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Nature products

Chemical Structure Cat. No. Product Name CAS No.
Wogonoside Chemical Structure
 BCP31664 Wogonoside 51059-44-0
Wogonoside, a flavonoid glycoside isolated from Huangqin, possesses anti-inflammatory effects. Wogonoside induces autophagy in breast cancer cells by regulating MAPK-mTOR pathway.
Gypsogenin-3-O-glucuronide Chemical Structure
 BCP31663 Gypsogenin-3-O-glucuronide 96553-02-5
Gypsogenin-3-O-glucuronide is a ubiquitous saponin precursor in plants of the genus Gypsophila.
Chrysin-7-O-Beta-D-glucoronide Chemical Structure
 BCP31659 Chrysin-7-O-Beta-D-glucoronide 35775-49-6
Chrysin-7-O-Beta-D-glucoronide is isolated and purified from the roots of Astragalus membranaceus
Taraxasterol Chemical Structure
 BCP31649 Taraxasterol 1059-14-9
Taraxasterol isolated from the herbs of Taraxacum officinale. It inhibits NO, PGE(2), TNF-α, IL-1β and IL-6 production in LPS-induced RAW 264.7 macrophages in a dose-dependent manner.
Spinosin Chemical Structure
 BCP31651 Spinosin 72063-39-9
Spinosin is isolated and purified from the seeds of Zizyphus jujuba
Britanin Chemical Structure
 BCP31650 Britanin 33627-28-0
Britannin, isolated from Inula aucheriana, is a sesquiterpene lactone. Britannin has anti-proliferative and anti-inflammatory activities.
Bergamotine Chemical Structure
 BCP31566 Bergamotine 7380-40-7
Bergamottin is a potent and competitive CYP1A1 inhibitor with a Ki of 10.703 nM.Bergamottin is a furanocoumarin found in grapefruit juice and lemon, lime, and bergamot oils that has diverse biological activities.
Hyperoside Chemical Structure
 BCP31552 Hyperoside 482-36-0
Hyperoside isolated from the herb of Hypericum perforatum L. It maybe as a candidate therapeutic agent for the treatment of vascular inflammatory and occlusive vascular diseases, inhibiting HMGB1 signaling pathway and activating Nur77 receptor.
L-Sulforaphane Chemical Structure
 BCP31547 L-Sulforaphane 142825-10-3
(R)-Sulforaphane is a highly potent inducer of the Keap1/Nrf2/ARE pathway. (R)-Sulforaphane is a far more potent inducer of the carcinogen-detoxifying enzyme systems in rat liver and lung than the S-isomer.
Phaseoloidin Chemical Structure
 BCP31533 Phaseoloidin 118555-82-1
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