Natural and semi-synthetic antibiotics

<p>Applications An carbapenem antibacterial.<br>References Shigemi, A., et al.: Int. J. Antimicrob. Agents, 34, 589 (2009), Miguet, L., et al.: J. Med. Chem., 52, 5926 (2009), Zhao, W., et al.: J. Med. Microbiol., 58, 1080 (2009), Sanbongi, Y., et al.: Microbiol. Immunol., 53, 361 (2009),<br></p>

<p>Applications Labelled Tylosin (T947650). Tylosin is a macrolide antibiotic isolated from a strain of Streptomycetes fradiae found in soil from Thailand. Antibacterial.<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 Hamill, et al.: Antibiot. Chemother., 11, 328 (1961), Corcoran, J.W., et al.: J. Antibiot., 30, 1012 (1977), Seno, E.T., et al.: Antimicrob. Agents. Chemother., 11, 455 (1977),<br></p>

<p>Applications Enrofloxacin-d5 is a labelled fluorinated quinolone antibacterial.<br>References Altreuther, P., et al.: Vet. Med. Rev., 2, 87 (1987),<br></p>

<p>Applications D-Cycloserine inhibits cell wall biosynthesis (D-Ala peptide bond formation). D-Cycloserine also prevents conversion of D-Ala to L-Ala. D-Cycloserine is an bacteriostatic. D-Cycloserine is an antibiotic against Gram-negative bacteria. There is evidence that D-cycloserine can enhance neuronal changes that lead to learning.<br>References Lamb., J.W., et al.: Anal. Profiles Drug Subs., 1, 53 (1972), Gentry-Weeks, C., et al.: J. Biol. Chem., 268, 7298 (1993), Alexander, F., et al.: Eur. J. Biochem., 219, 953 (1994), Auger, S., et al.: Biochimie, 87, 231 (2005); Chem and Eng. News p. 12, Dec. 7/14 (2015)<br></p>

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

<p>Stability Hygroscopic<br>Applications BB-K 6 is a semi-synthetic aminoglycoside antibiotic derived from Kanamycin A (K137500).<br>References Naito, T. et al.: J. Antibiot., 26, 297 (1973); Cron, M.J. et al.: J. Chem. Soc. Chem. Comm., 6, 266 (1979); Nakagawa, S. et al.: Mircob. Drug Resist., 2, 269 (1979);<br></p>

<p>Applications Mutational biosynthetic antiparasitic antibiotic structurally related to the avermectins.<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 Dutton, C.J., et al.: J. Antibiot., 44, 357 (1991), Lavy, E., et al.: Res. Vet. Sci., 75, 217 (2003)<br></p>

<p>Applications Moxifloxacin (M745000) impurity.<br>References Martel, A., et al.: Drugs Fut., 22, 109 (1997), Tobin, C., et al.: J. Antimicrob. Chemother., 42, 278 (1998),<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.<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 An antibacterial.<br>References Hirai, K., et al.: Antimicrob. Ag. Chemother., 29, 1059 (1986), Weidekamm, E., et al.: Antimicrob. Ag. Chemother., 31, 1909 (1987), Boerema, J.B.J., et al.: J. Antimicrob. Chemother., 21, 140 (1988)<br></p>

<p>Applications An impurity of Rifampamycin (R508000).<br></p>

<p>Applications 4'-O-2,6-Dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl 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>Stability Hygroscopic, Light Sensitive<br>Applications Rifabutin N-Oxide is a metabolite of Rifabutin (R505000) and like its parent compound it exhibits antibacterial activity.<br>References Medeiros, M., et al.: PCT Int. Appl., 44, (2004); Anand, R., et al.: Antimicrob. AG. Chemother., 32 (684 (1988), Skinner, M.H., et al.: Antimicrob. Agent Chemother., 33, 1237 (1989),<br></p>

<p>Applications Cefquinome (cas# 84957-30-2) is a compound useful in organic synthesis.<br></p>

<p>Applications Labelled Ceftiofur (C244700). An antibacterial.<br>References Yancey, R.J., et al.: Am. J. Vet. Res., 48, 1050 (1987)<br></p>

<p>Stability Hygroscopic<br>Applications A macrolide compound which is known to have antibacterial activity, and is useful in the therapy of bacterial infections in mammals. Antibiotic.<br>References Broto, P., et al.: Eur. J. Med. Chem., 19, 71 (1984), Farrar, V., et al.: J. Med. Chem., 36, 3517 (1993), Clark, D., et al.: J. Pharm. Sci., 88, 807 (1999),<br></p>

