ChemicalBook--->CAS DataBase List--->99674-26-7

99674-26-7

99674-26-7 Structure

99674-26-7 Structure
IdentificationBack Directory
[Name]

esperamicin A1
[CAS]

99674-26-7
[Synonyms]

esperamicin A1
[Molecular Formula]

C59H80N4O22S4
[MDL Number]

MFCD34469160
[MOL File]

99674-26-7.mol
[Molecular Weight]

1325.55
Chemical PropertiesBack Directory
[density ]

1.43±0.1 g/cm3(Predicted)
[pka]

6.67±0.70(Predicted)
[CAS DataBase Reference]

99674-26-7
Hazard InformationBack Directory
[Definition]

ChEBI: A naturally occurring antibiotic and antitumor agent isolated from Actinomadura verrucosopora. Its chemical structure consists of a core bicyclo[7.3.1]tridecadiynene moiety containing a 1,5-diyn-3-ene as part of a ten-membered ring, a lpha,beta-unsaturated ketone with a bridgehead double bond and an attached allylic trisulfide. This ring system is attached at one end by a trisaccharide moiety and at the opposite end by a 2-deoxy-L-fucose-anthra ilate moiety. The trisaccharide consists of a hydroxyamino sugar which is connected to a isopropylamino sugar through a glycosidic linkage and a thiomethyl sugar through an NH1O linkage.
[Uses]

Esperamicin A1, as an extremely potent antitumor antibiotic, is isolated from cultures of Actinomadura verrucosospora. Esperamicin A1 can be used for the research of antitumor[1]. Eesperamicin A1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
[References]

[1] Lam, K. S., et al. Biosynthesis of esperamicin A1, an enediyne antitumor antibiotic. Journal of the American Chemical Society, 115(26), 12340–12345.
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