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Results for "

Escin

" in MedChemExpress (MCE) Product Catalog:

12

Inhibitors & Agonists

12

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-B2114
    Escin
    2 Publications Verification

    		 Apoptosis Metabolic Disease Inflammation/Immunology Cancer
    Escin, a natural compound of triterpenoid saponins that can be isolated from horse chestnut (Aesculus hippocastanum) seeds, can be used as a vasoprotective anti-inflammatory, anti-edematous and anti-nociceptive agent .
    Escin
  • HY-N0555
    Escin IB

    		Others Metabolic Disease
    Escin IB is a saponin isolated from skin and the endosperm of seeds of horse chestnut (Aesculus hippocastanum). Escin IB shows inhibitory effect on pancreatic lipase activity .
    Escin IB
  • HY-N0554
    Escin IA

    		HIV Protease Infection Cancer
    Escin IA is a triterpene saponin isolated from Aesculus hippocastanum, which inhibits HIV-1 protease with IC50 values of 35 μM. Escin IA has anti-TNBC metastasis activity, and its action mechanisms involved inhibition of epithelial-mesenchymal transition process by down-regulating LOXL2 expression .
    Escin IA
  • HY-N0557
    Isoescin IB

    		Others Cancer
    Isoescin IB is an isomer of Escin IB. Isoescin IB and Escin IB are the chief active ingredients in escin .
    Isoescin IB
  • HY-N0555R
    Escin IB (Standard)

    		Others Metabolic Disease
    Escin IB (Standard) is the analytical standard of Escin IB. This product is intended for research and analytical applications. Escin IB is a saponin isolated from skin and the endosperm of seeds of horse chestnut (Aesculus hippocastanum). Escin IB shows inhibitory effect on pancreatic lipase activity .
    Escin IB (Standard)
  • HY-N0554R
    Escin IA (Standard)

    		HIV Protease Infection Cancer
    Escin IA (Standard) is the analytical standard of Escin IA. This product is intended for research and analytical applications. Escin IA is a triterpene saponin isolated from Aesculus hippocastanum, which inhibits HIV-1 protease with IC50 values of 35 μM. Escin IA has anti-TNBC metastasis activity, and its action mechanisms involved inhibition of epithelial-mesenchymal transition process by down-regulating LOXL2 expression .
    Escin IA (Standard)
  • HY-107248
    Escin IIa

    		Others Inflammation/Immunology
    Escin IIa, isolated from horse chestnut, the seeds of Aesculus hippocastanum L., has positive effects on acute inflammation in animals. Escin IIa has gastroprotections on ethanol-induced gastric mucosal lesions in rats .
    Escin IIa
  • HY-107247
    Escin IIb

    		Others Inflammation/Immunology
    Escin IIb, isolated from horse chestnut, the seeds of Aesculus hippocastanum L., has positive effects on acute inflammation in animals . Escin IIb showed potent protective effects against ethanol-induced gastric mucosal lesions .
    Escin IIb
  • HY-N7706
    Escin Ie

    		Others Others
    Escin Ie is a derivative of Aescine in Aesculi Semen extract .
    Escin Ie
  • HY-N0557R
    Isoescin IB (Standard)

    		Others Cancer
    Isoescin IB (Standard) is the analytical standard of Isoescin IB. This product is intended for research and analytical applications. Isoescin IB is an isomer of Escin IB. Isoescin IB and Escin IB are the chief active ingredients in escin .
    Isoescin IB (Standard)
  • HY-N7497
    Protoescigenin

    		Others Others
    Protoescigenin is the main aglycone of horse chestnut saponin mixture known as escin. Protoescigenin is selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene .
    Protoescigenin
  • HY-N7497R
    Protoescigenin (Standard)

    		Others Others
    Protoescigenin (Standard) is the analytical standard of Protoescigenin. This product is intended for research and analytical applications. Protoescigenin is the main aglycone of horse chestnut saponin mixture known as escin. Protoescigenin is selected as substrate for exploratory chemistry towards selective protection, followed by propargyl ether formation and subsequent condensation with azido-monosaccharides, to obtain novel triazole linked conjugates of the triterpene .
    Protoescigenin (Standard)

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