<p>Applications A metabolite of Roxithromycin (R700850).<br>References Lindstrom, T., et al.: Antimicrob. Agents Chemother., 37, 265 (1993), Shimada, T., et al.: J. Pharmacol. Exp. Ther., 270, 414 (1994), Yamazaki, H., et al.: J. Toxicol. Sci., 21, 215 (1996),<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>Applications T 2588G Sodium Bisulfite is a more stable form of T 2588G (Cefepime EP Impurity C) (T003100) which is a metabolite of Cefditorin (ME1207) (C242700), a new oral cephem.<br>References Sugioka, T., et al.: Chem. Pharmaceut. Bull., 38, 1998 (1990)<br></p>

<p>Impurity Azithromycin EP Impurity J<br>Applications Descladinose Azithromycin (Azithromycin EP Impurity J) is a metabolite of the semi-synthetic macrolide antibiotic Azithromycin (A927000).<br>References Luke, D.R. et al.: Clin. Pharmacol. Therap., 61, 641 (1997); Foulds, G. et al.: Infect. Dis. THer., 18, 367 (1995);<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 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>Impurity Fosfomycin EP Impurity C (Barium Salt)<br>Stability Hygroscopic<br>Applications 2-Amino-3-hydroxy-2-(hydroxymethyl)propyl Phosphate Barium Salt (Fosfomycin EP Impurity C (Barium Salt)) is a Fosfomycin (F727500) impurity. Fosfomycin is an antibiotic that exerts a broad spectrum of antibacterial activity.<br>References McGrath, J.W., et al.: Org. Biomolec. Chem., 7, 9 (1944); Goto, M., et al.: Antimicrob. Agents Chemother., 20, 393 (1981);<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>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>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 Linezolid USP Related Compound A<br>Applications An impurity of Linezolid (L466500), as antimycobacterial agent. Linezolid USP Related Compound A.<br>References Sato, K., et al.: Eur. J. Pharmacol., 347, 231 (1998), Maignan, S., et al.: J. Med. Chem., 43, 3226 (2000), Tokuyama, R., et al.: Chem. Pharm. Bull., 49, 353 (2001),<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 Florfenicol (F405750) intermediate as antibacterial agent.<br>References Kim, E, et al.: Microbiol. Immunol., 40, 665, (1996), Keyes, K.: Antimicrob. Agents Chemother., 44, 421 (2000)<br></p>

<p>Applications Aztreonam intermediate.<br>References Indelicato, J., et al.: J. Pharm. Sci., 75, 304 (1986), Kline, T., et al.: Bioorg. Med. Chem., 8, 73 (2000),<br></p>

<p>Impurity Amoxicillin EP Impurity H ; Amoxicillin USP Related Compound H<br>Stability Hygroscopic<br>Applications (R)-α-[(2,2-Dimethyl-1-oxopropyl)amino]-4-hydroxybenzeneacetic Acid (Amoxicillin EP Impurity H), is an Amoxicillin (A634235) related compound.<br>References Valvo, L., et al.: J. Chromatography A, 797, 311 (1998); 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 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>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>

<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 Novel intermediate of Azithromycin that acts as antibiotic.<br>References Krajacic, M.B., et al.: J. Antibiot., 58, 380 (2005),<br></p>

<p>Stability Hygroscopic<br>Applications Single factor antibiotic comprising about 10% of nebramycin, the aminoglycosidic antibiotic complex produced by Streptomyces tenebrarius. Antibacterial.A representative lot contains d4, d5, d6, d7, d8, and d9.<br>References 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 Cefalotin EP Impurity B<br>Applications Deacetylcephalothin (Cefalotin EP Impurity B) is an intermediate and the free acid analogue of Deacetylcephalothin Sodium Salt (D198210), which is an impurity in the synthesis of Cefalonium (C236800) and an analog of Cephalothin (C261150) a first-generation cephalosporin antibiotic used as a long-acting intramammary cerate for infusion of dairy cows.<br>References Shibata, K., et al.: J. Antibiot., 50, 135 (1997); Farra, A., et al.: Int. J. Antimicrob. Agents., 31, 427 (2008); Pichardo, C., et al.: Eur. J. Clin. Microbiol. Infect. Dis., 30, 289 (2011);<br></p>

<p>Applications An inactive metabolite of Linezolid (L466500).<br>References Shinabarger, D., et al.: Antimicrob. Agents Chemother., 41, 2132 (1997), Wynalda, M., et al.: Drug Metab. Dispos., 28, 1014 (2000),<br></p>

