: Antimicrob. Agents Chemother., 29, 1067 (1986), Hirai, S., et al.: Jpn. J. Antibiot., 39, 958 (1986), Lentz, K., et al.: Int. J. Pharm., 200, 41 (2000), Takagi, T., et al.: Mol. Pharmaceutics, 3, 631 (2006), Gu, C., et al.: Pharm. Res., 24, 1118 (2007),<br></p>

<p>Impurity Terbinafine BP Impurity A; Terbinafine USP Related Compound A<br>Applications N-Methyl-1-naphthalenemethanamine hydrochloride (Terbinafine BP Impurity A; Terbinafine USP Related Compound A) is an intermediate used in the synthesis of various pharmaceuticals such as Terbinafine hydrochloride (T107500) and Butenafine hydrochloride (B690195).<br>References Petranyi, G., et al.: Science, 224, 1239 (1984); Ryder, N.S., et al.: Antimicrob. Agents Chemother., 27, 252 (1985); Evans, E.G.V., et al.: Br. Med. J., 318, 1031 (1999); Kokjohn, K., et al.: Int. J. Dermatol., 42, 11 (2003); Sumikawa, M., et al.: J. Dermatol., 34, 456 (2007)<br></p>

<p>Stability Hygroscopic<br>Applications Polyether antibiotic. Coccidiostat.<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 Day, et al.: Antimicrob. Agents Chemother., 4, 410 (1973), Buchko, S., et al.: J. Food Prot., 63, 1467 (2000), De Leener, E., et al.: Microb. Drug Resist., 10, 341 (2004), Sanderson, M., et al.: Vet. Microbiol., 110, 125 ( 2005),<br></p>

<p>Stability Hygroscopic<br>Applications Desfuroyl Ceftiofur Dimer is an impurity of the drug Ceftiofur (C244695), a third generation cephalosporin antibiotic used in veterinary medicine.<br>References Donaldson, S.C. et al.: Appl. Environ. Microbiol., 72, 3940 (2006); Yancey, R.J. et al.: Am. J. Vet. Res., 48, 1050 (1987);<br></p>

<p>Stability Hygroscopic<br>Applications Delactamimipenem Monosodium is an impurity found in imipenem (I465200).<br>References Ratcliffe, R.W., et. al.: J. Org. Chem., 54, 653 (1989)<br></p>

<p>Applications Linezolid (L466500) intermediate.<br></p>

<p>Applications An impurity of Tobramycin (T524000(P)), which is a single factor antibiotic comprising about 10% of nebramycin, the aminoglycosidic antibiotic complex produced by Streptomyces tenebrarius; antibacterial.<br>References Brandl, M. et al.: Drug Dev. Ind. Pharm., 18, 1423 (1992); Murase, M. et al.: Prog. Antimicrob. Anticancer Chemother., Proc. Int. Congr. Chemother., 6, 1098 (1970); Koch, K.F., et al.: Antimicrob. Agents Chemother., 309 (1970); Welles, J.S., et al.: Toxicol. Appl. Pharmacol., 22, 332 (1972); Dash, A.K., et al.: Anal. Profiles Drug Subs. Excip., 24, 579 (1996)<br></p>

<p>Impurity Selamectin Impurity B<br>Stability Hygroscopic<br>Applications 22,23-Didehydro Selamectin is an impurity of Selamectin (S247990) which is a topical parasiticide. Selamectin (S247990) is also used as a veterinary antihelminithic agent on animals.<br>References Eshar, D., et al.: J. Am. Veterin. Med. Association., 241, 1056 (2012); Geis-Asteggiante, L., et al.: J. Chromatograph., 1258, 43 (2012);<br></p>

<p>Impurity Terbinafine EP Impurity E Dihydrochloride Salt<br>Applications A Terbinafine dimeric impurity of the antifungal agent Terbinafine (T107500), an orally active, antimycotic allylamine related to Naftifine. A specfic inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Antifungal. Also an impurity of SF 86-327 an antimycotic agent (2).<br>References 1. Petranyi G. et al.: Science. 1984 Jun 15;224(4654):1239-41. 2. Ryder, N et al.: Antimicrob Agents Chemother. 1985 Feb;27(2):252-6.<br></p>

<p>Impurity Azithromycin EP Impurity N<br>Stability Hygroscopic<br>Applications Azithromycin (A927000) impurity. A degradation products of Azithromycin.<br>References Anon., et al.: Pharmaeuropa, 13, 750 (2001),<br></p>

