Home > Name List By l > L-glycero-a-D-galacto-2-Nonulopyranose,O-2,6-dideoxy-3-O-methyl-b-D-arabino-hexopyranosyl-(1®

CAS No 194874-06-1 , L-glycero-a-D-galacto-2-Nonulopyranose,O-2,6-dideoxy-3-O-methyl-b-D-arabino-hexopyranosyl-(1®

  • Name: L-glycero-a-D-galacto-2-Nonulopyranose,O-2,6-dideoxy-3-O-methyl-b-D-arabino-hexopyranosyl-(1®
  • Synonyms: FU 40A;4)-O-2,6-dideoxy-3-C-methyl-a-L-arabino-hexopyranosyl-(1®Apoptolidin A;8)-3,5,7-trideoxy-1-C-[(2S,4S,5S,8E,10E,12R,13R,14E,16E,18E)-12-[(6-deoxy-4-O-methyl-a-L-glucopyranosyl)oxy]-5-hydroxy-4-methoxy-9,13,15,17,19-pentamethyl-20-oxooxacycloeicosa-8,10,14,16,18-pentaen-2-yl]-3,5-dimethyl-9-O-methyl-,(1R)-;Apoptolidin;L-glycero-a-D-galacto-2-Nonulopyranose,O-2,6-dideoxy-3-O-methyl-b-D-arabino-hexopyranosyl-(1®
  • CAS Registry Number:
  • Molecular Weight: 1129.38
  • Molecular Formula: C58H96 O21
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194874-06-1 APOPTOLIDIN

  • Germany Cfm Oskar Tropitzsch [Manufacturer]
  • Tel: +49-9231-9619-0
  • Fax: +49-9231-9619-60
  • Address: Cfm Oskar Tropitzsch
    Waldershofer Str. 49-51
    95615 Marktredwitz
    Germany null,nullGermany
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194874-06-1 SC-202062 APOPTOLIDIN

  • United States Santa Cruz Biotechnology, Inc. [Manufacturer]
  • Tel: 831-457-3800/ 800-457-3801
  • Fax: 831-457-3801
  • Address: Santa Cruz Biotechnology, Inc.
    2145 Delaware Ave.
    Santa Cruz, CA 95060 null,nullUnited States
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References of L-glycero-a-D-galacto-2-Nonulopyranose,O-2,6-dideoxy-3-O-methyl-b-D-arabino-hexopyranosyl-(1®
Title: Apoptolidin
CAS Registry Number: 194874-06-1
CAS Name: O-2,6-Dideoxy-3-O-methyl-b-D-arabino-hexopyranosyl-(1?4)-2,6-dideoxy-3-C-methyl-a-L-arabino-hexopyranosyl-(1?8)-3,5,7-trideoxy-1-C-[(2S,4S,5S,8E,10E,12R,13R,14E,16E,18E)-12-[(6-deoxy-4-O-methyl-a-L-glucopyranosyl)oxy]-5-hydroxy-4-methoxy-9,13,15,17,19-pentamethyl-20-oxooxacycloeicosa-8,10,14,16,18-pentaen-2-yl]-3,5-dimethyl-9-O-methyl-L-glycero-a-D-galacto-2-nonulopyranose
Manufacturers' Codes: FU-40A
Molecular Formula: C58H96O21
Molecular Weight: 1129.37
Percent Composition: C 61.68%, H 8.57%, O 29.75%
Literature References: Natural product isolated from Nocardiopsis sp.; specifically induces apoptosis in transformed tumor cells. Isoln, properties and bioactivity: J. W. Kim et al., J. Antibiot. 50, 628 (1997). Structure: Y. Hayakawa et al., J. Am. Chem. Soc. 120, 3524 (1998). Partial synthesis: J. Schuppan et al., Tetrahedron Lett. 41, 621 (2000); K. C. Nicolaou et al., Chem. Commun. 2000, 307. Review of synthetic methods: P. T. Daniel et al., Angew. Chem. Int. Ed. 45, 872-893 (2006).
Properties: Colorless powder, mp 128-130°. [a]21D -5.2° (c = 1.0 in methanol). uv max (methanol): 234, 320 nm (e 28300, 22000).
Melting point: mp 128-130°
Optical Rotation: [a]21D -5.2° (c = 1.0 in methanol)
Absorption maximum: uv max (methanol): 234, 320 nm (e 28300, 22000)