<p>Applications A phosphocholine ester metabolite of the immunosuppressant macrolide SDZ RAD (also known as Everolimus E945400) which is an analog of the parent drug Rapamycin (R124000).<br>References Zollinger, M. et al.: Drug. Metab. Disp., 36, 1457 (2008); Kovarik, J. M., et al.: Clin. Pharmacol. Ther., 69, 48 (2001);<br></p>

<p>Impurity Moxidectin EP Impurity K<br>Applications 5-O-(4-nitrobenzoyl)moxidectin is an impurity of moxidectin (M744800), 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>Ledipasvir (GS-5885) is a Hepatitis C Virus NS5A Inhibitor.</p>

<p>Applications 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>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>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>Applications Lasalocid is an anticancer supplement agent comprising of polyether antibiotic for treating brain tumors, also inhibits mitochondrial GPD2 activity and elicits anti-proliferative effects on cancer cells.<br>References Singh, G., et al.: Pharmaceuticals, 7, 192 (2014); Choi, G. S., et al.: Repub. Korean Kongkae Taeho Kongbo (2015), KR 2015033201 A 20150401<br></p>

<p>Applications Intermediate in the semi-synthetic cephalosporins synthesis. Found in Acremonium chrysogenum.<br>References Fukagawa, M. et al.; Agr. Biol. Chem. 55, 2163 (1991)<br></p>

<p>Applications Mupirocin, is a major component of the pseudomonic acid, an antibiotic complex produced by Pseudomonas fluorescens NCIB 10586. Topical antibacterial.<br>References Hughes, J., et al.: J. Antibiot., 31, 330 (1978), Ward, A., et al.: Drugs, 32, 425 (1986), Casewell, M.W., et al.: J. Antimicrob. Chemother., 19, 1 (1987),<br></p>

<p>Applications A selective HIV protease inhibitor. An analogue of Ritonavir.<br>References Adkins, J.C., et al.: Drugs, 55, 837 (1998)<br></p>

<p>Impurity Clavulanate Potassium EP Impurity A<br>Applications 2,5-Pyrazinediethanol (Clavulanate Potassium EP Impurity A) 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 Polyene antifungal antibiotic complex containing 3 biologically active components, A1, A2, A3. Increases the permeability of the cell membrane of sensitive fungi by binding to sterols. Cell culture tested. Growth promotant.Nystatin A1 is shown.<br>References Brautaset, T., et al.: Chem. Biol., 7, 395 (2000), Brautaset, T., et al.: J. Biol. Chem., 278, 14913 (2003), Bruheim, P., et al.: Antimicrob. Agents Chemother., 48, 4120 (2004), Scott, L., et al.: Drugs, 67, 269 (2007),<br></p>

<p>Impurity Azithromycin EP Impurity G<br>Applications 3’-N-Desmethyl-3’-N-tosyl Azithromycin (Azithromycin EP Impurity G) is an Azithromycin (A927000) impurity.<br>References Kirst, H., et al.: Antimicrob. Agents Chemother., 33, 1419 (1989), Gandhi, R., et al.: J. Pharm. Biomed. Anal., 23, 1073 (2000),<br></p>

<p>Stability Hygroscopic<br>Applications A labelled metabolite of Cephapirin (C261500) in bovine milk.<br>References Moats, W., et al.: J. Agric. Food Chem., 48, 498 (2000),<br></p>

<p>Applications N-Ethylpiperazine is an intermediate in the production of Enrofloxacin.<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 Chao, Q., et al.: J. Med. Chem., 52, 7808 (2009), Bebbington, D., et al.: Bioorg. Med. Chem. Lett., 19, 3586 (2009),<br></p>

<p>Impurity Azithromycin EP Impurity I<br>Stability Hygroscopic<br>Applications N’-Desmethyl Azithromycin (Azithromycin EP Impurity I) is a metabolite of Azithromycin (A927000) as potential anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agent.<br>References Bright, G., et al.: J. Antibiot., 41, 1029 (1988), Goldman, R., et al.: Antimicrob. Agents Chemother., 34, 426 (1990), Gandhi, R., et al.: J. Pharm. Biomed. Anal., 23, 1073 (2000),<br></p>

<p>Applications L-Penicillamine is a metabolite of penicillin. L-Penicillamine is used in the treatment of Wilson’s disease, Cystinuria, Scleroderma and arsenic poisoning.<br>References Marti-Prats, L., et al.: Neurosci. Lett., 483, 143 (2010), Singh, A., et al.: J. Pharm. Sci., 99, 3931 (2010), Everette, J., et al.: J. Agric. Food Chem., 58, 8139 (2010),<br></p>