<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>

<p>Applications Labelled Azithromycin, a semi-synthetic macrolide antibiotic; related to Erythromycin A. Antibacterial.<br>References Langtry, H.D., et al.: Drugs, 56, 273 (1998),<br></p>

<p>Applications 7-Amino-3-(1-pyridylmethyl)-3-cephem-4-carboxylic acid Hydroiodide, is an impurity of Ceftazidime (C244100). Ceftazidime impurity B.<br>References Miyake, A., et al.: Antimicrob. Agents Chemother., 486, 182 (1989), Seibert, G., et al.: Arzneim.-Forsch., 33, 1084 (1983),<br></p>

<p>Applications N-Desmethyl Doxycycline is a metabolite of Doxycycline (D561500); an antibacterial agent.<br>References Fabre, et al.: Chemotherapia, 11, 73 (1966); Goldenthal, et al.: Toxicol. Appl. Pharmacol., 18, 185 (1971); Polson, A.M., et al.: J. Periodontol., 68, 110 (1997); Boecker, R., et al.: Drug. Exp. Clin. Res., 9, 813 (1983)<br></p>

<p>Alvespimycin (17-DMAG) is a potent Hsp90 inhibitor with potential anticancer activity, which acts by binding to Hsp90.</p>

<p>Applications Moenomycin complex is an antibiotic and selective inhibitor of the transglycosylation step. Flavomycin (bambermycins) is an antibiotic complex obtained from Streptomyces bambergiensis containing mainly Moenomycins A and C. They are used as feed additives and growth promoters for swine, poultry and cattle.<br>References Crossland, W. et al.: J. Animal Sci., 95, 4554 (2017);<br></p>

<p>Applications 11-Desmethyl Rifaximin is a compound useful in organic synthesis.<br></p>

<p>Applications Abamectin is a mixture of avermectins, containing at least 80% of avermectin B1a (C48H72O14) and not more than 20% of avermectin B1b (C47H70O14). Used as acaricide, insecticide, Cannabis pesticide detection.<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 Wang, S., et al.: Prog. Clin. Biol. Res., 97, 373 (1982); Greenblatt, J.A., et al.: J. Agric. Entomol., 3, 233 (1986); Drexler, G., et al.: Eur. J. Pharmacol., 99, 269 (1984);<br></p>

<p>Applications An orally active, antimycotic allylamine related to Naftifine. A specfic inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Antifungal.<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 Petranyi, G., et al.: Science, 224, 1239 (1984), Ryder, N.S., et al.: Antimicrob. Agents Chemother., 27, 252 (1985), Evans, E.G.V., et al.: Br. Med. J., 318, 1031 (1999),<br></p>

<p>Applications Homoharringtonine (HHT) combined with some botanical drugs could induce cancer cells to resemble normal cells. HHT was prepared by a semi-synthetic method from Cephalotaxine, a major alkaloid of Cepahlotaxus species through the formation of α-ketoester harringtonine.<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 Baaske, D., et al.: Antimicrob. Agents Chemother., 12, 298 (1977), Tipping, A., et al.: Leukemia, 16, 2349 (2002), Marin, D., et al.: Cancer, 103, 1850 (2005), Levy, V., et al.: Br. J. Cancer, 95, 253 (2006), de Lavallade, H., et al.: Blood, 2779 (2007),<br></p>

<p>Applications Tilmicosin Phosphate Salt is the phosphate salt of the semi-synthetic antibiotic derivative. It can be used in biological study and pharmacological activity of bactericidal effects of various concentrations of enrofloxacin, florfenicol, tilmicosin phosphate, and tulathromycin on clinical isolates of Mannheimia haemolytica from cattle.<br>References Blondeau, J., et al.: Am J Vet Res, 76, 860 (2015)<br></p>

<p>Applications Nebramine Sulfate is a degradation product on the antibiotic Tobramycin (T524000).<br>References Brandl, M. et al.: Drug Dev. Indust. Pharm., 18, 1423 (1992); Ghinami, C. et al.: J. Chrom. A, 1139, 52 (2007);<br></p>

<p>Applications Intermediate in the production of Lumefantrine.<br>References Washburn, L., et al.: J. Med. Chem., 17, 676 (1974), Nakamura, H., et al.: Environ. Sci. Technol., 41, 2190 (2007),<br></p>

