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Results for "

Dysidea

" in MedChemExpress (MCE) Product Catalog:

6

Inhibitors & Agonists

6

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-121794
    Avarol

    (+)-Avarol

    		 Apoptosis NF-κB Cancer
    Avarol is a sesquiterpene hydroquinone that can be isolated from Dysidea avara sponge. Avarol has the potential for the research of ehrlich carcinoma (EC) and cervical cancer (CC-5) .
    Avarol
  • HY-N1032
    (+)-12α-Hydroxyisodrimenin

    		Others Others
    (+)-12α-Hydroxyisodrimenin (compound 7) is a drimanic sesquiterpene that can be found in sponge Dysidea fusca .
    (+)-12α-Hydroxyisodrimenin
  • HY-135771
    Avarone

    (+)-Avarone

    		 Others Cancer
    Avarone ((+)-Avarone) is a sesquiterpenoidal quinone that can be isolated from Dysidea avara. Avarone shows cytotoxicity. Avarone shows antileukemic activity .
    Avarone
  • HY-N20658
    ent-Yahazunol

    		Others Cancer
    ent-Yahazunol is a sesquiterpene hybrid growth inhibitor present in sponges of the genus Dysidea. ent-Yahazunol selectively inhibits the growth of human mammary adenocarcinoma cells and human lung cancer cells. ent-Yahazunol can be used in studies related to mammary adenocarcinoma and lung cancer .
    ent-Yahazunol
  • HY-N20664
    (+)-Chromazonarol

    (+)-ent-Chromazonarol

    		 Fungal Infection
    (+)-Chromazonarol ((+)-ent-Chromazonarol) is a marine sesquiterpene hybrid terpene and pimarane-type hybrid terpene Antifungal agent. (+)-Chromazonarol is isolated from the marine sponge Dysidea pallescens. (+)-Chromazonarol inhibits the mycelial growth of Sclerotinia sclerotiorum and Rhizoctonia solani. (+)-Chromazonarol is applicable to research related to Sclerotinia sclerotiorum infection and Rhizoctonia solani infection .
    (+)-Chromazonarol
  • HY-N17788
    6-Hydroxy-2,2′,4,4′-tetrabromodiphenyl ether

    		Tie Cancer
    6-Hydroxy-2,2′,4,4′-tetrabromodiphenyl ether is a selective inhibitor of Tie2 kinase, with an IC50 value of 2.1 μM. 6-Hydroxy-2,2′,4,4′-tetrabromodiphenyl ether interacts with the ATP binding site of Tie2 kinase, inhibiting kinase activity and subsequently blocking tumor angiogenesis. 6-Hydroxy-2,2′,4,4′-tetrabromodiphenyl ether can be isolated from sponges of the genus Dysidea .
    6-Hydroxy-2,2′,4,4′-tetrabromodiphenyl ether

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