<p>Applications Florfenicol is a fluorinated derivative of thiamphenicol. Florfenicol inhibits bacterial protein synthesis by binding to ribosome 50S and 70S subunits. Florfenicol is used as an antibacterial.<br>References Kim, E and Aoki, T.: Microbiol. Immunol., 40, 665, (1996), Keyes, K.: Antimicrob. Agents Chemother., 44, 421 (2000)<br></p>

<p>Applications 6-Chloro-6-defluoro Ciprofloxacin is an impurity of Ciprofloxacin (C482500), which is a fluorinated quinolone antibacterial.<br>References Hoffken, G., et al.: Antimicrob. Ag. Chemother., 27, 375 (1985), Scully, B.E., et al.: Lancet, 1, 819 (1986)<br></p>

<p>Impurity Cefixime EP Impurity A<br>Stability Light Sensitive, Temperature Sensitive<br>Applications Cefixime Impurity is an impurity of Cefixime (C242800); an orally active third generation cephalosporin antibiotic.<br>References Kamimura, T., et al.: Antimicrob. Agents Chemother., 25, 98 (1984); Yamanaka, H., et al.: J. Antibiot., 38, 1738 (1985); Guay, D.R.P., et al.: Antimicrob. Agents Chemother., 30, 485 (1986)<br></p>

<p>Stability Light Sensitive<br>Applications Moxidectin-d3 is a the labelled form of Moxidectin (M744800). Moxidectin 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> 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 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>Stability Very Hygroscopic<br>Applications Nebramine is a degradation product of 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>Impurity Mupirocin EP Impurity E<br>Stability Hygroscopic<br>Applications Mupirocin (M794000) impurity. The rearrangement isomer of Mupirocin is prepared using an enzyme-catalyzed, selective deesterification.<br>References Sime, J.T., et al.: Tetrahedron Lett., 28, 5169 (1987),<br></p>

<p>Applications Cefodizime is a third generation cephalosporin with a broad spectrum of antibacterial activity. Cefodizime maybe useful in the treatment of otitis media, sinusitis and gynaecological infections, and for the prophylaxis or treatment of surgical infections.<br>References Barradel, L.B. et al.: Drugs, 44, 800 (1992); Kasai, K. et al.: Jap. J. Antibiot., 37, 1306 (1984);<br></p>

<p>Applications Validamycin A (&gt;70%) Hydrochloride Salt is a metabolite of Validamycin A (&gt;70%) (V943430) which is an antibiotic fungicide that inhibits trehalase activity in plants, insects, and fungi.<br></p>

<p>Applications Cefdinir Sulfoxide is the oxide derivative of Cefdinir (C242670); a Cephalosporin antibiotic structurally similar to Cefixime.<br>References Inamoto, Y., et al.: J. Antibiot., 41, 828 (1988)<br></p>

<p>Applications D-threo-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol is an impurity of Chloramphenicol (C325030), a broad spectrum antibiotic agent obtained from cultures of the soil bacterium Streptomyces venezuelae.<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 Mehta, J., et al.: J. Biotechnol., 155, 361 (2011); Samsonova, J.V., et al.: Anal. Lett., 43, 133 (2010); Cravedi, J. P., et al.: Chem. Res. Toxciol., 8, 642 (1995); Wal, J.M., et al.: Antimicrob. Agent. Chemother., 24, 89 (1983);<br></p>

<p>Applications 3(2H)-Isoxazolone is a 3-hydroxyisoxazole with fungicidal activity. 3(2H)-Isoxazolone is an impurity of Cycloserine (C988800).<br>References Takahi, Y.: San. Kenk. Nen., 25, 8 (1973);<br></p>

<p>Applications A fluoroquinolone used in the synthesis of Gatifloxacin (G250000).<br>References Sunderland, J., et al.: J. Antimicrob. Chemother., 47, 271 (2001), Herzler, M., et al.: J. Anal. Toxicol., 27, 233 (2003), Li, Y., et al.: J. Pharm. Biomed. Anal., 35, 1101 (2004),<br></p>

<p>Applications Isotope labelled Erythromycin (E649950), an antibiotic useful for the treatment of a number of bacterial infection, usually prescribed to patients with allergy to penicillin.<br>References Koch, W.L., et al.: Anal. Profiles Drug Subs., 8, 157 (1979),<br></p>