<p>Impurity Terbinafine EP Impurity C<br>Stability Hygroscopic<br>Applications N-[(2E)-6,6-Dimethyl-2-hepten-4-yn-1-yl]-N-methyl-2-naphthalenemethanamine Hydrochloride (Terbinafine EP Impurity C<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 Petranyi, G., et al.: Science, 224, 1239 (1984); Ryder, N.S., et al.: Antimicrob. Agents Chemother., 27, 252 (1985); Evans, E.G.V., et al.: Br. Med. J., 318, 1031 (1999);<br></p>

<p>Applications Bacitracin Zinc is a peptide antibiotic effective against gram-postive bacteria. Bacitracin is an inhibitor of peptidoglycan synthesis. Bacitracin disrupts bacterial cell wall synthesis by inhibiting dephosphorylation of lipid pyrophosphate. Bacitracin also strongly inhibits proline endopeptidase from human muscle.<br>References Ward, J.B. et al.: Biochem. J., 141, 227 (1974); Anastasi, A. et al.: Biochem. J., 290, 601 (1993); Daly, D.J. et al.: Biochem. Soc. Trans., 13, 1161 (1985); Weinberg, E.D. et al.: Antibiot. Ber., 90, (1967);<br></p>

<p>Applications Pipecolic acid is involved in synaptic transmission in the central nervous system. The l-form occurs in plants.<br>References Nomura Y., et al.: Neurochem. Res., 6, 391 (1981),<br></p>

<p>Applications Moxidectin EP L is an impurity of Moxidectin (M744800) which is a macrocyclic lactone and semisynthetic derivative of nemadectin. Moxidectin is a parasiticide used for the prevention and control of heartworm and intestinal worms. Moxidectin is found in veterinary medicine used to treat animals such as dogs, cats, horses, cattle and sheep.<br>References Bisset, S.A. et al.: New Zeal. Vet. J., 40, 97 (1992); Monahan, C.M. et al.: Vet. Parasitol., 63, 225 (1996); Glickman, L.T. et al.: Int. J. Appl. Res. Vet. Med., 3, 49 (2005);<br></p>

<p>Applications The major glucuronide metabolite of Chloramphenicol (C325030).<br>References Simons, P., et al.: Xenobiotica, 22, 1267 (1992), Kaji, H., et al.: Drug Metab. Dispos., 33, 60 (2005),<br></p>

<p>Stability Store in Freezer<br>Applications Clarithromycin is a semi-synthetic macrolide antibiotic. Clarithromycin is a derivative of Erythromycin (E650000).<br>References Benson, C., et al.: Eur. J. Clin. Microbiol., 6, 173 (1987), Boyanova, L., et al.: J. Med. Microb., 61, 85 (2012), Lin, Z., et al.: Toxicol. Sci., 126, 114 (2012),<br></p>

<p>Applications Cephalosporin 87/359 is an impurity of Cefoxitin (C243190). Cefoxitin is a semi-synthetic antibiotic derived from Cephamycin C, possessing high resistance to β-lactamase inactivation. An antibacterial.<br>References Wallick, H., et al.: Antimicrob. Agents Chemother., 5, 25 (1974), Brenner, G.S., et al.: Anal. Profiles Drug Subs., 11, 169 (1982),<br></p>

<p>Applications N-Demethyl Rifampicin is a metabolite of Rifampicin (R508000).<br>References Marsili, L., et al.: J. Antibiot., 37, 1209 (1984), Nikaido, H., et al.: Antimicrob. Ag. Chemother., 37, 1393 (1993), Piddock, L., et al.: J. Antimicrob. Chemother., 45, 159 (2000),<br></p>

<p>Applications Anidulafungin Open-chain Degradant is an impurity of Anidulafungin (A673000) which is used as an antifungal drug.<br>References Denning, D. W., et al.: J. Antimicrob. Chemother, 40, 611 (1997); Vazquez, J. A., et al.: Clin. Ther., 27(6), 657 (2005);<br></p>

<p>Applications 1-butylpiperidine-2-carboxylic acid (cas# 856838-98-7) is a useful research chemical.<br></p>

<p>Applications Bacitracin A is a peptide antibiotic.<br>References Eppelmann, K., et al.: J. Biol. Chem., 276, 34824 (2001); Mei, L., et al.: Biomat., 34, 10328 (2013);<br></p>