Title:  Epirubicin 
CAS Registry Number:  56420-45-2 
CAS Name:  (8S,10S)-10-[(3-Amino-2,3,6-trideoxy-a-L-arabino-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-8-(hydroxyacetyl)-1-methoxy-5,12-naphthacenedione 
Additional Names:  3-glycoloyl-1,2,3,4,6,11-hexahydro-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1-naphthacenyl-3-amino-2,3,6-tridioxy-a-L-arabino-hexopyranoside;  4¢-epidoxorubicin;  4¢-epiadriamycin;  pidorubicin;  4¢-epi-DX 
Manufacturers' Codes:  IMI-28 
Molecular Formula:  C27H29NO11 
Molecular Weight:  543.52 
Percent Composition:  C 59.66%, H 5.38%, N 2.58%, O 32.38% 
Literature References:  Analog of the anthracycline antibiotic doxorubicin, q.v., differing only in the position of the C-4 hydroxy group of the sugar moiety.  Prepn:  F. Arcamone et al., DE 2510866; eidem, US 4058519 (1975, 1977 both to Soc. Farmaceut. Italia); eidem, J. Med. Chem. 18, 703 (1975); S. Penco, Process Biochem. 15(5), 12 (1980).  Purification:  E. Oppici et al., BE 898506; eidem, GB 2133005 (both 1984 to Farmitalia Carlo Erba).  Comparison with doxorubicin of in vitro activity:  A. Di Marco et al., Cancer Res. 36, 1962 (1976).  Tissue distribution:  C. Italia et al., Br. J. Cancer 47, 545 (1983); F. Arcamone et al., Cancer Chemother. Pharmacol. 12, 157 (1984).  HPLC determn in biological fluids:  P. E. Deesen, B. Leyland-Jones, Drug Metab. Dispos. 12, 9 (1984); G. Cassinelli et al., ibid. 506.  Clinical trials in solid tumors:  K. Kolaric et al., J. Cancer Res. Clin. Oncol. 106, 148 (1983).  Review of activity in experimental tumors:  A. Goldin et al., Invest. New Drugs 3, 3-21 (1985).  Review of pharmacology and clinical efficacy:  F. Ganzina, Cancer Treat. Rev. 10, 1-22 (1983); R. J. Cersosimo, W. K. Hong, J. Clin. Oncol. 4, 425-439 (1986); P. Hurteloup, F. Ganzina, Drugs Exp. Clin. Res. 13, 233-246 (1986).  Review of epirubicin and other anthracycline antineoplastics:  R. B. Weiss et al., Cancer Chemother. Pharmacol. 18, 185-97 (1986). 
  
Derivative Type:  Hydrochloride  
CAS Registry Number:  56390-09-1 
Trademarks:  Ellence (Pharmacia & Upjohn);  Farmorubicina (Pharmacia) 
Molecular Formula:  C27H29NO11.HCl 
Molecular Weight:  579.98 
Percent Composition:  C 55.91%, H 5.21%, N 2.42%, O 30.34%, Cl 6.11% 
Properties:  Red-orange crystals, mp 185° (dec).  [a]D20 +274° (c = 0.01 in methanol).  Solution should be protected from sunlight. 
Melting point:  mp 185° (dec) 
Optical Rotation:  [a]D20 +274° (c = 0.01 in methanol) 
  
Therap-Cat:  Antineoplastic. 
Keywords:  Antineoplastic; Antibiotics and Analogs; Anthracyclines; Topoisomerase II Inhibitor.   |