408358-51-0

Procumbenoside A Chemical Structure
408358-51-0

Chemical Structure

Procumbenoside A

  • CAS No.: 408358-51-0
  • Formula:C31H32O15
  • Molecular Weight:644.58

IUPAC Name: 9-(benzo[d][1,3]dioxol-5-yl)-4-(((2S,3R,4R)-4-hydroxy-4-(hydroxymethyl)-3-(((2S,3R,4S,5S)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)oxy)tetrahydrofuran-2-yl)oxy)-6,7-dimethoxynaphtho[2,3-c]furan-1(3H)-one

InChIKey: HBUCXSOGVZJQHH-IJZDSENBSA-N

SMILES: O=C1C2=C(C=3C(C(O[C@H]4[C@H](O[C@H]5[C@H](O)[C@@H](O)[C@@H](O)CO5)[C@](CO)(O)CO4)=C2CO1)=CC(OC)=C(OC)C3)C=6C=C7C(=CC6)OCO7

Biological Activity: Procumbenoside A is a lignan glycoside discovered in Justicia procumbens. Procumbenoside A inhibits HIV-1 replication with an IC50 of 4.95 μM. Procumbenoside A exerts cytotoxic effects on various cancer cells. Procumbenoside A induces Cu (II)-mediated strand breaks in supercoiled plasmid DNA, generating the relaxed circular DNA form, while no linear form is detected. Procumbenoside A is used in studies related to liver cancer, colon adenocarcinoma, and HIV-1 infection[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-N21692
Procumbenoside A Procumbenoside A is a lignan glycoside discovered in Justicia procumbens. Procumbenoside A inhibits HIV-1 replication with an IC50 of 4.95 μM. Procumbenoside A exerts cytotoxic effects on various cancer cells. Procumbenoside A induces Cu (II)-mediated strand breaks in supercoiled plasmid DNA, generating the relaxed circular DNA form, while no linear form is detected. Procumbenoside A is used in studies related to liver cancer, colon adenocarcinoma, and HIV-1 infection.
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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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References