Home > Name List By 2 > 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-...

CAS No 71628-96-1 , 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-,(2R,3S,4R,5R,6R,11R,13R)-

  • Name: 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-,(2R,3S,4R,5R,6R,11R,13R)-
  • Synonyms: NSC 269148; 7-OMEN; 7(R)-O-Methylnogarol; 7-O-Methylnogarol; U 52047;2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-,(2R,3S,4R,5R,6R,11R,13R)-;2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-,[2R-(2a,3b,4a,5b,6a,11a,13a)]-;Menogaril; TUT 7;7-Con-O-methylnogarol; 7-con-O-Methylnogarol;
  • CAS Registry Number:
  • Flash Point: 437.7°C
  • Boiling Point: 800.1°C at 760 mmHg
  • Density: 1.59g/cm3
  • Refractive index: 1.719
  • Safety Statements: Poison by intravenous and intraperitoneal routes. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx.
  • Flash Point: 437.7°C
  • Molecular Weight: 0
  • InChI: InChI=1/C28H31NO10/c1-27(36)8-10-6-11-16(21(32)15(10)14(9-27)37-5)22(33)17-13(30)7-12-24(18(17)20(11)31)38-26-23(34)19(29(3)4)25(35)28(12,2)39-26/h6-7,14,19,23,25-26,30,32,34-36H,8-9H2,1-5H3/t14-,19+,23+,25-,26-,27-,28-/m1/s1
  • Molecular Formula: C28H31 N O10
  • Molecular Structure:CAS No:71628-96-1 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-,(2R,3S,4R,5R,6R,11R,13R)-

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71628-96-1 Menogaril

  • United States LGM Pharma [Manufacturer]
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  • Address: 922 Clint Moore Road
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71628-96-1 MENOGARIL

  • China Nanjing Chemlin Chemical Industry Co.,Ltd. [Manufacturer]
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References of 2,6-Epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione,4-(dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-,(2R,3S,4R,5R,6R,11R,13R)-
Title: Menogaril
CAS Registry Number: 71628-96-1
CAS Name: (2R,3S,4R,5R,6R,11R,13R)-4-(Dimethylamino)-3,4,5,6,11,12,13,14-octahydro-3,5,8,10,13-pentahydroxy-11-methoxy-6,13-dimethyl-2,6-epoxy-2H-naphthaceno[1,2-b]oxocin-9,16-dione
Synonyms: 7-con-O-methylnogarol; 7-OMEN; 7(R)-O-methylnogarol; menogarol; TUT-7
Manufacturers' Codes: NSC-269148; U-52047
Molecular Formula: C28H31NO10
Molecular Weight: 541.55
Percent Composition: C 62.10%, H 5.77%, N 2.59%, O 29.54%
Literature References: Antitumor antibiotic; semi-synthetic derivative of nogalamycin. Prepn: P. F. Wiley, D. J. Houser, US 4086245 (1978 to Upjohn). Total synthesis: M. Kawasaki et al., Tetrahedron 44, 5727 (1988). Antitumor activity: G. L. Neil et al., Cancer Treat. Rep. 63, 1971 (1979). HPLC determn in plasma: J. E. Brown et al., J. Chromatogr. 226, 521 (1981); J. P. McGovren et al., Anal. Chem. 56, 1587 (1984). Pharmacokinetics and metabolism: M. J. Egorin et al., Cancer Res. 46, 1513 (1986). Mechanism of action: K. Wierzba et al., Jpn. J. Cancer Res. 81, 842 (1990). Clinical studies in non-small cell lung cancer: R. B. Vance et al., Invest. New Drugs 9, 73 (1991); in non-Hodgkin's lymphoma: J. Skillings et al., ibid., 79. Brief review of antitumor, biochemical, and toxicological studies: J. P. McGovren et al., ibid. 2, 359-367 (1984).
Properties: Orange crystals, mp 247-249° (dec). [a]D20 +857° (c = 0.112 in CHCl3). Also reported as mp 250-254° (dec). [a]D20 +867° (c = 0.045 in CHCl3); [a]D +958° (c = 0.163 in CHCl3). uv max (ethanol): 235, 251, 257, 290, 479 nm (e 41200, 25500, 24150, 10500, 15530).
Melting point: mp 247-249° (dec); mp 250-254° (dec)
Optical Rotation: [a]D20 +857° (c = 0.112 in CHCl3); [a]D20 +867° (c = 0.045 in CHCl3); [a]D +958° (c = 0.163 in CHCl3)
Absorption maximum: uv max (ethanol): 235, 251, 257, 290, 479 nm (e 41200, 25500, 24150, 10500, 15530)
 
 
Status: This monograph has been retired and is no longer subject to revision or update.