99674-26-7
Chemical Structure
Eesperamicin A1
- CAS No.: 99674-26-7
- Formula:C59H80N4O22S4
- Molecular Weight:1325.54
IUPAC Name: (2S,3R,4S,6S)-3-hydroxy-6-(((2S,5Z,9R,10S,13E)-9-hydroxy-2-(((2R,3R,4S,5S,6R)-4-hydroxy-5-((((2S,4S,5S,6R)-4-hydroxy-6-methyl-5-(methylthio)tetrahydro-2H-pyran-2-yl)oxy)amino)-3-(((2S,4S,5S)-5-(isopropylamino)-4-methoxytetrahydro-2H-pyran-2-yl)oxy)-6-meth
InChIKey: LJQQFQHBKUKHIS-IIZLOWFNSA-N
SMILES: CSSSC/C=C1C2=C(C([C@@H](O[C@@]3([H])C[C@@H]([C@H](O)[C@H](C)O3)OC(C4=C(C=C(OC)C(OC)=C4)NC(C(OC)=C)=O)=O)[C@]\1(C#C/C=C\C#C[C@@H]2O[C@@]5([H])[C@@H]([C@H]([C@H](NO[C@H]6C[C@@H]([C@H](SC)[C@@H](C)O6)O)[C@@H](C)O5)O)O[C@@]7([H])C[C@@H]([C@@H](NC(C)C)CO7)OC)O)=O)NC(OC)=O
Biological Activity: 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.
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Eesperamicin A1 | 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. 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. | |||||||||||||||||||||
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Keywords
