67005-97-4

N-Propargyladenosine Chemical Structure
67005-97-4

Chemical Structure

N-Propargyladenosine

  • CAS. Nr.: 67005-97-4
  • Formula:C13H15N5O4
  • Molecular Weight:305.29

IUPAC Name: (2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-(prop-2-yn-1-ylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diol

InChIKey: JCLIMDWHRZIHMW-QYVSTXNMSA-N

SMILES: OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N2C(N=CN=C3NCC#C)=C3N=C2)O1

Biological Activity: N-Propargyladenosine is an adenosine analogue. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. The popular products in this series are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277)[1]. N-Propargyladenosine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-152562 		N-Propargyladenosine 99.13% N-Propargyladenosine is an adenosine analogue. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. The popular products in this series are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277). N-Propargyladenosine 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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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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Structural Analogs

References

Keywords